New therapies for fungal pneumonia

被引:14
|
作者
Maertens, Johan [1 ]
Meersseman, Wouter [2 ]
Van Bleyenbergh, Pascal [3 ]
机构
[1] Katholieke Univ Leuven Hosp, Dept Hematol, Acute Leukemia & Stem Cell Transplantat Unit, B-3000 Louvain, Belgium
[2] Katholieke Univ Leuven Hosp, Dept Gen Med, B-3000 Louvain, Belgium
[3] Katholieke Univ Leuven Hosp, Dept Resp Med, B-3000 Louvain, Belgium
关键词
antifungal prophylaxis; aspergillosis; drug monitoring; galactomannan; beta-D-glucan; preemptive therapy; INVASIVE PULMONARY ASPERGILLOSIS; LIPOSOMAL AMPHOTERICIN-B; BETA-D-GLUCAN; PREEMPTIVE ANTIFUNGAL THERAPY; POLYMERASE-CHAIN-REACTION; MYCOSES STUDY-GROUP; COMPUTED-TOMOGRAPHY; EUROPEAN-ORGANIZATION; NEUTROPENIC PATIENTS; CROSS-REACTIVITY;
D O I
10.1097/QCO.0b013e328328cfff
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Purpose of review This review summarizes recent developments in the diagnosis and treatment of fungal pneumonia, with an emphasis on invasive pulmonary aspergillosis. Recent findings Improvements in nonculture-based fungal diagnostics, early implementation of pulmonary high resolution, or spiral computed tomography scanning and a recent expansion of the antifungal armamentarium have greatly improved the outcome of immunocompromised patients with invasive aspergillosis. However, the field is changing: new pathogens (such as Zygomycetes) are emerging, and novel risk groups (ICU patients in particular) are being identified. Summary Galactomannan antigen detection is a valuable tool for evaluating patients at risk for invasive aspergillosis (as a screening assay on serum samples from neutropenic patients or as a confirmatory assay on bronchoalveolar lavage fluid samples, in general), but should be used in conjunction with modern imaging techniques. beta-D-Glucan and PCR assays are still investigational. Voriconazole is the drug of choice for invasive aspergillosis, whereas liposomal amphotericin B at 3 mg/kg per day is the preferred alternative in case of contraindication, drug-related side-effects, or intolerance. Whenever possible, optimal antifungal therapy should be complemented by surgical debridement of necrotic tissue. The added value of combination therapy is still unproven. Therapeutic drug monitoring of mold-active azoles should be implemented in order to minimize toxicity and maximize efficacy. Lipid-based formulations of amphotericin B, and to a lesser extent voriconazole, are the drugs of choice for non-Aspergillus related fungal pneumonia. Although active in prophylaxis, the efficacy of posaconazole in confirmed infections remains controversial.
引用
收藏
页码:183 / 190
页数:8
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