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Aortic dissection

Aortic dissection
Classification and external resources
Dissection of the descending part of the aorta (3), which starts from the left subclavian artery and extends to the abdominal aorta (4). The ascending aorta (1) and aortic arch (2) are not involved.
ICD-10 I71.0
ICD-9 441.0
OMIM 607086
DiseasesDB 805
MedlinePlus 000181
eMedicine emerg/28
  • Thoracic Aortic Aneurysms and Aortic Dissections

Aortic dissection occurs when a tear in the inner wall of the cardiac failure, and sometimes rupture of the aorta. Aortic dissection is more common in those with a history of high blood pressure, a known thoracic aortic aneurysm, and in a number of conditions that affect blood vessel wall integrity such as Marfan syndrome and the vascular subtype of Ehlers–Danlos syndrome. The diagnosis is made with medical imaging (computed tomography, magnetic resonance imaging or echocardiography).

The treatment of aortic dissection depends on the part of the aorta involved. Surgery is usually required for dissections that involve the aortic arch, while dissections of the part further away from the heart may be treated with blood pressure lowering only. Since the 1990s endovascular aneurysm repair (carried out from inside the blood vessels) has been used in specific cases.

Aortic dissection is relatively rare, occurring at an estimated rate of 2–3.5 per 100,000 people every year. It is more common in males for unknown reasons. Mean age at diagnosis is 63, although all age groups may be affected. Many cases of aortic dissection (40%) lead to death so rapidly that the person does not reach a hospital in time. The first case of aortic dissection described was in the post-mortem examination of King George II of Great Britain in 1760. Surgery for aortic dissection was introduced in the 1950s.


  • Signs and symptoms 1
    • Blood pressure 1.1
    • Aortic insufficiency 1.2
    • Myocardial infarction 1.3
    • Pleural effusion 1.4
  • Causes 2
  • Pathophysiology 3
  • Diagnosis 4
    • D-dimer 4.1
    • Chest X-ray 4.2
    • Computed tomography 4.3
    • MRI 4.4
    • Transesophageal echocardiography 4.5
    • Aortogram 4.6
    • Classification 4.7
      • DeBakey 4.7.1
      • Stanford 4.7.2
  • Prevention 5
  • Management 6
    • Medication 6.1
    • Surgical 6.2
    • Follow-up 6.3
  • Epidemiology 7
  • Prognosis 8
  • History 9
  • References 10
  • External links 11

Signs and symptoms

About 96% of individuals with aortic dissection present with severe pain that had a sudden onset. It may be described as tearing, stabbing, or sharp in character. 17% of individuals will feel the pain migrate as the dissection extends down the aorta. The location of pain is associated with the location of the dissection. Anterior chest pain is associated with dissections involving the ascending aorta, while interscapular (back) pain is associated with descending aortic dissections. If the pain is pleuritic in nature, it may suggest acute pericarditis caused by hemorrhage into the pericardial sac. This is a particularly dangerous eventuality, suggesting that acute pericardial tamponade may be imminent. Pericardial tamponade is the most common cause of death from aortic dissection.

While the pain may be confused with the pain of a myocardial infarction (heart attack), aortic dissection is usually not associated with the other signs that suggest myocardial infarction, including heart failure and ECG changes.

Individuals with aortic dissection who do not present with pain have chronic dissection.

Less common symptoms that may be seen in the setting of aortic dissection include congestive heart failure (7%), syncope (9%), stroke (6%), ischemic peripheral neuropathy, paraplegia, cardiac arrest, and sudden death.[1] If the individual had a syncopal episode, about half the time it is due to hemorrhage into the pericardium leading to pericardial tamponade.

Neurologic complications of aortic dissection (i.e., cerebrovascular accident (CVA) and paralysis) are due to involvement of one or more arteries supplying portions of the central nervous system.

If the aortic dissection involves the abdominal aorta, compromise of the branches of the abdominal aorta is possible. In abdominal aortic dissections, compromise of one or both renal arteries occurs in 5–8% of cases, while mesenteric ischemia (ischemia of the large intestines) occurs 3–5% of the time.

