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In the fetal heart, the foramen ovale allows blood to enter the left atrium from the right atrium.
It is one of two fetal cardiac shunts, the other being the ductus arteriosus, which allows blood that still escapes to the right ventricle to bypass the pulmonary circulation.
Allows right to left intracardiac shunting.
In most individuals, the foramen ovale closes at birth., and it later forms the fossa ovalis.
The foramen ovale forms in the late fourth week of gestation, as a small passageway between the septum secundum and the ostium secundum.
Initially the atria are separated from one another by the septum primum except for a small opening below the septum, the ostium primum.
As the septum primum grows, the ostium primum narrows and eventually closes.
Bloodflow from the inferior vena cava wears down a portion of the septum primum, forming the ostium secundum.
The ostium secundum provides communication between the atria after the ostium primum closes completely.
Subsequently, a second wall of tissue, the septum secundum, grows over the ostium secundum in the right atrium.
Blood then passes from the right to left atrium only by way of a small passageway in the septum secundum and then through the ostium secundum.
This passageway is called the foramen ovale.
Occurs in about one fourth of the general population.
Is present in more than 25% of the adult population at autopsy.
The foramen ovale normally closes at birth.
No cause is established for a foramen ovale to remain open instead of closing naturally, but heredity and genetics may play a role.
At birth, when the lungs become functional, the pulmonary vascular pressure decreases and the left atrial pressure exceeds that of the right, which forces the septum primum against the septum secundum, functionally closing the foramen ovale.
In time the septa eventually fuse, leaving a remnant of the foramen ovale, the fossa ovalis.
The fetus receives oxygen not from its lungs, but from the mother’s oxygen-rich blood via the placenta.
Oxygenated blood from the placenta travels through the umbilical cord to the right atrium of the fetal heart.
As the fetal lungs are non-functional.
The blood bypasses them through two cardiac shunts.
The first is the foramen ovale which shunts blood from the right atrium to the left atrium.
The second is the ductus arteriosus which shunts blood from the pulmonary artery to the descending aorta.
In about 25% of adults the foramen ovale does not close completely, but remains as a small patent foramen ovale.
In most of these individuals, the PFO causes no problems and remains undetected throughout life.
PFO has a role in paradoxical embolism that may lead to a stroke or transient ischemic attack.
Transesophageal echocardiography is considered the most accurate investigation to demonstrate a patent foramen ovale.
A patent foramen ovale may also be an incidental finding.
Generally asymptomatic.
Can be a source of paroxidal embolism.
Can be associated with stroke.
May comprise 10% of ischemic strokes and young a middle-aged adults aged 18 to 60 years.
Prevalence decreases with advancing age.
More frequent in young patients with cryptogenic strokes than in the general population.
It is presumed that cryptogenic strokes are due to paradoxical embolisms that result due to a passage of a venous thrombus across a patent foremen ovale to enter the systemic circulation
Prevalence of 34% in first 3 decades of life and down to 20% by the ninth decade.
Patent foramen ovale seen in 15-35% of people, but associated paradoxical embolism is rare
Associated with cryptogenic strokes.
Associated with an increased risk of migraines, particular in those with a sizable shunt fraction.
Research suggests that a proportion of cases of migraine may be caused by PFO, and closure of a PFO can reduce symptoms in certain cases.
This remains controversial; 20% of the general population has a PFO, which for the most part, is asymptomatic.
About 20% of the female population has migraines, and the placebo effect in migraine typically averages around 40%.
The high frequency of these facts make finding statistically significant relationships between PFO and migraine difficult.
In a large randomized controlled trial, migraine headache cessation was not more prevalent in the group of migraine patients who underwent closure of their PFOs.
Present in 35-45% of patients with cryptogenic strokes compare with 25% in the general population.
Associated with strokes at all ages.
Systemic embolic events occur in increased frequency among patients with a patent foramen ovale, even in the absence of right to left shunting.
Can cause ischemic stroke by paradoxical embolic means.
Incidence of cryptogenic strokes without evidence of cardiac or cerebrovascular disease is approximately 200,000 per year
From 70-90,000 of cryptogenic strokes have a patent foramen ovale.
Size of shunt is correlated with risk of stroke.
Risk of stroke increased in patients with pulmonary embolism and a patent foramen ovale.
Increased in risk in patients with cryptogenic strokes.
The mechanism by which a PFO may play a role in stroke is called paradoxical embolism: a blood clot from the venous circulatory system is able to pass from the right atrium directly into the left atrium via the PFO, rather than being filtered by the lungs, and thereupon into systemic circulation toward the brain.
PFO is common in patients with an atrial septal aneurysm (ASA), a much rarer condition, which is also linked to cryptogenic stroke.
While PFO is present in 25% in the general population, the probability of someone having a PFO increases to about 40 to 50% in those who have had a cryptogenic stroke.
Increased age associated with increased risk of paradoxical embolism.
Diameter of the lesion increases with age.
Can lead to ischemic limb infarction, visceral infarction, myocardial infarction, TIAs, and pulmonary embolism.
In the presence of aspirin or warfarin therapy associated with increase risk of adverse events in older but, but not in younger individuals.
Lower prevalence of patent foramen ovale in older individuals than in younger patients with cryptogenic strokes, as alternative causes more likely in older patients.
The concomitant presence of an atrial septal aneurysm with a patent foramen ovale increases the risk of paradoxical embolism and stroke.
Closure of a patent foramen ovale in patients with ischemic stroke may reduce risk of recurrent stroke compared with medical therapy alone (Schuchlemz HW et al, Wahl A et al).
Catheter closure of patent foramen may be inferior management to medical therapy according to meta analyses.
In a multicenter study of patients with patent foramen ovale and ischemic stroke, TIA, or a peripheral thromboembolic event were randomly treated with the Amplatzer PFO Occluder or medical therapy: no significant reduction in risk of recurrent embolic events or death occurred as compared to medical therapy (Meier B et al).
Three randomized clinical trials comparing patent foremen ovale closure with medical therapy failed to show a significant advantage of patent foremen ovale closure.
Presently there is no current known difference in stroke incidence between antiplatelet and anticoagulation strategies in patients who have had a stroke and not having patent foramen closure.
However, studies show that patients with a patent foremen ovale closure who have in addition atrial septal aneurysm have a significant decrease in cryptogenic strokes, and without an aneurysm of the atrial septum, patent foramen ovale closure is not indicated.
In the CLOSE study 663 patients with patent foramen ovale and large interatrial shunts are atrial septal aneurysm were randomized to a patent foramen ovale device closure or medical therapy and followed for a mean of 5.3 years: significantly fewer strokes occurred in the patent foramen ovale closed group.
In the Septal Occluder and Antiplatelet Medical Management for Reduction of Recurrent Stroke or Imaging-Confirmed TIA in Patients with foramen ovale trial. 664 patients
With patent foramen ovale, of whom 81% had moderate to large interatrial shunts were randomized to patent foramen ovale closure plus antiplatelet therapy or antiplatelet therapy alone and followed for a mean of 3.2 years: there were significantly fewer clinical ischemic strokes in the patent foramen ovale closure group.