Skip to main content

Adverse pregnancy outcomes during the COVID-19 lockdown. A descriptive study

Abstract

Background

The ongoing spread coronavirus disease worldwide has caused major disruptions and led to lockdowns. Everyday lifestyle changes and antenatal care inaccessibility during the coronavirus disease 2019 (COVID-19) pandemic have variable results that affect pregnancy outcomes. This study aimed to assess the alterations in stillbirth, neonatal-perinatal mortality, preterm birth, and birth weight during the COVID-19 national lockdown.

Methods

We used the data from the Jordan stillbirths and neonatal death surveillance system to compare pregnancy outcomes (gestational age, birth weight, small for gestational age, stillbirth, neonatal death, and perinatal death) between two studied periods (11 months before the pandemic (May 2019 to March 2020) vs. 9 months during the pandemic (April 2020 to March 1st 2020). Separate multinomial logistic and binary logistic regression models were used to compare the studied outcomes between the two studied periods after adjusting for the effects of mother’s age, income, education, occupation, nationality, health sector, and multiplicity.

Results

There were 31106 registered babies during the study period; among them, 15311 (49.2%) and 15795 (50.8%) births occurred before and during the COVID-19 lockdown, respectively. We found no significant differences in preterm birth and stillbirth rates, neonatal mortality, or perinatal mortality before and during the COVID-19 lockdown. Our findings report a significantly lower incidence of extreme low birth weight (ELBW) infants (<1kg) during the COVID-19 lockdown period than that before the lockdown (adjusted OR 0.39, 95% CI 0.3-0.5: P value <0.001)

Conclusions

During the COVID-19 lockdown period, the number of infants born with extreme low birth weight (ELBW) decreased significantly. More research is needed to determine the impact of cumulative socio-environmental and maternal behavioral changes that occurred during the pandemic on the factors that contribute to ELBW infants.

Peer Review reports

Background

Numerous coronavirus outbreaks posing a great public health threat have occurred throughout the years, including the Middle East respiratory syndrome and severe acute respiratory syndrome (SARS-CoV). The current alarming worldwide spread of SARS-CoV-2 has caused worldwide disarray, with the World Health Organization (WHO) declaring it a public emergency in January 2020 [1].

The coronavirus disease (COVID-19) pandemic has caused an international outcry, leading to lockdowns, as well as health care and economic crises, in many countries [2]. Globally, numerous countrywide methods have been implemented to limit the virus spread, including social distancing and quarantine, as well as partial or complete lockdowns.

Individual studies and systematic reviews are increasingly giving evidence on the influence of other recent viral epidemics on pregnancy outcomes. According to the current literature, pregnancy may worsen the course of COVID-19 infection when compared to non-pregnant women of the same age. COVID-19 has been linked to an increase in obstetric complications like fetal distress, cesarean delivery, and both iatrogenic and spontaneous preterm birth [3]. The reported mechanism is vertical transmission of SARS-CoV-2, either in utero via the hematogenous transplacental route, resulting in an increased rate of decidual arteriopathy and other features of maternal vascular malperfusion. It may be rarely transmitted as intrapartum ascending route with aspiration of amniotic fluid or even the early postnatal period [3,4,5].

In the context of the 2014-2019 Ebola outbreak in West Africa, evidence suggests that nearly all pregnant women who contract Ebola have a negative pregnancy outcome. Perinatal mortality among Ebola-infected women's infants is extremely high, with only a small percentage surviving the neonatal period [6]. A comprehensive review and meta-analysis published in 2016 found a positive relationship between symptomatic dengue virus infections during pregnancy, preterm delivery, and low birth weight. Moreover, an increase in the risk of stillbirth was recorded in Brazil (2006–2012) [6,7,8]. A causal relationship between prenatal Zika Virus (ZIKV) infection and a variety of congenital brain abnormalities, including microcephaly. In this context, other negative fetal outcomes (such as preterm, low birth weight, small-for-gestational-age, and fetal death) related with ZIKV infection during pregnancy have not been well quantified [9]. There is limited data on the impact and likelihood of MERS-CoV during pregnancy emerged in 2012. There was a higher rate of fetal death (27%) among 12 reported pregnant women with MERS women compared to 0% among COVID-19 [10].

