Smith Clarissa B, Shi Xiaosong, Liesman Rachael M, Thomas Laura A, Bahr Nathan C, Brownback Kyle R
Department of Internal Medicine, University of Kansas Medical Center, Kansas City, Kansas, USA.
Division of Pulmonary, Critical Care and Sleep Medicine, Department of Internal Medicine, The University of Kansas Medical Center, Kansas City, Kansas, USA.
Open Forum Infect Dis. 2022 Dec 6;9(12):ofac646. doi: 10.1093/ofid/ofac646. eCollection 2022 Dec.
Pulmonary infections due to , Mucorales, and have high morbidity and mortality, in part due to diagnostic challenges. Commercially available molecular assays on bronchoalveolar lavage fluid (BALF) may have increased sensitivity over currently available diagnostic options. Our aim was to characterize the diagnostic performance of assays for each of these pathogens in our patient population.
The medical records of patients whose BALF was tested by polymerase chain reaction (PCR) for , Mucorales, and between 2019 and 2021 were reviewed in a cross-sectional manner. European Organization for Research and Treatment of Cancer and the Mycoses Study Group (EORTC/MSG) definitions of "proven," "probable," and "possible" infection were used, including histopathology, serology, and culture. We used (1) "proven" or "probable" infection by EORTC criteria, (2) improvement or stabilization on targeted antimicrobial therapy, and (3) absence of a more likely diagnosis as the reference standard.
The PCR assay demonstrated the highest agreement with the diagnostic reference standard, with 31.25% (10/32) sensitivity and 97.17% (206/212) specificity. Positive and negative predictive values were 62.50% (10/16) and 90.35% (206/228), respectively. No Mucorales or infections were identified by the diagnostic reference standard, so the sensitivity could not be calculated. The specificity of Mucorales and targets was 98.35% and 96.69%, respectively.
Our data demonstrated relatively poor clinical sensitivity for all 3 constituent PCR assays in our patient population, suggesting a limited role for this test in the diagnosis of , Mucorales, or .
由毛霉目真菌和其他病原体引起的肺部感染具有较高的发病率和死亡率,部分原因是诊断存在挑战。支气管肺泡灌洗液(BALF)上的商业分子检测可能比目前可用的诊断方法具有更高的灵敏度。我们的目的是在我们的患者群体中表征针对每种这些病原体的检测的诊断性能。
对2019年至2021年间其BALF通过聚合酶链反应(PCR)检测毛霉目真菌和其他病原体的患者的病历进行横断面回顾。采用欧洲癌症研究与治疗组织和真菌病研究组(EORTC/MSG)对“确诊”、“很可能”和“可能”感染的定义,包括组织病理学、血清学和培养。我们使用(1)根据EORTC标准“确诊”或“很可能”感染,(2)靶向抗微生物治疗后病情改善或稳定,以及(3)不存在更可能的诊断作为参考标准。
该PCR检测与诊断参考标准的一致性最高,灵敏度为31.25%(10/32),特异性为97.17%(206/212)。阳性和阴性预测值分别为62.50%(10/16)和90.35%(206/228)。诊断参考标准未识别出毛霉目真菌或其他病原体感染,因此无法计算灵敏度。毛霉目真菌和其他病原体靶点的特异性分别为98.35%和96.69%。
我们的数据表明,在我们的患者群体中,所有3种组成PCR检测的临床灵敏度相对较差,表明该检测在诊断毛霉目真菌、其他病原体感染方面作用有限。