Bicuspid aortic valve: long-term morbidity and mortality

被引:20
|
作者
Yang, Li-Tan [1 ,2 ]
Ye, Zi [1 ]
Ullah, Muhammad Wajih [1 ]
Maleszewski, Joseph J. [3 ]
Scott, Christopher G. [4 ]
Padang, Ratnasari [1 ]
Pislaru, Sorin V. [1 ]
Nkomo, Vuyisile T. [1 ]
Mankad, Sunil V. [1 ]
Pellikka, Patricia A. [1 ]
Oh, Jae K. [1 ]
Roger, Veronique L. [1 ]
Enriquez-Sarano, Maurice [1 ]
Michelena, Hector I. [1 ]
机构
[1] Mayo Clin, Dept Cardiovasc Med, 200 First St SW, Rochester, MN 55905 USA
[2] Natl Taiwan Univ Hosp, Cardiol Div, Taipei 100, Taiwan
[3] Mayo Clin, Dept Anat Pathol, Rochester, MN 55905 USA
[4] Mayo Clin, Div Biomed Stat & Informat, Rochester, MN 55905 USA
关键词
Bicuspid aortic valve; Community; Morbidity; Mortality; ADULTS; OUTCOMES; RECOMMENDATIONS; AORTOPATHY; CHILDREN; HISTORY; COHORT;
D O I
10.1093/eurheartj/ehad477
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background and Aims Bicuspid aortic valve (BAV) is the most common congenital heart anomaly. Lifetime morbidity and whether long-term survival varies according to BAV patient-sub-groups are unknown. This study aimed to assess lifetime morbidity and long-term survival in BAV patients in the community. Methods The authors retrospectively identified all Olmsted County (Minnesota) residents with an echocardiographic diagnosis of BAV from 1 January 1980 to 31 December 2009, including patients with typical valvulo-aortopathy (BAV without accelerated valvulo-aortopathy or associated disorders), and those with complex valvulo-aortopathy (BAV with accelerated valvulo-aortopathy or associated disorders). Results 652 consecutive diagnosed BAV patients [median (IQR) age 37 (22-53) years; 525 (81%) adult and 127 (19%) paediatric] were followed for a median (IQR) of 19.1 (12.9-25.8) years. The total cumulative lifetime morbidity burden (from birth to age 90) was 86% (95% CI 82.5-89.7); cumulative lifetime progression to >= moderate aortic stenosis or regurgitation, aortic valve surgery, aortic aneurysm >= 45 mm or z-score >= 3, aorta surgery, infective endocarditis and aortic dissection was 80.3%, 68.5%, 75.4%, 27%, 6% and 1.6%, respectively. Survival of patients with typical valvulo-aortopathy [562 (86%), age 40 (28-55) years, 86% adults] was similar to age-sex-matched Minnesota population (P = .12). Conversely, survival of patients with complex valvulo-aortopathy [90 (14%), age 14 (3-26) years, 57% paediatric] was lower than expected, with a relative excess mortality risk of 2.25 (95% CI 1.21-4.19) (P = .01). Conclusion The BAV condition exhibits a high lifetime morbidity burden where valvulo-aortopathy is close to unavoidable by age 90. The lifetime incidence of infective endocarditis is higher than that of aortic dissection. The most common BAV clinical presentation is the typical valvulo-aortopathy with preserved expected long-term survival, while the complex valvulo-aortopathy presentation incurs higher mortality.
引用
收藏
页码:4549 / 4562
页数:14
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