Retrospective analysis of our ECV experiences
Among 84 ECV operations, 76 (90.48%) successed and only 8 (9.52%) failed. Detailed information of the 84 patients was shown in Table 1. Mean maternal age was 31.50 years in total. In detail, 31.63 years in the successful team and 30.25 years in the failed group (P = 0.339). The mean gestational age was 37.01weeks, 37.02 weeks and 37.01 weeks in total, successful and failed group, respectively. The proportion of multiparous women was higher in successful group than in failed group (40.79% vs 12.5%), but not statistically significant (P = 0.117). The women in successful group were not with obviously different with those patients in failed group on stature, with BMI 25.37 vs 25.02 (P = 0.903). Ultrasonographic findings of placental location, presentation and umbilical cord around neck of fetus are also collected, results were delineated in Table 1. As the results shown, proportion of posterior placenta location in the successful group was obviously higher than the failed group (61.84% vs 37.5%, P = 0.029). And as compared with women in failed group, those in successful group had higher amniotic fluid index (AFI) value (137.92 vs 100.38, P = 0.001). Only one patient was performed with a second time of ECV among all the included women due to recovery of breech presentation after a period of loose of the belly band. We considered the variables, such as, maternal parity (multiparous), AFI, placental location (posterior), fetal breech presentation type (frank)in ECV, which might determine the success or failure of ECV. Then through multiple logistic regression analysis of these factors, AFI were separately found to affect the success of ECV (HR = 0.965, 95%CI:0.937–0.995, P = 0.021) with our data. And 84.52% patients were anesthetized with chloroprocaine. Others accepted ropivacaine, also with no statistical meaning.
The delivery information of the 84 included women was obtained, as shown in Fig. 1. The 76 patients with successful ECV all came through smooth delivery. One had CS because the fetus reverts to breech presentation. Among 46 patients with spontaneous labour, 44 patients had vaginal deliveries, 2 patients had cesarean section because of rupture of the placental marginal sinus and protracted descent. Among 29 patients with induced labour, 23 patients had vaginal deliveries, 6 patients had cesarean section, two were due to intrauterine infection, one was because of failure of induction, one was owing to protracted descent and two was on account of fetal distress. Another 8 failed ECV women, 5 had emergency CS, four were due to fetal bradycardia, one was because of placental abruption. Other 4 had elective cesarean delivery with persistent breech presentation on termination of pregnancy.
Other information of patients at delivery was also obtained and listed in Table 2. Obviously and reasonably, gestational age of patients with successful ECV was higher than patients with failed ECV, same to birth weight of the fetuses. Only one woman underwent successful ECV delivered with premature infant’s Apgar score of 8, and the neonate was admitted into NICU. Apgar score of others were all 10, but one fetus was admitted into NICU because of hypoglycemia. Complications within 24 h between the two groups were significantly different ( 10.53% vs 62.5%, P = 0.005). Five patients had transient fetal brachycardia in successful ECV group, and they were discharged with satisfied FHR monitoring. In the group of failed ECV, 4 patients had fetal brachycardia. After informing the conditions to the family, they requested emergency CS. Another 2 patients also accepted emergency CS, one was because of rupture of placental marginal sinus after successful ECV and one was because of placental abruption. The babies were both with apgar score of 10. As for other complications during pregnancy, including PROM, GDM, DM, hypothyroidism and hypertension, incidence between the two groups were not statistically variant.
Result Of The Bayesian Network Meta-analysis
Through literature retrieve with the descriptive search strategy, 492 studies were found. Amongst them, 432 records were excluded because of incongruent content, case-reports, reviews, meta-analysis or duplicates based on the titles and abstracts. Then, 38 studies were excluded on account of case-control studies, cohort studies or not comparing tocolytic agents during ECV process after reading the full articles. Besides, 6 records were removed owing to repetitive administration of different tocolytic agents to one patient. Finally, 16 RCTs[18–33]with 3468 patients were included in our study, details of the studies were summarized in Table 3. And the common adverse effects of the tocolytic agents were shown in Table 4. The workflow is shown in Fig. 2. All of these eligible records were RCTs and the quality of evidence was evaluated by the cochrane Handbook scoring system, and potential bias was graded as high, low or unclear. The detailed results of the evaluation were shown in Fig. 3a,b. Network meta-analysis was conducted based on the clinical outcomes, including ECV success, vaginal delivery and common complications of tocolytic agents retrospectively.
