Logo Medical Science Monitor

Call: +1.631.470.9640
Mon - Fri 10:00 am - 02:00 pm EST

Contact Us

Logo Medical Science Monitor Logo Medical Science Monitor Logo Medical Science Monitor

03 April 2024: Review Articles  

Advances in Treating Cesarean Scar Pregnancy: A Comprehensive Review of Techniques, Clinical Outcomes, and Fertility Preservation

Bartosz Kłobuszewski1ABCDEF, Maciej Szmygin ORCID logo12ABCDEF*, Karolina Nieoczym ORCID logo3ABCDE, Olga Kłobuszewska4ABDE, Sławomir Woźniak ORCID logo5BCF, Krzysztof Konrad Pyra ORCID logo1ABEF

DOI: 10.12659/MSM.943550

Med Sci Monit 2024; 30:e943550




ABSTRACT: Cesarean scar pregnancy (CSP) is a rare but potentially dangerous condition that occurs when an embryo implants and develops within the scar tissue from a previous cesarean section. Treatment of cesarean scar pregnancy depends on several factors, including the gestational age of the pregnancy, the presence of complications, and the individual patient’s circumstances. We performed a systematic review of the published literature on management of cesarean scar pregnancy and the outcomes, complications, and effects on fertility. A systematic review of recent scientific literature published up to April 2023 in the databases PubMed, Google Scholar, and Web of Science was performed according to the PRISMA guidelines. We used the search keywords “cesarean scar pregnancy,” “methotrexate,” “systemic,” “chemoembolization,” and “uterine artery embolization.” The baseline search resulted in 413 articles. After the exclusion of 342 irrelevant articles, the abstracts and titles of the remaining 71 articles were read for potential inclusion, resulting in exclusion of a further 16 articles. Therefore, the full texts of 55 articles were investigated. Finally, 42 papers were included in the study. The main finding was that chemoembolization is more successful than systemic methotrexate therapy, and is associated with less blood loss and shorter hospital stay. Transarterial chemoembolization appears to be safe and effective method of treatment in patients with CSP and should thus be considered during multidisciplinary evaluation of these patients.

Keywords: Pregnancy, Ectopic, endovascular procedures, review


Cesarean scar pregnancy (CSP) is one of the rarest types of ectopic pregnancy; it occurs when an embryo implants at the site of a cesarean section scar [1]. The incidence is estimated to range from 1/1000 to 1/2500 and correlates closely with the number of previous pregnancies terminated by cesarean section [2]. According to He et al, the most important factors influencing the occurrence of CSP are multiparity, number of previously performed abortions, uterus position, and vaginal bleeding [3]. Modern diagnosis is based on ultrasound criteria [4,5]. Two-dimensional (2D) B-mode transvaginal ultrasound (TVS) alone or in conjunction with three-dimensional (3D) ultrasound and color Doppler has been generally considered to be the criterion standard for diagnosis of CSP [6]. Ultrasound can help visualize the gestational sac within the cesarean scar, measure its size, and determine its location and viability [7,8].

Cesarean scar pregnancies can be categorized based on their location within the cesarean scar or niche [8], determined during the first-trimester transvaginal ultrasound examination [7]. There are 2 main categories:

In 2022, a new advanced standardized system for sonographic assessment and reporting of CSP in early pregnancy was created [7]. Depending on the location of the gestational sac (GS), the following types of CSP can be diagnosed:

It is important to note that the type of CSP can change with advancing gestation, meaning that the location of the gestational sac can shift as the pregnancy progresses [9]. The type of CSP and its location can have implications for the management and treatment of the condition, and should be evaluated and monitored by a healthcare provider [7].

Early diagnosis of cesarean scar pregnancy is particularly important in selecting appropriate treatment [10]. Expectant management of a cesarean scar pregnancy has a poor prognosis due to potential complications such as massive bleeding, disseminated intravascular coagulation, and uterine rupture [11]. It has been recommended to terminate the pregnancy in the first trimester soon after diagnosis to improve the prognosis [12]. Hysterectomy was often considered the only treatment option for CSP [13]. However, in recent years, more conservative approaches have been developed and are increasingly being used as an alternative to hysterectomy [14,15]. Contemporary treatment methods include surgical methods such as laparoscopic removal, hysteroscopic evacuation, dilation and curettage, sac aspiration by suction, selective uterine arterial chemoembolization (UAC), and open surgery [16]. Other methods used to treat cesarean scar pregnancy include methotrexate (MTX) administered locally or systemically and potassium chloride, sodium chloride, hyperosmolar glucose, or crystalline trichosanthin under ultrasonography guidance [16].

The choice of treatment approach for CSP depends on various factors, including the size and location of the pregnancy, the patient’s fertility desires, and the presence of any complications or risk factors [17]. At present, there is no universal treatment for CSP. The biggest challenge is to select and carry out the treatment properly, damaging the normal structures of the reproductive organs as little as possible, while effectively allowing fertility preservation [18].

