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Published on: August 6, 2015
Myocardial preservation using lidocaine blood cardioplegia
A C Fiore1, K S Naunheim, J Taub
1Department of Surgery, St. Louis University Medical Center, MO 63110-0250.
Insights
Lidocaine hydrochloride added to cold potassium blood cardioplegia significantly reduces ventricular fibrillation after aortic unclamping in heart surgery. This safe additive also lowered the need for defibrillation attempts and tended to decrease new atrial fibrillation.
Area of Science:
- Cardiology
- Cardiac Surgery
- Pharmacology
Background:
- Ventricular fibrillation (VF) is a risk after aortic unclamping during myocardial revascularization.
- Current methods to prevent VF may have limitations.
Purpose of the Study:
- To evaluate the efficacy of lidocaine hydrochloride as an additive to cold potassium blood cardioplegia for preventing VF post-aortic unclamping.
- To assess the safety and impact on clinical outcomes.
Main Methods:
- Prospective study of 46 patients undergoing elective myocardial revascularization.
- Comparison between patients receiving lidocaine-enhanced cardioplegia (n=23) and control group (n=23).
- Key metrics included VF incidence, cardioversion attempts, cardiac enzyme release, hemodynamics, and clinical outcomes.
Main Results:
- Lidocaine group showed a significant reduction in VF incidence (22% vs. 74%, p < 0.0005).
- Fewer cardioversion attempts were needed in the lidocaine group (0.5 vs. 1.9, p < 0.0005).
- No significant differences in cardiac enzyme release, hemodynamics, or overall clinical outcome were observed.
Conclusions:
- Lidocaine hydrochloride is a safe additive to potassium blood cardioplegia.
- It significantly reduces the incidence of ventricular fibrillation after aortic unclamping.
- Lidocaine may also reduce the incidence of new postoperative atrial fibrillation.
Abstract:
Prevention of ventricular fibrillation after aortic unclamping using lidocaine hydrochloride as an additive to cold potassium blood cardioplegia was studied prospectively in 46 patients undergoing elective myocardial revascularization. Patients were similar with respect to age, ventricular function, severity of coronary artery disease, cross-clamp time, completeness of revascularization, frequency of internal thoracic artery grafting, systemic temperature at the time of cross-clamp removal, and mean infusate volume and temperature. Patients receiving lidocaine blood cardioplegia (group 1, 23 patients) had a significant reduction in the incidence of ventricular fibrillation (22% versus 74%; p less than 0.0005) and in the mean number of cardioversion attempts required to defibrillate the heart (0.5 +/- 1.3 versus 1.9 +/- 0.97; p less than 0.0005) after cross-clamp removal compared with controls (group 2, 23 patients). There were no differences between the two groups postoperatively with regard to cardiac enzyme release, hemodynamic measurements, or clinical outcome. Patients receiving lidocaine blood cardioplegia tended to have a lower incidence of new postoperative atrial fibrillation (9% versus 26%). Ventricular function was preserved equally in both groups. We conclude that lidocaine is a safe additive to potassium blood cardioplegia and significantly reduces the incidence of ventricular fibrillation after aortic unclamping.
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