与葡萄糖酸氯己定联合使用的外用阴离子制剂不相容的证据:一项系统综述

G. Tran, T. Huynh, F. M. Bruins, Najeah Ahmad, W. Budris, Alba L. Posligua, J. Hammel, B. Nardone, D. West
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引用次数: 4

摘要

葡萄糖酸氯己定(CHG)是一种广泛应用于皮肤和伤口消毒的防腐剂。CHG的阳离子性质可能允许其在常用的外用剂中被阴离子剂失活和沉淀。我们通过检索PubMed、Cochrane Library和Web of Science数据库和精选的报告CHG不相容(定义为失活或沉淀)的原创研究文章进行了系统综述。研究结果显示,22篇论文通过以下途径证明了CHG的不相容性:1)抗菌活性降低(卡波姆、丙烯酸酯/C10-C30烷基丙烯酸酯交聚物、牙本质、牛血清白蛋白、共聚物M239144、十二烷基硫酸钠、热杀微生物、三乙醇胺和树皮软木);2)可见沉淀物的形成(次氯酸钠、EDTA、生理盐水、乙醇和制霉菌素)。只有三篇出版物报道了皮肤病学中CHG的不相容性,特别是卡波姆、三乙醇胺和丙烯酸酯/C10-C30烷基丙烯酸酯交聚物。虽然有有限的证据表明CHG不相容与阴离子药物有关,但如果同时使用CHG,临床医生应仔细考虑所使用的局部药物的性质。提高对CHG不相容的认识可能会导致更好的抗菌活性,从而确保最佳的患者管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evidence of incompatibility for topical anionic agents used in conjunction with chlorhexidine gluconate: A systematic review
Chlorhexidine gluconate (CHG) is a widely used antiseptic agent for skin and wound disinfection. The cationic properties of CHG may allow its inactivation and precipitation by anionic agents in commonly used topical agents. We conducted a systematic review by searching through PubMed, Cochrane Library, and Web of Science databases and selected original research articles reporting on CHG incompatibility, defined as inactivation or precipitation. The search yielded 22 publications that demonstrated CHG incompatibility via: 1) reduced antibacterial activity (carbomer, acrylates/C10-C30 alkyl acrylate crosspolymer, dentin, bovine serum albumin, copolymer M239144, sodium lauryl sulfate, heat-killed microbes, triethanolamine, and bark cork); and 2) visible precipitate formation (sodium hypochlorite, EDTA, saline, ethanol, andnystatin). Only three publications reported on CHG incompatibility in dermatology, specifically for carbomer, triethanolamine, and acrylates/C10-C30 alkyl acrylate crosspolymer. Although limited evidence linking CHG incompatibility and anionic agents exists, clinicians should carefully consider the nature of topical agents used if CHG is concurrently applied. Increased awareness of CHG incompatibility may result in better antibacterial activity thus ensuring optimal patient management.
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