Blood pressure

While some patients with an aortic dissection have a history of hypertension, the blood pressure is quite variable at presentation with acute aortic dissection, and tends to be higher in individuals with a distal dissection. In individuals with a proximal aortic dissection, 36% present with hypertension, while 25% present with hypotension. In those who present with distal aortic dissections, 70% present with hypertension while 4% present with hypotension.

Severe hypotension at presentation is a grave prognostic indicator. It is usually associated with pericardial tamponade, severe aortic insufficiency, or rupture of the aorta. Accurate measurement of the blood pressure is important. Pseudohypotension (falsely low blood pressure measurement) may occur due to involvement of the brachiocephalic artery (supplying the right arm) or the left subclavian artery (supplying the left arm).

Aortic insufficiency

Aortic insufficiency (AI) occurs in half to two-thirds of ascending aortic dissections, and the murmur of aortic insufficiency is audible in about 32% of proximal dissections. The intensity (loudness) of the murmur is dependent on the blood pressure and may be inaudible in the event of hypotension.

There are multiple etiologies for AI in the setting of ascending aortic dissection. The dissection may dilate the annulus of the aortic valve, so that the leaflets of the valve cannot coapt. Another mechanism is that the dissection may extend into the aortic root and detach the aortic valve leaflets. The third mechanism is that if there was an extensive intimal tear, the intimal flap may prolapse into the LV outflow tract, causing intimal intussusception into the aortic valve preventing proper valve closure.

Myocardial infarction

Myocardial infarction (heart attack) occurs in 1–2% of aortic dissections. The etiology of the infarction is involvement of the coronary arteries (the arteries that supply the heart) in the dissection. The right coronary artery is involved more commonly than the left coronary artery. If the myocardial infarction is treated with thrombolytic therapy, the mortality increases to over 70%, mostly due to hemorrhage into the pericardial sac causing pericardial tamponade.

Because aortic dissection may present to the emergency room physician similar to a myocardial infarction, the physician must be careful to make the proper diagnosis prior to initiating treatment for myocardial infarction, since the treatment regimen for myocardial infarction can be lethal to an individual presenting with aortic dissection.

Pleural effusion

A pleural effusion (fluid collection in the space between the lungs and the chest wall or diaphragm) can be due to either blood from a transient rupture of the aorta or fluid due to an inflammatory reaction around the aorta. If a pleural effusion were to develop due to an aortic dissection, it is more commonly in the left hemithorax rather than the right hemithorax.


Aortic dissection is associated with hypertension (high blood pressure) and many connective tissue disorders. Vasculitis (inflammation of an artery) is rarely associated with aortic dissection. It can also be the result of chest trauma. 72 to 80% of individuals who present with an aortic dissection have a previous history of hypertension.

A bicuspid aortic valve (a type of congenital heart disease involving the aortic valve) is found in 7–14% of individuals who have an aortic dissection. These individuals are prone to dissection in the ascending aorta. The risk of dissection in individuals with bicuspid aortic valve is not associated with the degree of stenosis of the valve.

Marfan syndrome is noted in 5–9% of individuals who suffer from aortic dissection. In this subset, there is an increased incidence in young individuals. Individuals with Marfan syndrome tend to have aneurysms of the aorta and are more prone to proximal dissections of the aorta.

Turner syndrome also increases the risk of aortic dissection, by aortic root dilatation.[2]

Chest trauma leading to aortic dissection can be divided into two groups based on etiology: blunt chest trauma (commonly seen in car accidents) and iatrogenic. Iatrogenic causes include trauma during cardiac catheterization or due to an intra-aortic balloon pump.

Aortic dissection may be a late sequela of cardiac surgery. 18% of individuals who present with an acute aortic dissection have a history of open heart surgery. Individuals who have undergone aortic valve replacement for aortic insufficiency are at particularly high risk. This is because aortic insufficiency causes increased blood flow in the ascending aorta. This can cause dilatation and weakening of the walls of the ascending aorta.

Syphilis will only potentially cause aortic dissection in its tertiary stage.[3]


Blood penetrates the intima and enters the media layer.

