Skip to main content

Women who smoke during pregnancy are more likely to be referred to an obstetrician during pregnancy and birth: results from a cohort study

Abstract

Background

Women who smoke during pregnancy make less use of prenatal care; the relation of smoking behavior with the use of other forms of maternal healthcare is unknown. The objective of this study is to investigate the association between women’s smoking behavior and their use of healthcare during pregnancy, birth and six weeks postpartum.

Methods

We analyzed data from the Dutch Midwifery Case Registration System (VeCaS), period 2012–2019. We included women with a known smoking status, singleton pregnancies, and who had their first appointment before 24 weeks of gestation with the primary care midwife. We compared three groups: non-smokers, early stoppers (stopped smoking in the first trimester), and late- or non-stoppers (stopped smoking after the first trimester or continued smoking). Descriptive statistics were used to report maternal healthcare utilization (during pregnancy, birth and six weeks postpartum), statistical differences between the groups were calculated with Kruskal–Wallis tests. Multivariable logistic regression was conducted to assess the association between smoking behavior and referrals to primary, secondary or tertiary care.

Results

We included 41 088 pregnant women. The groups differed significantly on maternal healthcare utilization. The late- or non-stoppers initiated prenatal care later and had less face-to-face consultations with primary care midwives during pregnancy. Compared to the non-smokers, the early- and late- or non-stoppers were statistically signficiantly more likely to be referred to the obstetrician during pregnancy and birth. Postpartum, the early- and late- or non-stoppers were statistically signficantly less likely to be referred to the obstetrician compared to the non-smokers.

Conclusions

Although the early- and late- or non-stoppers initiated prenatal care later than the non-smokers, they did receive adequate prenatal care (according to the recommendations). The results suggest that not smoking during pregnancy may decrease the likelihood of referral to secondary or tertiary care. The large population of smokers being referred during pregnancy underlines the important role of the collaboration between healthcare professionals in primary and secondary or tertiary care. They need to be more aware of the importance of smoking as a medical and as a non-medical risk factor.

Peer Review reports

Background

Research has shown that women who smoke during pregnancy have fewer contact moments with their midwives, and start prenatal care later compared to women who do not smoke during pregnancy, despite equal availability of prenatal care [1, 2]. Less contact moments with the midwife and later initiation of prenatal care for women who smoke during pregnancy has a twofold impact: both smoking during pregnancy and insufficient prenatal care are associated with an increased risk of low birth weight, neonatal death and stillbirth [3, 4]. Therefore, early initiation and adequate use of prenatal care should be pursued for women who smoke during pregnancy [5]. In the Netherlands it is common (more than 80%) that women start prenatal care with an independent primary care midwife [6]. If the midwife detects a serious risk factor during pregnancy or birth, she refers the woman to secondary or tertiary care [7]. A few studies reported an increase in referrals of pregnant women to secondary and tertiary care in the Netherlands, compared to years ago [8,9,10,11]. The main indications for this increase in referrals are fetal distress, a need for pain relief, meconium-stained amniotic fluid, and postpartum hemorrhage [8,9,10,11]. The influence of smoking status on the course of healthcare utilization has not been addressed in previous studies. Although we know that women who smoke during pregnancy begin later with prenatal care and pay less visits to the midwife [1, 2], we know little about their further maternal care trajectory. The association between smoking status, referrals and indications for referrals has not been studied before. Furthermore, the association between smoking cessation in the first trimester and referrals during the postpartum period are not examined in previous studies. The reported associations between smoking during pregnancy and increased risks of stillbirth, and operative birth interventions imply that women who smoke have more high-risk pregancies and require more specialized care [3, 12, 13]. Therefore, in the present study we aim to gain insight into the association between smoking status and healthcare utilization during pregnancy, birth, and six weeks postpartum. We aim to investigate initiation of maternal healthcare, number of contact moments with the midwife (contact in person or via telephone), frequency of referrals to primary, secondary and tertiary care, and the association of these factors with smoking status and the main indications for referrals. For this study we will use three groups: 1) pregnant women who do not smoke, 2) women who stopped smoking in the first trimester and 3) women who stopped smoking after the first trimester or who continued smoking during pregnancy. Insight into the course of healthcare utilization and referrals of pregnant women that differ in smoking status will increase our understanding of the impact of smoking on the maternal care trajectory. Based on the results of this study, recommendations for maternal care of women who smoke during pregnancy will be given.

