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Pak J Biol Sci ; 16(9): 443-5, 2013 May 01.
Artigo em Inglês | MEDLINE | ID: mdl-24498810

RESUMO

The aim of this study was to compare the efficacy of atropine and hyoscine-N-butyl bromide in reducing the pain and time length of the first stage of labour. In a single blind randomized clinical trial, 120 term pregnancies were enrolled from July 2009 to March 2011. A parallel design was used to randomly assign subjects into two equal groups including 60 participants in each group. Hyoscine-N-butylbromide was administered 40 mg intravenously in the first group and intravenous atropine was given in second group at a dose of 0.5 mg. The participants of the two trial arms were similar according to the distribution of background variables. The pain trend through the study follow up was found to be different between groups (p < 0.05). Mean length of the first stage of labor was 218.5 min (SD: 81.4) in hyoscine versus 339 min (SD: 83.3) in atropine group (p < 0.001). Mean 1st and 5th min APGAR score was similar in both groups. Drug side effects were less frequent in hyoscine group observed in 13 cases compared to atropine group observed in 56 cases (p < 0.001). Hyoscine appeared to be preferable to atropine specially in reducing the length of first stage of pregnancy.


Assuntos
Analgesia Obstétrica/métodos , Analgésicos/uso terapêutico , Atropina/uso terapêutico , Brometo de Butilescopolamônio/uso terapêutico , Dor do Parto/tratamento farmacológico , Primeira Fase do Trabalho de Parto/efeitos dos fármacos , Trabalho de Parto Induzido/métodos , Parassimpatolíticos/uso terapêutico , Administração Intravenosa , Adulto , Analgésicos/administração & dosagem , Analgésicos/efeitos adversos , Atropina/administração & dosagem , Atropina/efeitos adversos , Brometo de Butilescopolamônio/efeitos adversos , Distribuição de Qui-Quadrado , Feminino , Humanos , Irã (Geográfico) , Dor do Parto/diagnóstico , Dor do Parto/fisiopatologia , Medição da Dor , Parassimpatolíticos/administração & dosagem , Parassimpatolíticos/efeitos adversos , Gravidez , Método Simples-Cego , Fatores de Tempo , Resultado do Tratamento , Adulto Jovem
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