Real-world bleeding in patients with acute coronary syndrome (ACS) undergoing percutaneous coronary intervention (PCI) and prescribed different combinations of dual antiplatelet therapy (DAPT) in England: a population-based cohort study emulating a 'target trial'.
Acute Coronary Syndrome
/ diagnosis
Adolescent
Aspirin
/ adverse effects
Clopidogrel
/ adverse effects
Cohort Studies
Dinucleoside Phosphates
Hemorrhage
/ chemically induced
Humans
Percutaneous Coronary Intervention
/ adverse effects
Platelet Aggregation Inhibitors
/ adverse effects
Prasugrel Hydrochloride
/ adverse effects
Retrospective Studies
ST Elevation Myocardial Infarction
/ diagnosis
Ticagrelor
/ adverse effects
acute coronary syndrome
electronic health records
epidemiology
percutaneous coronary intervention
pharmacology, clinical
Journal
Open heart
ISSN: 2053-3624
Titre abrégé: Open Heart
Pays: England
ID NLM: 101631219
Informations de publication
Date de publication:
08 2022
08 2022
Historique:
received:
22
02
2022
accepted:
12
05
2022
entrez:
12
8
2022
pubmed:
13
8
2022
medline:
17
8
2022
Statut:
ppublish
Résumé
To estimate the incidence and HRs for bleeding for different dual antiplatelet therapies (DAPT) in a real-world population with acute coronary syndrome (ACS) undergoing percutaneous coronary intervention (PCI) in England. A retrospective, population-based cohort study emulating a target randomised controlled trial (tRCT). Linked Clinical Practice Research Datalink (CPRD) and Hospital Episode Statistics (HES). Primary and secondary care. Patients ≥18 years old with ACS undergoing emergency PCI. Aspirin and clopidogrel (AC, reference) versus aspirin and prasugrel (AP) or aspirin and ticagrelor (AT); AP evaluated only in patients with ST-elevation myocardial infarction (STEMI). Primary: any bleeding up to 12 months after the index event (HES- or CPRD- recorded). Secondary: HES-recorded bleeding, CPRD-recorded bleeding, all-cause and cardiovascular mortality, mortality from bleeding, myocardial infarction, stroke, additional coronary intervention and major adverse cardiovascular and cerebrovascular events (MACCE). In ACS, the rates of any bleeding for AC and AT were 89 per 1000 person years and 134 per 1000 person years, respectively. In STEMI, rates for AC, AP and AT were 93 per 1000 person years, 138 per 1000 person years and 143 per 100 person years, respectively. In ACS, compared with AC, AT increased the hazard of any bleeding (HR: 1.47, 95% CI 1.19 to 1.82) but did not reduce MACCE (HR: 1.06, 95% CI 0.89 to 1.27). In STEMI, compared with AC, AP and AT increased the hazard of any bleeding (HR: 1.77, 95% CI 1.21 to 2.59 and HR: 1.50, 95% CI 1.10 to 2.05, respectively) but did not reduce MACCE (HR: 1.10, 95% CI 0.80 to 1.51 and HR: 1.21, 95% CI 0.94 to 1.51, respectively). Non-adherence to the prescribed DAPT regimen was 28% in AC (29% in STEMI only), 31% in AP (STEMI only) and 33% in AT (32% in STEMI only). In a real-world population with ACS, DAPT with ticagrelor or prasugrel are associated with increased bleeding compared with DAPT with clopidogrel. ISRCTN76607611.
Identifiants
pubmed: 35961692
pii: openhrt-2022-001999
doi: 10.1136/openhrt-2022-001999
pmc: PMC9379532
pii:
doi:
Substances chimiques
Dinucleoside Phosphates
0
Platelet Aggregation Inhibitors
0
2'-deoxythymidylyl-(3'-5')-2'-deoxyadenosine
19192-40-6
Clopidogrel
A74586SNO7
Prasugrel Hydrochloride
G89JQ59I13
Ticagrelor
GLH0314RVC
Aspirin
R16CO5Y76E
Banques de données
ISRCTN
['ISRCTN76607611']
Types de publication
Journal Article
Randomized Controlled Trial
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Department of Health
ID : 14/192/89
Pays : United Kingdom
Organisme : British Heart Foundation
Pays : United Kingdom
Informations de copyright
© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY. Published by BMJ.
Déclaration de conflit d'intérêts
Competing interests: TWJ reports grants, personal fees and other from AstraZeneca and Bayer, personal fees and other from Daiichi Sankyo and personal fees from The Medicines Company, outside the submitted work.
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