With an increasing number of pregnant women being diagnosed with COVID-19 worldwide, our understanding of the effect of COVID-19 on fetal outcomes at population level remains limited. As healthcare services become overwhelmed by COVID-19 cases and means of addressing them, there is a threat of the already fragile infrastructure collapsing. There are concerns regarding whether these services can provide adequate antenatal care, especially in low- and middle-income countries [3].

During the early months of 2020, COVID-19 caused a worldwide healthcare emergency. Among other countries, it affected Jordan, a Middle Eastern upper-middle-income country with approximately 10 million inhabitants in 2020 [11]. The state of emergency and lockdown measures implemented by the government due to the pandemic caused limitations and challenges for healthcare providers. The restricted mobility of patients, including pregnant women and medical staff, as well as the lack of accessibility to diagnostic tools, were among the obstacles faced. These measures warranted further expansion of telemedicine use to guarantee that patients, including pregnant women, retain access to health care providers and attend regular follow-up appointments. Moreover, round-the-clock access to emergency departments was guaranteed [12,13,14,15].

Given the novelty of the virus, only modeling studies have investigated whether the COVID-19 pandemic affects mothers and their babies, with many of them anticipating decreased accessibility to health services. Several studies have attributed maternal mortality during the COVID-19 pandemic to comorbidities; on the other hand, neonatal mortality has been attributed to prematurity rather than infection [16,17,18]. The pandemic could affect the neonatal mortality rate due to the anticipated decline in health care services and possibly due to fear of mothers visiting health care facilities due to COVID-19 [19].

Prematurity is the leading cause of death in children aged < 5 years [20] and is associated with high morbidity and mortality [21]. In 2020, the reported preterm birth rate in Jordan was 11% [10]. Low birth weight (low, very low, and extremely low) is a predictive indicator of neonatal health. It concomitantly occurs with preterm births; therefore, it increases the long-term risk of complications. In 2020, the rate of low birth weight was 13% [22].

Although this is a sudden and unfortunate occurrence, it is important to identify a silver lining. Specifically, the pandemic provides a unique opportunity to evaluate its effects as a “natural experiment” [23]. Like the rest of the world. Jordan has been affected by the recent and ongoing changes brought about by the COVID-19 pandemic, including complete or partial lockdowns, stay-at-home orders, increased hand hygiene awareness, wearing masks, maintaining social distancing, changes in work stress, and inaccessibility of antenatal care, are likely to have had an effect on neonatal mortality, preterm birth, and low birth weight rates. This study take advantage of this unique situation and evaluate alterations in these rates, which could facilitate future studies on the underlying causes since low birth weight and preterm birth present different health outcomes when classified in different birth weight and gestation age strata. This study aimed to the assess the alterations in stillbirth, neonatal-perinatal mortality, preterm birth, and birth weight rate trends during COVID-19 national lock down. The present study is valuable as it reflects a large population in a middle-low-income country

Methods

Setting

On March 14th, 2020, the Jordanian government suspended schools, banned public gatherings, and closed borders and airports. During this period, the Ministry of Health advised the public to adhere to social distancing and proper hand hygiene. The government announced a lockdown on March 17th, 2020, which subsequently turned into a strictly enforced curfew with stay-at-home orders. The more cautious relaxation measures, driven by data, were applied on 30th April 2020, where the Jordanian government moved to ease the lockdown . On 5th May 2020, the government issued a defense order, punishing those who do not abide by safety regulations and by wearing of masks in public with a fine. These unique conditions could pose environmental risks or benefits to pregnant women. Using a prospective maternal and newborn health registry study, we analyzed data collected from May 2019 to December 2020. Stillbirth, neonatal-perinatal mortality, gestational age of preterm births, and low birth weight trends were collected from five pilot hospitals in Jordan over the set period during the COVID-19 pandemic. Subsequently, we compared these trends with the data of pre-lockdown trends.

