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Barry J. Maron, MD Director, Hypertrophic Cardiomyopathy Center Minneapolis Heart Institute Foundation Minneapolis, Minnesota Disclosures: Medtronic (Grantee) GeneDx (Consultant) State of the Art: Hypertrophic Cardiomyopathy 2015

Hypertrophic cardiomyopathy state of the art

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Page 1: Hypertrophic cardiomyopathy state of the art

Barry J. Maron, MD

Director, Hypertrophic Cardiomyopathy Center

Minneapolis Heart Institute Foundation

Minneapolis, Minnesota

Disclosures:

Medtronic (Grantee)

GeneDx (Consultant)

State of the Art:

Hypertrophic Cardiomyopathy

2015

Page 2: Hypertrophic cardiomyopathy state of the art

New HCM Paradigms:

1. Contemporary Treatable Disease

Compatible w/ Low Mortality &

Extended/Normal Longevity

2. RX Interventions Change Clinical

Course of Disease

Page 3: Hypertrophic cardiomyopathy state of the art

“At this time we are aware of no method

of management that can specifically and

favorably influence the course of a patient

with idiopathic ventricular hypertrophy.”

Eugene Braunwald

Edwin C. Brockenbrough

Andrew G. Morrow

Circulation, Volume XXVI, August 1962

Page 4: Hypertrophic cardiomyopathy state of the art

0

5

10

15

20

25

70 years 75 years 80 years 90 years

Survival to Advanced Age in HCM: Many (Most) Patients Don’t Require Much (Anything)

% H

CM

Pati

en

ts

Survival Age

19%

14%

8%

2%

Page 5: Hypertrophic cardiomyopathy state of the art

Sudden

Death Progressive

Heart Failure

AF

&

Stroke

End-

Stage

Profiles in Prognosis for HCM

Benign/Stable

(normal longevity)

Page 6: Hypertrophic cardiomyopathy state of the art

HCM

(36%)

Coronary

Anomalies

(17%)

Dilated CM (2%)

Sudden Death in Young Athletes

Maron, BJ et. al.

Circulation 2009;

119:1085-1092

Page 7: Hypertrophic cardiomyopathy state of the art

Prevention of Sudden Death in HCM

Page 8: Hypertrophic cardiomyopathy state of the art

Highest

Intermediate

Lowest

2° prevention

Cardiac arrest/sustained VT

1° prevention

Family history HCM-SD

Unexplained syncope

Multiple-repetitive NSVT (Holter)

Abnormal exercise BP response

LGE ≥ 15% of LV mass

Massive LVH ≥ 30 mm

Rare subgroups/potential arbitrators

End-stage (EF < 50%)

LV apical aneurysm

Marked LV outflow obstruction (rest)

Modifiable

Intense competitive sports

CAD

LGE ≥ 15% of LV mass

Age ≥ 60y

Alcohol septal ablation (?)

ICD

Page 9: Hypertrophic cardiomyopathy state of the art

Maron BJ et. al.

JAMA 2007

Page 10: Hypertrophic cardiomyopathy state of the art

0

10

20

30

40

50

60

70

Alive Non-

Cardiac

Death

Non-HCM

Cardiac

Death

Embolic

Stroke

Heart

Failure

SCD

% o

f H

CM

Co

ho

rt

65%

13% 12%

2% 1%

0.2%/y

Outcome of HCM Patients First Evaluated ≥ 60 Years

1%

HCM Death

Aging is Good in HCM

Maron BJ et. al.

Circ 2013; 127: 585

Page 11: Hypertrophic cardiomyopathy state of the art

Intermediate

Low Risk

Risk Stratification for Sudden Death in HCM

Moderate

High

No risk factors

Family history of sudden death

Nonsustained VT

Unexplained syncope

Extreme LVH

Abnormal BP response to Ex

0.5%/year

Page 12: Hypertrophic cardiomyopathy state of the art

VS

LV

A B

C

LGE as the Only Risk Factor

Maron BJ et. al.

AJC 2008; 101(4):544-7

Page 13: Hypertrophic cardiomyopathy state of the art

L

G

E

LGE LGE

Extent of LGE vs. Sudden Death Risk in HCM

Follow-up (years)

Su

rviv

al

LGE (-) LGE < 10%

LGE 10-20%

LGE > 20%

Chan RH et. al.

