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Design and rationale of Heart and Lung Failure – Pediatric INsulin Titration Trial (HALF-PINT): A randomized clinical trial of tight glycemic control in hyperglycemic critically ill children()

OBJECTIVES: Test whether hyperglycemic critically ill children with cardiovascular and/or respiratory failure experience more ICU-free days when assigned to tight glycemic control with a normoglycemic versus hyperglycemic blood glucose target range. DESIGN: Multi-center randomized clinical trial. SE...

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Autores principales: Agus, Michael SD, Hirshberg, Ellie, Srinivasan, Vijay, Faustino, Edward Vincent, Luckett, Peter M, Curley, Martha AQ, Alexander, Jamin, Asaro, Lisa A, Coughlin-Wells, Kerry, Duva, Donna, French, Jaclyn, Hasbani, Natalie, Sisko, Martha T, Soto-Rivera, Carmen L, Steil, Garry, Wypij, David, Nadkarni, Vinay M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5285511/
https://www.ncbi.nlm.nih.gov/pubmed/28042054
http://dx.doi.org/10.1016/j.cct.2016.12.023
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author Agus, Michael SD
Hirshberg, Ellie
Srinivasan, Vijay
Faustino, Edward Vincent
Luckett, Peter M
Curley, Martha AQ
Alexander, Jamin
Asaro, Lisa A
Coughlin-Wells, Kerry
Duva, Donna
French, Jaclyn
Hasbani, Natalie
Sisko, Martha T
Soto-Rivera, Carmen L
Steil, Garry
Wypij, David
Nadkarni, Vinay M
author_facet Agus, Michael SD
Hirshberg, Ellie
Srinivasan, Vijay
Faustino, Edward Vincent
Luckett, Peter M
Curley, Martha AQ
Alexander, Jamin
Asaro, Lisa A
Coughlin-Wells, Kerry
Duva, Donna
French, Jaclyn
Hasbani, Natalie
Sisko, Martha T
Soto-Rivera, Carmen L
Steil, Garry
Wypij, David
Nadkarni, Vinay M
author_sort Agus, Michael SD
collection PubMed
description OBJECTIVES: Test whether hyperglycemic critically ill children with cardiovascular and/or respiratory failure experience more ICU-free days when assigned to tight glycemic control with a normoglycemic versus hyperglycemic blood glucose target range. DESIGN: Multi-center randomized clinical trial. SETTING: Pediatric ICUs at 35 academic hospitals. PATIENTS: Children aged 2 weeks to 17 years receiving inotropic support and/or acute mechanical ventilation, excluding cardiac surgical patients. INTERVENTIONS: Patients receive intravenous insulin titrated to either 80–110 mg/dL (4.4–6.1 mmol/L) or 150–180 mg/dL (8.3–10.0 mmol/L). The intervention begins upon confirmed hyperglycemia and ends when the patient meets study-defined ICU discharge criteria or after 28 days. Continuous glucose monitoring, a minimum glucose infusion, and an explicit insulin infusion algorithm are deployed to achieve the BG targets while minimizing hypoglycemia risk. MEASUREMENTS AND MAIN RESULTS: The primary outcome is ICU-free days (equivalent to 28-day hospital mortality-adjusted ICU length of stay). Secondary outcomes include 90-day hospital mortality, organ dysfunction scores, ventilator-free days, nosocomial infection rate, neurodevelopmental outcomes, and nursing workload. To detect an increase of 1.25 ICU-free days (corresponding to a 20% relative reduction in 28-day hospital mortality and a one-day reduction in ICU length of stay), 1414 patients are needed for 80% power using a two-sided 0.05 level test. CONCLUSIONS: This trial tests whether hyperglycemic critically ill children randomized to 80–110 mg/dL benefit more than those randomized to 150–180 mg/dL. This study implements validated bedside support tools including continuous glucose monitoring and a computerized algorithm to enhance patient safety and ensure reproducible bedside decision-making in achieving glycemic control.