Methods

Study design

We performed a cohort study based on data from the Midwifery Case Registration System (Verloskundig Casusregistratie Systeem, VeCaS) [14], initiated by the Midwifery Science Department from Zuyd University Maastricht, and the Midwifery Academy Amsterdam Groningen (AVAG). The VeCaS data consists of routinely extracted data from two different electronic healthcare registration systems: Orfeus and Vrumun [15, 16], both used by Dutch midwifery care practices. The database contains data from 44 primary midwifery care practices spread across the Netherlands. The data for this study were collected in the period from January 1, 2012 until December 31, 2019. All women in the database provided informed consent for the use of their anonymized data. The women in the VeCaS database are comparable to the national population of women in primary midwife-led care in the Netherlands [14]. We obtained ethical approval for use of the database from the regional Medical Research Ethics Committee Maastricht (nr 09–4–061) [14].

Participants

For this study we selected women with singleton pregnancies, a known smoking status, a known parity and whose first appointment with their primary care midwife took place before 24 weeks of gestation. The threshold of 24 weeks was chosen because we wanted to have a sufficient amount of data of women’s pregnancy to be able to investigate their maternal healthcare utilization. Moreover, women who initiated care after 24 weeks of gestation likely started care at another midwifery care practice because they moved to another residence. We compared three groups of women based on smoking status, based on the categorisation of smoking behavior in the healthcare registration systems: non-smokers, early stoppers (women who stopped smoking during the first trimester), and late- or non-stoppers (women who stopped smoking after the first trimester or continued smoking during the entire pregnancy).

Outcomes

From the electronic healthcare registration systems we extracted routinely collected data about the healthcare utilization of women during pregnancy, birth, and up to six weeks postpartum. We also extracted data regarding demographic characteristics: maternal age, Body Mass Index (BMI), ethnic background (Dutch, Western non Dutch, Non-Western or other), marital status (single, in a relationship), parity (nulliparous or multiparous), gestational age at birth (extremely preterm, very preterm, moderate to late preterm, term, and post term) [17], lifestyle characteristics (alcohol and drug consumption), socioeconomic status (SES), and smoking status. SES was calculated based on data from the Netherlands Institute for Social Research (SCP), including employment, education, and income level of the residential postal code area. Combined with the number of inhabitants per residential postal code area, based on data from Statistics Netherlands (CBS), we calculated national percentiles. We divided SES into low, middle, and high, based on percentile cut-off points: SES below the 25th percentile we classified as low, and SES above the 75th percentile as high. Smoking status was self-reported and divided into three categories: no smoking, stopped smoking in the first trimester, and stopped smoking after the first trimester or continued smoking during the entire pregnancy. Next, we collected data of pregnancy and birth characteristics: gestational diabetes mellitus, hypertensive disorder, placenta previa and fetal growth restriction [18,19,20]. Hypertensive disorder was defined based on the Dutch guideline as two blood pressure measurements after 20 weeks gestation with a diastolic pressure ≥ 90 and/or a systolic pressure ≥ 140 mmHg [21]. We also collected data regarding the mode of birth (spontaneous vaginal, instrumental, cesarean delivery), the maternal outcome postpartum hemorrhage > 1000 ml, and infant characteristics (sex, birth weight, and mortality). For mortality, we defined neonatal death as death during the first 28 days postpartum. We assessed maternal healthcare utilization based on the number of appointments with the primary care midwife, including specific details like week of gestation and mode of contact (face-to-face or via the telephone). Besides face-to-face contact, we decided to report telephone appointments since this is an important part of the provision of midwifery care. Dutch women can call the midwife for minor and for major issues. We defined initiation of care as the first personal appointment with the primary care midwife, indicated by both a registered blood pressure measurement and a known term date, expressed in gestational weeks.

Furthermore, we examined maternal healthcare utilization based on frequency of referrals from the primary care midwife to the general practitioner in primary care, or to the obstetrician, pediatrician or other specialist in secondary or tertiary care. We classified referrals to the obstetrician as either incidental referrals or referrals resulting in handover of care. The data in the healthcare registration system did not provide the ability to distinguish between referrals to secondary or tertiary care. From the data we derived the indications for referrals for each group, based on smoking status during pregnancy, birth, and postpartum.

Statistical analysis

To report baseline characteristics we used descriptive statistics. To assess differences in baseline characteristics between the three groups of women based on smoking status we used chi-square tests. The data of initiation of care in gestational weeks, number of face-to-face contact moments, and number of telephonic contact moments were not normally distributed, we reported the medians (interquartile range) and calculated statistical differences between the three groups by means of Kruskal–Wallis tests. We performed multivariable logistic regression analyses to examine associations between smoking status and referrals during pregnancy, birth, and up to six weeks postpartum. Smoking status (non-smokers, early stoppers and late- or non-stoppers) was taken as independent variable, with non-smokers as reference category. Referrals to primary care (general practitioner) and secondary or tertiary care (incidental referrals, referrals resulting in handover of care by the obstetrician, referrals to the pediatrician, and referrals to an other specialist), were taken as dependent variables. We first calculated crude Odds Ratios (OR) with corresponding 95% Confidence Intervals (95% CI). We subsequently calculated adjusted Odds Ratios, and adjusted for possible confounders: BMI (continuous), maternal age (continuous), SES (using dummies with middle SES as reference category), and dichotomous variables: ethnicity (Dutch or non-Dutch) and parity (nulliparous or multiparous) [22, 23]. We did not control for pregnancy complications, because these are reason for referral and are causally associated with smoking behavior. Furthermore, we were not able to control for e-cigarette use during pregnancy because no women in our dataset reported using the e-cigarrette. Main indications for referrals are described according to a selection of the five main reasons for referral, based on smoking behavior during pregnancy, during birth, and up to six weeks postpartum. All data were analysed in SPSS version 26.0 (SPSS Inc., Chicago, IL, USA). A p-value of 0.05 was considered statistically significant.

