Remote intermittent ischemia before coronary artery bypass graft surgery: a strategy to reduce injury and inflammation?

被引:115
作者
Karuppasamy, Partheeban [1 ]
Chaubey, Sanjay [2 ]
Dew, Tracy [3 ]
Musto, Rebecca [3 ]
Sherwood, Roy [3 ]
Desai, Jatin [2 ]
John, Lindsay [2 ]
Shah, Ajay M. [4 ]
Marber, Michael S. [5 ]
Kunst, Gudrun [1 ]
机构
[1] Kings Coll Hosp NHS Fdn Trust, Dept Anaesthet Intens Care Med & Pain Therapy, London SE5 9RS, England
[2] Kings Coll Hosp NHS Fdn Trust, Dept Cardiothorac Surg, London SE5 9RS, England
[3] Kings Coll Hosp NHS Fdn Trust, Dept Clin Biochem, London SE5 9RS, England
[4] Kings Coll London, Cardiovasc Div, James Black Ctr, BHF Ctr Excellence, London SE5 9NU, England
[5] Kings Coll London, Cardiovasc Div, Rayne Inst, St Thomas Hosp,BHF Ctr Excellence, London SE1 7EH, England
关键词
Cardioprotection; Coronary artery disease; Bypass surgery; Inflammation; Myocardial ischemia; Preconditioning; MITOCHONDRIAL-PERMEABILITY; MYOCARDIAL PROTECTION; NONCARDIAC SURGERY; GROWTH-FACTOR; HEART; MUSCLE; REPAIR; MICROEMBOLIZATION; CARDIOMYOCYTES; ASSOCIATION;
D O I
10.1007/s00395-011-0185-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Perioperative myocardial ischemia contributes to postoperative morbidity and mortality. Remote intermittent ischemia (RI) has been shown to benefit patients undergoing coronary artery bypass graft (CABG) surgery by decreasing postoperative cardiac troponin levels. In addition, there is evidence that volatile anesthetics may provide myocardial protection. In this prospective randomized controlled trial we tested the hypothesis that RI is cardioprotective under a strict anesthetic regime with volatile anesthesia until cardiopulmonary bypass (CPB). We also assessed whether RI modulates postoperative cytokine and growth factor concentrations. Fifty-four patients referred for elective CABG surgery without concomitant valve or aortic surgery were randomized to three 5-min cycles of left upper limb ischemia by cuff inflation (RI) or placebo without cuff inflation (Plac). All patients received the volatile anesthetic isoflurane (1.15-1.5 vol%) before CPB and the intravenous anesthetic propofol (3-4 mg/kg/h) thereafter until the end of surgery. Cardiac arrest during CPB was induced by intermittent cross-clamp fibrillation, or by blood cardioplegia. We excluded patients older than 85 years, with unstable angina, significant renal disease, and those taking sulfonylureas. Troponin I (cTnI) was measured preoperatively and after 6, 12, 24 and 48 h. In addition, brain natriuretic peptide (BNP), creatine kinase (CKMB) and a panel of cytokines and growth factors were analyzed perioperatively. Although cTnI, BNP and CKMB all increased post-CABG, there were no significant differences between RI and Plac groups; area under the curve for cTnI 189.4 (183.6) ng/mL/48 h and 183.0 (155.2) ng/mL/48 h mean (SD), p = 0.90, respectively, despite a tendency to a shorter (p < 0.07) cross-clamp time in the treatment group. Similarly, there were no differences between groups in the central venous concentrations of numerous cytokines and growth factors. In patients undergoing CABG surgery RI does not provide myocardial protection under a strict anesthetic regime with volatile anesthesia until CPB, and RI was not associated with changes in cytokines.
引用
收藏
页码:511 / 519
页数:9
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