Izumoto H, Kawazoe K, Kitahara H, Kamata J
Department of Cardiovascular Surgery, Iwate Medical University Memorial Heart Center, Iwate Medical University, Morioka, Japan.
Ann Thorac Surg. 1998 Sep;66(3):800-4. doi: 10.1016/s0003-4975(98)00590-6.
There have been few reports on postoperative morbidity and mortality analyses after concomitant mitral valve operation and the Cox/maze procedure.
Between April 1993 and August 1995, 87 consecutive patients with chronic atrial fibrillation underwent a mitral valve operation and concomitant Cox/maze procedure at Iwate Medical University. The patients were divided into the replacement group (n = 31) and repair group (n = 56) according to the method of mitral valve replacement. Our initial experience with the combined operative procedures is presented along with the operative mortality and morbidity rates. Univariate analysis on preoperative and intraoperative variables affecting early mortality and morbidity is carried out retrospectively.
Total cardiopulmonary bypass time in all patients was 177.2 +/- 70.1 minutes. Total aortic cross-clamp time was 121.7 +/- 30.8 minutes. Total intensive care unit stay was 5.3 +/- 7.9 days. The average intubation period was 55.5 +/- 187.6 hours. The intensive care unit stay and the intubation period of the replacement group were longer than those of the repair group. There were four operative deaths among the 87 patients (4.6%). All repair group patients survived operation, whereas 4 replacement group patients died after operation. In all patients, the New York Heart Association functional class was higher (p = 0.028) in those who died than in those who survived. The overall restoration rate from atrial fibrillation was 79.5% (66 of 83 survivors). Seventeen patients (20.5%) had persistent atrial fibrillation postoperatively. Sick sinus syndrome occurred in 7 patients (8.4%). In the repair group, the restoration rate was 76.8%, whereas in the replacement group it was 85.2% for the survivors.
The Cox/maze procedure can be combined with a mitral valve operation with acceptably low operative risk. Analysis of risk factors of early mortality revealed that the type of mitral valve operation (replacement versus repair) and higher preoperative New York Heart Association functional class were associated with mortality. Long-term results from this combined procedure should be clearly demonstrated before its universal acceptance.
关于二尖瓣手术与Cox迷宫手术同期进行后的术后发病率和死亡率分析的报道较少。
1993年4月至1995年8月期间,87例连续性慢性房颤患者在岩手医科大学接受了二尖瓣手术及同期Cox迷宫手术。根据二尖瓣置换方法,将患者分为置换组(n = 31)和修复组(n = 56)。介绍了我们在联合手术操作方面的初步经验以及手术死亡率和发病率。对影响早期死亡率和发病率的术前及术中变量进行回顾性单因素分析。
所有患者的体外循环总时间为177.2±70.1分钟。主动脉阻断总时间为121.7±30.8分钟。重症监护病房总住院时间为5.3±7.9天。平均插管时间为55.5±187.6小时。置换组的重症监护病房住院时间和插管时间比修复组更长。87例患者中有4例手术死亡(4.6%)。所有修复组患者手术存活,而4例置换组患者术后死亡。在所有患者中,死亡患者的纽约心脏协会心功能分级高于存活患者(p = 0.028)。房颤总体恢复率为79.5%(83例存活者中的66例)。17例患者(20.5%)术后仍有持续性房颤。7例患者(8.4%)发生病态窦房结综合征。在修复组中,恢复率为76.8%,而在置换组中,存活者的恢复率为85.2%。
Cox迷宫手术可与二尖瓣手术联合进行,手术风险可接受且较低。早期死亡率危险因素分析显示,二尖瓣手术类型(置换与修复)及术前较高的纽约心脏协会心功能分级与死亡率相关。在该联合手术被广泛接受之前,应明确展示其长期结果。