Diagnosis and Management of Aortic Regurgitation
SUMMARY:
Aortic regurgitation (AR) is a condition where the aortic valve does not close properly, either due to primary disease of aortic valve leaflets and/or dilatation of aortic root and ascending aorta.
- Causes of AR
- Signs and Symptoms of AR
- Diagnosis and Follow-Up
- Stages of Aortic Regurgitation
- Medical Therapy of AR
- Intervention of Acute AR
- Intervention of Chronic AR
- Antiplatelet/Anticoagulant Therapy Post AVR
Causes of AR
- Primary leaflet abnormalities
- Rheumatic disease | Congenital (i.e., bicuspid) | Infective Endocarditis | Myxomatous valve disease | Trauma
- Aortic root abnormalities:
- Chronic hypertension | Marfan syndrome, | Aortic Dissection | Ehlers-Danlos syndrome | Syphilitic aortitis | Systemic inflammatory disorders
Signs and Symptoms of AS:
- Symptoms: Exertional dyspnea | orthopnea| Paroxysmal nocturnal dyspnea |Angina late in course
- Signs:
- Wide pulse pressure
- Apical impulse is hyperdynamic and displaced laterally and inferiorly
- Harsh systolic flow murmur (from increased total stroke volume) and high frequency diastolic murmur
- 3rd heart sound (S3) may be heard
Diagnosis and Follow-Up:
- A transthoracic and/or transesophageal echocardiogram to confirm presence, severity and possibly etiology of AR.
- Severe AR is defined by echocardiography as short deceleration time on aortic flow velocity curve (<300 msec)
- In the chronic setting, severe AR is associated with dilation of left ventricular size
- Frequency of TTE in asymptomatic patients with AR:
| Severity | Frequency |
| Mild | Every 3-5 years |
| Moderate | 1-2 years |
| Severe (asymptomatic) | Every 6 months to 1 year. (If LV is dilated more frequently) |
Stages of Aortic Regurgitation:
- Stage A: At risk of AR. Patients with bicuspid aortic valve | history of rheumatic fever or known rheumatic heart disease |diseases of the aortic sinuses or ascending aorta.
- Stage B: Progressive AR: mild to moderate AR
- Stage C: Asymptomatic Severe AR
- Stage D: Symptomatic Severe AR
Medical Therapy of AR:
- Stage B-C patients: Hypertension (SBP > 140 mmHg) should be treated accordingly. In the absence of systemic hypertension, vasodilating drug are not indicated
- Stage D patients and/or LV systolic dysfunction but prohibitive surgical risk, heart failure guideline directed medical therapy is recommended.
Intervention of Acute AR:
- Acute severe AR from infective endocarditis or aortic dissection, medical therapy to reduce LV afterload can be employed as a TEMPORIZING measure, but surgery should not be delayed especially if hypotension, pulmonary edema, or evidence of hypoperfusion.
Intervention of Chronic AR:
- Aortic Valve Replacement (AVR) is indicated in patients with SYMPTOMATIC severe AR
- AVR is indicated in ASYMPTOMATIC patients with severe AR and LVEF ≤ 55%
- AVR is indicated in ASYMPTOMATIC patients with severe AR if undergoing cardiac surgery for other indications
- AVR can be considered in ASYMPTOMATIC patients with severe AR and normal LVEF >55% if LV is severely enlarged (LV end systolic diameter >50 mm or LV end systolic diameter > 25 mm/m2)
Antiplatelet/Anticoagulant Therapy Post AVR:
- Patients with a bioprosthetic AVR , daily low-dose aspirin is recommended lifelong in addition to VKA anticoagulation with INR goal of 2.5 for first 3-6 months
- Patients with a mechanical AVR, anticoagulation ONLY with vitamin K antagonist (VKA) is recommended. *DOACs (Direct Oral Anticoagulants) are contraindicated*
- INR goals for patients with mechanical valves:
| Mechanical AVR | INR goal |
| Mechanical AVR with On-X valve | 1.5-2 |
| Mechanical AVR with no other risk factors* | 2.5 |
| Mechanical AVR with other risk factors* | 3 |
*Risk factors: older generation valve | atrial fibrillation | previous thromboembolism | hypercoagulable state |LV dysfunction
Learn More – Primary Sources:
2020 ACC/AHA Guideline for the Management of Patients with Valvular Heart Disease
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