Medical University Vienna, Department of Psychiatry and Psychotherapy, Währinger Gürtel 18-20, 1090, Vienna, Austria.
Eur J Pain. 2012 Apr;16(4):574-84. doi: 10.1016/j.ejpain.2011.08.008.
Increased pain sensitivity and the development of opioid tolerance complicate the treatment of pain experiencedby opioid maintained pregnantwomenduring delivery and the perinatal period. Theaim of the present study was to investigate differences in pain management of opioid maintained compared to nondependent pregnant women during delivery and the postpartum period. 40 deliveries of 37 opioid dependent women enrolled in a double-blind, double-dummy randomized controlled trial (RCT) examining the safety and efficacy of methadone (mean dose at the time of delivery = 63.89 mg) and buprenorphine (mean dose at the time of delivery = 14.05 mg) during pregnancy were analyzed and participants were matched to a non-dependent comparison group of 80 pregnant women. Differences in pain management (opioid and non-opioid analgesic medication) during delivery and perinatal period were analyzed. Following cesarean delivery opioid maintained women received significantly less opioid analgesics (day of delivery p = 0.038; day 1: p = 0.02), NSAIDs were administered more frequently to opioid dependent patients than to the comparison group during cesarean section and on the third day postpartum. Significantly higher nicotine consumption in the group of opioid dependentwomenhad a strong influence onthe retrieved results, and might be considered as an independent factor of altered pain experience. Differences in pain treatment became evident when comparing opioid maintained women to healthy controls. These differences might be based on psychosocial consequences of opioid addiction along with the lack of an interdisciplinary consensus on pain treatment protocols for opioid dependent patients.
在分娩和围产期,阿片类药物维持的孕妇疼痛敏感性增加和阿片类药物耐受的发展使疼痛治疗复杂化。本研究的目的是调查与非依赖孕妇相比,阿片类药物维持孕妇在分娩和产后期间疼痛管理的差异。对 37 名接受双盲、双模拟随机对照试验(RCT)的阿片类药物依赖孕妇的 40 次分娩进行了分析,该试验检查了美沙酮(分娩时的平均剂量为 63.89mg)和丁丙诺啡(分娩时的平均剂量为 14.05mg)在怀孕期间的安全性和疗效,参与者与 80 名非依赖孕妇的对照组相匹配。分析了分娩和围产期疼痛管理(阿片类和非阿片类镇痛药物)的差异。剖宫产后,阿片类药物维持的女性接受的阿片类镇痛药物明显较少(分娩当天:p=0.038;第 1 天:p=0.02),与对照组相比,阿片类药物依赖患者在剖宫产和产后第 3 天更频繁地使用非甾体抗炎药。阿片类药物依赖组中尼古丁消耗的显著增加对检索结果有很大影响,并且可以被认为是改变疼痛体验的一个独立因素。与健康对照组相比,阿片类药物维持的女性的疼痛治疗差异明显。这些差异可能基于阿片类药物成瘾的心理社会后果,以及缺乏针对阿片类药物依赖患者的疼痛治疗方案的跨学科共识。