β-D-glucan Surveillance with Preemptive Anidulafungin for Invasive Candidiasis in Intensive Care Unit Patients: A Randomized Pilot Study

被引:85
作者
Hanson, Kimberly E. [1 ,2 ]
Pfeiffer, Christopher D. [3 ]
Lease, Erika D. [4 ]
Balch, Alfred H. [5 ]
Zaas, Aimee K. [4 ]
Perfect, John R. [4 ]
Alexander, Barbara D. [4 ]
机构
[1] Univ Utah, Dept Med, Salt Lake City, UT 84112 USA
[2] Univ Utah, Dept Pathol, Salt Lake City, UT USA
[3] Oregon Hlth & Sci Univ, Dept Med, Portland, OR USA
[4] Duke Univ, Dept Med, Durham, NC USA
[5] Univ Utah, Dept Pediat, Salt Lake City, UT USA
关键词
BLOOD-STREAM INFECTIONS; NEUTROPENIC CRITICALLY-ILL; FUNGAL-INFECTIONS; LIMULUS TEST; CANDIDEMIA; DIAGNOSIS; PLASMA; ASSAY; COLONIZATION; PROPHYLAXIS;
D O I
10.1371/journal.pone.0042282
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Invasive candidiasis (IC) is a devastating disease. While prompt antifungal therapy improves outcomes, empiric treatment based on the presence of fever has little clinical impact. B-D-Glucan (BDG) is a fungal cell wall component detectable in the serum of patients with early invasive fungal infection (IFI). We evaluated the utility of BDG surveillance as a guide for preemptive antifungal therapy in at-risk intensive care unit (ICU) patients. Methods: Patients admitted to the ICU for >= 3 days and expected to require at least 2 additional days of intensive care were enrolled. Subjects were randomized in 3:1 fashion to receive twice weekly BDG surveillance with preemptive anidulafungin in response to a positive test or empiric antifungal treatment based on physician preference. Results: Sixty-four subjects were enrolled, with 1 proven and 5 probable cases of IC identified over a 2.5 year period. BDG levels were higher in subjects with proven/probable IC as compared to those without an IFI (117 pg/ml vs. 28 pg/ml; p<0.001). Optimal assay performance required 2 sequential BDG determinations of >= 80 pg/ml to define a positive test (sensitivity 100%, specificity 75%, positive predictive value 30%, negative predictive value 100%). In all, 21 preemptive and 5 empiric subjects received systemic antifungal therapy. Receipt of preemptive antifungal treatment had a significant effect on BDG concentrations (p<0.001). Preemptive anidulafungin was safe and generally well tolerated with excellent outcome. Conclusions: BDG monitoring may be useful for identifying ICU patients at highest risk to develop an IFI as well as for monitoring treatment response. Preemptive strategies based on fungal biomarkers warrant further study.
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