CASE 1 • • Usia : 63 tahun • Pasien baru pertama kali mengalami hal ini, riwayat mudah lelah saat aktivitas Pasien masuk dengan keluhan nyeri dada sejak 2 jam SMRS, terus menerus seperti ditekan benda berat, tidak menjalar, muntah (-)keringat dingin (+) hingga basah kuyup. Keluhan timbul saat sedang menunggu di bandara ,sesak (-), jantung berdebar (-) Faktor risiko • • • • • Hipertensi Kolesterol tinggi Merokok (-) DM (-) FH (-) Proprietary and Confidential. © AstraZeneca 2011. Document intended for internal discussion purposes. Physical Examination and ECG • • • • KU nyeri dada TD 134/78 mmHg Nadi 90 x / menit RR 16 x / menit Lab • • • • 3 Hb 13.6 mg/dl Lekosit 11.450 Hs Trop T 32 GDS 173 Proprietary and Confidential. © AstraZeneca 2011. Document intended for internal discussion purposes. Case 2 • Laki-laki 73 tahun • Dikirim dari sejawat dengan riwayat NSTEMI, DM ,CKD CABG 1996 • EF 63 % • Diagnostik Angio RCA distal CTO stent patent, LM stenosis 95%, LAD CTO, LCx CTO. LIMA Patent, SVG-RCA total oklusi, SVG-LCx total oklusi, LIMA patent Proprietary and Confidential. © AstraZeneca 2011. Document intended for internal discussion purposes. Atherothrombosis: A Generalized and Progressive Disease Atherothrombosis Unstable angina MI Ischemic stroke/TIA Critical leg ischemia Intermittent claudication Atherosclerosis CV death Stable angina/Intermittent claudication From first decade From third decade Growth mainly by lipid accumulation Adapted from Libby P. Circulation 2001; 104: 365–372 From fourth decade Smooth muscle and collagen Thrombosis, haematoma ACS – Adhesion – Activation – Aggregation 2 3 Adherent platelet become activated 1 Plaque rupture leads to platelet adhesion to the exposed subendothelium Vorchheimer DA, et al. Mayo Clin Proc. 2006;81:59-68; Davies MJ. Heart. 2000;83:361-366. Activated platelets aggregate and assemble a critical mass of activated, pro-thrombotic platelet membrane at the site of injury ACS with persistent ST segment elevation Troponin Elevated ACS without persistent ST segment elevation Troponin Elevated or not ACS with persistent ST segment elevation ACS without persistent ST segment elevation Management : Management : 1. Primary PCI 1. Risk Stratification 2. Fibrinolytic 2. Optimal DAPT 3. Early invasive Predictor Score Age, years Predictor Score Predictor Score Killip class Systolic Blood Pressure (mmHg) < 40 0 < 80 63 I 0 40 - 49 18 80 – 99 58 II 21 50 - 59 36 100 - 119 47 III 43 60 - 69 55 120 - 139 37 IV 64 70 - 79 73 140 - 159 26 80 91 160 - 199 11 > 200 0 Predictor Score Heart Rate , beats/min Predictor Score Creatinine (µmol/L) < 70 0 0 - 34 2 70-89 7 35 – 70 5 90-109 13 71 – 105 8 110 - 149 23 106 – 140 11 150 - 199 36 141 – 176 14 > 200 46 177 – 353 23 ≥ 354 31 Khalill R et al. Exp Clin Cardiol.2009; 14(2): e25 – e30 Predictor Score Cardiac arrest at admission 43 Elevated cardiac markers 15 ST Segment deviation 30 Khalill R et al. Exp Clin Cardiol.2009; 14(2): e25 – e30 • Play a major role in the early care of acute myocardial infarction • Often the first to be contacted by patients • What GP should do • Can perform and interpret the ECG • Alert EMS • Administer opioids and antithrombotic drugs (including fibrinolytic) • Undertake defibrillation if needed Steg PG, et al. European Heart Journal. 