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Dosage of oxytocin for augmentation of labor and women's childbirth experiences: A randomized controlled trial.
Selin, Lotta; Berg, Marie; Wennerholm, Ulla-Britt; Dencker, Anna.
Afiliación
  • Selin L; Institute of Health and Care Sciences, Sahlgrenska Academy, Gothenburg, Sweden.
  • Berg M; Department of Obstetrics and Gynecology, Region Vastra Gotaland , NU-Hospital Group, Trollhättan, Sweden.
  • Wennerholm UB; Institute of Health and Care Sciences, Sahlgrenska Academy, Gothenburg, Sweden.
  • Dencker A; Department of Obstetrics and Gynecology, Region Vastra Gotaland, Sahlgrenska University Hospital, Gothenburg, Sweden.
Acta Obstet Gynecol Scand ; 100(5): 971-978, 2021 05.
Article en En | MEDLINE | ID: mdl-33176392
INTRODUCTION: The aim of this study was to compare childbirth experiences and experience of labor pain in primiparous women who had received high- vs low-dose oxytocin for augmentation of delayed labor. MATERIAL AND METHODS: A multicenter, parallel, double-blind randomized controlled trial took place in six Swedish labor wards. Inclusion criteria were healthy primiparous women at term with uncomplicated singleton pregnancies, cephalic fetal presentation, spontaneous onset of labor, confirmed delayed labor progress and ruptured membranes. The randomized controlled trial compared high- vs low-dose oxytocin used for augmentation of a delayed labor progress. The Childbirth Experience Questionnaire version 2 (CEQ2) was sent to the women 1 month after birth. The CEQ2 consists of 22 items in four domains: Own capacity, Perceived safety, Professional support and Participation. In addition, labor pain was reported with a visual analog scale (VAS) 2 hours postpartum and 1 month after birth. The main outcome was the childbirth experience measured with the four domains of the CEQ2. The clinical trial number is NCT01587625. RESULTS: The CEQ2 was sent to 1203 women, and a total of 1008 women (83.8%) answered the questionnaire. The four domains of childbirth experience were scored similarly in the high- and low-dose oxytocin groups of women: Own capacity (P = .36), Perceived safety (P = .44), Professional support (P = .84), Participation (P = .49). VAS scores of labor pain were reported as similar in both oxytocin dosage groups. Labor pain was scored higher 1 month after birth compared with 2 hours postpartum. There was an association between childbirth experiences and mode of birth in both the high- and low-dose oxytocin groups. CONCLUSIONS: Different dosage of oxytocin for augmentation of delayed labor did not affect women's childbirth experiences assessed through CEQ2 1 month after birth, or pain assessment 2 hours or 1 month after birth.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Oxitócicos / Oxitocina / Parto / Dolor de Parto Tipo de estudio: Clinical_trials / Qualitative_research Aspecto: Patient_preference Límite: Adult / Female / Humans / Pregnancy País/Región como asunto: Europa Idioma: En Revista: Acta Obstet Gynecol Scand Año: 2021 Tipo del documento: Article País de afiliación: Suecia Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Oxitócicos / Oxitocina / Parto / Dolor de Parto Tipo de estudio: Clinical_trials / Qualitative_research Aspecto: Patient_preference Límite: Adult / Female / Humans / Pregnancy País/Región como asunto: Europa Idioma: En Revista: Acta Obstet Gynecol Scand Año: 2021 Tipo del documento: Article País de afiliación: Suecia Pais de publicación: Estados Unidos