Division of Infectious Diseases, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland; Division of Mycology, Department of Microbiology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Division of Infectious Diseases, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
J Heart Lung Transplant. 2023 Jul;42(7):953-963. doi: 10.1016/j.healun.2023.02.005. Epub 2023 Feb 19.
Respiratory viral infections (RVI) are associated with chronic lung allograft dysfunction (CLAD) and mortality in lung transplant recipients (LTRs). However, the prevalence and impact of secondary invasive fungal infections (IFIs) post RVIs in LTRs have not been investigated.
We performed a single center retrospective study including LTRs diagnosed with 5 different respiratory viral pathogens between January 2010 to May 2021 and evaluated their clinical outcomes in 1 year. The risk factors of IFIs were evaluated by logistic regression. The impact of IFIs on CLAD stage progression/death was examined by Cox regression.
A total of 202 RVI episodes (50 influenza, 31 severe acute respiratory syndrome coronavirus-2, 30 metapneumovirus, 44 parainfluenza, and 47 respiratory syncytial virus) in 132 patients was included for analysis. Thirty-one episodes (15%) were associated with secondary IFIs, and 27 occurred in LTRs with lower respiratory tract infection (LRTI; 28% from 96 LRTI episodes). Aspergillosis was the most common IFI (80%). LTRs with IFIs had higher disease severity during RVI episodes. In multivariable analysis, RVI with LTRI was associated with IFI (adjusted odds ratio [95% confidence interval (CI)] of 7.85 (2.48-24.9). Secondary IFIs were associated with CLAD stage progression/death after accounting for LRTI, pre-existing CLAD, intensive care unit admission, secondary bacterial pneumonia and underlying lung diseases pre-transplant with adjusted hazard ratio (95%CI) of 2.45 (1.29-4.64).
This cohort demonstrated 15% secondary IFI prevalence in LTRs with RVIs. Importantly, secondary IFIs were associated with CLAD stage progression/death, underscoring the importance of screening for fungal infections in this setting.
呼吸道病毒感染(RVI)与肺移植受者(LTR)的慢性肺移植物功能障碍(CLAD)和死亡率相关。然而,LTR 继发侵袭性真菌感染(IFI)的患病率和影响尚未得到研究。
我们进行了一项单中心回顾性研究,纳入了 2010 年 1 月至 2021 年 5 月期间诊断为 5 种不同呼吸道病毒病原体的 LTR,并在 1 年内评估了他们的临床结局。通过逻辑回归评估 IFI 的危险因素。通过 Cox 回归检验 IFI 对 CLAD 阶段进展/死亡的影响。
共纳入 132 例患者的 202 例 RVI 发作(50 例流感、31 例严重急性呼吸综合征冠状病毒 2 型、30 例副流感病毒、44 例副流感病毒和 47 例呼吸道合胞病毒)进行分析。31 例(15%)与继发 IFI 相关,27 例发生于下呼吸道感染(LRTI;96 例 LRTI 发作中有 28%)的 LTR 中。曲霉菌病是最常见的 IFI(80%)。IFI 组 RVI 发作时疾病严重程度更高。多变量分析显示,RVI 合并 LRTI 与 IFI 相关(调整后比值比 [95%置信区间(CI)]为 7.85(2.48-24.9)。在考虑到 LRTI、预先存在的 CLAD、重症监护病房入院、继发细菌性肺炎和移植前基础肺部疾病后,继发性 IFI 与 CLAD 阶段进展/死亡相关,调整后的危险比(95%CI)为 2.45(1.29-4.64)。
本队列显示 LTR 中 RVI 继发 IFI 的患病率为 15%。重要的是,继发 IFI 与 CLAD 阶段进展/死亡相关,这凸显了在这种情况下筛查真菌感染的重要性。