Trial design: Computer guided normal-low versus normal-high potassium control in critically ill patients: Rationale of the GRIP-COMPASS study

<p>Abstract</p> <p>Background</p> <p>Potassium depletion is common in hospitalized patients and can cause serious complications such as cardiac arrhythmias. In the intensive care unit (ICU) the majority of patients require potassium suppletion. However, there are no dat...

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Main Authors: van der Maaten Joost MAA, Lansink Annemieke, van der Horst Iwan CC, Vogelzang Mathijs, Hoekstra Miriam, Ismael Farouq, Zijlstra Felix, Nijsten Maarten WN
Format: Article
Language:English
Published: BMC 2010-12-01
Series:BMC Anesthesiology
Online Access:http://www.biomedcentral.com/1471-2253/10/23
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spelling doaj-f1ad3569f18c43d3bd93ebfef1e234c12020-11-25T01:21:40ZengBMCBMC Anesthesiology1471-22532010-12-011012310.1186/1471-2253-10-23Trial design: Computer guided normal-low versus normal-high potassium control in critically ill patients: Rationale of the GRIP-COMPASS studyvan der Maaten Joost MAALansink Annemiekevan der Horst Iwan CCVogelzang MathijsHoekstra MiriamIsmael FarouqZijlstra FelixNijsten Maarten WN<p>Abstract</p> <p>Background</p> <p>Potassium depletion is common in hospitalized patients and can cause serious complications such as cardiac arrhythmias. In the intensive care unit (ICU) the majority of patients require potassium suppletion. However, there are no data regarding the optimal control target in critically ill patients. After open-heart surgery, patients have a strongly increased risk of atrial fibrillation or atrial flutter (AFF). In a novel trial design, we examined if in these patients different potassium control-targets within the normal range may have different effects on the incidence of AFF.</p> <p>Methods/Design</p> <p>The "computer-driven Glucose and potassium Regulation program in Intensive care Patients with COMparison of PotASSium targets within normokalemic range (GRIP-COMPASS) trial" is a single-center prospective trial in which a total of 1200 patients are assigned to either a potassium control-target of 4.0 mmol/L or 4.5 mmol/L in consecutive alternating blocks of 50 patients each. Potassium levels are regulated by the computer-assisted potassium suppletion algorithm called GRIP-II (Glucose and potassium regulation for Intensive care Patients). Primary endpoint is the in-hospital incidence of AFF after cardiac surgery. Secondary endpoints are: in-hospital AFF in medical patients or patients after non-cardiac surgery, actually achieved potassium levels and their variation, electrolyte and glucose levels, potassium and insulin requirements, cumulative fluid balance, (ICU) length of stay, ICU mortality, hospital mortality and 90-day mortality.</p> <p>Discussion</p> <p>The GRIP-COMPASS trial is the first controlled clinical trial to date that compares potassium targets. Other novel methodological elements of the study are that it is performed in ICU patients where both targets are within the normal range and that a computer-assisted potassium suppletion algorithm is used.</p> <p>Trial registration</p> <p>NCT 01085071 at ClinicalTrials.gov</p> http://www.biomedcentral.com/1471-2253/10/23
collection DOAJ
language English
format Article
sources DOAJ
author van der Maaten Joost MAA
Lansink Annemieke
van der Horst Iwan CC
Vogelzang Mathijs
Hoekstra Miriam
Ismael Farouq
Zijlstra Felix
Nijsten Maarten WN
spellingShingle van der Maaten Joost MAA
Lansink Annemieke
van der Horst Iwan CC
Vogelzang Mathijs
Hoekstra Miriam
Ismael Farouq
Zijlstra Felix
Nijsten Maarten WN
Trial design: Computer guided normal-low versus normal-high potassium control in critically ill patients: Rationale of the GRIP-COMPASS study
BMC Anesthesiology
author_facet van der Maaten Joost MAA
Lansink Annemieke
van der Horst Iwan CC
Vogelzang Mathijs
Hoekstra Miriam
Ismael Farouq
Zijlstra Felix
Nijsten Maarten WN
author_sort van der Maaten Joost MAA
title Trial design: Computer guided normal-low versus normal-high potassium control in critically ill patients: Rationale of the GRIP-COMPASS study
title_short Trial design: Computer guided normal-low versus normal-high potassium control in critically ill patients: Rationale of the GRIP-COMPASS study
title_full Trial design: Computer guided normal-low versus normal-high potassium control in critically ill patients: Rationale of the GRIP-COMPASS study
title_fullStr Trial design: Computer guided normal-low versus normal-high potassium control in critically ill patients: Rationale of the GRIP-COMPASS study
title_full_unstemmed Trial design: Computer guided normal-low versus normal-high potassium control in critically ill patients: Rationale of the GRIP-COMPASS study
title_sort trial design: computer guided normal-low versus normal-high potassium control in critically ill patients: rationale of the grip-compass study
publisher BMC
series BMC Anesthesiology
issn 1471-2253
publishDate 2010-12-01
description <p>Abstract</p> <p>Background</p> <p>Potassium depletion is common in hospitalized patients and can cause serious complications such as cardiac arrhythmias. In the intensive care unit (ICU) the majority of patients require potassium suppletion. However, there are no data regarding the optimal control target in critically ill patients. After open-heart surgery, patients have a strongly increased risk of atrial fibrillation or atrial flutter (AFF). In a novel trial design, we examined if in these patients different potassium control-targets within the normal range may have different effects on the incidence of AFF.</p> <p>Methods/Design</p> <p>The "computer-driven Glucose and potassium Regulation program in Intensive care Patients with COMparison of PotASSium targets within normokalemic range (GRIP-COMPASS) trial" is a single-center prospective trial in which a total of 1200 patients are assigned to either a potassium control-target of 4.0 mmol/L or 4.5 mmol/L in consecutive alternating blocks of 50 patients each. Potassium levels are regulated by the computer-assisted potassium suppletion algorithm called GRIP-II (Glucose and potassium regulation for Intensive care Patients). Primary endpoint is the in-hospital incidence of AFF after cardiac surgery. Secondary endpoints are: in-hospital AFF in medical patients or patients after non-cardiac surgery, actually achieved potassium levels and their variation, electrolyte and glucose levels, potassium and insulin requirements, cumulative fluid balance, (ICU) length of stay, ICU mortality, hospital mortality and 90-day mortality.</p> <p>Discussion</p> <p>The GRIP-COMPASS trial is the first controlled clinical trial to date that compares potassium targets. Other novel methodological elements of the study are that it is performed in ICU patients where both targets are within the normal range and that a computer-assisted potassium suppletion algorithm is used.</p> <p>Trial registration</p> <p>NCT 01085071 at ClinicalTrials.gov</p>
url http://www.biomedcentral.com/1471-2253/10/23
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