López-Olivencia Marina, de Pablo Raúl, de Dios Noemí Paredes, García-Plaza Susana, Sáez-Noguero Sergio, de la Fuente Javier Sáez, Fortún Jesús, Cuesta María Cruz Soriano
Department of Intensive Care Medicine, Ramón y Cajal University Hospital, Madrid, Spain.
Department of Medicine and Medical Specialties, University of Alcalá, Madrid, Spain.
Infection. 2025 Mar 19. doi: 10.1007/s15010-025-02499-8.
To assess the incidence and clinical impact of CMV infection in critically ill COVID-19 patients, examining ICU and hospital mortality, and length of hospital stay.
In this single-center, prospective observational study (March 2020 - September 2022), 431 patients with COVID-19 pneumonia and moderate to severe ARDS were included. An active CMV surveillance protocol was implemented, analyzing CMV DNA in plasma and bronchoalveolar lavage (BAL). Clinical characteristics and outcomes were compared between CMV-COVID co-infected patients and those without CMV reactivation.
CMV-COVID co-infection was detected in 14.8% (64/431) of the cohort. Patients with CMV-COVID co-infection exhibited significantly higher ICU mortality (43.8% vs. 13.6%; p < 0.001) and hospital mortality (48.4% vs. 13.6%; p < 0.001) compared to patients without CMV. CMV infection was an independent predictor of hospital mortality (OR 4.91; 95% CI 2.76-8.75; p = 0.019). Earlier CMV reactivation was associated with an increased risk of hospital mortality (HR = 0.94; 95% CI: 0.90-0.98; p = 0.003). Additionally, CMV-COVID patients had a higher incidence of ICU-acquired infections and a prolonged hospital stay.
In critically ill patients with SARS-CoV-2 pneumonia, CMV infection was frequently observed, and associated with increased ICU and hospital mortality. CMV co-infection correlated with a higher incidence of ICU-acquired bacterial and fungal infections and prolonged hospital stays. This emphasizes the importance of early CMV monitoring upon ICU admission, as timely detection and intervention could potentially mitigate its impact on patient outcomes.
评估重症新型冠状病毒肺炎(COVID-19)患者中巨细胞病毒(CMV)感染的发生率及其临床影响,研究重症监护病房(ICU)死亡率、医院死亡率和住院时间。
在这项单中心前瞻性观察性研究(2020年3月至2022年9月)中,纳入了431例患有COVID-19肺炎且伴有中度至重度急性呼吸窘迫综合征(ARDS)的患者。实施了一项主动CMV监测方案,分析血浆和支气管肺泡灌洗(BAL)中的CMV DNA。比较了CMV-COVID合并感染患者与未发生CMV再激活患者的临床特征和结局。
该队列中14.8%(64/431)的患者检测到CMV-COVID合并感染。与未感染CMV的患者相比,CMV-COVID合并感染的患者表现出显著更高的ICU死亡率(43.8%对13.6%;p<0.001)和医院死亡率(48.4%对13.6%;p<0.001)。CMV感染是医院死亡率的独立预测因素(比值比4.91;95%置信区间2.76 - 8.75;p = 0.019)。更早的CMV再激活与医院死亡风险增加相关(风险比=0.94;95%置信区间:0.90 - 0.98;p = 0.003)。此外,CMV-COVID患者发生ICU获得性感染的发生率更高,住院时间更长。
在重症SARS-CoV-2肺炎患者中,经常观察到CMV感染,且与ICU死亡率和医院死亡率增加相关。CMV合并感染与ICU获得性细菌和真菌感染的发生率更高以及住院时间延长相关。这强调了在ICU入院时早期进行CMV监测的重要性,因为及时检测和干预可能会减轻其对患者结局的影响。