Prognosis of critically ill immunocompromised patients with virus-detected acute respiratory failure.

Immunocompromised Influenza Mechanical ventilation Pneumonia Respiratory virus

Journal

Annals of intensive care
ISSN: 2110-5820
Titre abrégé: Ann Intensive Care
Pays: Germany
ID NLM: 101562873

Informations de publication

Date de publication:
13 Oct 2023
Historique:
received: 07 07 2023
accepted: 26 09 2023
medline: 14 10 2023
pubmed: 14 10 2023
entrez: 13 10 2023
Statut: epublish

Résumé

Acute respiratory failure (ARF) is the leading cause of ICU admission. Viruses are increasingly recognized as a cause of pneumonia in immunocompromised patients, but epidemiologic data are scarce. We used the Groupe de Recherche en Réanimation Respiratoire en Onco-Hématologie's database (2003-2017, 72 intensive care units) to describe the spectrum of critically ill immunocompromised patients with virus-detected ARF and to report their outcomes. Then, patients with virus-detected ARF were matched based on clinical characteristics and severity (1:3 ratio) with patients with ARF from other origins. Of the 4038 immunocompromised patients in the whole cohort, 370 (9.2%) had a diagnosis of virus-detected ARF and were included in the study. Influenza was the most common virus (59%), followed by respiratory syncytial virus (14%), with significant seasonal variation. An associated bacterial infection was identified in 79 patients (21%) and an invasive pulmonary aspergillosis in 23 patients (6%). The crude in-hospital mortality rate was 37.8%. Factors associated with mortality were: neutropenia (OR = 1.74, 95% confidence interval, CI [1.05-2.89]), poor performance status (OR = 1.84, CI [1.12-3.03]), and the need for invasive mechanical ventilation on the day of admission (OR = 1.97, CI [1.14-3.40]). The type of virus was not associated with mortality. After matching, patients with virus-detected ARF had lower mortality (OR = 0.77, CI [0.60-0.98]) than patients with ARF from other causes. This result was mostly driven by influenza-like viruses, namely, respiratory syncytial virus, parainfluenza virus, and human metapneumovirus (OR = 0.54, CI [0.33-0.88]). In immunocompromised patients with virus-detected ARF, mortality is high, whatever the species, mainly influenced by clinical severity and poor general status. However, compared to non-viral ARF, in-hospital mortality was lower, especially for patients with detected viruses other than influenza.

Sections du résumé

BACKGROUND BACKGROUND
Acute respiratory failure (ARF) is the leading cause of ICU admission. Viruses are increasingly recognized as a cause of pneumonia in immunocompromised patients, but epidemiologic data are scarce. We used the Groupe de Recherche en Réanimation Respiratoire en Onco-Hématologie's database (2003-2017, 72 intensive care units) to describe the spectrum of critically ill immunocompromised patients with virus-detected ARF and to report their outcomes. Then, patients with virus-detected ARF were matched based on clinical characteristics and severity (1:3 ratio) with patients with ARF from other origins.
RESULTS RESULTS
Of the 4038 immunocompromised patients in the whole cohort, 370 (9.2%) had a diagnosis of virus-detected ARF and were included in the study. Influenza was the most common virus (59%), followed by respiratory syncytial virus (14%), with significant seasonal variation. An associated bacterial infection was identified in 79 patients (21%) and an invasive pulmonary aspergillosis in 23 patients (6%). The crude in-hospital mortality rate was 37.8%. Factors associated with mortality were: neutropenia (OR = 1.74, 95% confidence interval, CI [1.05-2.89]), poor performance status (OR = 1.84, CI [1.12-3.03]), and the need for invasive mechanical ventilation on the day of admission (OR = 1.97, CI [1.14-3.40]). The type of virus was not associated with mortality. After matching, patients with virus-detected ARF had lower mortality (OR = 0.77, CI [0.60-0.98]) than patients with ARF from other causes. This result was mostly driven by influenza-like viruses, namely, respiratory syncytial virus, parainfluenza virus, and human metapneumovirus (OR = 0.54, CI [0.33-0.88]).
CONCLUSIONS CONCLUSIONS
In immunocompromised patients with virus-detected ARF, mortality is high, whatever the species, mainly influenced by clinical severity and poor general status. However, compared to non-viral ARF, in-hospital mortality was lower, especially for patients with detected viruses other than influenza.

