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ICD-10
Q21.1
ICD-9
745.5-745.6
OMIM
108800
DiseasesDB
1089
eMedicine
med/3519
MeSH
C14.240.400.560.375
This article's introductory section may be too technical for most readers to understand. Please help improve this article to make it understandable to non-experts, without removing the technical details. The talk page may contain suggestions. (January
2009)
Atrial septal defect (ASD) is a form of congenital heart defect that enables blood flow between the left and right atria via the interatrial septum. The interatrial septum is the tissue that divides the right and left atria. Without this septum, or if there is a defect in this septum, it is possible for blood to travel from the left side of the heart to the right side of the heart, or vice versa.[1] This results in the mixing of arterial and venous blood, which may or may not be clinically significant. This mixture of blood may or may not result in what is known as a "shunt". The amount of shunting present, if any, dictates hemodynamic significance (see Pathophysiology below). A "right-to-left-shunt" typically poses the more dangerous scenario (see Pathophysiology below). The right side of the heart contains venous blood with a low oxygen content, and the left side of the heart contains arterial blood with a high oxygen content. A normal heart has an interatrial septum that prevents oxygen-rich blood and oxygen-deficient blood from mixing together. During development of the fetus, the interatrial septum develops to separate the left and right atrium. However, the foramen ovale ( /fremn ovli/) allows blood from the right atrium to the left atrium during fetal development. This opening allows blood to bypass the nonfunctional fetal lungs when the fetus obtains its oxygen from the placenta. A layer of tissue called the septum primum acts as a valve over the foramen ovale during fetal development. After birth, the pressure in the pulmonary circulatory system drops, thus causing the foramen ovale to close entirely. In approximately 25% of adults,[2] the foramen ovale does not entirely seal.[3] In this case, elevation of pressure in the pulmonary circulatory system (i.e.: pulmonary hypertension due to various causes, or transiently during a cough) can cause the foramen ovale to remain open. This is known as a patent foramen ovale (PFO).
Contents
[hide]
1 Pathophysiology 2 Epidemiology 3 Types of atrial septal defects o 3.1 Ostium secundum atrial septal defect 3.1.1 Natural history 3.1.2 Patent foramen ovale o 3.2 Ostium primum atrial septal defect
3.3 Sinus venosus atrial septal defect 3.4 Common or single atrium 3.5 Mixed Atrial septal defect 4 Diagnosis o 4.1 Diagnosis in children o 4.2 Diagnosis in adults 4.2.1 Physical exam auscultation of the heart 4.2.2 Echocardiography 4.2.3 Transesophageal Doppler (TCD) Bubble study 4.2.4 Electrocardiogram 5 Treatment o 5.1 Evaluation prior to correction o 5.2 Catheter Procedure o 5.3 Surgical ASD closure o 5.4 Percutaneous ASD closure 6 Associated conditions o 6.1 Decompression sickness o 6.2 Paradoxical emboli o 6.3 Migraine 7 See also 8 External links 9 References
o o o
[edit] Pathophysiology
Atrial septal defect with left-to-right shunt In unaffected individuals, the chambers of the left side of the heart are under higher pressure 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. This extra blood from the left atrium may cause a volume overload of both the right atrium and the right ventricle. If untreated, this condition can result in enlargement of the right side of the heart and ultimately heart failure.[4] Any process that increases the pressure in the left ventricle can cause worsening of the left-toright 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 pulmonary hypertension may develop. 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). 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.
[edit] Epidemiology
As a group, atrial septal defects are detected in 1 child per 1500 live births. PFO are quite common (appearing in 10 - 20% of adults) but asymptomatic and therefore undiagnosed. ASDs make up 30 to 40% of all congenital heart diseases that are seen in adults.[5] The ostium secundum atrial septal defect accounts for 7% of all congenital heart lesions. This lesion shows a female preponderance, with a male : female ratio of 1:2.[6]
Schematic drawing showing the location of different types of ASD, the view is into an opened right atrium. HV: right ventricle; VCS: superior vena cava; VCI: inferior vena cava; 1: upper sinus venosus defect; 2: lower sinus venosus defect; 3: secundum defect; 4: defect involving coronary sinus; 5; primum defect. There are many types of atrial septal defects. They are differentiated from each other by whether they involve other structures of the heart and how they are formed during the developmental process during early fetal development.
