Remote ischaemic preconditioning protects against cardiopulmonary bypass-induced tissue injury: a preclinical study

被引:67
作者
Kharbanda, R. K.
Li, J.
Konstantinov, I. E.
Cheung, M. M. H.
White, P. A.
Frndova, H.
Stokoe, J.
Cox, P.
Vogel, M.
Van Arsdell, G.
MacAllister, R.
Redington, A. N.
机构
[1] Univ Cambridge, Cambridge, England
[2] Hosp Sick Children, Toronto, ON M5G 1X8, Canada
[3] Papworth Hosp, Cambridge CB3 8RE, England
[4] UCL, London, England
关键词
D O I
10.1136/hrt.2004.042366
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: To test the hypothesis that remote ischaemic preconditioning (rIPC) reduces injury after cardiopulmonary bypass (CPB). Design: Randomised study with an experimental model of CPB (3 h CPB with 2 h of cardioplegic arrest). Twelve 15 kg pigs were randomly assigned to control or rIPC before CPB and followed up for 6 h. Intervention: rIPC was induced by four 5 min cycles of lower limb ischaemia before CPB. Main outcome measures: Troponin I, glial protein S-100B, lactate concentrations, load-independent indices (conductance catheter) of systolic and diastolic function, and pulmonary resistance and compliance were measured before and for 6 h after CPB. Results: Troponin I increased after CPB in both groups but during reperfusion the rIPC group had lower concentrations than controls (mean area under the curve -57.3 (SEM 7.3) v 89.0 (11.6) ng center dot h/ml, p = 0.02). Lactate increased after CPB in both groups but during reperfusion the control group had significantly more prolonged hyperlactataemia (p = 0.04). S-100B did not differ between groups. Indices of ventricular function did not differ. There was a tendency to improved lung compliance (p = 0.07), and pulmonary resistance changed less in the rIPC than in the control group during reperfusion (p = 0.02). Subsequently, peak inspiratory pressure was lower (p = 0.001). Conclusion: rIPC significantly attenuated clinically relevant markers of myocardial and pulmonary injury after CPB. Transient limb ischaemia as an rIPC stimulus has potentially important clinical applications.
引用
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页码:1506 / 1511
页数:6
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