Zimmerli W, Widmer A F, Blatter M, Frei R, Ochsner P E
Department of Internal Medicine, University Hospitals, Basel, Switzerland.
JAMA. 1998 May 20;279(19):1537-41. doi: 10.1001/jama.279.19.1537.
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.
To evaluate the clinical efficacy of a rifampin combination in staphylococcal infections associated with stable orthopedic devices.
A randomized, placebo-controlled, double-blind trial conducted from 1992 through 1997.
Two infectious disease services in tertiary care centers in collaboration with 5 orthopedic surgeons in Switzerland.
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).
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.
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.
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.
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.
基于体外和体内观察,含利福平的治疗方案能够治愈葡萄球菌植入物相关感染。然而,这一证据尚未得到对照临床试验的证实。
评估利福平联合用药治疗与稳定骨科器械相关的葡萄球菌感染的临床疗效。
1992年至1997年进行的一项随机、安慰剂对照、双盲试验。
瑞士三级医疗中心的两个传染病科室与5名骨科外科医生合作开展。
共有33例经培养证实为葡萄球菌感染且与稳定骨科植入物相关、感染症状持续时间较短(排除时限<1年;实际病程0 - 21天)的患者。
初始清创,给予氟氯西林或万古霉素联合利福平或安慰剂进行为期2周的静脉治疗,随后给予环丙沙星 - 利福平或环丙沙星 - 安慰剂进行长期治疗。
治愈定义为:(1)无感染的临床体征和症状;(2)C反应蛋白水平低于5mg/L;(3)在24个月的最终随访时无松动或感染的影像学表现。失败定义为:(1)存在持续的感染临床和/或实验室体征;(2)初始微生物持续存在或再次分离。
共有18例患者被分配至环丙沙星 - 利福平组,15例患者被分配至环丙沙星 - 安慰剂组。24例患者完成了试验,随访时间分别为35个月和33个月。环丙沙星 - 利福平组12例患者中有12例(100%)治愈,而环丙沙星 - 安慰剂组12例患者中有7例(58%)治愈(P = 0.02)。33例患者中有9例因不良事件(n = 6)、不依从(n = 1)或违反方案(n = 2)退出。退出的9例患者中有7例随后接受了利福平联合用药治疗,其中5例在未取出器械的情况下治愈。
在植入物稳定、感染持续时间短且进行了初始清创的患者中,能够耐受利福平 - 环丙沙星长期(3 - 6个月)治疗的患者,感染得以治愈且无需取出植入物。