Arom K V, Emery R W, Nicoloff D M, Flavin T F, Emery A M
Department of Cardiothoracic Surgery, Minneapolis Heart Institute, Minnesota, USA.
Ann Thorac Surg. 1997 Jun;63(6 Suppl):S48-52. doi: 10.1016/s0003-4975(97)00136-7.
This communication briefly details the goals, indications, surgical approaches, and limitations of minimally invasive direct coronary artery bypass grafting (MIDCABG). The experimental experiences from various institutions are summarized.
The clinical experiences of 72 consecutive MIDCABG procedures performed at our institutions between June 5, 1995, and August 13, 1996, were analyzed. We have divided patients into two groups. Group A consists of healthy low-risk patients with single lesions of the left anterior descending coronary artery or the right coronary artery, or with both lesions of both arteries. Group B consists of high-risk patients who had major contraindications to conventional cardiopulmonary bypass procedures. There were 55 patients in group A and 17 patients in group B. Using The Society of Thoracic Surgeons preoperative predicted risk module, group A had a 1% predicted mortality versus 4% in group B.
The 30-day mortality was 2% in group A and 6% in group B. The mean postoperative length of stay was 4 days for group A and 5 1/2 days for group B. Short-term follow-up of the survivors appears promising, and 81% of patients were angina free at the time of last follow-up.
The MIDCABG techniques are still developing. The short-term results during the learning period appear to be quite good, but long-term results remain yet to be seen. The addition of new equipment to facilitate construction of the anastomosis will enhance application and results. The lessons learned from these approaches are already being applied to other areas of cardiac surgery including valve replacement and the repair of congenital heart defects.
本交流简要详述了微创直接冠状动脉旁路移植术(MIDCABG)的目标、适应证、手术方法及局限性。总结了各机构的实验经验。
分析了1995年6月5日至1996年8月13日在我们机构连续进行的72例MIDCABG手术的临床经验。我们将患者分为两组。A组由健康的低风险患者组成,这些患者有左前降支冠状动脉或右冠状动脉单处病变,或两支动脉均有病变。B组由对传统体外循环手术有主要禁忌证的高风险患者组成。A组有55例患者,B组有17例患者。使用胸外科医师协会术前预测风险模块,A组预测死亡率为1%,而B组为4%。
A组30天死亡率为2%,B组为6%。A组术后平均住院时间为4天,B组为5.5天。对幸存者的短期随访结果似乎很有希望,81%的患者在最后一次随访时无心绞痛症状。
MIDCABG技术仍在发展。学习期的短期结果似乎相当不错,但长期结果仍有待观察。增加有助于构建吻合口的新设备将提高其应用和效果。从这些方法中学到的经验教训已被应用于心脏外科的其他领域,包括瓣膜置换和先天性心脏缺陷修复。