Circ 2014; 130(6):

484-95

Page 14: Hypertrophic cardiomyopathy state of the art

Highest

Intermediate

Lowest

2° prevention

Cardiac arrest/sustained VT

1° prevention

Family history HCM-SD

Unexplained syncope

Multiple-repetitive NSVT (Holter)

Abnormal exercise BP response

LGE ≥ 15% of LV mass

Massive LVH ≥ 30 mm

Rare subgroups/potential arbitrators

End-stage (EF < 50%)

LV apical aneurysm

Marked LV outflow obstruction (rest)

Modifiable

Intense competitive sports

CAD

LGE ≥ 15% of LV mass

Age ≥ 60y

Alcohol septal ablation (?)

ICD

Page 15: Hypertrophic cardiomyopathy state of the art

Evidence for Decreased

HCM Mortality:

1000 Patients Presenting

in Mid-Life (30-59y)

MHIF/Tufts

What is Possible…..

Page 16: Hypertrophic cardiomyopathy state of the art

0.0

0.2

0.4

0.6

0.8

1.0

1.2

1.4

General Population "Historic Mortality"

0.8%/y

32 ICD

interventions

% D

ea

th P

er

Year

1.5%/y

Maron BJ et. al.

JACC in press

Page 17: Hypertrophic cardiomyopathy state of the art

0.0

0.2

0.4

0.6

0.8

1.0

1.2

1.4

General Population "Historic Mortality"

0.8%/y

% D

eath

Per

Year

0.8%/y

Page 18: Hypertrophic cardiomyopathy state of the art

0.0

0.2

0.4

0.6

0.8

1.0

1.2

1.4

General Population "Historic Mortality"

0.8%/y

14

Transplants

% D

eath

Per

Year

0.8%/y

Page 19: Hypertrophic cardiomyopathy state of the art

0.0

0.2

0.4

0.6

0.8

1.0

1.2

1.4

General Population "Historic Mortality"

% D

eath

Per

Year

0.8%/y

0.6%/y

Page 20: Hypertrophic cardiomyopathy state of the art

0.0

0.2

0.4

0.6

0.8

1.0

1.2

1.4

General Population "Historic Mortality"

0.8%/y

6 OHCA

(with

hypothermia) % D

eath

Per

Year

0.6%/y

Page 21: Hypertrophic cardiomyopathy state of the art

0.8%/y

0.5%/y

Current Mortality

2014

% D

eath

Per

Year

p = 0.46

Page 22: Hypertrophic cardiomyopathy state of the art

0.0

0.2

0.4

0.6

0.8

1.0

1.2

1.4

0.5%/y

Current Mortality

2014

Advanced

Heart Failure

(n = 21)

SCD

(n = 15)

% D

eath

Per

Year

Stroke (n=1)

Page 23: Hypertrophic cardiomyopathy state of the art

0.0

0.2

0.4

0.6

0.8

1.0

1.2

1.4

0.5%/y

Current Mortality

2014

Advanced

Heart Failure

(n = 21)

SCD

(n = 15)

% D

eath

Per

Year

Stroke (n=1)

15 SCDs but…

5 declined ICD

7 pre-ICD era

Page 24: Hypertrophic cardiomyopathy state of the art

Sudden

Death

Advanced

HF

Page 25: Hypertrophic cardiomyopathy state of the art

Paradigm Change in Causes of Death: Advanced Heart Failure w/o

Obstruction (transplant/transplant candidates)

All HCM Patients

Current Causes of HCM Mortality (2015)

3%

(60%)

Page 26: Hypertrophic cardiomyopathy state of the art

Surgical Septal Myectomy:

Quality of Life/Survival

0.5

0.6

0.7

0.8

0.9

1.0

0 1 2 3 4 5 6 7 8 9 10

Years Post-op

Su

rviv

al

Isolated Myectomy Nonoperated obstructive Expected ---US population P<0.001

83%

61%

Ommen S et. al.

JACC 2006

(Operative mortality: 0.4%)

Page 27: Hypertrophic cardiomyopathy state of the art

CONTEMPORARY HCM MORTALITY

BY AGE: MHIF/Tufts

2015

<29 y 30-59 y >60 y Total

No.