Study population

Regarding the current pandemic, data were retrieved from the J-SANDS (Jordan Stillbirths and Neonatal Death Surveillance and Auditing System). The J-SANDS is a secure electronic surveillance system that was established in 2019 to collect and report standardized perinatal and neonatal mortality data from five main hospitals in Jordan. The system uses the WHO application of International Classification of Diseases, ICD-10, to classify deaths during the perinatal period (ICD-PM). These five hospitals include a university teaching hospital, a private hospital, and three public hospitals in three major governorates in Jordan. We included all births, as well as maternal demographic data, obtained from May 2019 to December 2020. We analysed data collected 11 months before the pandemic (May 2019 to March 2020) and 9 months during the pandemic (April 2020 to December 2020). The inclusion criteria were neonates born between 24 and 42 gestation weeks, with no further exclusion criteria being applied.

Variables

Data on mothers’ socio-demographic characteristics including age, nationality, hospital birth site, income, multiple pregnancies, and parity were extracted from the JSANDS. Multiplicity was divided into singleton, twin, and triplet pregnancies, while parity included primiparous, low multiparity (having 2–4 births), and grand multiparity (having ≥ 5 births).

Prematurity was classified into extremely preterm infants (born at < 28 weeks), very preterm (born at 28–32 weeks), and moderate-to-late preterm (born at 32–37 weeks). Birth weight was divided into normal, low (< 2500 g), very low (< 1500 g), and extremely low birth weight (< 1000 g). Stillbirth was defined as delivery at ≥ 24 gestation weeks or with a birth weight of ≥ 500 g without signs of life, irrespective of death. Stillbirths include antepartum stillbirth (death before labor onset) and intrapartum stillbirth (known to be alive at labor onset). Neonatal death was defined as a live-born baby at ≥ 24 gestation weeks or with a birth weight of ≥ 500 g who died before 28 completed days after birth. In the JSANDS, neonatal deaths are divided into early neonatal death (death before 7 completed days after birth) and late neonatal death (death between 8 and 47 completed days after birth). Perinatal death was defined as fetal death after 24 gestation weeks and before 7 post-birth days.

Ethics approval and consent to participate

This study was approved by the Institutional Review Board at Jordan University of Science and Technology (approval number 130/137/2020). To ensure data privacy, the data were exported without identifying information (e.g. name or phone number). Informed consent was obtained from all participated mothers. All methods were carried out in accordance with relevant guidelines and regulations of the Institutional Review Board of Jordan University of Science and Technology.

Statistical analysis

Statistical analyses were performed using SPSS version 24 (IBM Corp. Armonk, NY, USA). Data were described using means (SD) and percentages. Chi-square test was used to compare percentages. Separate binary logistic regression analyses (models) were used to compare the dichotomous outcome variables (small for gestational age, stillbirth, neonatal death, and perinatal death) between the two studied periods (during the COVID-19 lockdown vs. before COVID-19). For nominal outcome variables (gestational age and birth weight), we conducted separate multinomial logistic regression analysis for each outcome to compare the outcome between the two studied periods. The main independent variable in each model was the period (during the COVID-19 lockdown vs. before COVID-19). The differences in the pregnancy outcomes between two study periods were adjusted for mother’s age, income, education, occupation, nationality, health sector, and multiplicity. These variables were selected and included in the models based on the Wald Chi-Square test statistic. A p-value of less than 0.05 was considered statistically significant.

