Glucose-insulin-potassium improves left ventricular performances after aortic valve replacement: a secondary analysis of a randomized controlled trial

Abstract Background Patients with left ventricular (LV) hypertrophy may suffer ischemia-reperfusion injuries at the time of cardiac surgery with impairment in left ventricular function. Using transesophageal echocardiography (TEE), we evaluated the impact of glucose-insulin potassium (GIK) on LV per...

Full description

Bibliographic Details
Main Authors: Marc Licker, John Diaper, Tornike Sologashvili, Christoph Ellenberger
Format: Article
Language:English
Published: BMC 2019-09-01
Series:BMC Anesthesiology
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12871-019-0845-0
id doaj-5b2b5d28580a44a38ed6ff8894a43801
record_format Article
spelling doaj-5b2b5d28580a44a38ed6ff8894a438012020-11-25T03:45:19ZengBMCBMC Anesthesiology1471-22532019-09-0119111110.1186/s12871-019-0845-0Glucose-insulin-potassium improves left ventricular performances after aortic valve replacement: a secondary analysis of a randomized controlled trialMarc Licker0John Diaper1Tornike Sologashvili2Christoph Ellenberger3Department of Anesthesiology, Pharmacology and Intensive Care, University Hospital of GenevaDepartment of Anesthesiology, Pharmacology and Intensive Care, University Hospital of GenevaDivision of Cardiovascular Surgery, University Hospital of GenevaDepartment of Anesthesiology, Pharmacology and Intensive Care, University Hospital of GenevaAbstract Background Patients with left ventricular (LV) hypertrophy may suffer ischemia-reperfusion injuries at the time of cardiac surgery with impairment in left ventricular function. Using transesophageal echocardiography (TEE), we evaluated the impact of glucose-insulin potassium (GIK) on LV performances in patients undergoing valve replacement for aortic stenosis. Methods In this secondary analysis of a double-blind randomized trial, moderate-to-high risk patients were assigned to receive GIK (20 IU insulin with 10 mEq KCL in 50 ml glucose 40%) or saline over 60 min upon anesthetic induction. The primary outcomes were the early changes in 2-and 3-dimensional left ventricular ejection fraction (2D and 3D-LVEF), peak global longitudinal strain (PGLS) and transmitral flow propagation velocity (Vp). Results At the end of GIK infusion, LV-FAC and 2D- and 3D-LVEF were unchanged whereas Vp (mean difference [MD + 7.9%, 95% confidence interval [CI] 3.2 to 12.5%; P <  0.001) increased compared with baseline values. After Placebo infusion, there was a decrease in LV-FAC (MD -2.9%, 95%CI − 4.8 to − 1.0%), 2D-LVEF (MD -2.0%, 95%CI − 2.8 to − 1.3%, 3D-LVEF (MD -3.0%, 95%CI − 4.0 to − 2.0%) and Vp (MD − 4.5 cm/s, 95%CI − 5.6 to − 3.3 cm/s). After cardiopulmonary bypass, GIK pretreatment was associated with preserved 2D and 3D-LVEF (+ 0.4%, 95% 95%CI − 0.8 to 1.7% and + 0.4%, 95%CI − 1.3 to 2.0%), and PGLS (− 0.9, 95%CI − 1.6 to − 0.2) as well as higher Vp (+ 5.1 cm/s, 95%CI 2.9 to 7.3), compared with baseline. In contrast, in the Placebo group, 2D-LVEF (− 2.2%, 95%CI − 3.4 to − 1.0), 3D-LVEF (− 6.0%, 95%CI − 7.8 to − 4.2), and Vp (− 7.6 cm/s, 95%CI − 9.4 to − 5.9), all decreased after bypass. Conclusions Administration of GIK before aortic cross-clamping resulted in better preservation of systolic and diastolic ventricular function in patients with LV hypertrophy undergoing aortic valve replacement. Trial registration ClinicalTrials.gov: NCT00788242 , registered on November 10, 2008.http://link.springer.com/article/10.1186/s12871-019-0845-0Aortic valve stenosisEchocardiographyMyocardial protection
collection DOAJ
language English
format Article
sources DOAJ
author Marc Licker
John Diaper
Tornike Sologashvili
Christoph Ellenberger
spellingShingle Marc Licker
John Diaper
Tornike Sologashvili
Christoph Ellenberger
Glucose-insulin-potassium improves left ventricular performances after aortic valve replacement: a secondary analysis of a randomized controlled trial
BMC Anesthesiology
