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]
日期:2019-03-25
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI