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NEWER ANTI-
PLATELET DRUGS
VORAPAXOR/A
TOPAXAR
CLOPIDOGREL-
 MOST WIDELY USED –causes irreversible alterations in
p2y12 receptor mediated platelet inhibition.
 It has addictive effects when combined with aspirin due to
different mechanism of actions.
 Now used commonly in ACS with aspirin.
 Drawbacks- prodrug- delayed onset of action(4-6
hours),irreversible platelet inhibition (increased
hemmorhage)and has marked interindividual variability in
anti-platelet action called clopidogrel resistance( increased
stent thrombosis and MI)
 Also has interaction with PPI , hence lead to reduced clinical
effects,PANTOPRAZOLE IS SAFE, because no interaction
with CYP2C19 cytochrome enzyme.
PRASUGREL
 THEINOPYRIDINE group
 Acts through P2Y12 receptor.
 Prodrug- but acts more rapidly in 30 mins.
 TRITOM-TIMI trial compared prasugrel and
clopidogrel in 13608 patients.All patients received
aspirin.
 One group received Prasugrel 60 mg loading and
f/b 10 mg and other 300 mg clopi loading dose and
75 daily for 15 months.
 Prasugrel had 24 % risk reduction.
 BLEEDING risk is MORE.
 HENCE NOT RECOMMENDED IN -
 Elderly >75 years
 < 60 kgs
 History of previous strokes
 Planned for urgent surgery.
 Should only be given to patients whose coronary
anatomy is known after PCI, ONLY WHEN decision
to proceed to PTCA is made. NOT
RECOMMENDED FOR PATIENTS MANAGED
MEDICALLY.
TICAGRELOR-
 NOVEL directly acting oral platelet p2y12 receptor
antagonist and REVERSIBLE ACTION.
 FASTEST AND GREATER AND CONSISTENT anti-
platelet action.
 PLATO Trial-compared ticagrelor and clopitab ,
decreased deaths and MI in the Ticagrelor group.
 However NON-CABG and Intra-cranial bleeding higher.
 Increased Dyspnea.
 Increased Ventricular Phase of Holter Monitoring.
 Recommended in ALL PATIENTS BEING MANAGED
COSERVATIVELY OR WITH INTERVENTIONS.
CANGRELOR-
 Intravenous Platelet inhibitor.
 Rapid onset and offset.
 Reversible action and platelet function becomes
normal within 30- 60 minutes of stopping cangrelor.
 Used in patient who need to undergo CABG,Sinc it
acts for less time with rapid offfset.
PROTEASE ACTIVATED RECEPTOR
1(PAR1) INHIBITORS-
 Acts against THROMBIN induced Platelet
aggregation.
 VORAPAXOR AND ATOPAXAR selective and
potent.
 Reduces the risk of MI and death, but with
significant risk of bleeding.
GUIDELINES-
• Aspirin PLUS
• Clopitab, prasugrel or
ticagrelor
Acs with
planned
intervention
• Aspirin plus Clopidogrel
or ticagrelor
Medically
managed
ACS
• Aspirin plus clopidgrel
ELECTIVE
PCI
UNSTABLE ANGINA OR NSTEMI
 Aspirin
 PLUS
 BEFORE PCI- C/T/ OR IV GP 2B3A- Eptifibatide or
tirofiban
 At the time of PCI-
 Prasugrel /ticagrelor/clopidogrel or iv gp 2b3a
 Without stenting-aspirin for lifelong and C OR T
upto 12 months.
ESC GUIDELINES-
 Ticagrelor is recommended in all patients at
moderate to high risk ischaemic events (elevated
troponins ) irrespective of initial strategy.
 Prasugrel only in whom coronary anatomy is known
proceeding to PTCA
 Clopidogrel in all whom P OR T cant be given
STEMI
• Aspirin loading
• Plus clopidogrel 300 or prasugrel 60
or ticagrelor 180
Undergoing
Pami
• Aspirin plus clopidogrel 300 mg
loading if <75 years
Undergoing
Thrombolysising
• If pci performed within 24 hours
clopidogrel 300 mg loading and if
performed after 24hours- 600 mg
clopidogrel
Undergoing PCI
after
Thrombolysis
CLASS 1-
FOR ACS/NON STEMI /UA/ STEMI managed
medically-
Clopidogrel or ticagrelor- upto 12 months.
ACS undergoing PCI with stents-(bms or des)
clopidogrel or prasugrel or ticagrelor- upto 2- 3 years
ASPIRIN to be continued lifelong.
DURATION
CONCLUSION
 NEWER anti-platelets like prasugrel and ticagrelor
have shown promising results better than
clopidogrel.
 Other agents have shown reduction in clinical
events but increased risk of bleeding , hence still
under evaluation.