Patients 474 1000 428 1902

HCM

Mortality 0.5%/y 0.5%/y 0.6%/y 0.5%/y

Page 28: Hypertrophic cardiomyopathy state of the art

Estimated Decrease in

Predicted HCM Mortality

Over 50 Years

4-6%

1.5%

0.5%

Page 29: Hypertrophic cardiomyopathy state of the art

ICD

Sudden

Death

Progressive

Heart

Failure

(obstructive)

Advanced

Heart Failure

& End Stage

(non-

obstructive)

AF

&

Stroke

Benign/Stable (normal longevity)

Drugs

Septal Myectomy

(Alcohol Ablation)

Transplant Drugs

Anticoagulants

Ablation

Profiles in Prognosis for HCM

Page 30: Hypertrophic cardiomyopathy state of the art

Teare report

New disease (Braunwald; NIH)

Familial

Rare disease

“Interesting patients”

Controversy:

? Is obstruction

real

Echo Dx

↑ Recognition and

↑ risk

Common (1:500)

↑ Myectomy

Not as risky

Normal longevity

possible

Modern genetics

↓ Myectomy risk

↑ Alcohol ablation

SD prevention (ICD)

Genetic testing

Advanced imaging

Contemporary

Treatable

Disease

Phases of HCM History

Page 31: Hypertrophic cardiomyopathy state of the art

• It is literally a new day… for

the HCM patients

• Maturing perceptions of

HCM and effective

treatment interventions

Page 32: Hypertrophic cardiomyopathy state of the art
Page 33: Hypertrophic cardiomyopathy state of the art

ICD Performance in HCM

506

103

5.5%/y

Follow-up =

3.7 ± 3 years

ICD discharge

rate

Appropriate

Shocks (20%)

11%/y 4%/y

2º prevention 1º prevention

VT/VF

Maron BJ et. al.

JAMA 2007;

298:405-412

Page 34: Hypertrophic cardiomyopathy state of the art

ICD in HCM for Children / Adolescents

224

43

4.4% / yr

13%/yr 3%/yr

No. Patients

Appropriate ICD

Discharge (19%)

2° prevention 1° prevention

Follow-up=

4.3 ± 3.3 yr

Initial shock 9-23 y

(mean= 17 y)

Maron BJ et. al.

JACC 2013;

61:1527-35

Page 35: Hypertrophic cardiomyopathy state of the art

≤ 3

4 - 6

7 - 10

11-20

21-30

31-40 51-60

>90

Duration (months)

No

. P

ati

en

ts

0

2

4

6

8

10

12

14

16

61-70

71-90

41-50

ICD in HCM - II: Time to First Shock

Maron BJ et. al.

JAMA 2007;

298:405-412

Page 36: Hypertrophic cardiomyopathy state of the art

Profiles in Prognosis for

HCM

Sudden

Death

Risk

Symptom

Progression

End-

Stage AF

Page 37: Hypertrophic cardiomyopathy state of the art

0

0.5

1

1.5

2

% H

CM

Mo

rta

lity

HCM-Related Mortality

0

0.5

1.5

1

6

General U.S.

Population

0.8%/y

0.5%/y

1.5%/y

3-6%/y

Early HCM

Referral Cohorts

HCM Cohorts:

Prior to utilization

of current treatment

strategies/

interventions

ICD intervention

Heart transplant/myectomy

OHCA/defibrillation/hypothermia

Present HCM

Cohort:

Contemporary

treatment

Page 38: Hypertrophic cardiomyopathy state of the art

LA

LA

VS

RV

LV VS

A B C

D E F

Prevalence

of LGE = 55-70%

Page 39: Hypertrophic cardiomyopathy state of the art

HCM is Unpredictable

Page 40: Hypertrophic cardiomyopathy state of the art

Evidence for Reduced

HCM Mortality:

n=1000 Presenting 30-59y

What is possible………

Page 41: Hypertrophic cardiomyopathy state of the art

Beta-

blocker Verapamil

Beta-

blocker Verapamil

Verapamil

+ Diuretic Beta-blocker

+ Diuretic

Subaortic

Obstruction DDD

Pacing

Septal

Myectomy

Nonobstructive

Heart

Transplantation

Disopyramide

Diltiazem

Beta-blocker

+ Verapamil

Management of HCM

Asymptomatic

Mild-Moderate

Symptoms

Severe

Symptoms

? ?

