Atrial septal defect ostium secundum natural history, complications and prognosis

Jump to navigation Jump to search

Atrial septal defect ostium secundum Microchapters

Home

Overview

Anatomy

Pathophysiology

Epidemiology and Demographics

Natural History, Complications and Prognosis

Diagnosis

History and Symptoms

Physical Examination

Chest X Ray

Electrocardiogram

Echocardiography

Other Diagnostic Studies

Treatment

Medical Therapy

Indications for Surgical Repair

Surgical Closure

Percutaneous Closure

Case Studies

Case #1

Atrial septal defect ostium secundum natural history, complications and prognosis On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Atrial septal defect ostium secundum natural history, complications and prognosis

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Atrial septal defect ostium secundum natural history, complications and prognosis

CDC on Atrial septal defect ostium secundum natural history, complications and prognosis

Atrial septal defect ostium secundum natural history, complications and prognosis in the news

Blogs on Atrial septal defect ostium secundum natural history, complications and prognosis

Directions to Hospitals Treating Atrial septal defect ostium secundum

Risk calculators and risk factors for Atrial septal defect ostium secundum natural history, complications and prognosis

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Most individuals with an uncorrected secundum ASD are asymptomic or experience minimal symptoms through early adulthood. About 70% of all ostium secundum ASD patients' develop symptoms by the time they are in their 40s. Symptom onset and severity is largely dependent upon the size of the defect. Without intervention prior to the development of Eisenmenger's syndrome, the mortality rate for symptomatic adults is greater than 50%. Possible complications include atrial fibrillation, pulmonary hypertension and stroke.

Natural History

As many atrial septal defect ostium secundum patients are asymptomatic, it is common to survive into adulthood without any need for intervention. Many atrial septal defects smaller than 8 mm in diameter close spontaneously during infancy. Spontaneous closure is uncommon in children and adults. During adulthood there can be the onset of symptoms and an altered life expectancy. Beyond 40-50 years of age, survival without intervention is under 50% with a mortality rate of about 6% per year.

Complications

Atrial septal defect ostium secundum is associated with complications such as

Prognosis

The prognosis for most atrial septal defect patients, especially prior to the age of 40, is positive. As atrial septal defect patients age, symptoms and complications may advance and influence quality of life. With surgical intervention, the mortality rate is less than 1% for atrial septal defect patients under 45. Surgical intervention in older populations is equally promising and can result in longer longevity and improvements in quality of life. Left untreated, the prognosis for atrial septal defect patients is significantly less favorable and may lead to earlier death.

References

Template:WH Template:WS CME Category::Cardiology