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The Effect of a Liberal Approach to Glucose Control in Critically Ill Patients with Type 2 Diabetes: A Multicenter, Parallel-Group, Open-Label Randomized Clinical Trial.
Poole, Alexis P; Finnis, Mark E; Anstey, James; Bellomo, Rinaldo; Bihari, Shailesh; Biradar, Vishwanath; Doherty, Sarah; Eastwood, Glenn; Finfer, Simon; French, Craig J; Heller, Simon; Horowitz, Michael; Kar, Palash; Kruger, Peter S; Maiden, Matthew J; Mårtensson, Johan; McArthur, Colin J; McGuinness, Shay P; Secombe, Paul J; Tobin, Antony E; Udy, Andrew A; Young, Paul J; Deane, Adam M.
Afiliação
  • Poole AP; Discipline of Acute Care Medicine and.
  • Finnis ME; Intensive Care Unit and.
  • Anstey J; Australian and New Zealand Intensive Care Research Centre, School of Public Health and Preventive Medicine, Monash University, Prahran, Victoria, Australia.
  • Bellomo R; Discipline of Acute Care Medicine and.
  • Bihari S; Intensive Care Unit and.
  • Biradar V; Australian and New Zealand Intensive Care Research Centre, School of Public Health and Preventive Medicine, Monash University, Prahran, Victoria, Australia.
  • Doherty S; Department of Critical Care, Melbourne Medical School, The University of Melbourne, Parkville, Victoria, Australia.
  • Eastwood G; Department of Critical Care, Melbourne Medical School, The University of Melbourne, Parkville, Victoria, Australia.
  • Finfer S; Department of Intensive Care, Royal Melbourne Hospital, Parkville, Victoria, Australia.
  • French CJ; Australian and New Zealand Intensive Care Research Centre, School of Public Health and Preventive Medicine, Monash University, Prahran, Victoria, Australia.
  • Heller S; Department of Critical Care, Melbourne Medical School, The University of Melbourne, Parkville, Victoria, Australia.
  • Horowitz M; Department of Intensive Care, Austin Hospital, Heidelberg, Victoria, Australia.
  • Kar P; Department of Intensive and Critical Care Unit, Flinders Medical Centre, Bedford Park, South Australia, Australia.
  • Kruger PS; Department of Intensive Care, Lyell McEwin Hospital, Elizabeth Vale, South Australia, Australia.
  • Maiden MJ; Department of Intensive Care, Royal Melbourne Hospital, Parkville, Victoria, Australia.
  • Mårtensson J; Australian and New Zealand Intensive Care Research Centre, School of Public Health and Preventive Medicine, Monash University, Prahran, Victoria, Australia.
  • McArthur CJ; Department of Critical Care, Melbourne Medical School, The University of Melbourne, Parkville, Victoria, Australia.
  • McGuinness SP; Department of Intensive Care, Austin Hospital, Heidelberg, Victoria, Australia.
  • Secombe PJ; The George Institute for Global Health, University of New South Wales, Sydney, New South Wales, Australia.
  • Tobin AE; Department of Critical Care, Melbourne Medical School, The University of Melbourne, Parkville, Victoria, Australia.
  • Udy AA; Department of Intensive Care, Western Health, Footscray, Victoria, Australia.
  • Young PJ; Clinical Diabetes, Endocrinology, and Metabolism, University of Sheffield, Sheffield, United Kingdom.
  • Deane AM; Centre for Research Excellence in Translating Nutrition Science to Good Health, University of Adelaide, Adelaide, South Australia, Australia.
Am J Respir Crit Care Med ; 206(7): 874-882, 2022 10 01.
Article em En | MEDLINE | ID: mdl-35608484
ABSTRACT
Rationale Blood glucose concentrations affect outcomes in critically ill patients, but the optimal target blood glucose range in those with type 2 diabetes is unknown.

Objectives:

To evaluate the effects of a "liberal" approach to targeted blood glucose range during ICU admission.

Methods:

This mutlicenter, parallel-group, open-label randomized clinical trial included 419 adult patients with type 2 diabetes expected to be in the ICU on at least three consecutive days. In the intervention group intravenous insulin was commenced at a blood glucose >252 mg/dl and titrated to a target range of 180-252 mg/dl. In the comparator group insulin was commenced at a blood glucose >180 mg/dl and titrated to a target range of 108-180 mg/dl. The primary outcome was incident hypoglycemia (<72 mg/dl). Secondary outcomes included glucose metrics and clinical outcomes. Measurements and Main

Results:

By Day 28, at least one episode of hypoglycemia occurred in 10 of 210 (5%) patients assigned the intervention and 38 of 209 (18%) patients assigned the comparator (incident rate ratio, 0.21 [95% confidence interval (CI), 0.09 to 0.49]; P < 0.001). Those assigned the intervention had greater blood glucose concentrations (daily mean, minimum, maximum), less glucose variability, and less relative hypoglycemia (P < 0.001 for all comparisons). By Day 90, 62 of 210 (29.5%) in the intervention and 52 of 209 (24.9%) in the comparator group had died (absolute difference, 4.6 percentage points [95% CI, -3.9% to 13.2%]; P = 0.29).

Conclusions:

A liberal approach to blood glucose targets reduced incident hypoglycemia but did not improve patient-centered outcomes. Clinical trial registered with Australian New Zealand Clinical Trials Registry (ACTRN 12616001135404).
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 2 / Hipoglicemia Tipo de estudo: Clinical_trials Limite: Adult / Humans País/Região como assunto: Oceania Idioma: En Revista: Am J Respir Crit Care Med Assunto da revista: TERAPIA INTENSIVA Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 2 / Hipoglicemia Tipo de estudo: Clinical_trials Limite: Adult / Humans País/Região como assunto: Oceania Idioma: En Revista: Am J Respir Crit Care Med Assunto da revista: TERAPIA INTENSIVA Ano de publicação: 2022 Tipo de documento: Article