Results

From VeCaS we attained data of 61 717 women. From the dataset we excluded a total of 20 629 (33.4%) women. Reasons for exclusion were: no singleton pregnancy (n = 9278), not receiving care between 2012 and 2019 (i.e. these women received care after the inclusion period) (n = 7023), unknown smoking status (n = 2770), no first checkup with the primary care midwife (n = 448), starting prenatal care after 24 weeks of gestation (n = 1055) or unknown parity (n = 5) (illustrated in Fig. 1—Flowchart).

Fig. 1
figure 1

Flowchart of participants in the VeCaS data

Participants

In total, we included 41 088 pregnant women with a known smoking status and singleton pregnancies, and whose first appointment with the primary care midwife, before 24 weeks of gestation, took place between 2012 and 2019. Of this population, 83.0% were non-smokers, 7.8% were early stoppers, and 9.2% were late- or non-stoppers (Table 1). The three groups showed statistically significant differences on all maternal, birth and infant characteristics, except for the pregnancy complications gestational diabetes mellitus and placenta previa, and the infant characteristic mortality. Compared with the non-smokers, the late- or non-stoppers were of younger age, had a lower SES, were more often single, and showed a higher alcohol and drugs consumption. The late- or non-stoppers also showed higher proportions on maternal characteristics (preterm birth), pregnancy complications (fetal growth restriction) and infant characteristics (lower birthweight). The early stoppers were more often nulliparous, more likely to have hypertensive disorders, or had more often given birth by cesarean delivery.

Table 1 Maternal and infant characteristics by maternal smoking behavior during pregnancy; non-smokers, early stoppers and late- or non-stoppers

Initiation of maternal healthcare

The three groups differed significantly regarding the gestational age at initiation of maternal healthcare, number of face-to-face visits, and the number of contact moments by telephone with the midwife (p ≤ 0.001) (Table 2). The late- or non-stoppers started maternal care significantly later, at a median of 9.4 weeks of pregnancy (IQR 8.0–11.2), than the early stoppers, at a median of 9.1 weeks (IQR 8.0–10.7). Although the three groups differed significantly on the number of face-to-face visits, the medians and interquartile ranges were mostly similar. Based on the lower quartile, the late- or non-stoppers (IQR 8–14) had fewer face-to-face visits with the primary care midwife than the non-smokers (IQR 9–14) and early stoppers (IQR 9–14). With regard to the number of telephonic consultations, the non-smokers seem to have less consultations via telephone (IQR 0–3) than the early- (IQR 0–4) and the late- or non-stoppers (IQR 0–4) based on the upper quartile.

Table 2 Initation and frequency of antenatal consultations with the midwife by smoking behavior during pregnancy

Referrals

The results of referrals are indicated per stadium of pregnancy, birth, and six weeks postpartum. Concerning referrals to the obstetrician during pregnancy, the majority were referred for an incidental consult (40.0%), followed by handover of care (33.1%). Of the late- or non-stoppers, 40.5% were referred to the obstetrician, resulting in handover of care during pregnancy. Across all three groups, women were least often referred to an other specialist (0.6%) (Table 3). Compared to the non-smokers, both the early stoppers and the late- or non-stoppers were statistically significantly more likely to be referred to the obstetrician for an incidental referral, with Crude ORs of 1.15 (95%CI 1.07–1.24) and 1.24 (95%CI 1.16–1.33) respectively. This association remained significant after adjustment for confounders: aOR 1.11 (95% 1.03–1.20) for the early stoppers and 1.20 (95%CI 1.11–1.29) for the late- or non-stoppers. Compared to non-smokers, the early stoppers and late- or non-stoppers also were statistically significantly more likely to be referred to the obstetrician resulting in handover of care, with Crude ORs of 1.58 (95%CI 1.45–1.73) and 1.64 (95% CI 1.52–1.78), respectively. After adjusting for confounders, this remained significant: aOR 1.49 (95%CI 1.36–1.63) for early stoppers and aOR 1.58 (95%CI 1.45–1.73) for the late- or non-stoppers. During birth, for most women who had been referred to the obstetrician (22.6%), the referral resulted in handover of care. Compared to the non-smokers, the late- or non-stoppers were statistically significantly more likely to be referred to the obstetrician resulting in handover of care: OR 1.56 (95%CI 1.42–1.72) and OR 1.41 (95%CI 1.29–1.54), respectively. After adjusting for confounders, the associations remained statistically significant: aOR 1.30 (95%CI 1.17–1.44) for early stoppers and aOR 1.40 (95%CI 1.27–1.55) for late- or non-stoppers. Referrals to the general practitioner, pediatrician and other specialists were not taken into account, since these referrals were not applicable during birth.

