- Review of interventions
- Open Access
Reducing stillbirths: prevention and management of medical disorders and infections during pregnancy
BMC Pregnancy and Childbirth volume 9, Article number: S4 (2009)
An estimated two-thirds of the world's 3.2 million stillbirths occur antenatally, prior to labour, and are often overlooked in policy and programs. Poorly recognised, untreated or inadequately treated maternal infections such as syphilis and malaria, and maternal conditions including hypertensive disorders, are known risk factors for stillbirth.
We undertook a systematic review of the evidence for 16 antenatal interventions with the potential to prevent stillbirths. We searched a range of sources including PubMed and the Cochrane Library. For interventions with prior Cochrane reviews, we conducted additional meta-analyses including eligible newer randomised controlled trials following the Cochrane protocol. We focused on interventions deliverable at the community level in low-/middle-income countries, where the burden of stillbirths is greatest.
Few of the studies we included reported stillbirth as an outcome; most that did were underpowered to assess this outcome. While Cochrane reviews or meta-analyses were available for many interventions, few focused on stillbirth or perinatal mortality as outcomes, and evidence was frequently conflicting. Several interventions showed clear evidence of impact on stillbirths, including heparin therapy for certain maternal indications; syphilis screening and treatment; and insecticide-treated bed nets for prevention of malaria. Other interventions, such as management of obstetric intrahepatic cholestasis, maternal anti-helminthic treatment, and intermittent preventive treatment of malaria, showed promising impact on stillbirth rates but require confirmatory studies. Several interventions reduced known risk factors for stillbirth (e.g., anti-hypertensive drugs for chronic hypertension), yet failed to show statistically significant impact on stillbirth or perinatal mortality rates. Periodontal disease emerged as a clear risk factor for stillbirth but no interventions have reduced stillbirth rates.
Evidence for some newly recognised risk factors for stillbirth, including periodontal disease, suggests the need for large, appropriately designed randomised trials to test whether intervention can minimise these risks and prevent stillbirths. Existing evidence strongly supports infection control measures, including syphilis screening and treatment and malaria prophylaxis in endemic areas, for preventing antepartum stillbirths. These interventions should be incorporated into antenatal care programs based on attributable risks and burden of disease.
Of the world's 3.2 million annual stillbirths, at least 98% occur in low-/middle-income countries, and on average, as many as two-thirds of these stillbirths are thought to occur antenatally, prior to labour [1, 2]. Proportions of antenatal and intrapartum stillbirths may vary in different low- and middle-income country settings depending on the prevalence of risk factors and quality of antenatal and obstetric care. Antenatal stillbirths typically show signs of maceration, and result from an insult occurring in utero . Interventions targeting this period can play a major part in reducing the burden of stillbirths. Many known causes of antenatal stillbirths, including infections and maternal conditions including gestational diabetes and hypertension, are potentially preventable or treatable; relatively simple interventions may reduce their incidence. Known risk factors include syphilis, ascending bacterial vaginal infections, pre-existing and gestational maternal conditions like diabetes, inherited thrombophilias, and intrahepatic cholestasis; pre-eclampsia, placental abruption and other placental dysfunction; and maternal Rhesus disease .
Interventions targeting these risk factors may reduce stillbirth rates, especially in low- and middle-income countries. However, the evidence for impact of these interventions on stillbirth and perinatal mortality rates has not been extensively reviewed. This paper systematically examines the evidence for interventions to address or ameliorate the impact of known or biologically plausible clinical risk factors for stillbirth that are treatable or preventable during the antenatal period. Many of the risk factors examined are more prevalent in low- and middle-income countries than in high-income countries, including infections such as syphilis and malaria. Lack of access to health facilities providing antenatal care (ANC) or emergency obstetric care, especially in rural or otherwise remote areas, is associated with poor obstetric outcomes [5, 6]. Many of the interventions examined in this review are deliverable via outreach services at the community level, but some require equipped and functional facilities.
The methodology of the literature search, along with the data analysis strategy, has been detailed previously . We consulted PubMed and the Cochrane Library, including all human studies published after 1980. We included gray literature wherever possible. General search terms were used like "stillbirth", "fetal death" and "perinatal mortality", along with targeted terms like "antibiotics AND pregnancy" and "periodontal AND pregnancy". Interventions delivered during pregnancy for prevention or treatment of maternal infections or conditions are analyzed in this paper for their effect on stillbirths or perinatal mortality as shown in Table 1.
A total of 345 papers (35 systematic reviews and 310 individual studies) met the study criteria and were included in this paper.
Prevention and management of problems in pregnancy
Calcium supplementation to prevent pregnancy-induced hypertension (PIH) and pre-eclampsia
High blood pressure with or without proteinuria is a major cause of maternal morbidity and mortality , as well as perinatal morbidity and mortality, worldwide. Hypertension has been estimated to complicate 5% of all pregnancies and 11% of first pregnancies, half associated with pre-eclampsia, and accounting for up to 40,000 maternal deaths annually .
Pre-term birth, commonly associated with hypertensive disorders, is the leading cause of early neonatal death and infant mortality globally . Inverse relationships between calcium intake and hypertensive disorders of pregnancy were observed among the Mayan Indians in Guatemala , whose diet includes corn soaked in lime, and in Ethiopia, where dietary intake of calcium is also high ; both populations have low incidence of pre-eclampsia and eclampsia. This evidence, with other epidemiological and clinical studies [13, 14], suggested that increased calcium intake during pregnancy might reduce the incidence of hypertensive disorders, including pre-eclampsia, among women with low calcium intake. As supplementation is inexpensive and relatively straightforward, calcium supplementation is attractive as a potential intervention to reduce the risk of pre-eclampsia. The mechanisms involved in calcium-mediated effects on blood pressure reduction are not well understood, but it has been posited that parathyroid hormone might be involved in regulating this relationship .
Our literature search identified two systematic reviews and one Cochrane protocol, along with one other RCT (Table 2). Trumbo and Ellwood.  evaluated 7 moderate- to high-quality studies assessing the relationship between calcium intake and pregnancy-induced hypertension and/or pre-eclampsia (Additional file 1). The purpose of this review by the Food and Drug Administration (FDA) was to make recommendations for the US population and thus studies carried out in populations with low calcium intakes and undernutrition were specifically not included. Four studies showed no reduction in the incidence of pregnancy-induced hypertension as a result of calcium supplementation and three showed a reduction. Five of these studies also examined pre-eclampsia as an outcome and three of the five showed no reduction in the incidence of pre-eclampsia from calcium supplementation while the remaining two showed a reduction. Based on this review, the US Food and Drug Administration concluded that the relationship between calcium and risk of hypertension is inconsistent and inconclusive, and an impact of calcium intake on the risk of pregnancy-induced hypertension and pre-eclampsia is unlikely.
Hofmeyr et al.  reviewed 12 studies of good quality, including 5 of the studies in the Trumbo analysis, to assess the impact of calcium supplementation for preventing hypertensive disorders in pregnant women. The review found that calcium supplementation reduced the risk of high blood pressure (11 trials, N = 14,946 women: RR = 0.70, 95% CI: 0.57–0.86) and pre-eclampsia (12 trials, N = 15,206 women: RR = 0.48, 95% CI: 0.33–0.69) compared to placebo. Effect on pre-eclampsia was greatest for high-risk women (5 trials, N = 587 women: RR = 0.22, 95% CI: 0.12–0.42), and those with low baseline calcium intake (7 trials, N = 10,154 women: RR = 0.36, 95% CI: 0.18–0.70) (Additional file 2). Calcium supplementation also reduced the composite outcome "maternal death or serious morbidity" (4 trials, N = 9732 women; RR = 0.80, 95% CI: 0.65–0.97). However, there was no overall effect on the relative risk of a stillbirth or the baby dying before discharge from hospital (10 trials, N = 15,141 women: RR = 0.89, 95% CI: 0.73–1.09) [LOE: 1+]. Another Cochrane review on calcium supplementation other than for preventing or treating hypertension on pregnancy and infant outcomes is currently in progress .
In India, an RCT by Kumar et al.  found no significant difference in the percentage of stillbirths in healthy primigravidas supplemented with calcium compared to placebo (2.0% vs. 2.2%, respectively).
The evidence from a range of reasonable studies and a Cochrane review (Grade B evidence) indicated that calcium supplementation reduced the risk of pre-eclampsia by 31–67% and gestational hypertension by 30% in calcium-deficient individuals, and also had a concomitant benefit to maternal health. There was no significant effect of calcium supplementation in pregnant women on the risk of stillbirth or the baby dying before discharge from hospital, regardless of the mother's risk of hypertensive disorders of pregnancy. The evaluation of the evidence by Trumbo et al.  reflects a more guarded view on the role of calcium in prevention of hypertension in low-risk women. Both the Trumbo and the Cochrane review included a large NIH study (N = 4590)  in a well-nourished US population that found no evidence of benefit in preventing pre-eclampsia. However, the NIH participants made up a much larger proportion of the sample assessed in the Trumbo review than the Cochrane review, heavily influencing its findings. Reduction in pre-term birth due to calcium supplementation remains plausible, particularly given the reduction in the risk of pre-term birth observed among women at high risk of pre-eclampsia, but this impact remains unproven. The evidence for an impact of calcium supplementation varies based on the nutritional status of the population under study. It is plausible that calcium supplementation is effective in preventing pregnancy-induced hypertension and/or pre-eclampsia only in calcium-deficient individuals; the Cochrane review  included a number of studies among undernourished populations and found that the risk of pre-eclampsia was reduced by half. There are currently insufficient trials of calcium supplementation in calcium-deficient populations to assess impact on stillbirths conclusively. Future studies must evaluate the impact of calcium supplementation on a range of perinatal outcomes including stillbirths, focused wherever possible on calcium-deficient populations.
Anti-hypertensives for chronic maternal hypertension
Alone, high blood pressure has little impact on pregnancy outcomes–nearly 10% of normotensive women experience abnormally elevated blood pressure at some point during pregnancy–but sustained elevated blood pressure may be associated with other complications [21, 22]. Between 10 and 15% of maternal deaths in low-/middle-income countries are associated with hypertensive disorders of pregnancy [23–25], and these conditions also increase the risk of perinatal mortality as a consequence of prematurity, poor fetal growth, and other unknown mechanisms [26–28]. There are several major categories of hypertensive disorders, including gestational hypertension or pregnancy-induced hypertension (hypertension without proteinuria); pre-eclampsia (hypertension with proteinuria); chronic or essential hypertension (pre-existing hypertension); and chronic hypertension with superimposed pre-eclampsia . Hypertension, hypothesised to cause fetal distress due to vasoconstriction that reduces the blood supply across the placenta, or placental abruption, may result in poor growth or premature delivery, even when it is mild to moderate. Of all hypertensive disorders of pregnancy, pre-eclampsia/eclampsia has the highest impact on morbidity and mortality, including renal or liver failure, clotting disorders, stroke, pre-term delivery, stillbirth or neonatal death .
The pathophysiology of adverse pregnancy outcomes associated with hypertensive disorders is poorly understood. In pre-eclampsia, the prevailing theory is that poor placentation results in an ischemic placenta, which restricts blood and nutrient flow to the fetus. The dysfunctional placenta also releases factors into the mother's bloodstream that damage maternal organs and vasculature, and cause proteinuria [31, 32]. There are no reliable ways of predicting which women will develop pre-eclampsia, or which cases of pre-eclampsia will become eclamptic . However, women with severe hypertension prior to pregnancy, women who are hypertensive during the first trimester despite use of antihypertensives, and women who have had a prior adverse pregnancy outcome are known to be at high risk of super-imposed pre-eclampsia (50%–75%), fetal growth restriction (25%–40%), and placental abruption (10%–20%) .
The care of women with hypertensive disorders is complex . The rationale for administering anti-hypertensive drugs to pregnant women with high blood pressure is that these drugs could prevent progression of high blood pressure to pre-eclampsia, and pre-eclampsia to eclampsia (seizures), thus reducing the risk of pre-term delivery and placental abruption and improve fetal growth . The optimal treatment of chronic hypertension in pregnancy, including the effectiveness and safety of other anti-hypertensive drugs, such as calcium channel blockers and alpha agonists, which act primarily by causing vasodilatation, remains unclear .
Our literature search identified 6 Cochrane reviews and 2 other intervention/observational studies (Table 3). Abalos et al.  undertook a Cochrane review of all RCTs evaluating any anti-hypertensive drug treatment for mild to moderate hypertension during pregnancy defined using objective criteria. Comparisons were of one or more anti-hypertensive drug(s) with placebo, with no anti-hypertensive drug, or with another anti-hypertensive drug, where treatment was planned to continue for at least 7 days (Additional file 3). Forty-six trials (N = 4282 women) were included. Twenty-eight trials compared an anti-hypertensive drug with placebo/no anti-hypertensive drug (N = 3200 women), and found a 50% reduction in risk of developing severe hypertension (19 trials, N = 2409 women; RR = 0.50; 95% CI: 0.41–0.61; risk difference (RD) -0.10 (-0.12 to -0.07); number needed to treat (NNT) to prevent a case of severe hypertension was 10 (range: 8–13) but no evidence was found for a difference in the risk of pre-eclampsia (22 trials, N = 2702 women; RR = 0.97, 95% CI: 0.83–1.13). No significant impact on stillbirths was found (RR = 1.14, 95% CI: 0.60–2.17) [LOE: 1++]. Another Cochrane review by Magee and Duley  compared the effect on perinatal mortality of beta-blocker vs. placebo/no beta-blocker. Based on 13 trials (N = 1429 women), there was no effect of beta-blocker usage on PMR (RR = 1.01, 95% CI: 0.46–2.22) [LOE: 1++](Additional file 4). Similarly, Duley et al.  reported a non-significant effect of labetalol vs. hydralazine (RR = 0.50, 95% CI: 0.05–4.94) or similar calcium channel blockers vs. hydralazine (RR = 1.36, 95% CI: 0.42–4.41) on risk of fetal or neonatal deaths in pregnant women [LOE: 1++](Additional file 5).
In another Cochrane review comparing the impact of calcium channel blockers to any other tocolytic agent in inhibiting pre-term labour, King et al. 2003  found no statistically significant difference in PMR (10 trials; N = 810 pregnant women, RR = 1.65, 95% CI: 0.74–3.64) [LOE: 1+](Additional file 6). Similarly, Say et al. 1996  compared flunarizine vs. no treatment in pregnant women either at high risk or with suspected impaired fetal growth and found a large but non-significant reduction in PMR (OR = 0.14, 95% CI: 0.00–6.82) [LOE: 1+](Additional file 7). Other Cochrane reviews of the effect of hypertensive treatments on pregnancy outcome are in progress [38, 39].
Among other studies, an RCT in an Australian tertiary referral maternity hospital by Hennessy et al  compared different anti-hypertensive drugs in hypertensive women (N = 124) and reported three perinatal deaths in the group given IV hydralazine (5 mg doses) compared to one perinatal death in the group given mini-bolus diazoxide (15 mg doses), but the study was too small for the results to reach statistical significance [LOE: 1+]. Another meta-analysis by Meher et al.  assessed the impact of nitric oxide in preventing pre-eclampsia (N=4 RCTs) and computed a non-significant decrease in risk of perinatal and neonatal mortality combined compared to untreated controls (RR = 0.25, 95% CI: 0.03–2.34 [NS]) [LOE: 1+](Additional file 8).
While optimal pharmacological therapy of chronic maternal hypertension is highly desirable to improve maternal outcomes, uncertainty remains about the most optimal agent and duration of therapy. Among women with mild to moderate hypertension, anti-hypertensives are effective in reducing the risk of severe hypertensive episodes in pregnant women and the evidence from available studies is of reasonable quality (Grade B evidence). However, if reductions in severe hypertension were clinically important, a downstream impact of reduced perinatal mortality, pre-term births and caesarean section could be anticipated, yet there is no evidence of such an effect . One possible explanation for this lack of impact is the possibility of over-treatment with anti-hypertensives. The degree to which placental blood flow is autoregulated is still unknown, and some anti-hypertensives are known to increase the risk of fetal distress arising from reduced uteroplacental, umbilical or fetal blood flow [42, 43]. Because of these side effects, particularly when treating severe hypertension, it is possible that modest reductions in blood pressure could be of greater benefit to the fetus than achievement of normal maternal blood pressure using anti-hypertensives.
Women allocated to an anti-hypertensive, especially beta-blockers, were less likely to need another agent but more likely to experience side effects than those allocated placebo or no anti-hypertensive treatment. Between 8 and 13 women need to be treated with an anti-hypertensive drug to prevent an episode of severe hypertension. Whether anti-hypertensive treatment is worthwhile depends on whether there are associated reductions in the consequences of severe hypertension, such as pre-eclampsia, eclampsia, maternal stroke, and pre-term birth or associated outcomes, but the limited data suggest a lack of impact on stillbirths and perinatal mortality, and preclude any firm conclusions about intermediate outcomes such as pre-eclampsia and eclampsia.
The impact of various pharmacological agents on perinatal outcomes and stillbirths is unclear and further studies are needed to define optimal approaches to prevention and treatment of hypertension in pregnant women in appropriate community settings. Despite the wealth of studies and information available on the impact of anti-hypertensive therapy on maternal outcomes, there is no evidence that these drugs reduce the risk of stillbirth.
Pre-eclampsia is a common and serious complication of pregnancy that can lead to maternal renal or liver failure, placental abruption, maternal seizures, and fetal complications from placental dysfunction and hypoxia including LBW, SGA, stillbirth, and pre-term delivery . Theorised to arise from a poorly implanted or otherwise abnormal placenta that becomes hypoxic, the factors released by the damaged placenta into the maternal circulation are thought to activate platelets and the maternal clotting system [45–47]. This platelet activity may occur before symptoms of pre-eclampsia develop. Pre-eclampsia has also been characterised by insufficient levels of the vasodilator prostacyclin, and excessive production of thromboxane, a platelet-derived vasoconstrictor which stimulates platelet aggregation . The role of platelets in pre-eclampsia suggests that anti-platelet agents, including aspirin, could prevent or slow development of pre-eclampsia and its associated adverse pregnancy outcomes.
Biochemically, the anti-thrombotic effect of aspirin resluts from its suppression of cyclo-oxygenase. This disruption interferes with the production of thromboxane A2 (TXA2) and inhibits TXA2-dependent platelet aggregation . The reduced thromboxane production is thought to protect against vasoconstriction that can cause ischaemia, fetal growth restriction, and pathologic placental blood clots. Aspirin also carries risks: it crosses the placenta, it inhibits platelet function (thus increasing the risk of maternal and fetal bleeding), and has been linked with an increased risk of vascular disruptions including gastroschisis and possible premature closure of the ductus arteriosus . Given safety concerns, as well as clinical evidence that a daily dose as small as 30 to 50 mg of aspirin results in virtually complete suppression of platelet TXA2 synthesis after 7 to 10 days in normal subjects, low doses of aspirin have been considered sufficient to achieve anti-platelet activity with minimal risk . Indeed, large trials have consistently found low-dose aspirin in pregnancy to be relatively safe. There is no standard definition for "low-dose" aspirin, named in reference to standard aspirin (300 mg), but low-dose regimens typically range from 50–120 mg/day in pregnant patients.
