Antiplatelet drug: Difference between revisions
| Line 35: | Line 35: | ||
! Drug Group | ! Drug Group | ||
! Drug | ! Drug | ||
! Time to onset/peak action | |||
! Cost (UpToDate 08/2022) | ! Cost (UpToDate 08/2022) | ||
|- | |- | ||
|Thienopyridines | |Thienopyridines | ||
| Ticlopidine(first generation)<br/>Clopidogrel (second generation)<br/>Prasugrel (third generation) | | Ticlopidine(first generation)<br/>Clopidogrel (second generation)<br/>Prasugrel (third generation) | ||
| <br/><br/><30 minutes; 4 hours | |||
| $112<br/>$195<br/>$495 ($331 GoodRx) | | $112<br/>$195<br/>$495 ($331 GoodRx) | ||
|- | |- | ||
| Non-thienopyridines | | Non-thienopyridines | ||
| Ticagrelor | | Ticagrelor | ||
| <30 minutes; 2 hours | |||
| $511 | | $511 | ||
|} | |} | ||
Revision as of 19:51, 14 August 2022
|
WikiDoc Resources for Antiplatelet drug |
|
Articles |
|---|
|
Most recent articles on Antiplatelet drug Most cited articles on Antiplatelet drug |
|
Media |
|
Powerpoint slides on Antiplatelet drug |
|
Evidence Based Medicine |
|
Cochrane Collaboration on Antiplatelet drug |
|
Clinical Trials |
|
Ongoing Trials on Antiplatelet drug at Clinical Trials.gov Trial results on Antiplatelet drug Clinical Trials on Antiplatelet drug at Google
|
|
Guidelines / Policies / Govt |
|
US National Guidelines Clearinghouse on Antiplatelet drug NICE Guidance on Antiplatelet drug
|
|
Books |
|
News |
|
Commentary |
|
Definitions |
|
Patient Resources / Community |
|
Patient resources on Antiplatelet drug Discussion groups on Antiplatelet drug Patient Handouts on Antiplatelet drug Directions to Hospitals Treating Antiplatelet drug Risk calculators and risk factors for Antiplatelet drug
|
|
Healthcare Provider Resources |
|
Causes & Risk Factors for Antiplatelet drug |
|
Continuing Medical Education (CME) |
|
International |
|
|
|
Business |
|
Experimental / Informatics |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
An antiplatelet drug is a member of a class of pharmaceuticals that decreases platelet aggregation and inhibits thrombus formation. They are effective in the arterial circulation, where anticoagulants have little effect.
They are widely used in primary and secondary prevention of thrombotic cerebrovascular or cardiovascular disease.
The Most Important Antiplatelet Drugs
COX-2 inhibitor / Cyclooxygenase inhibitors
Phosphodiesterase inhibitors
- Cilostazol (Pletal)
Glycoprotein IIB/IIIA inhibitors (intravenous use only)
- Abciximab (ReoPro)
- Eptifibatide (Integrilin)
- Tirofiban (Aggrastat)
- Defibrotide
P2Y12 (Adenosine diphosphate receptors) inhibitors (thienopyridines)
- First generation: Ticlopidine (Ticlid)
- Second gereration:Clopidogrel (Plavix)
- Third gereration: Prasugrel
Non-thienopyridines
- Cangrelor (intravenous)
- Ticagrelor (oral)
| Drug Group | Drug | Time to onset/peak action | Cost (UpToDate 08/2022) |
|---|---|---|---|
| Thienopyridines | Ticlopidine(first generation) Clopidogrel (second generation) Prasugrel (third generation) |
<30 minutes; 4 hours |
$112 $195 $495 ($331 GoodRx) |
| Non-thienopyridines | Ticagrelor | <30 minutes; 2 hours | $511 |
Comparative studies
Are newer thienopyridine (third-generation) agents better than older thienopyridine (second-generation) agents?
Studies of all patients
The TRILOGY ACS randomized controlled trial found no benefit of prasugrel versus clopidogrel (primary outcome: 13.9% vs 16%; hazard ratio 0.91; 0.79 to 1.05; P=0.21) among "patients with unstable angina or myocardial infarction without ST-segment elevation who do not undergo revascularization"[1].
Are non-thienopyridines agents better than thienopyridine (second-generation) agents?
Studies of all patients
The ALPHEUS randomized controlled trial found no benefit of ticagrelor versus clopidogrel among stable coronary patients undergoing high-risk elective PCI (primary outcome in 35% vs 36% of patients)[2].
The POPular AGE randomized controlled trial found no benefit of ticagrelor versus clopidogrel among patients aged 70 years or older with non-ST-elevation acute coronary syndrome (MACE in 11% vs 12% of patients)[3]
The ISAR-REACT 5 randomized controlled trial found harm of ticagrelor versus prasugrel (primary outcome: 9.3% vs 6.9%; hazard ratio, 1.36; 95% confidence interval, 1.09 to 1.70; P = 0.006) among patients with "acute coronary syndromes and for whom invasive evaluation was planned"[4].