Results

From May 2019 to December 2020, 29592 women were admitted to the five pilot hospitals for delivery, with 31106 babies being born (15311 [49.2%] and 15795 [50.8%] before and during the COVID-19 lockdown, respectively). During the study period, 14989 (50.7%) vaginal births occurred, out of which 7228 (48.2%) and 7761 (51.8%) births occurred before and during the lockdown, respectively. Additionally, 14603 (49.3%) births occurred, by C-section out of which 7088 [48.5%] and 7515 [51.5%] were births before and during the lockdown, respectively. Table 1 presents the sociodemographic characteristics of women who delivered before and during the COVID-19 lockdown. The proportion of women with income > 500 JD was significantly lower during than that before the COVID-19 lockdown. There was no significant between-period difference in the proportion of preterm babies. Contrastingly, there was a significant between-period difference in the birth weight distribution (p <0.001).

Table 1 The characteristics of mothers who delivered before and during COVID-19 (N= 29592)

The proportion of babies born with low or very low birth weight was significantly lower during COVID-19 pandemic than that before the pandemic (Table 2). The percentage of babies with an appropriate weight for gestational age was significantly higher during, than before, the COVID-19 lockdown. There were no significant differences between the two periods in the rates of stillbirth, neonatal mortality, and perinatal mortality. The multinomial regression analysis for nominal pregnancy outcomes between two study periods were adjusted for the mother’s age, income, education, occupation, nationality, health sector, and multiplicity revealed no significant difference in the odds of extremely preterm, very preterm, and moderate-to-late preterm between the two periods (Table 3). However, babies born during the COVID-19 lockdown were significantly less likely (OR = 0.39) to be born with extremely low birth weight. In addition, there were no significant between-period differences in the rates of stillbirth, neonatal mortality, and perinatal mortality.

Table 2 Birth outcomes for women delivered before and during COVID-19 (N= 31106)
Table 3 Logistic regression analysis of differences in birth outcomes between babies born before and during the COVID-19 lockdown (During vs. Before)

Discussion

Very low birth weight (VLBW) and extremely low birth weight (ELBW) infants contribute significantly to under-5 mortality. In this context, it is important to have a better understanding of the impact of the COVID-19 pandemic on outcomes associated with preterm gestation age and low birth weight based on more appropriately standardized perinatal and neonatal mortality data. This would allow provision of more qualified care to pregnant women and the newborn. The current study reports that babies born during the period of COVID-19 were significantly less likely to be born with extremely low birth weight (0.56% vs 1.52%), even after adjusting for sociodemographic confounders. Similarly, Philip et al. reported that a significant reduction in the rate of ELBW and VLBW in Ireland includes multiple gestations (73% reduction in live births of VLBW infants and a 100% reduction of ELBW infants [24]. Their findings were reported to be possibly attributed to reduced working hours, infection avoidance due to mobility and crowding restriction, and nutritional support. In contrast, a study by Arnaez et al. from Spain [25] showed an increase in the rate of ELBW among all live births including multiple gestations during the complete lockdown period (OR: 2.21; 95% CI: 1.16–4.21; p = 0.016). Unexpectedly, these findings were not observed when both the lockdown and the de-escalation periods were considered. The differences in outcomes according to the period may be attributable to changes that occurred as a result of the COVID-19 pandemic, including infection prevention and control measures, the presence of around-the-clock access to emergency departments, life style and eating pattern changes, and restricted mobility of pregnant women with persistent stay home orders

At population-level reports offer conflicting data on a decrease or stability in the overall rate of preterm births during the pandemic. This study found no significant difference in the rate of preterm births, including preterm births of different gestational age strata, before and during the lockdown due to the COVID-19 pandemic. These findings are consistent with the findings of a study by Li et al. [26], conducted in Wuhan, China (9% vs 8%). In contrast with our findings, studies conducted in the United States [27] Australia [19], and the Netherlands [28], found a substantial reduction in the number of preterm births following implementation of the first national COVID-19 mitigation measures. These reductions were consistent across various degrees of prematurity. According to Been et al. [28], the reduction in the prematurity rates was probably due to a combination of factors including stopping work, increased hygiene measures, social distancing resulting in fewer infections by common pathogens, and less air pollution. Similarly, additional national studies done in Ireland and Denmark showed a significant decrease in the rate of extremely preterm births since the start of the COVID-19 pandemic [24, 29]. No change was reported in the incidence of preterm births in four hospitals in the United States [30], and one hospital in London [31].

