Wertheim Heiman F L, Vos Margreet C, Ott Alewijn, Voss Andreas, Kluytmans Jan A J W, Vandenbroucke-Grauls Christina M J E, Meester Marlene H M, van Keulen Peter H J, Verbrugh Henri A
Department of Medical Microbiology and Infectious Diseases, Erasmus University Medical Center, Rotterdam, The Netherlands.
Ann Intern Med. 2004 Mar 16;140(6):419-25. doi: 10.7326/0003-4819-140-6-200403160-00007.
Staphylococcus aureus nasal carriage is a major risk factor for nosocomial S. aureus infection. Studies show that intranasal mupirocin can prevent nosocomial surgical site infections. No data are available on the efficacy of mupirocin in nonsurgical patients.
To assess the efficacy of mupirocin prophylaxis in preventing nosocomial S. aureus infections in nonsurgical patients.
Randomized, double-blind, placebo-controlled trial.
3 tertiary care academic hospitals and 1 nonacademic hospital.
1602 culture-proven S. aureus carriers hospitalized in nonsurgical departments.
Therapy with mupirocin 2% nasal ointment (n = 793) or placebo ointment (n = 809), twice daily for 5 days, started 1 to 3 days after admission.
Nosocomial S. aureus infections according to defined criteria, in-hospital mortality, duration of hospitalization, and time to nosocomial S. aureus infection. Staphylococcus aureus isolates were genotyped to assess whether infection was caused by endogenous strains.
The mupirocin and placebo groups did not statistically differ in the rates of nosocomial S. aureus infections (mupirocin, 2.6%; placebo, 2.8%; risk difference, 0.2 percentage point [95% CI, -1.5 to 1.9 percentage points]), mortality (mupirocin, 3.0%; placebo, 2.8%; risk difference, -0.2 percentage point [CI, -1.9 to 1.5 percentage points]), or duration of hospitalization (median for both, 8 days). However, time to nosocomial S. aureus infection was decreased in the mupirocin group from 12 to 25 days (P > 0.2). A total of 77% of S. aureus nosocomial infections were endogenous.
A few infections in both groups may have been missed because investigators assessed a patient for infection only if microbiology culture results were positive for S. aureus.
Routine culture for S. aureus nasal carriage at admission and subsequent mupirocin application does not provide effective prophylaxis against nosocomial S. aureus infections in nonsurgical patients.
金黄色葡萄球菌鼻腔定植是医院内金黄色葡萄球菌感染的主要危险因素。研究表明,鼻用莫匹罗星可预防医院内手术部位感染。目前尚无关于莫匹罗星在非手术患者中疗效的数据。
评估莫匹罗星预防非手术患者医院内金黄色葡萄球菌感染的疗效。
随机、双盲、安慰剂对照试验。
3家三级医疗学术医院和1家非学术医院。
1602名在非手术科室住院的经培养证实的金黄色葡萄球菌携带者。
使用2%莫匹罗星鼻软膏(n = 793)或安慰剂软膏(n = 809)治疗,每天两次,共5天,入院后1至3天开始。
根据既定标准判断的医院内金黄色葡萄球菌感染、住院死亡率、住院时间以及发生医院内金黄色葡萄球菌感染的时间。对金黄色葡萄球菌分离株进行基因分型,以评估感染是否由内源性菌株引起。
莫匹罗星组和安慰剂组在医院内金黄色葡萄球菌感染率(莫匹罗星组为2.6%;安慰剂组为2.8%;风险差异为0.2个百分点[95%CI,-1.5至1.9个百分点])、死亡率(莫匹罗星组为3.0%;安慰剂组为2.8%;风险差异为-0.2个百分点[CI,-1.9至1.5个百分点])或住院时间(两组中位数均为8天)方面无统计学差异。然而,莫匹罗星组发生医院内金黄色葡萄球菌感染的时间从12天降至25天(P>0.2)。总共77%的医院内金黄色葡萄球菌感染是内源性的。
两组中可能有一些感染未被发现,因为研究人员仅在微生物培养结果显示金黄色葡萄球菌呈阳性时才对患者进行感染评估。
入院时常规检测金黄色葡萄球菌鼻腔定植并随后应用莫匹罗星不能有效预防非手术患者医院内金黄色葡萄球菌感染。