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Cardiology

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Answer
Pseudoaneurysm   well defined collection of blood & conn tissue outside vessel wall  
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Most common site of AAA formation:   infrarenal abdominal aorta  
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Atherosclerotic dz of aorta may produce:   stenotic obstruction or aneurysmal dilatation  
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Aneurysm types   Saccular; fusiform  
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Most common aneurysm type   Fusiform: symmetrical dilation (involves full circumference of aortic wall)  
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Aneurysm defn:   1.5x or > the normal diameter of the vessel.  
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Aneurysm type: comparative prevalence   Abdominal (85%) > thoracic aneurysm (15%)  
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Half of newly detected AAAs are:   <5cm (& 2/3 eventually require repair)  
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AAAs usually involve:   aortic bifurcation (& often involve common iliac arteries)  
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AAA & Rupture   80% rupture into left retroperitoneum (may contain it); remainder rupture into peritoneal cavity (=> uncontrolled hemorrhage & rapid circulatory collapse)  
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Healthy, young normal aorta: size   about 2 cm  
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Considered Aneurysm at size:   > 3 cm  
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AAAs arise in areas of:   dense athero-sclerosis, eroding & weakening the wall which leads to dilatation then rupture  
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90% of AAAs originate where:   below renal arteries (infrarenal); 10% suprarenal  
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Infrarenal aneurysm may exhibit:   stenosis (narrowing) of aorta  
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AAA: Surgery recommended when:   >5 cm; women: appropriate at 4.5 - 5.0 cm  
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Decline of aortic elasticity & distensibility is accelerated in pts with:   HTN, hyperlipidemia, & atherosclerosis of coronaries & other arteries.  
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AAA: Risk Factors   Tobacco; Age; HTN; lipid; Atherosclerosis; Male; FH  
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FH in AAA:   1/4 of AAA pts have first degree relative with hx of AAA  
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AAA Risk Factors for Rupture   Size (5cm female, 6 cm male); rapid progression (>1cm/yr); female; FH; unctrld HTN; SMK; COPD  
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AAA: what may prompt earlier endovasc repair?   Rapid expansion (>1 cm/yr) & pt preference (in 4.5-5.5 cm range)  
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AAA Prognosis   80% mortality with rupture  
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Cystic medial necrosis occurs most frequently in:   ascending aorta; aortic wall weakening => fusiform aneurysm  
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Cystic medial necrosis assoc with:   conn tissue dz (Marfan, Ehlers-Danlos syndrome, RA); aortic valve replacement  
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Asc TA: Etiologies   CMN, Bicuspid valve; AI; Arteritis/ Vasculitis; Collagen vasc dz (RA, Marfan, Ehlers-Danlos, Reiter); HTN; Syphilis; Atherosclerosis  
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Desc TA: predominant cause =   atherosclerosis  
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Desc TA: called thoracoabdominal if they:   extend below level of diaphram into abd aorta  
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TAA: Tx: >5 cm   surgery (if Sx or rapid expansion: then sooner)  
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TAA: Clinical Findings   > 50% pts ASx at dx; Sx due to vascular consequence or mass effect  
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TAA: if surgery required, need:   coronary angiography  
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TAA: Inc rupture risk at smaller diameters with:   Marfan; bicuspid valve  
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TAA: Asc Aorta: surgery indicated at:   ≥ 5.5 cm (=/> 5.5)  
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TAA Marfan/ Bicuspid Valve: surgery indicated at:   ≥ 5.0 cm (=/> 5.0)  
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TAA Aortic valve replacement: surgery indicated at:   ≥ 4.0 cm (=/> 4.0)  
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TAA Desc Aorta: surgery indicated at:   ≥ 6.0 cm (=/> 6.0)  
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TAA: Prognosis   M&M higher than with AAA; 5 yr if unrepaired (>6 cm) is 20-25% (most deaths due to rupture or CAD)  
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Aortic dissection: usual direction of extension   antegrade (driven by the forward force of aortic blood flow); sometimes retrograde from site of intimal tear  
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Aortic dissection: intimal tear in aorta creates a false lumen between:   media & adventitia  
