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Impact of spontaneous abortion history and induced abortion history on perinatal outcomes of singleton pregnancies

Abstract

Background

At present, there are several studies on abortion history and perinatal outcomes, but there is no unified conclusion whether the history of abortion and different types of abortion are related to perinatal complications of subsequent pregnancy. We aim to study the impact of different types of abortion history on perinatal outcomes of singleton pregnancies.

Methods

This was a retrospective study from a maternity and infant hospital in Shanghai, China from 2016 to 2020. Pregnant women who gave birth to live singleton infant were included (n = 75,773). We classified abortion into spontaneous abortion (SAB) and induced abortion (IA). We compared the perinatal outcomes of singleton pregnancies with different abortion histories and used Logistic regression analysis to evaluate the associations between pre-pregnancy abortion history with perinatal outcomes.

Results

We observed that pregnant women with a history of abortion were more likely to have a premature delivery (0.99% VS 0.45%), gestational diabetes mellitus (GDM) (13.40% VS 10.29%), placenta abnormality (8.16% VS 5.06%), placenta previa (5.65% VS 3.75%), placenta accreta (0.18% VS 0.04%), and placenta adhesion (2.79% VS 1.03%) than those who obtained singleton pregnancies without a history of abortion. When confounding factors were adjusted, differences in placenta abnormality still existed (excluding placenta abruption). The odds ratios and 95% confidence interval of placenta previa, placenta accreta, and placenta adhesion in pregnant women with only SAB history, only IA history, and both abortion history were 1.294(1.174–1.427), 1.272(1.159–1.396), and 1.390(1.188–1.625), 2.688(1.344–5.374), 2.549(1.268–5.125), and 5.041(2.232–11.386), 2.170(1.872–2.515), 2.028(1.738–2.366), and 3.580(2.917–4.395), respectively.

Conclusions

Our research showed that pregnant women who have a history of abortion before pregnancy were more likely to have premature birth, GDM, placenta previa, placenta accreta, and placenta adhesion. After adjusting for confounding factors, we found that the history of SAB, IA, and both SAB and IA history were related to the increased risk of placenta previa, placenta accreta, and placenta adhesion.

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Introduction

Abortion services have made progress in recent decades. In particular, the development of medical abortion can facilitate an early abortion for women. But complications caused by abortion are still an important cause of maternal mortality worldwide [1,2,3]. Research data in the United States suggested that abortion affected 1/3 of women each year. And by the age of 45, one in four American women has had an abortion [4, 5]. Therefore, it is necessary to continue the research related to abortion. According to the classification of abortion, it can be divided into spontaneous abortion and induced abortion. There is no unified conclusion on whether the history of abortion and different types of abortion are related to perinatal complications of the subsequent pregnancy.

At present, there are some studies on abortion and perinatal outcomes worldwide, but the conclusions are different. A study in the United States believed that there was a strong connection between the first abortion and the possibility of a second abortion in subsequent pregnancy [6]. According to a study from Britain, pregnant women with a history of abortion were more likely to have preeclampsia, premature delivery, and low birth weight in a subsequent pregnancy than those without a history of abortion [7]. Liran Hiersch et al. found that pregnant women with a history of miscarriage were more likely to develop GDM in subsequent pregnancies. Multivariate analysis showed that the history of abortion would lead to a higher cesarean section rate and placental retention rate [8]. Some studies have also explored the association between IA and pregnancy outcomes. A Finnish study explored the association of abortion history with obstetric pregnancy outcomes. The study found that premature delivery and low birth weight were more common among women who had abortions, but after Logistic regression analysis, they found no correlation between them, so the study considered that abortion was not an independent risk factor for obstetric adverse outcomes [9]. However, Alison Lowit and others from Britain believed that the history of IA was related to the increased risk of placenta previa, placental abruption, and low birth weight [10]. In addition, there were some studies on SAB history and pregnancy outcomes, especially on recurrent abortion, but the relevant conclusions were not unified [11, 12].

In view of the fact that there is no unified conclusion on the study of whether abortion history and different types of abortion history are related to perinatal complications of subsequent pregnancy. Therefore, this study was based on the large delivery volume of the class A tertiary obstetrics and gynecology hospital in Shanghai, China, and explored the association between the obstetrical outcomes of subsequent pregnancy with only SAB history, only IA history, and both history of SAB and IA.

