1 / 42

Valvular Heart Disease and the Cardiac Exam

Valvular Heart Disease and the Cardiac Exam. 2009. Overview. Clinical syndromes Overview of cardiac murmurs and maneuvers Left sided valvular lesions Aortic stenosis and sclerosis Mitral stenosis Rheumatic fever prophylaxis Acute and chronic aortic regurgitation

karif
Download Presentation

Valvular Heart Disease and the Cardiac Exam

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. Valvular Heart Disease and the Cardiac Exam 2009

  2. Overview • Clinical syndromes • Overview of cardiac murmurs and maneuvers • Left sided valvular lesions • Aortic stenosis and sclerosis • Mitral stenosis • Rheumatic fever prophylaxis • Acute and chronic aortic regurgitation • Acute and chronic mitral regurgitation • Right sided valvular lesions • Tricuspid valve disease • Prosthetic valves • Endocarditis prophylaxis • Questions

  3. Marfan Syndrome Tall, long extremities Associated with: aortic root dilitation, MV prolapse Acromegaly Large stature, coarse facial features, “spade” hands Associated with: Cardiac hypertrophy Turner Syndrome Web neck, hypertelorism, short stature Associated with: Aortic coarctation, pulmonary stenosis Pickwickian Syndrome Severe obesity, somnolence Associated with: Pulmonary hypertension Fredreich ataxia Lurching gait, hammertoe, pes cavus Associated with: hypertrophic cardiomyopathy Duchenne type muscular dystrophy Pseudohypertrophy of the calves Cardiomyopathy Ankylosing spondylitis Straight back syndrome, stiff (“poker”) spine Associated with: AI, CHB (rare) Lentigines (LEOPARD syndrome) Brown skin macules that do not increase with sunlight Associated with: HOCM, PS General Appearance

  4. “Spade” hands in acromegaly

  5. Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu) Small capillary hemangiomas on the face or mouth Associated with: Pulmonary arteriovenous fistula Lupus Butterfly rash on face, Raynaud phenomenon- hands, Livedo reticularis Associated with: Verrucous endocarditis, Myocarditis, Pericarditis Pheochromocytoma Pale diaphoretic skin, neurofibromatosis- café-au-lait spots Associated with: Catecholamine-induced secondary dilated CM Sarcoidosis Cutaneous nodules, erythema nodosum Associated with: Secondary cardiomyopathy, heart block Tuberous Sclerosis Angiofibromas (face; adenoma sebaceum) Associated with: Rhabdomyoma Myxedema Coarse, dry skin, thinning of lateral eyebrows, hoarseness of voice Associated with: Pericardial effusion, LV dysfunction General Appearance- 2

  6. Grading the Intensity of Cardiac Murmurs • Grade 1 • Murmur heard with stethoscope, but not at first • Grade 2 • Faint murmur heard with stethoscope on chest wall • Grade 3 • Murmur hears with stethoscope on chest wall, louder than grade 2 but without a thrill • Grade 4 • Murmur associated with a thrill • Grade 5 • Murmur heard with just the rim held against the chest • Grade 6 • Murmur heard with the stethoscope held away and in from the chest wall

  7. Cardiac Murmurs • Most mid systolic murmurs of grade 2/6 intensity or less are benign • Associated with physiologic increases in blood velocity: • Pregnancy • Elderly • In contrast, the following murmurs are usually pathologic: • Systolic murmurs grade 3/6 or greater in intensity • Continuous murmurs • Any diastolic murmur

  8. Diagnostic Testing • ECHOCARDIOGRAM • Exercise testing • To assess the clinical severity of valvular heart disease • Those with inconsistent resting hemodynamics • Equivocal history of symptoms • Exercise testing in AS patients • Should be ended promptly if: • Cardiac symptoms provoked • Decrease or minimal increase (<20 mmHg) in blood pressure • Prior history of angina, congestive heart failure, or exertional syncope absolute contraindications to exercise testing • Cardiac catheterization • Usually not needed for primary evaluation