Therefore, we performed a systematic review of the published literature on management of cesarean scar pregnancy and the outcomes, complications, and effects on fertility.

Material and Methods


Local institutional review board approval was not required for this type of study. The study was conducted in compliance with the Declaration of Helsinki.


Two independent reviewers (B.K. and K.N.) conducted a comprehensive search in 3 electronic databases (PubMed, Google Scholar, and Web of Science) using the following keywords in combinations: “cesarean scar pregnancy,” “methotrexate,” “systematic,” “chemoembolization,” and “uterine artery embolization.” The search was restricted to articles published in English from 2010 to the present. The search strategy was adapted to each database.


The inclusion criteria for the studies were: (1) original articles, reviews, and meta-analyses that evaluated the treatment of patients with cesarean scar pregnancy either with systemic methotrexate or uterine artery chemoembolization, and (2) studies published in English.



The baseline search resulted in 413 articles. All of them were initially reviewed on the title and abstract level according to PRISMA guidelines. After the exclusion of 312 irrelevant articles, the abstracts and titles of remaining 91 articles were read for potential inclusion, resulting in the further exclusion of 24 articles. Therefore, the full texts of 67 articles were further investigated. Finally, 60 papers were included in the study.


Chemoembolization is one of the newest methods used to treat CSP [19]. Embolization of the uterine arteries with intra-arterial infusion of methotrexate is a minimally invasive technique performed endovascularly [20]. This method allows concentrated administration of methotrexate directly into the arteries supplying the gestational foci, while occluding the vessel with occlusive agents such as polyvinyl alcohol and Gelfoam particles administered through a catheter [21].

Indications for chemoembolization for CSP include: presence of a live or viable embryo located in the cesarean scar, gestational age less than 12 weeks, absence of significant maternal symptoms or complications such as heavy vaginal bleeding or signs of hemodynamic instability, and refractory to or contraindications to other treatments such as methotrexate injection or dilation and curettage (D&C) [22]. Many authors have described successful chemoembolization procedures despite the presence of fetal heart activity, so it is not a contraindication to the procedure [23–25].

Uterine artery embolization as a treatment modality is influenced by factors such as high arterial flow associated with GS, uterine myometrial thickness between the sac and bladder less than 2 mm, or serum beta-human chorionic gonadotropin (β-hCG) levels above 10 000 mIU/ml [21].

The chemoembolization procedure is performed by experienced interventional radiologists under local anesthesia from the femoral access. Intraoperative angiography allows effective imaging of the anatomy with special attention to the uterine arteries and the possible presence of anastomoses that could hinder the procedure [23]. The standard dose used in the next step of the procedure is 50 mg of methotrexate, 25 mg in each of the uterine arteries, which directly supply blood to the embryo [26]. After the MTX is administered, occlusive agents such as polyvinyl alcohol and Gelfoam are injected through a delivery catheter to block the feeding vessel, prevent further blood flow to the gestational foci, and MTX migration.

When selecting an embolic agent, it is important to consider various factors, including the patient’s age, their risk for hemorrhage, hemodynamic conditions, and their desire to protect ovarian function and fertility. Ultimately, the selection of an embolic agent should be tailored to the individual needs and preferences, and should involve a comprehensive discussion between the patient and their healthcare provider to weigh the potential benefits and risks of different options [27]. Embolization is continued until complete occlusion of the gestational follicle’s feeding arteries is achieved. This procedure combines chemotherapy with tissue ischemia, which allows for a higher concentration of MTX to target the gestational foci for a longer period of time. This can result in more effective embryocide (destruction of the developing embryo), with fewer systemic toxic effects than other treatments [28].

A prospective observational study by Stępniak et al found that 20/22 (90%) women undergoing chemoembolization followed by suction curettage were successfully treated with this method [1]. The abnormal bleeding that occurred in one patient and the rich vascularization of the CSP originating from the ovarian artery in the other required repeated embolization. Of the 41 patients described by Pyra et al, treatment was successful in 34 patients (83%), and 7 patients required secondary treatment [23]. A retrospective study of 383 patients who underwent chemoembolization showed treatment success in 379 patients (99%) [24]. Treatment efficacy was found to be influenced by size of the gestational mass, presence of fetal heartbeat, and type of CSP. Yu et al evaluated the effectiveness of chemoembolization by comparing it with an injection of methotrexate combined with uterine curettage [26]. They found that the total effective rate was significantly higher in the group of patients treated with chemoembolization (P<0.05). Apart from this, compared to the group of patients treated with methotrexate injection, patients treated with chemoembolization showed better outcomes in terms of intraoperative blood loss, hospitalization period, time to return of menstruation, time to disappearance of the mass, and time to return of normal β-HCG level (P<0.05).

