Background

Early pregnancy failure (EPF) is estimated to occur in 10–20% of all clinical pregnancies and is one of the most common complications of early pregnancy [1]. While traditionally surgical intervention, i.e. dilatation and curettage (D&C) was considered to be the preferred treatment option, over the past two decades, medical treatment has become increasingly popular showcasing high efficacy and safety with few adverse events [2,3,4,5,6]. Moreover, medical treatment does not appear to impair future fertility potential [7, 8]. Several studies have compared medical treatment to surgical intervention for treatment of EPF showing favorable results [9,10,11]. This has led to a shift in paradigm and nowadays medical treatment is considered the primary approach for treatment of EPF.

The common medical treatment for EPF is misoprostol (PGE1) which can be administered orally, buccally or vaginally. Side effects are for the most part mild with few reports of major adverse events [10]. Advantages of vaginal administration compared to the oral route include decreased side effects such as nausea, diarrhea, vomiting and abdominal pain [12].

Success rate of treatment with misoprostol for EPF has been reported to range from 50 to 84% [13,14,15]. Previous studies have attempted to discover variables which may affect treatment efficacy. Dosage, route of administration, gestational age, gestational sac size and fetal size have all been suggested as factors which may influence treatment success [16,17,18,19].

Retained placenta affects 0.5-3% of all vaginal deliveries [20]. This clinical scenario is associated with substantial morbidity for women following vaginal delivery mostly due to post-partum hemorrhage. Several mechanisms have been proposed to explain retained placenta such as failed myometrial contraction and partial placenta accreta preventing placental detachment [20, 21]. Notably, treatment with misoprostol has not previously been shown to increase risk of placental complications [22]. Instead, it is plausible that there may be similar mechanisms, such as abnormal implantation or impaired uterine contractility, that may be associated with both failure of medical treatment of EPF and retained placenta after vaginal delivery. However, to date, the association between retained placenta and treatment success rate of misoprostol for EPF has yet to be evaluated.

The aim of this study was to test the hypothesis that patients with a history of complete or partial retained placenta were more likely to have failed medical management of EPF compared to women without a history of retained placenta. We further investigated the connection between medical, clinical and sonographic parameters and treatment success.

Methods

We conducted a retrospective cohort study at a tertiary university medical center from 2006 to 2021. Institutional ethical review board approval was received (0627-22-HMO).

The cohort included women up to 13 weeks gestation diagnosed with EPF who underwent medical management. Women with a case of manual placental extraction or uterine cavity inspection at time of delivery or retained placenta with need for medical intervention post-partum in a previous pregnancy comprised the study group. The control group included cases collected for a previous study we conducted, comprised of women who underwent treatment with misoprostol for EPF without history of retained placenta between January 2011 and June 2012. Excluded from both groups were non-singleton pregnancies, cases of scar pregnancy, patients with allergy to prostaglandins and women who did not complete the full protocol of medical treatment.

Early pregnancy failure was defined as missed abortion or blighted ovum up to 13 weeks gestation. Diagnosis of missed abortion was made according to the criteria established by Doubilet et al. [23]. Crown rump length (CRL) of 7 mm and mean sac diameter of 25 mm with the absence of cardiac activity on trans-vaginal ultrasound (TVUS) were considered indicative of missed abortion. Further criteria included absence of a visible heartbeat over 2 weeks after a scan showing a gestational sac without a yolk sac or over 11 days after a scan showing a gestational sac with a yolk sac [23].

Confirmation of EPF was established by TVUS scan performed in our medical center reviewed by a specialist in obstetrics and gynecology. According to our routine clinical pathway, following diagnosis each woman was offered one of three options: expectant management, surgical treatment (dilatation and curettage) or medical treatment with vaginal misoprostol. Women were counselled regarding benefits and risks of each option. Those who opted for medical treatment with vaginal misoprostol were eligible for inclusion in the study.

Our department’s protocol for administration of misoprostol has been described previously [24]. In short, following examination by a gynecologist and receipt of informed consent, 800 mcg of misoprostol (4 tablets of Cytotec 200 mcg each) are placed in the posterior vaginal fornix. All patients are asked to present again to the hospital 48–72 h after treatment for an ultrasound scan. If this ultrasound shows a gestational sac or endometrial thickness of above 20 mm, an additional dose of 800 mcg of misoprostol is administered in the same fashion described above. Patients are then instructed to undergo another ultrasound after two weeks or after the next period and if there is still evidence of retained products of conception, they are referred for surgical management. According to our department’s protocol, when the gestational sac is present, women are referred to undergo D&C as opposed to cases of increased endometrial thickness for which operative hysteroscopy is the treatment of choice.

Women in the study group had at least one case of retained placenta following delivery during a previous pregnancy. Retention of placental products included the need for manual placental removal, partial placental evacuation requiring manual inspection of the uterine cavity or retained products of conception diagnosed during the post-partum period. Patients with any one of these clinical scenarios were eligible for inclusion in our study group. Diagnosis of placental retention was made by the most senior physician in the labor and delivery ward at the time. Diagnosis of post-partum retained products of conception was confirmed with pelvic ultrasound.