Our literature search identified one Cochrane, two other systematic reviews and five other observational/intervention studies on the use of anti-platelet agents to improve pregnancy outcomes (Table 4). Duley et al.  reviewed 59 RCTs (N = 37,560 women) comparing the use of any anti-platelet agent (e.g., low-dose aspirin or dipyridamole) with either placebo or no anti-platelet agent in pregnant women at risk of pre-eclampsia (Additional file 9). Anti-platelet agents were associated with a statistically significant 17% reduction in the risk of pre-eclampsia (46 trials, N = 32,891 women, RR = 0.83, 95% CI: 0.77–0.89), with statistically significantly greater risk reduction for high-risk compared to moderate-risk women [risk difference (RD) 5.2% (-7.5 to -2.9%) vs. RD -0.84% (-1.37 to -0.3%), respectively]. Higher doses of anti-platelet agents appeared more effective in preventing pre-eclampsia, as 75 mg/day or less of aspirin (21 trials, N = 26,984 women) reduced risk of pre-eclampsia by 12% (RR = 0.88, 95% CI: 0.81–0.95), compared to reductions of 36% (RR = 0.64, 95% CI: 0.51–0.80) and 70% (RR = 0.30, 95% CI: 0.15–0.60) for trials evaluating more than 75 mg/day of aspirin, and trials combining high doses of aspirin with dipyridamole, respectively. Anti-platelet agents statistically significantly reduced the RR of pre-term birth (8% reduction), PMR (14% reduction), and SGA (10% reduction). However, rates of fetal loss were not statistically different between the two groups (RR = 0.96, 95% CI: 0.78–1.18) [LOE: 1++].
Askie et al.  in a recent meta-analysis evaluated individual patient data (N = 32,217 women, N = 32,819 offspring) involved in 31 RCTs of pre-eclampsia primary prevention (Additional file 10). Comparing women receiving anti-platelet agents to controls, they confirmed a significant reduction in risk of pre-eclampsia (RR = 0.90, 95% CI: 0.84–0.97), very pre-term delivery (< 34 weeks) (RR = 0.90, 95% CI: 0.83–0.98), and pregnancy with a serious adverse outcome (RR = 0.90, 95% CI: 0.85–0.96). Anti-platelet agents had no significant impact on PMR (RR = 0.91, 95% CI: 0.81–1.03) [NS]), though a slight trend toward reduced risk was observed [LOE: 1++].
The overall evidence of anti-platelet agents for pre-eclampsia is Grade B. Among high-risk women, there is some evidence from the Cochrane meta-analysis by Duley et al.  that use of low-dose aspirin reduces risk of PIH, but more research is needed to determine those women for whom aspirin therapy would be effective. There is strong evidence that anti-platelet treatment for high-risk women reduces the risk of pre-eclampsia, though the number needed to treat is high. The optimal choice and dosage of anti-platelet agent is unclear, but dosages of low-dose aspirin appear to be important, and higher doses in the low-dose range may be more efficacious. In the Cochrane meta-analysis, dosages of low-dose aspirin of 75 mg/day or more were associated with greater reductions in risk of pre-eclampsia, pre-term birth, and small-for-gestational age babies than preparations with 75 mg/day or less. The safety of dosages of aspirin exceeding this low-dose range remains unproven and requires further research.
The impact of anti-platelet agents on risk of stillbirths is less convincing, although the analysis shows a slight trend in the direction of benefit. Combination treatment with aspirin and heparin leads to a higher live birth rate among women with recurrent miscarriage and anti-phospholipid antibodies, but the results are statistically non-significant. Given the many small studies with poor allocation concealment and inadequate blinding, there is a need for more well-designed RCTs in varied settings and populations to assess the true effectiveness of aspirin in preventing fetal loss.
Heparin and other anti-coagulants in high-risk pregnancies
Pregnancy and the puerperium are associated with an increased risk of venous thromboembolism, which may be treated or prevented using anti-coagulants including unfractionated or low molecular weight heparin (LMWH) administered intravenously or subcutaneously. Anti-coagulants may also be used prophylactically for women with a history of deep venous thrombosis, clotting disorders, pulmonary embolism, anti-phospholipid antibodies, or systemic lupus erythematosis, or to preserve pregnancy in women with a history of unexplained spontaneous pregnancy losses. Thrombosis of placental vessels associated with many of these conditions can cause placental insufficiency and consequent fetal death .
A chief concern regarding anti-coagulant therapy in pregnancy is that warfarin, the anti-coagulant of choice for many chronic conditions, is known to be teratogenic. Historically, many pregnant women receiving heparin treatment have also had underlying conditions associated with stillbirth and adverse fetal outcomes, making clear data scarce on the impact of heparin (whether unfractionated or LMWH) in pregnancy, as well as the efficacy of heparin and other anti-coagulants in preventing pregnancy loss in women with coagulation disorders or a history of pregnancy loss.
Our literature search identified three Cochrane reviews, one Cochrane protocol, and 19 other intervention/observational studies (Tables 5, 6). Most studies tested the efficacy of any form of heparin to other anti-coagulants for indications including anti-phospholipid antibodies with prior loss, thrombophilias, unexplained repeated pregnancy loss, and cardiac indications.
Anti-phospholipid antibodies (including lupus coagulant, anti-cardiolipids, etc.)
A Cochrane review by Empson et al.  evaluated trials of heparin (N = 13) in pregnant women (N = 849) with a history of pregnancy loss and anti-phospholipid antibodies or lupus coagulant (Additional file 11). Intravenous immunoglobulin with or without unfractionated heparin and aspirin (2 trials; N = 58) was associated with higher rates of stillbirth and prematurity compared to unfractionated heparin or LMWH combined with aspirin (RR = 2.51, 95% CI: 1.27–4.95), similar to prednisone or aspirin (1 trial; N = 82) [LOE: 1+]. For reducing pregnancy loss, unfractionated heparin appeared superior to LMWH when combined with aspirin compared to aspirin alone (RR = 0.46, 95% CI: 0.29–0.71 for unfractionated heparin vs. RR = 0.78, 95% CI: 0.39–1.57 for LMWH). Varying the dosage of heparin had no impact on pregnancy loss (1 trial; N = 50). In India, a more recent RCT  also documented higher live birth rates and birth weights with heparin in combination with aspirin versus aspirin alone in a study population with poor obstetric history and elevated anti-cardiolipin antibodies. However, when comparing the relative impact on pregnancy loss (miscarriages + stillbirths) of LMWH versus unfractionated heparin by Stephenson et al. (1 RCT, N = 26 women)  in women with anti-phospholipid antibodies or lupus anti-coagulant, while a trend towards reduced pregnancy loss using LMWH was observed (RR = 0.44, 95% CI: 0.18–1.08 [NS]), the results did not reach statistical significance. Several other small studies comparing heparin plus low-dose aspirin to aspirin alone reported no difference in live birth rates or fetal loss between groups [54–57].
Several studies compared heparin treatment to no treatment for anti-phospholipid antibodies. A cohort study in Israel of enoxaparin versus no treatment  showed a three-fold higher odds of having a live birth among women given enoxaparin compared to controls (OR = 3.03; 95% CI: 1.12–8.36). Among primary aborters, the odds of live birth were improved even more dramatically with enoxaparin compared to controls. Ruffatti et al  assessed the efficacy and safety of calcium heparin versus no treatment to prevent fetal loss in women with a history of pregnancy loss and anti-phospholipid antibodies (N = 53), and reported a 100% live birth rate in patients receiving heparin versus 24.52% live birth rate in patients receiving no treatment (P < 0.001) [LOE: 3].
Two reviews included analyses of the impact of aspirin versus placebo or no treatment in patients with anti-phospholipid antibodies. Di Nisio et al.  reviewed RCTs and quasi-RCTs that assessed the effect of anti-coagulant treatment (either aspirin, unfractionated heparin and low molecular weight heparin compared to placebo or other treatment) on the live-birth rate in women with a history of at least two spontaneous miscarriages or one later intrauterine fetal death without apparent causes other than inherited thrombophilias (Additional file 12). Extracting relevant data from two eligible trials (N = 242), the study found no impact of aspirin vs. placebo on live birth rate (RR = 1.00, 95% CI: 0.78–1.29) [LOE: 1+]. Empson et al.  examined outcomes of aspirin given to maintain pregnancy in women with prior miscarriage and anti-phospholipid syndrome (APL) (N = 11 RCTs), and found no statistical difference in impact compared with placebo or usual care (RR = 1.05, 95% CI: 0.66–1.68) [LOE: 1+].
A Cochrane protocol by Dodd et al.  indicates that a review evaluating anti-thrombotic therapy for improving maternal or infant health outcomes in women at risk of placental dysfunction is in progress, and another Cochrane review by Gates et al.  of heparin as prophylaxis for thromboembolic disease did not identify enough deaths to conduct statistical analysis (Additional file 13). We also reviewed an observational study of anti-thrombotic therapy  including antithrombin, protein C or protein S deficient women (N = 37), which compared thromboprophylaxis with either LMWH or unfractionated heparin before 16 weeks and after 36 weeks' gestation plus a Vitamin K antagonist from 16 to 36 weeks until after delivery. The study documented no fetal losses among antithrombin, protein C or protein S deficient women who received treatment, 7% losses among non-deficient women who received treatment, and 45% in untreated antithrombin-deficient women (adj. RR = 0.07, 95% CI: 0.001–0.7, P = 0.02 in women who received treatment vs. women who did not, respectively).
Di Nisio et al.  conducted a Cochrane review of RCTs and quasi-RCTs of anti-coagulant treatments in women with a history of fetal loss without apparent causes other than inherited thrombophilias (2 trials; N = 242 women with inherited thrombophilias and prior loss). The review included a study in France by Gris et al.  that determined that enoxaparin was superior to low-dose aspirin in preventing stillbirth, as the live birth rate among women with prior pregnancy losses was 10 times higher in the enoxaparin group compared to controls given low-dose aspirin (RR = 10.00, 95% CI: 1.56–64.20) [LOE: 1-]. Another RCT  testing tinzaparin sodium (an LMWH) versus aspirin showed a lower rate of miscarriage in the LMWH group (N = 31) compared to the aspirin group (N = 31), though the difference was statistically non-significant (RR = 0.55, 95% CI: 0.23–1.29) [LOE: 2+]. When compared to no treatment, LMWH was associated with dramatically lower risk of fetal death. Significantly lower risk of fetal death was reported by a small study (N = 52) comparing LMWH plus aspirin to no treatment (OR = 0.10, 95% CI: 0.002–0.98) [LOE:2-]. In a cohort study in the Netherlands , thromboprophylaxis with heparin or LMWH reduced the fetal death rate to 0% in antithrombin-protein-C- or protein-S-deficient women, compared with 45% in deficient women given no treatment (P = 0.01) [LOE:2-].
Other observational studies have evaluated fetal outcomes after anti-coagulant therapy for cardiac problems or following cardiac surgery. Several studies explored pregnancies in women after cardiac valve replacement, including a Korean study  which compared the impact on birth outcomes of warfarin (N = 5), heparin (N = 18) and heparin for the first trimester followed by warfarin until 20 weeks gestation (N = 18). The lowest SBR occurred in the heparin-only group (5.6% in the heparin versus 40.0% and 44.4% in the warfarin and heparin-warfarin groups, respectively) [LOE:2-]. In a safety study of nadroparin among women with replaced heart valves, Lee et al.  reported a significantly lower fetal death rate (8.7% vs 50%, P = 0.01) among women treated with nadroparin (N = 23) compared with coumarin plus aspirin (N = 8) [LOE: 3]. Kawamata et al.  reported that among women with heart valve replacements (N = 12; N = 16 pregnancies) switched from warfarin to heparin treatment from 6–13 weeks of gestation until delivery, only one fetal death occurred [LOE: 3].
Repeated unexplained prior loss(es)
Only one study was identified that tested low molecular weight heparin in women with repeated unexplained losses excluding women with thrombophilias or anti-phospholipid antibodies. This RCT by Dolitzky et al. in Israel among women with at least 3 prior first-trimester or at least 2 prior second-trimester losses  (N = 107) found no difference in live birth rates between enoxaparin and aspirin.
Heparin appears to be safe throughout pregnancy. In Denmark, Sorensen et al.  used national prescription, birth registry, and hospital discharge data to analyze the safety of LMWH use in pregnancy, finding no increased risk of stillbirth, malformations, or LBW among pregnant women treated with LMWH compared with women who received no prescription drugs in pregnancy [LOE: 2+].
We conducted independent meta-analyses on available RCTs (N = 2) comparing the efficacy of LMWH enoxaparin (N = 64) to aspirin (N = 60) on live birth rate in women with recurrent pregnancy loss; finding no improvement of LMWH over aspirin in live birth rates (RR [fixed] = 1.17, 95% CI: 0.96–1.42) (RR [random] = 2.37, 95% CI: 0.22–24.93) (Figures 1, 2).
We also compared the impact on pregnancy loss of unfractionated heparin plus aspirin versus aspirin alone (3 RCTs; N = 212 women) in women with antiphospholipid antibody or lupus anticoagulant. The combination treatment with unfractionated heparin was associated with a 56% reduction in pregnancy loss (RR [Fixed] = 0.44, 95% CI: 0.29–0.65)(RR [Random] = 0.44, 95% CI: 0.30–0.66) (Figures 3 and 4).
The use of thromboprophylaxis in women with a history of at least two miscarriages or one later intrauterine fetal death without apparent causes other than inherited thrombophilia remains a matter of debate (overall evidence Grade C). While some clinicians prescribe anti-thrombotic agents as the last therapeutic resort in these women, this approach is largely based on data from non-randomised trials and on indirect evidence of an anti-coagulation benefit in women with anti-phospholipid antibody syndrome and recurrent pregnancy loss. According to a recent review , insufficient evidence exists (only 2 poorly controlled RCTs with questionable external validity, within which only a small subgroup of women met the inclusion criteria) to recommend the use of anti-thrombotic agents in women with unexplained recurrent pregnancy losses without anti-phospholipid antibodies. While aspirin appears not to improve gestational outcomes in these women [72, 73], LMWH appeared to increase the live birth rate relative to aspirin .
Despite the small size of the study groups, our results support the assertion that heparin, whether unfractionated or LMWH, is not teratogenic and can be safely used throughout pregnancy where indicated for maternal conditions including thrombophilias. For women with anti-phospholipid antibodies, unfractionated heparin plus aspirin is superior to aspirin alone . In women without anti-phospholipid syndrome, LMWH alone was more effective than aspirin . Used appropriately as anti-coagulant therapy for clotting disorders and anti-phospholipid syndrome, heparin shows strong evidence of benefit in reducing stillbirths and perinatal mortality.
Anti-oxidant treatment to prevent or treat pre-eclampsia
Anti-oxidants, including free radical scavengers and enzymes that inhibit peroxidase reactions which produce free radicals , protect proteins and enzymes from oxidation and destruction by free radicals, and help to maintain cellular membrane integrity. Examples include vitamin C (ascorbate), vitamin E (tocopherols), carotenoids, glutathione, glutathione peroxidase, catalase, and superoxide dismutase. Women with pre-eclampsia have been documented to have lower plasma and placental concentrations of anti-oxidants [75, 76], hypothesised to be due to placental underperfusion. Theoretically, anti-oxidants could increase women's resistance to oxidative stress, which depletes maternal stores of anti-oxidants. In cases where placental ischaemia causes subsequent oxidative stress, such supplements might limit systemic and uteroplacental endothelial damage to maternal vasculature and organs, thus slowing or preventing the progression of pre-eclampsia.
Our literature search identified three related Cochrane reviews, and one RCT (Table 7). Rumbold et al.  (10 RCTs, 5 high-quality, N = 6533 women) identified trials of anti-oxidants and found that most tested combined vitamin C and E therapy (Additional file 14). There was no significant difference between anti-oxidant and control groups in risk of pre-eclampsia (RR = 0.73, 95% CI: 0.51–1.06; 9 RCTs, N = 5446 women) or any other primary outcome, including severe pre-eclampsia (RR = 1.25, 95% CI: 0.89–1.76; 2 RCTs, N = 2495 women), pre-term birth (< 37 weeks) (RR = 1.10, 95% CI: 0.99–1.22; 5 RCTs, N = 5198 women), SGA infants (RR = 0.83, 95% CI: 0.62–1.11; 5 RCTs, N = 5271 babies) or pregnancy loss (RR 1.32, 95% CI 0.92 to 1.90; four trials, 5144 babies). Women allocated to anti-oxidants were more likely to self-report abdominal pain late in pregnancy (RR = 1.61, 95% CI: 1.11–2.34; 1 RCT, N = 1745 women), require anti-hypertensive therapy (RR = 1.77, 95% CI: 1.22–2.57; 2 RCTs, N = 4272 women) and require an antenatal hospital admission for hypertension (RR = 1.54, 95% CI: 1.00–2.39 [NS]; 1 RCT, N = 1877 women). However, for the latter two outcomes, this was not clearly reflected in an increase in any other hypertensive complications. An earlier Cochrane review by Rumbold and Crowther  (Additional file 15) assessed the impact of Vitamin C supplementation alone during pregnancy (5 RCTs, N = 766 women). No difference was seen between women supplemented with vitamin C alone or in combination with other supplements compared with placebo for the risk of stillbirth (RR = 0.87, 95% CI: 0.41–1.87, 3 RCTs, N = 539 women), PMR (RR = 1.16, 95% CI: 0.61–2.18, 2 RCTs, N = 238 women), birth weight (weighted mean difference (WMD) -139.00 g, 95% CI: -517.68 to 239.68, 1 RCT, N = 100 women) or IUGR (RR = 0.72, 95% CI: 0.49–1.04, 2 RCTs, N = 383 women). Women supplemented with vitamin C compared with placebo were at increased risk of pre-term birth (RR = 1.38, 95% CI: 1.04–1.82, 3 RCTs, N = 583 women). Rumbold and Crowther  (Additional file 15) also examined the impact of Vitamin E supplementation (4 RCTs, N = 566 women at risk of, or with, pre-eclampsia). All trials assessed vitamin E in combination with other supplements and two trials were published as abstracts only. Meta-analysis showed no impact of Vitamin E on risk of stillbirth (RR = 0.77, 95% CI: 0.35–1.71, 2 RCTs, N = 339 women), neonatal death (RR = 5.00, 95% CI: 0.64–39.06, 1 RCT, N = 40 women), PMR (RR = 1.29, 95% CI: 0.67–2.48, 1 RCT, N = 56 women), pre-term birth (RR = 1.29, 95% CI: 0.78–2.15, 2 RCTs, N = 383 women), IUGR (RR = 0.72, 95% CI: 0.49–1.04, 2 RCTs, N = 383 women) or birth weight (weighted mean difference -139.00 g, 95% CI: (-)517.68-239.68 g, 1 RCT, N = 100 women), using fixed-effect models.
Roberts et al.  reported results from a double-blind RCT of Vitamins C and E versus placebo administered to low-risk nulliparous women (N = 9969). The study found no differences in the primary outcome, defined as either severe hypertension or pregnancy-related hypertension with at least one of the following: SGA, hepatic or renal dysfunction, eclampsia, stillbirth, or neonatal death before discharge (6.1% vs. 5.8% in antioxidant vs. placebo groups, respectively). Additionally, there was no impact on the incidence of pre-eclampsia (7.2% vs. 6.7% in antioxidant vs. placebo groups, respectively).
The overall level of evidence for these studies for impact on pregnancy outcomes is Grade D. Based on this limited evidence, with no trials conducted in under-nourished populations, there appears to be little benefit of anti-oxidants for the prevention of pre-eclampsia and its related complications, as studies have not reported consistent impact. There is no evidence suggesting that anti-oxidant supplements, specifically vitamins C or E or both, avert stillbirths or other perinatal complications such as SGA or neonatal death. Given that the studies reviewed here may not be generalisable to under-nourished populations, studies are needed that test anti-oxidant supplementation in such populations to ascertain whether treatment can impact rates of adverse pregnancy outcomes. Interventions included in this section and paper have aimed to prevent pre-eclampsia/eclampsia; the management of pre-eclampsia/eclampsia in pregnancy has been dealt with in Paper 5 .