Up to six weeks postpartum, most women (1.7%) were referred to the obstetrician resulting in handover of care; followed by referrals to the pediatrician (1.5%). A small number of women were referred to the general practitioner (n = 33) or an other specialist (n = 21). The late- or non-stoppers were statistically significantly less likely to be referred for an incidental referral to the obstetrician: OR 0.69 (95%CI 0.49–0.99), compared to the non-smokers. This association remained statistically significant after adjusting for confounders: aOR 0.69 (0.47–0.99). The early stoppers were statistically signficiantly less likely to be referred to the obstetrician resulting in handover of care: OR 0.69 (95%CI 0.47–0.99), compared to the non-smokers. After adjusting for confounders, this association remained statistically significant, aOR 0.63 (95%CI 0.43–0.93). Due to the low frequencies of referrals, we omitted the general practitioner and the other specialist from the calculation.

Table 3 Association between smoking status and referrals to maternal care professionals

Indications for referral

During pregnancy, the five main indications for referral were decreased fetal movements, post-date pregnancy, hypertension/(pre)eclampsia, previous cesarean delivery and ultrasound for determination of the due date (Fig. 2). The main indications for the non-smokers and the early stoppers were similar; only the ranking differed. The main indications for referral were the same for the late- or non-stoppers, except for the indication suspicion of fetal growth restriction. Instead of five indications we reported six indications for referral for the late- or non-stoppers, because the percentages of some indications (previous cesarean delivery and hypertension/(pre)eclampsia) were equal. During birth, the main indications for referral were: need for pain relief, meconium-stained amniotic fluid, failure to progress in first stage of labor, failure to progress in second stage of labor, and prelabor rupture of membranes (Fig. 3). The late- or non-stoppers were less often referred for failure to progress in second stage of labor compared to the other groups. Postpartum, the main indications for referral were 3rd or 4th degree perineal tear, post partum hemorrhage > 1000 ml, various physical symptoms, and other problems (Fig. 4). These indications were the same for the non-smokers and the early stopppers, the late- or non-stoppers also had admission to the neonatal intensive care unit (NICU) as main indication for referral.

Fig. 2
figure 2

The five main indications for referral during pregnancy

Fig. 3
figure 3

The five main indications for referral during birth

Fig. 4
figure 4

The five main indications for referral postpartum

Discussion

Main findings

The aim of this study was to investigate maternal healthcare utilization for three groups of women, classified according to smoking status: non-smokers, early stoppers, and late- or non-stoppers. These groups showed statistically significant differences in the gestational age at initiation of maternal healthcare and number of contact moments, and in referrals during pregnancy, birth, and postpartum. First, we found that the late- or non-stoppers initiate maternal care later, and have fewer face-to-face visits with the midwife, compared to non-smokers or early stoppers. The non-smokers have less telephonic consultations with the midwife compared to the early stoppers and the late- or non-stoppers. Second, compared to the non-smokers, the early stoppers and the late- or non-stoppers were statistically significantly more likely to be referred to the obstetrician during pregnancy and birth. This seems to be reversed postpartum, the early stoppers and the late- or non-stoppers were statistically significantly less likely to be referred to the obstetrician compared to the non-smokers. Third, we identified the main indications for referral during pregnancy, birth, and postpartum; these were mostly similar for the three groups.

