Liu Fengqi, Zhuang Yiqi, Huang Xiaohan, Papazian Laurent, Cai Hongliu, Shao Huanzhang, Chen Qiong, Xie Chao, Tang Kankai, Li KangChen, Wang Mingqiang, Xu Yinghe, Shen Peng, Wang Qianqian, He Xuwei, Wang Nan, Wang Hongyu, Dai Muhua, Xiong Yonghui, Zhong Lin, Pan Yujie, Chu Lihong, Yang Bin, Zhang Gensheng, Zhou Hua, Xu Jinfu, Jiang Chao, Huang Lingtong
Department of Critical Care Medicine, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Department of Critical Care Medicine, The First Peoples Hospital of Huzhou, First Affiliated Hospital of Huzhou University, Huzhou, China.
Crit Care. 2025 Jun 20;29(1):254. doi: 10.1186/s13054-025-05496-3.
Herpesviruses are widely distributed in the lower respiratory tract, yet no study has comprehensively characterized their clinical features and prognostic impact in severe pneumonia.
In this multicenter, retrospective study, we included severe pneumonia patients who underwent bronchoalveolar lavage fluid (BALF) metagenomic testing in intensive care units across 17 medical centers from January 2019 to June 2023. Based on metagenomic results, patients were categorized into herpesvirus-negative, HSV-1, EBV, CMV, HHV-6B, and HHV-7 groups. Propensity score matching and multivariable Cox regression were used to compare mortality between herpesvirus-positive and -negative patients. Interaction analyses were conducted to assess the impact of co-detection of different herpesviruses. Besides, main findings were validated using data from a prospective multicenter cohort.
Among 1,737 enrolled patients, the 28-day mortality rate was 41.3% (718/1,737). Herpesviruses were detected in 828 patients. Detection frequencies were: HSV-1 (26.8%), CMV (17.8%), EBV (16.6%), HHV-7 (5.3%), HHV-6B (2.2%), and VZV (0.5%). Clinical characteristics varied across herpesvirus groups. No single herpesvirus was independently associated with increased mortality compared to the negative group. However, co-detection of HSV-1 and CMV was significantly associated with higher 28-day mortality (vs. both negative: adj-HR = 1.439, 95% CI: 1.093-1.894, P = 0.009). This finding was validated in a prospective cohort (adj-HR = 1.656, 95% CI: 1.061-2.585, P = 0.026).
Herpesviruses are frequently detected in the lower respiratory tract of patients with severe pneumonia, with distinct clinical features across virus types. Co-detection of HSV-1 and CMV was associated with increased 28-day mortality.
疱疹病毒在下呼吸道广泛分布,但尚无研究全面描述其在重症肺炎中的临床特征和预后影响。
在这项多中心回顾性研究中,我们纳入了2019年1月至2023年6月期间在17个医疗中心的重症监护病房接受支气管肺泡灌洗术(BALF)宏基因组检测的重症肺炎患者。根据宏基因组结果,将患者分为疱疹病毒阴性、HSV-1、EBV、CMV、HHV-6B和HHV-7组。采用倾向评分匹配和多变量Cox回归比较疱疹病毒阳性和阴性患者的死亡率。进行交互分析以评估不同疱疹病毒共同检测的影响。此外,使用来自前瞻性多中心队列的数据验证主要发现。
在1737名入组患者中,28天死亡率为41.3%(718/1737)。828名患者检测到疱疹病毒。检测频率分别为:HSV-1(26.8%)、CMV(17.8%)、EBV(16.6%)、HHV-7(5.3%)、HHV-6B(2.2%)和VZV(0.5%)。不同疱疹病毒组的临床特征各不相同。与阴性组相比,没有单一疱疹病毒与死亡率增加独立相关。然而,HSV-1和CMV共同检测与28天死亡率显著升高相关(与两者均为阴性相比:校正风险比=1.439,95%置信区间:1.093-1.894,P=0.009)。这一发现在前瞻性队列中得到验证(校正风险比=1.656,95%置信区间:1.061-2.585,P=0.026)。
疱疹病毒在重症肺炎患者的下呼吸道中经常被检测到,不同病毒类型具有不同的临床特征。HSV-1和CMV共同检测与28天死亡率增加相关。