ABSTRACT
Background and Aim
Cesarean scar pregnancy (CSP) is rare but poses a potentially life‐threatening complication. There is currently insufficient evidence in the literature regarding the impact of CSP treatment on future fertility due to limited clinical studies on a large scale. Here, we investigated the future reproductive outcomes of women with CSP.
Methods
From December 2019 to July 2023, women diagnosed with CSP at the Hospital of Obstetrics and Gynaecology of Fudan University, Shanghai, China, were followed up by telephone calls. Data on future fertility and outcomes were collected.
Results
Among 302 women, excluding three who did not answer the question, 234 (77.5%) did not express their intention to conceive in future, while only 65 (22%) expressed an intention to conceive again. Among these 65 women intending to conceive, 14 (21.5%) achieved pregnancy. In contrast, among women who did not intend to conceive, 31 (15.4%) achieved pregnancy. After excluding women within 12 months of treatment, the analysis showed no statistical difference in successful conception between women who intended to conceive again and those who did not (p = 0.0523). Additionally, among the 45 who achieved pregnancy, 26 resulted in live births. In women with successful conception, there was no statistical difference in the association between CSP treatment or CSP subtype and successful conception (p = 0.6913 or p = 0.5823).
Conclusion
Our study found that 22% of women with CSP intended to conceive, and 29% of our study cohort had a subsequent pregnancy. There was no association between treatment options or CSP subtype and successful conception. Additionally, the incidence of complications in subsequent pregnancies was comparable to that reported in the literature for women without a history of CSP. Our findings suggest that surgical treatments for CSP may not negatively affect future fertility.
Keywords: cesarean scar pregnancy, fertility, optimal treatment, reproductive outcomes, subtypes of CSP
1. Introduction
Cesarean scar pregnancy (CSP) is a life‐threatening complication of pregnancy, occurring in approximately 1:1800 to 1:2200 of all pregnancies [1], and up to 1:500 in women with a prior cesarean section [2, 3]. Because of the risk of severe complications, early termination is usually recommended in clinical practice. However, in CSP literature, there is still no “gold standard” treatment option, and management remains a clinical challenge [4, 5]. In clinical practice, medical treatment such as methotrexate and several surgical approaches, including transvaginal resection, laparoscopy, uterine artery embolization (UAE) combined with dilatation and curettage (D&C) with or without hysteroscopy, and hysteroscopy alone, are commonly used [6, 7, 8, 9, 10].
Approximately 40%–70% of women with a history of cesarean section develop cesarean scar defects (or “niches”) [11, 12]. These defects are increasingly recognized as both structural and functional sequelae that may interfere with implantation, promote local inflammation, and cause mechanical disruption, leading to adverse outcomes such as miscarriages [13]. Systematic review studies have recently suggested that niches can impair fertility because they can be a physical barrier [14, 15], and niche resection may improve conception rates in women with subfertility [16] and is safe [15]. These findings indirectly support a possible association between CSP and subsequent fertility outcomes.
Despite the increasing incidence of CSP worldwide, data on subsequent pregnancy outcomes after CSP treatment remain limited. This is largely due to the small sample size and the reluctance of women with a prior CSP to pursue another pregnancy. Prior reports indicate varying rates of reproductive desire post‐treatment, with up to 64% of women opting against future pregnancy [17, 18]. As a result, data on outcomes of subsequent pregnancy are limited, even though the low incidence of recurrence of CSP, miscarriage, ectopic pregnancy, preterm birth, placenta accreta, and uterine rupture in a subsequent pregnancy is reported [19].
Fertility outcomes after initial treatment of CSP are also not well characterized in the literature. A systematic review reported a subsequent pregnancy rate of 74% for surgical treatment and 69% for non‐surgical treatment of CSP [20]. However, that study did not address whether different management approaches affect future fertility (reviewed in [19]). Studies with a relatively small sample size reported that 15%–40% of women failed to conceive after 12 months of trying [17, 21]. Our previous study with a medium sample size similarly found that 14% of women with a history of CSP did not conceive without any contraception use [18].
The management strategies of CSP are entirely dependent on individual cases and different hospital protocols, which may influence fertility outcomes in future pregnancies. CSP has traditionally been divided into two subtypes, type 1 and type 2, based on the implantation site of the gestational sac and the thickness of the remaining myometrium [5, 22, 23]. This classification primarily helps to guide the potential treatment options. More recently, a study further proposed three types of CSP, type 1, type 2 and type 3, according to the surgical management strategy [24]. In contrast, the newer Crossover Sign (COS) classification focuses on the relationship between the gestational sac and the previous scar to better predict the risk of placenta accreta spectrum and uterine rupture [25, 26]. Therefore, we conducted this study to evaluate the reproductive outcomes of women with a history of CSP surgically treated in a tertiary hospital.