A meta-analysis evaluating the effectiveness of treatment with UAC in China showed that the mean time for β-hCG levels normalization was 29.8 days [14]. As far as the overall mean hospital stay was concerned, the average time hospitalization was 9 days. Authors also evaluated the estimated intraprocedural blood loss which was 41.2 ml. Finally, the counted the overall proportion of severe complication rate which was 0.012

The most commonly reported problems after the procedure are uterine cramping, nausea, and vomiting [1]. However, it is important to note that 5% of patients experience hemorrhage and 3% need a hysterectomy [1]. In a comparative study of UAC followed by curettage (UC) vs patients receiving intra-arterial MTX infusion followed by UAC and curettage (MUC), the use of intra-arterial MTX infusion had a positive impact on treatment outcomes [29]. Patients had a higher success rate (88.9%) without the need for additional medical interventions, and average blood loss during curettage was also lower in patients receiving MTX infusion directly into the arteries. Vaginal bleeding occurred in about 6% of patients.

Chemoembolization also shows similar efficacy as high-intensity focused ultrasound [30]. Wang et al compared the clinical outcome and rate of procedural compilations of high-intensity focused ultrasound (HIFU) vs UAC for the treatment of CSP, and no serious adverse effects were observed in either group. Interestingly, although HIFU was associated with a lower incidence of minor complications, the overall hospital stay was longer compared with patients who underwent endovascular embolization [31]. Overall, the most commonly occurring adverse effect of the treatment was lower abdominal pain [25].

In patients who desire to preserve fertility, performing chemoembolization is debatable because of the risk of ovarian failure and infertility, as well as the increased risk of miscarriage, preterm labor, and postpartum hemorrhage [22,26]. Czuczwar et al compared the effects of treatment with supracervical hysterectomy, ulipristal acetate, and uterine artery embolization on ovarian reserve [32]. The result of treatment was a significant reduction in the values of antral follicle count, anti-Mullerian hormone, and serum inhibin B and E2, while follicle stimulating hormone was significantly increased. They concluded that chemoembolization affects ovarian reserve to the greatest extent and should not be offered to patients who wish to become pregnant in the future. There are also reports of a decrease in menstrual blood volume or lack of menstruation after uterine artery embolization, which can negatively affect patients’ quality of life and subsequent fertility [32,33].

On the other hand, successful pregnancy rates of 30% following the uterine artery chemoembolization have been reported [23]. A large study found a 54% success rate of live births among patients seeking pregnancy [24]. Despite the many reports of successful pregnancies, more research is needed on the effects of UAC on fertility [23,24,32].

Cases of repeat pregnancies in the scar have been reported, which is currently one of the more serious challenges in treating this condition, so patients should always be informed of the risk of recurrence. Recurrent scar pregnancies are influenced by the surgical technique and incision closure technique used in cesarean section. However, based on the current study, the effect of a particular CSP treatment therapy on an episode of recurrence cannot be unanimously confirmed or denied. Most papers indicate that the method of treatment was an independent predictor of the risk of CSP recurrence [34]. CSP recurrence can be successfully treated with chemoembolization [35].


Methotrexate is a medication that works by inhibiting the synthesis of folic acid, which is essential for DNA synthesis and cell proliferation [36]. By disrupting these processes, it can halt the growth of an ectopic pregnancy and promote its absorption by the body. Pharmaceutical treatment with methotrexate is often preferred by patients over surgical treatment for ectopic pregnancy due to its non-invasive nature and lower risk of complications, and it can also be a cost-effective alternative to surgery [37].

There is a risk of treatment failure, which ranges from 22% to 48%, because the success of the treatment depends on several factors, including advanced gestational age, larger gestational sac diameter and crown–rump length, location of the ectopic pregnancy, the level of β-hCG in the blood, the individual patient’s response to the medication, and the presence of embryonic cardiac activity, which were associated with methotrexate failure or need for additional therapy [37,38].

MTX has been shown to be highly effective and safe, despite no exclusion criteria for β-hCG level, gestational sac diameter, or presence of embryonic cardiac activity [38]. Specific indications for treating CSP with methotrexate include contraindications to surgery or general anesthesia, high body mass index (BMI), or previous surgical history [38]. Patients in whom systemic administration of MTX does not have the intended result often undergo second-line surgical management UAE or laparotomy, and, in special cases, hysteroscopic resection [39,40].

Methotrexate in the systemic treatment of CSP is most often administered intramuscularly or intravenously [37]. A single dose of methotrexate was most commonly reported, with a second dose given 1 week apart if necessary [36]. The standard dose administered intramuscularly was 50 mg/m2 body surface area. Tanaka et al administered 100 mg methotrexate IV push over 5–10 min was used, with 200 mg methotrexate in 500 mL normal saline IV infusion over 12 h [38]. The selection of the appropriate treatment dose is influenced by the β-hCG level. If a β-hCG level of less than 1500 IU/L (less than 12 000 mIU/mL) is found, a single-dose regimen is preferred, while a multi-dose regimen is preferred for β-hCG levels under 3000 IU/L [37]. The literature describes the systemic intramuscular administration of MTX at a dose of 25 mg completed successfully in patients with the hCG levels 2781–15 700 milliunits/mL [41].

