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COVID-19 危重症患者曲霉检测谱与死亡率。

Aspergillus Test Profiles and Mortality in Critically Ill COVID-19 Patients.

机构信息

Center of Expertise in Mycology Radboudumc/CWZ, Radboud University Medical Center, Nijmegen, The Netherlands.

Department of Medical Microbiology, Radboud University Medical Center, Nijmegen, The Netherlands.

出版信息

J Clin Microbiol. 2021 Nov 18;59(12):e0122921. doi: 10.1128/JCM.01229-21. Epub 2021 Sep 8.

Abstract

The literature regarding COVID-19-associated pulmonary aspergillosis (CAPA) has shown conflicting observations, including survival of CAPA patients not receiving antifungal therapy and discrepancy between CAPA diagnosis and autopsy findings. To gain insight into the pathophysiology of CAPA, we performed a case-control study in which we compared Aspergillus test profiles in CAPA patients and controls in relation to intensive care unit (ICU) mortality. This was a multinational case-control study in which Aspergillus test results, use of antifungal therapy, and mortality were collected from critically ill COVID-19 patients. Patients were classified using the 2020 European Confederation for Medical Mycology and the International Society for Human and Animal Mycology (ECMM/ISHAM) consensus case definitions. We analyzed 219 critically ill COVID-19 cases, including 1 proven, 38 probable, 19 possible CAPA cases, 21 Aspergillus-colonized patients, 7 patients only positive for serum (1,3)-β-d-glucan (BDG), and 133 cases with no evidence of CAPA. Mortality was 53.8% in CAPA patients compared to 24.1% in patients without CAPA ( = 0.001). Positive serum galactomannan (GM) and BDG were associated with increased mortality compared to serum biomarker-negative CAPA patients (87.5% versus 41.7%,  = 0.046; 90.0% versus 42.1%,  = 0.029, respectively). For each point increase in GM or 10-point BDG serum concentration, the odds of death increased (GM, odds ratio [OR] 10.208, 95% confidence interval [CI], 1.621 to 64.291,  = 0.013; BDG, OR, 1.247, 95% CI, 1.029 to 1.511,  = 0.024). CAPA is a complex disease, probably involving a continuum of respiratory colonization, tissue invasion, and angioinvasion. Serum biomarkers are useful for staging CAPA disease progression and, if positive, indicate angioinvasion and a high probability of mortality. There is need for a biomarker that distinguishes between respiratory tract colonization and tissue-invasive CAPA disease.

摘要

COVID-19 相关肺曲霉病 (CAPA) 的文献报道存在相互矛盾的观察结果,包括未接受抗真菌治疗的 CAPA 患者的生存率以及 CAPA 诊断与尸检结果之间的差异。为了深入了解 CAPA 的病理生理学,我们进行了一项病例对照研究,比较了 CAPA 患者和对照组在重症监护病房 (ICU) 死亡率方面的曲霉检测谱。这是一项多中心的病例对照研究,收集了来自重症 COVID-19 患者的曲霉检测结果、抗真菌治疗使用情况和死亡率。患者使用 2020 年欧洲医学真菌学联合会和国际人类与动物真菌学协会 (ECMM/ISHAM) 共识病例定义进行分类。我们分析了 219 例重症 COVID-19 病例,包括 1 例确诊、38 例可能、19 例可疑 CAPA 病例、21 例曲霉定植患者、7 例仅血清 (1,3)-β-D-葡聚糖 (BDG) 阳性患者和 133 例无 CAPA 证据的患者。与无 CAPA 的患者相比,CAPA 患者的死亡率为 53.8%(CAPA 患者死亡率为 53.8%,无 CAPA 患者死亡率为 24.1%)(=0.001)。与血清生物标志物阴性 CAPA 患者相比,血清 GM 和 BDG 阳性与死亡率增加相关(GM:87.5%比 41.7%,=0.046;BDG:90.0%比 42.1%,=0.029)。GM 或 10 点 BDG 血清浓度每增加 1 分,死亡的几率就会增加(GM:比值比[OR]10.208,95%置信区间[CI]1.621 至 64.291,=0.013;BDG:OR,1.247,95%CI,1.029 至 1.511,=0.024)。CAPA 是一种复杂的疾病,可能涉及呼吸道定植、组织侵袭和血管侵袭的连续过程。血清生物标志物可用于分期 CAPA 疾病进展,如果阳性,表明血管侵袭和高死亡率。目前需要一种能够区分呼吸道定植和组织侵袭性 CAPA 疾病的生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b9c/8601217/c8d71b82bbb0/jcm.01229-21-f001.jpg

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