Management of intrahepatic cholestasis in pregnancy
Maternal intrahepatic chlolestasis is a liver disorder that causes maternal morbidity during pregnancy, usually manifested as itching (pruritis) as well as an increased risk of associated perinatal mortality. Cholestasis is the most common liver disorder specific to pregnancy and is a principal cause of jaundice in the third trimester. Cholestasis is associated with significantly increased risk of fetal distress, pre-term delivery and stillbirth; however, the mechanisms by which cholestasis causes these complications are still unclear, and treatment strategies are thus largely empiric. The risks of adverse pregnancy outcomes associated with cholestasis increase near term and are unrelated to the severity of symptoms. Early delivery (at 36 weeks gestation) is an intervention that may be considered in cases of severe intrahepatic cholestasis, particularly if there is suspected fetal distress and lung maturity has been confirmed. Administering Vitamin K to the baby immediately after birth may help prevent intracranial bleeding. There is limited evidence about the effectiveness of other treatments, including guar gum, activated charcoal, S-adenosyl-L-methionine (SAMe) and ursodeoxycholic acid (UDCA), in alleviating maternal itching or improving perinatal outcomes.
Our literature search identified no Cochrane reviews and four trials assessing interventions for maternal intrahepatic cholestasis in pregnancy (Table 8). Three of these four were RCTs and compared the impact of different treatments for intrahepatic cholestasis on stillbirths or perinatal mortality. Binder et al.  compared S-adenosyl-L-methionine (SAMe) monotherapy (N = 78), ursodeoxycholic acid (UDCA) (N = 78) and combined therapy (N = 78) and documented no perinatal deaths in any group. Comparing UDCA, dexamethasone, and placebo in a cohort of women (N = 130), Glantz et al.  recorded only one intrauterine fetal death, which occurred in the placebo group. In Chile, Palma et al.  tested UDCA versus placebo, reporting only one perinatal death in the placebo group (0/8 in the UDCA group versus 1/7 in the placebo group).
The fourth trial that we identified  prospectively evaluated the effect of a management protocol for cholestasis including surveillance for presence of meconium using transcervical amnioscopy after 36 weeks, semi-weekly non-stress testing and amniotic fluid indices, and induction of labour at 37 weeks. Comparing the study's rate of fetal death with historical series data using expectancy and conventional monitoring of fetal well-being in pregnancies complicated by cholestasis, the fetal death rate was significantly lower in the study group than in the series data (1/218 vs. 14/888, respectively, P = 0.045), and the Caesarean section rate was not significantly different [LOE: 2+].
The intervention trial reviewed above that compared a management protocol in patients with intrahepatic obstetric cholestasis to standard monitoring of fetal well-being suggests that such protocols can reduce the SBR without increasing the cesarean delivery rate. However, this evidence is inconclusive (overall Grade D), and more studies are needed. There remains a need for studies to identify the mechanisms by which cholestasis causes perinatal mortality, as well as safety and efficacy studies for optimal pharmacological treatment regimens to treat cholestasis. The impact of different treatments for cholestasis vis-à-vis stillbirths or perinatal mortality remains inconclusive, as there are only a few trials on the subject.
Maternal plasma exchange
Maternal autoimmune or coagulation disorders may trigger the production of embryotoxic antibodies, which jeopardise pregnancy and lead to intrauterine death. These conditions include anti-D antibodies produced following maternal Rhesus alloimmunisation, lupus anti-coagulant and anti-cardiolipin that mark anti-phospholipid syndrome, and anti-Ro/SSA and anti-La/SSB antibodies in systemic lupus erythematosus, among others . Plasma exchange, or plasmapheresis, often in conjunction with steroid treatment or intravenous administration of immunoglobulins, is a means to remove or suppress circulating autoimmune or anti-coagulation factors in the blood and have been employed in a range of situations . Reducing these embryotoxic factors could prevent pregnancy loss, and provide an important alternative when intrauterine transfusion for Rhesus alloimmunisation, or anti-coagulant therapy (e.g., heparin +/- low dose aspirin) for anti-phospholipid syndrome fails. In recurrent abortion involving the presence of anti-P antibodies in mothers with the rare P blood group , plasmapheresis has proven effective in reducing pregnancy loss.
Our review identified two observational studies. No Cochrane or other systematic review was identified on the subject. El-Haieg et al.  conducted a study which assessed plasmapheresis plus low dose prednisone on obstetric and neonatal outcomes among unsuccessfully treated pregnant women with documented anti-phospholipid syndrome. There were no perinatal deaths [LOE: 3]. According to the study of Angela et al. , fourteen high-risk cases of Rh alloimmunised women were treated by intensive plasma exchange on the cell separator throughout their pregnancies. The expected stillbirth rate in this series as determined by their past obstetric histories and anti-D levels was 62%. Intrauterine transfusion was given to only two of the infants and both were later stillborn [LOE: 3].
Only two case series were identified, one on plasma exchange for severe Rh disease and the other (prednisone and plasmapheresis) for anti-phospholipid syndrome (Grade D evidence). Further large-scale studies are needed to investigate the effect of plasma exchange on stillbirths/perinatal mortality. Although robust evidence of an impact on stillbirths and perinatal deaths is lacking, plasma exchange commenced early in pregnancy may be an alternative therapy for severe Rh haemolytic disease and anti-phospholipid syndrome and may be useful in preventing stillbirths.
Cervical incompetence is estimated to occur in approximately 1% of the obstetric population, and 8% of women who experience repeated spontaneous abortions ; true rates are difficult to assess given a range of definitions but are likely higher. Cervical incompetence is increasingly recognised as associated with a continuum of complications including second-trimester miscarriage as well as pre-term birth. Incompetent cervix may be diagnosed presumptively following recurrent unexplained second trimester losses or pre-term births. However, increasingly, incompetent cervix is assumed when a short cervix is diagnosed via transvaginal ultrasound. Cervical cerclage, the surgical process of stitching the cervix closed to prevent further shortening and dilatation, can be either planned (history-indicated), urgent (ultrasound-indicated) or emergent (exam-indicated, generally in an emergency situation) . In women with 3 or more pre-term births or second-trimester losses, history-indicated cerclage is typically placed between 12–14 weeks of gestation. Evidence suggests that ultrasound-indicated cerclage, on the other hand, may be most effective when placed after 14 weeks but before 24 weeks of gestation .
The two most common transvaginal methods for placement of a cervical stitch are modifications of procedures developed by Shirodkar and McDonald [94, 95]. The Shirodkar technique involves an incision in the cervix at the level of the internal os and requires dissecting the bladder free; the cervix is then encircled with a purse-string suture through the broad cervical ligament. The McDonald technique does not require dissecting the bladder free, using an encircling suture around the cervix to approximate the level of the internal os. Ultrasound examination post-cerclage has shown that the Shirodkar procedure achieves longer cervical length than the McDonald procedure , but no differences in rates of pre-term birth have been observed between the two methods . In women with short and/or scarred cervixes, or where vaginal cervical cerclage has not worked, placement of the stitch can be difficult; in these women, transabdominal cervical cerclage can be performed, but patients require caesarean section delivery.
Despite being widely practiced, cerclage is controversial because its benefits in maintaining pregnancy and preventing pre-term birth have been marginal. A number of meta-analyses and reviews including pooled estimates of cerclage impact have found conflicting evidence of impact on pre-term birth rates associated with cerclage [92, 98]. However, recent good-quality trials of ultrasound-indicated cerclage for short cervix, including a large, rigorous RCT, have demonstrated a statistically significant impact of cervical cerclage in reducing pre-term birth rates . Cerclage has been studied primarily for its impact on pre-term birth. The procedure may also reduce stillbirth, though this has not been a principal focus of cerclage studies to date.
For this review, we identified two systematic reviews and 5 other intervention and observational studies of cervical cerclage that reported impact on stillbirths and/or perinatal mortality (Table 9). One Cochrane review by Drakeley et al.  compiled all adequately randomised RCTs (6 trials, N = 2175 women) comparing cervical cerclage with expectant management or no cerclage during pregnancy, as well as trials comparing different cerclage techniques, alone or with other interventions (Additional file 16). In the 4 included trials of prophylactic cerclage versus no cerclage, pooled results revealed no overall reduction in perinatal death (RR = 0.80, 95% CI: 0.48–1.36), pregnancy loss, or pre-term delivery rates before 28 and before 34 weeks. Cervical cerclage was associated with mild pyrexia, increased tocolytic use, and increased hospital admissions, but had no associated serious morbidities [LOE: 1++]. Another meta-analysis of RCTs of cerclage  (N = 7 trials, N = 2091 women) found no significant impact of cerclage on pregnancy loss or death before discharge from hospital in singleton pregnancies (OR = 0.81; 95% CI: 0.60–1.10 [NS]), though the small sample size indicated a need for additional large trials (Additional file 17). However, in the logistic regression analysis, an adverse association of cerclage with perinatal deaths was observed for multiple pregnancies (OR 5.88; 95% CI 1.14–30.19), suggesting cerclage should be avoided in multiple pregnancies. Neither indication for cerclage nor obstetric history was found to have a statistically significant impact on the effect of cerclage [LOE: 1++]. The only other RCT compared the impact of outpatient versus inpatient cerclage ; live birth rate was slightly higher among the inpatient group but the difference was not statistically significant.
A retrospective study of prophylactic cerclage in multiple gestation by Strauss et al. reported no impact on perinatal mortality, and a non-statistically significantly elevated risk of perinatal morbidity in higher-order gestations (quadruplets and quintuplets) [LOE: 2-].
Three observational studies highlighted the effectiveness of transabdominal cerclage as an alternative after unsuccessful transvaginal cerclage. Fick et al.  [LOE: 2+], and Gesson-Paute et al. [LOE: 2-]reported live birth rates after transabdominal cerclage of 96%, and 93% respectively, compared to 18%  and 17%  before the procedure. Debbs et al.  conducted a similar study and reported a 93% live birth rate after the procedure [LOE: 3].
The systematic reviews on cervical cerclage are of sufficiently high quality to permit a Grade B assessment, but are concerned primarily with impact on pre-term birth, and report statistically non-significant impact on stillbirth. Perinatal mortality outcomes reported by the large meta-analysis on cerclage  showed no conclusive evidence of benefit on stillbirth. The largest reviewed study in this meta-analysis by the MRC/RCOG  reported a significant reduction in very pre-term deliveries, and more recent data from a large RCT  has demonstrated a positive impact on pre-term birth in pregnant women with ultrasound-confirmed short cervix. This definitive trial indicates that ultrasound-indicated cervical cerclage is of benefit to reduce risk of preterm birth. Cerclage is not routinely indicated in multiple pregnancies . It is possible that cervical cerclage may reduce pregnancy loss in singleton pregnancies , particularly high-risk pregnancies, but it is unlikely that another large RCT like the Owen study  will be conducted to evaluate the impact of cerclage on stillbirth. It should be noted that measurement of the impact of cerclage on pregnancy outcomes is biased by the frequent exclusion from studies of women with true cervical incompetence. Cervical cerclage is currently inconclusive evidence of benefit for preventing stillbirth despite its proven impact on pre-term birth. Future studies may confirm reductions in perinatal mortality and help identify the sub-groups of women in whom it is most effective (e.g., ultrasound-indicated cerclage).
Infection control and treatment
Anti-helminthics during pregnancy in hookworm-endemic regions
Two species of hookworm, Ancylostoma duodenale and Necator Americanus, typically infect humans. Found throughout the tropics and subtropics, hookworm infestation is significantly associated with anaemia in women and children in endemic areas. Anaemia during pregnancy is associated with premature delivery, LBW, maternal ill health, and maternal death . In areas endemic for hookworm, routine antenatal anti-helminthic therapy could reduce the prevalence of anaemia in pregnancy, hypothetically preventing pregnancy losses associated with anaemia. In two studies of anti-helminthic treatment of women in pregnancy, the mean decrease in haemoglobin concentration from the first to the third trimester in women receiving a single dose of albendazole was 6.6 g/L less than women receiving placebo (P = 0.003) [107, 108], but another study showed no impact on haemoglobin level . Where the prevalence of hookworm is more than 20% to 30%, the WHO recommends that pregnant women receive treatment (mebendazole, albendazole, levamisole or pyrantel) after the first trimester. At present, however, this is not a widely accepted control strategy in part because of a lack of data on the safety of anti-helminthics. Potential teratogenicity is the principal concern surrounding use of anti-helminthics, as side effects are few . The limited studies on this subject have found no evidence of fetal malformations attributable to anti-helminthics used during pregnancy, but some studies have recommended that anti-helminthics not be used during the first trimester as a precaution until larger safety studies in pregnancy are available [111–113].
Several studies of deworming in pregnancy have demonstrated benefits on maternal nutrition outcomes and anaemia [109, 114, 115]. Our literature review identified two intervention studies and one observational study (Table 10).
De Silva et al.  assessed the effect of mebendazole therapy during pregnancy on birth outcomes in a cross-sectional retrospective study in Sri Lanka in 1995. Stillbirths and perinatal deaths were significantly less common in the mebendazole group (19/1000 vs. 33/1000; RR = 0.55, 95% CI: 0.4–0.77), as was the proportion of LBW infants (1.1 vs. 2.3%, RR = 0.47, 95% CI: 0.32–0.71). A slightly higher, but statistically non-significant, rate of congenital defects was found in women who had taken the drug in the first trimester [LOE: 2+]. In contrast, another study by Gyorkos et al.  comparing antenatal mebendazole (500 mg single dose) given with iron supplements vs. placebo with iron supplementation did not show any statistically significant differences between the mebendazole group (N = 28) and the placebo group (N = 31) in rates of miscarriages, malformations, stillbirths, early neonatal deaths and pre-term births [LOE: 2+]. However, unpublished data from a study of anti-helminthic treatment, maternal anaemia, and birth weight in Nepal  showed a statistically significant reduction in neonatal mortality associated with 2 doses of albendazole during pregnancy compared to controls (OR = 0.54, 95% CI: 0.37–0.78) [LOE: 2++].
Mebendazole therapy should be avoided during the first trimester pending further evidence on safety. The overall quality of evidence from the literature reviewed is Grade C, however there is some evidence of impact of deworming on stillbirths and other perinatal outcomes. Maternal deworming holds promise for improving the health of pregnant women in low-/middle-income countries where intestinal helminthiases are endemic. Consonant with the findings of the studies we reviewed, the Lancet Maternal and Child Undernutrition Series recommends deworming during pregnancy in specific, situational contexts (i.e., where prevalence of helminthiases and iron-deficiency anaemia are high) . Given the promising but inconclusive findings of a recent Cochrane review , further RCTs, especially effectiveness trials, of maternal anti-helminthic therapy reporting a range of pregnancy and infant outcomes are needed.
Syphilis screening and treatment
Reported rates of syphilis vary greatly worldwide. Prevalence is generally lower in high-income countries than in low-/middle-income countries. In 1990, the incidence of primary and secondary syphilis in the United States was 20 per 100,000 population, far less than the disease burden of 360 per 100,000 estimated for parts of Africa [119, 120]. Syphilis remains a major cause of avoidable perinatal death in many low-/middle-income countries despite being treatable, and despite the WHO recommendation that all pregnant women be tested as part of routine ANC. Among pregnant women with untreated early syphilis, 25% of pregnancies result in stillbirth and 14% in neonatal death, an overall perinatal mortality of about 40% . In early untreated syphilis, a pregnant woman has a 70% chance of transmitting the infection to her fetus . Even after effective screening, many pregnant women with syphilis remain inadequately treated because of delays in initiating treatment or patient non-adherence. Testing for syphilis within antenatal clinics is a strategy that makes test results available immediately so that early treatment can be administered, which could improve treatment of syphilis and reduce perinatal mortality .
We identified 1 Cochrane review and 8 interventional, quasi-experimental, or observational studies (Table 11) addressing the impact of syphilis screening and treatment on perinatal outcomes, the effectiveness of recommended penicillin treatment regimens, and issues associated with testing and treatment adherence. Unfortunately, the Cochrane review by Walker  assessing the impact of antibiotic treatment of syphilis in pregnancy did not report perinatal mortality outcomes, as none of the studies identified (N = 29) met the review's eligibility criteria for comparability.
Impact of screening and treatment on perinatal mortality
In a Swaziland hospital, Guinness et al  assessed how testing results and subsequent treatment for maternal prenatal syphilis serostatus impacted outcomes. Almost one-third of women (87/283; 31%) were possibly syphilis seropositive (TPHA-positive and RPR-negative); a smaller proportion (37/283; 13%) showed conclusive syphilis infection (TPHA-positive and RPR-positive) at prenatal testing. Perinatal mortality was highest among women with untreated active syphilis (7/24; PMR = 290/1000). Among women with possibly active syphilis, PMR was 50/1000, compared with 30/1000 among seronegative women. Screening and treatment reduced PMR by 34%, but the intervention would have been even more effective if treatment had reached the 65% of mothers with active syphilis who were missed, as well as study participants' sexual partners [LOE: 3].
In Kenya, Temmerman et al.  assessed the impact of an antenatal syphilis control programme on pregnancy outcome, confirming the adverse effect of syphilis infection on stillbirth. Of patients tested for syphilis (N = 12,414), 3% (N = 377) were RPR-positive; 296 of these were also TPHA-positive. Syphilis seropositive women had a higher risk of adverse obstetric outcome, defined as stillbirth or LBW (OR 4.1, 95% CI: 2.4–7.2). Antenatal treatment of RPR reactive women with single-dose benzathine penicillin G (2.4 million units) reduced the risk of adverse outcome, but women who remained RPR-positive after treatment had worse outcomes than uninfected mothers (OR = 2.5, P < 0.05). There was no statistical difference in pregnancy outcome based on gestational age at treatment [LOE: 3].
Syphilis treatment strategies
Treatment for maternal syphilis with single-dose IM benzathine penicillin is being implemented in many parts of sub-Saharan Africa in conformity with the 1993 Centers for Disease Control and Prevention (CDC) treatment guideline recommending a single dose of benzathine penicillin G (2.4 million units) for primary, secondary, and early latent syphilis in pregnancy, and three doses one week apart for late latent syphilis and latent syphilis of unknown duration. Watson Jones et al.  studied the effectiveness of this regimen in a Tanzanian cohort (N = 1688 pregnant women), comparing birth outcomes between high-titer, low-titer, and seronegative women. When treated, there was no statistically significant increased risk of adverse pregnancy outcome (stillbirth or LBW) comparing high-titer (OR = 0.76, 95% CI: 0.4–1.4) or low-titer women (OR = 0.95, 95% CI: 0.6–1.5) to seronegative women. [LOE: 2+].
Donders et al.  administered 0, 1, 2 or 3 benzathine penicillin G intramuscular (IM) injections to HIV-negative black urban women with syphilis (N = 180) in South Africa. Pregnancy outcomes were significantly better among women receiving 2 or more doses of penicillin than women receiving 0 or 1 dose. However, excluding patients treated with oral penicillin derivatives and adjusting for duration of treponemicidal levels, the study found an association of treponemicidal coverage of 3 weeks or less with decreased birth weight (2748 vs. 3130 g, P = 0.004) and higher rates of perinatal mortality (RR = 20.5; 95% CI: 2.3–184) and pre-term birth (RR = 8.5; 95% CI: 2.5–28) compared with treponemicidal coverage lasting longer than 3 weeks [LOE: 2-].
Rotchford et al.  demonstrated the impact on perinatal mortality of inadequate treatment for maternal syphilis despite adequate screening. In a study population with 9% syphilis prevalence, Rotchford used linear and categorical modeling to confirm a dose response protective relationship of penicillin on PMR. One dose reduced the risk by 41%, two doses by 65% and three doses by 79%, compared with no doses. Among those receiving at least one dose, mean delay to the first dose was 20 days. Among those fully treated, mean delay to treatment completion was 34 days [LOE: 2++].