High efficacy in the treatment of CSP has been reported in patients who received a treatment regimen that included an intravenous bolus dose of methotrexate followed by methotrexate infusion over 12 h [38]. Treatment with high doses of methotrexate was effective and well tolerated by patients, without serious adverse effects. A retrospective cohort study comparing outcome assessment of single-dose methotrexate versus multiple-dose MTX protocols found no significant differences in need for additional surgical treatment [42], and there was no significant difference between the single-dose and multiple-dose groups in blood product administration and total days of hospitalization. On this basis, both single-dose and multiple-dose MTX treatment protocols are considered to have high success rates with relatively low rates of complications. In 2020, a systematic review found that the mean hospital stay was 11.7±1.2 days. The rate of success in pharmacotherapy of ectopic pregnancy by MTX is diverse and ranges from 71% to 100% [37]. In contrast, a systematic review published in 2017 reported a success rate of 56% for MTX treatment alone [43]. Numerous reports have shown that treatment of CSP with systemic MTX monotherapy alone is ineffective, but treatment success can be achieved by combining systemic MTX administration with other described treatment options [43].

The success of systemic treatment with methotrexate is influenced by β-hCG level. Mitsui et al assessed the influence of hCG level and gestational sac size, reporting that in patients who succeeded with treatment, bhCG levels were lower than in those for whom treatment failed [39]. This allowed them to determine that hCG levels less than 17 757.0 mIU/mL and GS sizes less than 10.4 mm are indications that MTX medical treatment is likely to successfully treat CSP patients. Shai et al described an MTX treatment success rate of 61.3% and found that a short time interval from the last cesarean delivery (CD) was a factor that directly influenced treatment outcome [44].

The success of systemic MTX treatment of patients described in a retrospective cohort study by Delplanquea et al was 87.5% (21/24). The remaining patients received second-line surgical treatment due to failure of methotrexate therapy [40]. The risk of failure may be influenced by the time interval between the previous cesarean delivery and CSP [44].

The use of MTX as first-line treatment is controversial, as better efficacy and safety of MTX treatment has been noted only in early pregnancy [42].

Methotrexate, which is a folic acid antagonist, competitively inhibits nucleic acid synthesis in its folate-dependent phase and effectively kills cells and tissues with a high-turnover such as trophoblasts, leading to decreased β-hCG levels [37]. According to a study by Seow et al, the mean time for complete gestational tissue regression after systemic MTX monotherapy is approximately 2 months, but it can take up to 1 year in some cases [45]. This means that even if the patient’s β-hCG levels return to normal relatively quickly after treatment, it may take several months for all of the remaining gestational tissue to be eliminated from the uterus.

Adverse effects occurring during systemic administration of MTX can affect various systems and organs due to the drug’s effects on the entire body, with adverse effects including nausea and vomiting, stomatitis, oral ulceration, vaginal spotting and bleeding, pneumonia, and alopecia [39,46–48].

Complications were more frequent in women with a history of 3 or more cesarean section deliveries and with a myometrial thickness thinner than 2 mm [42,49]. The risk of hemorrhage during MTX treatment was 10% [22]. Genital bleeding was also observed to occur in up to 70% of patients treated with systemic MTX [39]. The advantage of MTX administered directly into the gestational sac is its local action, thus limiting the effect of MTX on the whole body [48]. To date, there are very few reports comparing the adverse effects of CSP treatment using UAC vs systemic MTX. Doses of systemically administered methotrexate are often repeated to achieve an adequate response to treatment; thus, the patient is exposed to higher doses of this drug compared to the chemoembolization procedure [50]. In a study by Li et al compared systemic treatment with MTX as well as chemoembolization, showing that patients treated by chemoembolization had much less bleeding during uterine suction curettage, a shorter time until serum β-hCG resolution, and a shorter hospital stay than those receiving systemic MTX treatment [50]. Moreover, chemoembolization followed by uterine suction curettage was not associated with a higher incidence of complications as compared with MTX treatment.

Successful pregnancies after MTX treatment have been reported, but reliable data confirming the effect of MTX on subsequent female fertility and the incidence of recurrent CSP are still lacking [39,49]. Based on the available publications, conception outcomes are much lower than with chemoembolization treatment or were not analyzed. Tanakaa et al described only 1 healthy birth, which accounted for 3% of all patients [42]. In contrast, Takashi Mitsui et al reported a pregnancy success rate of 30% [39]. Because of these widely varying rates, further analysis is needed of fertility rates in patients treated with systemic MTX.

