Pseudoaneurysms
CASE 10-1
Aortic pseudoaneurysm after avr with anterior extension
This 41-year-old man with Reiter’s syndrome underwent mechanical aortic valve replacement 9 years ago for aortic regurgitation. Four months ago he developed prosthetic valve endocarditis. He was treated with antibiotics and repeat aortic valve replacement with that procedure complicated by a paravalvular abscess requiring placement of a pericardial patch in the periannular region. Postoperatively, he had persistent paravalvular regurgitation and repeat echocardiography showed “rocking” of the prosthesis and a possible pseudoaneurysm. A preoperative transesophageal echocardiogram demonstrated valve dehiscence with blood flow from the aorta into an anterior echo-free space that also communicated with the left ventricle. He was referred for surgery.
CASE 10-2
Aortic pseudoaneurysm after AVR with posterior extension
12 years prior to admission, this 44-year-old male underwent bioprosthetic AVR for endocarditis. Seven years later he underwent redo sternotomy and second replacement for aortic valve bioprosthesis failure. Four days prior to this admission he developed increasing shortness of breath, and presented to the Emergency Department where examination showed pulmonary edema and lab data including an elevated B-type natriuretic peptide level of 386 pg/mL (Normal <101). TTE and TEE revealed a dilated LV with severe aortic regurgitation and an unstable bioprosthesis with posterior dehiscence and a posterior aortic pseudoaneurysm. His EF was 50-55%. He denied chest pain, syncope, PND, orthopnea, swelling, significant DOE, fevers, chills, nausea, vomiting, diarrhea, and rash. At surgery, the prosthetic valve was explanted, the opening to the pseudoaneurysm patched, and a new bioprosthetic valve placed.
CASE 10-3
Aortic pseudoaneurysm after ascending aortic graft dehiscence
This 43-year-old male originally presented 2 years before the current admission with an acute Type A aortic dissection that originated above the aortic valve and extended to the iliac bifurcation. At that time his ascending aorta was replaced with a tube graft and the native aortic valve preserved. He was readmitted to our institution with chest pain and Staph aureus bacteremia. CT scan revealed a large mediastinal hematoma; anterior and posterior pseudoaneurysms were seen at the proximal end of the aortic graft.
Comments
A pseudoaneurysm is a contained aortic rupture that may be due to infection of an aortic valve prosthesis with abscess formation and tissue destruction or to dehiscence of a suture line at the anastomosis of an aortic tube graft. At the site of rupture, adhesions and scarring limit the extravasation of blood resulting in a contained space. In most cases, the only communication is from the aorta into the pseudoaneurysm space. However, when valve dehiscence extends both above and below the valve plane, blood enters the pseudoaneurysm from the aorta, and exits into the LV outflow tract, simulating aortic regurgitation. In contrast to a true aneurysm, the walls of a pseudoaneurysm are not composed of aortic tissue. Because a pseudoaneurysm is due to rupture of the aorta, albeit “contained,” treatment is surgical.
Suggested reading
- 1.
Evangelista A: Imaging aortic aneurysmal disease, Heart 100:909–915, 2014.
- 2.
Ekici F, Kocabaş A, Aktaş D, etin I, Eminoğlu S: Native aortic valve endocarditis complicated by pseudoaneurysm of mitral-aortic intervalvular fibrosa, Echocardiography 31:E60–E63, 2014.
Aortic dissection
CASE 10-4
Ascending and aortic arch dissection
This 57-year-old male patient presented to an outside hospital with the sudden onset of substernal chest pain, described as constant, nonradiating, and worse with movement. He had not had similar pain in the past. He denied trauma, shortness of breath, nausea, vomiting, numbness, tingling, weakness, back pain, abdominal pain, or syncope. His only risk factor for coronary disease was hypertension. He was taken urgently to the cardiac catheterization laboratory for what was suspected acute myocardial infarction and was found to have a normal left coronary system. The right coronary system could not be engaged; however, a dissection flap was seen in the ascending aorta. The patient urgently underwent computed tomographic angiography (CTA) of the aorta demonstrating an acute Type A aortic dissection extending from the aortic sinuses into the ascending aorta, around the arch and down into the descending thoracic aorta. The diameter of the aortic sinuses was severely enlarged at 5.3 cm. At the time of the CTA scan, there was no significant pericardial effusion or involvement of the head vessels. The patient was transferred to our institution for definitive management. At surgery, the aortic sinuses and ascending aorta were resected, and replaced with a composite valve, root, and aortic graft. The coronary arteries were implanted into the graft.
Comments
The initial diagnosis of acute aortic dissection often is made with CTA imaging because this modality is rapidly available 24/7 at most medical centers with an ED. Both CTA and MRI are equivalent to TEE in terms of sensitivity and specificity and both have the advantage of allowing evaluation of distal vessels and a wide field of view in the mediastinum. The choice of diagnostic modality in an individual patient often depends on the speed with which the study can be obtained and the expertise of each particular institution. Once the diagnosis is made, the patient is rapidly transferred or moved to the OR with minimal additional interim evaluation.
