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Prognosis of critically ill immunocompromised patients with virus-detected acute respiratory failure.
Dumas, Guillaume; Bertrand, Maxime; Lemiale, Virginie; Canet, Emmanuel; Barbier, François; Kouatchet, Achille; Demoule, Alexandre; Klouche, Kada; Moreau, Anne-Sophie; Argaud, Laurent; Wallet, Florent; Raphalen, Jean-Herlé; Mokart, Djamel; Bruneel, Fabrice; Pène, Frédéric; Azoulay, Elie.
Afiliação
  • Dumas G; Service de Médecine Intensive-Réanimation, CHU Grenoble-Alpes; Université Grenoble-Alpes, INSERM U1300-HP2, Grenoble, France. dumas.guillaume1@gmail.com.
  • Bertrand M; Medical Intensive Care Unit, Saint-Louis Teaching Hospital, AP-HP, Paris, France.
  • Lemiale V; ECSTRA Team, Biostatistics and Clinical Epidemiology, UMR 1153 (Center of Epidemiology and Biostatistics Sorbonne Paris Cité, CRESS), INSERM, Université de Paris, Paris, France.
  • Canet E; Medical Intensive Care Unit, Saint-Louis Teaching Hospital, AP-HP, Paris, France.
  • Barbier F; ECSTRA Team, Biostatistics and Clinical Epidemiology, UMR 1153 (Center of Epidemiology and Biostatistics Sorbonne Paris Cité, CRESS), INSERM, Université de Paris, Paris, France.
  • Kouatchet A; Nantes Université, CHU Nantes, Médecine Intensive Réanimation, 44000, Nantes, France.
  • Demoule A; Medical Intensive Care Unit, La Source Hospital, CHR Orleans, Orleans, France.
  • Klouche K; Medical Intensive Care Unit, Angers Teaching Hospital, Angers, France.
  • Moreau AS; 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.
  • Argaud L; Medical Intensive Care Unit, CHU de Montpellier, Montpellier, France.
  • Wallet F; Service de Réanimation Polyvalente, CHRU de Lille - Hôpital Roger Salengro, Lille, France.
  • Raphalen JH; Medical Intensive Care Unit, Hospices Civils de Lyon, Hopital Edouard Herriot, Lyon, France.
  • Mokart D; Intensive Care Unit, Lyon Sud Medical Center, Lyon, France.
  • Bruneel F; Department of Anesthesia and Critical Care, Necker Hospital, Paris, France.
  • Pène F; Intensive Care Unit, Institut Paoli Calmettes, Marseille, France.
  • Azoulay E; Medical Intensive Care Unit, Andre Mignot Hospital, Versailles, France.
Ann Intensive Care ; 13(1): 101, 2023 Oct 13.
Article em En | MEDLINE | ID: mdl-37833435
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: 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: 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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Ann Intensive Care Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Ann Intensive Care Ano de publicação: 2023 Tipo de documento: Article