On-site testing and treatment compliance
On-site syphilis testing in ANC clinics may prove an effective strategy to circumvent problems initiating and completing antibiotic treatment. Myer et al.  studied the impact of on-site syphilis testing on treatment delays and rates as well as perinatal mortality. Among women seeking ANC with available test results (N = 7134), 793 (11.1%) tested positive for syphilis. Women at intervention clinics completed treatment 16 days sooner on average (95% CI: 11–21 days), though there was no significant difference in the proportion receiving adequate treatment at intervention and control clinics (64 vs. 69%, respectively), or in PMR (3.3% vs 5.1% in intervention vs. control clinics; adjusted risk difference [RD]: (-)0.9%; 95% CI: (-)4.4-2.7) [LOE: 2++].
Bique et al.  assessed treatment initiation and compliance following RPR testing in seropositive pregnant women (N = 929) attending intervention or control clinics. Women attending intervention clinics were given health education about syphilis, on-site RPR testing and post-test counseling from a specially trained nurse-midwife, with encouragement to notify partners to come for free treatment. Women attending control clinics had standard RPR testing, entailing a multi-step, multi-provider process over a longer time period, and had to pay for their own treatment, resulting in compliance below 50%. PMR was significantly higher in the control group than in the intervention group (1.3% vs. 3.4% in intervention vs. control groups, respectively; P = 0.030) [LOE: 2-].
The nature of studies available for syphilis screening and treatment do not permit more than a Grade D evidence rating and it is recognised that classic RCTs are not possible. However, syphilis during pregnancy is a major cause of avoidable stillbirth and other adverse birth outcomes in many low-/middle-income countries, and interventions in terms of screening and treating syphilis are recommended for inclusion in endemic populations, as syphilis testing and treatment shows some evidence of impact on stillbirth. When treated with the appropriate dose of intramuscular benzathine penicillin, treatment effectively reduces perinatal mortality [129, 128] without risk of drug resistance. However, operational issues associated with treatment complicate the formulation of screening and treatment recommendations. Allergy to penicillin may pose problems for acceptability of treatment, but can be addressed with desensitisation therapy. There are a few studies on antibiotics other than penicillin for treatment of maternal syphilis; other drugs may offer alternative treatment options. In terms of service delivery, the studies reported did not support using on-site syphilis testing in addition to laboratory-based testing, although on-site testing may be the only feasible way to offer syphilis interventions in settings where laboratory facilities are lacking or of poor quality. More studies are needed to test the effectiveness of on-site syphilis testing and treatment and its impact on perinatal outcomes, as this strategy appears to improve compliance with treatment. Additionally, given interactions between syphilis and HIV co-infections, current testing and treatment guidelines may be inappropriate for individuals co-infected with HIV .
Antibiotics and antisepsis for urinary and reproductive tract infections (bacterial vaginosis, asymptomatic bacteriuria, and Group B streptococcus)
Maternal genital tract infection or colonisation by pathogenic organisms predisposes women to maternal and perinatal mortality and morbidity. Antibiotics and antiseptic agents have applications during pregnancy to prevent and treat reproductive tract infections, particularly presumptively for suspected or proven bacterial vaginosis (BV) and treatment of asymptomatic bacteriuria, as well as during the intrapartum period for Group B streptococcus (GBS) colonisation to prevent perinatal infection.
Bacterial vaginosis, an imbalance of normal vaginal flora with an overgrowth of anaerobic bacteria and a lack of normal lactobacillary flora, has been associated with poor perinatal outcome, particularly pre-term birth. Documented prevalence in pregnant women is common, ranging from 14% to 21% in Western countries; studies from Asian countries have reported prevalence ranges from 13.6–18% . Asymptomatic bacteriuria, generally defined as true bacteriuria in the absence of specific symptoms of acute urinary tract infection (UTI), occurs in 2% to 10% of all pregnancies in high-income countries . There is considerable evidence that bacteriuria and occult UTIs are more common in low-/middle-income countries, though estimates of prevalence are prone to wide margins of error. A urinalysis study from rural Tanzania using a variety of diagnostic methods found that 40% of nitrite tests and 65% of leukocyte esterase tests were positive at the first antenatal visit . One study reported significant bacteriuria in 86.6% of samples in an antenatal population in rural Nigeria, [134, 133]; other African studies have reported prevalences of bacteriuria in similar populations of 10–24% [135–137]. Some evidence from low- and middle-income countries that suggests that UTIs may be frequently missed, misdiagnosed, or improperly treated pharmacologically in these settings . Asymptomatic bacteriuria can lead to symptomatic UTIs, maternal pyelonephritis and septicemia, and is associated with higher rates of pre-term rupture of membranes (PROM) and chorioamnionitis.
Maternal colonisation with GBS infection is a recognised risk factor for neonatal colonisation and sepsis. GBS-colonised women who experience either a long duration of membrane rupture, premature delivery or intrapartum fever are at particularly high risk for transmitting GBS to their infants. Prevalence of colonisation with GBS is closely associated with socioeconomic status and is similar in both pregnant and non-pregnant women [132, 139].
We identified four Cochrane reviews, one other review, and 2 observational studies (Table 12). King et al.  conducted a Cochrane meta-analysis (N = 11 RCTs, N = 7428 women), including the ORACLE study, of the effect of maternal antibiotics in pre-term labour with intact membranes (Additional file 18). The Cochrane meta-analysis found that prophylactic antibiotics reduced rates of maternal infection (RR = 0.74, 95% CI: 0.64–0.87) but had no impact on PMR (RR = 1.22, 95% CI: 0.88–1.70) [LOE: 1++]. In another Cochrane review, McDonald et al.  compared antibiotic treatment to placebo/no treatment in cases of BV or intermediate vaginal flora, as well as comparisons between two or more antibiotic regimens (N = 15 RCTs, N = 5888 women) (Additional file 19). Antibiotic therapy effectively eradicated BV (OR = 0.17, 95% CI: 0.15–0.20; 10 RCTs, N = 4357 women), but did not reduce rates of pre-term premature rupture of membranes (PPROM) (OR = 0.88, 95% CI: 0.61–1.28; 4 RCTs, N = 2579 women). Antibiotics did not reduce the risk of pre-term birth before 37 weeks (OR = 0.91, 95% CI: 0.78–1.06; 15 RCTs, N = 5888 women), unless treatment was administered prior to 20 weeks' gestation (OR = 0.63, 95% CI: 0.48–0.84; 5 RCTs, N = 2387 women) or women had confirmed intermediate flora or BV (OR = 0.51, 95% CI: 0.32–0.81; 2 RCTs, N = 894 women). In women with previous pre-term birth, treatment did not affect the risk of subsequent pre-term birth (OR = 0.83, 95% CI: 0.59–1.17, 5 RCTs, N = 622 women). The three studies assessing the impact of metronidazole treatment for BV on perinatal mortality found no significant impact (OR = 0.96, 95% CI: 0.53–1.73) [LOE: 1++]
A Cochrane review by Lumbiganon et al.  found that vaginal chlorhexidine washing had no effect on perinatal mortality (RR = 1.00, 95% CI: 0.17–5.79) due to maternal and neonatal infections (excluding GBS and HIV) compared to placebo [LOE: 1++](Additional file 20). A systematic review by Goldenberg et al.  of the use of vaginal chlorhexidine treatment included two large, non-randomised, non-blinded trials from low-/middle-income countries that reported neonatal outcomes [LOE: 2+](Additional file 21). One quasi-experimental trial (N = 6965 women) included in this review from Malawi by Taha et al. , found that 0.25% chlorhexidine wipes at each vaginal examination during labour, followed by a neonatal wipe of the same concentration soon after birth, was associated with significant reductions in early neonatal deaths (29/1000 vs 37/1000 in intervention vs. control groups, respectively, RR = 0.78) and neonatal mortality due to infections (OR = 0.5, CI 0.29–0.88, 2.4 versus 7.3 per 1000, P < 0.005). A trial in Egypt included in the Goldenberg review using an almost identical study design and treatment plan as the Malawi study  (N = 4415 women), found significant decreases in infant death (2.8 vs. 4.2% in intervention vs. control groups, respectively, P = 0.01), and infant death due to infection (0.22% vs. 0.84% in intervention vs. control groups, respectively, P = 0.004). Neither study reported intrapartum stillbirth rates, which chlorhexidine treatment could theoretically impact by reducing infectious causes.
Thinkhamrop et al.  conducted a Cochrane review of the effects of prophylactic antibiotic administration in the second and third trimester (N = 6 RCTs, N = 2184 women) (Additional file 22). Antibiotic prophylaxis clearly reduced the risk of PROM (OR = 0.32, 95% CI: 0.14–0.73). Among women with a previous pre-term birth, antibiotics were associated with reduced odds of LBW (OR = 0.48, 95% CI: 0.27–0.84), as well as pre-term delivery (OR = 0.48, 95% CI: 0.28–0.81) in the subgroup of women with BV. Women with previous pre-term birth but without BV had no reduction in odds of pre-term birth (OR = 1.06, 95% CI: 0.68–1.64). The 3 trials that reported PMR yielded only non-significant effects (OR = 0.52, 95% CI: 0.16–1.71). [LOE: 1++].
The evidence to date does not suggest any benefit in screening and treating all pregnant women for asymptomatic BV to prevent pre-term birth (Grade D evidence); however, there is limited evidence that treatment with antibiotics early in pregnancy, particularly for women with confirmed intermediate flora or BV, may reduce pre-term births. The results of treatment trials for pregnant women with BV have been mixed, ranging from an 80% reduction to a two-fold increase in pre-term birth among women who received treatment, despite large numbers of women in the included trials. This heterogeneity of effect may be attributable to differences in participants' genetic background, diagnosis criteria, timing of treatment and antibiotic choice.
Chlorhexidine washes have long been linked to decreased maternal positivity for GBS , but this intervention also appears effective against other organisms. There is highly promising evidence from Egypt and Malawi to support the use of vaginal chlorhexidine washing during labour (and of the neonate after birth) in preventing adverse maternal and neonatal outcomes associated with infection, including neonatal death from sepsis and overall neonatal mortality, but stillbirths were not reported by studies to date. Two RCTs of maternal vaginal plus newborn skin cleansing have just been completed in South Africa and in Pakistan, but results of these trials have not yet been reported.
Although it appears that antibiotic prophylaxis during the second or third trimester of pregnancy may reduce the risk of PROM, LBW, and transmission of infection to the neonate in high-risk pregnant women, more data are needed to assess the risks of routine use of antibiotics in pregnancy and to confirm whether their use can prevent these and other substantive adverse pregnancy outcomes.
Antibiotics for pre-term premature rupture of membranes (PPROM) and premature rupture of membranes (PROM) in high-risk pregnancies
Premature rupture of membranes (PROM) is a condition where the placental membranes rupture at term prior to the onset of labour, which is of clinical concern if labour does not quickly become established thereafter, as the risk of maternal and fetal infection mounts. A related problem is when membranes rupture prior to 37 weeks (term). This condition precedes one-third of pre-term births, and has proven difficult to prevent: despite socio-economic improvements and the development of a large range of therapeutic interventions in high-income countries, the rate of pre-term births remains at 6 to 8 percent.
The causes of PROM and PPROM are multifactorial. Infection appears to play a major role, either as a cause or as a consequence of PROM/PPROM. Some organisms may produce collagenases, mucinases and proteases, which weaken the amnion and chorion and may lead to membrane rupture. Infection may also occur secondary to membrane rupture if ascending infection leads to occult deciduitis, intra-amniotic infection or fetal infection. A possible mechanism for the link between infection and pre-term delivery is bacterial stimulation of the biosynthesis of prostaglandins, either directly via phospholipase A2 and C , or indirectly via substances such as interleukin-1, tumour necrosis factor and platelet activating factor, all of which have been identified in infected amniotic fluid .
Theoretically, antibiotic therapy could improve perinatal outcome by two processes. Prevention or treatment of infection may minimise maternal or fetal infectious morbidity, which would have a direct impact on stillbirth incidence. Secondly, in cases of PPROM, suppression of the prostaglandin response may slow the progression to pre-term birth described above, which could provide a window of time for fetal lung maturation and other fetal changes that could impact incidence of complications of prematurity.
The literature search identified two Cochrane reviews, and one other intervention study (Table 13). Kenyon et al.  assessed the effects of administering antibiotics to women with PROM on fetal and neonatal morbidity and mortality, including both trials that compared antibiotic to placebo, as well as trials without placebo (22 trials, N = 6000 women) (Additional file 23). Antibiotic administration following PROM was associated with a statistically significant reduction in chorioamnionitis (RR = 0.57, 95% CI: 0.37–0.86), births <48 hours after membrane rupture (RR = 0.71, 95% CI: 0.58–0.87), and births < 7 days after randomisation (RR = 0.80, 95% CI: 0.71–0.90). There was no apparent impact on perinatal mortality or death before discharge (13 trials; RR = 0.90, 95% CI: 0.74–1.10) [LOE: 1++].
Another Cochrane review by Flenady and King  examined trials that tested the impact on maternal, fetal, and neonatal outcomes of antibiotics administered prophylactically to women with PROM ≥ 36 weeks' gestation (2 trials, N = 838 women) (Additional file 24). Antibiotic use was significantly associated with a decreased incidence of maternal infectious morbidity (chorioamnionitis or endometritis) (RR = 0.43, 95% CI: 0.23–0.82), RD = (-)4%, 95% CI: (-)7%, (-)1%), number needed to treat [NNT] = 25, 95% CI: 14–100). The two studies reporting perinatal outcomes showed no impact of antibiotic treatment on PMR (RR = 0.98, 95% CI: 0.14–6.89) [LOE: 1+].
Although the two Cochrane reviews on the subject were given a Grade B rating, they report no benefit of antibiotic administration in cases of PROM to reduce stillbirths. Antibiotic treatment following PPROM was associated with a statistically significant delay in women giving birth and reductions in major markers of neonatal morbidity (although not perinatal mortality). This delay in delivery would allow sufficient time for prophylactic prenatal corticosteroids to take effect. These data support the routine use of antibiotics in this clinical situation. The increase in the numbers of babies who developed neonatal necrotising enterocolitis with prenatal co-amoxiclav treatment suggests that erythromycin rather than co-amoxiclav is the antibiotic of choice in women at risk of pre-term delivery . In cases of term PROM, the Cochrane review by Flenady and King  indicates that there is insufficient evidence to justify the routine use of antibiotics prior to the onset of labour. Although antibiotics reduced rates of chorioamnionitis and endometritis, the low rate of maternal infection in the control population (~7 percent) suggests that exposure of all women with term PROM to antibiotics is unwarranted if treatment can be restricted to those who develop clinical indications for antibiotic treatment. Because these studies do show that antibiotics significantly reduce maternal infectious morbidity including chorioamnionitis, which is a known risk factor for stillbirth, more research is required to evaluate the potential impact of antibiotic administration after membrane rupture.
Anti-malarials in malaria-endemic areas
Globally, malaria affects almost 10% of the world's population, and of the nearly 500 million annual cases, approximately 1 million people die annually . Particularly in areas where malaria is endemic, malaria is a key cause of maternal illness and anaemia in pregnancy, especially in primiparas [153, 154]. Administration of anti-malarial drugs, whether presumptively through strategies such as intermittent preventive treatment (IPT) or as treatment for diagnosed parasitemia in pregnancy, is generally recommended in areas endemic for malaria.
The literature review identified one Cochrane review comprised of nine RCTs, as well as two other intervention and observational studies (Table 14). In the Cochrane review (N = 16 RCTs, N = 12,638 women), Garner and Gülmezoglu  found that anti-malarials reduced antenatal parasitemia when given to all pregnant women, but had no impact on PMR (RR = 1.02, 95% CI: 0.73–1.43, 4 RCTs, N = 2890 participants) or stillbirths specifically (RR = 1.51, 95% CI: 0.80–2.84) (Additional file 25). However, among women in their first or second pregnancy, a strategy of IPT reduced the risk of perinatal mortality (RR = 0.73, 95% CI: 0.53–0.99; 1 RCT, N = 1986 participants) but not stillbirth (RR = 0.87, 95% CI: 0.62–1.21, N = 3454 participants) [LOE: 1+].
An additional double-blind, placebo-controlled RCT not included in the reviews on malaria treatment during pregnancy in endemic areas was conducted by Hamer et al.  in which HIV-positive mothers were randomised in blocks of 20 to one of two dosing schedules: one treatment course of sulfadoxine-pyrimethamine (SP) per month; or one course of SP per trimester. There were slightly more stillbirths among the group receiving monthly SP compared to the once-per-trimester group, but this difference was not significant (2/191 vs. 5/203 total deliveries; RR = 0.43, 95% CI: 0.1–2.2) [LOE: 1+].
Prophylaxis with a variety of anti-malarial drugs or IPT with SP in women having their first or second baby is associated with a 38% lower incidence of severe anaemia and 27% fewer perinatal deaths, according to the Cochrane review on IPT and chemoprophylaxis  (Grade B evidence). There was no obvious impact on anaemia or perinatal outcomes when prophylaxis or IPT was given to all women regardless of the number of previous pregnancies. Malaria parasitaemia in the blood or the placenta is also less common with prophylaxis or IPT.
This evidence relates to a reasonable number of good quality studies although the data show no significant evidence of direct impact on stillbirths, largely owing to the studies being underpowered to detect differences. However, the myriad maternal and perinatal benefits observed justify the use of malaria chemoprophylaxis in women of low parity in malaria endemic regions. SP is currently the first-line drug for IPT in many countries according to the WHO Treatment Guidelines , but patterns of drug resistance are emerging rapidly. Although the WHO guidelines now recommend artesunate for most parasitemias, many new treatment drugs and regimens are available for the treatment of malaria; however, little information is available about their pharmacokinetics, safety, and effectiveness in pregnant women, as trials have excluded these women for fear of embryotoxicity . More research is underway to expand the arsenal of anti-malarial drugs, potentially to include other artemisinin-based treatments than artesunate, which are also safe to use in pregnancy .
Use of insecticide-treated nets (ITNs) during pregnancy
Every year, an estimated 50 million pregnant women are exposed to malaria. Pregnancy renders women more susceptible to malaria, and both the mother and fetus are at risk of adverse consequences of malarial infection, including maternal death from malaria, maternal anaemia and LBW in the fetus . Although the use of insecticide-treated nets (ITNs) during pregnancy has been touted as a key strategy for preventing malaria in pregnancy, the evidence of benefit has been mixed . The use of ITNs is known to decrease maternal and placental parasitemia, and raise haemoglobin concentrations in women with their first to fourth pregnancies . ITNs are recommended by the WHO in conjunction with IPT and case management of malarial infection  to prevent malaria in pregnant women living in malaria-endemic areas of Africa and Asia.
One systematic review, published in two journals and comprised of 5 RCTs, was identified in our literature search (Table 15). This review by Gamble et al.  assessed ITN use during pregnancy (N = 5 RCTs, with cluster- and individual-randomised designs) (Additional file 26). Four trials from sub-Saharan Africa compared the use of ITNs with no nets, and one trial from Asia compared ITNs with untreated nets. In Africa, ITNs reduced placental malaria in all pregnancies compared with no nets (RR = 0.79, 95% CI: 0.63–0.98). The use of ITNs also reduced LBW incidence (RR = 0.77, 95% CI: 0.61–0.98) and fetal loss (miscarriages plus stillbirths) in the first to fourth pregnancy (RR = 0.67, 95% CI: 0.47–0.97), but not in fifth and higher-order pregnancies. ITNs also appeared to have a beneficial impact on anaemia and clinical malaria but these trends were not statistically significant [LOE: 1++]. The updated systematic review by the same author in 2007 mentions four trials in which stillbirth outcomes are reported (Additional file 26). Summary estimates for the effect of ITN use were estimated from 3 studies [163–165] reporting fetal death (miscarriage plus stillbirths). ITNs compared to no nets reduced fetal death (by 33% (RR = 0.67, 95% CI: 0.47–0.97) in the first or second pregnancy [LOE: 1++].