Riley et al. [32] reported that a reduction of as little as 10% in the provision of antenatal health services in low- and middle-income countries during the COVID-19 pandemic, could lead to an increase in the rates of maternal and neonatal mortality, an increase in the number of women suffering from major obstetric complications, and an increase in newborns with major health-problems being deprived of suitable care. In Jordan, Muhaidat et al. [33] reported a significant increase in the percentage of pregnant women who did not receive antenatal care during the pandemic (from 4% to 59.5%), due to national mitigation measures in Jordan.

In this study, we did not observe differences between the two periods in neonatal mortality, perinatal mortality, or stillbirth. Inconsistent with this finding, a Nepalese study showed an increase in stillbirth and neonatal mortality during the COVID-19 pandemic compared with before [34]. Furthermore, middle-to-low-income countries reported a slight decrease in neonatal mortality, which could be attributed to increased severity of maternal infection or preterm birth [35], whereas we found no significant increase in prematurity.

To our knowledge, our study is by far the largest to have assessed the impact of COVID-19 mitigation measures on birth outcomes in a middle-income country. Given the large sample size of our study (n=31,106), our findings are representative of Jordan’s population and could facilitate further studies on the effect of cumulative socioenvironmental and maternal behavioral alteration on the factors contributing to extremely low birth weight, which has adverse effects on neonatal wellbeing and added long-term morbidity during the coronavirus pandemic [36]. Additionally, our findings could facilitate comparison with other data worldwide to elucidate the significance of these findings and the underlying causes of extremely low birth weight to minimize undesired future outcomes.

Our study has several limitations. First, we could not compare our results to previous Jordanian findings since the J-SANDS was only recently established in August 2019. A longer analysis period could have yielded more reliable rates since Jordan has a limited data system in place documenting stillbirths and other neonatal outcomes.

Second, the J-SANDS only includes five hospitals in Jordan, which could limit the generalizability of the results nationwide.

Conclusion

After adjustment for sociodemographic factors, the study found that there were significant differences in the populations of the two periods in terms of the rate of extreme low birth weight infants, but no difference in the rates of preterm birth, neonatal-perinatal death, and stillbirth. To see if the changes persist, birth outcomes must be tracked throughout the second year of the COVID-19 pandemic and beyond. Future epidemiological and experimental research is needed to better understand the effects of socioeconomic, maternal behavioral, and nutritional factors on the variable reported birth outcomes that occurred worldwide during the pandemic in order to develop effective preventive strategies.

Availability of data and materials

The datasets generated and/or analysed during the current study are not publicly available due to limitations of ethical approval involving the patient data and anonymity but are available from from yskhader@just.edu.jo on reasonable request.

Abbreviations

COVID-19:

Coronavirus disease 2019

ELBW:

Extremely low birth weight

ICD-10:

International Classification of Diseases-10

ICD-PM:

WHO application of ICD-10 to perinatal mortality

J-SANDS:

Jordan stillbirths and neonatal death surveillance and auditing system

SARS-CoV-2:

Severe acute respiratory syndrome coronavirus 2

References

  1. 1.

    WHO. Novel Coronavirus ( 2019-nCoV): situation report, 3. 2020. https://apps.who.int/iris/bitstream/handle/10665/330762/nCoVsitrep23Jan2020-eng.pdf?sequence=1&isAllowed=y

  2. 2.

    Nicola M, Alsafi Z, Sohrabi C, Kerwan A, Al-Jabir A, Iosifidis C, et al. The socio-9 coronavirus and COVID-19 pandemic: a review. Int J Surg. 2020;78:185–93.

    Article  Google Scholar 

  3. 3.