2012;33:2569-2619 10-questions strategy in selecting oral antiplatelet in ACS Admit to ICCU Continue diagnostic tests No antiplatelet therapy Q#1:Definite ACS Q#2 : STEMI ? Aspirin : oral 150-300 or IV 80-150 mg Q#4 : Invasive strategy for NSTE-ACS ? Q#3 : Reperfusion ? Probable non Invasive No Reperfusion Reperfusion Clopidogrel 75 mg Thrombolysis Age ≤ 75 : Clopidogrel 300 mg Age > 75 : Clopidogrel 75 mg Primary PCI Ticagrelor 180 mg Or Clopidogrel 600 mg if high bleeding risk Ticagrelor 180 mg Or clopidogrel 75 mg if high bleeding risk Confirmed non invasive Definite Invasive Ticagrelor 180 mg Or Clopidogrel 600 mg if high bleeding risk Switch to invasive Q#8 : normal coronary arteries? Q#5 : Large thrombus burden? Q#7 : Adequate antiplatelet Rx for PCI ? Clopidogrel pre Rx No Clopidogrel Yes : Thrombectomy ICU and Long Term Cath Laboratory First Medical Contact Q#1:ACS Diagnosis doubtful Low Bleeding Risk ? If yes, then GPIIb/IIIa inhibitor according to renal function Confirmed ACS ? If not, stop DAPT Q#10 : Stent Thombosis Risk ? Clopidogrel or switch to Ticagrelor Discuss Tirofiban or Eptifibatide Ticagrelor or Clopidogrel Discuss Tirofiban or Eptifibatide Q#6 : Surgery ? Stop P2Y12 : Clopidogrel or ticagrelor 5 days before. Resume DAPT after CABG Q#9 : Low Bleeding Risk ? If yes, continue Ticagrelor 90 mg/12h if ongoing OR switch from clopidogrel to ticagrelor 90 mg/12h. If no, Clopidogrel 75 mg/d if ongoing OR discuss switch from Prasugrel to Clopidogrel Francois Schiele and Nicolas Meneveau. European Heart Journal: Acute Cardiovascular Care 1(2) 170–176 Dual Antiplatelet Therapy is the STANDARD for ACS Recommendation Class & level Aspirin should be given to all patients without contraindications at an initial loading dose of 150–300 mg, and at a maintenance dose of 75–100 mg daily long-term regardless of treatment strategy. 1A A P2Y12 inhibitor should be added to aspirin as soon as possible and maintained over 12 months, unless there are contraindications such as excessive risk of bleeding. 1A Hamm CW et al. Eur Heart J 2011;32:2999 – 3054 0.04 0.03 0.02 0.01 Cumulative Hazard HR 0.96 (0.851.08) P = 0.489 0.0 ASA 81-100 mg ASA 300-325 mg 0 3 6 9 12 15 Days 18 Mehta SR et al. N Engl J Med. 2010;10:930-42 21 24 27 30 ESC STEMI GUIDELINES : P2Y12 Inhibitor Aspirin oral or iv (if unable to swallow) is recommended Kelas Level 1 B Kelas Level 1 B Kelas Level 1 C P2Y12 inhibitor is recommended in addition to aspirin : Ticagrelor Clopidogrel, preferably when prasugrel or ticagrelor are either not available or contraindicated Steg GS et al. doi:10.1093/eurheartj/ehs215 NSTEMI ACS Guidelines : P2Y12 Inhibitor Ticagrelor (180-mg loading dose, 90 mg twice daily) is recommended for all patients at moderate-to-high risk of ischaemic events (e.g. elevated troponins) , regardless of initial treatment strategy and including those pre-treated with clopidogrel (which should be discontinued when ticagrelor is commenced). Kelas Level 1 B Clopidogrel (300-mg loading dose, 75-mg daily dose) is recommended for patients who cannot receive ticagrelor or prasugrel. Kelas Level 1 A Kelas Level 1 B A 600-mg loading dose of clopidogrel (or a supplementary 300-mg dose at PCI following an initial 300-mg loading dose) is recommended for patients scheduled for an invasive strategy when ticagrelor or prasugrel is not an option. Hamm CW, et al. European Heart Journal (2011) 32, 2999–3054 Limitation of clopidogrel • Dual antiplatelet therapy (DAPT) with aspirin & clopidogrel is the current standard treatment in patients with ACS1 – With or without ST segment elevation1 • Poor platelet inhibition response to clopidogrel is seen in approximately 15% - 40% of patients2 – Contribute to residual high risk of recurrent results • Clopidogrel has slow onset of action1 – Prodrug that requires conversion to active metabolite1 • Variable metabolism results in interindividual variability in inhibition of platelet agregation1 1. Bassand JP . European Heart Journal Supplements (2008) 10 (Supplement D), D3–D11; 2. Gurbel PA, Tantry US. Thrombosis Research. 