2. Materials and Methods
The Ethics Committee of The Hospital of Obstetrics and Gynaecology, Fudan University, China, approved this prospective study (reference numbers: KYY2019‐76, KYY2020‐185, and KYY2024‐20). The signed consent form was obtained at the time of recruitment. This study was performed in accordance with the Medical Association Declaration of Helsinki.
2.1. Study Population
The Hospital of Obstetrics and Gynaecology, Fudan University, China, is located in Shanghai, a city with a population of 25,000,000. Our hospital is one of the largest Obstetrics and Gynaecology specialized hospitals in the country, ranked among the top three nationally. With a capacity of more than 820 beds, we manage more than 100,000 births and more than 1,000,000 gynecological outpatient visits annually.
This prospective cohort study followed the STROBE guidelines. From December 2019 to July 2023, 345 women were diagnosed with CSP at our hospital and received treatments. CSP confirmation was primarily achieved using transvaginal ultrasound (HITACHI ARTETTA, Japan or Philips) with key diagnostic criteria including the presence of a gestational sac or at least a large part of the gestational sac in the area of the scar, in addition to a history of a prior cesarean section and a positive test of serum β‐hCG. Based on the site of implantation and the gestational sac's growth direction, the CSP was subdivided into two types. Type 1 CSP is when the gestational sac is implanted in the myometrium and growing toward the cervico‐isthmic space or uterine cavity (Figure 1A). Type 2 CSP is when the gestational sac implants deeply into the previous cesarean scar defect and grows toward the myometrium and the uterine serosal layer (Figure 1B) [5, 22, 23]. The initial treatment, mainly performed in our hospital, included ultrasound‐guided suction curettage, ultrasound‐guided suction curettage after uterine artery embolization (referred to as UAE) using a 5‐F angiographic catheter, hysteroscopy or laparoscopy, or a combination of hysteroscopy and laparoscopy. Patients were discharged on Day 2 after treatment and were followed up in outpatient clinics. To confirm successful treatment, postoperative serum hCG testing was performed once a week for 2–4 times. Additionally, a follow‐up ultrasound was performed every 2 weeks for a total of two times.
Figure 1.

Transvaginal ultrasound images showing type 1 (A) and type 2 CSP (B). The gestational sac (red arrow) is implanted at the site of the previous cesarean scar (yellow arrow), located below and separate from the uterine cavity (green arrow).
Clinical data, including age at diagnosis, body mass index (BMI), blood loss during previous treatment, subtype of CSP, initial treatment option, parity, gestational age, the number of surgical abortions, and the interval between the current CSP and the last cesarean section, were collected from our hospital electronic databases.
By the end of November 2023, of these 345 cases, 302 (87.5%) women were followed up by telephone calls. Self‐reported information on a subsequent pregnancy, including pregnancy outcomes, whether intended to conceive again, menstrual cycle length and menses, and menstrual flow, was collected. Not conceiving is defined, according to the World Health Organization (WHO), as the failure to achieve a clinical pregnancy after 12 months or more of regular unprotected sexual intercourse. Therefore, in this study, women who were within 12 months of their initial treatment were excluded from the analysis of the probability of having a subsequent pregnancy.
2.2. Statistical Analysis
Among 302 women with CSP who were successfully followed up, 299 provided complete follow‐up data (Figure 2). To assess the efficacy of our sample size, we calculated 95% confidence intervals (CIs) for primary fertility outcomes in subsequent pregnancy. For women who intended to conceive again (n = 65), the pregnancy rate was 21.5% (95% CI: 12.5%, 33.3%). While the sample size was determined by the available clinical cohort rather than a prospective power calculation for statistical analysis, the high follow‐up rate (87.5%) and the resulting precision of the CIs allow for a reliable estimate of post‐CSP fertility trends in subsequent pregnancy. Additionally, 43 (12.5%) women were lost to follow‐up. There was no statistical difference in the baseline of clinical parameters, including age at diagnosis, parity, surgical abortions, number of previous cesarean sections and initial CSP subtype between women who were followed up and who lost (p > 0.05).
Figure 2.

