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剖检研究致死性侵袭性肺曲霉病:生前常漏诊。

Autopsy study of fatal invasive pulmonary aspergillosis: Often undiagnosed premortem.

机构信息

Division of Pulmonary, Critical Care, & Sleep Medicine, Mayo Clinic, Rochester, MN, USA.

Department of Radiology, Mayo Clinic, Rochester, MN, USA.

出版信息

Respir Med. 2022 Aug;199:106882. doi: 10.1016/j.rmed.2022.106882. Epub 2022 May 20.

Abstract

Invasive aspergillosis (IA) is a serious complication in immunocompromised and critically ill patients but is difficult to diagnose. We sought to examine how often cases go undiagnosed and to understand the presenting clinical and radiologic features associated with fatal IA. We reviewed cases of fatal IA confirmed at autopsy (N = 67) between 1999 and 2019 at a tertiary academic hospital. At autopsy, pulmonary involvement was present in 97% of cases--46% were limited to the lungs and 51% had concomitant extrapulmonary involvement. Immunosuppression with either glucocorticoids and/or other immunosuppressive agents was present in 85%. Among those not immunocompromised (15%), chronic lung disease was present in 70%, and a respiratory coinfection was found in 50%. Chest imaging abnormalities including consolidation, ground glass opacities, halo sign, cavitation, and air crescent sign were present in 49%, 49%, 37%, 22%, and 7% of cases, respectively. Diagnostic bronchoscopy was performed in 61% of cases and yielded aspergillus in 63% of those cases by either bronchoalveolar lavage (galactomannan and/or culture), bronchial washings, or transbronchial biopsy cultures. Either a respiratory coinfection or other systemic coinfection was diagnosed in 64%. The performance of diagnostic bronchoscopy was associated with accurate pre-mortem identification of IA (p = 0.001). Clinicians correctly identified IA as the cause of death in only 27% of fatal IA cases identified at autopsy. Complex presenting features, high rates of co-infections, and low rates of invasive diagnostic procedures may have led to missed diagnoses of IA.

摘要

侵袭性曲霉病(IA)是免疫功能低下和危重病患者的严重并发症,但难以诊断。我们旨在研究有多少病例未被诊断,并了解与致命性 IA 相关的临床表现和影像学特征。我们回顾了 1999 年至 2019 年在一家三级学术医院进行尸检证实的致命性 IA 病例(N=67)。尸检时,97%的病例存在肺部受累——46%的病例局限于肺部,51%的病例有肺外合并感染。85%的病例存在糖皮质激素和/或其他免疫抑制剂的免疫抑制。在无免疫抑制的病例(15%)中,70%存在慢性肺部疾病,50%存在呼吸道合并感染。胸部影像学异常包括实变、磨玻璃影、晕征、空洞和空气新月征,分别出现在 49%、49%、37%、22%和 7%的病例中。61%的病例进行了诊断性支气管镜检查,通过支气管肺泡灌洗(半乳甘露聚糖和/或培养)、支气管冲洗或经支气管镜活检培养,在 63%的病例中发现了曲霉菌。64%的病例诊断为呼吸道合并感染或其他全身合并感染。诊断性支气管镜检查的实施与生前准确识别 IA 有关(p=0.001)。临床医生仅在 27%的尸检确定的致命性 IA 病例中正确识别 IA 为死亡原因。复杂的临床表现、高合并感染率和低侵袭性诊断程序可能导致 IA 的漏诊。

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