The available studies and Cochrane review provide strong evidence of benefit of ITN use in pregnancy (Grade A evidence). ITNs significantly decreased maternal and placental parasitaemia, increased mean birth weight in most trials, and reduced rates of fetal loss and other negative pregnancy outcomes in women in their first or second pregnancy, with some benefit likely through the fourth pregnancy. Thus, ITNs are recommended for pregnant women, particularly primigravidae, in malaria-endemic areas. As four of the five trials considered were conducted in Africa, and the only trial conducted in Asia compared ITNs with untreated nets on the Thai-Burmese border, further efficacy studies of ITNs to prevent malaria in pregnancy are recommended in areas with less intense (as well as Plasmodium vivax) transmission in Asia and Latin America.
Prevention of mother-to-child transmission of HIV
High maternal viral load, which measures the level of HIV RNA in the plasma, is a strong independent risk factor for vertical (mother-to-child) transmission of HIV. In addition, breastfeeding, young maternal age, other STDs, advanced maternal HIV disease, low CD4 cell count, chorioamnionitis, prolonged rupture of membranes, vaginal delivery and associated events increasing maternal bleeding, and history of stillbirth also increase the risk of vertical transmission . Anti-retroviral (ARV) drugs, primarily zidovudine, nevirapine, or a combination of the two, are recommended during pregnancy to reduce mother-to-child transmission of HIV because by reducing viral replication, they effectively reduce maternal viral load. Additionally, the drugs provide some measure of pre-exposure prophylaxis for the fetus because they cross the placenta, and can be administered directly to the baby after delivery (usually within 72 hours of birth) as post-exposure prophylaxis. In developed countries, rates are around 1–2% thanks to the availability of highly active ARV therapy (HAART) . HAART availability remains limited in low and middle-income countries, but simpler and less expensive ARVs are now widely available. While numerous studies have been conducted on the efficacy of ARVs for PMTCT, few have reported stillbirth outcomes.
We identified three systematic reviews (3 reviews and meta-analyses comprised of 18 RCTs) and 8 other studies (Table 16). The studies assessed a range of different ARV drug choices, dosages, and timing of administration to mother, infant, or both. In a Cochrane review by Volmink et al. comparing ARVs administered to mothers and their infants to placebo , all 6 eligible RCTs reported statistically non-significant reductions in stillbirths (results were not pooled: see Table 16 for RRs and CIs) (Additional file 27). Comparing longer vs. shorter ARV regimens, 3 RCTs showed statistically non-significant reductions in stillbirths for longer regimens (results were not pooled, see Table 16 for RRs and CIs) [LOE: 1++]. Another systematic review by Suksomboon et al.  supported the efficacy of zidovudine to prevent vertical HIV transmission (RR = 0.57, 95% CI: 0.45–0.71 in zidovudine vs. placebo groups, respectively) as well as to reduce LBW (Pooled RR = 0.75, 95% CI: 0.57–0.99, P = 0.039), but found no significant effects of zidovudine on stillbirth or pre-term delivery (Additional file 28). The Suksomboon et al. review also found no differences between short-long and long-long regimens of zidovudine therapy in rates of perinatal HIV transmission, infant death, stillbirth, or pre-term birth. However, in the African studies in this review, zidovudine plus lamivudine combination therapy was very effective in preventing vertical transmission (adj. OR = 0.23, P < 0.0001). One included trial found that 2-dose nevirapine prophylaxis (intrapartum plus newborn dose, given in combination with zidovudine) reduced the death rate of live-born babies by 80% (RR = 0.20, 95% CI: 0.05–0.90) versus nevirapine placebo plus zidovudine; however, this regimen had no impact on SBR (RR = 1.11, 95% CI: 0.48–2.56) [LOE: 1++].
Similarly, comparing HIV-1-infected pregnant women given monotherapy, combination therapy without protease inhibitors, and combination therapy with protease inhibitors to women who did not receive ARVs, Tuomala et al.  reported similar SBRs between all groups [LOE: 2+]. Efavirenz therapy also appears to be ineffective in preventing stillbirths; in a comparison of 6 treatment regimens, 3 of which contained efavirenz, Bussmann et al.  reported no impact of efavirenz on SBR (P = 0.7) [LOE: 1-].
HAART, the administration strategy of choice for HIV disease where available, is associated with improved maternal and infant outcomes, but does not appear to impact stillbirth incidence. Townsend et al.  compared women on HAART with women on mono/dual therapy. In comparison with exposure to mono/dual therapy, exposure to HAART was associated with a non-significant increased risk of stillbirth (adj. OR = 2.27, 95% CI: 0.96–5.41; P = 0.063) [LOE 2+]; this trend was not observed by Tonwe-Gold et al. , who found that compared to women on short-course anti-retroviral (scARV) PMTCT regimens, women on HAART had no difference in SBR (P = 1.00) [LOE: 2+]. Sharma et al.  found that the total live birth rate increased by 150% (P = 0.001) in HIV-positive women given HAART compared to the pre-HAART era, compared with a mere 5% increase during the same time period in HIV uninfected women, but the study design was unable to determine stillbirth rates before or during HAART administration [LOE: 3].
A third PMTCT-related Cochrane review by Wiysonge et al.  reviewed the potential for vitamin A supplementation to reduce vertical transmission of HIV infection (4 RCTs, N = 3033 HIV-positive pregnant women), but found no evidence of impact of vitamin A supplementation on stillbirths (OR = 0.99, 95% CI: 0.67–1.46) [LOE: 1++](Additional file 29).
Overall, while there is no consensus on the ideal regimen for preventing vertical transmission, there is considerable evidence that in resource-poor settings, zidovudine alone or in combination with other ARVs such as lamivudine or nevirapine reduces the risk of vertical transmission and infant death, as well as positively impacts birth weight (overall Grade C evidence). In mothers already receiving zidovudine prophylaxis, a single dose of nevirapine to mothers during labour and to infants after birth further decreases the risk of vertical transmission and infant death. Wherever available, HAART appears to be associated with statistically significant improvement in live birth rate. However, there is no evidence that any regimen of PMTCT impacts stillbirth incidence. Additionally, there is no evidence for any impact of vitamin A supplementation on stillbirths in HIV-positive mothers. As PMTCT regimens are of clear benefit to maternal health (when administered to pregnant women) and infants (when administered during pregnancy and the postnatal period), we recommend their inclusion in ANC programs based on these benefits alone, with the caveat that there is no evidence of their efficacy in preventing stillbirths.
Periodontal care during pregnancy
Periodontal disease, including gingivitis and periodontitis, is one of the most common chronic disorders of infectious origin known in humans, with a reported prevalence varying between 10 and 60% in adults, depending on diagnostic criteria. Periodontal disease is initiated by overgrowth of certain bacterial species, with a majority of Gram-negative, anaerobic bacteria growing in subgingival sites and producing lipopolysaccharide (LPS) endotoxins and other bacterial substances. The host response to periodontal pathogens causes persistent inflammation with high levels of proinflammatory cytokines, contributing locally to periodontal disease as well as to systemic effects including increased risk of atherosclerosis, myocardial infarction, stroke, diabetes mellitus. Several studies have highlighted the relationship between maternal periodontal disease and birth outcomes, including prematurity [174, 175]. A large number of studies have explored the mechanisms by which periodontal disease might impact LBW, miscarriage, and pre-eclampsia . Most of these studies have centered on prematurity, and although several RCTs have reported an association between periodontal care and reduced rates of pre-term birth or pre-term LBW, systematic reviews and meta-analyses on the subject have been unable to determine conclusively whether there are any associations with these outcomes . There has been much less attention to date as to whether periodontal care could prevent stillbirth.
Our literature search identified 2 systematic reviews, and 4 other observational/intervention studies, that reported stillbirth or perinatal mortality outcomes (Table 17). None of the systematic reviews reported a conclusive association between periodontal disease and stillbirth or perinatal mortality. In a systematic review by Xiong et al. , only one cohort study  reported stillbirth or miscarriage as an outcome. Regression analysis revealed no significant relationships between the severity of periodontal disease and pre-term birth or LBW, but did elucidate a significant correlation between poorer periodontal health and those that experienced a late miscarriage (adj. OR = 2.54, 95% CI: 1.20–5.39) (Additional file 30). An update of this analysis  which included 2 studies reported an effect size ranging from 2.54–3.84 times increased risk of fetal loss attributable to periodontal disease (Additional file 31). Tarannum et al.  also reported a convincing link between periodontal disease and adverse pregnancy outcome (OR = 5.5, 95% CI: 1.4–21.2; P = 0.014). A more recent prospective cohort study from Pakistan  involving a periodontal examination at 20–26 weeks' gestation for study subjects (N = 1152 women) found that 76% of participants had moderate to severe periodontal disease. Stillbirth rates tended to be higher in the fourth quartile versus the first quartile of severity of periodontal disease (for stillbirth: 19/1000 vs. 41/1000 in 1st vs. 4th quartiles, respectively, P = 0.069). The same was true for perinatal and neonatal mortality rates. While some evidence supported an association between periodontal disease and early pre-term birth, the association was not statistically significant. Late pre-term birth and LBW were not associated with measures of periodontal disease.
While published data convincingly demonstrate a linkage between periodontal disease and stillbirth incidence, the limited literature on interventions for periodontal disease has not yet shown any evidence of impact on pre-term birth or perinatal mortality. An RCT by Macones et al. , which provided scaling and root planing to an intervention group versus tooth polishing for controls, reported no impact of periodontal disease treatment on pre-term birth rate at less than 35 weeks gestation (RR = 1.55, 95% CI: 0.90–2.67), and no difference in rates of the composite outcome of major neonatal mortality or morbidity between the intervention and control groups (RR = 1.30, 95% CI: 0.83–2.03) . In a competing-risks analysis by Michalowicz et al. , neither the risk of pre-term birth (P = 0.51) nor of spontaneous abortion or stillbirth (P = 0.08) differed significantly between women who were given periodontal care (scaling and root planing) at 21 weeks' gestation versus women whose care was delayed until after they gave birth.
There appears to be a relatively consistent association between periodontal disease and risk of adverse pregnancy outcome in some populations . Many studies have explored the potential association of periodontal disease and periodontal care with pre-term birth or pre-term LBW, but the evidence is conflicting. The observational studies that reported statistically significant results lack the design strength to eliminate confounding and definitively attribute causation. Variability in definition of periodontal disease, as well as design flaws in published studies, suggest that the available findings should be viewed with caution (overall Grade C evidence). Very few RCTs have assessed the impact of interventions for periodontal disease on stillbirth and perinatal mortality, and most have been designed with pre-term birth as the primary outcome and have been underpowered to detect impact on perinatal deaths. Although clinical trial data suggest that non-surgical periodontal treatment in the second trimester is a safe and effective strategy to improve periodontal indicators, there is currently insufficient evidence to recommend routine periodontal care as an effective strategy to prevent stillbirths or pre-term birth [183, 184, 182]. This emerging area of research warrants further study, however, particularly in low-/middle-income countries. Care for periodontal disease provided prior to pregnancy may offer more significant benefits, but this strategy has not yet been tested.
An additional mechanism by which periodontal care could prevent stillbirths is the emerging and clinically important link between periodontal disease and pre-eclampsia. A recent meta-analysis by Vergnes et al. 2008 reported that women with periodontal disease had almost double the risk of pre-eclampsia compared with women without periodontal disease (OR = 1.76, 95% CI: 1.43–2.18) . This linkage, if it can be confirmed, would be particularly relevant to low-/middle-income country settings given high rates of periodontal disease as well as higher incidence of pre-eclampsia than in high-income countries. Verifying this association and identifying the physiological mechanisms involved will require further studies.
While high-quality Cochrane or other published reviews or meta-analyses were available for many interventions, few of these reviews or their component studies reported stillbirths specifically, and evidence from different studies and different reviews was frequently conflicting. Additionally, comparing findings even for the same intervention was often difficult due to differing study objectives and design issues including study incommensurability, differences in outcome definitions, and differences in allocation technique. Even rigorous intervention trials were usually conducted in tertiary care centres where even controls received ANC, often of better quality than women who do not enroll in such trials; in such trials with appropriate care and monitoring, stillbirths are more rare than in the general population (e.g., use of anti-hypertensive agents in pregnant women with hypertension). This bias limits generalisability of findings and further hinders demonstration of impact attributable to an intervention. To bridge the evidence gap, there is a need for large research trials to report stillbirths–disaggregated from the perinatal mortality composite measure–as an outcome whenever feasible, and for rigorous RCTs in low-resource settings. The recommendation of each intervention for inclusion in programs is given in Table 18.
In many low-/middle-income countries, stillbirths associated with infection comprise a large proportion of stillbirths. Preventing stillbirth associated with maternal infection is appealing because it targets a large proportion of the burden, and interventions and service delivery needs are relatively straightforward, short-term, and noninvasive compared with behavioural, surgical, or nutritional interventions. While the evidence base for prevention of stillbirths with interventions prior to or during pregnancy is limited, evidence strongly supports a benefit of syphilis screening and treatment and malaria prophylaxis in endemic areas, and these interventions should be incorporated into ANC programs where epidemiological evidence indicates women are at risk. Some estimates suggest that better syphilis screening and treatment could prevent as many as half of all stillbirths in areas with high syphilis prevalence . When women are treated for syphilis successfully, their risk of stillbirth is similar to uninfected women . The logistical challenges of providing syphilis screening and treatment, particularly at the community level, are many, including training workers to perform a complex test or tests, evaluating ambiguities in diagnosis, preventing test and pharmaceutical supply stock outs, managing the occasional penicillin sensitivity, and ensuring that clients receive both test results and treatment. However, the high rates of ANC attendance (one or more visits) in much of sub-Saharan Africa and South Asia provide a potential infrastructural framework to provide access to this important intervention.
Given the endemicity of malaria in much of sub-Saharan Africa and South Asia, where stillbirth rates are concomitantly high, the three-pronged approach to malaria prevention and treatment advocated by the WHO (ITNs, IPT, and treatment of parasitemia with artemisinin-based therapies) appears prudent, though further research is needed about the safety of artemisinin-based drugs other than artesunate and the impact of timing of dosage on stillbirth rates.
Other interventions, such as anti-helminthic treatment, showed promising impact on stillbirth rates but require more studies to confirm effectiveness. While we recommend the continued practice of PMTCT for HIV, and malaria chemoprophylaxis in women of low parity, these recommendations are based primarily on demonstrated benefit for maternal or other fetal/neonatal outcomes, rather than definitive impact on stillbirths or perinatal mortality.
The area of stillbirth prevention, particularly the development of interventions that address the multifactorial causes of antepartum stillbirths, is a ripe area for new research (Table 19). In this review, we found evidence that several interventions brought about reductions in known risk factors for stillbirth, yet failed to bring about statistically significant improvements in stillbirth rates. For example, anti-platelet agents clearly reduced rates of PIH and pre-eclampsia, yet no statistically significant impact on stillbirths was noted. Similarly, antibiotic treatment for PROM was associated with a significant reduction in chorioamnionitis, yet yielded no statistically significant reduction in stillbirth rates. These findings are most likely attributable to studies underpowered to detect impact of the intervention on stillbirth rates, but could also be due to intervention at a point too distal in a multi-causal pathway, a deleterious effect of the intervention itself, including adverse effects of drugs, etc. For these interventions and others (Table 19), further research specifically designed to measure stillbirth as an outcome is needed.
Large gaps remain in the basic science of stillbirth causation and many of the maternal conditions and pathologies that lead to stillbirth, including pathophysiological mechanisms involved in pre-eclampsia, autoimmune and inflammatory responses that threaten pregnancy, still-unknown risk factors, and drug safety and efficacy studies. These studies will guide development of appropriate interventions for maternal conditions and infections associated with stillbirth causation.
Evidence for some newly recognised risk factors for stillbirth, such as periodontal disease, suggests the need for large, appropriately designed randomised trials to assess whether effective interventions can be designed to minimise these risks.
Knowledge and evidence gaps in the dynamics and prevention of antepartum stillbirth are numerous and deep. At present, there is no standard international classification system for stillbirth causation, and disagreement persists about the lower benchmarks of birth weight and gestational age used to define stillbirth. These ambiguities complicate measurement of stillbirths, comparison of different studies measuring stillbirth, and tracking trends over time . Development of practical, standardised templates to assess causes of stillbirth is underway, which, if adopted internationally, will help to more accurately measure the burden of intrapartum versus antepartum stillbirths and their associated causes. These data are crucial to inform the development of appropriate interventions. Meanwhile, the numerous gaps in the growing list of stillbirth risk factors, the pathophysiology of certain maternal infections and conditions, and the many interventions for which there is conflicting evidence of benefit suggest the need for greater investment in large studies powered to measure stillbirth rate reductions. Armed with more definitive knowledge of which interventions are effective and prevent the most stillbirths in particular settings, we can more effectively select and implement these interventions and prevent unnecessary loss of life.
Programmatically, the clearest evidence of impact in stillbirth prevention is adequate prevention and treatment of maternal infections such as syphilis and malaria. Given the enormous human burden of both of these diseases in many countries with the world's highest stillbirth rates, effective prevention and treatment of syphilis and malaria have the potential to greatly reduce global stillbirth rates.
Efforts prior to and during pregnancy to prevent stillbirth will be most effective in conjunction with effective monitoring interventions in pregnancy, prompt recognition and management of high-risk pregnancies and complications, and a system of interlinked facilities capable of prompt referral to ensure that complications are capably managed to prevent unnecessary loss of life for mothers or their babies.
diastolic blood pressure
early neonatal mortality rate
Food and Drug Administration
female genital mutilation
fetal growth restriction
Group B Streptococcus
highly active anti-retroviral therapy
human immunodeficiency virus
intrauterine growth restriction
low birth weight
low molecular weight
level of evidence
National Institutes of Health
neonatal mortality rate
neural tube defect
perinatal mortality rate
prevention of mother-to-child transmission
pre-term premature rupture of membranes
premature rupture of membranes
partial thromboplastin time
randomised controlled trial
recommended dietary allowance
rapid plasma reagin
systolic blood pressure
small for gestational age
Treponema pallidum haemagglutination test
vaginal birth after Caesarean
World Health Organization
Smith GC: Predicting antepartum stillbirth. Curr Opin Obstet Gynecol. 2006, 18 (6): 625-630. 10.1097/GCO.0b013e32801062ff.
Stanton C, Lawn JE, Rahman H, Wilczynska-Ketende K, Hill K: Stillbirth rates: delivering estimates in 190 countries. The Lancet. 2006, 367: 1487-1494. 10.1016/S0140-6736(06)68586-3.
Feresu SA, Harlow SD, Welch K, Gillespie BW: Incidence of stillbirth and perinatal mortality and their associated factors among women delivering at Harare Maternity Hospital, Zimbabwe: a cross-sectional retrospective analysis. BMC Pregnancy Childbirth. 2005, 5 (1): 9-10.1186/1471-2393-5-9.
Goldenberg RL, Kirby R, Culhane JF: Stillbirth: a review. J Matern Fetal Neonatal Med. 2004, 16 (2): 79-94. 10.1080/14767050400003801.
Yakoob MY, Menezes EV, Soomro T, Haws RA, Darmstadt GL, Bhutta ZA: Reducing stillbirths: behavioural and nutritional interventions before and during pregnancy. BMC Pregnancy and Childbirth. 2009, 9 (Suppl 1): S3-10.1186/1471-2393-9-S1-S3.
Menezes EV, Yakoob MY, Soomro T, Haws RA, Darmstadt GL, Bhutta ZA: Reducing stillbirths: prevention and management of medical disorders and infections during pregnancy. BMC Pregnancy and Childbirth. 2009, 9 (Suppl 1): S4-10.1186/1471-2393-9-S1-S4.
Lawn JE, Yakoob MY, Haws RA, Soomro T, Darmstadt GL, Bhutta ZA: 3.2 million stillbirths: epidemiology and overview of the evidence review. BMC Pregnancy and Childbirth. 2009, 9 (Suppl 1): S2-10.1186/1471-2393-9-S1-S2.