Outcomes of successful conception (*three women did not answer the question regarding the intention of conceiving again).
Mean, standard deviation (SD), or percentage were used for data presented in Table 1. To compare the probability of subsequent pregnancy between women who intended and those who did not, or to examine the association between previous treatment options or CSP subtypes and subsequent pregnancy (Tables 2, 3, 4), Chi‐square tests were performed using GraphPad Prism (version 10.1.2). Statistical significance was considered when p < 0.05.
Table 1.
Clinical parameters of the study cohort who were followed up (n = 302).
| Age at diagnosis of CSP (years, mean/SD) | 35.2 ± 4 |
| BMI (Kg/m2, mean/SD) | 22.73 ± 3.4 |
| Parity (n, %) | |
| 1 | 164 (54%) |
| 2 | 127 (42%) |
| ≥ 3 | 11 (4%) |
| Surgical abortions (n, %) | |
| 0 | 26 (9%) |
| 1 | 116 (38%) |
| 2 | 96 (32%) |
| ≥ 3 | 64 (21%) |
| Number of previous cesarean sections (n, %) | |
| 1 | 177 (59%) |
| 2 | 116 (38%) |
| ≥ 3 | 9 (3) |
| Subtypes of CSP (n, %) | |
| Type 1 | 123 (41%) |
| Type 2 | 179 (59%) |
| Treatment options (n, %) | |
| Suction curettage | 196 (65%) |
| UAE | 85 (28%) |
| Others* | 21 (7%) |
| Blood loss during operation (ml, mean/SD) | 40 ± 212 |
| Pelvic pain after the previous operation | |
| No change | 56 (18.5%) |
| No pelvic pain | 231 (76.5%) |
| Had pelvic pain | 15 (5%) |
| Menstrual cycle after the previous operation | |
| Menses (days, mean/SD) | 5 (± 1.7) |
| Days between cycles | 28 (± 3) |
Other referred to as hysteroscopy or laparoscopy or a combination of hysteroscopy and laparoscopy.
Table 2.
The comparison of subsequent pregnancy in CSP women who intend to have a pregnancy and who did not.
| Pregnancy intention after CSP treatment | Became pregnant (n, %) | Did not become pregnant (n, %) | p value (Chi‐square test) |
|---|---|---|---|
| Intended to conceive (n = 49)* | 14 (28.6%) | 35 (71.4%) | p = 0.0317 |
| Did not intend to conceive (n = 201)* | 31 (15.4%) | 170 (84.6%) |
Women within 12 months after initial CSP treatment were excluded.
Table 3.
The association of previous treatment options and subsequent pregnancy.
| Previous treatment options | Became pregnant (n, %) | Did not become pregnant (n, %) | p value (Chi‐square test) |
|---|---|---|---|
| Suction curettage (n = 196) | 33 (16.8%) | 163 (83.2%) | 0.6913 |
| UAE (n = 85) | 7 (8.2%) | 78 (91.8%) | |
| Others (n = 21) | 5 (23.8%) | 16 (76.2%) |
Note: Other referred to as hysteroscopy or laparoscopy or a combination of both; UAE: ultrasound‐guided suction curettage after uterine artery embolization (UAE).
Table 4.
The comparison of subsequent pregnancy outcomes between women with different types of previous CSP.
| Overall | Type 1 CSP ( n = 123) | Type 2 CSP ( n = 179) | p value (Chi‐square test) |
|---|---|---|---|
| Became pregnant (n, %) | 20 (16.3%) | 25 (14.0%) | 0.5823 |
| Did not become pregnant (n, %) | 103 (83.7%) | 154 (86.0%) | |
| Live birth (n = 26) | |||
| With live birth (n, %) | 9 (7.3%) | 17 (9.5%) | 0.5069 |
| Without live birth (n, %) | 114 (92.7%) | 162 (90.5%) |
3. Results
Of the 345 women diagnosed with CSP, 302 (87.5%) were successfully followed up. The general clinical characteristics of these women are listed in Table 1. The mean age at diagnosis was 35.2 (± 4) years, and the median age at diagnosis was 35 years, ranging from 24 to 47 years. The mean BMI was 22.73 (± 3.6) Kg/m2, and the median BMI was 22.2 Kg/m2 (ranging from 16 to 36). The mean blood loss during the previous operation was 40 ml (± 212), and the median was 10 mL, ranging from 1 to 3500 mL. 123 (41%) women were diagnosed with type 1 CSP, and 196 (65%) received suction curettage.