As with all other arteries, the aorta is made up of three layers, the intima, the media, and the adventitia. The intima is in direct contact with the blood inside the vessel, and mainly consists of a layer of endothelial cells on a basement membrane; the media contains connective and muscle tissue, and the vessel is protected on the outside by the adventitia, comprising connective tissue.[4]

In an aortic dissection, blood penetrates the intima and enters the media layer. The high pressure rips the tissue of the media apart along the laminated plane splitting the inner 2/3 and the outer 1/3 of the media apart. This can propagate along the length of the aorta for a variable distance forward or backwards. Dissections that propagate towards the iliac bifurcation (with the flow of blood) are called anterograde dissections and those that propagate towards the aortic root (opposite of the flow of blood) are called retrograde dissections. The initial tear is usually within 100 mm of the aortic valve so a retrograde dissection can easily compromise the pericardium leading to a hemocardium. Anterograde dissections may propagate all the way to the iliac bifurcation of the aorta, rupture the aortic wall, or recanalize into the intravascular lumen leading to a double barrel aorta. The double barrel aorta relieves the pressure of blood flow and reduces the risk of rupture. Rupture leads to hemorrhaging into a body cavity and prognosis depends on the area of rupture. Retroperitoneal and pericardial ruptures are both possible.

Histopathological image of dissecting aneurysm of thoracic aorta in a patient without evidence of Marfan syndrome. The damaged aorta was surgically removed and replaced by artificial vessel. Victoria blue & HE stain.

The initiating event in an aortic dissection is a tear in the intimal lining of the aorta. Due to the high pressures in the aorta, blood enters the media at the point of the tear. The force of the blood entering the media causes the tear to extend. It may extend proximally (closer to the heart) or distally (away from the heart) or both. The blood will travel through the media, creating a false lumen (the true lumen is the normal conduit of blood in the aorta). Separating the false lumen from the true lumen is a layer of intimal tissue. This tissue is known as the intimal flap.

The vast majority of aortic dissections originate with an intimal tear in either the ascending aorta (65%), the aortic arch (10%), or just distal to the ligamentum arteriosum in the descending thoracic aorta (20%).

As blood flows down the false lumen, it may cause secondary tears in the intima. Through these secondary tears, the blood can re-enter the true lumen.

While it is not always clear why an intimal tear may occur, quite often it involves degeneration of the collagen and elastin that make up the media. This is known as cystic medial necrosis and is most commonly associated with Marfan syndrome and is also associated with Ehlers-Danlos syndrome.

In about 13% of aortic dissections, there is no evidence of an intimal tear. It is believed that in these cases the inciting event is an intramural hematoma (caused by hemorrhage within the media). Since there is no direct connection between the true lumen and the false lumen in these cases, it is difficult to diagnose an aortic dissection by aortography if the etiology is an intramural hematoma. An aortic dissection secondary to an intramural hematoma should be treated the same as one caused by an intimal tear.


Because of the varying symptoms and signs of aortic dissection depending on the initial intimal tear and the extent of the dissection, the proper diagnosis is sometimes difficult to make.

While taking a good history from the individual may be strongly suggestive of an aortic dissection, the diagnosis cannot always be made by history and physical signs alone. Often the diagnosis is made by visualization of the intimal flap on a diagnostic imaging test. Common tests used to diagnose an aortic dissection include a CT scan of the chest with iodinated contrast material and a trans-esophageal echocardiogram. The proximity of the aorta to the esophagus allows the use of higher-frequency ultrasound for better anatomic images. Other tests that may be used include an aortogram or magnetic resonance angiogram (MRA) of the aorta. Each of these tests have varying pros and cons and they do not have equal sensitivities and specificities in the diagnosis of aortic dissection.

In general, the imaging technique chosen is based on the pre-test likelihood of the diagnosis, availability of the testing modality, patient stability, and the sensitivity and specificity of the test.