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Aortic dissection: >95% occur in the:   Ascend aorta just distal to aortic valve or just distal to left subclavian at ligamentum arteriosum  
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Aortic Dissection: Increased risk in:   pregnancy (1/4 of all female cases <40 yrs & most in last trimester); conn tissue dz (Marfan, Ehlers Danlos); Bicuspid Aortic Valve or Coarctation  
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Aortic Dissection: Debakey I =   Ascending A extending to distal  
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Aortic Dissection: Debakey II =   Ascending aorta only  
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Aortic Dissection: Debakey III =   Descending aorta only  
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Aortic Dissection: Stanford A =   Any involvement of ascending aorta  
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Aortic Dissection: Stanford B =   Not involving ascending aorta  
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Aortic Dissection: Proximal =   DeBakey Types I & II or Stanford Type A  
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Aortic Dissection: Distal =   DeBakey Type III & Stanford type B  
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Aortic Dissection: Clinical Findings   Acute: sudden, severe excruciating ripping chest pain (ascending) or scapular (descending); most hypertensive or nml  
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Aortic Dissection: PE   Increased or decreased BP; pt may be in shock; wide pulse pressure; diminished / asymmetric peripheral pulses; aortic insufficiency murmur if ascending aorta; syncope  
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Aortic Dissection: poss Sx devt   Acute aortic regurgitation (CHF indicates valve involvement); focal neuro (CVA may develop)  
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Aortic Dissection: mgmt: Type A =   Surgical repair, may require AVR  
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Aortic Dissection: mgmt: Type B =   Medical therapy (IV propranolol or nitroprusside)  
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Aortic Dissection: mgmt: All pts =   aggressive BP control; yearly imaging or if increased Sx  
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Aortic Dissection: Prognosis   Op mortality of type B 2x that of type A (bc comorbid illness); 30% have prog enlarging aneurysm that eventually req repair  
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Sudden onset ripping, tearing chest pain, diminished pulses =   Aortic dissection  
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Flank pain, hypotension, pulsatile abdominal mass =   AAA  
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RF/etiology of ascending aortic aneurysm:   CMT (cystic medial necrosis)  
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RF for TAA/AAA:   In order: tobacco, age, HTN, HLD, other atherosclerosis  
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2 components of Aorta   thoracic (ascending, arch, descending); Abdominal  
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3 layers of aorta:   Intima; Media; Adventitia  
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Intima:   thin, inner layer (delicate, easily traumatized)  
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Media:   thick middle layer (*strength of the aorta comes from media)  
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Adventitia:   somewhat thin outer layer (contains mainly collagen)  
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Strength of the aorta lies in:   media (= laminated, intertwining elastic tissue/ multiple layers, in a spiral manner, max tensile strength w/ distensible & elastic  
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Pseudoaneursym   well defined collection of blood & conn tissue outside vessel wall  
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Atherosclerotic vs inflammatory   inflame = extreme of atherosclerotic aneurysm  
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pathogenesis of AAAs:   multifactorial: genetic, environ, hemodynamic & immunological; Chlamydia pneumoniae?  
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Aorta most affected by atherosclerotic process:   infrarenal abdominal aorta  
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most common site of AAA formation:   infrarenal abdominal aorta  
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Atherosclerotic dz of aorta may produce:   stenotic obstrusion or aneurysmal dilatation  
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Aneurysm types   Saccular; fusiform  
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Most common aneurysm type   Fusiform  
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Has a fairly symmetrical dilation (involves full circumference of aortic wall)   Fusiform  
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More localized dilation (outpouching of a portion of aortic wall)   Saccular aneurysms  
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Flow disturbance thru the aneurysmal aortic segment:   blood may stagnate along walls, cause mural thrombus (may embolize)  
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Aneurysm defn:   1.5x or > the normal diameter of the vessel.  