The CHAMPION PCI randomized controlled trial found no benefit of cangrelor versus clopidogrel among patients "before percutaneous coronary intervention (PCI) in patients with acute coronary syndromes" (MACE in 7.5% vs 7.1% of patients)[5].
The CHAMPION PLATFORM randomized controlled trial found no benefit of cangrelor added to clopidogrel among patients with acute coronary syndrome before percutaneous coronary intervention (PCI) (MACE in 7% vs 8% of patients) percutaneous coronary intervention (PCI).
Studies of patients with CYP2C19 loss-of-function
The CHANCE-2 randomized controlled trial found benefit of ticagrelor versus clopidogrel (primary outcome: 6% vs 7.6%; hazard ratio, 0.77; 95% confidence interval, 0.64 to 0.94; P = 0.008) among Chinese patients with minor ischemic stroke or transient ischemic attack (TIA) who carried CYP2C19 loss-of-function alleles[4].
Is there a best non-thienopyridine antiplatelet drug?
The POPular Genetics randomized controlled trial found faster onset of action but no benefit of cangrelor versus ticagrelor among patients with "ST-elevation myocardial infarction (STEMI) population treated with primary percutaneous coronary intervention (PPCI"[6].
Should drug selection be driven by genetic testing and platelet function testing?
Guided therapy (drug choice based on genetic testing and platelet function testing may improve outcomes according to a systematic reveiw[7].
However, the key POPular Genetics randomized controlled trial found no benefit from a CYP2C19 guided therapy (primary outcome: 5.1 vs 5.9%;P = 0.44) among patients undergoing primary PCI with stent implantation[8].
See also
External links
References
- ↑ Roe MT, Armstrong PW, Fox KA, White HD, Prabhakaran D, Goodman SG; et al. (2012). "Prasugrel versus clopidogrel for acute coronary syndromes without revascularization". N Engl J Med. 367 (14): 1297–309. doi:10.1056/NEJMoa1205512. PMID 22920930.
- ↑ Silvain J, Lattuca B, Beygui F, Rangé G, Motovska Z, Dillinger JG; et al. (2020). "Ticagrelor versus clopidogrel in elective percutaneous coronary intervention (ALPHEUS): a randomised, open-label, phase 3b trial". Lancet. 396 (10264): 1737–1744. doi:10.1016/S0140-6736(20)32236-4. PMID 33202219 Check
|pmid=value (help). - ↑ Gimbel M, Qaderdan K, Willemsen L, Hermanides R, Bergmeijer T, de Vrey E; et al. (2020). "Clopidogrel versus ticagrelor or prasugrel in patients aged 70 years or older with non-ST-elevation acute coronary syndrome (POPular AGE): the randomised, open-label, non-inferiority trial". Lancet. 395 (10233): 1374–1381. doi:10.1016/S0140-6736(20)30325-1. PMID 32334703 Check
|pmid=value (help). Review in: Ann Intern Med. 2020 Sep 15;173(6):JC28 - ↑ 4.0 4.1 Wang Y, Meng X, Wang A, Xie X, Pan Y, Johnston SC; et al. (2021). "Ticagrelor versus Clopidogrel in CYP2C19 Loss-of-Function Carriers with Stroke or TIA". N Engl J Med. 385 (27): 2520–2530. doi:10.1056/NEJMoa2111749. PMID 34708996 Check
|pmid=value (help). Review in: Ann Intern Med. 2022 Mar;175(3):JC30 - ↑ Harrington RA, Stone GW, McNulty S, White HD, Lincoff AM, Gibson CM; et al. (2009). "Platelet inhibition with cangrelor in patients undergoing PCI". N Engl J Med. 361 (24): 2318–29. doi:10.1056/NEJMoa0908628. PMID 19915221.
- ↑ Ubaid S, Ford TJ, Berry C, Murray HM, Wrigley B, Khan N; et al. (2019). "Cangrelor versus Ticagrelor in Patients Treated with Primary Percutaneous Coronary Intervention: Impact on Platelet Activity, Myocardial Microvascular Function and Infarct Size: A Randomized Controlled Trial". Thromb Haemost. 119 (7): 1171–1181. doi:10.1055/s-0039-1688789. PMID 31129911.
- ↑ Galli M, Benenati S, Capodanno D, Franchi F, Rollini F, D'Amario D; et al. (2021). "Guided versus standard antiplatelet therapy in patients undergoing percutaneous coronary intervention: a systematic review and meta-analysis". Lancet. 397 (10283): 1470–1483. doi:10.1016/S0140-6736(21)00533-X. PMID 33865495 Check
|pmid=value (help). - ↑ Claassens DMF, Vos GJA, Bergmeijer TO, Hermanides RS, van 't Hof AWJ, van der Harst P; et al. (2019). "A Genotype-Guided Strategy for Oral P2Y12 Inhibitors in Primary PCI". N Engl J Med. 381 (17): 1621–1631. doi:10.1056/NEJMoa1907096. PMID 31479209.