Atrial septal defect pathophysiology

Jump to navigation Jump to search

WikiDoc Resources for Atrial septal defect pathophysiology

Articles

Most recent articles on Atrial septal defect pathophysiology

Most cited articles on Atrial septal defect pathophysiology

Review articles on Atrial septal defect pathophysiology

Articles on Atrial septal defect pathophysiology in N Eng J Med, Lancet, BMJ

Media

Powerpoint slides on Atrial septal defect pathophysiology

Images of Atrial septal defect pathophysiology

Photos of Atrial septal defect pathophysiology

Podcasts & MP3s on Atrial septal defect pathophysiology

Videos on Atrial septal defect pathophysiology

Evidence Based Medicine

Cochrane Collaboration on Atrial septal defect pathophysiology

Bandolier on Atrial septal defect pathophysiology

TRIP on Atrial septal defect pathophysiology

Clinical Trials

Ongoing Trials on Atrial septal defect pathophysiology at Clinical Trials.gov

Trial results on Atrial septal defect pathophysiology

Clinical Trials on Atrial septal defect pathophysiology at Google

Guidelines / Policies / Govt

US National Guidelines Clearinghouse on Atrial septal defect pathophysiology

NICE Guidance on Atrial septal defect pathophysiology

NHS PRODIGY Guidance

FDA on Atrial septal defect pathophysiology

CDC on Atrial septal defect pathophysiology

Books

Books on Atrial septal defect pathophysiology

News

Atrial septal defect pathophysiology in the news

Be alerted to news on Atrial septal defect pathophysiology

News trends on Atrial septal defect pathophysiology

Commentary

Blogs on Atrial septal defect pathophysiology

Definitions

Definitions of Atrial septal defect pathophysiology

Patient Resources / Community

Patient resources on Atrial septal defect pathophysiology

Discussion groups on Atrial septal defect pathophysiology

Patient Handouts on Atrial septal defect pathophysiology

Directions to Hospitals Treating Atrial septal defect pathophysiology

Risk calculators and risk factors for Atrial septal defect pathophysiology

Healthcare Provider Resources

Symptoms of Atrial septal defect pathophysiology

Causes & Risk Factors for Atrial septal defect pathophysiology

Diagnostic studies for Atrial septal defect pathophysiology

Treatment of Atrial septal defect pathophysiology

Continuing Medical Education (CME)

CME Programs on Atrial septal defect pathophysiology

International

Atrial septal defect pathophysiology en Espanol

Atrial septal defect pathophysiology en Francais

Business

Atrial septal defect pathophysiology in the Marketplace

Patents on Atrial septal defect pathophysiology

Experimental / Informatics

List of terms related to Atrial septal defect pathophysiology

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

Please Take Over This Page and Apply to be Editor-In-Chief for this topic: There can be one or more than one Editor-In-Chief. You may also apply to be an Associate Editor-In-Chief of one of the subtopics below. Please mail us [2] to indicate your interest in serving either as an Editor-In-Chief of the entire topic or as an Associate Editor-In-Chief for a subtopic. Please be sure to attach your CV and or biographical sketch.

Pathophysiology

In unaffected individuals, the chambers of the left side of the heart make up a higher pressure system than the chambers of the right side of the heart. This is because the left ventricle has to produce enough pressure to pump blood throughout the entire body, while the right ventricle only has to produce enough pressure to pump blood to the lungs.

In the case of a large ASD (>9mm), which may result in a clinically remarkable left-to-right shunt, blood will shunt from the left atrium to the right atrium causing excessive interatrial communication (In the case of hemodynamically significant ASD (Qp:Qs > 1.5:1), the patient is often found to be notably symptomatic and ASD repair may be indicated). This extra blood from the left atrium may cause a volume overload of both the right atrium and the right ventricle, which if left untreated, can result in enlargement of the right side of the heart and ultimately heart failure.

Any process that increases the pressure in the left ventricle can cause worsening of the left-to-right shunt. This includes hypertension, which increases the pressure that the left ventricle has to generate in order to open the aortic valve during ventricular systole, and coronary artery disease which increases the stiffness of the left ventricle, thereby increasing the filling pressure of the left ventricle during ventricular diastole.

The right ventricle will have to push out more blood than the left ventricle due to the left-to-right shunt. This constant overload of the right side of the heart will cause an overload of the entire pulmonary vasculature. Eventually the pulmonary vasculature will develop pulmonary hypertension to try to divert the extra blood volume away from the lungs.

The pulmonary hypertension will cause the right ventricle to face increased afterload in addition to the increased preload that the shunted blood from the left atrium to the right atrium caused. The right ventricle will be forced to generate higher pressures to try to overcome the pulmonary hypertension. This may lead to right ventricular failure (dilatation and decreased systolic function of the right ventricle) or elevations of the right sided pressures to levels greater than the left sided pressures.

When the pressure in the right atrium rises to the level in the left atrium, there will no longer be a pressure gradient between these heart chambers, and the left-to-right shunt will diminish or cease.

If left uncorrected, the pressure in the right side of the heart will be greater than the left side of the heart. This will cause the pressure in the right atrium to be higher than the pressure in the left atrium. This will reverse the pressure gradient across the ASD, and the shunt will reverse; a right-to-left shunt will exist. This phenomenon is known as Eisenmenger's syndrome.

Once right-to-left shunting occurs, a portion of the oxygen-poor blood will get shunted to the left side of the heart and ejected to the peripheral vascular system. This will cause signs of cyanosis.

References

Template:WH

Template:WS