Strenghts and limitations

This study has some strenths and limitiations to consider when interpreting the results. One strength is its use of primary midwifery care registration data; the women in the VeCaS data are comparable to the Dutch national population of women in primary midwife-led care [14]. The observed prevalence of smokers is a bit higher than that of the average population in the Netherlands [24], but the observed rates of referral are comparable to those in a previous Dutch study [9]. In addition, the large sample size made it possible to investigate differences in maternal healthcare utilization among the three groups of smokers. A first limitation of our study is that referrals to the general practitioner and the other specialist may be underreported, as pregnant women may visit general practitioners and an other specialist without referral by the midwife. The results of a previous study, using general practitioner registration data, imply that 65% of pregnant women contact their general practitioner [25]. This percentage is much higher than the 1.1% of women in our study who were referred to the general practitioner. The previous study offers a possible explanation for this difference by stating that pregnant women might contact their general practitioner first before they contact their midwife, because women are more familiar with their general practitioner or do not know whether a symptom is pregnancy related. It could also be that referrals to the general practitioner are underreported in VeCaS, since pregnant women can contact the general practitioner by themselves and do not need interference from a midwife. Second, in our study we have not taken the number of cigarettes into account. The number of cigarettes smoked is known to influence health outcomes of the baby [26], and thereby possibly maternal healthcare utilization. Third, we were not able to make a distinction between women who stopped smoking after the first trimester and women who continued smoking, because the VeCaS data only contains data about the three groups of smokers. Fourth, we do not have data of women who find out they were pregnant during birth, although this will be a very small percentage of women. Data of these women is available in Perined, a Dutch data registry that captures primary, secondary and tertiary care data. We decided not to use Perined data for our study because smoking status is heavily underreported in this dataset [27]. Lastly, we are aware that the association between smoking behavior and healthcare utilization is complex (e.g. smoking behavior is also related to other lifestyle factors like diet and physical activity). In our study we decided to take a pragmatic approach, focusing only on the association between smoking behavior and healthcare utilization.

Interpretation

Our finding that late- or non-stoppers initiate prenatal care later and have fewer face-to-face visits with the midwife could possibly be explained by the pregnancy recognition time. Previous studies reported that smoking during pregnancy is associated with unplanned pregnancy [28], leading to a later initiation of care and less prenatal visits [29]. Although the late- or non-stoppers initiate maternal care significantly later, our results do not indicate that either early stoppers or late- or non- stoppers have inadequate use of care. This finding partly corresponds to the results of previous studies, reporting that women who smoke during pregnancy initiate prenatal care later [1, 2, 30, 31]. In accordance with the recommendations in the Dutch guideline, the early stoppers and late- or non-stoppers in our study have a median initiation of care before 10 weeks of gestation, and a median of 12 face-to-face visits with the midwife [32]. Therefore, the late- or non-stoppers still meet the recommendations, despite the statistically significant differences between the groups on their use of maternal care; the differences are therefore not clinically relevant. This also applies to the number of face-to-face visits and telephonic consultations. The statistically significant differences, despite the similarities in medians, could be explained by skewed distributions and the large group sizes. We found that compared to the non-smokers, women who are early stoppers or late- or non-stoppers have more telephone consultations with the primary care midwife. Telephone consultations are often peformed at the initiative of the pregnant women themselves, and are used by midwives to provide education, support, and triage [33]. Based on the telephone consults, midwives can decide to refer women to secondary or tertiary care [33]. This higher number of telephonic consultations may be related to the increased referral rates of early- and late- or non-stoppers. Secondly, we found that pregnant women who smoke at the beginning of pregnancy, both early stoppers- and late- or non-stoppers, are more likely to be referred to the obstetrician during pregnancy and birth. Previous studies reported a positive effect of early smoking cessation on birth outcomes [26, 34], implying that early stoppers would be less likely to be referred to the obstetrician than late- or non-stoppers. However, we did not find large differences in referrals between the early stoppers and the late- or non-stoppers. This finding could be explained by the relatively higher proportions of fetal growth restriction, preterm births, and lower birth weights of infants that we found in our population of early stoppers and late- or non-stoppers, compared to the non-smokers. These are all possible negative health consequences of smoking during pregnancy [3], and indications for referral to secondary or tertiary care [35]. Postpartum, the association between smoking behavior during pregnancy and birth, and referrals, seems to be reversed. The early- and late- or non-stoppers are less likely to be referred to the obstetrician. A possible explanation may be the higher rates of referral to the obstetrician during pregnancy and birth, resulting in the handover of care. This might imply that women with higher risk pregnancies are already in secondary or tertiary care and therefore are not referred again postpartum. Therefore, additional referral postpartum is not applicable. This could also be illustrated by the differences in mode of birth between the groups [8, 9]. The early stoppers more often have an instrumental birth or cesarean delivery, implying that they already receive care from an obstetrician during birth in secondary or tertiary care. Third, among the three groups we did not find differences in indications large enough to explain the significant differences in referral rates. Women’s smoking behavior might be unrelated to the main indications for referral. Our identified indications for referrals are generally comparable to those reported in previous studies [8, 9]. Nevertheless, despite these similar indications for referral in the three groups, our results show that women who smoke during pregnancy are more often referred to the obstetrician. Considering the negative health effects of smoking [3], it may be that, for smokers, the indications for referral involve more serious health consequences, leading to higher referral rates. Furthermore, other concomitant non-medical risk factors associated with smoking during pregnancy may possibly influence the higher referral rates, such as a lower SES, lower education level, higher alcohol and drug use, and higher levels of anxiety and depression [5, 36]. These factors are also associated with adverse pregnancy outcomes, such as small for gestational age, preterm delivery and stillbirth [37,38,39], which could lead to higher referral rates to secondary and tertiary care. The higher prevalence of these factors in women who smoke during pregnancy might imply that they form a vulnerable group with a higher risk for adverse pregnancy outcomes, requiring more specialized care. In the Netherlands, special care paths are available that describe how vulnerable pregnant women can receive specialized care during pregnancy. The care for vulnerable pregnant women also involves consultations in which interdisciplinary healthcare professionals collaborate in the care for vulnerable women. However, a previous study reports that interdisciplinary care for vulnerable pregnant women still should be improved [40]. The study recommends that interdisciplinary healthcare professionals should take both medical risk factors (pregnancy outcomes) and non-medical risk factors (such as a low SES and poor lifestyle behaviors) into account [40]. The results of our study indicate the importance of smoking as a risk factor, related to both medical and non-medical factors, that should be taken into account in the care for (vulnerable) pregnant women.