Treatment

Failure

Refractory

Severe

Symptoms

Alcohol

Septal

Ablation

Page 42: Hypertrophic cardiomyopathy state of the art

Evidence for Reduced

HCM Mortality:

n=1000 Presenting 30-59y

What is possible………

Page 43: Hypertrophic cardiomyopathy state of the art
Page 44: Hypertrophic cardiomyopathy state of the art

0

2

4

6

8

10

12

14

16

<15 16-19 20-24 25-29 30

Max. LV Wall Thickness (mm)

% P

ati

en

ts W

ith

SC

D

Relation Between LV Thickness &

SCD in 482 HCM Patients

Page 45: Hypertrophic cardiomyopathy state of the art

Highest

Intermediate

Lowest

2° prevention

Cardiac arrest/sustained VT

1° prevention

Family history HCM-SD

Unexplained syncope

Multiple-repetitive NSVT (Holter)

Abnormal exercise BP response

LGE ≥ 15% of LV mass

Massive LVH ≥ 30 mm

Rare subgroups/potential arbitrators

End-stage (EF < 50%)

LV apical aneurysm

Marked LV outflow obstruction (rest)

Modifiable

Intense competitive sports

CAD

LGE ≥ 15% of LV mass

Age ≥ 60y

Alcohol septal ablation (?)

ICD

Page 46: Hypertrophic cardiomyopathy state of the art

A C

D E F

LA

P

D D

P

VS

VS

B

P

D

* * *

* *

*

Figure 1.

Page 47: Hypertrophic cardiomyopathy state of the art

0

1

2

3

4

5

6

7

1 2 ≥ 3 No. of Risk Factors for Primary Prevention

Ra

te o

f A

pp

rop

ria

te In

terv

en

tio

ns

pe

r 1

00

pe

rso

n-y

r

3.8

3.0

4.1

Overall p=0.88

Appropriate

Shocks

(35%)

Page 48: Hypertrophic cardiomyopathy state of the art

High

risk

Some

risk

Cardiologist

Patient

Autonomy

TRANSPARENCY / FULL DISCLOSURE / INFORMED CONSENT

?

Risk Factors

Primary Prevention Decision Tree: ICD In HCM

Page 49: Hypertrophic cardiomyopathy state of the art

% H

CM

Mo

rta

lity

HCM-Related Mortality

0

0.5

1.5

1

6

General U.S.

Population

0.8%/y

0.5%/y

1.5%/y

3-6%/y

Early HCM

Referral Cohorts

HCM Cohorts:

Prior to utilization

of current

treatment strategies/

interventions

Present HCM

Cohort:

Contemporary

treatment

ICD intervention

Cardiac transplant

OHCA/defibrillation/hypothermia

Page 50: Hypertrophic cardiomyopathy state of the art

% P

ati

en

ts W

ith

/Wit

ho

ut

ICD

In

terv

en

tio

n/S

ud

den

Death

Appropriate

ICD

Intervention

No Appropriate

ICD

Intervention

ESC Risk Score

<4% <4% 4-6% 4-6% >6% >6%

Risk/5y Risk/5y

<4% 4-6% >6%

Risk/5y

Sudden Death

Assessment of ESC Sudden Death Risk Score

(n = 1649)

60%

26%

63%

9%

Page 51: Hypertrophic cardiomyopathy state of the art

ICD

Sudden

Death

Progressive

Heart

Failure

(obstructive)

Advanced

Heart Failure

& End Stage

(non-

obstructive)

AF

&

Stroke

Benign/Stable (normal longevity)

Drugs

Septal Myectomy

(Alcohol Ablation)

Transplant Drugs

Anticoagulants

Ablation

Profiles in Prognosis for HCM

Page 52: Hypertrophic cardiomyopathy state of the art

Highest

Intermediate

Lowest

2° prevention

Cardiac arrest/sustained VT

1° prevention

Family history HCM-SD

Unexplained syncope

Multiple-repetitive NSVT (Holter)

Abnormal exercise BP response

LGE ≥ 15% of LV mass

Massive LVH ≥ 30 mm

Rare subgroups/potential arbitrators

End-stage (EF < 50%)

LV apical aneurysm

Marked LV outflow obstruction (rest)

Modifiable

Intense competitive sports

CAD

LGE ≥ 15% of LV mass

Age ≥ 60y

Alcohol septal ablation (?)

