Population-based treated prevalence, risk factors, and outcomes of bicuspid aortic valve in a pediatric Medicaid cohort
- PMID: 29922007
- PMCID: PMC5963224
- DOI: 10.4103/apc.APC_137_17
Population-based treated prevalence, risk factors, and outcomes of bicuspid aortic valve in a pediatric Medicaid cohort
Abstract
Background: We investigated the treated prevalence of bicuspid aortic valve in a pediatric population with congenital heart disease and its incident complications.
Materials and methods: A 15-year retrospective data set was analyzed. Selection criteria included age ≤17 years, enrollees in the South Carolina State Medicaid program and diagnosed as having bicuspid aortic valve on one or more service visits.
Results: The 15-year-treated prevalence of predominantly isolated bicuspid aortic valve was 2% (20/1000) of pediatric congenital heart disease cases, with a non-African American: African-American ratio of 3.5:1, and a male:female ratio of 1.6:1. Aortic stenosis (28.0%), ventricular septal defect (20.6%), and coarctation of the aorta (20.6%) were the most prevalent coexisting congenital heart lesions. Of the 378 bicuspid aortic valve cases examined, 10.3% received aortic valve repair/replacement, which was significantly more likely to be performed in children with diagnosed aortic stenosis (adjusted odds ratio = 12.90; 95% confidence interval = 5.66-29.44). Cohort outcomes over the study period indicated that 9.5% had diagnosed heart failure, but <1% had diagnosed supraventricular tachycardia, infective endocarditis, aneurysm, dissection, or death.
Conclusions: The majority of isolated bicuspid aortic valve cases without aortic stenosis did not require surgical intervention. Outcomes for cases requiring repair/replacement were relatively benign.
Keywords: Aortic valve repair; bicuspid aortic valve; complications; pediatrics.
Conflict of interest statement
There are no conflicts of interest.
References
-
- Sabet HY, Edwards WD, Tazelaar HD, Daly RC. Congenitally bicuspid aortic valves: A surgical pathology study of 542 cases (1991 through 1996) and a literature review of 2,715 additional cases. Mayo Clin Proc. 1999;74:14–26. - PubMed
-
- Bruckner BA, Reardon MJ. Bicuspid aortic valve and associated aortopathy: Surgical considerations. Methodist Debakey Cardiovasc J. 2010;6:29–32. - PubMed
-
- Sani UM, Jiya NM, Ahmed H, Waziri UM. Profile and outcome of congenital heart diseases in children: A preliminary experience from a tertiary center in Sokoto, North Western Nigeria. Niger Postgrad Med J. 2015;22:1–8. - PubMed
-
- Ciotti GR, Vlahos AP, Silverman NH. Morphology and function of the bicuspid aortic valve with and without coarctation of the aorta in the young. Am J Cardiol. 2006;98:1096–102. - PubMed
-
- Gupta-Malhotra M, Dave A, Sturhan BC, McNiece K, Syamasundar Rao P, Portman R, et al. Prevalence of undiagnosed congenital cardiac defects in older children. Cardiol Young. 2008;18:392–6. - PubMed
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