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==[[Atrial septal defect treatment | Treatment]]==
==[[Atrial septal defect treatment | Treatment]]==


[[Atrial septal defect evaluation prior to correction | Evaluation prior to correction]]
[[Atrial septal defect evaluation prior to correction | Evaluation prior to correction]] | [[Atrial septal defect surgical closure | Surgical ASD closure]]
 
===Surgical ASD closure===
Surgical closure of an [[ASD]] involves opening up at least one [[atrium (anatomy)|atrium]] and closing the defect with a patch under direct visualization.


===Percutaneous ASD closure===
===Percutaneous ASD closure===

Revision as of 14:22, 24 June 2011

Atrial septal defect
Heart of human embryo of about thirty-five days
ICD-10 Q21.1
ICD-9 745.5-745.6
OMIM 108800
DiseasesDB 1089
eMedicine med/3519 
MeSH C14.240.400.560.375

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Editors-In-Chief: Claudia Hochberg, M.D.; C. Michael Gibson, M.S., M.D. [1] Phone:617-525-6884

Associate Editors-In-Chief: Cafer Zorkun, M.D., Ph.D. [2]; Keri Shafer, M.D. [3]

Please Join in Editing This Page and Apply to be an 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 [4] 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.

Overview

Embryology

Pathophysiology

Epidemiology

Genetic

Types of atrial septal defects

Ostium primum atrial septal defect | Ostum secundum atrial septal defect | Patent foramen ovale | Sinus venosus atrial septal defect | Common or single atrium

Diagnosis

Physical examination | Auscultation of the heart | Chest X-ray | Electrocardiography | Echocardiography | Trans-cranial doppler ultrasound | MRI

Treatment

Evaluation prior to correction | Surgical ASD closure

Percutaneous ASD closure

Percutaneous closure of an ASD is currently only indicated for the closure of ostium secundum ASDs with a sufficient rim of tissue around the septal defect so that the closure device does not impinge upon the SVC, IVC, or the tricuspid or mitral valves. The Amplatzer Septal Occluder is commonly used to close ASD's. The ASO consists of two self-expandable round discs connected to each other with a 4-mm waist, made up of 0.004–0.005´´ nitinol wire mesh filled with Dacron fabric. Implantation of the device is relatively easy. The prevalence of residual defect is low. The disadvantages are a thick profile of the device and concern related to a large amount of nitinol (a nickel-titanium compound) in the device and consequent potential for nickel toxicity.

Percutaneous closure is the method of choice in most centers.[1]

Amplatzer Septal Occluder
Amplatzer Septal Occluder


Associated conditions

Due to the communication between the atria that occurs in ASD's, disease entities or complications from the condition, are possible.

Decompression sickness

ASDs, and particularly PFOs, are a predisposing risk factor for decompression sickness in divers because a proportion of venous blood carrying inert gases, such as helium or nitrogen does not pass through the lungs.[2][3] The only way to release the excess inert gases from the body is to pass the blood carrying the inert gases through the lungs to be exhaled. If some of the inert gas-laden blood passes through the PFO, it avoids the lungs and the inert gas is more likely to form large bubbles in the arterial blood stream causing decompression sickness.

Paradoxical emboli

Venous thrombi (clots in the veins) are quite common. Embolization (dislodgement of thrombi) normally go to the lung and cause pulmonary emboli. In an individual with ASD, these emboli can potentially enter the arterial system. This can cause any phenomenon that is attributed to acute loss of blood to a portion of the body, including cerebrovascular accident (stroke), infarction of the spleen or intestines, or even a distal extremity (i.e.: finger or toe).

This is known as a paradoxical embolus because the clot material paradoxically enters the arterial system instead of going to the lungs.

Migraine

Some recent research has suggested that a proportion of cases of migraine may be caused by patent foramen ovale. While the exact mechanism remains unclear, closure of a PFO can reduce symptoms in certain cases.[4][5] This remains controversial. 20% of the general population have a PFO, which for the most part, is asymptomatic. 20% of the female population have migraines. And, the placebo effect in migraine typically averages around 40%. The high frequency of these facts makes statistically significant relationships between PFO and migraine difficult (i.e., the relationship may just be chance or coincidence).

See also

References

  1. Bjørnstad P (2006). "Is interventional closure the current treatment of choice for selected patients with deficient atrial septation?". Cardiol Young. 16 (1): 3–10. PMID 16454871.
  2. Lier H, Schroeder S, Hering R (2004). "[Patent foramen ovale: an underrated risk for divers?]". Dtsch Med Wochenschr. 129 (1–2): 27–30. PMID 14703578.
  3. Saary M, Gray G (2001). "A review of the relationship between patent foramen ovale and type II decompression sickness". Aviat Space Environ Med. 72 (12): 1113–20. PMID 11763113.
  4. Adams H (2004). "Patent foramen ovale: paradoxical embolism and paradoxical data". Mayo Clin Proc. 79 (1): 15–20. PMID 14708944.
  5. Azarbal B, Tobis J, Suh W, Chan V, Dao C, Gaster R (2005). "Association of interatrial shunts and migraine headaches: impact of transcatheter closure". J Am Coll Cardiol. 45 (4): 489–92. PMID 15708691.

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