A blood D-dimer level less than 500 ng/ml may be able to rule out the diagnosis of aortic dissection, avoiding the need for further imaging.[5] This only applies if the test is done within 24 hours of the onset of symptoms.[6] The American Heart Association does not advise using this test in making the diagnosis, as evidence is still tentative.[7]

Chest X-ray

Aortic dissection on CXR. Note is made of a wide aortic knob.

Widening of the mediastinum on an x-ray of the chest has moderate sensitivity in the setting of an ascending aortic dissection. However, it has low specificity, as many other conditions can cause a widening of the mediastinum on chest x-ray.

The calcium sign is a finding on chest x-ray that suggests aortic dissection. It is the separation of the intimal calcification from the outer aortic soft tissue border by 10 mm.

Pleural effusions may be seen on chest x-ray. They are more commonly seen in descending aortic dissections. If seen, they are typically in the left hemithorax.

Other findings include obliteration of the aortic knob, depression of the left mainstem bronchus, loss of the paratracheal stripe, and tracheal deviation.

About 12 to 20% of individuals presenting with an aortic dissection have a "normal" chest x-ray; therefore, a normal chest radiograph does NOT rule out aortic dissection. If the clinical index of suspicion is high, it is imperative to rule out dissection with another imaging modality (CT angiogram, MRA, aortogram, or transesophageal echo)

Computed tomography

CT with contrast demonstrating aneurysmal dilation and a dissection of the ascending aorta (Type A Stanford)

Computed tomography angiography is a fast non-invasive test that will give an accurate three-dimensional view of the aorta. These images are produced by taking rapid thin cut slices of the chest and abdomen, and combining them in the computer to create cross-sectional slices. In order to delineate the aorta to the accuracy necessary to make the proper diagnosis, an iodinated contrast material is injected into a peripheral vein. Contrast is injected and the scan performed using a Bolus Tracking method. This is a type of scan timed to an injection to capture the contrast as it enters the aorta. The scan will then follow the contrast as it flows though the vessel.

It has a sensitivity of 96 to 100% and a specificity of 96 to 100%. Disadvantages include the need for iodinated contrast material and the inability to diagnose the site of the intimal tear.


MRI of an aortic dissection
1 Aorta descendens with dissection
2 Aorta isthmus

Magnetic resonance imaging (MRI) is currently the gold standard test for the detection and assessment of aortic dissection, with a sensitivity of 98% and a specificity of 98%. An MRI examination of the aorta will produce a three-dimensional reconstruction of the aorta, allowing the physician to determine the location of the intimal tear, the involvement of branch vessels, and locate any secondary tears. It is a non-invasive test, does not require the use of iodinated contrast material, and can detect and quantitate the degree of aortic insufficiency.

The disadvantage of the MRI scan in the face of aortic dissection is that it has limited availability and is often located only in the larger hospitals, and the scan is relatively time consuming. Due to the high intensity magnetic fields used during MRI, an MRI scan is contraindicated in individuals with metallic implants. In addition, many individuals experience claustrophobia while in the MRI scanning tube.

Transesophageal echocardiography

An echocardiogram displaying the true lumen and false lumen of an aortic dissection. In the image to the left, the intimal flap can be seen separating the two lumens. In the image to the right, color flow during ventricular systole suggests that the upper lumen is the true lumen.

The transesophageal echocardiogram (TEE) is a relatively good test in the diagnosis of aortic dissection, with a sensitivity of up to 98% and a specificity of up to 97%. It has become the preferred imaging modality for suspected aortic dissection. It is a relatively non-invasive test, requiring the individual to swallow the echocardiography probe. It is especially good in the evaluation of AI in the setting of ascending aortic dissection, and to determine whether the ostia (origins) of the coronary arteries are involved. While many institutions give sedation during transesophageal echocardiography for added patient comfort, it can be performed in cooperative individuals without the use of sedation. Disadvantages of the TEE include the inability to visualize the distal ascending aorta (the beginning of the aortic arch), and the descending abdominal aorta that lies below the stomach. A TEE may be technically difficult to perform in individuals with esophageal strictures or varices.


An aortogram involves placement of a catheter in the aorta and injection of contrast material while taking x-rays of the aorta. The procedure is known as aortography. Previously thought to be the diagnostic "gold standard", it has been supplanted by other less invasive imaging modalities.