  9. Aortic Stenosis • Most common cause is calcific degeneration • Active disease process with risk factors of male sex, smoking, HTN, DM, older age, hypercholesterolemia • 2% of the general population have bicuspid aortic valves • Symptomatic or severe AS occurs earlier (age 40-60 years) • AS less commonly from rheumatic heart disease valvulitis • Invariably MV involved first • Associated AV involvement in <1/2 patients • AV sclerosis • Valve thickening without obstruction • Present in >20% of people >65 years • Associated with 50% increased risk of MI and CV death

  10. Progression of Aortic Sclerosis • Hemodynamic progression usually slow • Average rate of increase in aortic jet velocity of 0.3 m/s per year • Increase in mean transaortic gradient of 7 mmHg • Decrease in AVA of 0.1 cm2 per year • Severe AS • Aortic jet velocity > 4 m/s • Mean transvalvular pressure gradient > 50 mmHg • AVA < 1.0 cm2

  11. Pathophysiology of Aortic Stenosis • Obstruction of LV outflow increases intracavitary systolic pressures and leads to LV pressure overload • Initial compensatory mechanism is myocardial hypertrophy with preservation of systolic function • Diastolic function impaired as a consequence of increased wall thickness and abnormal myocardial relaxation • Increased wall stress and afterload causes eventual decrease in ejection fraction

  12. Pseudostenosis • Occurs in patients with impaired systolic function and aortic stenosis • Unable to generate transvalvular gradient • Careful diagnostic testing with dobutamine infusion protocols can aid in differentiating between true AS and pseudostenosis • If the calculated AVA increases with augmentation of cardiac output, then pseudostenosis present • If AVA does not increase with dobutamine, then obstruction fixed and true AS present

  13. Clinical Presentation of Aortic Stenosis • Cardinal symptoms: • Angina • Occurs in >50% of patients, not sensitive due to prevalence of CAD • Syncope • CHF • Sudden cardiac death rare, <1% per year • In earlier stages, AS presentation more subtle • Dyspnea • Decreased exercise tolerance • Rarely, AS diagnosed in the setting of GI bleeding • Heyde’s syndrome • Bleeding caused by AVM • Concurrent AS occurs at prevalence rate of 15-25% • Associated with an acquired von Willebrand syndrome due to disruption of vW multimers through a diseased AV

  14. Management of Aortic Stenosis • Prognosis in asymptomatic disease excellent • Conservative approach with monitoring for symptoms recommended • When severe stenosis present- • 38% of asymptomatic patients develop symptoms within 2 years • 79% are symptomatic within 3 years • Once symptoms occur, AVR needed • LV dysfunction and severe AS have increased perioperative mortality with AVR • But outcomes still favorable with surgery • Nitroprusside may transiently improve cardiac function as a bridge to valve replacement • Does not supplant AVR in symptomatic patients

  15. Bonow et al. J Am Coll Cardiol 2006; 47: 2141-51

  16. Aortic Valve Replacement • Prophylatic AVR in asymptomatic patients not routinely performed due to surgical risks • Thromboembolism, bleeding associated with anticoagulation, prosthetic valve dysfunction, and endocarditis • Occurs at a rate of 2-3% annually • Only should be considered: • If other cardiac surgery (such as CABG) planned • Severe LVH or systolic dysfunction • Women contemplating pregnancy • Patients remote from health care • Surgical valve replacement with operative morbidity and mortality of 10% • Percutaneous balloon aortic valvotomy rarely used

  17. Mitral Stenosis • Usually associated with history of rheumatic fever • >40% of cases of RHD result in mitral stenosis • Women affected more than men (2:1) • Presentation 20-40 years after the initial episode of rheumatic fever • If infected at a young age, latent period is a few years

  18. Clinical Presentation of Mitral Stenosis • Significant MS leads to ↑LA pressure and pulm HTN • Symptoms include dyspnea with ↑ cardiac demand • Exercise • Pregnancy • Survival excellent with asymptomatic or minimally symptomatic patients • >80% survival at 10 years • Survival in symptomatic patients much worse • 10 year survival drops to 15% or lower (if pulm HTN present) • Findings consistent with severe MS: • Transvalvular diastolic pressure gradient >10 mmHg • MVA <1.0 cm2 • Severe pulmonary hypertension (>60 mmHg)

