Bicuspid aortic stenosis epidemiology and demographics

Revision as of 15:51, 5 January 2017 by Usama Talib (talk | contribs)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Jump to navigation Jump to search

Bicuspid aortic stenosis Microchapters

Home

Patient Info

Overview

Anatomy

Historical Perspective

Pathophysiology

Epidemiology & Demographics

Risk Factors

Screening

Causes of Bicuspid aortic stenosis

Natural History, Complications & Prognosis

Diagnosis

History & Symptoms

Physical Examination

Lab Tests

Electrocardiogram

Chest X Ray

CT

MRI

Echocardiography

Cardiac Catheterization

Treatment

Overview

Medical Therapy

Surgery

Bicuspid aortic stenosis epidemiology and demographics On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Bicuspid aortic stenosis epidemiology and demographics

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Bicuspid aortic stenosis epidemiology and demographics

CDC on Bicuspid aortic stenosis epidemiology and demographics

Bicuspid aortic stenosis epidemiology and demographics in the news

Blogs on Bicuspid aortic stenosis epidemiology and demographics

Directions to Hospitals Treating Bicuspid aortic stenosis

Risk calculators and risk factors for Bicuspid aortic stenosis epidemiology and demographics

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Usama Talib, BSc, MD [2]

Overview

In this condition, instead of three valve cusps, the aortic valve has two cusps which results from the fusing of one of the commissures. Bicuspid aortic stenosis is the most common congenital abnormality of the heart accounting for 5% of congenital heart defects and it occurs in 1-2% of the population. It can be manifested as a murmur and usually has no long term health consequences, but if it does, the manifestation of aortic stenosis occurs 10 years earlier.

Genetics

Bicuspid aortic valve has been found to be an inheritable condition, with a demonstrated association with Notch 1.[1] Familial clustering as well as isolated valve defects have been documented. The incidence of bicuspid aortic valve can be as high as 10% to 20% in families affected with the valve problem[2]. Other congential heart defects are associated with bicuspid aortic valve at various frequencies.

Timing of Diagnosis

This condition is often undiagnosed until later in life when the person develops symptomatic aortic stenosis. Aortic stenosis occurs in this condition usually in patients in their 40s or 50s, an average of 10 years earlier than can occur in people with congenitally normal aortic valves. 30% of cases are diagnosed in adolescence.

Incidence of Bicuspid Aortic Valve Disease Versus Degenerative Disease Among Patients with Surgical AS

The congenital bicuspid aortic valve may become calcified, which may lead to half the cases of surgically important pure aortic stenosis in adults, with varying degrees of severity of aortic stenosis and aortic regurgitation.

Male Predominance

Bicuspid aortic stenosis is more common in men than women (3:1 to 5:1).[3]

References

  1. Garg V, Muth AN, Ransom JF; et al. (2005). "Mutations in NOTCH1 cause aortic valve disease". Nature. 437 (7056): 270–4. doi:10.1038/nature03940. PMID 16025100.
  2. Kerstjens-Frederikse WS, Du Marchie Sarvaas GJ, et al. Left ventricular outflow tract obstruction: should cardiac screening be offered to first-degree relatives?. Heart. Aug 2011;97(15):1228-32.
  3. Simard L, Côté N, Dagenais F, Mathieu P, Couture C, Trahan S; et al. (2016). "Sex-Related Discordance Between Aortic Valve Calcification and Hemodynamic Severity of Aortic Stenosis: Is Valvular Fibrosis the Explanation?". Circ Res. doi:10.1161/CIRCRESAHA.116.309306. PMID 27879282.

Template:WH Template:WS CME Category::Cardiology