In patients for whom methotrexate treatment fails or is not appropriate, surgical management may be necessary. The choice of treatment approach will depend on several factors, including the patient’s clinical presentation, their fertility desires, and the potential risks and benefits of each treatment option [37]. In 2020, the Society for Maternal-Foetal Medicine (SMFM) recommended that MTX should not be used alone in the treatment of CSP [51]. Comparing the 2 treatment methods, the administration of systemic MTX is more often associated with the need for patients to undergo additional medical interventions or to repeat the procedure. The highest complication rates were observed with intramuscular methotrexate alone [41]. Additionally, a shorter hospital stay for patients treated with UAC was noted [52].


The aim of this study was to systematically review the available literature on the management of cesarean scar pregnancy (CSP) and the outcomes, complications, and effects on fertility, with special attention to comparison of endovascular uterine artery chemoembolization (UAC) vs systemic methotrexate (MTX). We observed that UAC aiming to minimally invasive injection of methotrexate directly into uterine arteries is highly effective, especially if followed by suction curettage, whereas traditional therapy with systemic MTX is associated with a significantly higher risk of failure, increased risk of hemorrhage, and higher post-operative costs connected with longer hospital stays. Our findings agree with results reported by authors of other recent meta-analyses on CSP treatment [14,22,53].

The incidence of cesarean scar pregnancy (CSP) is increasing with the growing number of cesarean sections performed. Some projections show that by 2030 nearly 30% of all deliveries will by cesarean section [54]. Although there are reports of healthy deliveries among patients who received expectant management, it is associated with relatively high morbidity and mortality rates; therefore, termination of CSP is currently recommended [55]. Chemoembolization and systemic methotrexate are both treatments for cesarean scar pregnancy, but UAC might be contraindicated in patients with serious symptoms or complications (eg, vaginal bleeding or hemodynamic instability) [22].

UAC treatment is reported to have 83–99% efficacy [1,23,24]. Factors influencing final outcome include gestational size sac, presence of fetal heartbeat, and type of the cesarean scar pregnancy [24]. Beta-human chorionic gonadotropin (β-hCG) levels usually resolve within 1 month after treatment [24]. In their meta-analysis comparing UAC and systemic MTX in a Chinese population, Qiao et al [56] observed that β-hCG levels normalized significantly faster among patients treated with the endovascular method, with significant differences in hospital stay, blood loss, and rate of adverse events, which confirms the findings of our review. However, systemic methotrexate administration can still be successfully used, especially in patients presenting before 8 weeks’ gestation, with β-hCG levels <12 000 mlU/ml, and without fetal heart beat [43]. There are reports of safe and effective use of a combination of systemic and local administration of MTX for patients with CSP [57,58], but adverse effects (eg, nausea, vaginal spotting, and elevated liver enzymes) were noted. Having had more than 2 previous cesarean section and myometrial thickness <2 mm were independent factors associated with increased risk of complications and treatment failure [42,49].

A concern with any intervention involving the reproductive system in women is the potential impact on future fertility, regardless of their parity. In general, occlusion of uterine arteries carries a risk of ovarian failure and infertility, especially if dangerous utero-ovarian anastomoses are present [59]. Nonetheless, in case of CSP chemoembolization, the occlusion of the arteries is temporary if performed with Gelfoam [23,60]. Reported post-treatment pregnancy rates in patients who underwent UAC due to CSP range from 30% to 54% [23,24]. Interestingly, there are reports of CSP recurrence treated successfully with repeated embolization [35]. Regarding the impact of systemic MTX treatment on fertility, conception outcomes are lower compared with selective chemoembolization and range from 3% to 30% [39,42,49]. However, reliable data confirming the effect of MTX on subsequent female fertility and the incidence of recurrent CSP are still lacking and further research is needed.

Study Limitations

Our study has certain limitations. First, although we tried to include all relevant articles, the number of reviewed databases was limited. Secondly, we included only English language articles, which might be perceived as a potential drawback. Finally, our analysis focused primarily on systemic therapy and uterine artery chemoembolization and only briefly focused on other methods of treatment of cesarean scar pregnancy.


Individualization of treatment after thorough multidisciplinary evaluation remains the key to successful therapy of patients with cesarean scar pregnancy. Results of our review indicate that transarterial chemoembolization appears to be safe and effective method of treatment in patients with CSP and should therefore be considered during multidisciplinary evaluation of these patients. It is associated with higher percentage of successful therapy compared to systemic methotrexate alone, less blood loss, and shorter hospitalization. Nonetheless, due to the small number of randomized control trials included, further research with a larger number of studies and patients is needed.


