Initial micafungin treatment does not improve outcomes compared to fluconazole treatment in immunocompromised and critically ill patients with candidaemia

被引:0
|
作者
Theodore, Deborah A. [1 ]
Henneman, Amrita D. [2 ]
Loo, Angela [3 ]
Shields, Ryan K. [4 ]
Eschenauer, Gregory [5 ]
Sobieszczyk, Magdalena E. [1 ]
Kubin, Christine J. [1 ,3 ]
机构
[1] Columbia Univ, New York Presbyterian Hosp, Dept Med, Div Infect Dis,Med Ctr, 622 West 168th St,PH 8W-876, New York, NY 10032 USA
[2] 160 Hofstra Univ, Hofstra Northwell Sch Nursing & Phys Assistant Stu, Hempstead, NY 11549 USA
[3] New York Presbyterian Hosp, Dept Pharm, 630 168th St,3rd Floor, New York, NY 10032 USA
[4] Univ Pittsburgh, Dept Med, Falk Med Bldg,Suite 3A,3601 Fifth Ave, Pittsburgh, PA 15213 USA
[5] Coll Pharm, Dept Pharm, Michigan Med, 428 Church St, Ann Arbor, MI 48109 USA
基金
美国国家卫生研究院;
关键词
AMPHOTERICIN-B; ECHINOCANDIN RESISTANCE; INVASIVE CANDIDIASIS; RISK-FACTORS; CANDIDEMIA; MULTICENTER; MORTALITY; CARE; EPIDEMIOLOGY; INFECTIONS;
D O I
10.1093/jac/dkae175
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Candidaemia is associated with poor outcomes including high mortality rates. Controversy remains regarding whether fluconazole or an echinocandin is the optimal choice for initial candidaemia treatment, particularly among high-risk patients such as the immunocompromised or critically ill. Objectives: To understand optimal initial treatment of candidaemia. Methods: We conducted a retrospective study of immunocompromised or ICU adult patients with candidaemia from 2010 to 2014. Patients who received >= 3 consecutive days of initial treatment with fluconazole or micafungin were included. The primary outcome was complete response at day 14, defined as clinical improvement and blood culture sterilization. Secondary outcomes included microbiological and clinical success, survival and recurrent candidaemia. Results: A total of 197 patients were included; 76 received fluconazole and 121 received micafungin. There was no difference in complete response between the fluconazole and micafungin groups (ICU: 38% versus 40%, P = 0.87; immunocompromised: 57% versus 59%, P = 0.80). Secondary outcomes including survival were also similar. In multivariable analysis, among ICU patients, Pitt bacteraemia score < 4 (P = 0.002) and time to antifungal (P = 0.037) were associated with meeting the primary outcome; white blood cell count > 11 cells x 10(3)/mu L on day 0 (P < 0.001) and Candida isolated from a non-blood site (P = 0.025) were associated with not meeting the primary outcome. Among immunocompromised patients, white blood cells > 11 x 10(3)/mu L (P = 0.003) and Candida isolated from a non-blood site (P = 0.026) were associated with not meeting the primary outcome. Conclusions: These data suggest that among ICU or immunocompromised patients, severity of illness rather than initial antifungal choice drove clinical outcomes.
引用
收藏
页码:1877 / 1884
页数:8
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