Among the 302 women who were followed up, 3 did not indicate their future reproductive intentions. Of the remaining 299 women, 234 (78%) did not intend to conceive again, while 65 (22%) expressed intention to conceive again (Figure 2). 14 of these 65 women who intended to conceive again achieved pregnancy. After excluding 16 women within 12 months of their initial CSP treatment, the conception rate in the remaining 49 women was 28.6% (Table 2). In contrast, among women who did not intend to conceive again (n = 201, excluding 33 women within 12 months of treatment), 31 (15.4%) “accidentally” achieved pregnancy. A Chi‐square test showed a significantly higher proportion of women who intended to conceive and did so than of those who did not intend to conceive but did (28.6% vs. 15.4%, p = 0.0317, Table 2).
We next evaluated whether different treatment options for the initial CSP influenced the likelihood of subsequent pregnancy, regardless of whether women intended to conceive again or not. Among the 45 women who achieved pregnancy, 33 (73.3%) had previously undergone suction curettage, 7 (15.6%) underwent UAE followed by suction curettage, and 5 (11.1%) underwent hysteroscopy, laparoscopy, or both. As shown in Table 3, there was no statistical association between prior CSP treatment options and successful conception (p = 0.6913). Additionally, we further analyzed whether the subtypes of CSP were associated with successful conception. As shown in Table 4, no significant differences were observed between type 1 and type 2 CSP in achieving either a subsequent pregnancy (p = 0.5823) or a live birth (p = 0.5069). Detailed clinical parameters, including previous treatment options, parity, history of termination, and the interval between the last CSP and the current pregnancy, for the 45 women who achieved pregnancy are summarized in Table S1.
We also compared the clinical parameters of the previous CSP between women who intended to conceive and achieved pregnancy (n = 14) and those who intended to conceive but did not achieve pregnancy (n = 35) (Table 5). Although statistical testing was not performed due to the small sample size in some subgroups, no clear differences were observed in previous CSP treatment options, subtype distribution, parity, or number of prior surgical abortions. However, women who did not achieve pregnancy tended to report light menstrual bleeding more frequently than those who conceived (54% vs. 29%).
Table 5.
Clinical parameters in women who intended to conceive again.
| Parameters | Intended & achieved pregnancy (n = 14) | Intended but did not achieve pregnancy (n = 35)# |
|---|---|---|
| Treatment options for previous CSP | ||
| Suction curettage | 11 (78%) | 21 (60%) |
| UAE | 1 (7%) | 11 (31%) |
| Others* | 2 (14%) | 3 (9%) |
| Previous surgical abortions | ||
| Once | 7 (50%) | 27 (77%) |
| Twice | 7 (50%) | 7 (20%) |
| ≥ Three | 1 (3%) | |
| Subtype of previous CSP | ||
| Type 1 | 10 (71%) | 14 (40%) |
| Type 2 | 4 (29%) | 21 (60%) |
| Parity | ||
| One | 8 (57%) | 22 (63%) |
| ≥Two | 6 (43%) | 13 (37%) |
| Menstrual bleeding pattern after previous CSP treatment | ||
| Light | 4 (29%) | 19 (54%) |
| Same as before | 10 (71%) | 16 (46%) |
Other referred to as hysteroscopy or laparoscopy, or a combination of hysteroscopy and laparoscopy; UAE: ultrasound‐guided suction curettage after uterine artery embolization.
Women within 12 months after initial treatment were excluded.
Among the 45 women who achieved pregnancy, 26 had a live birth, 10 requested an elective abortion, 7 experienced early pregnancy loss, 1 developed recurrent CSP, and 1 experienced an ectopic pregnancy (Figure 2). None of the women who had live births developed major obstetric complications such as preeclampsia, gestational diabetes mellitus, or preterm birth.
4. Discussion
In this medium‐term follow‐up study (up to 48 months) with a relatively large sample size (n = 302), we found that the subsequent pregnancy rate was 28.6% among women who intended to conceive again, excluding those within 12 months of initial CSP treatment. While 15.4% of women who did not intend to conceive again but achieved pregnancy. The successful conception or live birth was not associated with the subtypes of CSP and previous treatment options.