Materials and methods

Study population

This was a retrospective study at a class A tertiary obstetrics and gynecology hospital in Shanghai, including women who obtained singleton live pregnancies in this hospital from 2016 to 2020 (n = 75,773). Women with twin and multiple pregnancies (n = 2,580), foreigners (n = 29), missing data (n = 1,784), pre-pregnancy hypertension or pre-pregnancy diabetes (n = 425) were excluded from the study. At last, a total of 75,773 women with live singleton births were included for analysis. Among them, 48,283had no history of abortion, 10,992 had only a history of SAB, 13,360had only a history of IA, and 3,138 had both a history of SAB and a history of IA (Fig. 1).

Fig. 1
figure 1

Flow chart of the participant recruitment process. (Abbreviation: SAB, spontaneous abortion)

Exposure

The primary explanatory variable was the history of abortion, and it was classified as only SAB history, only IA history, both SAB history and IA history, and no abortion history.

Outcomes

We were interested in perinatal complications, including placenta abnormality, premature delivery, GDM, pregnancy hypertension disorder, intrahepatic cholestasis of pregnancy, and oligohydramnios. Placenta abnormality included placenta previa, placenta abruption, placental accreta, and placental adhesion. Placenta previa means that the lower edge of the placenta reaches or covers the cervix, which is lower than the fetal presentation. Placenta abruption means that the placenta is partially or completely stripped from the uterine wall before the fetus is delivered. Placenta accreta means that placental villi penetrate the myometrium of the uterine wall. Placental adhesion means that the placenta adheres to the uterine wall in whole or in part and cannot be peeled off by itself. Pregnancy hypertension disorder included PIH and preeclampsia.

Statistical analysis

The basic characteristics of the study population were statistically analyzed by descriptive analysis. Count (%) was used for categorical variables. The cross table was used to test whether women with an abortion history were related to perinatal complications compared with women without an abortion history. P < 0.05 is considered statistically significant. Logistic regression analysis was used to estimate the associations between different classifications of abortions and adverse perinatal outcomes. Possible confounding factors included maternal age, pre-pregnancy BMI (< 18.5 kg/m2, 18.5 kg/m2- < 25 kg/m2, ≥ 25 kg/m2) [13], mode of delivery (vaginal delivery or cesarean section) and parity (primipara or multipara). The classification of BMI was based on the standard of WHO [13].

All analyses were processed by the SPSS26.0 software package (SPSS Inc, Chicago, IL, USA).

Results

Among the 75,773 included pregnant women, 48,283(63.72%) had no history of abortion, 10,992(14.51%) had only a history of SAB, 13,360(17.63%) had only a history of IA, and 3,138 (4.14%) had both history of SAB and history of IA. Compared with pregnant women without an abortion history, pregnant women with an abortion history were more likely to be old (age ≥ 35 years old) (23.02% VS 9.67%), and the probability of BMI ≥ 25 kg/m2 before pregnancy is greater (10.27% VS 7.94%). Moreover, pregnant women with a history of abortion had a higher probability of cesarean section (38.62% VS 29.20%), and the probability of multipara was higher (37.01% VS 17.55%). In addition, women with a history of abortion had a higher risk of placenta abnormality (8.16% VS 5.06%) (including placenta previa (5.65% VS 3.75%), placenta accreta (0.18% VS 0.04%), and placenta adhesion (2.79% VS 1.03%)), premature delivery (0.99% VS 0.45%), and GDM (13.40% VS 10.29%). However, there was no statistical difference in the incidence of placenta abruption (0.42% VS 0.51%), pregnancy hypertension disorder (4.53% VS 4.50%), intrahepatic cholestasis of pregnancy (1.12% VS 1.18%) and oligohydramnios (1.25% VS 1.22%). The detailed information of the research population are shown in Table 1.