Conclusion

In this study we aimed to gain insight into similarities and differences in maternal healthcare utilization for women who do not smoke during pregnancy, early stoppers, and late- or non-stoppers. Our results indicate that the three groups differ in their utilization of care. However, although the late- or non-stoppers initiate maternal care later, their use of prenatal care is adequate. Furthermore, women who smoke at the beginning of pregnancy are more often referred to the obstetrician during pregnancy and birth than non-smokers. The large population of smokers being referred during pregnancy underlines the important role of the collaboration between healthcare professionals in primary and secondary or tertiary care. They need to be more aware of the importance of smoking as a medical and as a non-medical risk factor. More research is needed on the influence of the amount of cigarettes smoked on maternal healthcare use. We recommend future studies to make a distinction between women who stopped smoking after the first trimester and women who continued smoking to investigate the association on referrals to secondary or tertiary care.

Availability of data and materials

The data that support the findings of this study are available from Zuyd University Maastricht or the Midwifery Academy Amsterdam Groningen but restrictions apply to the availability of these data, which were used under license for the current study, and so are not publicly available. Data are however available from the authors upon reasonable request and with permission of Zuyd University Maastricht and the Midwifery Academy Amsterdam Groningen.

References

  1. Kupek E, Petrou S, Vause S, Maresh M. Clinical, provider and sociodemographic predictors of late initiation of antenatal care in England and Wales. BJOG. 2002;109(3):265–73.

    Article  Google Scholar 

  2. Feijen-de Jong EI, Jansen DE, Baarveld F, Boerleider AW, Spelten E, Schellevis F, et al. Determinants of prenatal health care utilisation by low-risk women: a prospective cohort study. Women Birth. 2015;28(2):87–94.

    Article  Google Scholar 

  3. Abraham M, Alramadhan S, Iniguez C, Duijts L, Jaddoe VW, Den Dekker HT, et al. A systematic review of maternal smoking during pregnancy and fetal measurements with meta-analysis. PLoS ONE. 2017;12(2):e0170946.

    Article  Google Scholar 

  4. Raatikainen K, Heiskanen N, Heinonen S. Under-attending free antenatal care is associated with adverse pregnancy outcomes. BMC Public Health. 2007;7:268.

    Article  Google Scholar 

  5. Moore E, Blatt K, Chen A, Van Hook J, DeFranco EA. Factors Associated with Smoking Cessation in Pregnancy. Am J Perinatol. 2016;33(6):560–8.

    PubMed  Google Scholar 

  6. Rijksoverheid. Factsheet Zwangerschap en Geboorte 2018. 2019.

    Google Scholar 

  7. Perdok H, Jans S, Verhoeven C, van Dillen J, Batenburg R, Mol BW, et al. Opinions of professionals about integrating midwife- and obstetrician-led care in The Netherlands. Midwifery. 2016;37:9–18.

    Article  Google Scholar 

  8. Offerhaus PM, Hukkelhoven CW, de Jonge A, van der Pal-de Bruin KM, Scheepers PL, Lagro-Janssen AL. Persisting rise in referrals during labor in primary midwife-led care in the Netherlands. Birth (Berkeley, Calif). 2013;40(3):192–201.

    Article  Google Scholar 

  9. Amelink-Verburg MP, Rijnders ME, Buitendijk SE. A trend analysis in referrals during pregnancy and labour in Dutch midwifery care 1988–2004. BJOG. 2009;116(7):923–32.

    Article  CAS  Google Scholar 

  10. Ghardallou M, Limam M, Khelifi A, Khairi O, Khairi H, Mtiraoui A, et al. Obstetric referrals to a tertiary care maternity: a descriptive study. Pan Afr Med J. 2019;33:306.

