Casalino Stefano, Tesler Ugo F, Novelli Eugenio, Stelian Edmond, Renzi Luca, Alessi Claudio, Lanzillo Guido, Cerin Gheorghe, Diena Marco
Department of Anesthesiology, Casa di Cura San Gaudenzio, Novara, Italy.
J Card Surg. 2008 Sep-Oct;23(5):444-9. doi: 10.1111/j.1540-8191.2008.00647.x.
The need to intermittently discontinue the administration of cardioplegia in order to complete the surgical procedure is a major drawback of antegrade warm blood cardioplegia. An ischemic time of 15 minutes is generally considered safe based on empirical observation. The aim of this study was the evaluation of the efficacy and safety of an intermittent warm blood cardioplegia with intervals between administrations prolonged to 25 minutes.
Ninety-seven patients undergoing primary elective coronary artery revascularization were prospectively randomized into two groups. The first, Intermittent Antegrade Warm Blood Cardioplegia (IAWBC) group, comprising 49 patients, received standard intermittent antegrade warm blood cardioplegia repeated every 15 minutes. The second, Modified Intermittent Antegrade Warm Blood Cardioplegia (M-IAWBC) group, comprising 48 patients, received intermittent antegrade warm blood cardioplegia supplemented with magnesium sulfate (MgSO(4)), delivered in volumes proportional to the ventricular mass and repeated every 25 minutes. The clinical outcomes were evaluated. The levels of creatine kinase-MB (CK-MB) isoenzyme, in addition to the echocardiographic assessment of septal dyskinesia and tricuspid annulus plane systolic excursion (TAPSE), have been used as markers of myocardial damage.
There were no statistically significant differences in clinical outcomes, need for inotropes and vasodilators, length of stay in the intensive care unit, and postoperative levels of CK-MB between the two groups. Likewise, postoperative echocardiographic assessment showed no relevant differences.
Administration of warm antegrade cardioplegic solution supplemented with MgSO(4), delivered in volumes proportional to ventricular mass every 25 minutes, provides adequate myocardial protection for coronary artery surgery.
为完成手术操作而需间歇性停止心脏停搏液的输注是顺行性温血心脏停搏的一个主要缺点。基于经验观察,一般认为15分钟的缺血时间是安全的。本研究的目的是评估将给药间隔延长至25分钟的间歇性温血心脏停搏的有效性和安全性。
97例接受初次择期冠状动脉血运重建术的患者被前瞻性随机分为两组。第一组为间歇性顺行性温血心脏停搏(IAWBC)组,共49例患者,每15分钟重复接受标准的间歇性顺行性温血心脏停搏。第二组为改良间歇性顺行性温血心脏停搏(M-IAWBC)组,共48例患者,接受补充硫酸镁(MgSO₄)的间歇性顺行性温血心脏停搏,输注量与心室质量成比例,每25分钟重复一次。评估临床结局。肌酸激酶-MB(CK-MB)同工酶水平,以及室间隔运动障碍和三尖瓣环平面收缩期位移(TAPSE)的超声心动图评估,已被用作心肌损伤的标志物。
两组在临床结局、对正性肌力药和血管扩张剂的需求、重症监护病房的住院时间以及术后CK-MB水平方面均无统计学显著差异。同样,术后超声心动图评估也未显示出相关差异。
每25分钟输注与心室质量成比例的补充有MgSO₄的温顺行性心脏停搏液,可为冠状动脉手术提供充分的心肌保护。