[edit] Patent foramen ovale A patent foramen ovale (PFO) is a small channel that has some hemodynamic consequence; it is a remnant of the fetal foramen ovale. Clinically it is linked to decompression sickness, paradoxical embolism and migraine. On echocardiography, there may not be any shunting of blood noted except when the patient coughs. There is debate within the neurology and cardiology communities about the role of a PFO in cryptogenic (i.e. of unknown cause) neurologic events such as strokes and transient ischemia attacks (TIAs) without any other potential cause. Data suggests that PFOs are involved in the pathogenesis of some migraine headaches. Several clinical trials are currently underway to investigate the role of PFO in these clinical situations.
Ultrasound picture of the heart, seen in a subcostal view. The apex towards the right, atria to the left. ASD secundum seen as a discontinuation of the white band of the atrial septum. Enlarged right atrium below. Enlarged pulmonary veins seen entering left atrium above.
Common (or single) atrium is a failure of development of the embryologic components that contribute to the atrial septal complex. It is frequently associated with heterotaxy syndrome.[12]
[edit] Diagnosis
[edit] Diagnosis in children
Most individuals with a significant ASD are diagnosed in utero or in early childhood with the use of ultrasonography or auscultation of the heart sounds during physical examination.
allows the pulmonic valve to close earlier at the end of ventricular systole, causing P2 to occur earlier. In individuals with an ASD, there is a fixed splitting of S2. The reason that there is a fixed splitting of the second heart sound is that the extra blood return during inspiration gets equalized between the left and right atrium due to the communication that exists between the atria in individuals with ASD. The right ventricle can be thought of as continuously overloaded because of the left to right shunt, producing a widely split S2. Because the atria are linked via the atrial septal defect, inspiration produces no net pressure change between them, and has no effect on the splitting of S2. Thus, S2 is split to the same degree during inspiration as expiration, and is said to be fixed. [edit] Echocardiography In transthoracic echocardiography, an atrial septal defect may be seen on color flow imaging as a jet of blood from the left atrium to the right atrium. If agitated saline is injected into a peripheral vein during echocardiography, small air bubbles can be seen on echocardiographic imaging. It may be possible to see bubbles travel across an ASD either at rest or during a cough. (Bubbles will only flow from right atrium to left atrium if the RA pressure is greater than LA). Because better visualization of the atria is achieved with transesophageal echocardiography, this test may be performed in individuals with a suspected ASD which is not visualized on transthoracic imaging. Newer techniques to visualize these defects involve intracardiac imaging with special catheters that are typically placed in the venous system and advanced to the level of the heart. This type of imaging is becoming more common and involves only mild sedation for the patient typically. If the individual has adequate echocardiographic windows, it is possible to use the echocardiogram to measure the cardiac output of the left ventricle and the right ventricle independently. In this way, it is possible to estimate the shunt fraction using echocardiograpy. [edit] Transesophageal Doppler (TCD) Bubble study A less invasive method for detecting a PFO or other ASDs than transesophagal ultrasound is Transcranial Doppler with bubble contrast.[13] This method reveals the cerebral impact of the ASD or PFO. [edit] Electrocardiogram The ECG findings in atrial septal defect vary with the type of defect the individual has. Individuals with atrial septal defects may have a prolonged PR interval (a first degree heart block). The prolongation of the PR interval is probably due to the enlargement of the atria that is
common in ASDs and the increased distance due to the defect itself. Both of these can cause an increased distance of internodal conduction from the SA node to the AV node.[14] In addition to the PR prolongation, individuals with a primum ASD have a left axis deviation of the QRS complex while those with a secundum ASD have a right axis deviation of the QRS complex. Individuals with a sinus venosus ASD exhibit a left axis deviation of the P wave (not the QRS complex). A common finding in the ECG is the presence of incomplete RBBB (Right Bundle Branch Block). In fact this finding is so characteristic that if it is absent, the diagnosis of ASD should be revised.