    Article  Google Scholar 

  11. Amelink-Verburg MP, Verloove-Vanhorick SP, Hakkenberg RM, Veldhuijzen IM, Bennebroek Gravenhorst J, Buitendijk SE. Evaluation of 280,000 cases in Dutch midwifery practices: a descriptive study. BJOG. 2008;115(5):570–8.

    Article  CAS  Google Scholar 

  12. Lurie S, Ribenzaft S, Boaz M, Golan A, Sadan O. The effect of cigarette smoking during pregnancy on mode of delivery in uncomplicated term singleton pregnancies. J Matern Fetal Neonatal Med. 2014;27(8):812–5.

    Article  CAS  Google Scholar 

  13. Hackshaw A, Rodeck C, Boniface S. Maternal smoking in pregnancy and birth defects: a systematic review based on 173 687 malformed cases and 11.7 million controls. Human Reprod Update. 2011;17(5):589–604.

    Article  CAS  Google Scholar 

  14. Pouwels A, Offerhaus P, Merkx A, Zeegers B, Nieuwenhuijze MJ. Detailed registration of care in midwifery practices in the Netherlands: an opportunity for research within a healthy pregnant population. BMC Pregnancy Childbirth. 2020;20(1):366.

    Article  CAS  Google Scholar 

  15. Orfeus. [Computer software] 2022. Retrieved from: https://www.orfeus.nl/producten/orfeus-1e-lijn/.

  16. Vrumun. [Computer software] 2021. Retrieved from: https://www.vrumun.nl/index.html.

  17. Organization WH. Preterm birth 2018. Available from: https://www.who.int/news-room/fact-sheets/detail/preterm-birth#:~:text=Preterm%20is%20defined%20as%20babies,(32%20to%2037%20weeks.

  18. Adibelli D, Kirca N. The relationship between gestational active and passive smoking and early postpartum complications. J Matern Fetal Neonatal Med. 2020;33(14):2473–9.

    Article  Google Scholar 

  19. Nabet C, Lelong N, Ancel PY, Saurel-Cubizolles MJ, Kaminski M. Smoking during pregnancy according to obstetric complications and parity: results of the EUROPOP study. Eur J Epidemiol. 2007;22(10):715–21.

    Article  Google Scholar 

  20. Fernandez-Rodriguez B, Gomez AR, Jimenez Moreno BS, de Alba C, Galindo A, Villalain C, et al. Smoking influence on early and late fetal growth. J Perinat Med. 2022;50(2):200–6.

    Article  Google Scholar 

  21. (KNOV) KNOV. Hypertensieve aandoeningen tijdens de zwangerschap, bevalling en kraamperiode - Aanbevelingen voor risicoselectie, diagnostiek en beleid. Utrecht: Koninklijke Nederlandse Organisatie van Verloskundigen (KNOV); 2011.

  22. Flenady V, Koopmans L, Middleton P, Frøen JF, Smith GC, Gibbons K, et al. Major risk factors for stillbirth in high-income countries: a systematic review and meta-analysis. Lancet. 2011;377(9774):1331–40.

    Article  Google Scholar 

  23. Holness N. High-Risk Pregnancy. Nurs Clin North Am. 2018;53(2):241–51.

    Article  Google Scholar 

  24. Scheffers-van Schayck T, den Hollander W, van Belzen E, Monshouwer K, Tuithof M. Monitor Middelengebruik en Zwangerschap 2018. Trimbos-instituut; 2019.

  25. Feijen-de Jong EI, Baarveld F, Jansen DE, Ursum J, Reijneveld SA, Schellevis FG. Do pregnant women contact their general practitioner? A register-based comparison of healthcare utilisation of pregnant and non-pregnant women in general practice. BMC Fam Pract. 2013;14:10.

    Article  Google Scholar 

  26. Soneji S, Beltrán-Sánchez H. Association of Maternal Cigarette Smoking and Smoking Cessation With Preterm Birth. JAMA Netw Open. 2019;2(4):e192514.

    Article  Google Scholar 

  27. Perined. Aanlevering en terugkoppeling van informatie leefstijl zwangere. Utrecht 2020.

  28. Huynh ST, Yokomichi H, Akiyama Y, Kojima R, Horiuchi S, Ooka T, et al. Prevalence of and factors associated with unplanned pregnancy among women in Koshu, Japan: cross-sectional evidence from Project Koshu, 2011–2016. BMC Pregnancy Childbirth. 2020;20(1):397.

    Article  Google Scholar 

  29. Goossens J, Van Den Branden Y, Van der Sluys L, Delbaere I, Van Hecke A, Verhaeghe S, et al. The prevalence of unplanned pregnancy ending in birth, associated factors, and health outcomes. Hum Reprod. 2016;31(12):2821–33.

