Abstract:This randomised controlled trial was carried out over a 14-month period in a tertiary health institution in Nigeria, to determine the effectiveness of Foley catheter and synchronous low dose misoprostol for pre-labour cervical ripening. Term pregnant women with unfavourable cervices (Bishop's score < 6) requiring cervical ripening/induction of labour were assigned randomly into three groups: Group A, transcervical Foley catheter was used synchronously with low dose intravaginal misoprostol; Group B, transcervi… Show more
“…Four [15–18] were excluded because the treatment allocation was not randomized, one [19] was excluded because the full text could not be obtained, two [20,21] were excluded because they involved induction of labor in pregnancies with a nonviable fetus, and one [22] was excluded because misoprostol was not used concurrently with a Foley catheter in the combination treatment group. Therefore, eight eligible studies [9–12,23–26] with a total of 1153 patients were included in the present meta‐analysis (Table 1).…”
Section: Resultsmentioning
confidence: 99%
“…Among the included studies, seven [9–12,23–25] had a low risk of random sequence generation and allocation concealment and were judged to be of high quality (Table 2). One study [26] was judged to be of low quality.…”
Section: Resultsmentioning
confidence: 99%
“…All studies reported the time from induction to delivery. However, Ugwu et al [23] reported the data as patient numbers per time interval; because of this format, the data could not be pooled with those from the other studies. On the basis of random‐effects estimation, the use of Foley catheter plus misoprostol (combination group) was associated with a shorter mean time to delivery than was misoprostol alone, but the difference did not reach statistical significance (mean difference –1.46 hours, 95% CI –3.72 to 0.81; P = 0.21) (Fig.…”
The combined use of Foley catheter and misoprostol results in a reduced time to delivery, a reduced frequency tachysystole with fetal heart rate changes, and an increased incidence of chorioamnionitis.
“…Four [15–18] were excluded because the treatment allocation was not randomized, one [19] was excluded because the full text could not be obtained, two [20,21] were excluded because they involved induction of labor in pregnancies with a nonviable fetus, and one [22] was excluded because misoprostol was not used concurrently with a Foley catheter in the combination treatment group. Therefore, eight eligible studies [9–12,23–26] with a total of 1153 patients were included in the present meta‐analysis (Table 1).…”
Section: Resultsmentioning
confidence: 99%
“…Among the included studies, seven [9–12,23–25] had a low risk of random sequence generation and allocation concealment and were judged to be of high quality (Table 2). One study [26] was judged to be of low quality.…”
Section: Resultsmentioning
confidence: 99%
“…All studies reported the time from induction to delivery. However, Ugwu et al [23] reported the data as patient numbers per time interval; because of this format, the data could not be pooled with those from the other studies. On the basis of random‐effects estimation, the use of Foley catheter plus misoprostol (combination group) was associated with a shorter mean time to delivery than was misoprostol alone, but the difference did not reach statistical significance (mean difference –1.46 hours, 95% CI –3.72 to 0.81; P = 0.21) (Fig.…”
The combined use of Foley catheter and misoprostol results in a reduced time to delivery, a reduced frequency tachysystole with fetal heart rate changes, and an increased incidence of chorioamnionitis.
“…20 In other women, the bleeding resolved spontaneously and induction with the catheter was continued. 10,21 In three cases a caesarean section (CS) was performed due to severe bleeding and in one woman due to a marginal placenta praevia. 18,19,22 Two of these neonates had good Apgar scores and information of the third one was not available to us.…”
“…They did not find differences in the likelihood to choose the same method of cervical ripening for possible future inductions (91 vs. 100%; p ¼ 0.08). 18 Another explanation could be that more vaginal examinations were performed in the oral misoprostol group (mean: 8.1 vs. 6.8), thereby creating more contact moments with the attending physician that could lead to more satisfaction with the induction experience instead of the previously assumed disadvantage of vaginal examinations. Different cultural perceptions of induction of labor might influence the preference for an induction method.…”
Section: Women's Experiences With and Preference For Induction Of Labmentioning
Objective We assessed experience and preferences among term women undergoing induction of labor with oral misoprostol or Foley catheter. Study Design In 18 of the 29 participating hospitals in the PROBAAT-II trial, women were asked to complete a questionnaire within 24 hours after delivery. We adapted a validated questionnaire about expectancy and experience of labor and asked women whether they would prefer the same method again in a future pregnancy.
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