1. Stępniak A, Paszkowski T, Jargiełło T, Effectiveness, complications and reproductive outcome of selective chemoembolization with methotrexate followed by suction curettage for caesarean cesarean scar pregnancy – a prospective observational study: Eur J Obstet Gynecol Reprod Biol, 2019; 241; 56-59

2. Cali G, Timor-Tritsch I, Palacios-Jaraquemada J, Outcome of cesarean scar pregnancy managed expectantly: Systematic review and meta-analysis: Ultrasound Obstet Gynecol, 2018; 51; 169-75

3. He C, Zheng F, Lin J, A nomogram to predict the risk of cesarean scar pregnancy after caesarean section: J Obstet Gynaecol, 2023; 43; 2142767

4. Rotas M, Haberman S, Levgur M, Cesarean scar ectopic pregnancies: Etiology, diagnosis, and management: Obstet Gynecol, 2006; 107; 1373-81

5. Ash A, Smith A, Maxwell D, Cesarean scar pregnancy: BJOG, 2007; 114; 253-63

6. Noël L, Thilaganathan B, Caesarean scar pregnancy: Diagnosis, natural history and treatment: Curr Opin Obstet Gynecol, 2022; 34; 279-86

7. Jordans IPM, Verberkt C, De Leeuw RA, Definition and sonographic reporting system for Cesarean cesarean scar pregnancy in early gestation: Modified Delphi method: Ultrasound Obstet Gynecol, 2022; 59; 437-39

8. Kaelin Agten A, Cali G, Monteagudo A, The clinical outcome of cesarean scar pregnancies implanted “on the scar” versus “in the niche”: Am J Obstet Gynecol, 2017; 216; 510.e1-e6

9. Ban Y, Shen J, Wang X, Cesarean scar ectopic pregnancy clinical classification system with recommended surgical strategy: Obstet Gynecol, 2023; 141; 927-36

10. Timor-Tritsch IE, Monteagudo A, Cali G, Cesarean scar pregnancy: Diagnosis and pathogenesis: Obstet Gynecol Clin North Am, 2019; 46; 797-811

11. Kanat-Pektas M, Bodur S, Dundar O, Systematic review: What is the best frst-line approach for cesarean section ectopic pregnancy?: Taiwan J Obstet Gynecol, 2016; 55; 263-69

12. Gonzalez N, Tulandi T, Cesarean scar pregnancy: A systematic review: J Minim Invasive Gynecol, 2017; 24; 731-38

13. Gulino FA, Ettore C, Ettore G, A review on management of caesarean scar pregnancy: Curr Opin Obstet Gynecol, 2021; 33; 400-4

14. Marchand GJ, Masoud AT, Coriell C, Treatment of cesarean scar ectopic pregnancy in China with uterine artery embolization-a systematic review and meta-analysis: J Clin Med, 2022; 13(11); 7393

15. Hameed MSS, Wright A, Chern BSM, Cesarean scar pregnancy: Current understanding and treatment including role of minimally invasive surgical techniques: Gynecol Minim Invasive Ther, 2023; 12; 64-71

16. Long Y, Zhu H, Hu Y, Interventions for non-tubal ectopic pregnancy: Cochrane Database Syst Rev, 2020; 7; CD011174

17. Heidar Z, Zadeh Modarres S, Abediasl Z, Cesarean scar pregnancy treatment: A case series: J Med Case Rep, 2021; 15; 506

18. Al-Jaroudi D, Aboudi S, Baradwan S, Different treatment modalities for cesarean scar pregnancies: A single-center experience and literature review: Arch Gynecol Obstet, 2021; 303; 1143-51

19. Shen L, Tan A, Zhu H, Bilateral uterine artery chemoembolization with methotrexate for cesarean scar pregnancy: Am J Obstet Gynecol, 2012; 207; 386.e1-6

20. Cheng F, Shan D, Guo S, Risk factor for residue after uterine artery chemotherapy and embolization in combination with dilatation and curettage for treating caesarean scar pregnancy: Curr Mol Med, 2019; 19; 525-31

21. Zheng YJ, Chen Q, Li S, Cesarean scar pregnancies treated by uterine artery chemotherapy embolization combined with ultrasound-guided dilation and curettage: A retrospective study: J Ultrasound Med, 2023; 42; 27-33

22. Maheux-Lacroix S, Li F, Bujold E, Cesarean scar pregnancies: A systematic review of treatment options: J Minim Invasive Gynecol, 2017; 24; 915-25

23. Pyra K, Szmygin M, Bérczi V, Clinical outcome and analysis of procedural failure during uterine artery chemoembolisation as a treatment of caesarean scar pregnancy: Wideochir Inne Tech Maloinwazyjne, 2021; 16; 243-48

24. Li Y, Lu L, Wang W, Retrospective study of patients with cesarean scar pregnancies treated by uterine artery chemoembolization and curettage: Int J Gynaecol Obstet, 2018; 143; 172-77

25. Wang W, Chen Y, Yang Y, High-intensity focused ultrasound compared with uterine artery chemoembolization with methotrexate for the management of cesarean scar pregnancy: Int J Gynaecol Obstet, 2022; 158; 572-78

26. Yu K, Zhou H, Clinical curative effects and influencing factors of uterine artery chemoembolization combined with uterine curettage treating with cesarean cesarean scar pregnancy patients: Evid Based Complement Alternat Med, 2022; 2022; 7785573