The echocardiographic diagnosis of aortic dissection is based on visualization of a linear mobile echogenic structure within the aortic lumen, such as the initial flap. It is particularly important to evaluate the ascending aorta because treatment of a dissection that involves the ascending aorta (Type A) is surgery whereas treatment of a dissection limited to the descending aorta (Type B) often is medical.
On echocardiography, imaging artifacts may share some features of an aortic dissection so the echocardiographer should ensure that the mobile intraluminal echo is not due to reverberations. Dissection flaps may be missed if image quality is poor or if there is limited visualization of any aortic segment. The interface between the innominate vein and the aortic arch may be mistaken for a dissection flap. However, with a careful examination by an experienced echocardiography, TEE has a sensitivity of about 98% with a specificity of 98% for diagnosis of aortic dissection.
The TEE performed in the OR thus is critical in defining the exact location and extent of dissection, involvement of the coronary artery ostia, and the presence of a pericardial effusion (implying impending aortic rupture). The TEE also can evaluate aortic valve anatomy to identify those with a bicuspid valve and to evaluate the degree of aortic regurgitation. Even if evaluated before arriving in the OR, the clinical situation changes rapidly with aortic dissection so that reevaluation is critical. The baseline TEE is also helpful in surgical planning: when severe sinus dilation is present as in this case, the possibility of a connective tissue disorder (such as Marfan syndrome) must be considered. These patients require a Bentall procedure with stabilization of the aortic annulus, replacement of the sinuses as well as ascending aorta, valve replacement, and coronary reimplantation. In patients with an ascending aortic dissection but normal sinuses, the native aortic valve may be resuspended at the proximal anastomosis of the ascending aorta graft repair.
Suggested reading
- 1.
Tan CN, Fraser AG: Perioperative transesophageal echocardiography for aortic dissection, Can J Anesth 61:362–378, 2014.
- 2.
Pape LA, Awais M, Woznicki EM, et al: Presentation, diagnosis, and outcomes of acute aortic dissection: 17-year trends from the International Registry of Acute Aortic Dissection, J Am Coll Cardiol 66:350–358, 2015.
CASE 10-5
Bicuspid valve and aortic dissection
This 50-year-old man presented with the acute onset of bilateral leg weakness and numbness when lifting weights. His initial examination was unremarkable and he was discharged from the ED. Several days later he once again presented to hospital with persistent symptoms, but also with nausea and vomiting and bloody stools. Laboratory work revealed acute renal injury and elevated liver function tests. CTA revealed an aortic dissection flap that extended from the ascending aorta to the iliac bifurcation.
The patient underwent an aortic root and valve replacement using a composite graft with an aortic valve bioprosthesis and coronary reimplantation.
Comments
A congenitally bicuspid aortic valve is present in 1% to 2% of the entire population. Bicuspid aortic valve disease is not confined to the valve leaflets; the aorta also is abnormal. Histopathologic studies now support an underlying connective tissue disease process with elastin fragmentation, irregularities in smooth muscle integrity, and increased collagen deposition. Compared with normal adults with a trileaflet aortic valve, bicuspid aortic valve patients have larger dimensions of the aortic sinuses and ascending aorta, abnormal aortic elasticity, are at risk for progressive aortic dilation, and have an estimated age-adjusted relative risk of dissection of 8.4 compared with patients with a trileaflet valve, corresponding to an absolute risk of 3.1 cases per 10,000 patient-years. The risk factors for aortic dissection in bicuspid valve patients remain unclear but may include the specific morphology of the valve, in addition to a family history of dissection. In patients with a known bicuspid valve, periodic imaging is recommended for assessment of aortic size either with echocardiography (if the aorta is well seen) or with CT or MRI imaging. Prophylactic aortic root replacement is recommended when aortic diameter exceeds 5.5 cm if there are no other risk factors, and 5.0 cm if there is rapid progression or a family history of dissection.
Suggested reading
- 1.
Wojnarski CM, Svensson LG, Roselli EE, et al: Aortic dissection in patients with bicuspid aortic valve-associated aneurysms, Ann Thorac Surg 100:1666–1674, 2015.
- 2.
Adamo L, Braverman AC: Surgical threshold for bicuspid aortic valve aneurysm: a case for individual decision-making, Heart 101:1361–1367, 2015.
- 3.
Detaint D, Michelena HI, Nkomo VT, et al: Aortic dilatation patterns and rates in adults with bicuspid aortic valves: a comparative study with Marfan syndrome and degenerative aortopathy, Heart 100:126–134, 2014.
- 4.
Michelena HI, Khanna AD, Mahoney D, et al: Incidence of aortic complications in patients with bicuspid aortic valves, JAMA 306:1104–1112, 2011.
- 5.
Schaefer BM, Lewin MB, Stout KK, et al: The bicuspid aortic valve: an integrated phenotypic classification of leaflet morphology and aortic root shape, Heart 94:1634–1638, 2008.