Cruddas L, Baker D M
University College London Medical School, London, UK.
Department of Surgery, Royal Free Hospital, London, UK.
J Eur Acad Dermatol Venereol. 2017 Jun;31(6):952-963. doi: 10.1111/jdv.14081. Epub 2017 Feb 21.
Primary hyperhidrosis is a condition characterized by excessive sweating. Patients are treated off-license with oral anticholinergic medications and report adverse events associated with systemic anticholinergic interactions. This review assesses clinical evidence of efficacy, impact on quality of life and adverse events associated with oral anticholinergic therapy for primary hyperhidrosis. PRISMA guidelines were implemented to complete a systematic review (PROSPERO:CRD42016036326). MEDLINE, EMBASE and PubMed were searched from 1946 to 2015. Inclusion criteria included observational and experimental studies, anticholinergic medication use in primary hyperhidrosis, oral therapy and clear diagnostic and outcome measures. Twenty-three articles relevant to the inclusion criteria were analysed. Oxybutynin therapy improved symptoms in an average of 76.2% (range 60-97%) patients and improved QOL in 75.6% (range 57.6-100%) of patients. Methantheline bromide therapy was associated with a 41% reduction in axillary sweating, 16.4% reduction in palmar sweating, 25% decrease in HDSS score and 40.9% increase in DLQI score. Outcome measures of glycopyrrolate therapy were too variable to collate. Dry mouth was reported in 73.4% (range 43.3-100%) of participants taking oxybutynin 10 mg/day, 38.6% (range 27.8-63.2%) of patients taking glycopyrrolate and 68.8% of patients taking methantheline bromide. Nine studies reported that patients stopped therapy due to adverse events. In eight of these studies, a mean of 10.9% of total participants ceased treatment due to dry mouth. Evidence of oral anticholinergic therapy for hyperhidrosis is limited. However, its use is associated with improvement in quality of life and clinical symptoms but at the cost of considerable adverse events.
原发性多汗症是一种以出汗过多为特征的病症。患者使用未获许可的口服抗胆碱能药物进行治疗,并报告了与全身性抗胆碱能相互作用相关的不良事件。本综述评估了口服抗胆碱能疗法治疗原发性多汗症的疗效、对生活质量的影响以及不良事件的临床证据。采用PRISMA指南完成系统评价(国际前瞻性系统评价注册平台:CRD42016036326)。检索了1946年至2015年期间的MEDLINE、EMBASE和PubMed数据库。纳入标准包括观察性和实验性研究、原发性多汗症中抗胆碱能药物的使用、口服疗法以及明确的诊断和结局指标。分析了23篇符合纳入标准的文章。奥昔布宁治疗使平均76.2%(范围60 - 97%)的患者症状得到改善,75.6%(范围57.6 - 100%)的患者生活质量得到改善。溴甲贝那替秦治疗使腋窝出汗减少41%,手掌出汗减少16.4%,多汗症疾病严重程度评分降低25%,皮肤病生活质量指数评分增加40.9%。格隆溴铵治疗的结局指标差异太大,无法进行整理。服用10毫克/天奥昔布宁的参与者中有73.4%(范围43.3 - 100%)报告口干,服用格隆溴铵的患者中有38.6%(范围27.8 - 63.2%)报告口干,服用溴甲贝那替秦的患者中有68.8%报告口干。9项研究报告患者因不良事件停止治疗。在其中8项研究中,平均10.9%的总参与者因口干停止治疗。口服抗胆碱能疗法治疗多汗症的证据有限。然而,其使用与生活质量和临床症状的改善相关,但代价是出现相当多的不良事件。