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spelling pubmed-52855112018-02-01 Design and rationale of Heart and Lung Failure – Pediatric INsulin Titration Trial (HALF-PINT): A randomized clinical trial of tight glycemic control in hyperglycemic critically ill children() Agus, Michael SD Hirshberg, Ellie Srinivasan, Vijay Faustino, Edward Vincent Luckett, Peter M Curley, Martha AQ Alexander, Jamin Asaro, Lisa A Coughlin-Wells, Kerry Duva, Donna French, Jaclyn Hasbani, Natalie Sisko, Martha T Soto-Rivera, Carmen L Steil, Garry Wypij, David Nadkarni, Vinay M Contemp Clin Trials Article OBJECTIVES: Test whether hyperglycemic critically ill children with cardiovascular and/or respiratory failure experience more ICU-free days when assigned to tight glycemic control with a normoglycemic versus hyperglycemic blood glucose target range. DESIGN: Multi-center randomized clinical trial. SETTING: Pediatric ICUs at 35 academic hospitals. PATIENTS: Children aged 2 weeks to 17 years receiving inotropic support and/or acute mechanical ventilation, excluding cardiac surgical patients. INTERVENTIONS: Patients receive intravenous insulin titrated to either 80–110 mg/dL (4.4–6.1 mmol/L) or 150–180 mg/dL (8.3–10.0 mmol/L). The intervention begins upon confirmed hyperglycemia and ends when the patient meets study-defined ICU discharge criteria or after 28 days. Continuous glucose monitoring, a minimum glucose infusion, and an explicit insulin infusion algorithm are deployed to achieve the BG targets while minimizing hypoglycemia risk. MEASUREMENTS AND MAIN RESULTS: The primary outcome is ICU-free days (equivalent to 28-day hospital mortality-adjusted ICU length of stay). Secondary outcomes include 90-day hospital mortality, organ dysfunction scores, ventilator-free days, nosocomial infection rate, neurodevelopmental outcomes, and nursing workload. To detect an increase of 1.25 ICU-free days (corresponding to a 20% relative reduction in 28-day hospital mortality and a one-day reduction in ICU length of stay), 1414 patients are needed for 80% power using a two-sided 0.05 level test. CONCLUSIONS: This trial tests whether hyperglycemic critically ill children randomized to 80–110 mg/dL benefit more than those randomized to 150–180 mg/dL. This study implements validated bedside support tools including continuous glucose monitoring and a computerized algorithm to enhance patient safety and ensure reproducible bedside decision-making in achieving glycemic control. 2016-12-30 2017-02 /pmc/articles/PMC5285511/ /pubmed/28042054 http://dx.doi.org/10.1016/j.cct.2016.12.023 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Agus, Michael SD
Hirshberg, Ellie
Srinivasan, Vijay
Faustino, Edward Vincent
Luckett, Peter M
Curley, Martha AQ
Alexander, Jamin
Asaro, Lisa A
Coughlin-Wells, Kerry
Duva, Donna
French, Jaclyn
Hasbani, Natalie
Sisko, Martha T
Soto-Rivera, Carmen L
Steil, Garry
Wypij, David
Nadkarni, Vinay M
Design and rationale of Heart and Lung Failure – Pediatric INsulin Titration Trial (HALF-PINT): A randomized clinical trial of tight glycemic control in hyperglycemic critically ill children()
title Design and rationale of Heart and Lung Failure – Pediatric INsulin Titration Trial (HALF-PINT): A randomized clinical trial of tight glycemic control in hyperglycemic critically ill children()
title_full Design and rationale of Heart and Lung Failure – Pediatric INsulin Titration Trial (HALF-PINT): A randomized clinical trial of tight glycemic control in hyperglycemic critically ill children()
title_fullStr Design and rationale of Heart and Lung Failure – Pediatric INsulin Titration Trial (HALF-PINT): A randomized clinical trial of tight glycemic control in hyperglycemic critically ill children()
title_full_unstemmed Design and rationale of Heart and Lung Failure – Pediatric INsulin Titration Trial (HALF-PINT): A randomized clinical trial of tight glycemic control in hyperglycemic critically ill children()
title_short Design and rationale of Heart and Lung Failure – Pediatric INsulin Titration Trial (HALF-PINT): A randomized clinical trial of tight glycemic control in hyperglycemic critically ill children()
title_sort design and rationale of heart and lung failure – pediatric insulin titration trial (half-pint): a randomized clinical trial of tight glycemic control in hyperglycemic critically ill children()
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5285511/
https://www.ncbi.nlm.nih.gov/pubmed/28042054
http://dx.doi.org/10.1016/j.cct.2016.12.023
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