HMSO: Report on confidential enquiries into maternal deaths in the United Kingdom 1988–1990. Department of Health Welsh Office, Scottish Office Home and Health Department, Department of Health and Social Security, Northern Ireland. 1994, London: HMSO
Villar J, Say L, Shennan A, Lindheimer M, Duley L, Conde-Agudelo A, Merialdi M: Methodological and technical issues related to the diagnosis, screening, prevention, and treatment of pre-eclampsia and eclampsia. Int J Gynaecol Obstet. 2004, 85 (Suppl 1): S28-41. 10.1016/j.ijgo.2004.03.009.
Villar J, Ezcurra EJ, Gurtner de la Fuente V, Campodonico L: Preterm delivery syndrome: the unmet need. Research and Clinical Forums. 1994, 16: 9-39.
Belizan JM, Villar J: The relationship between calcium intake and edema-, proteinuria-, and hypertension-getosis: an hypothesis. Am J Clin Nutr. 1980, 33 (10): 2202-2210.
Hamlin R: Prevention of pre-eclampsia. Lancet. 1962, 1: 864-865. 10.1016/S0140-6736(62)91887-1.
Repke JT, Villar J: Pregnancy-induced hypertension and low birth weight: the role of calcium. Am J Clin Nutr. 1991, 54 (1 Suppl): 237S-241S.
Villar J, Belizan JM, Fisher PJ: Epidemiologic observation on the relationship between calcium intake and eclampsia. International Journal of Gynecology & Obstetrics. 1993, 21: 271-278. 10.1016/0020-7292(83)90016-4.
Villar J, Merialdi M, Gulmezoglu AM, Abalos E, Carroli G, Kulier R, de Onis M: Nutritional interventions during pregnancy for the prevention or treatment of maternal morbidity and preterm delivery: an overview of randomized controlled trials. J Nutr. 2003, 133 (5 Suppl 2): 1606S-1625S.
Trumbo PR, Ellwood KC: Supplemental calcium and risk reduction of hypertension, pregnancy-induced hypertension, and preeclampsia: an evidence-based review by the US Food and Drug Administration. Nutr Rev. 2007, 65 (2): 78-87. 10.1111/j.1753-4887.2007.tb00284.x.
Hofmeyr GJ, Atallah AN, Duley L: Calcium supplementation during pregnancy for preventing hypertensive disorders and related problems. Cochrane Database Syst Rev. 2006, 3: CD001059-
Buppasiri P, Lumbiganon P, Thinkhamrop J, Ngamjarus C: Calcium supplementation (other than for preventing or treating hypertension) for improving pregnancy and infant outcomes (Protocol). Cochrane Database of Systematic Reviews. 2008, CD007079-2
Kumar A, Devi SG, Batra S, Singh C, Shukla DK: Calcium supplementation for the prevention of pre-eclampsia. Int J Gynaecol Obstet. 2009, 104 (1): 32-36. 10.1016/j.ijgo.2008.08.027.
Levine RJ, Hauth JC, Curet LB, Sibai BM, Catalano PM, Morris CD, DerSimonian R, Esterlitz JR, Raymond EG, Bild DE, et al: Trial of calcium to prevent preeclampsia. N Engl J Med. 1997, 337 (2): 69-76. 10.1056/NEJM199707103370201.
Duley L, Henderson-Smart DJ, Meher S: Drugs for treatment of very high blood pressure during pregnancy. Cochrane Database Syst Rev. 2006, 3: CD001449-
Geographic variation in the incidence of hypertension in pregnancy: World Health Organization International Collaborative Study of Hypertensive Disorders of Pregnancy. Am J Obstet Gynecol. 1988, 158 (1): 80-83.
Moodley J: Maternal deaths due to hypertensive disorders in pregnancy: Saving Mothers report 2002–2004. Cardiovasc J Afr. 2007, 18 (6): 358-361.
Moodley J: Maternal deaths due to hypertensive disorders in pregnancy. Best Pract Res Clin Obstet Gynaecol. 2008, 22 (3): 559-567. 10.1016/j.bpobgyn.2007.11.004.
Chhabra S, Kakani A: Maternal mortality due to eclamptic and non-eclamptic hypertensive disorders: a challenge. J Obstet Gynaecol. 2007, 27 (1): 25-29. 10.1080/01443610601016800.
Yadav S, Saxena U, Yadav R, Gupta S: Hypertensive disorders of pregnancy and maternal and foetal outcome: a case controlled study. J Indian Med Assoc. 1997, 95 (10): 548-551.
Ananth CV, Savitz DA, Bowes WA: Hypertensive disorders of pregnancy and stillbirth in North Carolina, 1988 to 1991. Acta Obstet Gynecol Scand. 1995, 74 (10): 788-793. 10.3109/00016349509021198.
Rankhethoa NM, Moodley J, Adhikari M, Gouws E: Perinatal outcome of babies born to black South African women with hypertension. East Afr Med J. 1998, 75 (7): 388-391.
Abalos E, Duley L, Steyn DW, Henderson-Smart DJ: Antihypertensive drug therapy for mild to moderate hypertension during pregnancy. Cochrane Database Syst Rev. 2007, CD002252-1
Druzin ML, Charles B, Johnson AL: Editorial summary of symposium on hypertensive disorders of pregnancy. Curr Opin Obstet Gynecol. 2008, 20 (2): 91-
Redman CW: Current topic: pre-eclampsia and the placenta. Placenta. 1991, 12 (4): 301-308. 10.1016/0143-4004(91)90339-H.
Levine RJ, Thadhani R, Qian C, Lam C, Lim KH, Yu KF, Blink AL, Sachs BP, Epstein FH, Sibai BM, et al: Urinary placental growth factor and risk of preeclampsia. JAMA. 2005, 293 (1): 77-85. 10.1001/jama.293.1.77.
Duley L: Pre-eclampsia and the hypertensive disorders of pregnancy. Br Med Bull. 2003, 67: 161-176. 10.1093/bmb/ldg005.
Sibai BM: Caring for women with hypertension in pregnancy. JAMA. 2007, 298 (13): 1566-1568. 10.1001/jama.298.13.1566.
Magee LA, Duley L: Oral beta-blockers for mild to moderate hypertension during pregnancy. Cochrane Database Syst Rev. 2003, CD002863-3
King JF, Flenady VJ, Papatsonis DN, Dekker GA, Carbonne B: Calcium channel blockers for inhibiting preterm labour. Cochrane Database Syst Rev. 2003, CD002255-1
Say L, Gülmezoglu AM, Hofmeyr GJ: Calcium channel blockers for potential impaired fetal growth. Cochrane Database of Systematic Reviews. 1996, CD000049-1
Nabhan AF, Adel A: Tight versus very tight control of mild-moderate pre-existing or non-proteinuric gestational hypertension for improving outcomes. (Protocol). Cochrane Database of Systematic Reviews. 2008, CD006907-1
Mathew D, Khan K, Thornton JG, Todros T: Antibiotics for preventing hypertensive diseases in pregnancy. (Protocol). Cochrane Database of Systematic Reviews. 2007, CD006841-4
Hennessy A, Thornton CE, Makris A, Ogle RF, Henderson-Smart DJ, Gillin AG, Child A: A randomised comparison of hydralazine and mini-bolus diazoxide for hypertensive emergencies in pregnancy: the PIVOT trial. Aust N Z J Obstet Gynaecol. 2007, 47 (4): 279-285. 10.1111/j.1479-828X.2007.00738.x.
Meher S, Duley L: Nitric oxide for preventing pre-eclampsia and its complications. Cochrane Database Syst Rev. 2007, CD006490-2
Sibai BM: Treatment of hypertension in pregnant women. N Engl J Med. 1996, 335 (4): 257-265. 10.1056/NEJM199607253350407.
Podymow T, August P: Update on the use of antihypertensive drugs in pregnancy. Hypertension. 2008, 51 (4): 960-969. 10.1161/HYPERTENSIONAHA.106.075895.
Duley L, Henderson-Smart DJ, Meher S, King JF: Antiplatelet agents for preventing pre-eclampsia and its complications. Cochrane Database Syst Rev. 2007, CD004659-2
Anton L, Brosnihan KB: Systemic and uteroplacental renin – angiotensin system in normal and pre-eclamptic pregnancies. Ther Adv Cardiovasc Dis. 2008, 2 (5): 349-362. 10.1177/1753944708094529.
Burton GJ, Yung HW, Cindrova-Davies T, Charnock-Jones DS: Placental endoplasmic reticulum stress and oxidative stress in the pathophysiology of unexplained intrauterine growth restriction and early onset preeclampsia. Placenta. 2009, 30 (Suppl A): S43-S48. 10.1016/j.placenta.2008.11.003.
Gilbert JS, Nijland MJ, Knoblich P: Placental ischemia and cardiovascular dysfunction in preeclampsia and beyond: making the connections. Expert Rev Cardiovasc Ther. 2008, 6 (10): 1367-1377. 10.1586/14779072.6.10.1367.
James AH, Brancazio LR, Price T: Aspirin and reproductive outcomes. Obstet Gynecol Surv. 2008, 63 (1): 49-57. 10.1097/OGX.0b013e31815e8731.
Patrono C: Aspirin as an antiplatelet drug. N Engl J Med. 1994, 330 (18): 1287-1294. 10.1056/NEJM199405053301808.
Askie LM, Duley L, Henderson-Smart DJ, Stewart LA: Antiplatelet agents for prevention of pre-eclampsia: a meta-analysis of individual patient data. Lancet. 2007, 369 (9575): 1791-1798. 10.1016/S0140-6736(07)60712-0.
Empson M, Lassere M, Craig J, Scott J: Prevention of recurrent miscarriage for women with antiphospholipid antibody or lupus anticoagulant. Cochrane Database Syst Rev. 2005, CD002859-2
Goel N, Tuli A, Choudhry R: The role of aspirin versus aspirin and heparin in cases of recurrent abortions with raised anticardiolipin antibodies. Med Sci Monit. 2006, 12 (3): CR132-136.
Stephenson MD, Ballem PJ, Tsang P, Purkiss S, Ensworth S, Houlihan E, Ensom MH: Treatment of antiphospholipid antibody syndrome (APS) in pregnancy: a randomized pilot trial comparing low molecular weight heparin to unfractionated heparin. J Obstet Gynaecol Can. 2004, 26 (8): 729-734.
Bar J, Cohen-Sacher B, Hod M, Blickstein D, Lahav J, Merlob P: Low-molecular-weight heparin for thrombophilia in pregnant women. Int J Gynaecol Obstet. 2000, 69 (3): 209-213. 10.1016/S0020-7292(00)00202-2.
Glasnovic M, Bosnjak I, Vcev A, Soldo I, Kosuta M, Lenz B, Glasnovic-Horvatic E, Soldo-Butkovic S, Micunovic N: Antibody profile of pregnant women with antiphospholipid syndrome and pregnancy outcome after treatment with low dose aspirin and low-weight-molecular heparin. Coll Antropol. 2007, 31 (1): 173-177.
Malinowski A, Dynski MA, Maciolek-Blewniewska G, Glowacka E, Pawlowski T, Babula G: [Treatment outcome in women suffering from recurrent miscarriages and antiphospholipid syndrome]. Ginekol Pol. 2003, 74 (10): 1213-1222.
Noble LS, Kutteh WH, Lashey N, Franklin RD, Herrada J: Antiphospholipid antibodies associated with recurrent pregnancy loss: prospective, multicenter, controlled pilot study comparing treatment with low-molecular-weight heparin versus unfractionated heparin. Fertil Steril. 2005, 83 (3): 684-690. 10.1016/j.fertnstert.2004.11.002.
Carp H, Dolitzky M, Inbal A: Thromboprophylaxis improves the live birth rate in women with consecutive recurrent miscarriages and hereditary thrombophilia. J Thromb Haemost. 2003, 1 (3): 433-438. 10.1046/j.1538-7836.2003.00066.x.
Ruffatti A, Orsini A, Di Lenardo L, Nardelli GB, Patrassi GM, Truscia D, Brigato G, Grella P, Todesco S: A prospective study of fifty-three consecutive calcium heparin treated pregnancies in patients with antiphospholipid antibody-related fetal loss. Clin Exp Rheumatol. 1997, 15 (5): 499-505.
Di Nisio M, Peters L, Middeldorp S: Anticoagulants for the treatment of recurrent pregnancy loss in women without antiphospholipid syndrome. Cochrane Database Syst Rev. 2005, CD004734-2
Dodd JM, Kingdom J, McLeod A, Windrim RC: Antithrombotic therapy for improving maternal or infant health outcomes in women considered at risk of placental dysfunction. (Protocol). Cochrane Database of Systematic Reviews. 2007, CD006780-4
Gates S, Brocklehurst P, Davis LJ: Prophylaxis for venous thromboembolic disease in pregnancy and the early postnatal period. Cochrane Database Syst Rev. 2002, CD001689-2
Folkeringa N, Brouwer JL, Korteweg FJ, Veeger NJ, Erwich JJ, Holm JP, Meer van der J: Reduction of high fetal loss rate by anticoagulant treatment during pregnancy in antithrombin, protein C or protein S deficient women. Br J Haematol. 2007, 136 (4): 656-661. 10.1111/j.1365-2141.2006.06480.x.
Gris JC, Mercier E, Quere I, Lavigne-Lissalde G, Cochery-Nouvellon E, Hoffet M, Ripart-Neveu S, Tailland ML, Dauzat M, Mares P: Low-molecular-weight heparin versus low-dose aspirin in women with one fetal loss and a constitutional thrombophilic disorder. Blood. 2004, 103 (10): 3695-3699. 10.1182/blood-2003-12-4250.
Dendrinos S, Kalogirou I, Makrakis E, Theodoridis T, Mahmound EA, Christopoulou-Cokkinou V, Creatsas G: Safety and effectiveness of tinzaparin sodium in the management of recurrent pregnancy loss. Clin Exp Obstet Gynecol. 2007, 34 (3): 143-145.
Deligiannidis A, Parapanissiou E, Mavridis P, Tabakoudis G, Mavroudi A, Papastavrou T, Tabakoudis P: Thrombophilia and antithrombotic therapy in women with recurrent spontaneous abortions. J Reprod Med. 2007, 52 (6): 499-502.
Kim KH, Jeong DS, Ahn H: Anticoagulation in pregnant women with a bileaflet mechanical cardiac valve replacement. Heart Surg Forum. 2007, 10 (4): E267-270. 10.1532/HSF98.20071024.
Lee JH, Park NH, Keum DY, Choi SY, Kwon KY, Cho CH: Low molecular weight heparin treatment in pregnant women with a mechanical heart valve prosthesis. J Korean Med Sci. 2007, 22 (2): 258-261. 10.3346/jkms.2007.22.2.258.
Kawamata K, Neki R, Yamanaka K, Endo S, Fukuda H, Ikeda T, Douchi T: Risks and pregnancy outcome in women with prosthetic mechanical heart valve replacement. Circ J. 2007, 71 (2): 211-213. 10.1253/circj.71.211.
Dolitzky M, Inbal A, Segal Y, Weiss A, Brenner B, Carp H: A randomized study of thromboprophylaxis in women with unexplained consecutive recurrent miscarriages. Fertil Steril. 2006, 86 (2): 362-366. 10.1016/j.fertnstert.2005.12.068.
Sorensen HT, Johnsen SP, Larsen H, Pedersen L, Nielsen GL, Moller M: Birth outcomes in pregnant women treated with low-molecular-weight heparin. Acta Obstet Gynecol Scand. 2000, 79 (8): 655-659. 10.1034/j.1600-0412.2000.079008655.x.
Tulppala M, Marttunen M, Soderstrom-Anttila V, Ailus K, Palosuo T, Ylikorkala O: Low dose aspirin in the prevention of miscarriage in women with unexplained or autoimmune related recurrent miscarriage: effect on prostacyclin and thromboxane A2 production. Human Reproduction. 1997, 12: 191-10.1093/humrep/12.7.1567.
Tulppala M, Marttunen M, Soderstrom-Anttila V, Foudila T, Ailus K, Palosuo T, Ylikorkala O: Low-dose aspirin in prevention of miscarriage in women with unexplained or autoimmune related recurrent miscarriage: effect on prostacyclin and thromboxane A2 production. Hum Reprod. 1997, 12 (7): 1567-1572. 10.1093/humrep/12.7.1567.
Kontic-Vucinic O, Terzic M, Radunovic N: The role of antioxidant vitamins in hypertensive disorders of pregnancy. J Perinat Med. 2008, 36 (4): 282-290. 10.1515/JPM.2008.063.
Hubel CA, Kagan VE, Kisin ER, McLaughlin MK, Roberts JM: Increased ascorbate radical formation and ascorbate depletion in plasma from women with preeclampsia: implications for oxidative stress. Free Radic Biol Med. 1997, 23 (4): 597-609. 10.1016/S0891-5849(97)00010-5.
Wang Y, Walsh SW: Antioxidant activities and mRNA expression of superoxide dismutase, catalase, and glutathione peroxidase in normal and preeclamptic pregnancies. Journal of the Society for Gynecological Investigation. 1996, 3: 179-184. 10.1016/1071-5576(96)00015-9.
Rumbold A, Duley L, Crowther CA, Haslam RR: Antioxidants for preventing pre-eclampsia. Cochrane Database Syst Rev. 2008, CD004227-1
Rumbold A, Crowther CA: Vitamin C supplementation in pregnancy. Cochrane Database Syst Rev. 2005, CD004072-2
Rumbold A, Crowther CA: Vitamin E supplementation in pregnancy. Cochrane Database Syst Rev. 2005, CD004069-2
Roberts JM: A randomized controlled trial of antioxidant vitamins to prevent serious complications associated with pregnancy-related hypertension in low-risk nulliparous women. Am J Obstet Gynecol. 2008, 199 (6 Supplement 1): S4-10.1016/j.ajog.2008.09.034.
Darmstadt GL, Yakoob MY, Haws RA, Menezes EV, Soomro T, Bhutta ZA: Reducing stillbirths: interventions during labour. BMC Pregnancy and Childbirth. 2009, 9 (Suppl 1): S6-10.1186/1471-2393-9-S1-S6.
Binder T, Salaj P, Zima T, Vitek L: Randomized prospective comparative study of ursodeoxycholic acid and S-adenosyl-L-methionine in the treatment of intrahepatic cholestasis of pregnancy. J Perinat Med. 2006, 34 (5): 383-391. 10.1515/JPM.2006.077.
Glantz A, Marschall HU, Lammert F, Mattsson LA: Intrahepatic cholestasis of pregnancy: a randomized controlled trial comparing dexamethasone and ursodeoxycholic acid. Hepatology. 2005, 42 (6): 1399-1405. 10.1002/hep.20952.
Palma J, Reyes H, Ribalta J, Hernandez I, Sandoval L, Almuna R, Liepins J, Lira F, Sedano M, Silva O, et al: Ursodeoxycholic acid in the treatment of cholestasis of pregnancy: a randomized, double-blind study controlled with placebo. J Hepatol. 1997, 27 (6): 1022-1028. 10.1016/S0168-8278(97)80146-8.
Roncaglia N, Arreghini A, Locatelli A, Bellini P, Andreotti C, Ghidini A: Obstetric cholestasis: outcome with active management. Eur J Obstet Gynecol Reprod Biol. 2002, 100 (2): 167-170. 10.1016/S0301-2115(01)00463-8.
Lockshin MD: Pregnancy loss and antiphospholipid antibodies. Lupus. 1998, 7 (Suppl 2): S86-89. 10.1177/096120339800700219.
Yoshida H, Ito K, Kusakari T, Ida K, Ihara Y, Mori T, Matsumura M: Removal of maternal antibodies from a woman with repeated fetal loss due to P blood group incompatibility. Transfusion. 1994, 34 (8): 702-705. 10.1046/j.1537-2995.1994.34894353467.x.