Table 1 Basic characteristics and adverse outcomes of the study population by the history of abortion or not

We studied the association between different types of abortion and perinatal complications of singleton pregnancies and found that compared with pregnant women without abortion history, those with abortion history (including SAB history or IA history) were more likely to have premature delivery, GDM, pregnancy hypertension disorder, placenta previa, placenta accreta, and placenta adhesion, and there were statistical differences (P < 0.05). Compared with pregnant women without abortion history, women with a history of SAB were more likely to have premature delivery (0.76% VS 0.45%), GDM (15.00% VS 10.29%), pregnancy hypertension disorder (5.41% VS 4.50%), placenta abnormality (8.04% VS 5.06%), placenta previa (5.43% VS 3.75%), placental accreta (0.15% VS 0.04%) and placental adhesion (2.88% VS 1.03%), and there was a statistical difference (P < 0.05). Women with a history of IA were more likely to have premature delivery (1.04% VS 0.45%), GDM (11.75% VS 10.29%), pregnancy hypertension disorder (3.81% VS 4.50%), placenta abnormality (7.69% VS 5.06%), placenta previa (5.63% VS 3.75%), placental accreta (0.16% VS 0.04%) and placental adhesion (2.30% VS 1.03%). The difference was also statistically significant (P < 0.05). However, we did not observe the statistical difference between women with a history of both SAB and IA and women without a history of abortion in pregnancy hypertension disorder. The details were shown in Table 2.

Table 2 Basic characteristics and adverse outcomes of the study population by different classifications of abortions

Logistic regression analysis was used to evaluate the association between abortion history and premature delivery, GDM, pregnancy hypertension disorder, PIH, preeclampsia, placenta abnormality, placenta previa, placental accreta, and placental adhesion. The results showed that after adjusting for potential confounding factors (including pre-pregnancy BMI, maternal age, mode of delivery, and parity), differences in placenta abnormality (including placenta previa, placenta accreta, and placental adhesion) still existed. The odds ratios (ORs) and 95% confidence interval (CI) of placenta previa, placenta accreta, and placenta adhesion in pregnant women with only SAB history, only IA history, and both abortions history were 1.294(1.174–1.427), 1.272(1.159–1.396), and 1.390(1.188–1.625), 2.688(1.344–5.374), 2.549(1.268–5.125), and 5.041(2.232–11.386), 2.170(1.872–2.515), 2.028(1.738–2.366), and 3.580(2.917–4.395), respectively. We also found that women with only a SAB history had a higher risk of premature delivery and GDM. However, we did not observe the association between only IA history and premature delivery, GDM, and pregnancy hypertension disorder. The details are shown in Table 3.

Table 3 Crude and adjusted OR (95% CI) for the associations between classification of abortions and unfavorable outcomes

In addition, considering the strong correlation between abortion history and placenta abnormality, we also conducted a stratified analysis of maternal age and pre-pregnancy BMI to further observe whether the risk of placenta previa, placenta accreta, and placental adhesion changed with maternal age or pre-pregnancy BMI, and we found that compared with women under 35 years old, women over 35 years old with a history of abortion (including SAB and IA) have an increased risk of placenta abnormality, placenta previa and placental adhesion. But we did not find that the association between them changed with pre-pregnancy BMI. See Tables 4 and 5 for details.

Table 4 Crude and adjusted OR (95% CI) for the associations between the classification of abortions and unfavorable perinatal outcomes by pre-pregnancy BMI
Table 5 Crude and adjusted OR (95% CI) for the associations between the classification of abortions and unfavorable perinatal outcomes by maternal age

Discussion

As far as we know, this was the first large-scale study in China to explore the association between the history of abortion and perinatal outcomes after singleton pregnancies. After analyzing 75,773 women with singleton pregnancies, we found that women with only SAB history before pregnancy had a higher risk of premature delivery, GDM, placenta abnormality, placenta previa, placenta accreta, and placental adhesion in subsequent pregnancies. Women who only had IA history and had both SAB and IA history were at greater risk of placenta abnormality, placenta previa, placenta accreta, and placenta adhesion in subsequent pregnancies.

