Literature DB >> 27789517

Early Cessation of Adenosine Diphosphate Receptor Inhibitors Among Acute Myocardial Infarction Patients Treated With Percutaneous Coronary Intervention: Insights From the TRANSLATE-ACS Study (Treatment With Adenosine Diphosphate Receptor Inhibitors: Longitudinal Assessment of Treatment Patterns and Events After Acute Coronary Syndrome).

Emil L Fosbøl1, Christine Ju2, Kevin J Anstrom2, Marjorie E Zettler2, John C Messenger2, Ron Waksman2, Mark B Effron2, Brian A Baker2, David J Cohen2, Eric D Peterson2, Tracy Y Wang2.   

Abstract

BACKGROUND: Guidelines recommend the use of adenosine diphosphate receptor inhibitor (ADPri) therapy for 1 year postacute myocardial infarction; yet, early cessation of therapy occurs frequently in clinical practice. METHODS AND
RESULTS: We examined 11 858 acute myocardial infarction patients treated with percutaneous coronary intervention discharged alive on ADPri therapy from 233 United States TRANSLATE-ACS study (Treatment With Adenosine Diphosphate Receptor Inhibitors: Longitudinal Assessment of Treatment Patterns and Events After Acute Coronary Syndrome) participating hospitals to determine the prevalence of early ADPri cessation (within 1 year), patient-reported reasons for cessation, and associated risk of major adverse cardiovascular events at 1 year. Overall, 2514 (21.2%) of percutaneous coronary intervention-treated patients stopped ADPri by 1 year postmyocardial infarction; the median time from discharge to cessation was 200.5 days (25th, 75th percentiles: 71, 340). Among those with early ADPri cessation, 53.9% received drug-eluting stents and had a median duration of 301 treatment days (25th, 75th percentiles: 137, 353); 33.3% of drug-eluting stent patients stopped treatment within 6 months compared with 64.2% of bare metal stent patients. Those discharged on prasugrel (versus clopidogrel) had a slightly higher likelihood of early ADPri cessation (23.2% versus 21.0%; P=0.03; adjusted hazard ratio, 1.28; 95% confidence interval, 1.17-1.40). Patient-reported reasons for early ADPri cessation included physician-recommended discontinuation (54%), as well as patient self-discontinuation, because of cost (19%), medication side effects (9%), and procedural interruption (10%). Using a time-dependent covariate model, early cessation of ADPri therapy was associated with increased major adverse cardiovascular event (adjusted hazard ratio, 1.40; 95% confidence interval, 1.19-1.65; P<0.0001).
CONCLUSIONS: One in 5 percutaneous coronary intervention-treated myocardial infarction patients stopped ADPri treatment within 1 year. Early cessation was associated with increased major adverse cardiovascular event risk. CLINICAL TRIAL REGISTRATION: URL: http://www.clinicaltrials.gov. Unique identifier: NCT01088503.
© 2016 American Heart Association, Inc.

Entities:  

Keywords:  adenosine diphosphate; major adverse cardiovascular event; myocardial infarction; percutaneous coronary intervention; stent

Mesh:

Substances:

Year:  2016        PMID: 27789517     DOI: 10.1161/CIRCINTERVENTIONS.115.003602

Source DB:  PubMed          Journal:  Circ Cardiovasc Interv        ISSN: 1941-7640            Impact factor:   6.546


  7 in total

1.  Trends in Platelet Adenosine Diphosphate P2Y12 Receptor Inhibitor Use and Adherence Among Antiplatelet-Naive Patients After Percutaneous Coronary Intervention, 2008-2016.

Authors:  Elias J Dayoub; Matthew Seigerman; Sony Tuteja; Taisei Kobayashi; Daniel M Kolansky; Jay Giri; Peter W Groeneveld
Journal:  JAMA Intern Med       Date:  2018-07-01       Impact factor: 21.873

Review 2.  Management of Antithrombotic Therapy after Acute Coronary Syndromes.

Authors:  Fatima Rodriguez; Robert A Harrington
Journal:  N Engl J Med       Date:  2021-02-04       Impact factor: 176.079

3.  Antiplatelet Therapy Changes for Patients With Myocardial Infarction With Recurrent Ischemic Events: Insights Into Contemporary Practice From the TRANSLATE-ACS (Treatment With ADP Receptor Inhibitors: Longitudinal Assessment of Treatment Patterns and Events After Acute Coronary Syndrome) Study.

Authors:  Alexander C Fanaroff; Lisa A Kaltenbach; Eric D Peterson; Mohammed W Akhter; Mark B Effron; Timothy D Henry; Tracy Y Wang
Journal:  J Am Heart Assoc       Date:  2018-02-08       Impact factor: 5.501

4.  Incidence, Predictors, and Clinical Impact of Early Prasugrel Cessation in Patients With ST-Elevation Myocardial Infarction.

Authors:  Konstantinos C Koskinas; Thomas Zanchin; Roland Klingenberg; Baris Gencer; Fabrice Temperli; Andreas Baumbach; Marco Roffi; Aris Moschovitis; Oliver Muller; David Tüller; Stefan Stortecky; Francois Mach; Thomas F Lüscher; Christian M Matter; Thomas Pilgrim; Dik Heg; Stephan Windecker; Lorenz Räber
Journal:  J Am Heart Assoc       Date:  2018-04-13       Impact factor: 5.501

5.  Incidence, predictors, and prognosis of premature discontinuation or switch of prasugrel or ticagrelor: the ATLANTIS - SWITCH study.

Authors:  Max-Paul Winter; Dirk von Lewinski; Markus Wallner; Florian Prüller; Ewald Kolesnik; Christian Hengstenberg; Jolanta M Siller-Matula
Journal:  Sci Rep       Date:  2019-06-03       Impact factor: 4.379

6.  The effect of de-escalation of P2Y12 receptor inhibitor therapy after acute myocardial infarction in patients undergoing percutaneous coronary intervention: A nationwide cohort study.

Authors:  Jong-Shiuan Yeh; Chien-Yi Hsu; Chun-Yao Huang; Wan-Ting Chen; Yi-Chen Hsieh; Li-Nien Chien
Journal:  PLoS One       Date:  2021-01-25       Impact factor: 3.240

7.  Perceptions of generic medicines and medication adherence after percutaneous coronary intervention: a prospective multicentre cohort study.

Authors:  Trond Røed Pettersen; Jan Schjøtt; Heather G Allore; Bjørn Bendz; Britt Borregaard; Bengt Fridlund; Alf Inge Larsen; Jan Erik Nordrehaug; Svein Rotevatn; Tore Wentzel-Larsen; Tone Merete Norekvål
Journal:  BMJ Open       Date:  2022-09-20       Impact factor: 3.006

  7 in total

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