CSP is a rare but potentially life‐threatening complication of pregnancy, with high risks of catastrophic uterine rupture and massive hemorrhage, as well as placenta accreta spectrum [27]. Currently, some evidence reports a relatively lower rate of adverse outcomes in subsequent pregnancy in women with a history of CSP. However, a significant number (20%–80%) of women with a history of CSP do not intend to conceive again, which varies by ethnicity [17, 21, 28]. Our current follow‐up study also showed that 78% of women did not intend to conceive again. Although parity could be one factor influencing the intention of contraception, our data showed no difference in parity between women who intended to conceive again and those who did not (data not shown). Therefore, a higher number of women with a history of CSP did not intend to conceive again, resulting in a lack of evidence about the outcomes of subsequent pregnancy, including subfertility, in the literature.
Increasing evidence recently indicates that the presence of niches caused by cesarean section is potentially associated with infertility. Therefore, whether CSP itself or the treatment options could affect future fertility has not been well answered. Studies reported that 12.5%–40% of women were not pregnant after more than 12 months of attempting to conceive [17, 18, 21, 29]. In our study, in addition to 15.4% of women who did not intend to conceive again but achieved pregnancy, we found a higher proportion (28%) of women who intended to conceive again and did so, after excluding women within 12 months of their initial CSP treatment. Our data may suggest that CSP itself, after treatment, did not influence the probability of a subsequent pregnancy.
Surgical or non‐surgical treatments for CSP are recommended in the current international guidelines. A recent study reported that surgical treatment may cause uterine arteriovenous malformation or uterine artery pseudoaneurysm [30], which may lead to subfertility or recurrent miscarriage [31]. However, a meta‐analysis study reported a 74% subsequent pregnancy rate in CSP after surgical treatments [20]. Our current study found that the successful conception was not associated with the different surgical treatment options, including suction curettage, ultrasound‐guided suction curettage after UAE, hysteroscopy, laparoscopy, or a combination of both (Table 3). Additionally, the number of previous surgical abortions was also not associated with successful conception, even though surgical abortions could damage the endometrium, and the formation of scar tissue in the uterus may impede implantation in the future.
Two types of CSP are traditionally classified based on the site of implantation and the growth direction of the gestational sac [5, 22, 23]. This classification may result in a difference in scar tissue recovery in the uterus after CSP treatment. Whether this difference could affect a subsequent pregnancy has not been investigated. Our current study found that successful conception, including live births, was not associated with CSP subtypes. We also found that the interval between the last CSP treatment and the current pregnancy did not differ between women with different CSP subtypes. Taken together, our data indicate that successful conception was independent of prior surgical treatment and CSP subtypes.
Several factors can influence successful conception. We then compared clinical parameters between women who intended to conceive again and achieved pregnancy and those who did not. Due to the small sample size in some subgroups, our descriptive data showed no clear differences in previous treatment options, parity, history of termination, or interval between the last CSP and the current successful conception between the two groups. However, self‐reported data in the current study showed that a higher number of women with light menstrual bleeding was seen in women who intended to conceive again but did not (Table 5). Women with light menstrual bleeding are associated with a poor conception outcome [32], and changes in the uterine tree could cause dysfunctional menstrual bleeding [33]. A recent follow‐up study (up to 57 months) reported that 60% of women, after an initial treatment with UAE for CSP, experienced reduced menstrual blood volume or amenorrhea [34]. There is currently no evidence indicating CSP treatment results in light menstrual bleeding, suggesting additional research investigating uterine abnormalities and hormone levels in women after CSP treatment would be necessary to definitively establish the impact of CSP and its treatments on future fertility. Additionally, the comparison was not adjusted for other confounders, such as maternal age, inflammation status, and medical history.
Current literature suggests that the incidence of adverse outcomes or complicated pregnancies in subsequent pregnancies is relatively low in women with a history of CSP. Our findings also reported no adverse pregnancy outcomes in those with live births and a lower rate of complicated pregnancies, further suggesting that having a subsequent pregnancy is generally safe in women with a history of CSP.
We acknowledge several limitations in this study. The follow‐up data were obtained from self‐reports, which can introduce response bias [35]. Additionally, the analysis of the association between successful conception and previous CSP treatment options or CSP subtypes has a limitation. The intention to conceive was not controlled when evaluating the association. Some women who did not achieve pregnancy may not have intended to conceive, which could partly influence the observed association. Therefore, the absence of pregnancy in these women may not necessarily indicate reduced fertility potential. Future studies stratified by pregnancy intention could provide a clearer picture of the association. Although our study included a relatively large cohort of 329 women with CSP, the subgroup of women who actively intended to conceive again following CSP treatment was comparatively small (n = 65). However, this reflects a well‐documented trend in the literature. Many women after CSP treatment do not intend to conceive again due to the fear of recurrence and the associated psychological impact [18]. In our study, 78% of them chose not to conceive again, which aligns with current evidence.