With regard to SAB, recurrent abortion was the most studied. Many studies have shown that recurrent abortion was associated with a variety of adverse obstetrical outcomes, including preeclampsia, premature delivery, small for gestational-age infants, placental abruption, pregnancy complications related to placental dysfunction, etc. [14,15,16]. A new study in China has found that women with a history of SAB had an increased risk of GDM in subsequent pregnancies [17]. An Iranian study assessed the history of SAB and the risk of preterm birth in subsequent pregnancies. The results showed that the history of SAB was related to the increased probability of preterm delivery, that is, the more times of SAB, the greater the probability of preterm delivery [18], and other studies had similar results [19]. These findings were consistent with our conclusions because we found that women who had only SAB history before pregnancy had a higher risk of preterm delivery and GDM in subsequent pregnancies after adjusting for confounding factors. Although we did not observe that the history of IA was related to premature delivery and GDM, other studies suggested that the risk of premature delivery increased after IA [20,21,22]. It has been reported that women with abnormal glucose metabolism before pregnancy will have an increased risk of miscarriage in the following pregnancy [23, 24], which may explain the increased risk of GDM after SAB. However, because this study is retrospective and lacks enough detailed glucose metabolism information, we are not sure whether it is related to this reason. We speculate that the reason for the increase in the incidence of preterm delivery may be that the history of abortion could lead to cervical insufficiency and increase the risk of infection [25, 26]. However, there is no literature report on why the risk of premature delivery of SAB increases, but the risk of IA does not increase significantly.

We found that pregnant women with only SAB history were more likely to have PIH and preeclampsia, but pregnant women with only IA history were less likely to have PIH and preeclampsia, and these results were statistically different. After Logistic regression analysis, these differences still existed and had statistical differences. However after adjusting the potential confounding factors, these differences disappeared. Beck et al. found that the probability of preeclampsia in pregnant women with IA was significantly lower than that in pregnant women without abortion or with SAB history [27], and other studies had similar results [28, 29]. These were all consistent with our research results. However, other studies have suggested that a history of SAB can reduce the risk of preeclampsia [30, 31]. It has been suggested that normal pregnancy interrupted in the early stage of pregnancy may cause immune changes, thereby reducing the risk of preeclampsia in subsequent pregnancy [29]. Other studies have suggested that the interval between two pregnancies may be a major determinant [32, 33]. However, the mechanism of the relationship between SAB, IA and pregnancy induced hypertension needs to be further explored.

With regard to placenta abnormality, we mainly explored four placenta-related complications: placenta previa, placental abruption, placental accreta, and placental adhesion. We found that whether there was only a history of SAB, only a history of IA, or a history of both SAB and IA, they were associated with an increased risk of placenta previa, placental accreta, and placental adhesion, but not with placental abruption. Our conclusions were consistent with those of other studies [34]. Studies by W Zhou et al. have shown that there was a positive correlation between abortion and placental residues in subsequent singleton live births [35]. Zhu et al.'s study showed that women with a history of IA had a higher incidence of placental abruption. However, after considering confounding factors, the difference was not statistically significant [36]. In addition, other studies also believed that placenta previa, placenta residue, and other placenta abnormality were related to abortion [37, 38]. The placenta abnormality occurred in the subsequent pregnancy after abortion, and the mechanism may be that the operation damaged the endometrium and uterine cavity [39, 40].

Our study was the first large-scale study in China to explore the association between the history of abortion and multiple pregnancy complications after singleton pregnancy. However, our research had some limitations. First of all, this was a retrospective study. Abortion information was self-reported by pregnant women, and there may be underreporting. Secondly, some literature believed that the pregnancy interval after abortion will have an impact on perinatal complications [41], but we did not study the effect of pregnancy interval after abortion on the outcomes. Thirdly, we did not classify induced abortion to study the effects of drug abortion and surgical abortion on the results [42]. Finally, because the electronic medical record system did not record the gestational age at the time of abortion in detail and lacked the history of PE, GDM and placenta abnormality in their previous pregnancy, we did not study its influence on the pregnancy outcomes.

Conclusion

In a word, our research showed that pregnant women who had a history of abortion before pregnancy (including a history of SAB or IA) and then got singleton pregnancies were more likely to have premature delivery, GDM, placenta abnormality, placenta previa, placenta accreta, and placenta adhesion. After adjusting for confounding factors, it was found that the history of SAB and IA were still associated with placenta abnormality, placenta previa, placental accreta, and placental adhesion.

