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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...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2016
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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. |
format | Online Article Text |
id | pubmed-5285511 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
record_format | MEDLINE/PubMed |
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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