5. General evaluation documented or
suspected VT
1. Syncope
2. ECG / ETT
3. Ambulatory ECG
4. Implantable monitor
5. Imaging
6. Biomarkers
7. Genetic
8. Cath / CCTA
9. EP
5
6. General evaluation documented or
suspected VT1. Syncope
2. ECG / ETT
3. Ambulatory ECG
4. Implantable monitor
5. Imaging
6. Biomarkers
7. Genetic
8. Cath / CCTA
9. EP
ā¢ HISTORY
ā¢ FAMILY HOSTORY
ā¢ EXAMINATION
6
7. General evaluation documented or
suspected VT1. Syncope
2. ECG / ETT
3. Ambulatory ECG
4. Implantable monitor
5. Imaging
6. Biomarkers
7. Genetic
8. Cath / CCTA
9. EP
Stable VTļ 12 Lead ECG during WCT
ļ 12 Lead ECG Sinus
ETT for Exercise induced arrhythmias
1.Symptoms on exertion
2.IHD
3.CPVT
7
8. General evaluation documented or
suspected VT1. Syncope
2. ECG / ETT
3. Ambulatory ECG
4. Implantable monitor
5. Imaging
6. Biomarkers
7. Genetic
8. Cath / CCTA
9. EP
Symptoms
are caused by VA
8
9. General evaluation documented or
suspected VT1. Syncope
2. ECG / ETT
3. Ambulatory ECG
4. Implantable monitor
5. Imaging
6. Biomarkers
7. Genetic
8. Cath / CCTA
9. EP
Sporadic Symptoms
9
10. General evaluation documented or
suspected VT1. Syncope
2. ECG / ETT
3. Ambulatory ECG
4. Implantable monitor
5. Imaging
6. Biomarkers
7. Genetic
8. Cath / CCTA
9. EP
ECHO for structure and function
CT / MRI
10
11. General evaluation documented or
suspected VT1. Syncope
2. ECG / ETT
3. Ambulatory ECG
4. Implantable monitor
5. Imaging
6. Biomarkers
7. Genetic
8. Cath / CCTA
9. EP
BNP
NT Pro-BNP
For predicting SCA and SCD
11
12. General evaluation documented or
suspected VT1. Syncope
2. ECG / ETT
3. Ambulatory ECG
4. Implantable monitor
5. Imaging
6. Biomarkers
7. Genetic
8. Cath / CCTA
9. EP
Patients and family
Counselling
For those with
Recommended Genetic testing
See expert concensus document
12
13. General evaluation documented or
suspected VT1. Syncope
2. ECG / ETT
3. Ambulatory ECG
4. Implantable monitor
5. Imaging
6. Biomarkers
7. Genetic
8. Cath / CCTA
9. EP
SCA
13
14. General evaluation documented or
suspected VT1. Syncope
2. ECG / ETT
3. Ambulatory ECG
4. Implantable monitor
5. Imaging
6. Biomarkers
7. Genetic
8. Cath / CCTA
9. EP
Risk assessment in
1. ICM
2. NICM
3. ACHD
Not candidates for Primary ICD
1. ICD CANDIDIATES
2. LONG QT
3. SHORT QT
4. CPVT
5. Early Repolarization Syndrome
14
18. Therapies for Prevention
BB reduce mortality in
ā¢ HFrEF
ā¢ MI
ā¢ Polymorphic VT after MI
ā¢ Acute BB in MI increase mortality
ā¢ Medicines
ā¢ Defibs
ā¢ Catheter Ablation
ā¢ Surgical Ablation
ā¢ Autonomic Modulation
ā¢ Revasc.
18
19. Therapies for Prevention
In patients taking diuretics monitor both
ā¢ Potassium
ā¢ Magnessium
Replace both if deficient
IV Mg post MI ļ No mortality benefit at 30 days
ā¢ Medicines
ā¢ Defibs
ā¢ Catheter Ablation
ā¢ Surgical Ablation
ā¢ Autonomic Modulation
ā¢ Revasc.
19
20. Therapies for Prevention
PUFA
Initial studies showed mortality benefit and less SCD
Later studies showed no benefit, no harm
Statins
Benefit in IHD MADIT-CRT, SCD-HeFT, AVID, DEFINITE
No Benefit in HFļ Rosuvastatin in CORONA, GISSI-HF
ā¢ Medicines
ā¢ Defibs
ā¢ Catheter Ablation
ā¢ Surgical Ablation
ā¢ Autonomic Modulation
ā¢ Revasc.
20
25. Therapies for Prevention
ā¢ VA / SCA
ā¢ Anomalous origin of coronary is the cause
ā¢ Medicines
ā¢ Defibs
ā¢ Catheter Ablation
ā¢ Surgical Ablation
ā¢ Autonomic Modulation
ā¢ Revasc.
BUT Revasc alone is not enough in case of prior MI and Monomorphic VT
25
26. Acute Management Of VA / Cardiac
Arrest
ā¢ CPRļ ACLS
ā¢ IV Amiodarone after 1 max energy shock
ā¢ DCC
ā¢ STEMI + Polymorphic VT ļ Urgent C.Angiogram + Revasc.
