{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,16]],"date-time":"2026-02-16T18:36:05Z","timestamp":1771266965972,"version":"3.50.1"},"reference-count":33,"publisher":"Wiley","issue":"5","license":[{"start":{"date-parts":[[2021,1,28]],"date-time":"2021-01-28T00:00:00Z","timestamp":1611792000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/"}],"content-domain":{"domain":["obgyn.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Acta Obstet Gynecol Scand"],"published-print":{"date-parts":[[2021,5]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:title>Introduction<\/jats:title><jats:p>The aim of this study was to compare childbirth experiences and experience of labor pain in primiparous women who had received high\u2010 vs low\u2010dose oxytocin for augmentation of delayed labor.<\/jats:p><\/jats:sec><jats:sec><jats:title>Material and methods<\/jats:title><jats:p>A multicenter, parallel, double\u2010blind 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\u2010 vs low\u2010dose oxytocin used for augmentation of a delayed labor progress. The Childbirth Experience Questionnaire version 2 (CEQ2) was sent to the women 1\u00a0month after birth. The CEQ2 consists of 22 items in four domains: <jats:italic>Own capacity, Perceived safety, Professional support<\/jats:italic> and <jats:italic>Participation<\/jats:italic>. In addition, labor pain was reported with a visual analog scale (VAS) 2\u00a0hours postpartum and 1\u00a0month after birth. The main outcome was the childbirth experience measured with the four domains of the CEQ2. The clinical trial number is NCT01587625.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>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\u2010 and low\u2010dose oxytocin groups of women: <jats:italic>Own capacity<\/jats:italic> (<jats:italic>P<\/jats:italic>\u00a0=\u00a0.36), <jats:italic>Perceived safety<\/jats:italic> (<jats:italic>P<\/jats:italic>\u00a0=\u00a0.44), <jats:italic>Professional support<\/jats:italic> (<jats:italic>P<\/jats:italic>\u00a0=\u00a0.84), <jats:italic>Participation<\/jats:italic> (<jats:italic>P<\/jats:italic>\u00a0=\u00a0.49). VAS scores of labor pain were reported as similar in both oxytocin dosage groups. Labor pain was scored higher 1\u00a0month after birth compared with 2\u00a0hours postpartum. There was an association between childbirth experiences and mode of birth in both the high\u2010 and low\u2010dose oxytocin groups.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p>Different dosage of oxytocin for augmentation of delayed labor did not affect women\u2019s childbirth experiences assessed through CEQ2 1\u00a0month after birth, or pain assessment 2\u00a0hours or 1\u00a0month after birth.<\/jats:p><\/jats:sec>","DOI":"10.1111\/aogs.14042","type":"journal-article","created":{"date-parts":[[2020,11,11]],"date-time":"2020-11-11T20:11:15Z","timestamp":1605125475000},"page":"971-978","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":7,"title":["Dosage of oxytocin for augmentation of labor and women\u2019s childbirth experiences: A randomized controlled trial"],"prefix":"10.1111","volume":"100","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-9553-1274","authenticated-orcid":false,"given":"Lotta","family":"Selin","sequence":"first","affiliation":[{"name":"Institute of Health and Care Sciences Sahlgrenska Academy Gothenburg Sweden"},{"name":"Department of Obstetrics and Gynecology Region Vastra Gotaland , NU\u2010Hospital Group Trollh\u00e4ttan Sweden"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Marie","family":"Berg","sequence":"additional","affiliation":[{"name":"Institute of Health and Care Sciences Sahlgrenska Academy Gothenburg Sweden"},{"name":"Department of Obstetrics and Gynecology Region Vastra Gotaland, Sahlgrenska University Hospital Gothenburg Sweden"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ulla\u2010Britt","family":"Wennerholm","sequence":"additional","affiliation":[{"name":"Department of Obstetrics and Gynecology Region Vastra Gotaland, Sahlgrenska University Hospital Gothenburg Sweden"},{"name":"Center of Perinatal Medicine and Health Institute of Clinical Sciences Sahlgrenska Academy Gothenburg Sweden"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Anna","family":"Dencker","sequence":"additional","affiliation":[{"name":"Institute of Health and Care Sciences Sahlgrenska Academy Gothenburg Sweden"},{"name":"Center for Person\u2010centered Care Sahlgrenska Academy Gothenburg Sweden"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2021,1,28]]},"reference":[{"key":"e_1_2_10_2_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.midw.2005.01.001"},{"key":"e_1_2_10_3_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.0730-7659.2004.0270.x"},{"key":"e_1_2_10_4_1","doi-asserted-by":"publisher","DOI":"10.1017\/S0033291715002706"},{"key":"e_1_2_10_5_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.wombi.2018.07.004"},{"key":"e_1_2_10_6_1","doi-asserted-by":"publisher","DOI":"10.1111\/jan.13534"},{"key":"e_1_2_10_7_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1471-0528.2008.02020.x"},{"key":"e_1_2_10_8_1","doi-asserted-by":"publisher","DOI":"10.1080\/00016340701837744"},{"key":"e_1_2_10_9_1","doi-asserted-by":"publisher","DOI":"10.1080\/00016340902811001"},{"key":"e_1_2_10_10_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.wombi.2017.07.002"},{"key":"e_1_2_10_11_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.srhc.2012.12.002"},{"key":"e_1_2_10_12_1","doi-asserted-by":"publisher","DOI":"10.1186\/1471-2393-7-15"},{"key":"e_1_2_10_13_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.srhc.2012.03.003"},{"key":"e_1_2_10_14_1","first-page":"CD007123","article-title":"Oxytocin versus no treatment or delayed treatment for slow progress in the first stage of spontaneous labour","volume":"6","author":"Bugg GJ","year":"2013","journal-title":"Cochrane Database Syst Rev"},{"key":"e_1_2_10_15_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1471-0528.1998.tb09362.x"},{"key":"e_1_2_10_16_1","doi-asserted-by":"publisher","DOI":"10.1046\/j.1523-536x.1999.00089.x"},{"key":"e_1_2_10_17_1","doi-asserted-by":"publisher","DOI":"10.1097\/01.AOG.0000226862.78768.5c"},{"key":"e_1_2_10_18_1","first-page":"CD007201","article-title":"High\u2010dose versus low\u2010dose oxytocin for augmentation of delayed labour","volume":"7","author":"Kenyon S","year":"2013","journal-title":"Cochrane Database Syst Rev"},{"key":"e_1_2_10_19_1","doi-asserted-by":"publisher","DOI":"10.1111\/1471-0528.12331"},{"key":"e_1_2_10_20_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.wombi.2018.09.002"},{"key":"e_1_2_10_21_1","unstructured":"BergM DykesAK Nordstr\u00f6mL WennerholmU\u2010B.Indikation f\u00f6r v\u00e4rkstimulering med oxytocin under aktiv f\u00f6rlossning. 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