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Dosage of oxytocin for augmentation of labor and women’s childbirth experiences: A randomized controlled trial
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 plac...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8248083/ https://www.ncbi.nlm.nih.gov/pubmed/33176392 http://dx.doi.org/10.1111/aogs.14042 |
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author | Selin, Lotta Berg, Marie Wennerholm, Ulla‐Britt Dencker, Anna |
author_facet | Selin, Lotta Berg, Marie Wennerholm, Ulla‐Britt Dencker, Anna |
author_sort | Selin, Lotta |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-8248083 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82480832021-07-02 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 Acta Obstet Gynecol Scand Birth 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. John Wiley and Sons Inc. 2021-01-28 2021-05 /pmc/articles/PMC8248083/ /pubmed/33176392 http://dx.doi.org/10.1111/aogs.14042 Text en © 2020 The Authors. Acta Obstetricia et Gynecologica Scandinavica published by John Wiley & Sons Ltd on behalf of Nordic Federation of Societies of Obstetrics and Gynecology (NFOG) https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Birth Selin, Lotta Berg, Marie Wennerholm, Ulla‐Britt Dencker, Anna Dosage of oxytocin for augmentation of labor and women’s childbirth experiences: A randomized controlled trial |
title | Dosage of oxytocin for augmentation of labor and women’s childbirth experiences: A randomized controlled trial |
title_full | Dosage of oxytocin for augmentation of labor and women’s childbirth experiences: A randomized controlled trial |
title_fullStr | Dosage of oxytocin for augmentation of labor and women’s childbirth experiences: A randomized controlled trial |
title_full_unstemmed | Dosage of oxytocin for augmentation of labor and women’s childbirth experiences: A randomized controlled trial |
title_short | Dosage of oxytocin for augmentation of labor and women’s childbirth experiences: A randomized controlled trial |
title_sort | dosage of oxytocin for augmentation of labor and women’s childbirth experiences: a randomized controlled trial |
topic | Birth |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8248083/ https://www.ncbi.nlm.nih.gov/pubmed/33176392 http://dx.doi.org/10.1111/aogs.14042 |
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