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Hello!
Dr. Azim Anwar
Phase B Resident,
Cardiology, BSMMU
2
Dr. Md. Khurshed Ahmed
Associate Professor. Department of Cardiology
CHAIRPERSON
Todays Agenda
4
Todays Agenda
Assessment of Cancer patients before starting anticancer drugs
5
Todays Agenda
Assessment of Cancer patients before starting anticancer drugs
CV toxicity prevention strategy
6
Todays Agenda
Assessment of Cancer patients before starting anticancer drugs
CV toxicity prevention strategy
After chemotherapy management
7
“
Assessment of cancer patients
from cardiac POV before
starting chemotherapy is Class I
Indication.
8
Assessment before starting chemotherapy includes
History
Clinical Examination
Investigation
9
 History of Cancer
 Past H/O Cancer therapy :
Type of drugs***
Duration of use
Side effects
History
History of Heart disease :
 Cardiomyopathy
VHD
MI, CCS
PCI, CABG
PVD, DVT
Arrythmia- AF, Long QTS
Drugs : Antiplatelet,
Anticoagulant
10
CVRF Assessment:
 Age
10 Yr ASCVD Risk
DM, HTN, DL
Proteinuria
CKD
Family HO: Thrombophillia
Smoking , Obesity
. Clinical Examination:
*** BP
(VEGFi- Bevacizumab,
Monoclonal Ab-Ramucinumab)
11
▫ Anthracyclines
▫ HER2 inhibitor
▫ VEGFi
▫ BTK Inhibitor
(Bruton Tyrosine kinase)
 Proteosome Inhibitor
 RAFK & MAK Inhibitor
 (Rapidly accelereted fibrosarcoma,
 mitogen-activated protein kinase)
▫ Very High Risk
Chemotherapy
12
Investigations
 cTn (1)
Nt Pro BNP (1)
Echocardiography (1)
ECG (1)
HBA1c
RFT
F. Lipid profile
CMR
13
Echocardiography: What to look for ?
14
▫ Right Heart
 RV Dimension
 S’
 TAPSE
 FAC (Fractional Area Change)
 RV FWLS (Free Wall Long Strain)
 RA Area
 Peak TRV
 IVCd
 RV EF
▫ Left Heart
 LV Volume
 LV Mass
 LV EF
 Long & Circum strain
15
All HO
Negative but
ECG +
No
Cardiovascul
ar disease but
CVRF +
Preexisting CVD / CTRCD
Arrythmia / IHD
Cardiologist
Referrel
(1)
Symptomatic,
but cTn & ETT- N
CPET ?
Management
of RF with life
style
modification
and
medications
(1)
Baseline & 10 Yr CVD risk
assessment with Score &
Score 2 is recommended. Do
necessary Inv
cTn
Nt pro BNP
TTE
CMR
& Refer to cardiologist (1) 16
Scenario:
Positive History but ECG, cTN, TTE Normal.
What to do ?
17
Scenario:
Positive History but ECG, cTN, TTE Normal.
What to do ?
Ans: CPET
18
CPET
Lung Function: Flow volume loops
Oxygen Consumption during exercise (VO2 max)
Anaerobic Threshold
Heart performance during exercise
Blood gas measurement from blood sample taken from the earlobe
Exercise 12 lead ECG
19
All HO
Negative but
ECG +
No
Cardiovascul
ar disease but
CVRF +
Preexisting CVD / CTRCD
Arrythmia / IHD
Cardiologist
Referrel
(1)
Symptomatic,
but cTn & ETT- N
CPET
Management
of RF with life
style
modification
and
medications
(1)
Baseline & 10 Yr CVD risk
assessment with Score &
Score 2 is recommended. Do
necessary Inv
cTn
Nt pro BNP
TTE
CMR
& Refer to cardiologist (1) 20
21
Mild to Moderate
Risk:
Education &
Counseling (1)
Lifestyle modification
Supervised exercise
therapy
Risk fc Mx
Cardioonclogy Rehab
Adherence to rx
High / Very
High Risk
Minimize the use
of cardiotoxic
drugs
ACEI /ARB, BB
Statins
 Dexrazoxane
(Anthracyclines)
22
After Chemotherapy…………..