  19. Management of Mitral Stenosis • Atrial fibrillation • Prevalence >30% in symptomatic patients and associated with poorer long term outcome • Warfarin indicated: • In patients with AF and MS • Patients without history of AF but with MS and embolic CVA • In patients with prior history of AF who have mitral valve surgery, decreased postoperative AF observed if MAZE performed concominantly

  20. Mitral Valve Repair • Percutaneous valvotomy • Therapeutic intervention of choice if: • LAA thrombus excluded • MR less than moderate • Valvular characteristics favorable • Pliable leaflets, minimal commisural fusion, minimal valvular or subvalvular calcification • Pulmonary HTN not contraindication to valvotomy • Major complications include: severe MR (1-8%), systemic embolization (1-3%), and tamponade (1-2%) • Periprocedural mortality- 1% • Surgical commissurotomy or MVR can be performed in unfavorable anatomy

  21. Bonow et al. J Am Coll Cardiol 2006; 47: 2141-51

  22. Rheumatic Fever Prophylaxis • Primary prophylaxis • If living in an endemic area, with pharyngitis and a +test for group A strep or positive throat culture • Given once, may be repeated as needed: • PCN G 1.2 million U IM or PCN V 500 mg TID x 10d • Azithromycin 500 mg on day 1, 250 mg daily for 4d • Secondary prophylaxis • PCN G 1.2 million units IM every 4 weeks or PCN V 250 mg PO BID or erythromycin 250 mg BID • RHD without carditis- At least 5 years or until >21 y of age • RHD with carditis, no valvular HD- At least 10 y or well into adulthood • RHD with carditis and valvular HD- At least 10 years from last episode or until patient is older than 40 years

  23. Acute Aortic Regurgitation • Causes of acute aortic regurgitation: • Aortic dissection • Valve distruction from endocarditis • Traumatic rupture • Classic physical exam findings may be absent in the acute presentation • Diastolic murmur may not be present due to sudden increase of LVEDP • TTE, along with TEE, cath, CT or MRI may be used for diagnosis • Surgical AV repair or replacement should be performed emergently • Afterload reducing medications and inotropes may help to acutely stabilize the patient • IABP contraindicated

  24. Acute Mitral Regurgitation • Most often occurs in: • Chordae tendineae rupture due to myxomatous valve disease or endocarditis • Myocardial infarction with papillary muscle dysfunction or rupture • Symptoms almost always occur • Dyspnea and pulmonary edema • Systolic function may occur normal or hyperdynamic • IABP or afterload reducing drugs to temporize • Surgical intervention for treatment

  25. Chronic Valvular Regurgitation • Cardiac chamber size and function have time to compensate for dysfunction • May allow patients to remain asymptomatic for a long time • Both preload and afterload increases • Once increase in cardiac output insufficient→ systolic function declines → pulmonary HTN may develop and symptoms develop • LV enlargement and progressive systolic dysfunction are associated with significant morbidity and mortality • Serial echocardiography and evaluation by a cardiologist is indicated

  26. Chronic Aortic Regurgitation • Occurs most often in bicuspid AV • Other causes include ascending aortic aneurysm and Marfan’s Disease • Risk factors for poorer outcome: • Age • Cardiac symptoms • Atrial fibrillation • LV enlargement • Lower LVEF • Asymptomatic patients with normal LV size and function do not require prophylatic surgery • Surgery should be considered if: • LVESD > 55 mm • Ejection fraction <60% • Symptoms develop • Oral afterload reduction (nifedipine or ACE-I) may slow rate of LV dilation

