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Hypertrophic Cardiomyopathy
New advances in clinical management
and sudden death prevention
Prof. Franco Cecchi, MD
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Authors/Task Force members: Perry M. Elliott (Chairperson) (UK)
Aris Anastasakis (Greece), Michael A. Borger (Germany), Martin Borggrefe(Germany), Franco Cecchi (Italy), Philippe Charron (France), Albert Alain Hagege(France), Antoine Lafont (France), Giuseppe Limongelli (Italy), Heiko Mahrholdt(Germany), William J. McKenna (UK), Jens Mogensen (Denmark), PetrosNihoyannopoulos (UK), Stefano Nistri (Italy), Petronella G. Pieper (Netherlands), Burkert Pieske (Austria), Claudio Rapezzi (Italy), Frans H. Rutten (Netherlands), Christoph Tillmanns (Germany), and Hugh Watkins (UK).
Additional Contributor: Constantinos O'Mahony (UK).
Guidelines are developed to aid the practitioner
in pursuing the most appropriate healthcare response
for the clinical circumstances of a specific patient
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Prof. Franco Cecchi, MD
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Amyloid
LV Non CompactionLV wall tumor
SARCOMERIC HCM
Myofilament Protein Mutations65 – 80 %
MYBPC3‐MYH7‐TNN2‐TNNI3
Z‐disc and Ca++ regulMutations (2‐5%)
22 Genes > 1000 mutations
Non‐Sarcomeric HCM (5‐10% ?)
LSD α‐Galactosidase mutAnderson‐Fabry disease (~1%)
Syndromic (RAS): Noonan S.Leopard S.Freidreich Ataxia
GlycogenStorage disease
MitochondrialDisease
Metabolic Deficiency
HCM in adults
Danon
Prof. Franco Cecchi, MD
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1677 pts, 40 Italian centers mean FU 9,7 yrs
Atrial Fibrillation 22 %ACS + MI 3.5 %Sustained VT 3 %Syncope 7 %SA /AV‐block 5 %Others 4 %
Annual CV mortality 1% Sudden Death 0,3% Appropriate ICD discharge 0,3%
Progression to NYHA III/IV or CHF Death
129630
50
40
30
20
10
0Follow‐up (yrs)
Sudden Death
Progressionto FC II
CV EVENTS
Cumulative Risk (%
)
Progression to FC III‐IV/ Endstage HF
Prof. Franco Cecchi, MD
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HCM : RISK STRATIFICATION FOR SUDDEN DEATHANNUAL RISK OF SUDDEN DEATH : < 1% (range 0 ‐ 10% )
CMI END‐STAGE (stage IV) 10%
0%
1,4% CARDIAC ARREST SURVIVOR (2010)
7% CARDIAC ARREST SURVIVOR (1989‐1995)
Prof. Franco Cecchi, MD
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LIMITATIONS OF CLASSICAL RISK FACTORS (ICD Guidelines for HCM 2003 & 2011)
RISK FACTOR Sensitivity Specificity PPV NPV
Family history of SD 42 79 28 88
Max LV thickness > 30 mm 26 88 13 95
Non sustained VT (ECG D) 69 80 22 97
Abnormal pressure responseat exercise test age < 45
75 66 15 97
Syncope 29 83 25 86
Elliot P, W.McKenna, 2003 Level of evidence C
Prof. Franco Cecchi, MD
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41%40%15%3%0,6%
Pts %
Prof. Franco Cecchi, MD
• The aggregation of risk factors is associated with increased risk of SCD
• PPV remains low even in the presenceof multiple risk factors
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CHF
SD5,9%
Prof. Franco Cecchi, MD
…..these results underscore the need for a more accurate assessment of the sudden death risk in patients with HC
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Prof. Franco Cecchi, MD
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Prof. Franco Cecchi, MD
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2014
Multicenter study (6) 3675 pts
Age > 16 yrs at diagnosis
Prof. Franco Cecchi, MD
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http://www.doc2do.com/hcm/webHCM.html
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Prevention of Sudden Cardiac Death
Recommendations for ICD in each risk category take into account not only the absolute statistical risk, but also the age and general health of thepatient, socio-economic factors and the psychological impact of therapy.
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Extent of LGE (> 6 SD above the mean)is an additional risk factor in pts considered at low risk
Circulation 2014
Prof. Franco Cecchi, MD
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Prof. Franco Cecchi, MD
LGE extension + LVEF <60% are markers of disease progression
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SURVIVAL FREE OF SUDDEN DEATH
Ommen S, Maron BJ, Olivotto I et al, JACC 2005
(Rochester Mayo Clinic, versus Minneapolis + Florence)
RISK STRATIFICATION: risk factors modifications
Prof. Franco Cecchi, MD
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SUBCUTANEOUS ICD
Prof. Franco Cecchi, MD
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S‐ICD for SD PREVENTION in pts with HCM
It may : • improve LONG TERM RISK/BENEFIT RATIO + QOL • increase acceptance by children and adolescents• avoid lead fracture and sepsis• reduce implant complications and • inappropriate discharges due to SV arrhythmias
Prof. Franco Cecchi, MDProf. Franco Cecchi, MD
HEART RHYTHM CONGRESS 2014 AB06‐06 ‐ Combined Analysis of Subcutaneous ICD Outcomes in Hypertrophic Cardiomyopathy Patients from the EFFORTLESS Registry & IDE StudyLambiase P. et al.
96 HCM ptsConclusions: This pooled analysis shows the S‐ICD has equivalent conversion efficacy, appropriate rhythm discrimination & therapy in HCM vs non‐HCM pts‐ demonstrating satisfactory early performance in the HCM population
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Prof. Franco Cecchi, MD
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New areas of Clinical research and options
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HCM: RANOLAZINE EFFECTS ON CARDIOMYOCITES
Late Sodium Current Inhibition ReversesElectromechanical Dysfunction in Human Hypertrophic Cardiomyopathy
Circulation. 2013;127:575‐584,Coppini R et al.
Prof. Franco Cecchi, MD
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The reappraisal of complexGENE MUTATIONS
Prof. Franco Cecchi, MD
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Thanks !!
I. OLIVOTTO, B. TOMBERLI
NURSING K.Baldini, S.FantiniGENETICS F. Torricelli, F. Girolami CMR L.Rega, S.PradellaPET R. SciagràALCOHOL SA D. AntoniucciCARDIAC SURGERY M.Yacoub, PL.Stefano, G.Popoff, P. FerrazziISTOPATHOLOGY G. D’Amati, O.LeoneELECTROPHYSIOLOGY L. Padeletti, P.Pieragnoli, G.Ricciardi, F.Gaita, MG BongiorniPHYSIOLOGY C. Poggesi, C.Ferrantini, R. CoppiniNEUROLOGY W.BorsiniNEPHROLOGY L.CiramiIE METABOLISM M.A. Donati, A. Morrone, E. Pasquini