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Hypertrophic
Cardiomyopathy
Hypertrophic Cardiomyopathy
Definition:
WHO: left and/or right ventricular
hypertrophy, usually asymmetric and
involves the interventricular septum.
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
Stimulus:
• Unknown
• Disorder of intracellular calcium metabolism
• Neural crest disorder
• Papillary muscle malpositioned and misoriented
Genetic abnormality:
• Autosomal dominant.
• Mutations in genes for cardiac sarcomeric proteins.
• Polymorphism of ACE gene.
• ß-myosin heavy chain gene on chromosome 14.
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.
Hypertensive hypertrophic Cardiomyopathy
• Elderly women
• Simulates HCM
• Prognosis better than non-hypertensive HCM
Pathophysiology of HCM
• Dynamic LV outflow tract obstruction
• Diastolic dysfunction
• Myocardial ischemia
• Mitral regurgitation
• Arrhythmias
• 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.
Maneuvers that ↓ end-diastolic volume
(↓ venous return & afterload, ↑ contractility)
• Vasodilators
• Inotropes
• Dehydration
• Valsalva
• Amyl nitrite
• Exercise
→ ↑ HCM murmur
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.
Histology:
• Myocardial fiber disarray, endocardial plaques.
• Abnormal relaxation and diversely oriented myocardial fibers.
• Intimal hyperplasia of intramural coronary arteries,
endothelial dysfunction, myocardial perfusion defects.
Clinical presentation:
• Any age
• Leading cause of sudden death in competitive athletes
• Triad: DOE, angina, presyncope/syncope.
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
EKG:
Echocardiography:
2D-echo:
• Asymmetric septal hypertrophy
• Diffuse concentric or localized to apex/anterior wall
• Systolic anterior motion of MV (SAM)
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)
Cardiac cath:
• Not necessary
Brockenbrough response
• ↑ LV systolic pressure
• ↓ Ao systolic pressure
• ↑ gradient between LV & Ao
Post PVC
Brockenbrough response
Imitator of HCM
• Amyloidosis:
Thickened walls & low voltage on EKG.
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)
Genetic defect and prognosis
Management
• All first degree relatives: screening…
echocardiography/genetic counseling
• Avoid competitive athletics
• Prophylactic antibiotics before medical & dental procedures
• Holter x 48 hours
• 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
• Disopyramide: class I antiarrhythmic + strong –ive inotropic
effect
Non-responders to Medical
therapy
???
1- Surgery (Myotomy/Myectomy) +/- MVR
2- ICD
3- DDD pacemaker
4- NSRT (alcohol septal ablation)
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
Myotomy/Myectomy
2- ICD:
• Previous sudden death
• High risk of sudden death
• EPS use ?
3- DDD pacemaker
Substantial ↓ gradient(~ 50 %)
Effect of DDD pacemaker in HCM
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
• ↓ MR
• May favorably alter diastolic function
• LVH regression
Candidates for DDD
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
NSRT (Non Surgical Septal Reduction
Therapy)
The most appropriate candidates for NSRT should meet all of the
following 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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HOCM Hypertrophic cardiomyopathy

  • 3. Definition: WHO: left and/or right ventricular hypertrophy, usually asymmetric and involves the interventricular septum.
  • 4. 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
  • 5. Stimulus: • Unknown • Disorder of intracellular calcium metabolism • Neural crest disorder • Papillary muscle malpositioned and misoriented
  • 6. Genetic abnormality: • Autosomal dominant. • Mutations in genes for cardiac sarcomeric proteins. • Polymorphism of ACE gene. • ß-myosin heavy chain gene on chromosome 14.
  • 7. 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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  • 9. Hypertensive hypertrophic Cardiomyopathy • Elderly women • Simulates HCM • Prognosis better than non-hypertensive HCM
  • 10. Pathophysiology of HCM • Dynamic LV outflow tract obstruction • Diastolic dysfunction • Myocardial ischemia • Mitral regurgitation • Arrhythmias
  • 11. • 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.
  • 12. Maneuvers that ↓ end-diastolic volume (↓ venous return & afterload, ↑ contractility) • Vasodilators • Inotropes • Dehydration • Valsalva • Amyl nitrite • Exercise → ↑ HCM murmur
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  • 14. 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.
  • 15. Histology: • Myocardial fiber disarray, endocardial plaques. • Abnormal relaxation and diversely oriented myocardial fibers. • Intimal hyperplasia of intramural coronary arteries, endothelial dysfunction, myocardial perfusion defects.
  • 16. Clinical presentation: • Any age • Leading cause of sudden death in competitive athletes • Triad: DOE, angina, presyncope/syncope.
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  • 19. 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
  • 20. EKG:
  • 21. Echocardiography: 2D-echo: • Asymmetric septal hypertrophy • Diffuse concentric or localized to apex/anterior wall • Systolic anterior motion of MV (SAM)
  • 22. 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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  • 26. Brockenbrough response • ↑ LV systolic pressure • ↓ Ao systolic pressure • ↑ gradient between LV & Ao Post PVC
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  • 29. Imitator of HCM • Amyloidosis: Thickened walls & low voltage on EKG.
  • 30. 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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  • 32. Genetic defect and prognosis
  • 33. Management • All first degree relatives: screening… echocardiography/genetic counseling • Avoid competitive athletics • Prophylactic antibiotics before medical & dental procedures • Holter x 48 hours
  • 34. • 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
  • 35. • Disopyramide: class I antiarrhythmic + strong –ive inotropic effect
  • 36. Non-responders to Medical therapy ??? 1- Surgery (Myotomy/Myectomy) +/- MVR 2- ICD 3- DDD pacemaker 4- NSRT (alcohol septal ablation)
  • 37. 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
  • 39. 2- ICD: • Previous sudden death • High risk of sudden death • EPS use ?
  • 40. 3- DDD pacemaker Substantial ↓ gradient(~ 50 %)
  • 41. Effect of DDD pacemaker in HCM
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  • 43. 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
  • 44. • ↓ MR • May favorably alter diastolic function • LVH regression
  • 46. 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
  • 47. NSRT (Non Surgical Septal Reduction Therapy) The most appropriate candidates for NSRT should meet all of the following 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.