    Article  CAS  Google Scholar 

  30. Feijen-de Jong EI, Jansen DE, Baarveld F, van der Schans CP, Schellevis FG, Reijneveld SA. Determinants of late and/or inadequate use of prenatal healthcare in high-income countries: a systematic review. Eur J Pub Health. 2012;22(6):904–13.

    Article  Google Scholar 

  31. Petrou S, Kupek E, Vause S, Maresh M. Clinical, provider and sociodemographic determinants of the number of antenatal visits in England and Wales. Soc Sci Med (1982). 2001;52(7):1123–34.

    Article  CAS  Google Scholar 

  32. Verloskundigen KNOv. Prenatale verloskundige begeleiding. Aanbevelingen voor ondersteuning, interactie en voorlichting. Utrecht: KNOV; 2008.

  33. Koster L, Batterink M, Stoof R, Schipper M. Takenpakket verloskunde Onderzoek naar taken, tijdsbesteding en productie van verloskundigen. 2015.

    Google Scholar 

  34. Ratnasiri AWG, Gordon L, Dieckmann RA, Lee HC, Parry SS, Arief VN, et al. Smoking during Pregnancy and Adverse Birth and Maternal Outcomes in California, 2007 to 2016. Am J Perinatol. 2020;37(13):1364–76.

    Article  Google Scholar 

  35. zorgverzekeringen Cv. Verloskundig Vademecum. 2003. 2003.

    Google Scholar 

  36. Riaz M, Lewis S, Naughton F, Ussher M. Predictors of smoking cessation during pregnancy: a systematic review and meta-analysis. Addiction. 2018;113(4):610–22.

    Article  Google Scholar 

  37. Swaminathan A, Lahaie Luna M, Rennicks White R, Smith G, Rodger M, Wen SW, et al. The influence of maternal and paternal education on birth outcomes: an analysis of the Ottawa and Kingston (OaK) birth cohort. J Matern Fetal Neonatal Med. 2022:1–8. https://doi.org/10.1080/14767058.2022.2049751.

  38. Parpinel G, Rosso G, Galante A, Germano C, Aragno E, Girlando F, et al. Effect of depressive disorders and their pharmacological treatment during pregnancy on maternal and neonatal outcome. J Clin Med. 2022;11(6):1486. https://doi.org/10.3390/jcm11061486. Published 2022 Mar 9. 

  39. Azuine RE, Ji Y, Chang HY, Kim Y, Ji H, DiBari J, et al. Prenatal Risk Factors and Perinatal and Postnatal Outcomes Associated With Maternal Opioid Exposure in an Urban, Low-Income, Multiethnic US Population. JAMA Netw Open. 2019;2(6):e196405.

    Article  Google Scholar 

  40. Harmsen van der Vliet-Torij HW, Venekamp AA, van Heijningen-Tousain HJM, Wingelaar-Loomans E, Scheele J, de Graaf JP, et al. Development of a Blueprint for Integrated Care for Vulnerable Pregnant Women. Matern Child Health J. 2022;26(3):451–60.

    Article  CAS  Google Scholar 

Download references

Acknowledgements

We would like to thank the midwives who participate in the VeCaS project and the women who consented to use their data.

Funding

This work was supported by the Dutch institute ZonMW (number 531 003018) and is part of the broader project ‘Together we’ll quit smoking! Optimizing the implementation of the Trimbos guideline ‘smoking cessation counseling’ in daily practice of healthcare professionals supporting low SES pregnant women in the North or the Netherlands’. ZonMW had no involvement in the study design, the collection, analysis or interpretation of the data.

Author information

Authors and Affiliations

Authors

Contributions

SW: Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Project administration, Writing-original draft. LLP: Conceptualization, Data curation, Funding acquisition, Methodology, Project administration, Resources, Supervision, Writing-review & editing. MYB: Conceptualization, Funding acquisition, Project administration, Supervision, Writing-review & editing. JJHME: Conceptualization, Funding acquisition, Project administration, Resources, Supervision, Writing-review & editing. DEMCJ: Conceptualization, Funding acquisition, Methodology, Project administration, Resources, Supervision, Writing-review & editing. The author(s) read and approved the final manuscript.

Corresponding author

Correspondence to S. Weiland.

Ethics declarations

Ethics approval and consent to participate

We obtained ethical approval for use of the database from the regional Medical Research Ethics Committee Maastricht (nr 09–4–061). All women in the database provided informed consent for the use of their anonymized data. All methods were performed in accordance with the Declaration of Helsinki.

Consent for publication

Not applicable (there are no images or other personal or clinical details of participants that compromise anonymity).

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Weiland, S., Peters, L., Berger, M. et al. Women who smoke during pregnancy are more likely to be referred to an obstetrician during pregnancy and birth: results from a cohort study. BMC Pregnancy Childbirth 22, 479 (2022). https://doi.org/10.1186/s12884-022-04808-7

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12884-022-04808-7

Keywords