Classification of aortic dissection
Percentage 60% 10–15% 25–30%
Type DeBakey I DeBakey II DeBakey III
Stanford A (Proximal) Stanford B (Distal)

Several different classification systems have been used to describe aortic dissections. The systems commonly in use are based on either the anatomy of the dissection or the duration of onset of symptoms prior to presentation. The Stanford system is used more commonly now, as it is more attuned to the management of the patient.


The DeBakey system, named after surgeon and aortic dissection sufferer Michael E. DeBakey, is an anatomical description of the aortic dissection. It categorizes the dissection based on where the original intimal tear is located and the extent of the dissection (localized to either the ascending aorta or descending aorta, or involves both the ascending and descending aorta.[8]

  • Type I – Originates in ascending aorta, propagates at least to the aortic arch and often beyond it distally. It is most often seen in patients less than 65 years of age and is the most lethal form of the disease.
  • Type II – Originates in ascending aorta and is confined to the ascending aorta.
  • Type III – Originates in descending aorta, rarely extends proximally but will extend distally. It most often occurs in elderly patients with atherosclerosis and hypertension.


The Stanford classification is divided into two groups; A and B depending on whether the ascending aorta is involved.[9]

  • A – Involves the ascending aorta and/or aortic arch, and possibly the descending aorta. The tear can originate in the ascending aorta, the aortic arch, or, more rarely, in the descending aorta. It includes DeBakey types I and II.
  • B – Involves the descending aorta or the arch (distal to the left subclavian artery), without involvement of the ascending aorta. It includes DeBakey type III.

The Stanford classification is useful as it follows clinical practice, as type A ascending aortic dissections generally require primary surgical treatment whereas type B dissections generally are treated medically as initial treatment with surgery reserved for any complications.

The reason for surgical repair of Type A dissections is that ascending aortic dissections often involve the aortic valve, which, having lost its suspensory support, telescopes down into the aortic root, resulting in aortic incompetence. This needs resuspending to reseat the valve and repair / prevent coronary artery injury. Also the area of dissection is removed and replaced with a Dacron graft to prevent further dissection from occurring. However type B dissections are not improved, from a mortality point of view, by operation, unless there is leaking, rupture or compromise to other organs, e.g. kidneys.


Chronic enlargement of the ascending aorta from aneurysm or previously unrecognized and untreated aortic dissections is repaired electively when it reaches 6 cm (2.4 in) in size and surgery may be recommended between for as little as 4.5 cm (1.8 in) in size if the patient has one of several connective-tissue disorders or a family history of ruptured aorta.


In an acute dissection treatment choice depends on its location. For Stanford type A (ascending aortic) dissection, surgical management is superior to medical management. For uncomplicated Stanford type B (distal aortic) dissections (including abdominal aortic dissections), medical management is preferred over surgical.

The risk of death due to aortic dissection is highest in the first few hours after the dissection begins, and decreases afterwards. Because of this, the therapeutic strategies differ for treatment of an acute dissection compared to a chronic dissection. An acute dissection is one in which the individual presents within the first two weeks. If the individual has managed to survive this window period, his prognosis is improved. About 66% of all dissections present in the acute phase. Individuals who present two weeks after the onset of the dissection are said to have chronic aortic dissections. These individuals have been self-selected as survivors of the acute episode, and can be treated with medical therapy as long as they are stable.


Aortic dissection generally presents as a hypertensive emergency, and the prime consideration of medical management is strict blood pressure control. The target blood pressure should be a mean arterial pressure (MAP) of 60 to 75 mmHg, or the lowest blood pressure tolerated by the patient. Another factor is to reduce the shear-force dP/dt (force of ejection of blood from the left ventricle).

Beta blockers are first line treatment for patients with acute and chronic aortic dissection. In acute dissection, rapidly acting, titratable parenteral agents (such as esmolol, propranolol, or labetalol) are preferred. Vasodilators such as sodium nitroprusside can be considered for patients with ongoing hypertension, but they should never be used alone, as they generally cause reflex tachycardia.

