Hill R L, Fisher A P, Ware R J, Wilson S, Casewell M W
Department of Medical Microbiology, King's College Hospital and School of Medicine & Dentistry, London, UK.
J Hosp Infect. 1990 May;15(4):311-21. doi: 10.1016/0195-6701(90)90088-6.
In a prospective study, 218 cardiothoracic patients, in whom 'Abbocath-T' cannulae had been inserted preoperatively into the internal jugular vein, were randomized to receive skin preparation of the insertion site with tincture of iodine (108 controls) or tincture of iodine followed by application of sterile 2% calcium mupirocin ointment (110 test patients). Cannulae were usually removed within 48 h of the operation. Patients receiving mupirocin were less likely to develop significant colonization of one or more of their cannulae as judged by Maki's criterion of a yield of greater than 15 colony forming units (cfu) from a cannula segment rolled on an agar plate (17% of mupirocin treated patients compared with 54% of the controls, P less than 0.001). Coagulase-negative staphylococci, micrococci, or both, were the commonest isolates and were cultured from 70% of the 186 control cannulae compared with 24% of 172 cannulae inserted through mupirocin-treated skin (P less than 0.001). A count of more than 15 cfu was found on the tips of 25% control cannulae compared with 5% of the cannulae from mupirocin-treated patients, an effect which was independent of in-situ time (P less than 0.001). For cannulae with colonized tips, the same species was isolated from the skin of the insertion site in 67%, from the exterior of the hub in 61% and from the lumen in only 15%. There were no side effects attributed to mupirocin or superinfection with resistant organisms. We conclude that in cardiothoracic patients the application of mupirocin after standard skin preparation with tincture of iodine significantly reduces the colonization of central venous cannulae by organisms derived from the skin insertion site.
在一项前瞻性研究中,218例心胸外科患者术前已将“Abbocath - T”套管插入颈内静脉,这些患者被随机分为两组,一组用碘酊对插管部位进行皮肤准备(108例对照),另一组先用碘酊,然后涂抹无菌2%莫匹罗星钙软膏(110例试验患者)。套管通常在术后48小时内拔除。根据Maki标准,即从在琼脂平板上滚动的套管段中培养出的菌落形成单位(cfu)产量大于15,判断接受莫匹罗星治疗的患者其一根或多根套管发生显著定植的可能性较小(接受莫匹罗星治疗的患者中有17%,而对照组为54%,P<0.001)。凝固酶阴性葡萄球菌、微球菌或两者是最常见的分离菌,186根对照套管中有70%培养出这些菌,而通过用莫匹罗星处理过的皮肤插入的172根套管中只有24%培养出这些菌(P<0.001)。25%的对照套管尖端菌落计数超过15 cfu,而莫匹罗星治疗患者的套管中这一比例为5%,这一效应与在位时间无关(P<0.001)。对于尖端定植的套管,67%从插管部位皮肤分离出相同菌种,61%从针座外部分离出,仅15%从管腔内分离出。没有归因于莫匹罗星的副作用或耐药菌的二重感染。我们得出结论,在心胸外科患者中,在用碘酊进行标准皮肤准备后应用莫匹罗星可显著减少来自皮肤插管部位的微生物对中心静脉套管的定植。