Data were retrieved from the electronic medical record and included demographic, clinical and sonographic characteristics such as age, gravidity, parity, previous miscarriage, previous treatment with misoprostol, size of gestational sac, fetal crown-rump length (CRL), presence of fetal heart rate on ultrasound prior to diagnosis of EPF, uterine position and treatment success.

The primary outcome was successful medical treatment compared between women who had an event of retained placenta and women who did not. Successful treatment was defined as endometrial thickness of less than 20 mm with no evidence of retained products of conception after one or two doses of misoprostol.

Statistical analysis

To compare the study covariates chi-square and Fischer exact test were used for categorical variables and the Mann-Whitney test for continuous variables- all distributions were different from normal. Logistic regression was used for multivariate analysis adjusting for available baseline characteristics. The statistical software package SPSS 24.0 (SPSS Inc., Chicago, IL) was used for all data analyses. We report odds ratios (OR), 95% confidence interval (CI), and two-sided P values. P-values < 0.05 were considered statistically significant.

Results

A total of 271 patients with EPF were included in the study. Mean age and parity of participants were 32.7 ± 6.5 and 1.9 ± 2.2, respectively. Two-hundred and thirty-three women (86.0%) presented with missed abortion, and 38 (14.0%) with blighted ovum. Success rate after treatment with misoprostol was 76.4%.

The study group included 34 women diagnosed with EPF who had a previous case of retained placenta. The control group included 237 women diagnosed with EPF treated with misoprostol without such an event. A comparison of demographic and obstetric characteristics, as well as miscarriage related parameters are summarized in Tables 1 and 2. Women in the study group had higher parity, gravidity, were less likely to have presence of embryonic heartbeat and had a smaller gestational sac size length (mm) on TVUS. Regarding the primary outcome, success rate after treatment with misoprostol was found to be lower in the study group compared to the control group (61.8% vs. 78.5%, p = 0.032).

Table 1 Demographic and obstetric characteristics of the study population – patients with and without history of retained placenta
Table 2 Current early pregnancy failure characteristics and treatment outcomes

In the attempt to identify factors affecting misoprostol treatment failure, a univariate analysis was performed comparing successful vs. failed misoprostol treatment (Table 3). Advanced age, gravidity, parity, and gestational sac size length (mm) were associated with higher misoprostol treatment failure rate.

Table 3 Demographic and clinical characteristics of the study population – patients with success vs. failure of misoprostol treatment

A logistic regression multivariate analysis was performed in order to identify factors associated with misoprostol treatment failure (Table 4). Advanced age, parity and history of manual lysis or retained placenta entered the logistic regression model but did not reach statistical significance.

Table 4 Multivariate logistic regression analysis for misoprostol treatment failure

Discussion

In this study we found that women with EPF who have a history of retained placenta were at increased risk of misoprostol treatment failure. However, following multivariate analysis this finding as well as other parameters evaluated were no longer statistically significant.

Retained placenta following delivery may be complete or partial. Treatment of complete retained placenta entails manual removal of the placenta while partial retention requires uterine cavity examination to remove remaining placental tissue. When retained products of conception are diagnosed during the post-partum period, operative hysteroscopy is often the treatment of choice.

Several mechanisms have been suggested for retained placenta. One of these includes dysfunctional contractility in which the retro-placental myometrium contracts inadequately leading to failure of placental separation during the third stage of labor [25, 26]. Misoprostol treatment for EPF causes uterine contractions which often are sufficient to achieve complete evacuation of uterine content. If uterine contractility is impaired, this may decrease its ability to evacuate products of conception adherent to the uterine wall. Although during the first trimester the uterus is smaller with diminished contractile potential, inherent contractile dysfunction may play a role in failure of misoprostol during treatment of EPF.

Another possible mechanism for retained placenta is abnormally invasive placenta which incorporates a spectrum of clinical scenarios such as adherent placenta and placenta accreta. In this situation spontaneous placental detachment is inhibited leading to partial or whole placental retention. First trimester abortion complicated by placenta accreta is a rare event described in several case reports [27, 28]. In recent years the concept of partial placenta accreta has gained recognition during which only part of the placenta may be pathologically adherent [29]. This phenomenon could explain cases in which only part of the placenta remains intra-uterine following delivery. Such partial invasive attachment may exist during the first trimester, possibly hindering success of medical treatment for EPF, though this hypothesis requires further investigation.

To our knowledge this is the first study to assess the association between retained placenta and success rate of misoprostol treatment for EPF. Other strengths of the study include systematic collection of data, demographic as well as sonographic parameters, a relatively large control group and substantial clinical relevance for caregivers treating women with EPF.

However, apart from its retrospective nature the study has several limitations. The small study group may have caused certain parameters to fall short of reaching statistical significance. The control group was collected during a relatively short time period compared to the study group. However, we believe this had little effect on the results given that treatment protocols and routine follow-up have not changed in our department during the study period.

Conclusion

In Conclusion, in this study we found women who had an event of retained placenta to have decreased success rate of treatment with misoprostol for EPF. However, this difference was no longer significant following multivariate analysis. While we appreciate the results found here are preliminary, we believe they may help clinicians counsel women deliberating which treatment course to take following diagnosis of EPF. Future studies focusing on this clinical scenario are needed and will most certainly add to the sparse literature currently available.