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Aneurysm type cf prevalence   Abdominal more common than thoracic aneurysm  
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Half of newly detected AAAs are:   <5cm (& 2/3 eventually require repair)  
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AAA & COPD:   COPD pts: rupture of smaller AAAs more likely  
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AAAs usually involve:   aortic bifurcation (& often involve common iliac arteries)  
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AAA & Rupture   80% rupture into left retroperitoneum (may contain it); remainder rupture into peritoneal cavity (=> uncontrolled hemorrhage & rapid circulatory collapse)  
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Healthy, young normal aorta: size   about 2 cm  
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Considered Aneurysm at size:   > 3 cm  
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AAA Incidence in Men vs Women   10:1  
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AAA: men over 55   2%  
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AAAs arise in areas of:   dense athero-sclerosis, eroding & weakening the wall which leads to dilatation then rupture  
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90% of AAAs originate where:   below renal arteries (infrarenal); 10% suprarenal  
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Infrarenal aneurysm may exhibit:   stenosis (narrowing) of aorta  
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AAA: Surgery recommended when:   >5 cm or if growing >0.5cm in 6 months or >1cm per year  
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Decline of aortic elasticity & distensibility is accelerated in pts with:   HTN, hyperlipidemia, & atherosclerosis of coronaries & other arteries.  
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Loss of aortic elasticity   loss of elastin & increase in collagen (=> lack of distensibility)  
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AAA: Risk Factors   Tobacco; Age; HTN; lipid; Atherosclerosis; Male; FH  
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FH in AAA:   1/4 of AAA pts have first degree relative with hx of AAA  
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Initial dx test to screen for & follow known AAA =   Abdominal US:  
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Abdominal US: advantages   100% sensitivity, no contrast, low cost  
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AAA: CT scan   pre-op or if US indeterminate; better defines shape & location/ extent of AAA  
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AAA: Catheter aortography may:   underestimate diameter  
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AAA Risk Factors for Rupture   Size (5cm female, 6 cm male); rapid progression (>1cm/yr); female; FH; unctrld HTN; SMK; COPD  
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AAA Surveillance   Trend: bigger AAA, more frequent surveil  
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AAA: for average risk pts, a threshold of ?? cm in diameter is appropriate for elective repair   5.5 cm  
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AAA: what may prompt earlier endovasc repair?   Rapid expansion (>1 cm/yr) & pt preference (in 4.5-5.5 cm range)  
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AAA Endovascular repair: No justification for:   endovascular repair at smaller diameters  
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AAA: for women, elective endovasc repair is appropriate at:   4.5 or 5.0 cm  
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AAA Prognosis   80% mortality with rupture  
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AAA mgmt:   Risk factor mod (stop SMK, aggressive HTN & Lipid Rx), med mgmt to slow progression  
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AAA operative mortality:   Elective = 2-5%, Expanding = 5-15%, Ruptured: >50%  
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Criteria for Endovascular Repair: Proximal neck:   length: min 15 mm; diameter: max 28 mm; angulation: <60 degrees  
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Criteria for Endovascular Repair: Iliac arteries   Common iliac a.: variable diameters; ext iliac a. <7 mm  
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USPSTF Screening Guidelines for AAA: repair what in who?   large AAA (> 5.5 cm) in men btw 65-75 w/ Hx of SMK; No gdln for men 65-75 no hx SMK; gdln against screen in women  
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USPSTF AAA Screen Consensus stmt   All M 60-85; All F 60-85 w/ 1 or more CVD risk factor; M&F > 50 w/ FH AAA  
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Thoracic aneurysm: prevalence   Far less common than AAAs  
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Thoracic aneurysm: classified by:   pt of aorta involved ( ascending, arch or descending TA)  
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Thoracoabdominal AA =   desc TA extends distally to involve AA  
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TAA: prevalence   Less common than AAA w/ diff pathogenesis; 60% = aortic root & ascend A; 40% desc A; 10% arch  
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Sm mx cell drop out & elastic fiber degen w/ media of cystic spaces filled w/ mucoid matl =   Cystic medial necrosis  
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Cystic medial necrosis occurs most frequently in:   ascending aorta  
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Cystic medial necrosis leads to:   aortic wall weakening => fusiform aneurysm  
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Aneurysm from cystic medial necrosis often involve:   aortic root & may consequently result in AI  
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CMN is accelerated by:   HTN (occurs somewhat w/ aging)  
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CMN assoc with:   conn tissue dz (Marfan, Ehlers-Danlos syndrome, RA); aortic valve replacement  
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Ascending TA: Etiologies   CMN, Bicuspid valve; AI; Arteritis/ Vasculitis; Collagen vasc dz (RA, Marfan, Ehlers-Danlos, Reiter); HTN; Syphilis; Atherosclerosis  
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Ascending aneurysms usually caused by:   CMN  
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If Asc aneurysm due to atherosclerosis, assoc with:   diffuse aortic atherosclerosis  
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Aortic Arch aneurysms often contiguous with:   aneurysms of asc OR desc A & can be caused by any of the etiologies above.  
