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Do we need a 200 µg misoprostol vaginal insert? A retrospective cohort study comparing the misoprostol vaginal insert to oral misoprostol.
Wegener, Silke; Koenigbauer, Josefine T; Laesser, Claudia; Metz, Melanie; Pech, Luisa; Kummer, Julia; Daut, Julia; Jarchau, Ute; Wegener, Viktor; Hellmeyer, Lars.
Afiliação
  • Wegener S; Department of Obstetrics and Gynecology, Vivantes Klinikum im Friedrichshain, Berlin, Germany.
  • Koenigbauer JT; Department of Obstetrics and Gynecology, Vivantes Klinikum im Friedrichshain, Berlin, Germany.
  • Laesser C; Department of Obstetrics and Gynecology, Vivantes Klinikum im Friedrichshain, Berlin, Germany.
  • Metz M; Department of Obstetrics and Gynecology, Vivantes Klinikum im Friedrichshain, Berlin, Germany.
  • Pech L; Department of Obstetrics and Gynecology, Vivantes Klinikum im Friedrichshain, Berlin, Germany.
  • Kummer J; Department of Obstetrics and Gynecology, Vivantes Klinikum im Friedrichshain, Berlin, Germany.
  • Daut J; Department of Obstetrics and Gynecology, Vivantes Klinikum im Friedrichshain, Berlin, Germany.
  • Jarchau U; Department of Obstetrics and Gynecology, Vivantes Klinikum im Friedrichshain, Berlin, Germany.
  • Wegener V; Department of Anesthesiology and Operative Intensive Care Medicine (CCM, CVK), Charité - Universitätsmedizin Berlin, Berlin, Germany.
  • Hellmeyer L; Department of Obstetrics and Gynecology, Vivantes Klinikum im Friedrichshain, Berlin, Germany.
J Obstet Gynaecol Res ; 46(6): 851-857, 2020 Jun.
Article em En | MEDLINE | ID: mdl-32363787
ABSTRACT

AIM:

The misoprostol vaginal insert (MVI) was reported to be more effective than dinoprostone but discussed critically because of high rates of fetal heart rate changes due to uterine tachysystole. The aim of this study was to investigate the outcome of induced labor using the MVI compared to off-label orally-administered misoprostol (OM).

METHODS:

Retrospective study including a total of 401 patients with singleton pregnancies in whom labor was induced at ≥36 0/7 gestational weeks with MVI (203) or OM (198). Primary outcomes were the time from induction to delivery, vaginal delivery in 24 h and the mode of delivery and the neonatal outcome.

RESULTS:

Median time until any delivery was 833 min (645-1278) for MVI and 1076.5 min (698-1686.3) for OM group; 83.7% of the patients in the MVI group gave birth within 24 h versus 63.6% in the OM group. The MVI group needed significantly less pre-delivery oxytocin (29%). Tachysystole (6.4%) and pathological CTG (30.5%) occurred at a significantly higher frequency in the MVI group. The cesarean section rate was significantly higher in the MVI group amounting to 21.7% versus 14.6% in the OM group (P < 0.05). Neonatal outcome did not differ between the groups.

CONCLUSION:

The MVI might be an option if you are in need for an approved and faster method to induce labor. Although we observed a significantly higher rate of fetal heart rate changes and cesarean sections in the MVI group this did not affect the neonatal outcome.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Misoprostol / Trabalho de Parto Induzido Tipo de estudo: Etiology_studies / Observational_studies Limite: Adult / Female / Humans / Pregnancy Idioma: En Revista: J Obstet Gynaecol Res Assunto da revista: GINECOLOGIA / OBSTETRICIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Misoprostol / Trabalho de Parto Induzido Tipo de estudo: Etiology_studies / Observational_studies Limite: Adult / Female / Humans / Pregnancy Idioma: En Revista: J Obstet Gynaecol Res Assunto da revista: GINECOLOGIA / OBSTETRICIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Alemanha