▫ Low Risk
1. F/Up after 1
year of Rx
completion
(2b) by cTn &
TTE
2. CVRF
assessment
after 1 year
▫ Intermediate
Risk
1. F/Up after 1 year
of Rx completion
(2a) by cTn &
TTE
2. CVRF
assessment
after 1 year & 5
year, and 5
yearly.
▫ High Risk
1. F/Up after 3
months & 1 year
of Rx completion
(1) by cTn & TTE
2. CVRF
assessment by
TTE at 1,3,5 years
and 5 yearly 23
ACS in Cancer patient(60Y), Receiving Anthracyclines…………………
▫ History:
1. Cancer Type
2. Type &
Duration of
chemo
3. CVRF
4. Active CD
▫ Examination
1. Peripheral
pulses
2. BP
3. HF
▫ Investigation
1. ECG
2. cTnI
3. Echo
4. Nt Pro BNP
24
25
26
Management:
▫ CCU Admission
▫ Anti ischemic therapy
▫ Revascularization / Medical Mx
▫ Hold chemo upto clinically stable.
▫ MDT
Revascularization Noninvasive Mx (IIa)
 > 6 months survival
 High risk ST/NST ACS
 <6 months survival
 Low risk NST ACS
 Very high bleeding risk
27
PCI CABG
 Cardiogenic shock
 HF
 Vent Arrythmia
 PC > 30,000
(POBA if thrombocytopenia)
 FFR, IVUS, OCT
 Radial route
 Lower heparin dose, 30-50U/kg
▫ Extensive CAD not amenable
to PCI
▫ >12 Months survival
▫ PC > 50,000
▫ LIMA & RIMA viability
assessment needed
28
 Choice of DAPT: Preferred
▫ Aspirin (PC >10,000)
▫ Clopid (PC>30,000)
 DAPT Duration: 1-3 M [IIa]
 Tica (PC>50,000)
 Prasugrel (<75Y, >60Kg, Child
Pugh A-B hepatic impair)
[IIb]
▫ Anticoagulation:
▫ NOAC + DAPT, 1 week in
hospital
▫ Then, NOAC + Clopid
29
30
▫ Chemotherapy and CCS
▫ Chemotherapy and VHD
▫ Chemotherapy and arrythmia
▫ Chemotherapy and Implantable
devices
▫ Chemotherapy and HTN
▫ HSCT and cardiac risk

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18. Cardiac Onco Guideline 2022.pptx

  • 1.
  • 2. Hello! Dr. Azim Anwar Phase B Resident, Cardiology, BSMMU 2
  • 3. Dr. Md. Khurshed Ahmed Associate Professor. Department of Cardiology CHAIRPERSON
  • 5. Todays Agenda Assessment of Cancer patients before starting anticancer drugs 5
  • 6. Todays Agenda Assessment of Cancer patients before starting anticancer drugs CV toxicity prevention strategy 6
  • 7. Todays Agenda Assessment of Cancer patients before starting anticancer drugs CV toxicity prevention strategy After chemotherapy management 7
  • 8. “ Assessment of cancer patients from cardiac POV before starting chemotherapy is Class I Indication. 8
  • 9. Assessment before starting chemotherapy includes History Clinical Examination Investigation 9
  • 10.  History of Cancer  Past H/O Cancer therapy : Type of drugs*** Duration of use Side effects History History of Heart disease :  Cardiomyopathy VHD MI, CCS PCI, CABG PVD, DVT Arrythmia- AF, Long QTS Drugs : Antiplatelet, Anticoagulant 10
  • 11. CVRF Assessment:  Age 10 Yr ASCVD Risk DM, HTN, DL Proteinuria CKD Family HO: Thrombophillia Smoking , Obesity . Clinical Examination: *** BP (VEGFi- Bevacizumab, Monoclonal Ab-Ramucinumab) 11
  • 12. ▫ Anthracyclines ▫ HER2 inhibitor ▫ VEGFi ▫ BTK Inhibitor (Bruton Tyrosine kinase)  Proteosome Inhibitor  RAFK & MAK Inhibitor  (Rapidly accelereted fibrosarcoma,  mitogen-activated protein kinase) ▫ Very High Risk Chemotherapy 12
  • 13. Investigations  cTn (1) Nt Pro BNP (1) Echocardiography (1) ECG (1) HBA1c RFT F. Lipid profile CMR 13
  • 14. Echocardiography: What to look for ? 14
