TY - JOUR
T1 - Making cervical ripening EASI
T2 - A prospective controlled comparison of single versus double balloon catheters
AU - Mei-Dan, Elad
AU - Walfisch, Asnat
AU - Valencia, Constanza
AU - Hallak, Mordechai
N1 - Funding Information:
The study was approved by the Israeli Ministry of Health (reference number: HTA4174) and by the Hillel Yaffe local Institutional Review Board (reference number: 15/2007) 28 November 2007.
Publisher Copyright:
© 2014 Informa UK Ltd.
PY - 2014/11/1
Y1 - 2014/11/1
N2 - Objective: To compare the efficacy of two mechanical devices for cervical ripening: double versus single balloon catheters, both with extra-amniotic saline infusion (EASI). Methods: Women at term with a singleton pregnancy presenting for labor induction were assigned to receive the double balloon catheter (with EASI) or the single balloon catheter (with EASI). Outcomes included time from device insertion to delivery, rates of successful vaginal delivery and occurrence of adverse events. Results: One hundred and eighty-six women completed the study. Ripening success was comparable between the double and single balloon arms (96.4% versus 92.7%, p = 0.55, respectively). Balloon insertion to delivery interval was significantly shorter, and cesarean section rate was significantly lower in the double balloon arm compared with the single balloon arm (14.3 versus 15.8 h, p = 0.04 and 8.3% versus 20%, p = 0.05, respectively). There were no significant differences in maternal characteristics, satisfaction or adverse outcomes. Conclusions: This study is the first documented assessment of the double balloon catheter combined with EASI. Our findings suggest that the double balloon catheter results in reduced time to delivery and higher vaginal delivery rates, compared with the single balloon catheter with EASI, without compromising maternal or fetal safety.
AB - Objective: To compare the efficacy of two mechanical devices for cervical ripening: double versus single balloon catheters, both with extra-amniotic saline infusion (EASI). Methods: Women at term with a singleton pregnancy presenting for labor induction were assigned to receive the double balloon catheter (with EASI) or the single balloon catheter (with EASI). Outcomes included time from device insertion to delivery, rates of successful vaginal delivery and occurrence of adverse events. Results: One hundred and eighty-six women completed the study. Ripening success was comparable between the double and single balloon arms (96.4% versus 92.7%, p = 0.55, respectively). Balloon insertion to delivery interval was significantly shorter, and cesarean section rate was significantly lower in the double balloon arm compared with the single balloon arm (14.3 versus 15.8 h, p = 0.04 and 8.3% versus 20%, p = 0.05, respectively). There were no significant differences in maternal characteristics, satisfaction or adverse outcomes. Conclusions: This study is the first documented assessment of the double balloon catheter combined with EASI. Our findings suggest that the double balloon catheter results in reduced time to delivery and higher vaginal delivery rates, compared with the single balloon catheter with EASI, without compromising maternal or fetal safety.
KW - Balloon
KW - Extra-amniotic saline infusion
KW - Labor induction
UR - http://www.scopus.com/inward/record.url?scp=84911890563&partnerID=8YFLogxK
U2 - 10.3109/14767058.2013.879704
DO - 10.3109/14767058.2013.879704
M3 - Article
C2 - 24397244
AN - SCOPUS:84911890563
VL - 27
SP - 1765
EP - 1770
JO - Journal of Maternal-Fetal and Neonatal Medicine
JF - Journal of Maternal-Fetal and Neonatal Medicine
SN - 1476-7058
IS - 17
ER -