Your browser doesn't support javascript.
loading
The Labor Progression Study: The use of oxytocin augmentation during labor following Zhang's guideline and the WHO partograph in a cluster randomized trial.
Dalbye, Rebecka; Bernitz, Stine; Olsen, Inge Christoffer; Zhang, Jun; Eggebø, Torbjørn Moe; Rozsa, Daniella; Frøslie, Kathrine Frey; Øian, Pål; Blix, Ellen.
Afiliação
  • Dalbye R; Department of Obstetrics and Gynecology, Østfold Hospital Trust, Grålum, Norway.
  • Bernitz S; Department of Nursing and Health Promotion, Faculty of Health Sciences, Oslo Met-Oslo Metropolitan University, Oslo, Norway.
  • Olsen IC; Department of Obstetrics and Gynecology, Østfold Hospital Trust, Grålum, Norway.
  • Zhang J; Department of Nursing and Health Promotion, Faculty of Health Sciences, Oslo Met-Oslo Metropolitan University, Oslo, Norway.
  • Eggebø TM; Research Support Services, Clinical Trial Unit, Oslo University Hospital, Oslo, Norway.
  • Rozsa D; MOE-Shanghai Key Lab of Children's Environmental Health, Xinhua Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
  • Frøslie KF; National Center for Fetal Medicine, Trondheim University Hospital (St Olav's Hospital), Trondheim, Norway.
  • Øian P; Department of Obstetrics and Gynecology, Stavanger University Hospital, Stavanger, Norway.
  • Blix E; Department of Obstetrics and Gynecology, Stavanger University Hospital, Stavanger, Norway.
Acta Obstet Gynecol Scand ; 98(9): 1187-1194, 2019 09.
Article em En | MEDLINE | ID: mdl-31017306
ABSTRACT

INTRODUCTION:

This study aims to investigate the use of oxytocin augmentation during labor in nulliparous women following Zhang's guideline or the WHO partograph. MATERIAL AND

METHODS:

This is a secondary analysis of a cluster randomized controlled trial in 14 birth-care units in Norway, randomly assigned to either the intervention group, which followed Zhang's guideline, or to the control group, which followed the WHO partograph, for labor progression. The participants were nulliparous women who had a singleton full-term fetus in a cephalic presentation and spontaneous onset of labor, denoted as group 1 in the Ten Group Classification System.

RESULTS:

Between December 2014 and January 2017, 7277 participants were included. A total of 3219 women (44%) received augmentation with oxytocin during labor. Oxytocin was used in 1658 (42%) women in the Zhang group compared with 1561 (47%) women in the WHO group. The adjusted relative risk for augmentation with oxytocin was 0.98 (95% CI 0.84-1.15; P = .8) in the Zhang vs WHO group, with an adjusted risk difference of -0.8% (95% CI -7.8 to 6.1). The participants in the Zhang group were less likely to be augmented with oxytocin before reaching 6 cm of cervical dilatation (24%) compared with participants in the WHO group (28%), with an adjusted relative risk of 0.84 (95% CI 0.75-0.94; P = .003). Oxytocin was administered for almost 20 min longer in the Zhang group than in the WHO group, with an adjusted mean difference of 17.9 min (95% CI 2.7-33.1; P = .021). In addition, 19% of the women in the Zhang group and 23% in the WHO group received augmentation with oxytocin without being diagnosed with labor dystocia.

CONCLUSIONS:

Although no significant difference in the proportion of oxytocin augmentation was observed between the 2 study groups, there were differences in how oxytocin was used. Women in the Zhang group were less likely to receive oxytocin augmentation before 6 cm of cervical dilatation. The duration of augmentation with oxytocin was longer in the Zhang group than in the WHO group.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ocitócicos / Ocitocina / Guias de Prática Clínica como Assunto Tipo de estudo: Clinical_trials / Etiology_studies / Guideline / Risk_factors_studies Limite: Adult / Female / Humans / Pregnancy País como assunto: Europa Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ocitócicos / Ocitocina / Guias de Prática Clínica como Assunto Tipo de estudo: Clinical_trials / Etiology_studies / Guideline / Risk_factors_studies Limite: Adult / Female / Humans / Pregnancy País como assunto: Europa Idioma: En Ano de publicação: 2019 Tipo de documento: Article