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A Patient-Level Meta-Analysis of Intensive Glucose Control in Critically Ill Adults.
Adigbli, Derick; Li, Yang; Hammond, Naomi; Chatoor, Richard; Devaux, Anthony G; Li, Qiang; Billot, Laurent; Annane, Djillali; Arabi, Yaseen; Bilotta, Federico; Bohé, Julien; Brunkhorst, Frank Martin; Cavalcanti, Alexandre Biasi; Cook, Deborah; Engel, Christoph; Green-LaRoche, Deborah; He, Wei; Henderson, William; Hoedemaekers, Cornelia; Iapichino, Gaetano; Kalfon, Pierre; de La Rosa, Gisela; Lahooti, Afsaneh; Mackenzie, Iain; Mahendran, Sajeev; Mélot, Christian; Mitchell, Imogen; Oksanen, Tuomas; Polli, Federico; Preiser, Jean-Charles; Garcia Soriano, Francisco; Vlok, Ruan; Wang, Lingcong; Xu, Yuan; Delaney, Anthony P; Di Tanna, Gian Luca; Finfer, Simon.
Affiliation
  • Adigbli D; Critical Care Division, The George Institute for Global Health, Sydney.
  • Li Y; Department of Critical Care, Melbourne Medical School, University of Melbourne, Melbourne, VIC, Australia.
  • Hammond N; Medical School, Faculty of Medical Sciences, University College London, London.
  • Chatoor R; Department of Intensive Care, Austin Health, Melbourne, VIC, Australia.
  • Devaux AG; Critical Care Division, The George Institute for Global Health, Sydney.
  • Li Q; Critical Care Division, The George Institute for Global Health, Sydney.
  • Billot L; Royal North Shore Hospital, Malcolm Fisher Department of Intensive Care, St Leonards, NSW, Australia.
  • Annane D; Royal North Shore Hospital, Malcolm Fisher Department of Intensive Care, St Leonards, NSW, Australia.
  • Arabi Y; The George Institute for Global Health, Biostatistics and Data Science Division, Barangaroo, NSW, Australia.
  • Bilotta F; The George Institute for Global Health, Biostatistics and Data Science Division, Barangaroo, NSW, Australia.
  • Bohé J; The George Institute for Global Health, Biostatistics and Data Science Division, Barangaroo, NSW, Australia.
  • Brunkhorst FM; Department of Intensive Care, Hôpital Raymond-Poincare, Garches, France.
  • Cavalcanti AB; PROMETHEUS IHU, Université Paris-Saclay, Garches, France.
  • Cook D; Laboratory of Infection & Inflammation, School of Medicine Simone Veil Santé, Université Paris-Saclay, Montigny Le Bretonneux, France.
  • Engel C; FHU SEPSIS (Saclay and Paris Seine Nord Endeavour to PerSonalize Interventions for Sepsis), Garches, France.
  • Green-LaRoche D; Intensive Care Medicine, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
  • He W; Department of Anesthesiology and Intensive Care Medicine, University of Rome La Sapienza, Rome.
  • Henderson W; Service d'Anesthésie-Réanimation-Médecine Intensive, Hospices Civils de Lyon, Groupement Hospitalier Sud, Lyon, France.
  • Hoedemaekers C; Department of Anaesthesiology and Intensive Care Medicine, Jena University Hospital, Jena, Germany.
  • Iapichino G; HCor Research Institute, São Paulo, Brazil.
  • Kalfon P; Departments of Medicine, Clinical Epidemiology & Biostatistics (Division of Critical Care), McMaster University, Hamilton, ON, Canada.
  • de La Rosa G; Institute for Medical Informatics, Statistics and Epidemiology, Leipzig University, Leipzig, Germany.
  • Lahooti A; Department of Neurology, Tufts University School of Medicine, Boston.
  • Mackenzie I; Department of Critical Care Medicine, Beijing Tongren Hospital, Capital Medical University, Beijing.
  • Mahendran S; Faculty of Medicine, The University of British Columbia, Vancouver, BC, Canada.
  • Mélot C; Department of Intensive Care Medicine, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Mitchell I; Anestesiologia e Rianimazione, Università degli Studi di Milano, Milan.
  • Oksanen T; La Casamance Private Hospital, Aubagne, France.
  • Polli F; Hospital Pablo Tobon Uribe, Medellín, Colombia.
  • Preiser JC; Critical Care Division, The George Institute for Global Health, Sydney.
  • Garcia Soriano F; School of Science, Western Sydney University, Campbelltown, NSW, Australia.
  • Vlok R; InterSystems Corporation, Cambridge, MA.
  • Wang L; The George Institute for Global Health, Biostatistics and Data Science Division, Barangaroo, NSW, Australia.
  • Xu Y; Faculty of Medicine and Health, Northern Clinical School, The University of Sydney, St Leonards, NSW, Australia.
  • Delaney AP; Faculté de Médecine, Université Libre de Bruxelles, Brussels.
  • Di Tanna GL; Office of Research and Education, Canberra Health Services Library, Canberra, ACT, Australia.
  • Finfer S; School of Medicine and Psychology, Australian National University, Canberra, ACT, Australia.
NEJM Evid ; 3(8): EVIDoa2400082, 2024 Aug.
Article in En | MEDLINE | ID: mdl-38864749
ABSTRACT

BACKGROUND:

Whether intensive glucose control reduces mortality in critically ill patients remains uncertain. Patient-level meta-analyses can provide more precise estimates of treatment effects than are currently available.

METHODS:

We pooled individual patient data from randomized trials investigating intensive glucose control in critically ill adults. The primary outcome was in-hospital mortality. Secondary outcomes included survival to 90 days and time to live cessation of treatment with vasopressors or inotropes, mechanical ventilation, and newly commenced renal replacement. Severe hypoglycemia was a safety outcome.

RESULTS:

Of 38 eligible trials (n=29,537 participants), 20 (n=14,171 participants) provided individual patient data including in-hospital mortality status for 7059 and 7049 participants allocated to intensive and conventional glucose control, respectively. Of these 1930 (27.3%) and 1891 (26.8%) individuals assigned to intensive and conventional control, respectively, died (risk ratio, 1.02; 95% confidence interval [CI], 0.96 to 1.07; P=0.52; moderate certainty). There was no apparent heterogeneity of treatment effect on in-hospital mortality in any examined subgroups. Intensive glucose control increased the risk of severe hypoglycemia (risk ratio, 3.38; 95% CI, 2.99 to 3.83; P<0.0001).

CONCLUSIONS:

Intensive glucose control was not associated with reduced mortality risk but increased the risk of severe hypoglycemia. We did not identify a subgroup of patients in whom intensive glucose control was beneficial. (Funded by the Australian National Health and Medical Research Council and others; PROSPERO number CRD42021278869.).
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hospital Mortality / Critical Illness / Hypoglycemia Limits: Adult / Humans Language: En Journal: NEJM Evid Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hospital Mortality / Critical Illness / Hypoglycemia Limits: Adult / Humans Language: En Journal: NEJM Evid Year: 2024 Document type: Article