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Desc TA: predominant cause =   atherosclerosis  
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Desc TA: tend to originate:   just distal to origin of L subclavian; may be fusiform or accular  
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Aortic Arch Aneurysm: Etiologies   Ext of Asc or Desc aneurysms; Hx trauma or deceleration injury  
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Desc TA: called thoracoabdominal if they:   extend below level of diaphram into abd aorta  
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TAA: Spontaneous rupture prevalence   less common than AAA (bc inc of Sx due to compression of surrounding structures)  
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TAA: Tx: >5 cm   surgery (if Sx or rapid expansion: then sooner)  
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Sx pts or w/ AI:   Inc incidence of rupture  
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TAA: Clinical Findings   > 50% pts ASx at dx; Sx due to vascular consequence or mass effect  
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TAA: Vascular Sx   AI with CHF, or thromboembolism causing stroke, lower extremity or mesenteric ischemia, renal infarct  
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TAA: Mass Effect   SVC syndrome, tracheal deviation, cough, hemoptysis, dysphagia, hoarseness  
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Ascending or arch An can cause compression of:   SVC or innominate v. => obstruction of venous return  
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Desc/ arch An: may cause compression of:   trachea or main stem bronchus => tracheal deviation, wheezing, cough & positional dyspnea, hemoptysis or recurrent pneumonitis  
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Desc/ arch An: Compression of esophagus can cause:   dysphagia & compression of recurrent laryngeal n. can cause hoarseness  
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TAA: Clinical Findings   Pain ( 25% pts) from direct compression of intrathoracic structures or chest wall; substernal or in back/ neck; steady, deep & severe?  
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TAA Rupture:   excruciating pain; may be assoc w/ aortic dissection  
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Rupture occurs most commonly into:   L intrapleural space or mediastinum; results in severe hypotension  
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Desc An rupture into:   adjacent esophagus => life threatening hematemesis  
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TAA Evaluation   CXR (only rule in, cannot R/O); Echo (TTE vs TEE); CT/ MRI  
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TAA: Pos CXR:   Must differentiate from anterior mediastinal mass (ie thymoma, lung CA)  
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TAA: if surgery required, need:   coronary angiography  
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Echo: TTE vx TEE   TTE only good to visualize aortic root (good for Marfan); TEE to visualize entire aorta, but is semi invasive (CT/ MRI better)  
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TAA Mgmt: major factors in rupture risk   Size & rate of growth  
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TAA Mgmt: Annual growth rate for <5cm aneurysm   2%  
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TAA Mgmt: Annual growth rate for 5-5.9 cm   3%  
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TAA Mgmt: Annual growth rate for >6 cm   7%  
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TAA: Inc rupture risk at smaller diameters with:   Marfan; bicuspid valve  
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Asc Aorta: surgery indicated at:   ≥ 5.5 cm (=/> 5.5)  
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Marfan/ Bicuspid Valve: surgery indicated at:   ≥ 5.0 cm (=/> 5.0)  
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Aortic valve replacement: surgery indicated at:   ≥ 4.0 cm (=/> 4.0)  
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Desc Aorta: surgery indicated at:   ≥ 6.0 cm (=/> 6.0)  
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Aortic Root Replacement: Bentall:   Dacron graft w/ prosthetic valve sewn directly into aortic annulus; coronary arteries reimplanted into the graft (op mortality risk 5%)  
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Aortic Root Replacement: David =   valve sparing Bentall (re-implant native valve within dacron graft)  
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TAA: Prognosis   M&M higher than with AAA; 5 yr if unrepaired (>6 cm) is 20-25% (most deaths due to rupture or CAD)  
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TAA: 1 month op mortality =   8-20%  
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TAA: operative complications   pulmo comps & damage to laryngeal or phrenic n., carotid or subclavian a. poss  
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Tear in aortic intima usu preceded by medial wall degen/ CMN =   aortic dissection  
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Aortic dissection: intimal tear in aorta creates a false lumen between:   media & adventitia  
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Aortic dissection: time course   May be acute or chronic  
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Aortic dissection: >95% occur in the:   Ascend aorta just distal to aortic valve or just distal to L subclavian at lig arteriosum  
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Intimal tears resulting in dissection: prevalence:   65% Ascend A; 20% Desc A; 10% A Arch; 5% Abd A.  