  27. Bonow et al. J Am Coll Cardiol 2006; 47: 2141-51

  28. Chronic Mitral Regurgitation • Often caused by myxomatous disease or MVP • Myxomatous mitral valve disease with progressive MR associated with poor long term outcome • Higher risk of arrhythmias and sudden cardiac death • Mitral valve prolapse occurs in ~2% of the general population • Consists of the buckling of the mid portion of the valve leaflets into the LA • Usually asymptomatic, but may be associated with palpitations or chest discomfort • Prognosis usually benign • Antibiotic prophylaxis now not indicated

  29. Chronic Mitral Regurgitation • Other causes include secondary or acquired leaflet dysfunction • Endocarditis • Rheumatic heart disease • Annular tethering from LV dilation • Tethering of the chordal apparatus from ischemic heart disease • Rare cause: Fenfluramine and phentermine, also associated with AI • Compensatory increase in LV chamber size initially allows for increase in total stroke volume and restoration or total forward cardiac output

  30. Treatment of Chronic Mitral Regurgitation • Mitral valve repair preferred over mitral valve replacement • Avoids risk of anticoagulation • Preservation of subvalvular apparatus • Better postoperative LV function and long term survival • When MR occurs in volume overloaded states, afterload reduction can be beneficial • Dilated CM • CAD • Revascularization may improve dysfunction of the papillary muscle • Biventricular pacing may improve LV geometry

  31. Timing of Intervention for Left-Sided Valvular Conditions

  32. Tricuspid Valve Disease • Tricuspid stenosis is rare • Associated with rheumatic heart disease • TR usually occurs secondary to: • Pulmonary hypertension • RV chamber enlargement with annular dilatation • Endocarditis (associated with IV drug use) • Injury following pacer lead placement • Other secondary causes: carcinoid, radiation therapy, anorectic drug use, and trauma • Primary causes: Marfan’s syndrome and congenital disorders such as Ebstein’s anomaly and AV canal malformation • Echo is diagnostic in most cases

  33. Tricuspid Regurgitation • Severe tricuspid regurgitation is difficult to treat and carries a poor overall clinical outcome • Symptoms are manifestations of systemic venous congestion • Ascites • Pedal edema • Surgical intervention usually considered if other cardiac surgery planned • Surgical options include valvular annuloplasty or replacement • If replacement planned, bioprosthetic valve preferred

  34. Prosthetic Valves- Mechanical • Three types: • Ball-cage valve • Single tilting disk valve • Bileaflet valve • Durable but require life long anticoagulation • For operative procedures, warfarin typically is discontinued for 48-72 hours and restarted postop as soon as possible, except for: • Mechanical mitral prosthesis • Atrial fibrillation • Prior thromboembolic events

  35. Ball-cage valve Single tilting disk valve Bileaflet valve

  36. Prosthetic Valves- Biological • Biological Valves • Composed of autologous or xenograft biological material mounted on stents and a sewing ring • Warfarin therapy not required due to lower thromboembolic potential • Valve durability less when compared to mechanical valves • Newer stentless valves with increased longevity

  37. Anticoagulation Guidelines for Mechanical Valves Bonow et al. J Am Coll Cardiol 2006; 47: 2141-51

  38. Prosthetic Valve Complications • Common complications include: • Structural valve deterioration • Valve thrombosis • Embolism • Bleeding • Endocarditis • Endocarditis prophylaxis required for patients with all types of prosthetic valves • Suspect valve dehiscence or dysfunction in: • Acute CHF in the immediate postop period • New cardiac symptoms • Embolic phenomena • Hemolytic anemia • New murmurs • TEE is the diagnostic procedure of choice • Postop TTE should be done 2-3 months after surgery

  39. Valve Thrombosis • Incidence with mechanical prosthesis of 2-4 % per year • Suspect in patients with new murmur, change in cardiopulmonary symptoms, or an embolic event • Diagnosis based on clinical presentation, TTE/TEE, and fluroscopy • In small thrombus, treatment with heparin may be adequate • Optimal treatment for left sided thrombosis is emergency surgery • Consider thrombolytic therapy for right sided thrombosis or if surgery cannot be performed with left sided disease

  40. Endocarditis Prophylaxis 2007 AHA Prevention of Infective Endocarditis Guidelines

More Related