Identifiants

pubmed: 37833435
doi: 10.1186/s13613-023-01196-9
pii: 10.1186/s13613-023-01196-9
pmc: PMC10575827
doi:

Types de publication

Journal Article

Langues

eng

Pagination

101

Informations de copyright

© 2023. La Société de Réanimation de Langue Francaise = The French Society of Intensive Care (SRLF).

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Auteurs

Guillaume Dumas (G)

Service de Médecine Intensive-Réanimation, CHU Grenoble-Alpes; Université Grenoble-Alpes, INSERM U1300-HP2, Grenoble, France. dumas.guillaume1@gmail.com.

Maxime Bertrand (M)

Medical Intensive Care Unit, Saint-Louis Teaching Hospital, AP-HP, Paris, France.
ECSTRA Team, Biostatistics and Clinical Epidemiology, UMR 1153 (Center of Epidemiology and Biostatistics Sorbonne Paris Cité, CRESS), INSERM, Université de Paris, Paris, France.

Virginie Lemiale (V)

Medical Intensive Care Unit, Saint-Louis Teaching Hospital, AP-HP, Paris, France.
ECSTRA Team, Biostatistics and Clinical Epidemiology, UMR 1153 (Center of Epidemiology and Biostatistics Sorbonne Paris Cité, CRESS), INSERM, Université de Paris, Paris, France.

Emmanuel Canet (E)

Nantes Université, CHU Nantes, Médecine Intensive Réanimation, 44000, Nantes, France.

François Barbier (F)

Medical Intensive Care Unit, La Source Hospital, CHR Orleans, Orleans, France.

Achille Kouatchet (A)

Medical Intensive Care Unit, Angers Teaching Hospital, Angers, France.

Alexandre Demoule (A)

Service de Médecine Intensive et Réanimation (Département R3S), Sorbonne Université, INSERM, UMRS1158 Neurophysiologie Respiratoire Expérimentale et Clinique, and AP-HP, Groupe Hospitalier Universitaire APHP-Sorbonne Université, Site Pitié-Salpêtrière, 75013, Paris, France.

Kada Klouche (K)

Medical Intensive Care Unit, CHU de Montpellier, Montpellier, France.

Anne-Sophie Moreau (AS)

Service de Réanimation Polyvalente, CHRU de Lille - Hôpital Roger Salengro, Lille, France.

Laurent Argaud (L)

Medical Intensive Care Unit, Hospices Civils de Lyon, Hopital Edouard Herriot, Lyon, France.

Florent Wallet (F)

Intensive Care Unit, Lyon Sud Medical Center, Lyon, France.

Jean-Herlé Raphalen (JH)

Department of Anesthesia and Critical Care, Necker Hospital, Paris, France.

Djamel Mokart (D)

Intensive Care Unit, Institut Paoli Calmettes, Marseille, France.

Fabrice Bruneel (F)

Medical Intensive Care Unit, Andre Mignot Hospital, Versailles, France.

Frédéric Pène (F)

Medical Intensive Care Unit, Cochin Hospital, Hôpitaux Universitaires Paris Centre, AP-HP, Paris, France.
Institut Cochin, INSERM Unité 1016/Centre National de La Recherche Scientifique (CNRS) Unité Mixte de Recherche (UMR) 8104/Université de Paris, Paris, France.

Elie Azoulay (E)

Medical Intensive Care Unit, Saint-Louis Teaching Hospital, AP-HP, Paris, France.
ECSTRA Team, Biostatistics and Clinical Epidemiology, UMR 1153 (Center of Epidemiology and Biostatistics Sorbonne Paris Cité, CRESS), INSERM, Université de Paris, Paris, France.

Classifications MeSH