2007;120: 311–321 GRAVITAS Study (clopidogrel low responders) : No improve in CV outcome with increase dose of clopidogrel Observed event rates are listed; P value by log rank test. DISPERSE: Greater and more consistent IPA with ticagrelor than with clopidogrel (final extent) Clopidogrel 75 mg od 100 100 80 80 DAY 1 60 40 20 0 0 2 4 8 60 Mean Inhibition, % Mean Inhibition, % Ticagrelor 100 mg bd 12 100 80 40 20 0 0 2 4 8 12 100 80 60 60 DAY 14 40 20 40 20 2nd dose 0 0 0 2 4 8 12 Time, h 24 0 2 4 8 12 Time, h IPA = inhibition of platelet aggregation; od = once daily; bd = twice daily. Adapted from Husted SE, et al. Presented at: European Society of Cardiology Annual Congress 2005; 3-7 September, 2005; Stockholm, Sweden. 24 P2Y12 inhibitor Hamm CW et al. Eur Heart J 2011;32:2999 – 3054 Ticagrelor is direct acting whereas all thienopyridines are pro-drugs Active compound Intermediate metabolite Pro-drug Ticagrelor No in vivo biotransformation CYP-dependent oxidation CYP3A4/5 CYP2B6 CYP2C19 CYP2C9 Hydrolysis CYP2D6 by esterase Binding Platelet Prasugrel P2Y12 Clopidogrel CYP-dependent oxidation CYP1A2 CYP2B6 CYP2C19 Figure adapted from Schömig A (2009). CYP, cytochrome P450. Schömig A. N Engl J Med 2009;361:1108–1111. CYP-dependent oxidation CYP2C19 CYP3A4/5 CYP2B6 21 APPROVED NOV 2013 FOR USE BY ASTRAZENECA MEDICAL AFFAIRS PERSONNEL. MAY NOT BE USED FOR PRODUCT PROMOTIONAL PURPOSES. NOT FOR USE BY ASTRAZENECA SALES PERSONNEL. ONSET/OFFSET STUDY : TICAGRELOR FASTER ONSET and FASTER OFFSET VS Last HIGH DOSE CLOPIDOGREL Maintenance 100 90 80 Dose 90 mg bid 75 mg qd Loading Dose * 180 mg * * * * * 600 mg 70 IPA % Ticagrelor (n=54) * † Clopidogrel (n=50) * * P<0.0001 P<0.005 ‡ P<0.05 † 60 50 * 40 ‡ 30 † 20 10 0 0 0.5 1 2 4 Onset Time (Hours) Gurbel PA et al. Circulation 2009;120:2577-2585 8 24 6 weeks Maintenance 0 2 4 8 24 48 Offset Time (Hours) 72 120 168 240 All OAP proven to reduce CV event (CV death, MI dan Stroke ) Rate of composite CV event (CV death, MI atau Stroke)%) CURE1 TRITON TIMI 382 12.1 11.4 11.7 9.9 9.3 P < 0.001 Plasebo Clopidogrel n = 12.562 PLATO3 P < 0.001 Clopidogrel Prasugrel n = 13.608 9.8 P < 0.001 Clopidogrel BRILINTA n = 18.624 23 1.Yusuf S et al. N Engl J Med 2001;345; Wiviott SD e tal. N Engl J Med 2007;357:2001-15; Wallentin L, et al. N Engl J Med. 2009;361:1045–1057. Only ticagrelor proven to have mortality benefit vs clopidogrel composite of of Rate (%)death (%) CV deathCV Rate CURE1 TRITON TIMI 382 PLATO3 P = N/A 5.50 5.10 5.10 4.00 2.40 Plasebo Clopidogrel n = 12.562 NNT = 250 Clopidogrel 2.10 Prasugrel n = 13.608 NNT = 333 Clopidogrel Ticagrelor n = 18.624 NNT = 91 1.Yusuf S et al. N Engl J Med 2001;345; Wiviott SD e tal. N Engl J Med 2007;357:2001-15; Wallentin L, et al. N Engl J Med. 2009;361:1045–1057. K-M Estimated Rate (% Per Year) P = 0.008 Ticagrelor (n=9,235) 18 16 Clopidogrel (n=9,186) 16.1 NS 14.6 14 12 11.6 10 11.2 NS NS P = 0.03 8 6 5.8 5.8 4.5 4 7.4 3.8 NS 2 0.3 0.3 0 Major Bleeding Life-threatening/ Fatal Bleeding All values presented by PLATO criteria. Both groups included aspirin. Wallentin L, et al. N Engl J Med. 2009;361:1045–1057. Fatal Bleeding Major and Minor Bleeding Non-CABGMajor Bleeding CABG-Major Bleeding 7.9 Interruption and/or neutralization of both anticoagulant and antiplatelet therapies is indicated in case of major bleeding, unless it can be adequately controlled by specific haemostatic measures Minor bleeding should preferably be managed without interruption of active treatments. Co-medication of PPI and antithrombotic agents is recommended in patients at increased risk of GI