27. Ma Y, Yang C, Shao X, Efficacy comparison of transcatheter arterial embolization with gelatin sponge and polyvinyl alcohol particles for the management of cesarean scar pregnancy and follow-up study: J Obstet Gynaecol Res, 2017; 43; 682-88

28. Zhang XB, Zhong YC, Chi JC, Caesarean scar pregnancy: Treatment with bilateral uterine artery chemoembolization combined with dilation and curettage: J Int Med Res, 2012; 40; 1919-30

29. Gao L, Hou YY, Sun F, A retrospective comparative study evaluating the efficacy of adding intra-arterial methotrexate infusion to uterine artery embolisation followed by curettage for cesarean scar pregnancy: Arch Gynecol Obstet, 2018; 297; 1205-11

30. Liu Y, Yin Q, Xu F, Clinical efficacy and safety of high-intensity focused ultrasound (HIFU) ablation in treatment of cesarean scar pregnancy (CSP) I and II: BMC Pregnancy Childbirth 30, 2022; 22; 607

31. Wang X, Yang B, Chen W, Clinical efficacy and re-pregnancy outcomes of patients with previous cesarean scar pregnancy treated with either high-intensity focused ultrasound or uterine artery embolization before ultrasound-guided dilatation and curettage: A retrospective cohort study: BMC Pregnancy Childbirth, 2023; 23; 85

32. Czuczwar P, Stepniak A, Milart P, Comparison of the influence of three fibroid treatment options: Supracervical hysterectomy, ulipristal acetate and uterine artery embolization on ovarian reserve – an observational study: J Ovarian Res, 2018; 11; 45

33. Chen H, Zhou J, Wang H, The treatment of cesarean scar pregnancy with uterine artery embolization and curettage as compared to transvaginal hysterotomy: Eur J Obstet Gynecol Reprod Biol, 2017; 214; 44-49

34. Timor-Tritsch IE, Horwitz G, D’Antonio F, Recurrent cesarean scar pregnancy: Case series and literature review: Ultrasound Obstet Gynecol, 2021; 58; 121-26

35. Pyra K, Szmygin M, Wozniak S, Recurrent cesarean cesarean scar pregnancytreated successfully with uterine artery chemoembolization: Ginekol Pol, 2021; 92; 394-95

36. Mosconi C, Crocetti L, Bruno A, Scar pregnancy and extrauterine implants: Semin Ultrasound CT MR, 2021; 42; 46-55

37. Salari N, Kazeminia M, Shohaimi S, Evaluation of treatment of previous cesarean cesarean scar pregnancywith methotrexate: A systematic review and meta-analysis: Reprod Biol Endocrinol, 2020; 9(18); 108

38. Tanaka K, Coghill E, Ballard E, Management of caesarean cesarean scar pregnancy with high dose intravenous methotrexate infusion therapy: 10-year experience at a single tertiary centre: Eur J Obstet Gynecol Reprod Biol, 2019; 237; 28-32

39. Mitsui T, Mishima S, Ohira A, hCG values and gestational sac size as indicators of successful systemic methotrexate treatment in cesarean scar pregnancy: Taiwan J Obstet Gynecol, 2021; 60; 454-57

40. Delplanque S, Le Lous M, Flévin M, Effectiveness of conservative medical treatment for non-tubal ectopic pregnancies: A multicenter study: J Gynecol Obstet Hum Reprod, 2020; 20; 101762

41. Grechukhina O, Deshmukh U, Fan L, Cesarean scar pregnancy, incidence, and recurrence: Five-year experience at a single tertiary care referral center: Obstet Gynecol, 2018; 132; 1285-95

42. Giampaolino P, De Rosa N, Morra I, Management of cesarean scar pregnancy: A single-institution retrospective review: Biomed Res Int, 2018; 2018; 6486407

43. Bodur S, Özdamar Ö, Kılıç S, The efficacy of the systemic methotrexate treatment in caesarean scar ectopic pregnancy: A quantitative review of English literature: J Obstet Gynaecol, 2015; 35; 290-96

44. Shai D, Meyer R, Levin G, Single-dose methotrexate-based protocol for the treatment of caesarean cesarean scar pregnancy and successive pregnancy outcomes: Hum Fertil (Camb), 2021; 29; 1-7

45. Seow KM, Huang LW, Lin YH, Cesarean scar pregnancy: Issues in management: Ultrasound Obstet Gynecol, 2004; 23; 247-53

46. Kim YR, Moon MJ, Ultrasound-guided local injection of methotrexate and systemic intramuscular methotrexate in the treatment of cesarean scar pregnancy: Obstet Gynecol Sci, 2018; 61; 147-53

47. Pędraszewski P, Wlaźlak E, Panek W, Cesarean cesarean scar pregnancy – a new challenge for obstetricians: J Ultrason, 2018; 18; 56-62

