Department of Respiratory and Critical Care Medicine, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Department of Scientific Affairs, Vision Medicals for Infection Diseases, Guangzhou, China.
BMJ Open Respir Res. 2023 Feb;10(1). doi: 10.1136/bmjresp-2022-001358.
Invasive pulmonary aspergillosis (IPA) remains underestimated in patients with community-acquired pneumonia (CAP). This study aims to describe clinical features and outcomes of IPA in CAP patients, assess diagnostic performance of metagenomic next-generation sequencing (mNGS) for IPA and analyse lung microbiome via mNGS data.
This retrospective cohort study included CAP patients from 22 April 2019 to 30 September 2021. Clinical and microbiological data were analysed. Diagnostic performance of mNGS was compared with traditional detection methods. The lung microbiome detected by mNGS was characterised and its association with clinical features was evaluated.
IPA was diagnosed in 26 (23.4%) of 111 CAP patients. Patients with IPA displayed depressed immunity, higher hospital mortality (30.8% vs 11.8%) and intensive care unit mortality (42.1% vs 17.5%) compared with patients without IPA. The galactomannan (GM) antigen test had the highest sensitivity (57.7%) in detecting the spp, followed by mNGS (42.3%), culture (30.8%) and smear (7.7%). The mNGS, culture and smear had 100% specificity, while GM test had 92.9% specificity. The microbial structure of IPA significantly differed from non-IPA patients (p<0.001; Wilcoxon test). Nineteen different species were significantly correlated with clinical outcomes and laboratory biomarkers, particularly for , and .
Our results reveal that patients with infection tend to have a higher early mortality rate. The mNGS may be suggested as a complement to routine microbiological test in diagnosis of patients at risk of infection. The lung microbiota is associated with inflammatory, immune and metabolic conditions of IPA, and thus influences clinical outcomes.
社区获得性肺炎(CAP)患者中侵袭性肺曲霉病(IPA)仍然被低估。本研究旨在描述 CAP 患者 IPA 的临床特征和结局,评估宏基因组下一代测序(mNGS)对 IPA 的诊断性能,并通过 mNGS 数据分析肺部微生物组。
这是一项回顾性队列研究,纳入了 2019 年 4 月 22 日至 2021 年 9 月 30 日期间的 CAP 患者。分析了临床和微生物学数据。比较了 mNGS 与传统检测方法的诊断性能。通过 mNGS 对肺部微生物组进行了特征描述,并评估了其与临床特征的相关性。
在 111 例 CAP 患者中,诊断出 IPA 26 例(23.4%)。与无 IPA 患者相比,IPA 患者的免疫功能抑制更为明显,住院死亡率(30.8%比 11.8%)和重症监护病房死亡率(42.1%比 17.5%)更高。半乳甘露聚糖(GM)抗原检测对 spp 的检测灵敏度最高(57.7%),其次是 mNGS(42.3%)、培养(30.8%)和涂片(7.7%)。mNGS、培养和涂片的特异性均为 100%,而 GM 检测的特异性为 92.9%。IPA 患者的微生物结构与非 IPA 患者显著不同(p<0.001;Wilcoxon 检验)。19 种不同的物种与临床结局和实验室生物标志物显著相关,特别是 、 和 。
我们的结果表明,感染 的患者早期死亡率较高。mNGS 可能被建议作为常规微生物检测的补充,用于诊断有感染风险的患者。肺部微生物组与 IPA 的炎症、免疫和代谢状况相关,从而影响临床结局。