    Sahin D, Tanacan A, Erol SA, Anuk AT, Yetiskin FD, Keskin HL, et al. Updated experience of a tertiary pandemic center on 533 pregnant women with COVID-19 infection: a prospective cohort study from Turkey. Int J Gynecol Obstet. 2021 Mar;152(3):328–34.

    CAS  Article  Google Scholar 

  4. 4.

    Shanes ED, Mithal LB, Otero S, Azad HA, Miller ES, Goldstein JA. Placental pathology in COVID-19. Am J Clin Pathol. 2020;154(1):23–32.

    CAS  Article  Google Scholar 

  5. 5.

    Blumberg DA, Underwood MA, Hedriana HL, Lakshminrusimha S. Vertical transmission of SARS-CoV-2: what is the optimal definition? Am J Perinatol. 2020;37(8):769.

    Article  Google Scholar 

  6. 6.

    Haddad LB, Horton J, Ribner BS, Jamieson DJ. Ebola infection in pregnancy: a global perspective and lessons learned. Clin Obstet Gynecol. 2018;61(1):186.

    Article  Google Scholar 

  7. 7.

    Paixao ES, Teixeira MG, Mda CC, Rodrigues LC. Dengue during pregnancy and adverse fetal outcomes: a systematic review and meta-analysis. Lancet Infect Dis. 2016;16:857–65. https://doi.org/10.1016/s1473-3099(16)00088-8.

    Article  PubMed  Google Scholar 

  8. 8.

    Paixao ES, et al. Symptomatic dengue infection and the risk of stillbirth in Brazil, 2006–2012: a matched case–control study. Lancet Infect Dis. 2017;17:957–64.

    Article  Google Scholar 

  9. 9.

    Clemente NS, Brickley EB, Paixão ES, De Almeida MF, Gazeta RE, Vedovello D, et al. Zika virus infection in pregnancy and adverse fetal outcomes in São Paulo State, Brazil: a prospective cohort study. Sci Rep. 2020;10(1):1.

    Article  Google Scholar 

  10. 10.

    Alfaraj SH, Al-Tawfiq JA, Memish ZA. Middle East Respiratory Syndrome Coronavirus (MERS-CoV) infection during pregnancy: report of two cases & review of the literature

  11. 11.

    Online document. Population, Department of Statistics 2020. Accessed [12 Apr 2021]. http://www.doswebdosgovjo/population/population-2/

  12. 12.

    Alsharaydeh I, Rawashdeh H, Saadeh N, Obeidat B, Obeidat N. Challenges and solutions for maternity and gynecology services during the COVID-19 crisis in Jordan. Int J Gynecol Obstet. 2020;150(2):159–62.

    CAS  Article  Google Scholar 

  13. 13.

    Uwambaye P, Nyiringango G, Musabwasoni SM, Husain A, Nessa K, Razzaque MS. COVID-19 pandemic: adaptation in antenatal care for better pregnancy outcomes. Front Glob Womens Health. 2020;1:599327.

    Article  Google Scholar 

  14. 14.

    Boelig RC, Saccone G, Bellussi F, Berghella V. MFM guidance for COVID-19. Am J Obstet Gynecol MFM. 2020;2:100106.

    Article  Google Scholar 

  15. 15.

    Obeidat AZ, El-Salem K. A national telemedicine program in the Kingdom of Jordan–Editorial. Ann Med Surg. 2021;62:145–9.

    Article  Google Scholar 

  16. 16.

    Online document. Coronavirus infection and pregnancy. Information for Healthcare professionals Royal College of Obstetricians and Gynecologists. Coronavirus infection and pregnancy. Information for Healthcare professionals. 2021:13-19. https://www.rcog.org.uk/en/guidelines-research-services/guidelines/coronavirus-pregnancy/covid-19-virus-infection-and-pregnancy/.Accessed 12 Apr 2021

  17. 17.

    Nair M, Nelson-Piercy C, Knight M. Indirect maternal deaths: UK and global perspectives. Obstet Med. 2017;10:10–5.

