Fitzpatrick A P, Lesh M D, Epstein L M, Lee R J, Siu A, Merrick S, Griffin J C, Scheinman M M
University of California, Department of Medicine, San Francisco 94143.
Circulation. 1994 Jun;89(6):2503-8. doi: 10.1161/01.cir.89.6.2503.
Implantable cardioverter/defibrillators (ICDs) have conventionally been implanted in the operating room by surgeons. However, technological developments have reduced size and increased simplicity, bringing the procedure into the realm of the electrophysiologist. The purpose of this study was to evaluate the safety and efficacy of implantation of the entire ICD system by electrophysiologists in an electrophysiology laboratory.
Between July 1993 and February 1994, 23 patients (21 men; age, 64 +/- 11 years) underwent transvenous ICD implantation by electrophysiologists working alone, entirely in the electrophysiology laboratory. Indications for ICD were sudden death in 10 patients, uncontrolled life-threatening ventricular tachycardia in 12, and syncope with cardiomyopathy and familial sudden death in 1. Seventeen patients had coronary artery disease and a past history of acute myocardial infarction. Four patients had idiopathic dilated cardiomyopathy, 1 had coronary ectasia and poor left ventricular function, and another had poor left ventricular function related to valvular dysfunction. The mean left ventricular ejection fraction was 34 +/- 10% (range, 20% to 50%). General anesthesia was administered in 22 cases, and deep sedation was used in 1 elderly patient. After positioning of transvenous leads and subcutaneous patch/array lead positioning, defibrillation testing was performed. After transvenous and subcutaneous lead tunneling, all generators were placed subcutaneously in an abdominal pocket. The mean total time in the electrophysiology laboratory was 254 +/- 68 minutes (range, 150 to 375 minutes), with 104 +/- 42 minutes for anesthetic and other preparation, 159 +/- 45 minutes for implantation, and 8.7 +/- 5 minutes (range, 3 to 25 minutes) of fluoroscopy required for positioning of transvenous and subcutaneous lead systems. Implant times showed a significant improvement when the first 10 cases (188 +/- 44 minutes) were compared with the last 10 in the series (124 +/- 44 minutes, P < .01). The mean defibrillation threshold was 17 +/- 5 J (range, 5 to 25 J). There were 5 complications (22%): 1 patch-site hematoma, 1 pneumothorax related to subclavian venous puncture, 1 pulmonary embolism, and 2 patients requiring overnight ventilation after hemodynamic deterioration following defibrillation testing. There were no deaths, and there were no infections. The mean time to hospital discharge after the implant was 5.1 +/- 3.5 days. After 11.6 +/- 9 weeks of follow-up, all devices were functioning satisfactorily, all patients had successfully defibrillated at postimplant predischarge checkup with 29 +/- 5 J, and there had been no late complications.
This is the first report to show that nonthoracotomy ICD implantation may be successfully carried out by electrophysiologists working alone in the electrophysiology laboratory, with a high rate of success and few complications, even in high-risk patients. This high rate of success and safety probably relates to the availability of high-quality fluoroscopy and familiarity with electrophysiology laboratory equipment and personnel.
传统上,植入式心脏复律除颤器(ICD)由外科医生在手术室植入。然而,技术的发展减小了设备尺寸并提高了操作的简易性,使得该手术进入了电生理学家的领域。本研究的目的是评估电生理学家在电生理实验室植入整个ICD系统的安全性和有效性。
1993年7月至1994年2月期间,23例患者(21例男性;年龄64±11岁)由电生理学家单独操作,完全在电生理实验室接受经静脉ICD植入术。植入ICD的指征为:10例患者有猝死史,12例患者有无法控制的危及生命的室性心动过速,1例患者有心肌病合并晕厥及家族性猝死。17例患者有冠状动脉疾病及急性心肌梗死病史。4例患者有特发性扩张型心肌病,1例患者有冠状动脉扩张及左心室功能不全,另1例患者左心室功能不全与瓣膜功能障碍有关。平均左心室射血分数为34±10%(范围为20%至50%)。22例患者采用全身麻醉,1例老年患者采用深度镇静。经静脉导线定位及皮下贴片/阵列导线定位后,进行除颤测试。经静脉和皮下导线隧道置入后,所有发生器均置于腹部皮下囊袋中。在电生理实验室的平均总时间为254±68分钟(范围为150至375分钟),麻醉及其他准备时间为104±42分钟,植入时间为159±45分钟,经静脉和皮下导线系统定位所需透视时间为8.7±5分钟(范围为3至25分钟)。将系列中的前10例(188±44分钟)与后10例(124±44分钟,P<.01)比较,植入时间有显著改善。平均除颤阈值为17±5焦耳(范围为5至25焦耳)。发生5例并发症(22%):1例贴片部位血肿,1例与锁骨下静脉穿刺相关的气胸,1例肺栓塞,2例患者在除颤测试后血流动力学恶化需过夜通气。无死亡病例,无感染发生。植入后平均住院时间为5.1±3.5天。随访11.6±9周后,所有装置功能良好,所有患者在植入后出院前检查时均成功除颤,能量为29±5焦耳,无晚期并发症。
这是第一份表明非开胸ICD植入术可由电生理学家单独在电生理实验室成功实施的报告,成功率高且并发症少,即使在高危患者中也是如此。这种高成功率和安全性可能与高质量透视设备的可用性以及对电生理实验室设备和人员的熟悉程度有关。