Hypertrophic Cardiomyopathy Ahmad Yousre Msc cardiology.
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Transcript of Hypertrophic Cardiomyopathy Ahmad Yousre Msc cardiology.
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Hypertrophic Cardiomyopathy
Ahmad Yousre
Msc cardiology
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Hypertrophic Cardiomyopathy
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Definition:
WHO: left and/or right ventricular
hypertrophy, usually asymmetric and
involves the interventricular septum.
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Differential Diagnosis:
HCM Can be asymmetric Wall thickness: > 15 mm LA: > 40 mm LVEDD : < 45 mm Diastolic function: always
abnormal
Athletic heart Concentric & regresses < 15 mm < 40 mm > 45 mm Normal
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Stimulus:
Unknown Disorder of intracellular calcium metabolism Neural crest disorder Papillary muscle malpositioned and
misoriented
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Genetic abnormality:
Autosomal dominant. Mutations in genes for cardiac sarcomeric
proteins. Polymorphism of ACE gene. ß-myosin heavy chain gene on
chromosome 14.
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Variants of HCM:Most common location: subaortic , septal, and ant. wall.
Asymmetric hypertrophy (septum and ant. wall): 70 %.
Basal septal hypertrophy: 15- 20 %.
Concentric LVH: 8-10 %.
Apical or lateral wall: < 2 % (25 % in Japan/Asia): characteristic giant T-wave inversion laterally & spade-like left ventricular cavity: more benign.
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Hypertensive hypertrophic Cardiomyopathy
Elderly women Simulates HCM Prognosis better than non-hypertensive HCM
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Pathophysiology of HCM
Dynamic LV outflow tract obstruction Diastolic dysfunction Myocardial ischemia Mitral regurgitation Arrhythmias
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Left ventricular outflow tract gradient ↑ with decreased preload, decreased
afterload, or increased contractility. Venturi effect: anterior mitral valve leaflets &
chordae sucked into outflow tract →
↑ obstruction, eccentric jet of MR in mid-late systole.
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Maneuvers that ↓ end-diastolic volume(↓ venous return & afterload, ↑ contractility) Vasodilators Inotropes Dehydration Valsalva Amyl nitrite Exercise → ↑ HCM murmur
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Arrhythmias: Sustained V-Tach and V-Fib: most likely
mechanism of syncope/ sudden death.
Dependant on atrial kick: CO ↓ by 40 % if A. Fib present.
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Histology:
Myocardial fiber disarray, endocardial plaques.
Abnormal relaxation and diversely oriented myocardial fibers.
Intimal hyperplasia of intramural coronary arteries, endothelial dysfunction, myocardial perfusion defects.
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Clinical presentation:
Any age Leading cause of sudden death in
competitive athletes Triad: DOE, angina, presyncope/syncope.
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Physical exam:
Apex localized, sustained Palpable S4 Tripple ripple Prominent “a” wave Rapid upstroke carotid pulse, “jerky” bifid (spike-and-
dome pulse) Harsh systolic ejection murmur across entire
precordium → apex & heart base MR: separate murmur: severity of MR related to
degree of outflow obstruction
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EKG:
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Echocardiography:
2D-echo: Asymmetric septal hypertrophy Diffuse concentric or localized to
apex/anterior wall Systolic anterior motion of MV (SAM)
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Doppler Echocardiocraphy: Typical appearance: late-peaking signal
“dagger-shaped” Bernoulli for peak systolic gradient (+ maneuvers) Obstructive or non-obstructive Distinguish MR and intra-cavitary obstruction
(looking for the aortic closure signal)
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Cardiac cath:
Not necessary
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Brockenbrough response
↑ LV systolic pressure ↓ Ao systolic pressure ↑ gradient between LV & Ao
Post PVC
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Brockenbrough response
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Imitator of HCM
Amyloidosis:
Thickened walls & low voltage on EKG.
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Natural history of HCM
Mortality: 3 %/year (6-8 % with NSVTach) Poor prognosis: - Younger age - Male sex - + family hx. of sudden death - Hx. of syncope - Genetic markers (mutations of arginine gene) - Exercise-induced hypotension (worst)
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Genetic defect and prognosis
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Management
All first degree relatives: screening… echocardiography/genetic counseling Avoid competitive athletics Prophylactic antibiotics before medical &
dental procedures Holter x 48 hours
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β- Blockers: Propranolol 200-400 mg/d
(large doses)/ Selective β- B lose selectivity at high doses:
Slow HR → longer diastolic filling time →
↓ myocardial O2 consumption →
↓ myocardial ischemia & LVOT obstruction CaCh- Blockers: Verapamil 240-320 mg/d
(with caution for hemodynamic deterioration) Combination of both
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Disopyramide: class I antiarrhythmic + strong –ive inotropic effect
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Non-responders to Medical therapy???
1- Surgery (Myotomy/Myectomy) +/- MVR
2- ICD
3- DDD pacemaker
4- NSRT (alcohol septal ablation)
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1- Surgery:
Septal myotomy/myectomy: Patients < 40 years: mortality < 1 % Patients > 65 years: mortality 10-15 % Survival better than medically treated patients Should be considered in: resting gradient > 50 mmHg, or
refractory to medical Rx. Young patients, particularly those with severe disease Additional structural abnormalities affecting the mitral valve or
coronary arteries.
Complication (rare): Aortic incompetence
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Myotomy/Myectomy
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2- ICD:
Previous sudden death High risk of sudden death EPS use ?
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3- DDD pacemakerSubstantial ↓ gradient(~ 50 %)
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Effect of DDD pacemaker in HCM
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Potential Mechanisms of benefit of Pacing in HCM:
RV apical pacing & maintenance of AV synchrony → abnormal pattern of septal contraction → ↓ early systolic bulging of hypertrophic subaortic septum in LVOT &
↓ Venturi forces that produce SAM. ↑ LVOT width during systole ↓ systolic hypercontractility: ↑ end-systolic
volume → ↓ intraventricular pressure gradients & myocardial work
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↓ MR May favorably alter diastolic function LVH regression
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Candidates for DDD
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4- Alcohol septal ablation (NSRT)
Controlled myocardial infarction
of the basal ventricular septum
to ↓ gradient. First septal artery occluded with
a balloon catheter and ETOH
injected distally
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NSRT (Non Surgical Septal Reduction Therapy)
The most appropriate candidates for NSRT should meet all of thefollowing criteria : - HCM with severe symptoms of heart failure (NYHA class III to IV) despite adequate tolerated drug therapy
- An LVOT gradient 50 mmHg at rest or after exercise or >30 mmHg at rest or 60 mmHg under stress
- Basal septal thickness 18 mm
- NYHA class II heart failure with a resting LVOTgradient >50 mmHg or >30 mmHg at rest and 100 mmHg with stress .
- Elderly or comorbidities that may increase the risk of surgical correction.
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Thank you