Shorr Andrew F, Chung Kevin, Jackson William L, Waterman Paige E, Kollef Marin H
Washington Hospital Center, Medstar, Potomac, MD, USA.
Crit Care Med. 2005 Sep;33(9):1928-35; quiz 1936. doi: 10.1097/01.ccm.0000178352.14703.49.
To evaluate the impact of fluconazole prophylaxis on the incidence of fungal infections and on mortality among critically ill surgical patients.
Meta-analysis of randomized, placebo-controlled trials of fluconazole prophylaxis.
Subjects participating in the clinical trials in this area.
We identified four randomized studies comparing fluconazole to placebo for prevention of fungal infections in the surgical intensive care unit (SICU). The studies enrolled 626 patients and used differing dosing regimens of fluconazole. All trials were double-blind and two were multicenter studies. Fluconazole administration significantly reduced the incidence of fungal infections (pooled odds ratio, 0.44; 95% confidence interval, 0.27-0.72; p < .001). However, fluconazole prophylaxis was not associated with a survival advantage (pooled OR for mortality, 0.87; 95% confidence interval, 0.59-1.28; p = NS). Fluconazole did not statistically alter the rate of candidemia, as this was low across the studies and developed in only 2.2% of all participants. Performing a sensitivity analysis and including two additional studies that indirectly examined fluconazole prophylaxis in the critically ill did not change our observations. Data from the reports reviewed were insufficient to allow comment on the impact of fluconazole prophylaxis on resource utilization, the distribution of non-albicans species of Candida, and the emergence of antifungal resistance. Generally, fluconazole appeared to be safe for SICU patients.
Prophylactic fluconazole administration for prevention of mycoses in SICU patients appears to successfully decrease the rate of these infections, but this strategy does not improve survival. The absence of a survival advantage may reflect the few studies in this area and the possibility that this issue has not been adequately studied. Because of the potential for both resistance and emergence of non-albicans isolates, clinicians must consider these issues when evaluating fluconazole prophylaxis in the SICU. Future trials should focus on more precisely identifying patients at high risk for fungal infections and on determining if broader use of fluconazole alters the distribution of candidal species seen in the SICU and impacts measures of resource utilization such as length of stay and duration of mechanical ventilation.
评估氟康唑预防性用药对重症外科患者真菌感染发生率及死亡率的影响。
对氟康唑预防性用药的随机、安慰剂对照试验进行荟萃分析。
参与该领域临床试验的受试者。
我们确定了四项将氟康唑与安慰剂用于预防外科重症监护病房(SICU)真菌感染的随机研究。这些研究共纳入626例患者,并采用了不同的氟康唑给药方案。所有试验均为双盲试验,两项为多中心研究。氟康唑给药显著降低了真菌感染的发生率(合并比值比,0.44;95%置信区间,0.27 - 0.72;p < 0.001)。然而,氟康唑预防性用药与生存优势无关(死亡率的合并比值比,0.87;95%置信区间,0.59 - 1.28;p = 无统计学意义)。氟康唑对念珠菌血症发生率无统计学上的改变,因为在所有研究中该发生率都很低,仅在2.2%的所有参与者中出现。进行敏感性分析并纳入另外两项间接研究重症患者氟康唑预防性用药的研究后,我们的观察结果未改变。所审查报告中的数据不足以就氟康唑预防性用药对资源利用、非白色念珠菌属念珠菌的分布以及抗真菌耐药性的出现的影响发表评论。总体而言,氟康唑对SICU患者似乎是安全的。
在SICU患者中预防性使用氟康唑预防霉菌感染似乎成功降低了这些感染的发生率,但该策略并未改善生存率。缺乏生存优势可能反映了该领域研究较少,以及这个问题可能尚未得到充分研究。由于存在耐药性以及非白色念珠菌分离株出现的可能性,临床医生在评估SICU中氟康唑预防性用药时必须考虑这些问题。未来的试验应集中于更精确地识别真菌感染高危患者,并确定更广泛使用氟康唑是否会改变SICU中所见念珠菌种类的分布以及影响诸如住院时间和机械通气时间等资源利用指标。