ā¢ WCT is VT if unclear
ā¢ Stable VT ļ IV Procainamide (not in unstable)
ā¢ VF/ polymorph VT ļ CPR+ Defib + Adrenaline fail ļ LIDOCAINE
ā¢ Polymorphic VT due to Ischemia ļ IV BB ( trials on ACLS vs BB )
ā¢ Recent MI with VT/VF Storm despite DCC and Meds ļ IV BB
ā¢ Adrenaline 1mg every 3-5 min
ā¢ Stable VT ļ IV Amio / Sotalol
ā¢ HIGH dose Adrenaline
ā¢ Mg ( without torsades )
ā¢ Prophylactic lidocaine
ā¢ Verapamil/diltiazem
26
27. Sub Cutaneous - Defibs
ā¢ If Indication for PACING or CRT or ATP
ā¢ Inadequate vascular access / high risk for
infection
ā¢ Otherwise
27
28. Wearable Defib
ā¢ REMOVAL OF ICD
ā ICD + SCA/VA ( 2ndry Prevention )
ā¢ Not indication for ICD but Risk of SCD
ā Within 40/90 days with EF<35
ā Transplant candidates
ā Myocarditis
ā Secondary CM
ā Systemic Infection
28
29. Catheter Ablation
ā¢ Bundle Branch Reentrant VT
ā¢ Epicardial Ablation for SHD with failed
endocardial ablation
29
30. Post Mortem
ā¢ Cardiac specific autopsy for SCD
ā¢ SCD <40y
ā Cardiac evaluation
ā Genetic counselling
ā Genetic testing of 1st degree RELATIVES
ā¢ Post Mortem Genetic testing ( if confirm OR clue on autopsy)
30
31. Terminal Care
ā¢ Inform that it can be DEACTIVATED any time
ā At time of implatantion
ā¢ End of Life/ Terminally ill ļ Discuss
Deactivation
31
32. Shared Decision
ā¢ Shared Decision ( health goals & evidence )
ā¢ Inform Risk of SCD and non sudden DEATH,
Effectiveness, Complications
32
34. IHD
ā¢ ICD
Primary Prevention
Secondary Prevention
Coronary Spasm
Post CABG ā¢ 40/90 days post MI/ Revsc.
ā¢ GDMT
ā¢ Survival >1 yr
NYHA II-III
EF < 35
NYHA I
EF < 30
NSVT
EF <40
EP inducible
NYHA IV
LVAD/T
NYHA IV
NO LVAD/T
ECG; ECHO; SYMPTOMS
34
41. IHDPrimary Prevention
Secondary Prevention
Coronary Spasm
Post CABG
ā¢ Ca Ch. Blocker
ā¢ Smoking cessation
Trial used
1. Diltiazem
2. Verapamil
3. Amlodipine
4. Nifedipine
Ineffective medical therapyļ ICD
ICD in addition to Medical therapy
41
42. IHDPrimary Prevention
Secondary Prevention
Coronary Spasm
Post CABG
POLYMORPHIC (Treat the Cause : Ischemia)
MONOMORPHIC (Scar/graft for CTO)
Same recommendations for SCA/VA
Only LV dysfuntion NSVT with LV dysfunction
EP inducibleļ ICD
Reasses LV after 3 Months
LV improves
EARLY POST CABG PHASE
WCD meanwhile
VERY EARLY
Within 24 hours is due to Reperfusion
Acid base/electrolytes
42
43. NICM
VERY EARLY
Within 24 hours is due to Reperfusion
Acid base/electrolytes
MRI for risk of SCA/SCD
Suspected infiltration ļ MRI
NICM + Conduction disease / LV dys / FH of SCD + <40 yo ļ Genetic counselling and Testing
43
44. NICM
VERY EARLY
Within 24 hours is due to Reperfusion
Acid base/electrolytesPrimary Prevention ICD
Secondary Prevention
Recurrent
EF<35
NYHA II-III
NYHA IV
No LVAD/T
EF<35
NYHA I
Lamin A/C
Mutation plus
2 risk factors
ā¢ NSVT
ā¢ EF<45
ā¢ Nonmissense
ā¢ male
Should be on GDMT for 3 Months
Meanwhile WCD
44
45. NICM
VERY EARLY
Within 24 hours is due to Reperfusion
Acid base/electrolytesPrimary Prevention ICD
Secondary Prevention
Recurrent
SCA
NO reversible Cause
Syncope ļ EP +
SCA but
Inelligible for ICD
ļ Amiodarone
EP has less Value than in IHD.