48. Peng P, Gui T, Liu X, Comparative efficacy and safety of local and systemic methotrexate injection in cesarean scar pregnancy: Ther Clin Risk Manag, 2015; 27; 137-42

49. Levin G, Zigron R, Dior UP, Conservative management of caesarean scar pregnancies with systemic multidose methotrexate: Predictors of treatment failure and reproductive outcomes: Reprod Biomed Online, 2019; 39; 827-34

50. Li C, Li C, Feng D, Transcatheter arterial chemoembolization versus systemic methotrexate for the management of cesarean scar pregnancy: Int J Gynaecol Obstet, 2011; 113; 178-82

51. Miller R, Gyamfi-Bannerman CSociety for Maternal-Fetal Medicine (SMFM), Society for Maternal-Fetal Medicine Consult Series #63: Cesarean scar ectopic pregnancy: Am J Obstet Gynecol, 2022; 227; 9-20

52. Long Y, Zhu H, Hu Y, Interventions for non-tubal ectopic pregnancy: Cochrane Database Syst Rev, 2020; 7; CD011174

53. Birch Petersen K, Hoffmann E, Larsen Rifbjerg, Cesarean scar pregnancy: A systematic review of treatment studies: Fertil Steril, 2016; 105; 958-67

54. Betran AP, Ye J, Moller AB, Trends and projections of caesarean section rates: Global and regional estimates: BMJ Glob Health, 2021; 6; e005671

55. Silva B, Viana Pinto P, Costa MA, Cesarean scar pregnancy: A systematic review on expectant management: Eur J Obstet Gynecol Reprod Biol, 2023; 288; 36-43

56. Qiao B, Zhang Z, Li Y, Uterine artery embolization versus methotrexate for cesarean scar pregnancy in a Chinese population: A meta-analysis: J Minim Invasive Gynecol, 2016; 23; 1040-48

57. Van X, Bui T, Dinh HT, The effectiveness of combined local and systemic methotrexate treatment in cesarean scar pregnancy weeks 8 to 14: Gynecol Minim Invasive Ther, 2023; 12; 170-74

58. Naeh A, Shrim A, Shalom-Paz E, Cesarean scar pregnancy managed with local and systemic methotrexate: A single center case series: Eur J Obstet Gynecol Reprod Biol, 2019; 238; 138-42

59. Serres-Cousine O, Kuijper FM, Curis E, Clinical investigation of fertility after uterine artery embolization: Am J Obstet Gynecol, 2021; 225; 403.e1-e22

60. Munger DP, Gemery JM, Forauer AR, Short-interval recanalization after gelfoam occlusion: Radiol Case Rep, 2022; 17; 3835-37

In Press

Clinical Research  

Exploring the Educational Social and Physical Activities Among Health Care Undergraduates – a Cross-Section...

Med Sci Monit In Press; DOI: 10.12659/MSM.943399  


Clinical Research  

Percutaneous Coronary Intervention as a Non-Surgical Treatment for Ischemic Mitral Regurgitation in Patient...

Med Sci Monit In Press; DOI: 10.12659/MSM.943122  

Clinical Research  

Maxillary Canine Impaction: Assessing the Influence of Maxillary Anatomy Using Cone Beam Computed Tomography

Med Sci Monit In Press; DOI: 10.12659/MSM.944306  

Clinical Research  

Optimal Duration of Cold and Heat Compression for Forearm Muscle Biomechanics in Mixed Martial Arts Athlete...

Med Sci Monit In Press; DOI: 10.12659/MSM.944149  

Most Viewed Current Articles

17 Jan 2024 : Review article  

Vaccination Guidelines for Pregnant Women: Addressing COVID-19 and the Omicron Variant

DOI :10.12659/MSM.942799

Med Sci Monit 2024; 30:e942799


14 Dec 2022 : Clinical Research  

Prevalence and Variability of Allergen-Specific Immunoglobulin E in Patients with Elevated Tryptase Levels

DOI :10.12659/MSM.937990

Med Sci Monit 2022; 28:e937990


16 May 2023 : Clinical Research  

Electrophysiological Testing for an Auditory Processing Disorder and Reading Performance in 54 School Stude...

DOI :10.12659/MSM.940387

Med Sci Monit 2023; 29:e940387


01 Jan 2022 : Editorial  

Editorial: Current Status of Oral Antiviral Drug Treatments for SARS-CoV-2 Infection in Non-Hospitalized Pa...

DOI :10.12659/MSM.935952

Med Sci Monit 2022; 28:e935952


Your Privacy

We use cookies to ensure the functionality of our website, to personalize content and advertising, to provide social media features, and to analyze our traffic. If you allow us to do so, we also inform our social media, advertising and analysis partners about your use of our website, You can decise for yourself which categories you you want to deny or allow. Please note that based on your settings not all functionalities of the site are available. View our privacy policy.

Medical Science Monitor eISSN: 1643-3750
Medical Science Monitor eISSN: 1643-3750