Role of rifampin for treatment of orthopedic implant-related staphylococcal infections - A randomized controlled trial

被引:744
作者
Zimmerli, W
Widmer, AF
Blatter, M
Frei, R
Ochsner, PE
机构
[1] Univ Basel Hosp, Div Infect Dis, Dept Internal Med, CH-4031 Basel, Switzerland
[2] Univ Basel Hosp, Div Clin Epidemiol, CH-4031 Basel, Switzerland
[3] Univ Basel Hosp, Bacteriol Lab, CH-4031 Basel, Switzerland
[4] Kantonsspital, Clin Orthoped Surg, Liestal, Switzerland
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 1998年 / 279卷 / 19期
关键词
D O I
10.1001/jama.279.19.1537
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context.-Rifampin-containing regimens are able to cure staphylococcal implant-related infections based on in vitro and in vivo observations. However, this evidence has not been proven by a controlled clinical trial. Objective.-To evaluate the clinical efficacy of a rifampin combination in staphylococcal infections associated with stable orthopedic devices. Design.-A randomized, placebo-controlled, double-blind trial conducted from 1992 through 1997. Setting.-Two infectious disease services in tertiary care centers in collaboration with 5 orthopedic surgeons in Switzerland. Patients.-A total of 33 patients with culture-proven staphylococcal infection associated with stable orthopedic implants and with a short duration of symptoms of infection (exclusion limit <1 year; actual experience 0-21 days). Intervention.-Initial debridement and 2-week intravenous course of flucloxacillin or vancomycin with rifampin or placebo, followed by either ciprofloxacin-rifampin or ciprofloxacin-placebo long-term therapy. Main Outcome Measures.-Cure was defined as (1) lack of clinical signs and symptoms of infection, (2) C-reactive protein level less than 5 mg/L, and (3) absence of radiological signs of loosening or infection at the final follow-up visit at 24 months. Failure was defined as (1) persisting clinical and/or laboratory signs of infection or (2) persisting or new isolation of the initial microorganism. Results.-A total of 18 patients were allocated to ciprofloxacin-rifampin and 15 patients to the ciprofloxacin-placebo combination. Twenty-four patients fully completed the trial with a follow-up of 35 and 33 months. The cure rate was 12 (100%) of 12 in the ciprofloxacin-rifampin group compared with 7 (58%) of 12 in the ciprofloxacin-placebo group (P=.02), Nine of 33 patients dropped out due to adverse events (n=6), noncompliance (n=1), or protocol violation (n=2), Seven of the 9 patients who dropped out were subsequently treated with rifampin combinations, and 5 of them were cured without removal of the device. Conclusion.-Among patients with stable implants, short duration of infection, and initial debridement, patients able to tolerate long-term (3-6 months) therapy with rifampin-ciprofloxacin experienced cure of the infection without removal of the implant.
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收藏
页码:1537 / 1541
页数:5
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