Calcium channel blockers can be used in the treatment of aortic dissection, particularly if there is a contraindication to the use of beta blockers. The calcium channel blockers typically used are verapamil and diltiazem, because of their combined vasodilator and negative inotropic effects.

If the individual has refractory hypertension (persistent hypertension on the maximum doses of three different classes of antihypertensive agents), involvement of the renal arteries in the aortic dissection plane should be considered.


Indications for the surgical treatment of aortic dissection include an acute proximal aortic dissection and an acute distal aortic dissection with one or more complications. Complications include compromise of a vital organ, rupture or impending rupture of the aorta, retrograde dissection into the ascending aorta, and a history of Marfan syndrome or Ehlers-Danlos Syndrome.

The objective in the surgical management of aortic dissection is to resect (remove) the most severely damaged segments of the aorta, and to obliterate the entry of blood into the false lumen (both at the initial intimal tear and any secondary tears along the vessel). While excision of the intimal tear may be performed, it does not significantly change mortality.

Some methods of repair are:

  • Replacement of the damaged section with a tube graft (often made of dacron) when there is no damage to the aortic valve.
  • Bentall procedure — Replacement of the damaged section of aorta and replacement of the aortic valve.
  • David procedure — Replacement of the damaged section of aorta and reimplantation of the aortic valve.
  • Insertion of a stent graft (covered stent), e.g. in TEVAR (thoracic endovascular aortic repair). It is usually combined with on-going medical management
  • Replacement of the damaged section of aorta with a sutureless vascular ring connector-reinforced dacron graft. Vascular ring connector (VRC) is a titanic ring used as a stent in the vascular graft to achieve a quick, blood-sealed, and sutureless anastomosis. There are two furrows on the surface of the ring for fixation of the vascular graft and the aorta. The tapes used to tie against the ring provide a larger contact surface area than the traditional stitches, thus provides stronger anastomosis and better surgical results.

A number of comorbid conditions increase the surgical risk of repair of an aortic dissection. These include:

  • Prolonged pre-op evaluation (increased length of time prior to surgery)
  • Advanced age
  • Comorbid disease states (e.g.: coronary artery disease)
  • Aneurysm leakage
  • Cardiac tamponade
  • Shock
  • Past history of myocardial infarction or CVA
  • History of renal failure (either acute or chronic renal failure)


Closure of the lumen of a Type B aortic dissection following medical management

The long term follow-up in individuals who survive aortic dissection involves strict blood pressure control. The relative risk of late rupture of an aortic aneurysm is 10 times higher in individuals who have uncontrolled hypertension, compared to individuals with a systolic pressure below 130 mmHg.

The risk of death is highest in the first two years after the acute event, and individuals should be followed closely during this time period. 29% of late deaths following surgery are due to rupture of either the dissecting aneurysm or another aneurysm. In addition, there is a 17% to 25% incidence of new aneurysm formation. This is typically due to dilatation of the residual false lumen. These new aneurysms are more likely to rupture, due to their thinner walls.

Serial imaging of the aorta is suggested, with MRI being the preferred imaging technique.


It has been difficult to establish the incidence of aortic dissection because many cases are only diagnosed after death (which may have been attributed to another cause), and is often initially misdiagnosed. It is estimated that aortic dissection affects 2–3.5 people out of every 100,000 every year. Studies from Sweden suggest that the incidence of aortic dissection may be rising. Men are more commonly affected than women: 65% of all people with aortic dissection are male. The mean age at diagnosis is 63 years.[4] In females before the age of 40, half of all aortic dissections occur during pregnancy (typically in the 3rd trimester or early postpartum period).