Some prefer ICD even if EP is negative
45
46. NICM
VERY EARLY
Within 24 hours is due to Reperfusion
Acid base/electrolytesPrimary Prevention ICD
Secondary Prevention
Recurrent
RECURRENT VA despite Beta Blockers
ā¢ AMIODARONE / SOTALOL
ā¢ STORM & failed Amiodarone or others ļ Catheter Ablation
OPTIC TRIAL: most benefit with BB+A
46
51. Genetic diseases
VERY EARLY
Within 24 hours is due to Reperfusion
Acid base/electrolytes
ARVC
HCM
NMD
SCA ļ ICD
Genetic counselling and testing of patient
Genetic counselling and testing of 1st RELATIVES
Suspected ARVC
ā¢ MRI
ā¢ SAECG
SCA/ LVEF /RVEF<35
ā¢ BB
ā¢ Avoid Exercise
ā¢ ICD
ā¢ Genetic
LVEF >35
ā¢ BB
ā¢ EP
Syncope
ICD
51
52. Genetic diseases
VERY EARLY
Within 24 hours is due to Reperfusion
Acid base/electrolytes
ARVC
HCM
NMD
SCA ļ ICD
Genetic counselling and testing of patient
Genetic counselling and testing of 1st RELATIVES
Risk Stratification
RELATIVESļ ECG + ECHO
Established risk factor
ā¢ LVWT > 30mm
ā¢ Syncope < 6 m
ā¢ FH of SCD
NSVT/ abnormal ETT
+HIGH RISK or
RISK MODIFIER
ā¢ ANEURYSM
ā¢ <30 yo
ā¢ HOCM
ā¢ Syncope >5 y
ā¢ MRI
NO RISK Factor even if Gene + ļ ICD
52
NSVT/ abnormal ETT
Without HIGH RISK or
RISK MODIFIER
Amiodarone
If no ICD
EP
53. Genetic diseases
VERY EARLY
Within 24 hours is due to Reperfusion
Acid base/electrolytes
ARVC
HCM
NMD
Same as NICM
Emery- Dreifuss & Limb Girdle Type 1B ļ ICD
Follow up even asymptomatic
MD 1 + PPM ļ ICD ( like Sarcoidosis )
53
54. Channelopathiesā¢ Brugada
ā¢ CPVT
ā¢ LQT
ā¢ sQT
ā¢ J wave
SCA ļ ICD
Genetic counselling and testing of 1st RELATIVES
NO ICD for Asymptomatic low risk even with FH
NO Primary Prevention ICD
GeneticC/T of Pt
OBSERVE
SCAļ ICD
Recurrent ļ Quinidine / Ablation
NO ICDļ Quinidine / Ablation
EP for asymptomatic
Not in any other ch.pathy
54
55. Channelopathiesā¢ Brugada
ā¢ CPVT
ā¢ LQT
ā¢ sQT
ā¢ J wave
SCA ļ ICD
Genetic counselling and testing of 1st RELATIVES
NO ICD for Asymptomatic low risk even with FH
NO Primary Prevention ICD
GeneticC/T of Pt
BB
Recurrent despite BBļ ICD/ Denervation / Inc. MEDS
55
56. Channelopathiesā¢ Brugada
ā¢ CPVT
ā¢ LQT
ā¢ sQT
ā¢ J wave
SCA ļ ICD
Genetic counselling and testing of 1st RELATIVES
NO ICD for Asymptomatic low risk even with FH
Primary Prevention ICD
GeneticC/T of Pt
ECGļ lying/standing/ ETT
<470 ļ BB
>470 ļ BB
>500 Despite BB ļ Inc MEDS/ Denerve/ ICD
Recurrent VA despite BBļ ICD/ Denervation / Inc. MEDS
Recurrent VA after ICD & BB ļ Denerve/ Inc MEDS
QT Pr. DRUGS 56
57. Channelopathiesā¢ Brugada
ā¢ CPVT
ā¢ LQT
ā¢ sQT
ā¢ J wave
SCA ļ ICD
Genetic counselling and testing of 1st RELATIVES
NO ICD for Asymptomatic low risk even with FH
NO Primary Prevention ICD
GeneticC/T of Pt
OBSERVE
Recurrent ļ quinidine
Stormļ Isoprpterenol infusion
57
58. Channelopathiesā¢ Brugada
ā¢ CPVT
ā¢ LQT
ā¢ sQT
ā¢ J wave
SCA ļ ICD
Genetic counselling and testing of 1st RELATIVES
NO ICD for Asymptomatic low risk even with FH
NO Primary Prevention ICD
GeneticC/T of Pt
OBSERVE
58
59. Disease Primary Prevevntion CLASS Secondary Prevention CLASS
HCM
FH of SCD Iia
SCA
SYNCOPE
I
LVWT>30mm Iia
NSVT/BP
with HIGH RISK/MODIFIER
Iia
NSVT/BP Iib
ARC RVEF/LVEF<35% I
SCA I
Syncope Iia
LQT
High Risk despite BB I
SCA I
>500 IIb
CPVT
SCA I
Syncope
VT Despite BB
I
Brugada
SCA
Syncope
I
J wave SCA I
sQT SCA I
SARCOIDOSIS
LVEF<35% I SCA I
Scar ( MRI/ PET ) IIa
Syncope IIaPPM indication IIa
EP inducible IIa
HF Waiting for transplant IIa Cause dependent
NMD
Emery-Dreifuss/L-G 1B IIa
as NICM
MD 1 PPM indication IIb
59