Availability of data and materials

The datasets used and analyzed during the current study are available from the corresponding author upon reasonable request.

References

  1. Induced abortion. Hum Reprod. 2017;32(6):1160–1169. https://doi.org/10.1093/humrep/dex071.

  2. Harris LH, Grossman D. Complications of Unsafe and Self-Managed Abortion. N Engl J Med. 2020;382(11):1029–40.

    Article  CAS  PubMed  Google Scholar 

  3. Stevenson AJ. The Pregnancy-Related Mortality Impact of a Total Abortion Ban in the United States: A Research Note on Increased Deaths Due to Remaining Pregnant. Demography. 2021;58(6):2019–28.

    Article  PubMed  Google Scholar 

  4. Jones RK, Jerman J. Population Group Abortion Rates and Lifetime Incidence of Abortion: United States, 2008–2014. Am J Public Health. 2017;107(12):1904–9.

    PubMed  PubMed Central  Google Scholar 

  5. ACOG Practice Bulletin No. 200: Early Pregnancy Loss. Obstet Gynecol. 2018;132(5):e197-e207. https://doi.org/10.1097/AOG.0000000000002899.

  6. Studnicki J, Longbons T, Reardon DC, et al. The Enduring Association of a First Pregnancy Abortion with Subsequent Pregnancy Outcomes: A Longitudinal Cohort Study. Health Serv Res Manag Epidemiol. 2022;9:23333928221130944.

    PubMed  PubMed Central  Google Scholar 

  7. Bhattacharya S, Townend J, Shetty A, Campbell D, Bhattacharya S. Does miscarriage in an initial pregnancy lead to adverse obstetric and perinatal outcomes in the next continuing pregnancy? BJOG. 2008;115(13):1623–9.

    Article  CAS  PubMed  Google Scholar 

  8. Hiersch L, Ashwal E, Aviram A, Rayman S, Wiznitzer A, Yogev Y. The association between previous single first trimester abortion and pregnancy outcome in nulliparous women. J Matern Fetal Neonatal Med. 2016;29(9):1457–61.

    Article  PubMed  Google Scholar 

  9. Raatikainen K, Heiskanen N, Heinonen S. Induced abortion: not an independent risk factor for pregnancy outcome, but a challenge for health counseling. Ann Epidemiol. 2006;16(8):587–92.

    Article  PubMed  Google Scholar 

  10. Lowit A, Bhattacharya S, Bhattacharya S. Obstetric performance following an induced abortion. Best Pract Res Clin Obstet Gynaecol. 2010;24(5):667–82.

    Article  PubMed  Google Scholar 

  11. Ali N, Elbarazi I, Ghazal-Aswad S, et al. Impact of Recurrent Miscarriage on Maternal Outcomes in Subsequent Pregnancy: The Mutaba’ah Study. Int J Womens Health. 2020;12:1171–9.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Ausbeck EB, Blanchard C, Tita AT, Szychowski JM, Harper L. Perinatal Outcomes in Women with a History of Recurrent Pregnancy Loss. Am J Perinatol. 2021;38(1):10–5.

    Article  PubMed  Google Scholar 

  13. Appropriate body-mass index for Asian populations and its implications for policy and intervention strategies. Lancet. 2004;363(9403):157–163. https://doi.org/10.1016/S0140-6736(03)15268-3.

  14. Rasmark Roepke E, Christiansen OB, Källén K, Hansson SR. Women with a History of Recurrent Pregnancy Loss Are a High-Risk Population for Adverse Obstetrical Outcome: A Retrospective Cohort Study. J Clin Med. 2021;10(2). https://doi.org/10.3390/jcm10020179. 

  15. Gunnarsdottir J, Stephansson O, Cnattingius S, Akerud H, Wikström AK. Risk of placental dysfunction disorders after prior miscarriages: a population-based study. Am J Obstet Gynecol. 2014;211(1):34.e31-38.

