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[Cervical ripening at term. a randomized and prospective study: Misoprotol versus dinoprostone]
Tunisie Medicale [La]. 2012; 90 (5): 362-369
em Francês | IMEMR | ID: emr-131495
ABSTRACT
To compare the efficacy and safety of cervical ripening at term by vaginal Misoprostol and Dinoprostone. We performed a prospective randomized study on cervical ripening with misoprostol and dinoprostone in the third trimester of pregnancy. 300 patients have been divided into two groups one consisted by 150 patients who received Misoprostol [Cytotec registered] and the second consisted by 150 patients who received Dinoprostone [Pr‚pidil registered]. Analysis of our results allowed to reveal a significant decrease in the time of entry into work for the Misoprostol group [9.08 hours versus 12.51 hours, p = 0.007], a significant reduction delivery time [14.48 hours versus 19.30 hours, p = 0.001]. Moreover, the birth rate in the first 24 hours after the first dose was significantly higher in the Misoprostol group [86.7% versus 72.7%, p = 0.003]. The use of oxytocin was significantly reduced with Misoprostol [44% versus 58.7%, p = 0.01]. The mode of delivery was not influenced by membership in one or other of the two groups. Misoprostol seems an interesting molecule for cervical ripening and labor induction
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Índice: IMEMR (Mediterrâneo Oriental) Assunto principal: Dinoprostona / Ensaios Clínicos Controlados Aleatórios como Assunto / Estudos Prospectivos / Resultado do Tratamento / Misoprostol / Parto Obstétrico Tipo de estudo: Ensaio Clínico Controlado Limite: Feminino / Humanos Idioma: Francês Revista: Tunisie Med. Ano de publicação: 2012

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Índice: IMEMR (Mediterrâneo Oriental) Assunto principal: Dinoprostona / Ensaios Clínicos Controlados Aleatórios como Assunto / Estudos Prospectivos / Resultado do Tratamento / Misoprostol / Parto Obstétrico Tipo de estudo: Ensaio Clínico Controlado Limite: Feminino / Humanos Idioma: Francês Revista: Tunisie Med. Ano de publicação: 2012