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Aortic Dissection incidence   3/100,00/year (7,000 cases/year in US); most common in 6th-8th decade; M>F 2:1 2:1  
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Aortic Dissection: Increased risk in:   pregnancy (1/4 of all female cases <40 yrs & most in last trimester); conn tissue dz (Marfan, Ehlers Danlos); Bicuspid Aortic Valve or Coarctation  
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Aortic Dissection: 80% of pts are:   Hypertensive  
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Aortic Dissection: Clinical Findings   Acute: sudden, severe excruciating ripping chest pain (ascending) or scapular (descending); most hypertensive or nml  
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Aortic Dissection: poss Sx devt   Acute aortic regurgitation (CHF indicates valve involvement); focal neuro (CVA may develop)  
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Aortic Dissection Eval: CXR =   wide mediastinum, poss L sided pleural effusion  
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Aortic Dissection Eval: Echo =   98% sensitive, 99% specific, +/- pericardial effusion  
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Aortic Dissection Eval: CT helpful in:   acute presentation  
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Aortic Dissection Eval: MRA/MRI useful for:   serial follow up  
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Aortic Dissection Eval: EKG =   LVH, nonspecific or inferior abnormalities (dissections preferentially extend into Right coronary ostium)  
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Aortic dissection: CXR =   Wide aortic silhouette & mediastinum; Left pleural effusion; 10%-20% normal  
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Aortic Dissection: mgmt: Type A =   Surgical repair, may require AVR  
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Aortic Dissection: mgmt: Type B =   Medical therapy  
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Aortic Dissection: mgmt: Type B: Exceptions to med tx:   Rupture, Limb/ visceral ischemia, Saccular morphology, ongoing pain, uncontrolled HTN, Marfan, AI  
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Aortic Dissection: mgmt: Chronic & asymptomatic =   medical Rx  
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Aortic Dissection: mgmt: All pts =   aggressive BP control; yearly imaging or if increased Sx  
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Aortic Dissection: Prognosis   Op mortality of type B 2x that of type A (bc comorbid illness)  
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Aortic Dissection: 5 yr survival: repaired Type A =   70-80% repaired type A  
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Aortic Dissection: 5 yr survival: repaired Type B =   50-70% repaired type B  
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Aortic Dissection: Prognosis: chronic type B   30% => progressively enlarging aneurysm that eventually requires repair  
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Aortic aneurysm etiologies =   atherosclerosis (most common); Marfan (esp TAA); aortitis (mycotic, salmonella, syphilis, other infxn), giant cell arteritis  
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Complications of aortic aneurysm   rupture (esp if >5.5cm); thromboembolism; distal ischemia  
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Aortic aneurysm dx studies   U/S; CT; aortography (used before surgery); CXR (to show calcifications)  
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Aortic dissection etiologies:   HTN; Marfan; cystic medial necrosis; iatrogenic comp of cath  
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Aortic dissection pathophysiology   intimal tear with formation of false channel in media by hematoma  
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Aortic dissection on CXR =   wide superior mediastinum; displaced trachea; L pleural effusion; enlarged aortic knob  
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Which medication (ACE, diuretic, CCB, sotalol) will decrease morbidity of patient with AAA?   Sotalol  
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