Effect of continuous exenatide infusion on cardiac function and peri-operative glucose control in patients undergoing cardiac surgery: A single-blind, randomized controlled trial
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023001%3A_____%2F17%3A00076202" target="_blank" >RIV/00023001:_____/17:00076202 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/00023761:_____/17:N0000019 RIV/00216208:11110/17:10365061 RIV/00064165:_____/17:10365061
Výsledek na webu
<a href="http://onlinelibrary.wiley.com/doi/10.1111/dom.13029/full" target="_blank" >http://onlinelibrary.wiley.com/doi/10.1111/dom.13029/full</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1111/dom.13029" target="_blank" >10.1111/dom.13029</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Effect of continuous exenatide infusion on cardiac function and peri-operative glucose control in patients undergoing cardiac surgery: A single-blind, randomized controlled trial
Popis výsledku v původním jazyce
We performed a randomized controlled trial with the glucagon-like peptide-1 (GLP-1) receptor agonist exenatide as add-on to standard peri-operative insulin therapy in patients undergoing elective cardiac surgery. The aims of the study were to intensify peri-operative glucose control while minimizing the risk of hypoglycaemia and to evaluate the suggested cardioprotective effects of GLP-1-based treatments. A total of 38 patients with decreased left ventricular systolic function (ejection fraction <= 50%) scheduled for elective coronary artery bypass grafting (CABG) were randomized to receive either exenatide or placebo in a continuous 72-hour intravenous (i.v.) infusion on top of standard peri-operative insulin therapy. While no significant difference in postoperative echocardiographic variables was found between the groups, participants receiving exenatide showed improved peri-operative glucose control as compared with the placebo group (average glycaemia 6.4 +/- 0.5 vs 7.3 +/- 0.8 mmol/L; P < .001; percentage of time in target range of 4.5-6.5 mmol/L 54.8% +/- 14.5% vs 38.6% +/- 14.4%; P = .001; percentage of time above target range 39.7% +/- 13.9% vs 52.8% +/- 15.2%; P = .009) without an increased risk of hypoglycaemia (glycaemia < 3.3 mmol/L: 0.10 +/- 0.32 vs 0.21 +/- 0.42 episodes per participant; P = .586). Continuous administration of i.v. exenatide in patients undergoing elective CABG could provide a safe option for intensifying the peri-operative glucose management of such patients.
Název v anglickém jazyce
Effect of continuous exenatide infusion on cardiac function and peri-operative glucose control in patients undergoing cardiac surgery: A single-blind, randomized controlled trial
Popis výsledku anglicky
We performed a randomized controlled trial with the glucagon-like peptide-1 (GLP-1) receptor agonist exenatide as add-on to standard peri-operative insulin therapy in patients undergoing elective cardiac surgery. The aims of the study were to intensify peri-operative glucose control while minimizing the risk of hypoglycaemia and to evaluate the suggested cardioprotective effects of GLP-1-based treatments. A total of 38 patients with decreased left ventricular systolic function (ejection fraction <= 50%) scheduled for elective coronary artery bypass grafting (CABG) were randomized to receive either exenatide or placebo in a continuous 72-hour intravenous (i.v.) infusion on top of standard peri-operative insulin therapy. While no significant difference in postoperative echocardiographic variables was found between the groups, participants receiving exenatide showed improved peri-operative glucose control as compared with the placebo group (average glycaemia 6.4 +/- 0.5 vs 7.3 +/- 0.8 mmol/L; P < .001; percentage of time in target range of 4.5-6.5 mmol/L 54.8% +/- 14.5% vs 38.6% +/- 14.4%; P = .001; percentage of time above target range 39.7% +/- 13.9% vs 52.8% +/- 15.2%; P = .009) without an increased risk of hypoglycaemia (glycaemia < 3.3 mmol/L: 0.10 +/- 0.32 vs 0.21 +/- 0.42 episodes per participant; P = .586). Continuous administration of i.v. exenatide in patients undergoing elective CABG could provide a safe option for intensifying the peri-operative glucose management of such patients.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
30202 - Endocrinology and metabolism (including diabetes, hormones)
Návaznosti výsledku
Projekt
<a href="/cs/project/NV15-26854A" target="_blank" >NV15-26854A: Význam epikardiální tukové tkáně u onemocnění srdce: nové mechanizmy působení a jejich terapeutické ovlivnění</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2017
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Diabetes, obesity and metabolism
ISSN
1462-8902
e-ISSN
—
Svazek periodika
19
Číslo periodika v rámci svazku
12
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
5
Strana od-do
1818-1822
Kód UT WoS článku
000414514600021
EID výsledku v databázi Scopus
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