Aortic valve stenosis
Echocardiography
Myocardial protection
author_facet Marc Licker
John Diaper
Tornike Sologashvili
Christoph Ellenberger
author_sort Marc Licker
title Glucose-insulin-potassium improves left ventricular performances after aortic valve replacement: a secondary analysis of a randomized controlled trial
title_short Glucose-insulin-potassium improves left ventricular performances after aortic valve replacement: a secondary analysis of a randomized controlled trial
title_full Glucose-insulin-potassium improves left ventricular performances after aortic valve replacement: a secondary analysis of a randomized controlled trial
title_fullStr Glucose-insulin-potassium improves left ventricular performances after aortic valve replacement: a secondary analysis of a randomized controlled trial
title_full_unstemmed Glucose-insulin-potassium improves left ventricular performances after aortic valve replacement: a secondary analysis of a randomized controlled trial
title_sort glucose-insulin-potassium improves left ventricular performances after aortic valve replacement: a secondary analysis of a randomized controlled trial
publisher BMC
series BMC Anesthesiology
issn 1471-2253
publishDate 2019-09-01
description Abstract Background Patients with left ventricular (LV) hypertrophy may suffer ischemia-reperfusion injuries at the time of cardiac surgery with impairment in left ventricular function. Using transesophageal echocardiography (TEE), we evaluated the impact of glucose-insulin potassium (GIK) on LV performances in patients undergoing valve replacement for aortic stenosis. Methods In this secondary analysis of a double-blind randomized trial, moderate-to-high risk patients were assigned to receive GIK (20 IU insulin with 10 mEq KCL in 50 ml glucose 40%) or saline over 60 min upon anesthetic induction. The primary outcomes were the early changes in 2-and 3-dimensional left ventricular ejection fraction (2D and 3D-LVEF), peak global longitudinal strain (PGLS) and transmitral flow propagation velocity (Vp). Results At the end of GIK infusion, LV-FAC and 2D- and 3D-LVEF were unchanged whereas Vp (mean difference [MD + 7.9%, 95% confidence interval [CI] 3.2 to 12.5%; P <  0.001) increased compared with baseline values. After Placebo infusion, there was a decrease in LV-FAC (MD -2.9%, 95%CI − 4.8 to − 1.0%), 2D-LVEF (MD -2.0%, 95%CI − 2.8 to − 1.3%, 3D-LVEF (MD -3.0%, 95%CI − 4.0 to − 2.0%) and Vp (MD − 4.5 cm/s, 95%CI − 5.6 to − 3.3 cm/s). After cardiopulmonary bypass, GIK pretreatment was associated with preserved 2D and 3D-LVEF (+ 0.4%, 95% 95%CI − 0.8 to 1.7% and + 0.4%, 95%CI − 1.3 to 2.0%), and PGLS (− 0.9, 95%CI − 1.6 to − 0.2) as well as higher Vp (+ 5.1 cm/s, 95%CI 2.9 to 7.3), compared with baseline. In contrast, in the Placebo group, 2D-LVEF (− 2.2%, 95%CI − 3.4 to − 1.0), 3D-LVEF (− 6.0%, 95%CI − 7.8 to − 4.2), and Vp (− 7.6 cm/s, 95%CI − 9.4 to − 5.9), all decreased after bypass. Conclusions Administration of GIK before aortic cross-clamping resulted in better preservation of systolic and diastolic ventricular function in patients with LV hypertrophy undergoing aortic valve replacement. Trial registration ClinicalTrials.gov: NCT00788242 , registered on November 10, 2008.
topic Aortic valve stenosis
Echocardiography
Myocardial protection
url http://link.springer.com/article/10.1186/s12871-019-0845-0
work_keys_str_mv AT marclicker glucoseinsulinpotassiumimprovesleftventricularperformancesafteraorticvalvereplacementasecondaryanalysisofarandomizedcontrolledtrial
AT johndiaper glucoseinsulinpotassiumimprovesleftventricularperformancesafteraorticvalvereplacementasecondaryanalysisofarandomizedcontrolledtrial
AT tornikesologashvili glucoseinsulinpotassiumimprovesleftventricularperformancesafteraorticvalvereplacementasecondaryanalysisofarandomizedcontrolledtrial
AT christophellenberger glucoseinsulinpotassiumimprovesleftventricularperformancesafteraorticvalvereplacementasecondaryanalysisofarandomizedcontrolledtrial
_version_ 1724510193646043136