Rock JA, Shirey RS, Braine HG, Ness PM, Kickler TS, Niebyl JR: Plasmapheresis for the treatment of repeated early pregnancy wastage associated with anti-P. Obstet Gynecol. 1985, 66 (3 Suppl): 57S-60S.
El-Haieg DO, Zanati MF, El-Foual FM: Plasmapheresis and pregnancy outcome in patients with antiphospholipid syndrome. Int J Gynaecol Obstet. 2007, 99 (3): 236-241. 10.1016/j.ijgo.2007.05.045.
Angela E, Robinson E, Tovey LA: Intensive plasma exchange in the management of severe Rh disease. Br J Haematol. 1980, 45 (4): 621-631. 10.1111/j.1365-2141.1980.tb07185.x.
Simcox R, Shennan A: Cervical cerclage in the prevention of preterm birth. Best Pract Res Clin Obstet Gynaecol. 2007, 21 (5): 831-842. 10.1016/j.bpobgyn.2007.03.009.
Drakeley AJ, Roberts D, Alfirevic Z: Cervical stitch (cerclage) for preventing pregnancy loss in women. Cochrane Database Syst Rev. 2003, CD003253-1
Berghella V, Seibel-Seamon J: Contemporary use of cervical cerclage. Clin Obstet Gynecol. 2007, 50 (2): 468-477. 10.1097/GRF.0b013e31804bddfd.
Shirodkar VN: A new method of operative treatment for habitual abortions in the second trimester of pregnancy. Antiseptic. 1955, 52: 299-300.
McDonald IA: Suture of the cervix for inevitable miscarriage. J Obstet Gynaecol Br Emp. 1957, 64 (3): 346-350.
Rozenberg P, Senat MV, Gillet A, Ville Y: Comparison of two methods of cervical cerclage by ultrasound cervical measurement. J Matern Fetal Neonatal Med. 2003, 13 (5): 314-317. 10.1080/713605888.
Odibo AO, Berghella V, To MS, Rust OA, Althuisius SM, Nicolaides KH: Shirodkar versus McDonald cerclage for the prevention of preterm birth in women with short cervical length. Am J Perinatol. 2007, 24 (1): 55-60. 10.1055/s-2006-958165.
Drakeley AJ, Roberts D, Alfirevic Z: Cervical cerclage for prevention of preterm delivery: meta-analysis of randomized trials. Obstet Gynecol. 2003, 102 (3): 621-627. 10.1016/S0029-7844(03)00673-2.
Owen J: Multicenter randomized trial of cerclage for preterm birth prevention in high-risk women with shortened mid-trimester cervical length. Am J Obstet Gynecol. 2008, S3-10.1016/j.ajog.2008.09.030. Suppl
Jorgensen AL, Alfirevic Z, Tudur Smith C, Williamson PR: Cervical stitch (cerclage) for preventing pregnancy loss: individual patient data meta-analysis. BJOG. 2007, 114 (12): 1460-1476. 10.1111/j.1471-0528.2007.01515.x.
Blair O, Fletcher H, Kulkarni S: A randomised controlled trial of outpatient versus inpatient cervical cerclage. J Obstet Gynaecol. 2002, 22 (5): 493-497. 10.1080/0144361021000003618.
Fick AL, Caughey AB, Parer JT: Transabdominal cerclage: can we predict who fails?. J Matern Fetal Neonatal Med. 2007, 20 (1): 63-67. 10.1080/14767050601059156.
Gesson-Paute A, Berrebi A, Parant O: [Transabdominal cervico-isthmic cerclage in the management of cervical incompetence in high risk women]. J Gynecol Obstet Biol Reprod (Paris). 2007, 36 (1): 30-35.
Debbs RH, DeLa Vega GA, Pearson S, Sehdev H, Marchiano D, Ludmir J: Transabdominal cerclage after comprehensive evaluation of women with previous unsuccessful transvaginal cerclage. Am J Obstet Gynecol. 2007, 197 (3): 317-10.1016/j.ajog.2007.06.060. e311–314.
Final report of the Medical Research Council/Royal College of Obstetricians and Gynaecologists multicentre randomised trial of cervical cerclage. MRC/RCOG Working Party on Cervical Cerclage. Br J Obstet Gynaecol. 1993, 100 (6): 516-523.
Seshadri S: Nutritional anaemia in South Asia. Malnutrition in South Asia: a Regional Profile. Kathmandu. Edited by: Gillespie S. 1997, United Nations Children's Fund, 75-124.
Torlesse H, Hodges M: Albendazole therapy and reduced decline in Hb concentration during pregnancy (Sierra Leone). Trans R Soc Trop Med Hyg. 2001, 95: 195-201. 10.1016/S0035-9203(01)90164-6.
Torlesse HHM: Antihelminthic treatment and haemoglobin concentrations during pregnancy. Lancet. 2000, 356: 1083-10.1016/S0140-6736(00)02738-0.
Larocque R, Casapia M, Gotuzzo E, MacLean JD, Soto JC, Rahme E, Gyorkos TW: A double-blind randomized controlled trial of antenatal mebendazole to reduce low birthweight in a hookworm-endemic area of Peru. Trop Med Int Health. 2006, 11 (10): 1485-1495. 10.1111/j.1365-3156.2006.01706.x.
Haider BA, Bhutta ZA: Effects of interventions for helminthic infections in pregnancy (Protocol). Cochrane Database of Systematic Reviews. 2005, CD005547-DOI: 10.1002/14651858.CD005547., 4
Diav-Citrin O, Shechtman S, Arnon J, Lubart I, Ornoy A: Pregnancy outcome after gestational exposure to mebendazole: a prospective controlled cohort study. Am J Obstet Gynecol. 2003, 188 (1): 282-285. 10.1067/mob.2003.79.
Ndyomugyenyi R, Kabatereine N, Olsen A, Magnussen P: Efficacy of ivermectin and albendazole alone and in combination for treatment of soil-transmitted helminths in pregnancy and adverse events: a randomized open label controlled intervention trial in Masindi district, western Uganda. Am J Trop Med Hyg. 2008, 79 (6): 856-863.
Gyorkos TW, Larocque R, Casapia M, Gotuzzo E: Lack of risk of adverse birth outcomes after deworming in pregnant women. Pediatr Infect Dis J. 2006, 25 (9): 791-794. 10.1097/01.inf.0000234068.25760.97.
Torlesse H, Hodges M: Anthelminthic treatment and haemoglobin concentrations during pregnancy. Lancet. 2000, 356 (9235): 1083-10.1016/S0140-6736(00)02738-0.
Torlesse H, Hodges M: Albendazole therapy and reduced decline in haemoglobin concentration during pregnancy (Sierra Leone). Trans R Soc Trop Med Hyg. 2001, 95 (2): 195-201. 10.1016/S0035-9203(01)90164-6.
de Silva NR, Sirisena JL, Gunasekera DP, Ismail MM, de Silva HJ: Effect of mebendazole therapy during pregnancy on birth outcome. Lancet. 1999, 353 (9159): 1145-1149. 10.1016/S0140-6736(98)06308-9.
Christian P, Khatry SK, West KP: Antenatal anthelmintic treatment, birthweight, and infant survival in rural Nepal. Lancet. 2004, 364 (9438): 981-983. 10.1016/S0140-6736(04)17023-2.
Bhutta ZA, Ahmed T, Black RE, Cousens S, Dewey K, Giugliani E, Haider BA, Kirkwood B, Morris SS, Sachdev HP, et al: What works? Interventions for maternal and child undernutrition and survival. Lancet. 2008, 371 (9610): 417-440. 10.1016/S0140-6736(07)61693-6.
Hook EW: Treatment of syphilis: current recommendations, alternatives, and continuing problems. Rev Infect Dis. 1989, 11 (Suppl 6): S1511-1517.
Hook EW, Marra CM: Acquired syphilis in adults. N Engl J Med. 1992, 326 (16): 1060-1069. 10.1056/NEJM199204163261606.
Finelli L, Berman SM, Koumans EH, Levine WC: Congenital syphilis. Bull World Health Organ. 1998, 76 (Suppl 2): 126-128.
Walker GJ, Walker DG: Congenital syphilis: a continuing but neglected problem. Semin Fetal Neonatal Med. 2007, 12 (3): 198-206. 10.1016/j.siny.2007.01.019.
Myer L, Wilkinson D, Lombard C, Zuma K, Rotchford K, Karim SS: Impact of on-site testing for maternal syphilis on treatment delays, treatment rates, and perinatal mortality in rural South Africa: a randomised controlled trial. Sex Transm Infect. 2003, 79 (3): 208-213. 10.1136/sti.79.3.208.
Walker GJ: Antibiotics for syphilis diagnosed during pregnancy. Cochrane Database Syst Rev. 2001, CD001143-3
Guinness LF, Sibandze S, McGrath E, Cornelis AL: Influence of antenatal screening on perinatal mortality caused by syphilis in Swaziland. Genitourin Med. 1988, 64 (5): 294-297.
Temmerman M, Gichangi P, Fonck K, Apers L, Claeys P, Van Renterghem L, Kiragu D, Karanja G, Ndinya-Achola J, Bwayo J: Effect of a syphilis control programme on pregnancy outcome in Nairobi, Kenya. Sex Transm Infect. 2000, 76 (2): 117-121. 10.1136/sti.76.2.117.
Watson-Jones D, Gumodoka B, Weiss H, Changalucha J, Todd J, Mugeye K, Buve A, Kanga Z, Ndeki L, Rusizoka M, et al: Syphilis in pregnancy in Tanzania. II. The effectiveness of antenatal syphilis screening and single-dose benzathine penicillin treatment for the prevention of adverse pregnancy outcomes. J Infect Dis. 2002, 186 (7): 948-957. 10.1086/342951.
Donders GG, Desmyter J, Hooft P, Dewet GH: Apparent failure of one injection of benzathine penicillin G for syphilis during pregnancy in human immunodeficiency virus-seronegative African women. Sex Transm Dis. 1997, 24 (2): 94-101. 10.1097/00007435-199702000-00007.
Rotchford K, Lombard C, Zuma K, Wilkinson D: Impact on perinatal mortality of missed opportunities to treat maternal syphilis in rural South Africa: baseline results from a clinic randomized controlled trial. Trop Med Int Health. 2000, 5 (11): 800-804. 10.1046/j.1365-3156.2000.00636.x.
Bique Osman N, Challis K, Folgosa E, Cotiro M, Bergström S: An intervention study to reduce adverse pregnancy outcomes as a result of syphilis in Mozambique. Sexually Transmitted Infections. 2000, 76: 203-207. 10.1136/sti.76.3.203.
Thinkhamrop J: Antibiotics for treating bacterial vaginosis in pregnancy: RHL commentary. Geneva: World Health Organization, last revised: 4 July 2007.
Whalley P: Bacteriuria of pregnancy. Am J Obstet Gynecol. 1967, 97 (5): 723-738.
Olsen BE, Hinderaker SG, Lie RT, Gasheka P, Baerheim A, Bergsjo P, Kvale G: The diagnosis of urinary tract infections among pregnant women in rural Tanzania; prevalences and correspondence between different diagnostic methods. Acta Obstet Gynecol Scand. 2000, 79 (9): 729-736. 10.1034/j.1600-0412.2000.079009729.x.
Akerele J, Abhulimen P, Okonofua F: Prevalance of asymptomatic bacteriuria among pregnant women in Benin City, Nigeria. Journal of Obstetrics and Gynaecology. 2001, 21: 141-144. 10.1080/01443610020026038.
Akinloye O, Ogbolu DO, Akinloye OM, Terry Alli OA: Asymptomatic bacteriuria of pregnancy in Ibadan, Nigeria: a re-assessment. Br J Biomed Sci. 2006, 63 (3): 109-112.
Tadesse A, Negash M, Ketema LS: Asymtomatic bacteriuria in pregnancy: assesment of prevlence, microbial agents and ther antimicrobial sensitivty pattern in Gondar Teaching Hospital, north west Ethiopia. Ethiop Med J. 2007, 45 (2): 143-149.
Olusanya O, Ogunledun A, Fakoya TA: Asymptomatic significant bacteriuria among pregnant and non-pregnant women in Sagamu, Nigeria. West Afr J Med. 1993, 12 (1): 27-33.
Mathai E, Thomas RJ, Chandy S, Mathai M, Bergstrom S: Antimicrobials for the treatment of urinary tract infection in pregnancy: practices in southern India. Pharmacoepidemiol Drug Saf. 2004, 13 (9): 645-652. 10.1002/pds.950.
Turck MGB, Petersdorf RG: Bacteriuria in pregnancy; relationship to socioeconomic factors. N Engl J Med. 1962, 266: 857-860. 10.1056/NEJM196204262661703.
King J, Flenady V: Prophylactic antibiotics for inhibiting preterm labour with intact membranes. Cochrane Database Syst Rev. 2002, CD000246-4
McDonald HM, Brocklehurst P, Gordon A: Antibiotics for treating bacterial vaginosis in pregnancy. Cochrane Database Syst Rev. 2007, CD000262-1
Lumbiganon P, Thinkhamrop J, Thinkhamrop B, Tolosa JE: Vaginal chlorhexidine during labour for preventing maternal and neonatal infections (excluding Group B Streptococcal and HIV). Cochrane Database Syst Rev. 2004, CD004070-4
Goldenberg RL, McClure EM, Saleem S, Rouse D, Vermund S: Use of vaginally administered chlorhexidine during labor to improve pregnancy outcomes. Obstet Gynecol. 2006, 107 (5): 1139-1146.
Taha TE, Biggar RJ, Broadhead RL, Mtimavalye LA, Justesen AB, Liomba GN, Chiphangwi JD, Miotti PG: Effect of cleansing the birth canal with antiseptic solution on maternal and newborn morbidity and mortality in Malawi: clinical trial. BMJ. 1997, 315 (7102): 216-219. discussion 220.
Bakr AF, Karkour T: Effect of predelivery vaginal antisepsis on maternal and neonatal morbidity and mortality in Egypt. J Womens Health (Larchmt). 2005, 14 (6): 496-501. 10.1089/jwh.2005.14.496.
Thinkhamrop J, Hofmeyr GJ, Adetoro O, Lumbiganon P: Prophylactic antibiotic administration in pregnancy to prevent infectious morbidity and mortality. Cochrane Database Syst Rev. 2002, CD002250-4
Dykes AK, Christensen KK, Christensen P: Chlorhexidine for prevention of neonatal colonization with group B streptococci. IV. Depressed puerperal carriage following vaginal washing with chlorhexidine during labour. Eur J Obstet Gynecol Reprod Biol. 1987, 24 (4): 293-297. 10.1016/0028-2243(87)90154-7.
Bejar R, Curbelo V, Davis C, Gluck L: Premature labor. II. Bacterial sources of phospholipase. Obstet Gynecol. 1981, 57 (4): 479-482.
Yoon BH, Romero R, Park JS, Kim M, Oh SY, Kim CJ, Jun JK: The relationship among inflammatory lesions of the umbilical cord (funisitis), umbilical cord plasma interleukin 6 concentration, amniotic fluid infection, and neonatal sepsis. Am J Obstet Gynecol. 2000, 183 (5): 1124-1129. 10.1067/mob.2000.109035.
Kenyon S, Boulvain M, Neilson J: Antibiotics for preterm rupture of membranes. Cochrane Database Syst Rev. 2003, CD001058-2
Flenady V, King J: Antibiotics for prelabour rupture of membranes at or near term. Cochrane Database of Systematic Reviews. 2002, 3: CD001807-
Rugemalila JB, Wanga CL, Kilama WL: Sixth Africa Malaria Day in 2006: how far have we come after the Abuja Declaration?. Malar J. 2006, 5: 102-10.1186/1475-2875-5-102.
Uneke CJ: Impact of placental Plasmodium falciparum malaria on pregnancy and perinatal outcome in sub-Saharan Africa: part III: placental malaria, maternal health, and public health. Yale J Biol Med. 2008, 81 (1): 1-7.
Lagerberg RE: Malaria in pregnancy: a literature review. J Midwifery Womens Health. 2008, 53 (3): 209-215. 10.1016/j.jmwh.2008.02.012.
Garner P, Gulmezoglu AM: Drugs for preventing malaria in pregnant women. Cochrane Database Syst Rev. 2006, CD000169-4
Hamer DH, et al: Two-Dose versus monthly intermittent preventive treatment of malaria with sulfdoxine-pyrimethamine (SP) in HIV-seropositive pregnant Zambian women. J Infect Dis. 2007, 196: 1585-1594. 10.1086/522142.
WHO: Guidelines for the treatment of malaria. 2006, Geneva: World Health Organization
D'Alessandro U, ter Kuile FO: Amodiaquine, malaria, pregnancy: the old new drug. Lancet. 2006, 368 (9544): 1306-1307. 10.1016/S0140-6736(06)69532-9.
Hutagalung R, Paiphun L, Ashley EA, McGready R, Brockman A, Thwai KL, Singhasivanon P, Jelinek T, White NJ, Nosten FH: A randomized trial of artemether-lumefantrine versus mefloquine-artesunate for the treatment of uncomplicated multi-drug resistant Plasmodium falciparum on the western border of Thailand. Malar J. 2005, 4: 46-10.1186/1475-2875-4-46.
Guyatt HL, Snow RW: Malaria in pregnancy as an indirect cause of infant mortality in sub-Saharan Africa. Trans R Soc Trop Med Hyg. 2001, 95 (6): 569-576. 10.1016/S0035-9203(01)90082-3.
Gamble C, Ekwaru JP, ter Kuile FO: Insecticide-treated nets for preventing malaria in pregnancy. Cochrane Database Syst Rev. 2006, CD003755-2
World Health Organization: The African summit on Roll Back Malaria. accessed 21 November 2001., [http://mosquito.who.int/docs/abuja_declaration.pdf]
Njagi J: The effects of sulfadoxine-pyrimethamine intermittent treatment and pyrethroid impregnated bed nets on malaria morbidity and birth weight in Bondo district, Kenya [dissertation]. 2002, Nairobi: University of Nairobi; Copenhagen Danish Bilharziasis Laboratory, 129-
ter Kuile FO, Terlouw DJ, Phillips-Howard PA, Hawley WA, Friedman JF, Kariuki SK, Shi YP, Kolczak MS, Lal AA, Vulule JM, et al: Reduction of malaria during pregnancy by permethrin-treated bed nets in an area of intense perennial malaria transmission in western Kenya. Am J Trop Med Hyg. 2003, 68 (4 Suppl): 50-60.
Shulman CEDE, Talisuna AO, Lowe BS, Nevill C, Snow RW, et al: A community randomized controlled trial of insecticide-treated bednets for the prevention of malaria and anaemia among primigravid women on the Kenyan coast. Tropical Medicine and International Health. 1998, 3: 197-204. 10.1046/j.1365-3156.1998.00214.x.
Volmink J, Siegfried NL, Merwe van der L, Brocklehurst P: Antiretrovirals for reducing the risk of mother-to-child transmission of HIV infection. Cochrane Database Syst Rev. 2007, CD003510-1
Suksomboon N, Poolsup N, Ket-Aim S: Systematic review of the efficacy of antiretroviral therapies for reducing the risk of mother-to-child transmission of HIV infection. J Clin Pharm Ther. 2007, 32 (3): 293-311. 10.1111/j.1365-2710.2007.00825.x.
Tuomala RE, Shapiro DE, Mofenson LM, Bryson Y, Culnane M, Hughes MD, O'Sullivan MJ, Scott G, Stek AM, Wara D, et al: Antiretroviral therapy during pregnancy and the risk of an adverse outcome. N Engl J Med. 2002, 346 (24): 1863-1870. 10.1056/NEJMoa991159.
Bussmann H, et al: Pregnancy rates and birth outcomes among women on efavirenz-containing highly active antiretroviral therapy in Botswana. J Acquir Immune Defic Syndr. 2007, 45: 269-273.
