Evidence map›Paper›PMID 39014504›Full record

Observational studyCritical care (London, England)2024

Clinical characteristics and outcomes of immunocompromised critically ill patients with cytomegalovirus end-organ disease: a multicenter retrospective cohort study.

Sara Fernández, Ignacio Grafia, Olivier Peyrony, Emmanuel Canet, Clara Vigneron, Clément Monet, Nahéma Issa, Maxens Decavele, Anne-Sophie Moreau, Alexandre Lautrette and 14 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Critical care (London, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors.

Sara FernándezMedical Intensive Care Unit, Hospital Clínic of Barcelona, Barcelona, Spain. sfernanm@clinic.cat.
Ignacio GrafiaMedical Intensive Care Unit, Hospital Clínic of Barcelona, Barcelona, Spain.
Olivier PeyronyEmergency Department, Hôpital Saint-Louis, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
Emmanuel CanetService de Médecine Intensive Réanimation, CHU de Nantes, Université de Nantes, Nantes, France.
Clara VigneronMédecine Intensive et Réanimation, Hôpital Cochin, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
Clément MonetAnesthesia and Critical Care Department, St-Eloi Hospital, University of Montpellier, PhyMedExp, INSERM U1046, CNRS, Montpellier, France.
Nahéma IssaMedical Intensive Care Unit, Hôpital Saint André, CHU Bordeaux, Bordeaux, France.
Maxens DecaveleMedical Intensive Care Unit (Department R3S), Pitié-Salpêtrière University Hospital, Sorbonne University Hospitals, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
Anne-Sophie MoreauMedical Intensive Care Unit, CHU Lille, Lille, France.
Alexandre LautretteMedical Intensive Care Unit, Jean Perrin Oncology Institut and Montpied Teaching Hospital, Clermont-Ferrand, France.
Guillaume LacaveMedical-Surgical Intensive Care Unit, Versailles Hospital Center, Le Chesnay, France.
Guillaume MorelHematology Department, Institut Paoli-Calmettes, Marseille, France.
Cyril CadozRéanimation Polyvalente, CHR Metz-Thionville Hôpital de Mercy, Metz, France.
Laurent ArgaudMedical Intensive Care Unit, Hôpital Edouard Herriot, Hospices Civils de Lyon, Lyon, France.
Liran StatlenderGeneral Intensive Care Unit, Beilinson Hospital, Rabin Medical Center, Petah Tikva, Israel.
Karam AzemSchool of Medicine, Tel Aviv University, Tel Aviv, Israel.
Jean-Pierre QuenotDeparment of Intensive Care, Burgundy University Hospital, Dijon, France.
Olivier LesieurIntensive Care Unit, La Rochelle General Hospital, La Rochelle, France.
Javier FernándezLiver Intensive Care Unit, Hospital Clinic of Barcelona, Barcelona, Spain.
Marta FarreroHeart Failure Unit, Hospital Clinic of Barcelona, Barcelona, Spain.
Mª Ángeles MarcosMicrobiology Department, Hospital Clinic of Barcelona, University of Barcelona, Barcelona, Spain.
Virgine LemialeMedical Intensive Care Unit, Hôpital Saint-Louis, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
Pedro CastroMedical Intensive Care Unit, Hospital Clínic of Barcelona, Barcelona, Spain.
Élie AzoulayMedical Intensive Care Unit, Hôpital Saint-Louis, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCytomegalovirus (CMV) infection in patients with cellular immune deficiencies is associated with significant morbidity and mortality. However, data on CMV end-organ disease (CMV-EOD) in critically ill, immunocompromised patients are scarce. Our objective here was to describe the clinical characteristics and outcomes of CMV-EOD in this population.

methodsWe conducted a multicenter, international, retrospective, observational study in adults who had CMV-EOD and were admitted to any of 18 intensive care units (ICUs) in France, Israel, and Spain in January 2010-December 2021. Patients with AIDS were excluded. We collected the clinical characteristics and outcomes of each patient. Survivors and non-survivors were compared, and multivariate analysis was performed to identify risk factors for hospital mortality.

resultsWe studied 185 patients, including 80 (43.2%) with hematologic malignancies, 55 (29.7%) with solid organ transplantation, 31 (16.8%) on immunosuppressants, 16 (8.6%) with solid malignancies, and 3 (1.6%) with primary immunodeficiencies. The most common CMV-EOD was pneumonia (n = 115, [62.2%] including 55 [47.8%] with a respiratory co-pathogen), followed by CMV gastrointestinal disease (n = 64 [34.6%]). More than one organ was involved in 16 (8.8%) patients. Histopathological evidence was obtained for 10/115 (8.7%) patients with pneumonia and 43/64 (67.2%) with GI disease. Other opportunistic infections were diagnosed in 69 (37.3%) patients. Hospital mortality was 61.4% overall and was significantly higher in the group with hematologic malignancies (75% vs. 51%, P = 0.001). Factors independently associated with higher hospital mortality were hematologic malignancy with active graft-versus-host disease (OR 5.02; 95% CI 1.15-27.30), CMV pneumonia (OR 2.57; 95% CI 1.13-6.03), lymphocytes < 0.30 × 10

conclusionsMortality was high in critically ill, immunocompromised patients with CMV-EOD and varied considerably with the cause of immunodeficiency and organ involved by CMV. Three of the four independent risk factors identified here are also known to be associated with higher mortality in the absence of CMV-EOD. CMV pneumonia was rarely proven by histopathology and was the most severe CMV-EOD.

Indexed as

Critical IllnessCytomegalovirus InfectionsImmunocompromised HostAdultAgedCohort StudiesCytomegalovirusFemaleFranceHospital MortalityHumansIntensive Care UnitsIsraelMaleMiddle AgedRetrospective StudiesCytomegalovirusHematologic malignancyImmunocompromised hostIntensive careTransplantation

Identifiers

PMID39014504
PMCPMC11251242

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.