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症状性肥厚性梗阻性心肌病的管理——手术治疗后的长期结果

Management of symptomatic hypertrophic obstructive cardiomyopathy--long-term results after surgical therapy.

作者信息

Schulte H D, Borisov K, Gams E, Gramsch-Zabel H, Lösse B, Schwartzkopff B

机构信息

Department of Thoracic and Cardiovascular Surgery, Heinrich Heine University Medical Center, Düsseldorf, Germany.

出版信息

Thorac Cardiovasc Surg. 1999 Aug;47(4):213-8. doi: 10.1055/s-2007-1013146.

Abstract

BACKGROUND

The natural history of Hypertrophic Obstructive Cardiomyopathy (HOCM), is well known from earlier investigations. The yearly death rate of medically or non-treated patients with HOCM is between 1.7% and 4%. After conservative management with beta-blockers and/or calcium antagonist, early improvement is followed in many patients by a symptomatic and clinical impairment, which today may lead to surgical or interventional treatment.

METHODS

From 1963 to 12/1998 a total of 519 patients were operated by transaortic subvalvular myectomy (TSM). The mean age was 49 +/- 11 years (range 3 months - 82 years) in 292 males and 227 females.

RESULTS

The early risk was related to the clinical class (NYHA) and the need for additional cardiac procedures during the same intervention. Total early mortality was 4.4% (n=23), in isolated myectomy 3.6% (n= 11). During the last 10 years it could be reduced to 1.9%. The first complete (100%) reinvestigation of 346 patients up to 26 years after surgery (1963-1991) demonstrated a disease-related mortality rate of 5.2% (n=20). The analysis of late deaths showed that disease-related lethal complications (sudden death, life-threatening arrhythmias, valve endocarditis, secondary LV dilatation) were relatively rare, the age-related death rate nearly followed the natural course because of other causes. The cumulative survival rate after 10 years was 88%, after 20-26 years 72%. The yearly disease-related death rate could be reduced to 0.6%. The long-lasting, symptomatic clinical improvement (NYHA I-II), and also the physical and mental capacity with enlargement of the acitivity radius and improvement of quality of life were remarkable. The positive effects of surgical enlargement of the LVOT could be confirmed in the meantime by hemodynamic, rhythmological, echocardiographic investigations as well as endurance tests.

CONCLUSION

We have examined the outcome of a large series of patients treated surgically for HOCM since 1963. The majority of patients were in NYHA class III and came to surgery after long-term medical, but finally insufficient, management. The perioperative risk could be reduced considerably during recent years, despite the advanced cardiomyopathy status. The long-term postoperative observation of the patients demonstrated an unexpectedly continuing good outcome. Therefore these results may serve as a standard for assessing the results after the less invasive alcohol-induced transcoronary ablation of septal hypertrophy.

摘要

背景

肥厚型梗阻性心肌病(HOCM)的自然病史已在早期研究中得到充分了解。未经治疗或接受药物治疗的HOCM患者的年死亡率在1.7%至4%之间。在使用β受体阻滞剂和/或钙拮抗剂进行保守治疗后,许多患者早期症状改善,但随后出现症状和临床功能受损,如今这可能导致手术或介入治疗。

方法

1963年至1998年12月,共有519例患者接受了经主动脉瓣下肌切除术(TSM)。平均年龄为49±11岁(范围3个月至82岁),其中男性292例,女性227例。

结果

早期风险与临床分级(纽约心脏协会分级)以及同一手术中是否需要额外的心脏手术有关。早期总死亡率为4.4%(n = 23),单纯肌切除术的死亡率为3.6%(n = 11)。在过去10年中,该死亡率可降至1.9%。对1963年至1991年手术后长达26年的346例患者进行的首次全面(100%)复查显示,疾病相关死亡率为5.2%(n = 20)。对晚期死亡的分析表明,与疾病相关的致命并发症(猝死、危及生命的心律失常、瓣膜性心内膜炎、继发性左心室扩张)相对较少,与年龄相关的死亡率因其他原因几乎遵循自然病程。10年后的累积生存率为88%,20至26年后为72%。每年与疾病相关的死亡率可降至0.6%。持久的、有症状的临床改善(纽约心脏协会I-II级),以及身体和心理能力的提升,活动范围扩大和生活质量改善都非常显著。与此同时,通过血流动力学、节律学、超声心动图检查以及耐力测试,可以证实手术扩大左心室流出道的积极效果。

结论

我们研究了自1963年以来接受手术治疗的大量HOCM患者的治疗结果。大多数患者处于纽约心脏协会III级,在长期药物治疗但最终效果不佳后接受手术。尽管心肌病病情严重,但近年来围手术期风险已大幅降低。对患者的长期术后观察显示出意外的持续良好结果。因此,这些结果可作为评估侵入性较小的酒精诱导经冠状动脉间隔肥厚消融术后结果的标准。

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