Of all people with aortic dissection, 40% die almost straight away and do not reach hospital in time. Of the remainder, 1% die every hour, making prompt diagnosis and treatment a priorty. Even after diagnosis, 5–20% die during surgery or in the immediate postoperative period.[4] In ascending aortic dissection, if there is a decision that surgery is not appropriate, 75% die within 2 weeks. With aggressive treatment 30-day survival for thoracic dissections may be as high as 90%.[10]


The earliest fully documented case of aortic dissection is attributed to

  • Thoracic aortic disease coalition, American advocacy group

External links

  1. ^ Sheikh, AS; Ali, K; Mazhar, S (Sep 3, 2013). "Acute aortic syndrome.". Circulation 128 (10): 1122–7.  
  2. ^ Practice Committee of the American Society for Reproductive Medicine (Nov 2006). "Increased maternal cardiovascular mortality associated with pregnancy in women with Turner syndrome". Fertil Steril. 86 (5 Suppl): S127–8.  
  3. ^ Kamalakannan D, Rosman HS, Eagle KA (October 2007). "Acute aortic dissection". Crit Care Clin 23 (4): 779–800, vi.  
  4. ^ a b c Hiratzka LF, Bakris GL, Beckman JA, et al. (April 2010). "2010 ACCF/AHA/AATS/ACR/ASA/SCA/SCAI/SIR/STS/SVM guidelines for the diagnosis and management of patients with Thoracic Aortic Disease: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines, American Association for Thoracic Surgery, American College of Radiology, American Stroke Association, Society of Cardiovascular Anesthesiologists, Society for Cardiovascular Angiography and Interventions, Society of Interventional Radiology, Society of Thoracic Surgeons, and Society for Vascular Medicine". Circulation 121 (13): e266–369.  
  5. ^ Shimony, A; Filion, KB, Mottillo, S, Dourian, T, Eisenberg, MJ (2011-04-15). "Meta-analysis of usefulness of d-dimer to diagnose acute aortic dissection". The American journal of cardiology 107 (8): 1227–34.  
  6. ^ Bossone, E; Suzuki, T; Eagle, KA; Weinsaft, JW (May 2013). "Diagnosis of acute aortic syndromes : imaging and beyond.". Herz 38 (3): 269–76.  
  7. ^ Bruce M. Lo (December 2013). "An Evidence-Based Approach To Acute Aortic Syndromes". Emergency Medicine Practice 15 (12). 
  8. ^ DeBakey ME, Henly WS, Cooley DA, Morris GC Jr, Crawford ES, Beall AC Jr (Jan 1965). "Surgical management of dissecting aneurysms of the aorta".  
  9. ^ Daily PO, Trueblood HW, Stinson EB, Wuerflein RD, Shumway NE (Sep 1970). "Management of acute aortic dissections". Ann Thorac Surg. 10 (3): 237–47.  
  10. ^ Woo KM, Schneider JI (November 2009). "High-risk chief complaints I: chest pain--the big three". Emerg. Med. Clin. North Am. 27 (4): 685–712, x.  
  11. ^ Nicholls F (1761). "Observations concerning the body of his late majesty". Philosophical Transactions of the Royal Society 52: 265–274.  
  12. ^ a b c d Criado FJ (2011). "Aortic dissection: a 250-year perspective". Tex Heart Inst J 38 (6): 694–700.  
  13. ^ a b c Leonard JC (July 1979). "Thomas Bevill Peacock and the early history of dissecting aneurysm". Br Med J 2 (6184): 260–2.  
  14. ^ Altman LK (2006-12-25). "The Man on the Table Devised the Surgery". New York Times. Retrieved 2013-05-27. 


Surgery for aortic dissection was first introduced and developed by Michael E. DeBakey, Denton Cooley and Oscar Creech, cardiac surgeons associated with the Baylor College of Medicine, Houston, Texas in 1954. DeBakey developed aortic dissection himself at age 97 in 2005,[12] and underwent surgery in 2006.[14] Endovascular treatment of aortic dissection was developed in the 1990s.[12]

[13] The characteristic symptom of tearing pain in the chest was recognised in 1855, when a case was diagnosed in life.[13] contributed to the understanding of the condition by publishing two series of the cases described in the literature so far: nineteen cases in an 1843 review, and eighty in 1863.Thomas Bevill Peacock London cardiologist [13][12] labelled the condition "dissecting aneurysm".René Laennec The term "aortic dissection" was introduced by the French physician J.P. Maunoir in 1802, and [12][11]

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