  • 15. ▫ Right Heart  RV Dimension  S’  TAPSE  FAC (Fractional Area Change)  RV FWLS (Free Wall Long Strain)  RA Area  Peak TRV  IVCd  RV EF ▫ Left Heart  LV Volume  LV Mass  LV EF  Long & Circum strain 15
  • 16. All HO Negative but ECG + No Cardiovascul ar disease but CVRF + Preexisting CVD / CTRCD Arrythmia / IHD Cardiologist Referrel (1) Symptomatic, but cTn & ETT- N CPET ? Management of RF with life style modification and medications (1) Baseline & 10 Yr CVD risk assessment with Score & Score 2 is recommended. Do necessary Inv cTn Nt pro BNP TTE CMR & Refer to cardiologist (1) 16
  • 17. Scenario: Positive History but ECG, cTN, TTE Normal. What to do ? 17
  • 18. Scenario: Positive History but ECG, cTN, TTE Normal. What to do ? Ans: CPET 18
  • 19. CPET Lung Function: Flow volume loops Oxygen Consumption during exercise (VO2 max) Anaerobic Threshold Heart performance during exercise Blood gas measurement from blood sample taken from the earlobe Exercise 12 lead ECG 19
  • 20. All HO Negative but ECG + No Cardiovascul ar disease but CVRF + Preexisting CVD / CTRCD Arrythmia / IHD Cardiologist Referrel (1) Symptomatic, but cTn & ETT- N CPET Management of RF with life style modification and medications (1) Baseline & 10 Yr CVD risk assessment with Score & Score 2 is recommended. Do necessary Inv cTn Nt pro BNP TTE CMR & Refer to cardiologist (1) 20
  • 21. 21 Mild to Moderate Risk: Education & Counseling (1) Lifestyle modification Supervised exercise therapy Risk fc Mx Cardioonclogy Rehab Adherence to rx High / Very High Risk Minimize the use of cardiotoxic drugs ACEI /ARB, BB Statins  Dexrazoxane (Anthracyclines)
  • 22. 22
  • 23. After Chemotherapy………….. ▫ Low Risk 1. F/Up after 1 year of Rx completion (2b) by cTn & TTE 2. CVRF assessment after 1 year ▫ Intermediate Risk 1. F/Up after 1 year of Rx completion (2a) by cTn & TTE 2. CVRF assessment after 1 year & 5 year, and 5 yearly. ▫ High Risk 1. F/Up after 3 months & 1 year of Rx completion (1) by cTn & TTE 2. CVRF assessment by TTE at 1,3,5 years and 5 yearly 23
  • 24. ACS in Cancer patient(60Y), Receiving Anthracyclines………………… ▫ History: 1. Cancer Type 2. Type & Duration of chemo 3. CVRF 4. Active CD ▫ Examination 1. Peripheral pulses 2. BP 3. HF ▫ Investigation 1. ECG 2. cTnI 3. Echo 4. Nt Pro BNP 24
  • 25. 25
  • 26. 26 Management: ▫ CCU Admission ▫ Anti ischemic therapy ▫ Revascularization / Medical Mx ▫ Hold chemo upto clinically stable. ▫ MDT
  • 27. Revascularization Noninvasive Mx (IIa)  > 6 months survival  High risk ST/NST ACS  <6 months survival  Low risk NST ACS  Very high bleeding risk 27
  • 28. PCI CABG  Cardiogenic shock  HF  Vent Arrythmia  PC > 30,000 (POBA if thrombocytopenia)  FFR, IVUS, OCT  Radial route  Lower heparin dose, 30-50U/kg ▫ Extensive CAD not amenable to PCI ▫ >12 Months survival ▫ PC > 50,000 ▫ LIMA & RIMA viability assessment needed 28
  • 29.  Choice of DAPT: Preferred ▫ Aspirin (PC >10,000) ▫ Clopid (PC>30,000)  DAPT Duration: 1-3 M [IIa]  Tica (PC>50,000)  Prasugrel (<75Y, >60Kg, Child Pugh A-B hepatic impair) [IIb] ▫ Anticoagulation: ▫ NOAC + DAPT, 1 week in hospital ▫ Then, NOAC + Clopid 29
  • 30. 30 ▫ Chemotherapy and CCS ▫ Chemotherapy and VHD ▫ Chemotherapy and arrythmia ▫ Chemotherapy and Implantable devices ▫ Chemotherapy and HTN ▫ HSCT and cardiac risk