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Effect of glucose-insulin-potassium in severe acute heart failure after brain death
Armelle Nicolas-Robin1, Julien Amour, Cristina Ibanez-Esteve
1Department of Anesthesiology, Centre Hospitalo-Universitaire Pitie-Salpetriere, Assistance Publique-Hôpitaux de Paris, Université Pierre et Marie Curie, Paris, France. armelle.nicolas-robin@psl.aphp.fr
Insights
Glucose-insulin-potassium effectively improves heart function in brain-dead patients, similar to dobutamine but without adverse effects. This finding supports its use in managing myocardial dysfunction in potential organ donors.
Area of Science:
- Cardiology
- Organ Donation
- Critical Care Medicine
Background:
- Donor heart shortages necessitate using marginal donors.
- Brain death can cause myocardial dysfunction, potentially reversible.
- Dobutamine, used to support donors, may worsen ischemia.
Purpose of the Study:
- Compare dobutamine and glucose-insulin-potassium (GIK) for left ventricular systolic dysfunction in brain-dead patients.
- Evaluate GIK as a safer alternative to dobutamine.
Main Methods:
- Prospective screening of 135 brain-dead patients.
- Twelve patients with ejection fraction <30% received dobutamine (10 mcg/kg/min for 30 min).
- Following recovery, patients received GIK infusion (over 120 min).
Main Results:
- Dobutamine increased ejection fraction (21% to 39%) but decreased blood pressure and increased heart rate.
- GIK also increased ejection fraction (21% to 37%) without significant changes in blood pressure or heart rate.
- Both interventions improved systolic function, but GIK had a more favorable hemodynamic profile.
Conclusions:
- GIK is as effective as dobutamine in improving ventricular systolic function in brain-dead patients.
- GIK offers a safer alternative by avoiding dobutamine's side effects.
- This supports GIK for managing myocardial dysfunction in potential organ donors.
Background:
As a result of donor heart shortage, resorting to marginal heart donors is being promoted. Dobutamine is usually used to support these potential donors and has been proposed to identify the reversible part of the brain death-induced myocardial dysfunction before potential organ donation. But dobutamine impairs the oxygen supply-demand balance and may increase myocardial ischemia. The aim of this study was to compare the effects of dobutamine and glucose-insulin-potassium on the left ventricular systolic dysfunction in brain dead patients.
Methods And Results:
One hundred thirty-five consecutive brain dead patients were prospectively screened. Twelve of them with severe acute heart failure defined by an echocardiographic ejection fraction area <30% received 10 microg/kg/min dobutamine infusion over 30 min and, after return to baseline cardiac function, glucose-insulin-potassium infusion over 120 min. With dobutamine, ejection fraction area significantly increased (39 +/- 14 vs. 21 +/- 6%, p < 0.0001) whereas mean diastolic arterial pressure decreased (71 +/- 9 vs. 89 +/- 18 mm Hg, p < 0.05) and heart rate increased (150 +/- 16 vs. 118 +/- 24 beats/min, p < 0.01). After glucose-insulin-potassium infusion, ejection fraction area significantly increased (37 +/- 8 vs. 21 +/- 6%, p < 0.0001), without significant changes in mean arterial blood pressure (79 +/- 16 vs. 89 +/- 18 mm Hg, nonsignificant) and heart rate (116 +/- 18 vs. 118 +/- 24 beats/min, nonsignificant).
Conclusion:
Glucose-insulin-potassium was as efficient as dobutamine in improving ventricular systolic function in brain-dead patients, without the side effects of dobutamine.
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