[edit] Treatment
Once someone is found to have an atrial septal defect, a determination of whether it should be corrected has to be made. Surgical mortality due to closure of an ASD is lowest when the procedure is performed prior to the development of significant pulmonary hypertension. The lowest mortality rates are achieved in individuals with a pulmonary artery systolic pressure of less than 40 mmHg. If Eisenmenger's syndrome has occurred, there is significant risk of mortality regardless of the method of closure of the ASD. In individuals who have developed Eisenmenger's syndrome, the pressure in the right ventricle has raised high enough to reverse the shunt in the atria. If the ASD is then closed, the afterload that the right ventricle has to act against has suddenly increased. This may cause immediate right ventricular failure, since it may not be able to pump the blood against the pulmonary hypertension. Closure of an ASD in individuals under age 25 has been shown to have a low risk of complications, and individuals have a normal lifespan (comparable to a healthy age-matched population). Closure of an ASD in individuals between the ages of 25 and 40 who are asymptomatic but have a clinically significant shunt is controversial. Those that perform the procedure believe that they are preventing long-term deterioration in cardiac function and preventing the progression of pulmonary hypertension. Methods of closure of an ASD include surgical closure and percutaneous closure.
If pulmonary hypertension is present, the evaluation may include a right heart catheterization. This involves placing a catheter in the venous system of the heart and measuring pressures and oxygen saturations in the SVC, IVC, right atrium, right ventricle, pulmonary artery, and in the wedge position. Individuals with a pulmonary vascular resistance (PVR) of less than 7 wood units show regression of symptoms (including NYHA functional class). On the other hand, individuals with a PVR of greater than 15 wood units have increased mortality associated with closure of the ASD. If the pulmonary arterial pressure is more than 2/3 the systemic systolic pressure, there should be a net left-to-right shunt of at least 1.5:1 or evidence of reversibility of the shunt when given pulmonary artery vasodilators prior to surgery. (If eisenmenger's physiology has set in, it must be proven that the right-to-left shunt is reversible with pulmonary artery vasodilators prior to surgery.)
connected to each other with a 4 mm waist, made up of 0.0040.005 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 centres.[15]
[edit] Migraine
Main article: Migraine surgery#Patent foramen ovale closure 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.[18][19] 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). In a large randomized controlled trial the higher prevalence of patent foramen ovale in migraine patients was confirmed, but migraine headache
cessation was not more prevalent in the group of migraine patients that underwent closure of their patent foramen ovale.[20]
Atrioventricular septal defect Cardiac output Congenital heart disease Heart sounds Pulmonary hypertension Vascular resistance o Pulmonary vascular resistance Ventricular septal defect Illnesses of Ariel Sharon Minimally Invasive Heart Surgery
Pediatric Heart Surgery The Congenital Heart Surgery Video Project Pediatric Cardiac Surgery: Atrial Septal Defect Repair
[edit] References
1. 2. 3. 4. ^ Atrial septal defect at Mount Sinai Hospital ^ Robbins Basic Pathology, 8th Edition, p. 384 ^ Atrial Septal Defect in PediatriceMedicine ^ a b John, J; Abrol, S; Sadiq, A; Shani, J (2011 Jul 26). "Mixed atrial septal defect coexisting ostium secundum and sinus venosus atrial septal defect.". Journal of the American College of Cardiology 58 (5): e9. PMID 21777739. http://content.onlinejacc.org/cgi/content/full/58/5/e9. Retrieved 17 June 2012. 5. ^ Kaplan S (1993). "Congenital heart disease in adolescents and adults. Natural and postoperative history across age groups". Cardiol Clin 11 (4): 54356. PMID 8252558. 6. ^ Feldt R, Avasthey P, Yoshimasu F, Kurland L, Titus J (1971). "Incidence of congenital heart disease in children born to residents of Olmsted County, Minnesota, 1950-1969". Mayo Clin Proc 46 (12): 7949. PMID 5128021. 7. ^ Leachman R, Cokkinos D, Cooley D (1976). "Association of ostium secundum atrial septal defects with mitral valve prolapse". Am J Cardiol 38 (2): 1679. DOI:10.1016/0002-9149(76)90144-2. PMID 952260. 8. ^ "Atrial Septal Defect Types - Mayo Clinic". Archived from the original on 28 September 2007. http://www.mayoclinic.org/atrial-septal-defect/types.html. Retrieved 2007-10-14. 9. ^ Fix, James D.; Dudek, Ronald W. (1998). Embryology. Baltimore: Williams & Wilkins. pp. 52. ISBN 0683-30272-8. 10. ^ Q21.2 11. ^ Davia J, Cheitlin M, Bedynek J (1973). "Sinus venosus atrial septal defect: analysis of fifty cases". Am Heart J 85 (2): 17785. DOI:10.1016/0002-8703(73)90458-4. PMID 4569755. 12. ^ Valdes-Cruz LM, Cayre RO (1998). Echocardiographic diagnosis of congenital heart disease. Philadelphia.