In conclusion, this medium‐term follow‐up study with a relatively large sample size found that the initial treatment options for CSP or the subtype of CSP were not associated with successful conception in women with a history of CSP. The incidence of complicated subsequent pregnancy was similar to that in women without a history of CSP, as reported in the literature. Our findings suggest that surgical treatments for CSP did not negatively affect future fertility.
Author Contributions
Yunhui Tang: conceptualization, methodology, investigation. Jing Gao: investigation, formal analysis. Qi Chen: conceptualization, investigation, supervision, writing – original draft, writing – review and editing. Min Zhao: conceptualization, writing – review and editing.
Conflicts of Interest
The authors declare no conflicts of interest.
Transparency Statement
The lead author Qi Chen, Min Zhao affirms that this manuscript is an honest, accurate, and transparent account of the study being reported; that no important aspects of the study have been omitted; and that any discrepancies from the study as planned (and, if relevant, registered) have been explained.
Supporting information
Supporting File:
Acknowledgments
This study was supported by the Medical Innovations Project (20Y11907400) for study design, data collection, analysis and interpretation, and Shanghai Natural Science Foundation Project (23ZR1408100) for publication related cost, both funded by the Shanghai Science and Technology Committee of China. Open access publishing facilitated by The University of Auckland, as part of the Wiley ‐ The University of Auckland agreement via the Council of Australasian University Librarians.
Tang Y., Gao J., Chen Q., and Zhao M., “Surgical treatment options and the subtypes of cesarean scar pregnancy did not affect the probability of a subsequent pregnancy: a prospective cohort study,” Health Science Reports 9 (2026): e72451. 10.1002/hsr2.72451.
Yunhui Tang and Jing Gao equally contributed to this study.
Contributor Information
Qi Chen, Email: q.chen@auckland.ac.nz.
Min Zhao, Email: zmdoc2002@163.com.
Data Availability Statement
The datasets used and analyzed during the current study are available from the corresponding author upon reasonable request.
References
- 1. Jurkovic D., Hillaby K., Woelfer B., Lawrence A., Salim R., and Elson C. J., “First‐Trimester Diagnosis and Management of Pregnancies Implanted Into the Lower Uterine Segment Cesarean Section Scar,” Ultrasound in Obstetrics & Gynecology: The Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology 21, no. 3 (2003): 220–227. [DOI] [PubMed] [Google Scholar]
- 2. Hanáček J., Heřman H., Brandejsová A., et al., “Cesarean Scar Pregnancy ‐ A Retrospective Analysis of Cases in the Years 2012–2021,” Česká gynekologie 87, no. 4 (2022): 245–248. [DOI] [PubMed] [Google Scholar]
- 3. Litwicka K. and Greco E., “Caesarean Scar Pregnancy: A Review of Management Options,” Current opinion in obstetrics & gynecology 25, no. 6 (2013): 456–461. [DOI] [PubMed] [Google Scholar]
- 4. Ash A., Smith A., and Maxwell D., “Caesarean Scar Pregnancy,” BJOG: An International Journal of Obstetrics & Gynaecology 114, no. 3 (2007): 253–263. [DOI] [PubMed] [Google Scholar]
- 5. Gonzalez N. and Tulandi T., “Cesarean Scar Pregnancy: A Systematic Review,” Journal of Minimally Invasive Gynecology 24, no. 5 (2017): 731–738. [DOI] [PubMed] [Google Scholar]
- 6. Birch Petersen K., Hoffmann E., Rifbjerg Larsen C., and Nielsen H. S., “Cesarean Scar Pregnancy: A Systematic Review of Treatment Studies,” Fertility and Sterility 105, no. 4 (2016): 958–967. [DOI] [PubMed] [Google Scholar]
- 7. Miller R., Timor‐Tritsch I. E., and Gyamfi‐Bannerman C., “Society for Maternal‐Fetal Medicine (SMFM) Consult Series #49: Cesarean Scar Pregnancy,” American Journal of Obstetrics and Gynecology 222, no. 5 (2020): B2–B14. [DOI] [PubMed] [Google Scholar]
