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Association between continuous hyperosmolar therapy and survival in patients with traumatic brain injury – a multicentre prospective cohort study and systematic review

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  • معلومة اضافية
    • Contributors:
      Service d'anesthésie et réanimation chirurgicale Nantes; Hôtel-Dieu-Centre Hospitalier Universitaire de Nantes = Nantes University Hospital (CHU Nantes); Centre Hospitalier Universitaire de Nantes = Nantes University Hospital (CHU Nantes); Centre Hospitalier Universitaire d'Angers (CHU Angers); PRES Université Nantes Angers Le Mans (UNAM); Centre Hospitalier Universitaire de Rennes CHU Rennes = Rennes University Hospital Pontchaillou; Centre Hospitalier Universitaire de Toulouse (CHU Toulouse); Département d'Anesthésie-Réanimation Gui de Chauliac - CHU Montpellier; Centre Hospitalier Régional Universitaire Montpellier (CHRU Montpellier)-Hôpital Gui de Chauliac CHU Montpellier; Centre Hospitalier Régional Universitaire Montpellier (CHRU Montpellier); Centre hospitalier universitaire de Poitiers = Poitiers University Hospital (CHU de Poitiers La Milétrie ); Pharmacologie des anti-infectieux (PHAR Poitiers ); Université de Poitiers = University of Poitiers (UP)-Institut National de la Santé et de la Recherche Médicale (INSERM); Hôpital Beaujon; Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Université Paris Diderot - Paris 7 (UPD7)-Hôpital Beaujon AP-HP; Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP); Hôpital Henri Mondor; Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Henri Mondor-Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12); Service de réanimation médicale CHU HEGP; Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Européen Georges Pompidou APHP (HEGP); Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpitaux Universitaires Paris Ouest - Hôpitaux Universitaires Île de France Ouest (HUPO)-Hôpitaux Universitaires Paris Ouest - Hôpitaux Universitaires Île de France Ouest (HUPO); Equipe 2 : ECSTRA - Epidémiologie Clinique, STatistique, pour la Recherche en Santé (CRESS - U1153); Université Paris Diderot - Paris 7 (UPD7)-Centre de Recherche Épidémiologie et Statistique Sorbonne Paris Cité (CRESS (U1153 / UMR_A_1125 / UMR_S_1153)); Institut National de la Recherche Agronomique (INRA)-Université Paris Diderot - Paris 7 (UPD7)-Université Paris Descartes - Paris 5 (UPD5)-Université Sorbonne Paris Cité (USPC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut National de la Recherche Agronomique (INRA)-Université Paris Diderot - Paris 7 (UPD7)-Université Paris Descartes - Paris 5 (UPD5)-Université Sorbonne Paris Cité (USPC)-Institut National de la Santé et de la Recherche Médicale (INSERM); MethodS in Patients-centered outcomes and HEalth ResEarch (SPHERE); Université de Tours (UT)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Nantes - UFR des Sciences Pharmaceutiques et Biologiques; Université de Nantes (UN)-Université de Nantes (UN); Caractéristiques féminines des dysfonctions des interfaces cardio-vasculaires (EA 2992); Université Montpellier 1 (UM1)-Université de Montpellier (UM); Centre Hospitalier Universitaire de Nîmes (CHU Nîmes)
    • بيانات النشر:
      CCSD
      BioMed Central
    • الموضوع:
      2017
    • Collection:
      Université François-Rabelais de Tours: HAL
    • نبذة مختصرة :
      International audience ; Background : Intracranial hypertension (ICH) is a major cause of death after traumatic brain injury (TBI). Continuoushyperosmolar therapy (CHT) has been proposed for the treatment of ICH, but its effectiveness is controversial. Wecompared the mortality and outcomes in patients with TBI with ICH treated or not with CHT.Methods:We included patients with TBI (Glasgow Coma Scale≤12 and trauma-associated lesion on braincomputed tomography (CT) scan) from the databases of the prospective multicentre trials Corti-TC, BI-VILI andATLANREA. CHT consisted of an intravenous infusion of NaCl 20% for 24 hours or more. The primary outcome wasthe risk of survival at day 90, adjusted for predefined covariates and baseline differences, allowing us to reduce thebias resulting from confounding factors in observational studies. A systematic review was conducted includingstudies published from 1966 to December 2016. Results : Among the 1086 included patients, 545 (51.7%) developed ICH (143 treated and 402 not treated withCHT). In patients with ICH, the relative risk of survival at day 90 with CHT was 1.43 (95% CI, 0.99–2.06,p= 0.05). Theadjusted hazard ratio for survival was 1.74 (95% CI, 1.36–2.23,p< 0.001) in propensity-score-adjusted analysis. At day90, favourable outcomes (Glasgow Outcome Scale 4–5) occurred in 45.2% of treated patients with ICH and in 35.8%of patients with ICH not treated with CHT (p= 0.06). A review of the literature including 1304 patients from eightstudies suggests that CHT is associated with a reduction of in-ICU mortality (intervention, 112/474 deaths (23.6%) vs.control, 244/781 deaths (31.2%); OR 1.42 (95% CI, 1.04–1.95),p= 0.03,I2= 15%). Conclusions : CHT for the treatment of posttraumatic ICH was associated with improved adjusted 90-day survival.This result was strengthened by a review of the literature.
    • Relation:
      info:eu-repo/semantics/altIdentifier/pmid/29282104; PUBMED: 29282104; PUBMEDCENTRAL: PMC5745762
    • الرقم المعرف:
      10.1186/s13054-017-1918-4
    • الدخول الالكتروني :
      https://hal.umontpellier.fr/hal-01800039
      https://hal.umontpellier.fr/hal-01800039v1/document
      https://hal.umontpellier.fr/hal-01800039v1/file/s13054-017-1918-4.pdf
      https://doi.org/10.1186/s13054-017-1918-4
    • Rights:
      http://creativecommons.org/licenses/by/ ; info:eu-repo/semantics/OpenAccess
    • الرقم المعرف:
      edsbas.59E3E17F