haemorrhage. Hamm CW et al. Eur Heart J 2011;32:2999 – 3054 CLASS LEVEL 1 C CLASS LEVEL 1 C CLASS LEVEL 1 B Consistent result of ticagrelor in efficacy primary endpoint despite of PPI treatment Proton Pump Inhibitors (Rand.) P value interaction 0.69 KM % at Month 12 Hazard Ratio (95% CI) HR (95% CI) Ti. Cl. No n = 12,249 9.2 11.0 0.83 (0.74, 0.93) Yes n = 6375 11.0 12.9 0.86 (0.75, 1.00) 0.2 0.5 Ticagrelor better 1.0 2.0 Clopidogrel better KM : Kaplan–Meier Wallentin L, et al. N Engl J Med. 2009;361:1045–1057. + supplement CASE 1 Q#1:Definite ACS ICU and Long Term Cath Laboratory First Medical Contact Q#2 : STEMI ? Aspirin : oral 150-300 or IV 80-150 mg Q#3 : Reperfusion ? Reperfusion Primary PCI Ticagrelor 180 mg Or Clopidogrel 600 mg if high bleeding risk Which P2Y12 inhibitor preferred for this case ? 1. Faster onset 2. Low inter individual variability 3. No issue with low responders Q#5 : Large thrombus burden? Yes : Thrombectomy Low Bleeding Risk ? If yes, then GPIIb/IIIa inhibitor according to renal function •Reduced risk of stent thrombosis •Reduced CV mortality Q#10 : Stent Thombosis Risk ? Q#9 : Low Bleeding Risk ? If yes, continue Ticagrelor 90 mg/12h if ongoing OR switch from clopidogrel to ticagrelor 90 mg/12h. If no, Clopidogrel 75 mg/d if ongoing OR discuss switch from Prasugrel to Clopidogrel Francois Schiele and Nicolas Meneveau. European Heart Journal: Acute Cardiovascular Care 1(2) 170–176 Case 2 First Medical Contact Q#1:Definite ACS Aspirin : oral 150-300 or IV 80-150 mg Check GRACE RISK Score Q#4 : Invasive strategy for NSTE-ACS ? Definite Invasive Age : 73 years old CKD, Elevated CardiACS maker, ST segment deviation Ticagrelor 180 mg Or Clopidogrel 600 mg if high bleeding risk ICU and Long Term Cath Laboratory Moderate – high risk patients Guidelines Ticagrelor Mod – high risk NSTEMI patient Pre treated with clopi or naïve PCI or MM Q#7 : Adequate antiplatelet Rx for PCI ? 1B Clopidogrel If ticagrelor or prasugrel not available Clopidogrel pre Rx 1A Q#10 : Stent Thombosis Risk ? Clopidogrel or switch to Ticagrelor Discuss Tirofiban or Eptifibatide No Clopidogrel Ticagrelor or Clopidogrel Discuss Tirofiban or Eptifibatide Q#9 : Low Bleeding Risk ? If yes, continue Ticagrelor 90 mg/12h if ongoing OR switch from clopidogrel to ticagrelor 90 mg/12h. If no, Clopidogrel 75 mg/d if ongoing OR discuss switch from Prasugrel to Clopidogrel Francois Schiele and Nicolas Meneveau. European Heart Journal: Acute Cardiovascular Care 1(2) 170–176 ESC STEMI Guidelines 2012 DAPT and antithrombotic combination therapies after STEMI • Primary PCI and Fibrinolytic is up to 12 months • No reperfusion at least 1 month up to 12 months NTEMI Guidelines 2012 Continue for 12 months (unless at high risk of bleeding) Cessation of DAPT in Surgery patients • The risk of bleeding related to surgery must be balanced against the risk of recurrent ischaemic events related to discontinuation of therapy • it is reasonable to restart DAPT as soon as considered safe in relation to bleeding risk Steg GS et al. doi:10.1093/eurheartj/ehs215; Hamm CW, et al. European Heart Journal (2011) 32, 2999–3054 • Antiplatelet therapy key to reducing thrombus burden and plaque stabilisation during ACS • In STEMI patients, a loading dose of P2Y12 receptor inhibitor should be given as early as possible or at time of primary PCI • In NSTEMI patients, a strategy of risk stratification, optimal potent dual antiplatelet therapy (including the new oral P2Y12 inhibitors and early invasive approach is appropriate • Ticagrelor + aspirin has recommended in ESC and AHA guidelines as first line treatment in ACS and proven to reduced CV mortality