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Crit Care. 2025;29(1):177.

Cytomegalovirus reactivation in the lower respiratory tract as an independent risk factor for mortality in critically Ill patients.

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제1저자 김중엽, 이찬미 · 교신저자 강창경, 이진우

소속 (7)
  1. Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Seoul National University Hospital, Seoul, Republic of Korea.
  2. Department of Internal Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Republic of Korea.
  3. Department of Microbiology, Harvard Medical School, Boston, MA, USA.
  4. Department of Critical Care Medicine, Seoul National University Hospital, Seoul, Republic of Korea.
  5. Department of Internal Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Republic of Korea. voyager0@snu.ac.kr.
  6. Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Seoul National University Hospital, Seoul, Republic of Korea. realrain7@snu.ac.kr.
  7. Department of Internal Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Republic of Korea. realrain7@snu.ac.kr.

Abstract

BACKGROUND The clinical significance of cytomegalovirus reactivation in the lower respiratory tract (LRT) of critically ill patients remains unclear. We aimed to investigate the association between cytomegalovirus reactivation detected in LRT and intensive care unit (ICU) prognosis.

METHODS This study included critically ill patients admitted to a medical ICU at a tertiary referral center in South Korea between January 2021 and June 2023. Cytomegalovirus load in LRT samples collected via bronchoscopy was measured within 7 days of admission. Detection of cytomegalovirus DNA in LRT was defined as reactivation. Associations between cytomegalovirus reactivation and ICU, in-hospital, 30-day, and 90-day mortality were assessed using multivariable Fine-Gray model adjusted for major clinical factors.

RESULTS Of the 322 patients (median age 68 years, 66.8% male), 145 (45%) had cytomegalovirus reactivation in the LRT. Cytomegalovirus reactivation was independently associated with increased ICU (adjusted subdistribution hazard ratio [aSHR], 2.28; 95% confidence interval [CI], 1.46-3.56), in-hospital (aSHR, 2.00; 95% CI, 1.44-2.78), 30-day (aSHR, 2.11; 95% CI, 1.42-3.13), and 90-day mortality (aSHR, 2.05; 95% CI, 1.45-2.88). Anti-cytomegalovirus therapy was significantly associated with reduced ICU mortality in patients with radiologic findings suggestive of cytomegalovirus pneumonia (P for interaction = 0.001), but was linked to increased mortality in patients with positive bacterial cultures (P for interaction = 0.002).

CONCLUSION Cytomegalovirus reactivation in the LRT is associated with poor outcomes in critically ill patients. Anti-cytomegalovirus therapy was not associated with overall survival outcomes; however, the subgroup with radiologic findings of cytomegalovirus pneumonia suggested benefits, while the subgroup with bacterial co-infections suggested harmful effects. Randomized controlled trials are needed.

© 2025. The Author(s).

Keywords

CMVICULower respiratory tractPrognosisReactivation

Figures

Fig. 1
Fig. 1 Flow diagram. LRT, lower respiratory tract; CMV, cytomegalovirus; ICU, intensive care unit
Fig. 2
Fig. 2 Cumulative incidence of ICU mortality by LRT CMV positivity. LRT, lower respiratory tract; CMV, cytomegalovirus; ICU, intensive care unit. Cumulative incidence function plot for ICU mortality, stratified by LRT CMV positivity. The plot depicts ICU mortality trends over time, with CMV-positive cases represented in red and CMV-negative cases in blue. Statistical significance of the differences between groups was assessed using Gray’s test
Fig. 3
Fig. 3 Forest plot illustrating the subdistribution hazard ratios of anti-CMV therapy on ICU mortality across various subgroups. LRT, lower respiratory tract; CI, confidence interval; CMV, cytomegalovirus; SHR, subdistribution hazard ratio; ICU, intensive care unit. Each subgroup displays the count and number of antiviral users, along with SHRs and 95% CI. Lines to the left favor anti-CMV therapy, while those to the right disfavor it. Larger squares indicate greater weight in the analysis. The P for interaction assess whether the effect of anti-CMV therapy varies significantly across subgroups

그림 출처: PubMed Central 공개 논문 (PMC12048981)

Comment · 정정

Conflict of interest statement

Declarations. Competing interests: The authors declare no competing interests.

그 밖의 정보
출판 형태
Journal Article
저널
Critical care (London, England) · eISSN 1466-609X
전자 출판
2025-05-02
MeSH
Humans · Male · Female · Aged · Critical Illness / mortality · Republic of Korea / epidemiology · Cytomegalovirus* / pathogenicity · Middle Aged · Risk Factors · Intensive Care Units / organization & administration / statistics & numerical data · Cytomegalovirus Infections* / mortality · Virus Activation* / physiology · Mortality / trends
연구비
National Research Foundation of Korea 2021M3A9I2080498
참고문헌
32편