The 16 enrolled studies contains 3 kinds of tocolysis, beta stimulants (salbutamol, ritodrine and terbutaline), calcium channel blockers (nifedipine) and nitric oxide donors (nitroglycerine). They were compared in pairs or contrasted with placebo. Besides, as terbutaline was the most common tocolytic agent clinically, other drugs and placebo were also compared with it. According to variant treatments, the networks were plotted and the results were shown in Fig. 4a,b and c. The thickness of the connective lines were proportional to the number of comparisons, and the numbers were shown on the lines. No inconsistency was found between the direct and indirect comparisons from node-splitting analysis.
Success Of Ecv
The included 16 studies all recorded success and failed number of patients after ECV under the usage of different tocolytic agents or placebo. And the highest success rate is 70.18%, which was under the treatment of salbutamol in Vani’s study. The lowest success rate is 0.8%, which was under the treatment of placebo in Impey’s study. The efficacy of other tocolytic agents and placebo versus terbutaline, and different tocolytic agents versus placebo on the success rate of ECV were evaluated by ORs and corresponding 95% CrIs ( As displayed in Fig. 5a, b). And the rank probabilities of the different treatment strategies were shown in Fig. 6a. Accordingly, it isproved that terbutaline played better roles on ECV success rate than nifedipine (OR 0.53, 95% CrI 0.31 to 0.96), nitroglycerin (OR 0.44, 95% CrI 0.21 to 0.91), and placebo (OR 0.46, 95% CrI 0.24 to 0.93), but comparable with ritodrine (OR 0.79, 95% CrI 0.38 to 1.8) and salbutamol (OR 1.2, 95% CrI 0.47 to 3.0). When compared with placebo, ritodrine (OR 1.7, 95% CrI 1.2 to 2.6), sabultamol (OR 2.5, 95% CrI 1.4 to 4.7) and terbutaline (OR 2.1, 95% CrI 1.1 to 4.2) were identified to exert positive effect on ECV success rate, but nifedipine (OR 1.1, 95% CrI 0.63 to 2.1) and nitroglycerin (OR 0.94, 95% CrI 0.56 to 1.6) didn’t work better.
Vaginal Delivery
A total of 13 studies reported delivery condition of the included participants, with the highest vaginal delivery rate of 86.05% under the treatment of nifedipine in Ismail’s study and the lowest vaginal delivery rate of 14.51% under the treatment of placebo in Impey’s study. The efficacy of other tocolytic agents or placebo versus terbutaline, and different tocolytic agents versus placebo on the vaginal delivery rate were evaluated by ORs and corresponding 95% CrIs (As shown in Fig. 5c,d). And the rank probabilities of the different treatment strategies were shown in Fig. 6b. As the result showed that terbutaline didn’t work better obviously on vaginal delivery rate than other treatments. Besides, application of the tocolytic agents didn’t significantly improve the vaginal delivery rate compared with placebo. However, ORs of nitroglycerin (OR 1.4, 95% CrI 0.78 to 2.7), ritodrine (OR 1.4, 95% CrI 0.85 to 2.3), salbutamol (OR 1.4, 95% CrI 0.57 to 4.4) and terbutaline (OR 1.6, 95% CrI 0.83 to 3.5) were all above one compared with placebo, except for nifedipine (OR 0.98, 95% CrI 0.50 to 2.1).
Common Complications Of Tocolytic Agents
Eight studies recorded the incidence of common complications. ORs and CrIs used to evaluate the influence of the treatments on the emergency of common complications were displayed in Fig. 5e, f. Rank probabilities of the interventions were exhibited in Fig. 6c. Comparing with terbutaline, salbutamol (OR 8.4e + 06, 95% CrI 5.1 to 2.4e + 25) appeared evidently more complications, other interventions all had ORs less than one, but not with statistical meaning. Compared with placebo, sabutamol also had more complications (OR 1.6e + 08, 95% CrI 14 to8.8e + 21), terbutaline (OR 2.1, 95% CrI 0.27 to 14), nifedipine (OR 1.8, 95% CrI 0.29 to 10) and nitroglycerin (OR 1.7, 95% CrI 0.39 to 5.4) all had ORs lager than one, ritodrine (OR 0.92, 95% CrI 0.12 to 4.7) had OR less than one, but is not statistically significant.