Could a simple manual technique performed by a midwife reduce the incidence of episiotomy and perineal lacerations? A non-randomized pilot study

被引:0
作者
Taylor, Kathryn E. [1 ]
Stulz, Virginia [2 ]
机构
[1] Nepean Hosp, Kingswood, Australia
[2] Univ Canberra, Fac Hlth, Bruce, Australia
来源
EUROPEAN JOURNAL OF MIDWIFERY | 2024年 / 8卷
关键词
perineum; myofascial release; vaginal birth; labor; episiotomy; PELVIC PAIN; LABOR; RISK;
D O I
10.18332/ejm/191749
中图分类号
R47 [护理学];
学科分类号
1011 ;
摘要
INTRODUCTION Women experience medical interventions, episiotomy, and perineal lacerations during childbirth, impacting their physical, psychological, and sexual well-being. This study compares the perineal status of prospective women who had the midwifery intervention of perineal myofascial release during childbirth, to a matched retrospective control sample of women who received standard care during childbirth. METHODS A non-randomized pilot study with prospective data collected for 50 women after informed verbal consent was obtained to having the midwifery intervention of perineal myofascial release during childbirth, and the matched retrospective data for the control group of 49 women were collected from a random sample generated from the regression, and chi-squared analyses. Retrospective trial registration was granted with The Australian New Zealand Clinical Trials Registry ANZTR. RESULTS Women were six times (OR=0.15; 95% CI: 0.0-0.37) less likely to have a nonintact perineum and twice (OR=0.44; 95% CI: 0.35-0.56) less likely to have an episiotomy if they were in the intervention group. Chi-squared analysis found no statistically significant differences between groups for normal vaginal birth and instrumental births, excluding cesareans and waterbirth [chi 2(1)= -0.37, p=0.542]. CONCLUSIONS This study found perineal myofascial release benefits women by reducing perineal trauma and episiotomy. However, there were no significant differences in the duration of the active pushing stage of labor or mode of birth. This study has shown some promise in obtaining data for a larger, definitive, randomized controlled trial.
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