A prospective observational study of candidemia: Epidemiology, therapy, and influences on mortality in hospitalized adult and pediatric patients

被引:628
|
作者
Pappas, PG
Rex, JH
Lee, J
Hamill, RJ
Larsen, RA
Powderly, W
Kauffman, CA
Hyslop, N
Mangino, JE
Chapman, S
Horowitz, HW
Edwards, JE
Dismukes, WE
机构
[1] Univ Alabama Birmingham, Div Infect Dis, Birmingham, AL 35294 USA
[2] Univ Texas, Houston, TX USA
[3] Houston Vet Affairs Med Ctr, Houston, TX USA
[4] Washington Univ, St Louis, MO USA
[5] Univ Michigan, Ann Arbor, MI 48109 USA
[6] Ann Arbor Vet Affairs Med Ctr, Ann Arbor, MI USA
[7] Tulane Univ, New Orleans, LA 70118 USA
[8] Ohio State Univ, Columbus, OH 43210 USA
[9] Univ Mississippi, Med Ctr, Jackson, MS 39216 USA
[10] New York Med Coll, Westchester Cty Med Ctr, Valhalla, NY 10595 USA
[11] Univ Calif Los Angeles, Harbor Med Ctr, Los Angeles, CA 90024 USA
[12] Univ So Calif, Los Angeles, CA USA
关键词
D O I
10.1086/376906
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We conducted a prospective, multicenter observational study of adults (n = 1447) and children (n = 144) with candidemia at tertiary care centers in the United States in parallel with a candidemia treatment trial that included nonneutropenic adults. Candida albicans was the most common bloodstream isolate recovered from adults and children (45% vs. 49%) and was associated with high mortality (47% among adults vs. 29% among children). Three-month survival was better among children than among adults (76% vs. 54%; P < .001). Most children received amphotericin B as initial therapy, whereas most adults received fluconazole. In adults, Candida parapsilosis fungemia was associated with lower mortality than was non-parapsilosis candidemia (24% vs. 46%; P < .001). Mortality was similar among subjects with Candida glabrata or non-glabrata candidemia; mortality was also similar among subjects with C. glabrata candidemia who received fluconazole rather than other antifungal therapy. Subjects in the observational cohort had higher Acute Physiology and Chronic Health Evaluation II scores than did participants in the clinical trial (18.6 vs. 16.1), which suggests that the former subjects are more often excluded from therapeutic trials.
引用
收藏
页码:634 / 643
页数:10
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