Townsend CL, Cortina-Borja M, Peckham CS, Tookey PA: Antiretroviral therapy and premature delivery in diagnosed HIV-infected women in the United Kingdom and Ireland. AIDS. 2007, 21 (8): 1019-1026. 10.1097/QAD.0b013e328133884b.
Tonwe-Gold B, Ekouevi DK, Viho I, Amani-Bosse C, Toure S, Coffie PA, Rouet F, Becquet R, Leroy V, El-Sadr WM, et al: Antiretroviral treatment and prevention of peripartum and postnatal HIV transmission in West Africa: evaluation of a two-tiered approach. PLoS Med. 2007, 4 (8): e257-10.1371/journal.pmed.0040257.
Sharma A, Feldman JG, Golub ET, Schmidt J, Silver S, Robison E, Minkoff H: Live birth patterns among human immunodeficiency virus-infected women before and after the availability of highly active antiretroviral therapy. Am J Obstet Gynecol. 2007, 196 (6): 541.e1-6. 10.1016/j.ajog.2007.01.005.
Wiysonge CS, Shey MS, Sterne JA, Brocklehurst P: Vitamin A supplementation for reducing the risk of mother-to-child transmission of HIV infection. Cochrane Database Syst Rev. 2005, CD003648-4
Wimmer G, Pihlstrom BL: A critical assessment of adverse pregnancy outcome and periodontal disease. J Clin Periodontol. 2008, 35 (8 Suppl): 380-397. 10.1111/j.1600-051X.2008.01284.x.
Novak MJ, Novak KF, Hodges JS, Kirakodu S, Govindaswami M, Diangelis A, Buchanan W, Papapanou PN, Michalowicz BS: Periodontal bacterial profiles in pregnant women: response to treatment and associations with birth outcomes in the obstetrics and periodontal therapy (OPT) study. J Periodontol. 2008, 79 (10): 1870-1879. 10.1902/jop.2008.070554.
Xiong X, Buekens P, Fraser WD, Beck J, Offenbacher S: Periodontal disease and adverse pregnancy outcomes: a systematic review. BJOG. 2006, 113 (2): 135-143. 10.1111/j.1471-0528.2005.00827.x.
Jeffcoat MK, Geurs NC, Reddy MS, Goldenberg RL, Hauth JC: Current evidence regarding periodontal disease as a risk factor in preterm birth. Ann Periodontol. 2001, 6 (1): 183-188. 10.1902/annals.2001.6.1.183.
Farrell S, Ide M, Wilson RF: The relationship between maternal periodontitis, adverse pregnancy outcome and miscarriage in never smokers. J Clin Periodontol. 2006, 33 (2): 115-120. 10.1111/j.1600-051X.2005.00884.x.
Xiong X, Buekens P, Vastardis S, Yu SM: Periodontal disease and pregnancy outcomes: state-of-the-science. Obstet Gynecol Surv. 2007, 62 (9): 605-615. 10.1097/01.ogx.0000279292.63435.40.
Tarannum F, Faizuddin M: Effect of periodontal therapy on pregnancy outcome in women affected by periodontitis. J Periodontol. 2007, 78 (11): 2095-2103. 10.1902/jop.2007.060388.
Mobeen N, Jehan I, Banday N, Moore J, McClure EM, Pasha O, Wright LL, Goldenberg RL: Periodontal disease and adverse birth outcomes: a study from Pakistan. Am J Obstet Gynecol. 2008, 198 (5): 514-10.1016/j.ajog.2008.03.010. e511–518.
Macones G, Jeffcoat M, Parry S, Sammel M, Ludmir J, Cohen A, Nelson D, Stamilio D, Clothier B, Strauss J: Screening and treating periodontal disease in pregnancy does not reduce the incidence of preterm birth: results from the PIPS Study. Am J Obstet Gynecol. 2008, S3-10.1016/j.ajog.2008.09.031. Suppl
Offenbacher S, Beck J, Jared H, Mauriello S, Mendoza L, Couper D, Stewart D, Murtha A, Cochran D, Dudley D, et al: Maternal oral therapy to reduce obstetric risk (MOTOR): A report of a multi-centered periodontal therapy randomized-controlled trial on rate of preterm delivery. American Journal of Obstetrics and Gynecology. 2008, 199 (6 Supplement 1): S2-10.1016/j.ajog.2008.09.029.
Michalowicz BS, Hodges JS, DiAngelis AJ, Lupo VR, Novak MJ, Ferguson JE, Buchanan W, Bofill J, Papapanou PN, Mitchell DA, et al: Treatment of periodontal disease and the risk of preterm birth. N Engl J Med. 2006, 355 (18): 1885-1894. 10.1056/NEJMoa062249.
Vergnes JN: Studies suggest an association between maternal periodontal disease and pre-eclampsia. Evid Based Dent. 2008, 9 (2): 46-47. 10.1038/sj.ebd.6400580.
McClure EM, Saleem S, Pasha O, Goldenberg RL: Stillbirth in developing countries: a review of causes, risk factors and prevention strategies. J Matern Fetal Neonatal Med. 2009, 22 (3): 183-190. 10.1080/14767050802559129.
Watson-Jones D, Weiss HA, Changalucha JM, Todd J, Gumodoka B, Bulmer J, Balira R, Ross D, Mugeye K, Hayes R, et al: Adverse birth outcomes in United Republic of Tanzania – impact and prevention of maternal risk factors. Bull World Health Organ. 2007, 85 (1): 9-18.
Hofmeyr GJ, Duley L, Atallah A: Dietary calcium supplementation for prevention of pre-eclampsia and related problems: a systematic review and commentary. BJOG. 2007, 114 (8): 933-943. 10.1111/j.1471-0528.2007.01389.x.
Bott-Kanner G, Schweitzer A, Reisner SH, Joel-Cohen SJ, Rosenfeld JB: Propranolol and hydrallazine in the management of essential hypertension in pregnancy. Br J Obstet Gynaecol. 1980, 87 (2): 110-114.
Duley L, Henderson-Smart D, Knight M, King J: Antiplatelet drugs for prevention of pre-eclampsia and its consequences: systematic review. BMJ. 2001, 322 (7282): 329-333. 10.1136/bmj.322.7282.329.
Uzan S, Beaufils M, Breart G, Bazin B, Capitant C, Paris J: Prevention of fetal growth retardation with low-dose aspirin: findings of the EPREDA trial. Lancet. 1991, 337 (8755): 1427-1431. 10.1016/0140-6736(91)93124-R.
Tempfer CB, Kurz C, Bentz EK, Unfried G, Walch K, Czizek U, Huber JC: A combination treatment of prednisone, aspirin, folate, and progesterone in women with idiopathic recurrent miscarriage: a matched-pair study. Fertil Steril. 2006, 86 (1): 145-148. 10.1016/j.fertnstert.2005.12.035.
Backos M, Rai R, Baxter N, Chilcott IT, Cohen H, Regan L: Pregnancy complications in women with recurrent miscarriage associated with antiphospholipid antibodies treated with low dose aspirin and heparin. Br J Obstet Gynaecol. 1999, 106 (2): 102-107.
Leduc L, Dubois E, Takser L, Rey E, David M: Dalteparin and low-dose aspirin in the prevention of adverse obstetric outcomes in women with inherited thrombophilia. J Obstet Gynaecol Can. 2007, 29 (10): 787-793.
Brenner B, Hoffman R, Carp H, Dulitsky M, Younis J: Efficacy and safety of two doses of enoxaparin in women with thrombophilia and recurrent pregnancy loss: the LIVE-ENOX study. J Thromb Haemost. 2005, 3 (2): 227-229. 10.1111/j.1538-7836.2004.01090.x.
Sarig G, Blumenfeld Z, Leiba R, Lanir N, Brenner B: Modulation of systemic hemostatic parameters by enoxaparin during gestation in women with thrombophilia and pregnancy loss. Thromb Haemost. 2005, 94 (5): 980-985.
Franklin RD, Kutteh WH: Antiphospholipid antibodies (APA) and recurrent pregnancy loss: treating a unique APA positive population. Hum Reprod. 2002, 17 (11): 2981-2985. 10.1093/humrep/17.11.2981.
Jaswal A, Manaktala U, Sharma JB: Cervical cerclage in expectant management of placenta previa. Int J Gynaecol Obstet. 2006, 93 (1): 51-52. 10.1016/j.ijgo.2005.12.025.
Delport SD: On-site screening for maternal syphilis in an antenatal clinic. S Afr Med J. 1993, 83 (10): 723-724.
Tita AT, Cliver SP, Goepfert AR, Conner M, Goldenberg RL, Hauth JC, Andrews WW: Clinical trial of interconceptional antibiotics to prevent preterm birth: subgroup analyses and possible adverse antibiotic-microbial interaction. Am J Obstet Gynecol. 2007, 197 (4): 367-10.1016/j.ajog.2007.06.028. e361–366.
Kenyon S, Taylor DJ, Tarnow-Mordi WO, ORACLE Collaborative Group: ORACLE – antibiotics for preterm prelabour rupture of the membranes: short-term and long-term outcomes. Acta Paediatr Suppl. 2002, 91: 12-15. 10.1080/08035250260095735.
Verhoeff FH, Brabin BJ, Chimsuku L, Kazembe P, Broadhead RL: Malaria in pregnancy and its consequences for the infant in rural Malawi. Ann Trop Med Parasitol. 1999, 93 (Suppl 1): S25-33. 10.1080/00034989957718.
Gamble C: Insecticide-treated nets for the prevention of malaria in pregnancy: a systematic review of randomized controlled trials. PLoS Med. 2007, 4: e107-10.1371/journal.pmed.0040107.
Sperling RS, Shapiro DE, Coombs RW, Todd JA, Herman SA, McSherry GD, O'Sullivan MJ, Van Dyke RB, Jimenez E, Rouzioux C, et al: Maternal viral load, zidovudine treatment, and the risk of transmission of human immunodeficiency virus type 1 from mother to infant. Pediatric AIDS Clinical Trials Group Protocol 076 Study Group. N Engl J Med. 1996, 335 (22): 1621-1629. 10.1056/NEJM199611283352201.
Stiehm ER, Lambert JS, Mofenson LM, Bethel J, Whitehouse J, Nugent R, Moye J, Glenn Fowler M, Mathieson BJ, Reichelderfer P, et al: Efficacy of zidovudine and human immunodeficiency virus (HIV) hyperimmune immunoglobulin for reducing perinatal HIV transmission from HIV-infected women with advanced disease: results of Pediatric AIDS Clinical Trials Group protocol 185. J Infect Dis. 1999, 179 (3): 567-575. 10.1086/314637.
Onah HE, Obi SN, Agbata TA, Oguanuo TC: Pregnancy outcome in HIV-positive women in Enugu, Nigeria. J Obstet Gynaecol. 2007, 27 (3): 271-274. 10.1080/01443610701195108.
Oittinen J, Kurki T, Kekki M, Kuusisto M, Pussinen P, Vilkuna-Rautiainen T, Nieminen A, Asikainen S, Paavonen J: Periodontal disease and bacterial vaginosis increase the risk for adverse pregnancy outcome. Infect Dis Obstet Gynecol. 2005, 13 (4): 213-216.
This series was supported by the Saving Newborn Lives programme of Save the Children-US through a grant from the Bill & Melinda Gates Foundation.
This article has been published as part of BMC Pregnancy and Childbirth Volume 9 Supplement 1, 2009: Stillbirths – the global picture and evidence-based solutions. The full contents of the supplement are available online at http://www.biomedcentral.com/1471-2393/9?issue=S1.
The authors declare that they have no competing interests.
The paper was written and reviewed by all the authors.
Electronic supplementary material
Additional file 1: Web Table 1. Component studies in Trumbo et al. 2007 meta-analysis: Impact of calcium supplementation for prevention of PIH and pre-eclampsia on stillbirths/perinatal mortality. Component studies in Trumbo et al. 2007 meta-analysis showing impact on stillbirths/perinatal mortality (DOC 44 KB)
Additional file 2: Web Table 2. Component studies in Hofmeyr et al. 2007 meta-analysis: Impact of calcium supplementation for prevention of PIH. Component studies in Hofmeyr et al. 2007 meta-analysis reporting impact on stillbirths/perinatal mortality (DOC 76 KB)
Additional file 3: Web Table 3. Component studies in Abalos et al. 2007 meta-analysis: impact of antihypertensive drugs for chronic maternal hypertension. Component studies in Abalos et al. 2007 meta-analysis reporting impact on stillbirths/perinatal mortality (DOC 192 KB)
Additional file 4: Web Table 4. Component studies in Magee et al. 2003 meta-analysis: impact of anti-hypertensive drugs for chronic maternal hypertension. Component studies in Magee et al. 2003 meta-analysis reporting impact on stillbirths/perinatal mortality (DOC 135 KB)
Additional file 5: Web Table 5. Component studies in Duley et al. 2006 meta-analysis: impact of anti-hypertensive drugs for chronic maternal hypertension. Component studies in Duley et al. 2006 meta-analysis reporting impact on stillbirths/perinatal mortality (DOC 80 KB)
Additional file 6: Web Table 6. Component studies in King et al. 2003 meta-analysis: impact of anti-hypertensive drugs for chronic maternal hypertension. Component studies in King et al. 2003 meta-analysis reporting impact on stillbirths/perinatal mortality (DOC 69 KB)
Additional file 7: Web Table 7. Component studies in Say et al. 1996 meta-analysis: impact of anti-hypertensive drugs for chronic maternal hypertension. Component studies in Say et al. 1996 meta-analysis reporting impact on stillbirths/perinatal mortality (DOC 30 KB)
Additional file 8: Web Table 8. Component studies in Meher and Duley. 2007 meta-analysis: impact of anti-hypertensive drugs for chronic maternal hypertension. Component studies in Meher and Duley. 2007 meta-analysis reporting impact on stillbirths/perinatal mortality (DOC 36 KB)
Additional file 9: Web Table 9. Component studies in Duley et al. 2007 meta-analysis: impact of anti-platelet agents. Component studies in Duley et al. 2007 meta-analysis reporting impact on stillbirths/perinatal mortality (DOC 200 KB)
Additional file 10: Web Table 10. Component studies in Askie et al. 2007 meta-analysis: impact of anti-platelet agents. Component studies in Askie et al. 2007 meta-analysis reporting impact on stillbirths/perinatal mortality (DOC 144 KB)
Additional file 11: Web Table 11. Component studies in Empson et al. 2005 meta-analysis: Impact of treatment during pregnancy for lupus anti-coagulant or anti-phospholipid syndrome. Component studies in Empson et al. 2005 meta-analysis reporting impact on stillbirths/perinatal mortality (DOC 86 KB)
Additional file 12: Web Table 12. Component studes in Di Nisio et al. 2005: Impact of LMWH (enoxaparin) versus aspirin. Component studies in Di Nisio et al. 2005 review reporting impact on stillbirths/perinatal mortality (DOC 32 KB)
Additional file 13: Web Table 13. Component studies in Gates et al. 2002 meta-analysis: Impact of thromboprophylaxis during pregnancy. Component studies in Gates et al. 2002 meta-analysis reporting impact on stillbirths/perinatal mortality (DOC 42 KB)
Additional file 14: Web Table 14. Component studies in Rumbold et al. 2008: impact of anti-oxidant supplements. Component studies in Rumbold et al. 2008 meta-analysis reporting impact on stillbirths/perinatal mortality (DOC 42 KB)
Additional file 15: . Component studies in Rumbold and Crowther 2005 meta-analysis reporting impact on stillbirths/perinatal mortality (DOC 34 KB)
Additional file 16: Web Table 16. Component studies in Drakeley et al. 2003 meta-analysis: Impact of cervical cerclage on stillbirths and perinatal mortality. Component studies in Drakeley et al. 2003 meta-analysis reporting impact on stillbirths/perinatal mortality (DOC 52 KB)
Additional file 17: Web Table 17. Component studies in Jorgensen et al. 2007 meta-analysis: Impact of cervical cerclage. Component studies in Jorgensen et al. 2007 meta-analysis reporting impact on stillbirths/perinatal mortality (DOC 56 KB)
Additional file 18: Web Table 18. Component studies in King and Flenady 2002 meta-analysis: impact of anti-biotics in high-risk pregnancy. Component studies in King and Flenady 2002 meta-analysis reporting impact on stillbirths/perinatal mortality (DOC 62 KB)
Additional file 19: Web Table 19. Component studies in McDonald et al. 2007 meta-analysis: impact of anti-biotics in high-risk pregnancy. Component studies in McDonald et al. 2007 meta-analysis reporting impact on stillbirths/perinatal mortality (DOC 46 KB)
Additional file 20: Web Table 20. Component studies in Lumbiganon et al. 2004 meta-analysis: impact of anti-biotics in high-risk pregnancy. Component studies in Lumbiganon et al. 2004 meta-analysis reporting impact on stillbirths/perinatal mortality (DOC 34 KB)
Additional file 21: Web Table 21. Component studies in Goldenberg et al. 2006 meta-analysis: Impact of vaginally administered chlorhexidine during labour on stillbirths/perinatal mortality. Component studies in Goldenberg et al. 2006 meta-analysis reporting impact on stillbirths/perinatal mortality (DOC 36 KB)
Additional file 22: Web Table 22. Component studies in Thinkhamrop et al. 2002 meta-analysis: impact of anti-biotics in high-risk pregnancy. Component studies in Thinkhamrop et al. 2002 meta-analysis reporting impact on stillbirths/perinatal mortality (DOC 40 KB)
Additional file 23: Web Table 23. Component studies in Kenyon et al. 2003 meta-analysis: Impact of antibiotics for PPROM/PROM. Component studies in Kenyon et al. 2003 meta-analysis reporting impact on stillbirths/perinatal mortality (DOC 106 KB)
Additional file 24: Web Table 24. Component studies in Flenady and King 2002 meta-analysis: Impact of anti-biotics for PROM at or near term. Component studies in Flenady and King 2002 meta-analysis reporting impact on stillbirths/perinatal mortality (DOC 34 KB)
Web Table 25. Component studies in Garner and Gulmezoglu 2006 meta-analysis: impact of anti-malarials in malaria-endemic areas
Additional file 25: . Component studies in Garner and Gulmezoglu 2006 meta-analysis reporting impact on stillbirths/perinatal mortality (DOC 50 KB)
Additional file 26: Web Table 26. Component studies in Gamble et al. 2006 & 2007 meta-analyses: impact of ITNs. Component studies in Gamble et al. 2006, 2007 meta-analysis reporting impact on stillbirths/perinatal mortality (DOC 44 KB)
Additional file 27: Web Table 27. Component studies in Volmink et al. 2007 meta-analysis: impact of PMTCT. Component studies in Volmink et al. 2007 meta-analysis reporting impact on stillbirths/perinatal mortality (DOC 84 KB)
Additional file 28: meta-analysis: impact of PMTCT. Component studies in Suksomboon et al. 2007 meta-analysis reporting impact on stillbirths/perinatal mortality (DOC 55 KB)
Additional file 29: meta-analysis: impact of PMTCT. Component studies in Wiysonge et al. 2005 meta-analysis reporting impact on stillbirths/perinatal mortality (DOC 42 KB)
Additional file 30: : impact of periodontal disease. Component studies in Xiong et al. 2006 reporting impact on stillbirths/perinatal mortality (DOC 30 KB)
Additional file 31: : impact of periodontal disease. Component studies in Xiong et al. 2007 reporting impact on stillbirths/perinatal mortality (DOC 36 KB)
About this article
Cite this article
Menezes, E.V., Yakoob, M.Y., Soomro, T. et al. Reducing stillbirths: prevention and management of medical disorders and infections during pregnancy. BMC Pregnancy Childbirth 9, S4 (2009). https://doi.org/10.1186/1471-2393-9-S1-S4
- Periodontal Disease
- Bacterial Vaginosis
- Perinatal Mortality