13. ^ Glen, S.; J. Douglas. (1995). "Transcranial doppler monitoring. (letter to editor)". South Pacific Underwater Medicine Society Journal 25 (2). ISSN 0813-1988. OCLC 16986801. http://archive.rubiconfoundation.org/6409. Retrieved 2008-04-06. 14. ^ Clark E, Kugler J (1982). "Preoperative secundum atrial septal defect with coexisting sinus node and atrioventricular node dysfunction". Circulation 65 (5): 97680. DOI:10.1161/01.CIR.65.5.976. PMID 7074763. 15. ^ Bjrnstad P (2006). "Is interventional closure the current treatment of choice for selected patients with deficient atrial septation?". Cardiol Young 16 (1): 310. DOI:10.1017/S1047951105002027. PMID 16454871. 16. ^ Lier H, Schroeder S, Hering R (2004). "[Patent foramen ovale: an underrated risk for divers?]". Dtsch Med Wochenschr 129 (12): 2730. DOI:10.1055/s-2004-812652. PMID 14703578. 17. ^ 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): 111320. PMID 11763113. 18. ^ Adams H (2004). "Patent foramen ovale: paradoxical embolism and paradoxical data". Mayo Clin Proc 79 (1): 1520. DOI:10.4065/79.1.15. PMID 14708944. 19. ^ 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): 48992. DOI:10.1016/j.jacc.2004.09.075. PMID 15708691. 20. ^ "Migraine Intervention With STARFlex Technology (MIST) trial: a prospective, multicenter, doubleblind, sham-controlled trial to evaluate the effectiveness of patent foramen ovale closure with STARFlex septal repair implant to resolve refractory migraine headache. - Dowson A et al. 117 (11): 1397-1404 Circulation". Archived from the original on 26 October 2008. http://circ.ahajournals.org/cgi/content/full/117/11/1397. Retrieved 2008-10-26.
This article incorporates public domain material from the United States Department of Health and Human Services document "National Heart, Lung, and Blood Institute". [show]
v t e
Atrioventricular septal defect LR: Ostium primum Right Left pulmonary valves (stenosis, insufficiency) tricuspid valves (stenosis, atresia, Ebstein's anomaly) Hypoplastic right heart syndrome (Uhl anomaly) aortic valves (stenosis, insufficiency, bicuspid) mitral valves (stenosis, regurgitation) Hypoplastic left heart syndrome
M: HRT
anat/phys/devp [show]
v t e
Oxygen
Deep water blackout Hyperoxia Oxygen toxicity Shallow water blackout Atrial septal defect Avascular necrosis Decompression sickness Dysbaric osteonecrosis High-pressure nervous syndrome Hydrogen narcosis Isobaric counterdiffusion Nitrogen narcosis Taravana Uncontrolled decompression Hypercapnia
Inert gases
Aerosinusitis Air embolism Alternobaric vertigo Barodontalgia Barostriction Barotrauma Decompression illness Dental barotrauma Dysbarism Ear clearing Frenzel maneuver Valsalva maneuver Asphyxia
Immersion
Drowning Hypothermia Hypoxia (medical) Immersion diuresis Instinctive drowning response Salt water aspiration syndrome Swimming-induced pulmonary edema
List of signs and symptoms of diving disorders Seasickness Diving medicine Hyperbaric medicine In-water recompression Oxygen therapy Diving chamber
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