ICD

Page 53: Hypertrophic cardiomyopathy state of the art
Page 54: Hypertrophic cardiomyopathy state of the art

0

2

4

6

8

10

12

14

16

<15 16-19 20-24 25-29 30

Max. LV Wall Thickness (mm)

% P

ati

en

ts W

ith

SC

D

Relation Between LV Thickness &

SCD in 482 HCM Patients

Page 55: Hypertrophic cardiomyopathy state of the art

Highest

Intermediate

Lowest

2° prevention

Cardiac arrest/sustained VT

1° prevention

Family history HCM-SD

Unexplained syncope

Multiple-repetitive NSVT (Holter)

Abnormal exercise BP response

LGE ≥ 15% of LV mass

Massive LVH ≥ 30 mm

Rare subgroups/potential arbitrators

End-stage (EF < 50%)

LV apical aneurysm

Marked LV outflow obstruction (rest)

Modifiable

Intense competitive sports

CAD

LGE ≥ 15% of LV mass

Age ≥ 60y

Alcohol septal ablation (?)

ICD

Page 56: Hypertrophic cardiomyopathy state of the art

L

G

E

LGE LGE

Extent of LGE vs. Sudden Death Risk in HCM

Follow-up (years)

Su

rviv

al

LGE (-) LGE < 10%

LGE 10-20%

LGE > 20%

Page 57: Hypertrophic cardiomyopathy state of the art

ICD Performance in HCM

506

103

5.5%/y

Follow-up =

3.7 ± 3 years

ICD discharge

rate

Appropriate

Shocks (20%)

11% 4%

2º prevention 1º prevention

VT/VF

Page 58: Hypertrophic cardiomyopathy state of the art

0

1

2

3

4

5

6

7

1 2 ≥ 3 No. of Risk Factors for Primary Prevention

Ra

te o

f A

pp

rop

ria

te In

terv

en

tio

ns

pe

r 1

00

pe

rso

n-y

r

3.8

3.0

4.1

Overall p=0.88

Appropriate

Shocks

(35%)

Page 59: Hypertrophic cardiomyopathy state of the art

Beta-

blocker Verapamil

Beta-

blocker Verapamil

Verapamil

+ Diuretic Beta-blocker

+ Diuretic

Subaortic

Obstruction DDD

Pacing

Septal

Myectomy

Nonobstructive

Heart

Transplantation

Disopyramide

Diltiazem

Beta-blocker

+ Verapamil

Management of HCM

Asymptomatic

Mild-Moderate

Symptoms

Severe

Symptoms

? ?

Treatment

Failure

Refractory

Severe

Symptoms

Alcohol

Septal

Ablation

Page 60: Hypertrophic cardiomyopathy state of the art

Alcohol Septal

Ablation

Page 61: Hypertrophic cardiomyopathy state of the art

Septal Scarring

Septal Scar No Scar

Post-ablation Post-myectomy

VS=30%

LV 10% Valeti et. al. JACC 2007;49:350

Page 62: Hypertrophic cardiomyopathy state of the art

Cardiovascular Societies &

HCM Consensus Panels for

Myectomy vs. Alcohol Ablation

ACC 2003

ESC 2003

ACC 2011

AHA 2011

Myectomy

Myectomy

Myectomy

Myectomy

Page 63: Hypertrophic cardiomyopathy state of the art

0.0

0.2

0.4

0.6

0.8

1.0

1.2

1.4

General Population "Historic Mortality"

0.8%/y

32 ICD

interventions

% D

ea

th P

er

Ye

ar

1.5%/y

Page 64: Hypertrophic cardiomyopathy state of the art

0.0

0.2

0.4

0.6

0.8

1.0

1.2

1.4

General Population "Historic Mortality"

0.8%/y

% D

eath

Per

Year 0.8%/y

Page 65: Hypertrophic cardiomyopathy state of the art

0.0

0.2

0.4

0.6

0.8

1.0

1.2

1.4

General Population "Historic Mortality"

0.8%/y

14 Transplants

% D

eath

Per

Year 0.8%/y

Page 66: Hypertrophic cardiomyopathy state of the art

0.0

0.2

0.4

0.6

0.8

1.0

1.2

1.4

General Population "Historic Mortality"

0.8%/y

% D

eath

Per

Year 0.8%/y

0.6%/y

Page 67: Hypertrophic cardiomyopathy state of the art

0.0

0.2

0.4

0.6

0.8

1.0

1.2

1.4

General Population "Historic Mortality"

