Aortic Sentence Examples
The aortic trunk is very short, sends off the coronary arteries and then the left aorta brachiocephalica, while the rest divides into the right brachiocephalic and the aorta descendens.
The discovery of the Rntgen rays has also extended the physician's power of vision, as in cases of aortic aneurysm, and other thoracic diseases.
Left brachial artery arising from a common innominate trunk, instead of coming off separately from the aortic arch.
The drug is contra-indicated in all cases where the heart is already beating too slowly; in aortic incompetence - where the prolongation of diastole increases the amount of the blood that regurgitates through the incompetent valve; in chronic Bright's disease and in fatty degeneration of the heart - since nothing can cause fat to become contractile.
Alternatively, the presence of an aortic aneurysm may make you think twice about performing an anastomosis.Advertisement
Do you really think a mere ruptured aortic aneurysm is a good enough excuse to endanger Freedom?
The risk of death from a ruptured abdominal aortic aneurysm is about 50 per cent, even during operation.
Aortic aneurysm or aortic dissection occurred in 18 %, usually in the thoracic aorta (about 60% ).
Enlargement of the aorta can cause disturbance in the function of the aorta valve (leaky aortic valve ).
Aortic valve calcification occurs in up to 55% of patients, with aortic stenosis being present in 13% .Advertisement
There should be about 2mm of aorta visible below the aortic clamp.
Surgery is offered when the aortic diameter exceeds 55 mm.
The " dup " sound is caused by the closing of the aortic and pulmonary valves at the beginning of ventricular diastole.
Repeat scans of patients with an AAA of 3 to 5.9 cm were done at intervals determined by the aortic dilatation.
In the entire group with aortic dilation, 10 of 15 (67 %) patients were younger than 21 years.Advertisement
Aortic aneurysm, aortic dissection, or large artery stenosis occurred in 27% .
Flow enters the aorta at the aortic root, which is a relatively distensible portion of the aorta.
Diagnosis Thrombosis of the aorta and aortic graft Renal infarction Discussion The more distal images demonstrated the nature of his previous surgery.
Her cardiac history included a myocardial infarct 5 years previously, mixed aortic valve disease, hypertension and rheumatic fever in childhood.
Mixed valve disease is a combination of both aortic stenosis and aortic regurgitation.Advertisement
We have placed these in three categories; coronary artery bypass grafting (CABG ), aortic valve replacement (AVR) and other.
The outcome of traumatic aortic rupture varies from reports to reports, however, is still not satisfactory.
The risk of aneurysm rupture is related to aortic diameter.
F - the loudness of the murmur bears no relation to the severity of the aortic stenosis.
Tritace should not be used in patients with aortic or mitral valve stenosis or outflow obstruction (see Precautions section below ).Advertisement
The coronary arteries come out of the aorta just after the last heart valve (the aortic valve ).
The discovery of the RÃ¶ntgen rays has also extended the physician's power of vision, as in cases of aortic aneurysm, and other thoracic diseases.
Like pulmonic stenosis, aortic stenosis is a congenital heart defect in which a malformation impedes the flow of blood through the heart.
We have placed these in three categories; coronary artery bypass grafting (CABG), aortic valve replacement (AVR) and other.
Annually in the United States, 9000 deaths occur as result of rupture of an abdominal aortic aneurysm.
Tritace should not be used in patients with aortic or mitral valve stenosis or outflow obstruction (see Precautions section below).
An untreated ruptured thoracic aortic aneurysm is also always fatal.
Changes in the pattern of distribution of von Willebrand factor in rat aortic endothelial cells following thrombin generation in vivo.
The coronary arteries come out of the aorta just after the last heart valve (the aortic valve).
Aortic valve-The valve between the heart's left ventricle and ascending aorta that prevents regurgitation of blood back into the left ventricle.
These include defective heart valves, hypertrophic cardiomyopathy (enlarged heart muscle), holes or abnormal openings in the walls of the heart (septal defects), aortic aneurysm, or other congenital heart disease.
A septal defect or aortic aneurysm can cause heart murmurs.
An aortic aneurysm is an abnormal bulging of part of the aorta that may cause blood to leak through the aortic valve and flow the wrong direction.
This stretching increases the likelihood of an aortic dissection, which is a tear or separation between the layers of tissue that make up the aorta.
An aortic dissection usually causes severe pain in the abdomen, back, or chest, depending on the section of the aorta that is affected.
A weakened and enlarged aorta may allow some blood to leak back into the heart during each heartbeat; this condition is called aortic regurgitation.
Aortic regurgitation occasionally causes shortness of breath during normal activity.
This disturbed breathing pattern increases the risk of aortic dissection.
In cases involving a possible aortic dissection, the child may be given a TEE (transesophageal echocardiogram).
A child with Marfan may be given drugs called beta-blockers to slow down the rate of aortic enlargement and decrease the risk of dissection by lowering the blood pressure and decreasing the forcefulness of the heartbeat.
The most common surgical treatment involves replacing the child's aortic valve and several inches of the aorta itself with a composite graft, which is a prosthetic heart valve sewn into one end of a Dacron tube.
Many individuals with Williams syndrome have heart disorders, typically supravalvular aortic stenosis (SVAS), which is a narrowing of the aorta.
Supravalvular aortic stenosis (SVAS)-A narrowing of the aorta.
About 85 percent of all children and adults with COA have a double aortic valve (bicuspid aortic valve) in the heart.
The aortic arch is the first artery to carry blood as it leaves the heart.
High blood pressure (hypertension) affects parts of the body supplied by arteries that branch off the aortic arch above the narrowing.
The bicuspid aortic valve is usually present.
Complications in children who have not had surgery are hypertension, aortic rupture, intracranial bleeding, and congestive heart failure.
Undetected or untreated COA can also lead to early adulthood death due to congestive heart failure, systemic hypertension, coronary artery disease, and aortic aneurysm.
The most common obstruction defects are pulmonary valve stenosis, aortic valve stenosis, and coarctation of the aorta.
In aortic stenosis, the improperly formed aortic valve is narrowed.
Bicuspid aortic valve and subaortic stenosis are less common obstruction defects.
A bicuspid aortic valve has only two flaps instead of three, which can lead to stenosis in adulthood.
Subaortic stenosis is a narrowing of the left ventricle below the aortic valve that limits the flow of blood from the left ventricle.
Infants born with DiGeorge sequence can have heart defects such as a malformed aortic arch and tetralogy of Fallot.
It is sometimes used to treat aortic stenosis.
To correct aortic stenosis, the Ross procedure grafts the pulmonary artery to the aorta.
Defects such as coarctation of the aorta and aortic valve stenosis have the greatest risk of occurring in the child's offspring.
A catheter is passed through the needle across the fetus's aortic valve.
High blood pressure may be due to aortic constriction or to kidney abnormalities; however, in a majority of cases, no specific cause for high blood pressure can be identified.
As many as 15 percent of children with Turner syndrome have bicuspid aortic valves, where the major blood vessel from the heart has only two rather than three components to the valve regulating blood flow.
Because it is so dangerous, experts suggest early screening and surgery for aortic coarctation of the artery in girls with Turner syndrome.
Bicuspid aortic valves can deteriorate or become infected, so it is advised that all girls with Turner syndrome undergo annual cardiac evaluations.
Bicuspid aortic valve-A condition in which the major blood vessel from the heart has only two rather than three components to the valve regulating blood flow.