    Article  Google Scholar 

  18. 18.

    Sullivan E, Marshall D, Li Z, Knight M, Farquhar C, Schutte J, et al. Maternal mortality in high-income countries. J Paediatr Child Health. 2017;53(S2):61.

    Google Scholar 

  19. 19.

    Matheson A, McGannon CJ, Malhotra A, Palmer KR, Stewart AE, Wallace EM, et al. Prematurity rates during the coronavirus disease 2019 (COVID-19) pandemic lockdown in Melbourne, Australia. Obstet Gynecol. 2021;137:405–7.

    CAS  Article  Google Scholar 

  20. 20.

    Chawanpaiboon S, Vogel JP, Moller A-B, Lumbiganon P, Petzold M, Hogan D, et al. Global, regional, and national estimates of levels of preterm birth in 2014: a systematic review and modelling analysis. Lancet Glob Health. 2019;7(1):e37–46.

    Article  Google Scholar 

  21. 21.

    Schwartz DA, Dhaliwal A. Infections in pregnancy with COVID-19 and other respiratory RNA virus diseases are rarely, if ever, transmitted to the fetus: Experiences with coronaviruses, parainfluenza, metapneumovirus respiratory syncytial virus, and influenza. Arch Pathol Lab Med. 2020;144(8):920–8.

    CAS  Article  Google Scholar 

  22. 22.

    Al-sheyab NA, Khader YS, Shattnawi KK, Alyahya MS, Batieha A. Neonatal mortality in Jordan: Rate, determinants, and causes using Jordan stillbirth and neonatal surveillance system. 29 April 2020, PREPRINT (Version 1). 10.21203/rs.3.rs-24128/v1. Accessed [12 Apr 2021].

  23. 23.

    Been JV, Sheikh A. COVID-19 must catalyse key global natural experiments. J Glob Health. 2020;10(1):010104.

    Article  Google Scholar 

  24. 24.

    Philip RK, Purtill H, Reidy E, Daly M, Imcha M, McGrath D, et al. Unprecedented reduction in births of very low birthweight (VLBW) and extremely low birthweight (ELBW) infants during the COVID-19 lockdown in Ireland: a ‘natural experiment’allowing analysis of data from the prior two decades. BMJ Glob Health. 2020;5(9):e003075.

    Article  Google Scholar 

  25. 25.

    Arnaez J, Ochoa-Sangrador C, Caserío S, Gutiérrez EP, del Pilar Jiménez M, Castañón L, et al. Lack of changes in preterm delivery and stillbirths during COVID-19 lockdown in a European region. Eur J Pediatr. 2021:1–6.

  26. 26.

    Li M, Yin H, Jin Z, Zhang H, Leng B, Luo Y, et al. Impact of Wuhan lockdown on the indications of cesarean delivery and newborn weights during the epidemic period of COVID-19. PLoS One. 2020;15:e0237420.

    CAS  Article  Google Scholar 

  27. 27.

    Berghella V, Boelig R, Roman A, Burd J, Anderson K. Decreased incidence of preterm birth during coronavirus disease 2019 pandemic. Am J Obstet Gynecol. 2020;2:100258.

    Google Scholar 

  28. 28.

    Been JV, Ochoa LB, Bertens LC, Schoenmakers S, Steegers EA, Reiss IK. Impact of COVID-19 mitigation measures on the incidence of preterm birth: a national quasi-experimental study. Lancet Glob Health. 2020;5(11):e604–11.

    Article  Google Scholar 

  29. 29.

    Hedermann G, Hedley PL, Bækvad-Hansen M, Hjalgrim H, Rostgaard K, Poorisrisak P, et al. Danish premature birth rates during the COVID-19 lockdown. Arch Dis Childhood Fetal Neonatal Edn. 2021;106(1):93–5.

    Article  Google Scholar 

  30. 30.