0.8%/y

6 OHCA

(w/ hypothermia) % D

eath

Per

Year

0.6%/y

Page 68: Hypertrophic cardiomyopathy state of the art

0.8%/y

0.5%/y

Current Mortality

2014

% D

eath

Per

Year

p = 0.46

Page 69: Hypertrophic cardiomyopathy state of the art

0.0

0.2

0.4

0.6

0.8

1.0

1.2

1.4

0.5%/y

Current Mortality

2014

Advanced

Heart Failure

(n = 21)

SCD

(n = 15)

% D

eath

Per

Year

Stroke (n=1)

Page 70: Hypertrophic cardiomyopathy state of the art

0.0

0.2

0.4

0.6

0.8

1.0

1.2

1.4

0.5%/y

Current Mortality

2014

Advanced

Heart Failure

(n = 21)

SCD

(n = 15)

% D

eath

Per

Year

Stroke (n=1)

15 SCDs but…

5 declined ICD

7 pre-ICD era

Page 71: Hypertrophic cardiomyopathy state of the art

% H

CM

Mo

rta

lity

HCM-Related Mortality

0

0.5

1.5

1

6

General U.S.

Population

0.8%/y

0.5%/y

1.5%/y

3-6%/y

Early HCM

Referral Cohorts

HCM Cohorts:

Prior to utilization

of current

treatment strategies/

interventions

Present HCM

Cohort:

Contemporary

treatment

ICD intervention

Cardiac transplant

OHCA/defibrillation/hypothermia

Page 72: Hypertrophic cardiomyopathy state of the art

ICD

Sudden

Death

Progressive

Heart

Failure

(obstructive)

Advanced

Heart Failure

& End Stage

(non-

obstructive)

AF

&

Stroke

Benign/Stable (normal longevity)

Drugs

Septal Myectomy

(Alcohol Ablation)

Transplant Drugs

Anticoagulants

Ablation

Profiles in Prognosis for HCM

Page 73: Hypertrophic cardiomyopathy state of the art

Arrhythmogenic Myocardial Substrate in HCM

Page 74: Hypertrophic cardiomyopathy state of the art

HCM

(36%)

Coronary

Anomalies

(17%)

Dilated CM (2%)

Sudden Death in Young Athletes

Maron, BJ et. al.

Circulation 2009;

119:1085-1092

Page 75: Hypertrophic cardiomyopathy state of the art

Highest

Intermediate

Lowest

2° prevention

Cardiac arrest/sustained VT

1° prevention

Family history HCM-SD

Unexplained syncope

Multiple-repetitive NSVT (Holter)

Abnormal exercise BP response

LGE ≥ 15% of LV mass

Massive LVH ≥ 30 mm

Rare subgroups/potential arbitrators

End-stage (EF < 50%)

LV apical aneurysm

Marked LV outflow obstruction (rest)

Modifiable

Intense competitive sports

CAD

LGE ≥ 15% of LV mass

Age ≥ 60y

Alcohol septal ablation (?)

ICD

Page 76: Hypertrophic cardiomyopathy state of the art

A C

D E F

LA

P

D D

P

VS

VS

B

P

D

* * *

* *

*

Figure 1.

Page 77: Hypertrophic cardiomyopathy state of the art

Patients with

LVAA

(n=28)

Aborted

Cardiac

Arrest

(2)✝

Progressive

Heart Failure/

Death

(5)✝

Sudden

Death

(2)*

non-fatal

embolic

stroke

(1)

non-fatal

embolic

stroke

(1)

Appropriate

ICD Discharge

(3)*

Alive/

Clinically

Stable

(n = 16)*

Adverse

Events

(n = 12)

Cardiovascular Event Rate = 11%/year

Page 78: Hypertrophic cardiomyopathy state of the art

Highest

Intermediate

Lowest

2° prevention

Cardiac arrest/sustained VT

1° prevention

Family history HCM-SD

Unexplained syncope

Multiple-repetitive NSVT (Holter)

Abnormal exercise BP response

LGE ≥ 15% of LV mass

Massive LVH ≥ 30 mm

Rare subgroups/potential arbitrators

End-stage (EF < 50%)

LV apical aneurysm

Marked LV outflow obstruction (rest)

Modifiable

Intense competitive sports

CAD

LGE ≥ 15% of LV mass

Age ≥ 60y

Alcohol septal ablation (?)

