GDH and toxin immunoassay for the diagnosis of Clostridioides (Clostridium) difficile infection is not a 'one size fit all' screening test

被引:6
作者
Ashraf, Zuhha [1 ]
Rahmati, Elham [2 ]
Bender, Jeffrey M. [3 ]
Nanda, Neha [2 ]
She, Rosemary C. [1 ]
机构
[1] Univ Southern Calif, Keck Sch Med, Dept Pathol, Los Angeles, CA 90033 USA
[2] Univ Southern Calif, Keck Sch Med, Div Infect Dis, Dept Med, Los Angeles, CA 90033 USA
[3] Univ Southern Calif, Keck Sch Med, Div Infect Dis, Dept Pediat, Los Angeles, CA 90033 USA
关键词
Glutamate dehydrogenase; Algorithm; EIA; PCR; Immunocompromised; REAL-TIME PCR; ENZYME-IMMUNOASSAY; C; DIFFICILE; ASSAY; STRAIN; IMPACT; RISK;
D O I
10.1016/j.diagmicrobio.2018.12.010
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Diagnosing Clostridioides (Clostridium) difficile infection is challenged by lack of a clear gold standard. We sought to determine if the two-step algorithm (screening GDH and toxin lateral flow assay followed by tcdB PCR) would have adequate clinical performance at a tertiary care center. Of 486 patients, 310 (63.8%) were immunocompromised. Of 150 PCR-positive specimens, 52 (34.7%) were toxin-positive and 126 (84.0%) were GDH positive. Positive GDH or toxin results corresponded to lower PCR cycle threshold values (P < 0.01). PCR-positive patients had more frequently documented antibiotic usage (78.4% vs 66.9%, P = 0.05) and diarrhea (91.0% vs. 79.4%, P < 0.01) and less frequent alternate etiologies of diarrhea (27.3% vs. 41.1%, P = 0.004) or laxative use (24.6% vs 36.1%, P = 0.02). Toxin positivity was associated with antibiotic use (P < 0.01), but not with neutropenia, diarrhea, malignancy, or chemotherapy (P> 0.05). The application of the 2-step algorithm should be thoroughly evaluated in immunocompromised patient populations before implementation. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:109 / 112
页数:4
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