 Not recmommended in cerebrovascular or other
peripheral vascular illnesses.
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Newer anti platelet drugs

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  • 3.
  • 4.
  • 6. CLOPIDOGREL-  MOST WIDELY USED –causes irreversible alterations in p2y12 receptor mediated platelet inhibition.  It has addictive effects when combined with aspirin due to different mechanism of actions.  Now used commonly in ACS with aspirin.  Drawbacks- prodrug- delayed onset of action(4-6 hours),irreversible platelet inhibition (increased hemmorhage)and has marked interindividual variability in anti-platelet action called clopidogrel resistance( increased stent thrombosis and MI)  Also has interaction with PPI , hence lead to reduced clinical effects,PANTOPRAZOLE IS SAFE, because no interaction with CYP2C19 cytochrome enzyme.
  • 7. PRASUGREL  THEINOPYRIDINE group  Acts through P2Y12 receptor.  Prodrug- but acts more rapidly in 30 mins.  TRITOM-TIMI trial compared prasugrel and clopidogrel in 13608 patients.All patients received aspirin.  One group received Prasugrel 60 mg loading and f/b 10 mg and other 300 mg clopi loading dose and 75 daily for 15 months.  Prasugrel had 24 % risk reduction.
  • 8.  BLEEDING risk is MORE.  HENCE NOT RECOMMENDED IN -  Elderly >75 years  < 60 kgs  History of previous strokes  Planned for urgent surgery.  Should only be given to patients whose coronary anatomy is known after PCI, ONLY WHEN decision to proceed to PTCA is made. NOT RECOMMENDED FOR PATIENTS MANAGED MEDICALLY.
  • 9. TICAGRELOR-  NOVEL directly acting oral platelet p2y12 receptor antagonist and REVERSIBLE ACTION.  FASTEST AND GREATER AND CONSISTENT anti- platelet action.  PLATO Trial-compared ticagrelor and clopitab , decreased deaths and MI in the Ticagrelor group.  However NON-CABG and Intra-cranial bleeding higher.  Increased Dyspnea.  Increased Ventricular Phase of Holter Monitoring.  Recommended in ALL PATIENTS BEING MANAGED COSERVATIVELY OR WITH INTERVENTIONS.
  • 10. CANGRELOR-  Intravenous Platelet inhibitor.  Rapid onset and offset.  Reversible action and platelet function becomes normal within 30- 60 minutes of stopping cangrelor.  Used in patient who need to undergo CABG,Sinc it acts for less time with rapid offfset.
  • 11. PROTEASE ACTIVATED RECEPTOR 1(PAR1) INHIBITORS-  Acts against THROMBIN induced Platelet aggregation.  VORAPAXOR AND ATOPAXAR selective and potent.  Reduces the risk of MI and death, but with significant risk of bleeding.
  • 12. GUIDELINES- • Aspirin PLUS • Clopitab, prasugrel or ticagrelor Acs with planned intervention • Aspirin plus Clopidogrel or ticagrelor Medically managed ACS • Aspirin plus clopidgrel ELECTIVE PCI
  • 13.
  • 14. UNSTABLE ANGINA OR NSTEMI  Aspirin  PLUS  BEFORE PCI- C/T/ OR IV GP 2B3A- Eptifibatide or tirofiban  At the time of PCI-  Prasugrel /ticagrelor/clopidogrel or iv gp 2b3a  Without stenting-aspirin for lifelong and C OR T upto 12 months.
  • 15. ESC GUIDELINES-  Ticagrelor is recommended in all patients at moderate to high risk ischaemic events (elevated troponins ) irrespective of initial strategy.  Prasugrel only in whom coronary anatomy is known proceeding to PTCA  Clopidogrel in all whom P OR T cant be given
  • 16. STEMI • Aspirin loading • Plus clopidogrel 300 or prasugrel 60 or ticagrelor 180 Undergoing Pami • Aspirin plus clopidogrel 300 mg loading if <75 years Undergoing Thrombolysising • If pci performed within 24 hours clopidogrel 300 mg loading and if performed after 24hours- 600 mg clopidogrel Undergoing PCI after Thrombolysis
  • 17. CLASS 1- FOR ACS/NON STEMI /UA/ STEMI managed medically- Clopidogrel or ticagrelor- upto 12 months. ACS undergoing PCI with stents-(bms or des) clopidogrel or prasugrel or ticagrelor- upto 2- 3 years ASPIRIN to be continued lifelong. DURATION
  • 18. CONCLUSION  NEWER anti-platelets like prasugrel and ticagrelor have shown promising results better than clopidogrel.  Other agents have shown reduction in clinical events but increased risk of bleeding , hence still under evaluation.  Not recmommended in cerebrovascular or other peripheral vascular illnesses.