Brown Morgan L, Dearani Joseph A, Danielson Gordon K, Cetta Frank, Connolly Heidi M, Warnes Carole A, Li Zhuo, Hodge David O, Driscoll David J
Division of Cardiovascular Surgery, Mayo Clinic Center Congenital Heart Center, Mayo Clinic College of Medicine, Mayo Clinic and Foundation, Rochester, Minnesota, USA.
J Am Coll Cardiol. 2008 Aug 5;52(6):460-6. doi: 10.1016/j.jacc.2008.03.064.
The objective of this study was to review the long-term functional outcome of patients with Ebstein anomaly who had cardiac operation at our institution.
Ebstein anomaly is a spectrum of tricuspid valvular and right ventricular dysplasia. Many patients will require operation in an attempt to improve quality of life.
From April 1, 1972, to January 1, 2006, 539 patients with Ebstein anomaly underwent 604 cardiac operations at the Mayo Clinic in Rochester, Minnesota. Patient records were reviewed, and all patients known to still be alive were mailed a medical questionnaire or contacted by telephone.
At the initial operation at our institution, the mean age of the patients was 24 years (range 8 days to 79 years) and 53% were female patients. Survival at 5, 10, 15, and 20 years was 94%, 90%, 86%, and 76%, respectively. Survival free of late reoperation was 86%, 74%, 62%, and 46% at 5, 10, 15, and 20 years, respectively. Surveys were returned by 285 of 448 (64%) patients known to be alive at the time of this study. Two hundred thirty-seven (83%) patients were in New York Heart Association functional class I or II, and 34% were taking no cardiac medication. One hundred three patients (36%) reported an incident of atrial fibrillation or flutter, 5 patients (2%) reported having had endocarditis, and 1 patient (<1%) reported having a stroke. There were 275 pregnancies among 82 women. The recurrence of congenital heart disease was reported in 9 of 232 (3.9%) liveborn children.
Patients have good long-term survival and functional outcomes after undergoing surgery for Ebstein anomaly. Atrial arrhythmias are common both before and after surgery. Many patients have had one or more successful pregnancies with a low-recurrence risk of congenital heart disease.
本研究的目的是回顾在我们机构接受心脏手术的埃布斯坦畸形患者的长期功能结局。
埃布斯坦畸形是一系列三尖瓣和右心室发育异常。许多患者需要手术以改善生活质量。
从1972年4月1日至2006年1月1日,539例埃布斯坦畸形患者在明尼苏达州罗切斯特市的梅奥诊所接受了604次心脏手术。回顾了患者记录,并向所有已知仍在世的患者邮寄了一份医学问卷或通过电话联系。
在我们机构进行初次手术时,患者的平均年龄为24岁(范围为8天至79岁),53%为女性患者。5年、10年、15年和20年的生存率分别为94%、90%、86%和76%。5年、10年、15年和20年无晚期再次手术的生存率分别为86%、74%、62%和46%。在本研究进行时已知在世的448例患者中,有285例(64%)回复了调查问卷。237例(83%)患者属于纽约心脏协会心功能I级或II级,34%的患者未服用心脏药物。103例患者(36%)报告有心房颤动或扑动事件,5例患者(2%)报告有感染性心内膜炎,1例患者(<1%)报告有中风。82名女性中有275次妊娠。232例活产婴儿中有9例(3.9%)报告有先天性心脏病复发。
埃布斯坦畸形患者接受手术后有良好的长期生存和功能结局。心房心律失常在手术前后都很常见。许多患者有过一次或多次成功妊娠,先天性心脏病复发风险较低。