    Article  Google Scholar 

  16. Endler M, Saltvedt S, Cnattingius S, Stephansson O, Wikström AK. Retained placenta is associated with pre-eclampsia, stillbirth, giving birth to a small-for-gestational-age infant, and spontaneous preterm birth: a national register-based study. BJOG. 2014;121(12):1462–70.

    Article  CAS  PubMed  Google Scholar 

  17. Zhao Y, Zhao Y, Fan K, Jin L. Association of History of Spontaneous or Induced Abortion With Subsequent Risk of Gestational Diabetes. JAMA Netw Open. 2022;5(3): e220944.

    Article  PubMed  PubMed Central  Google Scholar 

  18. Omani-Samani R, Mansournia MA, Sepidarkish M, et al. Cross-sectional study of associations between prior spontaneous abortions and preterm delivery. Int J Gynaecol Obstet. 2018;140(1):81–6.

    Article  PubMed  Google Scholar 

  19. Makhlouf MA, Clifton RG, Roberts JM, et al. Adverse pregnancy outcomes among women with prior spontaneous or induced abortions. Am J Perinatol. 2014;31(9):765–72.

    PubMed  Google Scholar 

  20. Swingle HM, Colaizy TT, Zimmerman MB, Morriss FH Jr. Abortion and the risk of subsequent preterm birth: a systematic review with meta-analyses. J Reprod Med. 2009;54(2):95–108.

    PubMed  Google Scholar 

  21. Voigt M, Henrich W, Zygmunt M, Friese K, Straube S, Briese V. Is induced abortion a risk factor in subsequent pregnancy? J Perinat Med. 2009;37(2):144–9.

    Article  PubMed  Google Scholar 

  22. Zhou W, Sørensen HT, Olsen J. Induced abortion and subsequent pregnancy duration. Obstet Gynecol. 1999;94(6):948–53.

    CAS  PubMed  Google Scholar 

  23. Kawakita T, Bowers K, Coviello E, et al. Prepregnancy Weight in Women with Type I Diabetes Mellitus: Effect on Pregnancy Outcomes. Am J Perinatol. 2016;33(13):1300–5.

    Article  CAS  PubMed  Google Scholar 

  24. Wahabi HA, Esmaeil SA, Fayed A, Al-Shaikh G, Alzeidan RA. Pre-existing diabetes mellitus and adverse pregnancy outcomes. BMC Res Notes. 2012;5:496.

    Article  PubMed  PubMed Central  Google Scholar 

  25. Field K, Murphy DJ. Perinatal outcomes in a subsequent pregnancy among women who have experienced recurrent miscarriage: a retrospective cohort study. Hum Reprod. 2015;30(5):1239–45.

    Article  CAS  PubMed  Google Scholar 

  26. Oliver-Williams C, Fleming M, Wood AM, Smith G. Previous miscarriage and the subsequent risk of preterm birth in Scotland, 1980–2008: a historical cohort study. BJOG. 2015;122(11):1525–34.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  27. Beck I. Incidence of pre-eclampsia in first full-term pregnancies preceded by abortion. J Obstet Gynaecol. 1985;6(2):82–4.

    Article  CAS  Google Scholar 

  28. Seidman DS, Ever-Hadani P, Stevenson DK, Gale R. The effect of abortion on the incidence of pre-eclampsia. Eur J Obstet Gynecol Reprod Biol. 1989;33(2):109–14.

    Article  CAS  PubMed  Google Scholar 

  29. Trogstad L, Magnus P, Skjaerven R, Stoltenberg C. Previous abortions and risk of pre-eclampsia. Int J Epidemiol. 2008;37(6):1333–40.

    Article  PubMed  PubMed Central  Google Scholar 

  30. Mohamedain A, Rayis DA, AlHabardi N, Adam I. Association between previous spontaneous abortion and preeclampsia: a case-control study. BMC Pregnancy Childbirth. 2022;22(1):715.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  31. Eras JL, Saftlas AF, Triche E, Hsu CD, Risch HA, Bracken MB. Abortion and its effect on risk of preeclampsia and transient hypertension. Epidemiology. 2000;11(1):36–43.

    Article  CAS  PubMed  Google Scholar 

  32. Skjaerven R, Wilcox AJ, Lie RT. The interval between pregnancies and the risk of preeclampsia. N Engl J Med. 2002;346(1):33–8.