- 8. Diagnosis and Management of Ectopic Pregnancy: Green‐Top Guideline No. 21,” BJOG: An International Journal of Obstetrics and Gynaecology 123, no. 13 (2016): 15. [DOI] [PubMed] [Google Scholar]
- 9. Kaelin Agten A., Jurkovic D., Timor‐Tritsch I., et al., “First‐Trimester Cesarean Scar Pregnancy: A Comparative Analysis of Treatment Options From the International Registry,” American Journal of Obstetrics and Gynecology 230, no. 6 (2024): 669.e1–669.e19. [DOI] [PubMed] [Google Scholar]
- 10. Alameddine S., Lucidi A., Jurkovic D., et al., “Treatments for Cesarean Scar Pregnancy: A Systematic Review and Meta‐Analysis,” Journal of Maternal‐Fetal & Neonatal Medicine: The Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 37, no. 1 (2024): 2327569. [DOI] [PubMed] [Google Scholar]
- 11. Bij de Vaate A. J., van der Voet L. F., Naji O., et al., “Prevalence, Potential Risk Factors for Development and Symptoms Related to the Presence of Uterine Niches Following Cesarean Section: Systematic Review,” Ultrasound in Obstetrics & Gynecology: The Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology 43, no. 4 (2014): 372–382. [DOI] [PubMed] [Google Scholar]
- 12. Klein Meuleman S. J. M., Murji A., van den Bosch T., et al., “Definition and Criteria for Diagnosing Cesarean Scar Disorder,” JAMA Network Open 6, no. 3 (2023): e235321. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13. Keag O. E., Norman J. E., and Stock S. J., “Long‐Term Risks and Benefits Associated With Cesarean Delivery for Mother, Baby, and Subsequent Pregnancies: Systematic Review and Meta‐Analysis,” PLoS Medicine 15, no. 1 (2018): e1002494. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14. van den Tweel M. M., van der Struijs S., Le Cessie S., and Boers K. E., “The Impact of Caesarean Scar Niche on Fertility ‐ a Systematic Review,” Journal of Obstetrics and Gynaecology 44, no. 1 (2024): 2349714. [DOI] [PubMed] [Google Scholar]
- 15. Surico D., Vigone A., Monateri C., Tortora M., and Aquino C. I., Minimally Invasive Surgery for the Excision and Repair of Cesarean Scar Defect: A Scoping Review of the Literature (Medicina, 2025). 61(7). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16. Vissers J., Hehenkamp W. J. K., Brölmann H. A. M., Lambalk C. B., and Huirne J. A. F., “Reproductive Outcomes After Laparoscopic Resection of Symptomatic Niches in Uterine Cesarean Scars: Long‐Term Follow‐Up on the Prospective LAPNICHE Study,” Acta Obstetricia et Gynecologica Scandinavica 102, no. 12 (2023): 1643–1652. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17. Ben Nagi J., Helmy S., Ofili‐Yebovi D., Yazbek J., Sawyer E., and Jurkovic D., “Reproductive Outcomes of Women With a Previous History of Caesarean Scar Ectopic Pregnancies,” Human Reproduction 22, no. 7 (2007): 2012–2015. [DOI] [PubMed] [Google Scholar]
- 18. Sun X., Liu Y., Tang Y., Yu H., Zhao M., and Chen Q., “Subsequent Fertility in Women Treated for Caesarean Scar Pregnancy With Hysteroscopy: A 5‐Year Follow‐Up Descriptive Study in a Tertiary Hospital,” Frontiers in Endocrinology 12 (2021): 659647. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19. Morlando M., Conte A., and Schiattarella A., “Reproductive Outcome After Cesarean Scar Pregnancy,” Best Practice & Research Clinical Obstetrics & Gynaecology 91 (2023): 102362. [DOI] [PubMed] [Google Scholar]
- 20. Morlando M., Buca D., Timor‐Tritsch I., et al., “Reproductive Outcome After Cesarean Scar Pregnancy: A Systematic Review and Meta‐Analysis,” Acta Obstetricia et Gynecologica Scandinavica 99, no. 10 (2020): 1278–1289. [DOI] [PubMed] [Google Scholar]
- 21. Wang Q., Peng H. L., He L., and Zhao X., “Reproductive Outcomes After Previous Cesarean Scar Pregnancy: Follow Up of 189 Women,” Taiwanese Journal of Obstetrics and Gynecology 54, no. 5 (2015): 551–553. [DOI] [PubMed] [Google Scholar]
- 22. Vial Y., Petignat P., and Hohlfeld P., “Pregnancy in a Cesarean Scar,” Ultrasound in Obstetrics & Gynecology: The Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology 16, no. 6 (2000): 592–593. [DOI] [PubMed] [Google Scholar]
