School of Nursing and Midwifery, Griffith University, University Drive, Meadowbrook, Queensland 4131, Australia; School of Nursing and Midwifery, Trinity College Dublin, 24 D'Olier St., Dublin 2, Ireland.
School of Nursing and Midwifery, Trinity College Dublin, 24 D'Olier St., Dublin 2, Ireland.
Women Birth. 2021 Sep;34(5):e435-e441. doi: 10.1016/j.wombi.2020.09.001. Epub 2020 Sep 11.
To compare labour and birth outcomes between nulliparous women who used versus did not use intrapartum epidural analgesia.
Prospective cohort study.
Two maternity hospitals in Ireland.
A total of 1221 nulliparous women who gave birth vaginally or by emergency caesarean section.
Multinomial logistic regression was used to analyse categorical outcomes, with results presented as ratios of relative risks (RRR). For dichotomous outcomes we used logistic regression, with results presented as odds ratios (OR).
Mode of birth, IV syntocinon use, pyrexia (≥38°C), antibiotic treatment, first stage labour ≥10h, second stage labour ≥2h, blood loss (≥500mls, ≥1000mls), perineal trauma. Neonatal outcomes included Apgar score ≥7 at 1min and 5min, admission to neonatal intensive care unit, and infant feeding method.
Women using EA were more likely to require a vacuum-assisted birth (RRR 3.35, p<0.01) or forceps-assisted birth (RRR 11.69, p<0.01). Exposure to EA was associated with significantly greater risk of ≥10h first (OR 6.72, p=0.01) and ≥2h second (OR 2.25, p<0.01) stage labour, increased likelihood of receiving IV syntocinon (OR 9.38, p<0.01), antibiotics (OR 2.97, p<0.01) and a greater probability of pyrexia (OR 10.26, p<0.01). Women who used EA were half as likely to be breastfeeding at three months postpartum (OR 0.53, p<0.01). No differences were observed between groups in neonatal outcomes.
Our data shows significant associations between EA use and several intrapartum outcomes.
比较使用与不使用产时硬膜外镇痛的初产妇的分娩结局。
前瞻性队列研究。
爱尔兰的两家产科医院。
共有 1221 名经阴道分娩或急诊剖宫产的初产妇。
采用多项逻辑回归分析分类结局,结果表示为相对风险比(RRR)。对于二项结局,我们使用逻辑回归,结果表示为优势比(OR)。
分娩方式、静脉催产素使用、发热(≥38°C)、抗生素治疗、第一产程≥10 小时、第二产程≥2 小时、出血量(≥500ml、≥1000ml)、会阴创伤。新生儿结局包括 1 分钟和 5 分钟时 Apgar 评分≥7、新生儿重症监护病房入院和婴儿喂养方式。
使用 EA 的女性更有可能需要真空辅助分娩(RRR 3.35,p<0.01)或产钳辅助分娩(RRR 11.69,p<0.01)。暴露于 EA 与第一产程≥10 小时(OR 6.72,p=0.01)和第二产程≥2 小时(OR 2.25,p<0.01)的风险显著增加相关,更有可能接受静脉催产素(OR 9.38,p<0.01)、抗生素(OR 2.97,p<0.01),发热的可能性更大(OR 10.26,p<0.01)。使用 EA 的女性在产后 3 个月时母乳喂养的可能性减半(OR 0.53,p<0.01)。两组在新生儿结局方面无差异。
我们的数据显示 EA 使用与一些产时结局之间存在显著关联。