    Article  PubMed  Google Scholar 

  33. Basso O, Christensen K, Olsen J. Higher risk of pre-eclampsia after change of partner. An effect of longer interpregnancy intervals? Epidemiology. 2001;12(6):624–9.

    Article  CAS  PubMed  Google Scholar 

  34. Yang J, Wang Y, Wang XY, Zhao YY, Wang J, Zhao YY. Adverse Pregnancy Outcomes of Patients with History of First-Trimester Recurrent Spontaneous Abortion. Biomed Res Int. 2017;2017:4359424.

    Article  PubMed  PubMed Central  Google Scholar 

  35. Zhou W, Nielsen GL, Larsen H, Olsen J. Induced abortion and placenta complications in the subsequent pregnancy. Acta Obstet Gynecol Scand. 2001;80(12):1115–20.

    Article  CAS  PubMed  Google Scholar 

  36. Zhu QX, Gao ES, Chen AM, Luo L, Cheng YM, Yuan W. Mifepristone-induced abortion and placental complications in subsequent pregnancy. Hum Reprod. 2009;24(2):315–9.

    Article  PubMed  Google Scholar 

  37. Ganer Herman H, Volodarsky-Perel A, Nu TNT, et al. Does a history of recurrent pregnancy loss affect subsequent obstetric outcomes and placental findings in in vitro fertilization? J Assist Reprod Genet. 2022;39(12):2711–8.

    Article  PubMed  Google Scholar 

  38. Barrett JM, Boehm FH, Killam AP. Induced abortion: a risk factor for placenta previa. Am J Obstet Gynecol. 1981;141(7):769–72.

    Article  CAS  PubMed  Google Scholar 

  39. Ananth CV, Smulian JC, Vintzileos AM. The association of placenta previa with history of cesarean delivery and abortion: a metaanalysis. Am J Obstet Gynecol. 1997;177(5):1071–8.

    Article  CAS  PubMed  Google Scholar 

  40. Adelusi B, Soltan MH, Chowdhury N, Kangave D. Risk of retained placenta: multivariate approach. Acta Obstet Gynecol Scand. 1997;76(5):414–8.

    Article  CAS  PubMed  Google Scholar 

  41. El Behery MM, Siam S, Seksaka MA, Ibrahim ZM. Reproductive performance in the next pregnancy for nulliparous women with history of first trimester spontaneous abortion. Arch Gynecol Obstet. 2013;288(4):939–44.

    Article  PubMed  Google Scholar 

  42. Bhattacharya S, Lowit A, Bhattacharya S, et al. Reproductive outcomes following induced abortion: a national register-based cohort study in Scotland. BMJ Open. 2012;2(4). https://doi.org/10.1136/bmjopen-2012-000911.

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Acknowledgements

We thank Shanghai First Maternity and Infant Hospital for providing the patient records.

Funding

This work was supported by National Natural Science Foundation (grant No.82371693), Shanghai Municipal Health Commission (grant No.202340113), Pudong New Area Health Committee (grant No. PW2023E-04), and Shanghai Science and Technology Commission (grant No. 20Y11907900).

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Sun and Mao drafted the manuscript and analysed the data. Su interpreted data and conducted statistical analysis. Du critically revised the manuscript of important content. All authors were involved in writing of the paper and had final approval of the submitted and published versions.

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Correspondence to Qiaoling Du.

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This study was approved by the Ethics Committee of the Shanghai First Maternal and Infant Hospital, affiliated with Tongji University School of Medicine (KS1998). Written informed consent for participation was not required for this study per national legislation and the institution’s requirements. Due to the nature of this retrospective study and the preserved anonymity of patients, a waiver of informed consent was obtained. Shanghai First Maternal and Infant Hospital, affiliated with Tongji University School of Medicine waived for consent. We confirmed that all methods were carried out in accordance with relevant guidelines and regulations.

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Sun, H., Mao, J., Su, X. et al. Impact of spontaneous abortion history and induced abortion history on perinatal outcomes of singleton pregnancies. BMC Public Health 23, 2360 (2023). https://doi.org/10.1186/s12889-023-17264-5

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