Impact of preconditioning protocol on anesthetic-induced cardioprotection in patients having coronary artery bypass surgery

被引:64
作者
Fraessdorf, Jan [1 ,2 ]
Borowski, Andreas [3 ]
Ebel, Dirk [2 ,4 ]
Feindt, Peter [3 ]
Hermes, Manuel [2 ]
Meemann, Thomas [2 ]
Weber, Rene [2 ]
Muellenheim, Jost [5 ]
Weber, Nina C. [1 ]
Preckel, Benedikt [1 ,2 ]
Schlack, Wolfgang [1 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Anesthesiol, NL-1100 DD Amsterdam, Netherlands
[2] Univ Hosp Dusseldorf, Dept Anesthesiol, Dusseldorf, Germany
[3] Univ Hosp Dusseldorf, Dept Thorac & Cardiovasc Surg, Dusseldorf, Germany
[4] Slingeland Ziekenhuis, Dept Anesthesiol, Doetinchem, Netherlands
[5] S Tyneside Dist Hosp, Dept Anesthesiol, S Shields, England
关键词
MYOCARDIAL-INFARCTION; VOLATILE ANESTHETICS; TROPONIN-I; SEVOFLURANE; ISOFLURANE; PROTECTION; INJURY; DESFLURANE; ISCHEMIA;
D O I
10.1016/j.jtcvs.2008.04.034
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Anesthetic preconditioning may contribute to the cardioprotective effects of sevoflurane in patients having coronary artery bypass surgery. We investigated whether 2 different sevoflurane administration protocols can induce preconditioning in patients having coronary artery bypass. Methods: Thirty patients were randomly allocated to 1 of 3 groups. All patients received a total intravenous anesthesia with sufentanil (0.3 mu g(-1) (.) kg (.) h(-1)) and propofol as target controlled infusion (2.5 mu g/mL). The control group had no further intervention; 10 minutes prior to establishing the extracorporeal circulation, patients of the sevoflurane-I group received 1 minimum alveolar concentration of sevoflurane for 5 minutes. Patients of the sevoflurane-II group received (2 times) 5 minutes of sevoflurane, interspersed by 5-minute washout 10 minutes prior to extracorporeal circulation. Troponin I was measured as marker of cardiac cellular damage. Results: Peak levels of troponin I release were observed at 4 hours after cardiopulmonary bypass and were not affected by 1 cycle of sevoflurane administration (controls: 14 +/- 3 ng/mL vs sevoflurane-I group, 14 +/- 3 ng/mL). Two periods of sevoflurane preconditioning significantly reduced cellular damage compared with controls (peak troponin I level sevoflurane-II group, 7 +/- 2 ng/mL). Conclusion: These data show that sevoflurane-induced preconditioning is reproducible in patients having coronary artery bypass but depends on the preconditioning protocol used.
引用
收藏
页码:1436 / U171
页数:9
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