    Wood R, Sinnott C, Goldfarb I, Clapp M, McElrath T, Little S. Preterm birth during the coronavirus disease 2019 (COVID-19) pandemic in a large hospital system in the United States. Obstet Gynecol. 2021;137:403–4.

    CAS  Article  Google Scholar 

  31. 31.

    Khalil A, Von Dadelszen P, Draycott T, Ugwumadu A, O’Brien P, Magee L. Change in the incidence of stillbirth and preterm delivery during the COVID-19 pandemic. JAMA. 2020;324:705–6.

    CAS  Article  Google Scholar 

  32. 32.

    Riley T, Sully E, Ahmed Z, Biddlecom A. Estimates of the potential impact of the COVID-19 pandemic on sexual and reproductive health in low-and middle-income countries. Int Perspect Sex Reprod Health. 2020;46:73–6.

    Article  Google Scholar 

  33. 33.

    Muhaidat N, Fram K, Thekrallah F, Qatawneh A, Al-Btoush A. Pregnancy during COVID-19 outbreak: The impact of lockdown in a middle-income country on antenatal healthcare and wellbeing. Int J Women's Health. 2020;12:1065–73.

    Article  Google Scholar 

  34. 34.

    Ashish K, Gurung R, Kinney MV, Sunny AK, Moinuddin M, Basnet O, et al. Effect of the COVID-19 pandemic response on intrapartum care, stillbirth, and neonatal mortality outcomes in Nepal: a prospective observational study. Lancet Glob Health. 2020;8:e1273–81.

    Article  Google Scholar 

  35. 35.

    Caniglia EC, Magosi LE, Zash R, Diseko M, Mayondi G, Mabuta J, et al. Modest reduction in adverse birth outcomes following the COVID-19 lockdown. Am J Obstet Gynecol. 2020;S0002-9378(20):32574–6.

    Google Scholar 

  36. 36.

    Debevec T, Burtscher J, Millet GP. Preterm birth: potential risk factor for greater COVID-19 severity? Respir Physiol Neurobiol. 2020;280:103484.

    CAS  Article  Google Scholar 

Download references

Acknowledgments

We want to thank the King Abdullah II Fund for Development (KAFD) for participating in Partial funding this project (researcher transport and paper printing).

Funding

This study was partially funded by the King Abdullah II Fund for Development (KAFD).(Number 24/11.2020)

Author information

Affiliations

Authors

Contributions

EFB conceived the presented idea, supervised the project, and drafted the final manuscript. EFB, RMD, YK planned and supervised the project. RAM, FAS, LAY, NAB, MAJ, MAM in running the project and development of the initiate manuscript of the project. RAM, MAJ, MAM participated actively in running the technical parts of the project of the project and writing the final draft of the manuscript. YK contributed to the interpretation of the results and writing final draft. All authors provided critical feedback, participated in the research and analysis, and accepted the final manuscript.

Corresponding author

Correspondence to Eman F. Badran.

Ethics declarations

Ethics approval and consent to participate

Informed consent was obtained from all participated mothers. All methods were carried out in accordance with relevant guidelines and regulations of the Institutional Review Board of Jordan University of Science and Technology" for informed consent and guidelines in method section, Ethical approval was obtained from Institutional Review Board of Jordan university of science and Technology (Approval Number 13/137/2020). This manuscript does not contain any individual’s data in any form (including individual details, images, or videos). The process for the approval of the research authorization for use of the databases of the J-SANDS was done by JSANDS technical committee through contact with their project manager.

Consent for publication

Not applicable.

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

Verify currency and authenticity via CrossMark

Cite this article

Badran, E.F., Darwish, R.M., Khader, Y. et al. Adverse pregnancy outcomes during the COVID-19 lockdown. A descriptive study. BMC Pregnancy Childbirth 21, 761 (2021). https://doi.org/10.1186/s12884-021-04221-6

Download citation

Keywords

  • COVID-19
  • Extremely low birth weight
  • Lockdown
  • Neonates