- 23. Ghezzi F., Laganà D., Franchi M., Fugazzola C., and Bolis P., “Conservative Treatment by Chemotherapy and Uterine Arteries Embolization of a Cesarean Scar Pregnancy,” European Journal of Obstetrics & Gynecology and Reproductive Biology 103, no. 1 (2002): 88–91. [DOI] [PubMed] [Google Scholar]
- 24. Ban Y., Shen J., Wang X., et al., “Cesarean Scar Ectopic Pregnancy Clinical Classification System With Recommended Surgical Strategy,” Obstetrics & Gynecology 141, no. 5 (2023): 927–936. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25. Lin S. Y., Hsieh C. J., Tu Y. A., et al., “New Ultrasound Grading System for Cesarean Scar Pregnancy and Its Implications for Management Strategies: An Observational Cohort Study,” PLoS One 13, no. 8 (2018): e0202020. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26. Cali G., Forlani F., Timor‐Tritsch I. E., Palacios‐Jaraquemada J., Minneci G., and D'antonio F., “Natural History of Cesarean Scar Pregnancy on Prenatal Ultrasound: The Crossover Sign,” Ultrasound in Obstetrics & Gynecology: The Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology 50, no. 1 (2017): 100–104. [DOI] [PubMed] [Google Scholar]
- 27. Nguyen V. H., Huynh Q. H., Ha T. N., Nguyen M. C. N., and Nguyen P. N., “Additional Role of Magnetic Resonance Imaging to Ultrasound in Assessing Placenta Accreta Spectrum Disorders: A Retrospective Cross‐Sectional Study From Vietnam,” Oman Medical Journal 39, no. 6 (2024): e697. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28. Zhang C., Zhang Y., He J., and Zhang L., “Outcomes of Subsequent Pregnancies in Patients Following Treatment of Cesarean Scar Pregnancy With High Intensity Focused Ultrasound Followed by Ultrasound‐Guided Dilation and Curettage,” International Journal of Hyperthermia 36, no. 1 (2019): 925–930. [DOI] [PubMed] [Google Scholar]
- 29. Jurkovic D., Knez J., Appiah A., Farahani L., Mavrelos D., and Ross J. A., “Surgical Treatment of Cesarean Scar Ectopic Pregnancy: Efficacy and Safety of Ultrasound‐Guided Suction Curettage,” Ultrasound in Obstetrics & Gynecology: The Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology 47, no. 4 (2016): 511–517. [DOI] [PubMed] [Google Scholar]
- 30. Le N. D. and Nguyen P. N., “Uterine Arteriovenous Malformation or Uterine Artery Pseudoaneurysm Secondary to Uterine Aspiration in Cesarean Scar Ectopic Pregnancy: A Case Report and Review of the Literature,” Journal of Medical Case Reports 19, no. 1 (2025): 248. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31. Delplanque S., Le Lous M., Proisy M., et al., “Fertility, Pregnancy, and Clinical Outcomes After Uterine Arteriovenous Malformation Management,” Journal of Minimally Invasive Gynecology 26, no. 1 (2019): 153–161. [DOI] [PubMed] [Google Scholar]
- 32. Gao Y., Hong X., Wang Z., and Zhu Y., “Endometrial Receptivity and Conception Outcome Among Women With Light Menstrual Bleeding of Unidentified Etiology,” International Journal of Gynecology & Obstetrics 140, no. 1 (2018): 37–41. [DOI] [PubMed] [Google Scholar]
- 33. Åkerlund M., “Vascularization of Human Endometrium,” Annals of the New York Academy of Sciences 734 (1994): 47–56. [DOI] [PubMed] [Google Scholar]
- 34. Cao G.‐S., Liu R.‐Q., Liu Y.‐Y., et al., “Menstruation Recovery in Scar Pregnancy Patients Undergoing UAE and Curettage and Its Influencing Factors,” Medicine 97, no. 11 (2018): e9584. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35. Rosenman R., Tennekoon V., and Hill L. G., “Measuring Bias in Self‐Reported Data,” International Journal of Behavioural & Healthcare Research 2, no. 4 (2011): 320–332. [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Supporting File:
Data Availability Statement
The datasets used and analyzed during the current study are available from the corresponding author upon reasonable request.
