Combination of sepsis biomarkers may indicate an invasive fungal infection in haematological patients

降钙素原 中性粒细胞减少症 内科学 败血症 医学 发热性中性粒细胞减少症 生物标志物 菌血症 免疫学 队列 化疗 抗生素 生物 微生物学 生物化学
作者
Igor Stoma,Igor Karpov,Anatoly Uss,Svetlana Krivenko,Igor Iskrov,Natalia Milanovich,Svetlana Vlasenkova,Irina Lendina,Kristina Belyavskaya,Veronika Cherniak
出处
期刊:Biomarkers [Taylor & Francis]
卷期号:24 (4): 401-406 被引量:22
标识
DOI:10.1080/1354750x.2019.1600023
摘要

Background: Invasive fungal infections are a major threat to a large cohort of immunocompromised patients, including patients with chemotherapy-associated neutropenia. Early differential diagnosis with bacterial infections is often complicated, which leads to a delay in empirical antifungal therapy and increases risk for adverse outcome. Accessibility and performance of specific fungal antigen and PCR-tests are still limited, while sepsis biomarkers are more broadly used in most settings currently.Methods: Haematological patients hospitalized to receive chemotherapy with proven or probable invasive fungal infection or microbiologically proven bacterial bloodstream infection were included in the study. C-reactive protein was assessed daily during the profound neutropenia period, while procalcitonin or presepsin were measured during the first 48 hours after the onset of febrile episode.Results: There were totally 64 patients included in the study, 53 with bacterial bloodstream infections and 11 with invasive fungal infections. Combination of CRP >120 with PCT <1.25 or presepsin <170 was shown to be a possible combined biomarker for invasive fungal infections in immunocompromised patients, with areas under the ROC-curves: 0.962 (95% CI 0.868 to 0.995) for PCT-based combination and 0.907 (95% CI 0.692 to 0.990) for presepsin-based combination.
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