Beyersdorf F, Sarai K, Maul F D, Wendt T, Satter P
Department of Thoracic and Cardiovascular Surgery, Johann Wolfgang Goethe-University, Frankfurt, Germany.
J Thorac Cardiovasc Surg. 1991 Dec;102(6):856-66.
This study tests the hypothesis that contractile dysfunction that often develops after acute coronary occlusion despite emergency revascularization can be avoided by careful control of the composition of the initial reperfusate and the conditions of the reperfusion. Between January 1987 and May 1989, 31 consecutive patients with acute coronary occlusion (90% resulting from percutaneous transluminal coronary angioplasty failures) were reperfused during emergency myocardial revascularization according to one of two different protocols. In 23 patients the reperfusate was normal blood given at systemic pressure ("uncontrolled reperfusion"); in eight patients the ischemic segment was reperfused during the first 20 minutes with a regional blood cardioplegic solution (substrate-enriched, hyperosmotic, hypocalcemic, alkalotic, diltiazem-containing) at 37 degrees C at a pressure of 50 mm Hg. Thereafter total bypass was prolonged for an additional 30 minutes before extracorporeal circulation was discontinued ("controlled reperfusion"). Assessment of regional contractility (echocardiography, radionuclide ventriculography), electrocardiographic evidence of myocardial infarction, release of creatine kinase and isoenzyme of creatine kinase, and hospital mortality was performed. Regional contractility was quantified with a scoring system from 0 (normokinesis) to 4 (dyskinesis). Data are expressed as mean +/- standard error of the mean. Both groups were well matched for age, sex, and the distribution of the occluded artery. In the controlled-reperfusion group there was a greater prevalence of previous infarctions (63% versus 43%), additional significant stenosis (1.3 +/- 0.2 versus 0.8 +/- 0.2), and cardiogenic shock (38% versus 17%) compared with the uncontrolled-reperfusion group. Furthermore, the interval between coronary occlusion and reperfusion was significantly longer in the controlled-reperfusion group (4.0 +/- 0.5 versus 2.3 +/- 0.3 hr; p less than 0.05). Regional contractility returned to normal in all patients treated by controlled reperfusion (wall motion score = 0.8 +/- 0.3, normokinesis = 0, slight hypokinesis = 1). In contrast, regional contractility remained severely depressed after uncontrolled reperfusion with normal blood (score 2.5 +/- 0.2; p less than 0.05), with only four of 23 patients with a score less than 2 (2 = severe hypokinesis). Postoperatively enzymes and electrocardiographic changes were similar in both groups. One patient died of mitral insufficiency in the controlled-reperfusion group, despite complete recovery of wall motion in the angioplasty-related artery. Conversely, the four of 23 deaths after uncontrolled reperfusion occurred in patients who sustained infarct in the area of the coronary occlusion (mortality 13% versus 17%). In conclusion, these preliminary clinical results indicate that immediate recovery of segmental contractility can be achieved after acute coronary occlusion if the initial reperfusion is controlled.(ABSTRACT TRUNCATED AT 400 WORDS)
尽管进行了紧急血运重建,但急性冠状动脉闭塞后常出现的收缩功能障碍可通过仔细控制初始再灌注液的成分和再灌注条件来避免。在1987年1月至1989年5月期间,31例连续的急性冠状动脉闭塞患者(90%由经皮腔内冠状动脉成形术失败所致)在紧急心肌血运重建期间按照两种不同方案之一进行了再灌注。23例患者接受的再灌注液为全身压力下给予的正常血液(“非控制性再灌注”);8例患者在最初20分钟内用含底物、高渗、低钙、碱性、含地尔硫䓬的区域性血液心脏停搏液在37℃、50mmHg压力下对缺血节段进行再灌注。此后,在体外循环停止前,全旁路再延长30分钟(“控制性再灌注”)。进行了局部收缩功能评估(超声心动图、放射性核素心室造影)、心肌梗死的心电图证据、肌酸激酶及其同工酶的释放以及住院死亡率评估。局部收缩功能用0(正常运动)至4(运动障碍)的评分系统进行量化。数据以平均值±平均标准误差表示。两组在年龄、性别和闭塞动脉分布方面匹配良好。与非控制性再灌注组相比,控制性再灌注组既往梗死的发生率更高(63%对43%)、存在额外的明显狭窄(1.3±0.2对0.8±0.2)以及心源性休克(38%对17%)。此外,控制性再灌注组冠状动脉闭塞与再灌注之间的间隔明显更长(4.0±0.5对2.3±0.3小时;p<0.05)。所有接受控制性再灌注治疗的患者局部收缩功能均恢复正常(室壁运动评分=0.8±0.3,正常运动=0,轻度运动减弱=1)。相比之下,用正常血液进行非控制性再灌注后局部收缩功能仍严重受损(评分2.5±0.2;p<0.05),23例患者中只有4例评分低于2(2=严重运动减弱)。两组术后酶和心电图变化相似。控制性再灌注组有1例患者死于二尖瓣关闭不全,尽管与血管成形术相关的动脉室壁运动完全恢复。相反,非控制性再灌注后23例死亡患者中有4例发生在冠状动脉闭塞区域梗死的患者中(死亡率13%对17%)。总之,这些初步临床结果表明,如果初始再灌注得到控制,急性冠状动脉闭塞后节段性收缩功能可立即恢复。(摘要截短至400字)