Evidence map›Paper›PMID 41533748›Full record

Trial reportThe Journal of infectious diseases2026

Cytomegalovirus DNAemia in Hospitalized Adults With SARS-CoV-2 Infection Requiring Supplemental Oxygen: Virologic and Clinical Characteristics and Association With Outcomes.

Michael Boeckh, Hu Xie, Terry Stevens-Ayers, Linda Sircy, Danniel Zamora, Jason D Goldman, Christopher W Woods, Renee D Stapleton, Gordon Rubenfeld, Andre Kalil and 3 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in The Journal of infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Michael BoeckhVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.ORCID 0000-0003-1538-7984
Hu XieVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.ORCID 0000-0003-0556-6591
Terry Stevens-AyersVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.ORCID 0000-0002-7546-8439
Linda SircyVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.ORCID 0000-0003-3335-9258
Danniel ZamoraDepartment of Medicine, City of Hope Medical Center, Duarte, California, USA.ORCID 0000-0002-1318-2902
Jason D GoldmanDepartment of Medicine, University of Washington, Seattle, Washington, USA.ORCID 0000-0002-3825-6832
Christopher W WoodsDivision of Infectious Diseases, Center for Precision Health, Duke University, Durham, North Carolina, USA.
Renee D StapletonDepartment of Medicine, University of Vermont, Burlington, Vermont, USA.
Gordon RubenfeldDepartment of Medicine, University of Toronto, Toronto, Ontario, Canada.
Andre KalilDivision of Infectious Diseases, University of Nebraska, Lincoln, Nebraska, USA.ORCID 0000-0002-6489-6294
Keith R JeromeVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.ORCID 0000-0002-8212-3789
Sayan DasguptaVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.ORCID 0000-0001-5271-7247
Ajit P LimayeInfectious Disease Division, University of California San Francisco, San Francisco, California, USA.ORCID 0000-0002-5350-9025

Funding

Merck Investigator Study
6 · The paper itself

Abstract

backgroundCytomegalovirus (CMV) reactivation occurs in the context of coronavirus disease 2019 (COVID-19); however, the viral kinetics, risk factors, and clinical outcomes are poorly defined.

methodsWe examined the association of CMV DNAemia with clinical outcomes among participants of a randomized trial of remdesivir with or without baricitinib (National Institute of Allergy and Infectious Diseases [NIAID], Adaptive COVID-19 Treatment Trial 2 [ACTT-2]). Plasma CMV DNAemia from CMV-seropositive participants with COVID-19 (NIAID ordinal scale [OS] 5, 6, or 7 at entry) were assessed longitudinally by quantitative polymerase chain reaction. Factors associated with CMV DNAemia, and clinical outcomes were analyzed by Cox regression and proportional odds models.

resultsOf 772 trial participants with available samples, 643 (83%) were CMV seropositive. Baseline CMV serostatus was not associated with COVID-19 outcomes. The cumulative incidence of CMV DNAemia among seropositive persons by day 28 was overall 11% (baseline OS 5, 6.3%; OS 6, 16.4%; OS 7, 24.7%), and was associated with older age, baseline OS, male sex, lymphopenia, and systemic corticosteroid use, while remdesivir and baricitinib did not affect risk. CMV DNAemia was associated with a lower probability of improvement by day 29 (adjusted hazard ratio, 0.3 [95% confidence interval, .17-.56]), with a more pronounced delay of recovery with higher CMV viral load. CMV DNAemia was also associated with higher severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) viral load and death.

conclusionsIn hospitalized adults with COVID-19 requiring oxygen, CMV viremia occurs within well-defined clinical risks and is independently associated with delayed recovery from illness, higher SARS-CoV-2 viral load, and increased mortality.

Indexed as

COVID-19COVID-19 Drug TreatmentCytomegalovirusCytomegalovirus InfectionsDNA, ViralOxygen Inhalation TherapyAdenosine MonophosphateAdultAgedAlanineAntiviral AgentsAzetidinesFemaleHospitalizationHumansMaleAdenosine MonophosphateAlanineAntiviral AgentsAzetidinesbaricitinibDNA, ViralPurinesPyrazolesremdesivirSulfonamidescytomegalovirusrecoverySARS-CoV-2viral sheddingviremia

Identifiers

PMID41533748
PMCPMC13175614

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.