ICD

Page 79: Hypertrophic cardiomyopathy state of the art

0

10

20

30

40

50

60

70

Alive Non-

Cardiac

Death

Non-HCM

Cardiac

Death

Embolic

Stroke

Heart

Failure

SCD

% o

f H

CM

Co

ho

rt

65%

13% 12%

2% 1%

0.2%/y

Outcome of HCM Patients First Evaluated ≥ 60 Years

1%

HCM Death

Aging is Good in HCM

Page 80: Hypertrophic cardiomyopathy state of the art

Intermediate

Low Risk

Risk Stratification for Sudden Death in HCM

Moderate

High

No risk factors

Family history of sudden death

Nonsustained VT

Unexplained syncope

Extreme LVH

Abnormal BP response to Ex

0.5%/year

Page 81: Hypertrophic cardiomyopathy state of the art

LA

LA

VS

RV

LV VS

A B C

D E F

Prevalence

of LGE = 55-70%

Page 82: Hypertrophic cardiomyopathy state of the art

L

G

E

LGE LGE

Extent of LGE vs. Sudden Death Risk in HCM

Follow-up (years)

Su

rviv

al

LGE (-) LGE < 10%

LGE 10-20%

LGE > 20%

Page 83: Hypertrophic cardiomyopathy state of the art

Highest

Intermediate

Lowest

2° prevention

Cardiac arrest/sustained VT

1° prevention

Family history HCM-SD

Unexplained syncope

Multiple-repetitive NSVT (Holter)

Abnormal exercise BP response

LGE ≥ 15% of LV mass

Massive LVH ≥ 30 mm

Rare subgroups/potential arbitrators

End-stage (EF < 50%)

LV apical aneurysm

Marked LV outflow obstruction (rest)

Modifiable

Intense competitive sports

CAD

LGE ≥ 15% of LV mass

Age ≥ 60y

Alcohol septal ablation (?)

ICD

Page 84: Hypertrophic cardiomyopathy state of the art

(15%)

(15%)

(7%)

(7%)

(<1%)

(<1%)

(<1%)

(<1%)

(<1%)

(<1%)

Page 85: Hypertrophic cardiomyopathy state of the art

Unexplained LVH

Sarcomeric Protein

Mutations Non-Sarcomeric

Mutations

AMP-Kinase

(PRKAG2)

Lamp2

(Danon)

Storage Diseases

~ 11 Genes---

or more?

> 1400 mutations

Fabry

Disease

Page 86: Hypertrophic cardiomyopathy state of the art

Genetic

Testing

Prognosis

HCM

(w/o LVH)

HCM

(w/ LVH)

To

ide

ntify

“Genotype +

Phenotype - ”

Follow-up

Page 87: Hypertrophic cardiomyopathy state of the art

HCM—ICD Registry

29

(6%)

14

14

1

Deaths

ICD

Malfunction End-stage

Embolic stroke

Cancer, sepsis,

renal diseases,

suicide, CAD,

accidents

No HCM

HCM

HCM- Arrhythmias

(nl EF)

Maron, BJ et. al. JAMA 2007;298:405

Page 88: Hypertrophic cardiomyopathy state of the art

Evidence for Reduced

HCM Mortality:

n=1000 Presenting 30-59y

What is possible………

Page 89: Hypertrophic cardiomyopathy state of the art

Contemporary C-V treatment options

offer HC patients a reasonable

aspiration for reduced mortality and

extended longevity. The ICD has

altered clinical course affording the

possibility of normal or near normal

life expectancy.

Page 90: Hypertrophic cardiomyopathy state of the art

Contemporary C-V treatment options

offer HC patients a reasonable

aspiration for reduced mortality and

extended longevity. The ICD has

altered clinical course affording the

possibility of normal or near normal

life expectancy.

Page 91: Hypertrophic cardiomyopathy state of the art

0

0.5

1

1.5

2

% H

CM

Mo

rta

lity

HCM-Related Mortality

0

0.5

1.5

1

6

General U.S.

Population

0.8%/y

0.5%/y

1.5%/y

3-6%/y

Early HCM

Referral Cohorts

HCM Cohorts:

Prior to utilization

of current

treatment strategies/

interventions

Present HCM

Cohort:

Contemporary

treatment

ICD intervention

Heart transplant/myectomy

OHCA/defibrillation/hypothermia