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  3. Frequency, Reasons, and Impact of Premature Ticagrelor Discontinuation in Patients Undergoing Coronary Revascularization in Routine Clinical Practice: Results From the Bern Percutaneous Coronary Intervention Registry.
 

Frequency, Reasons, and Impact of Premature Ticagrelor Discontinuation in Patients Undergoing Coronary Revascularization in Routine Clinical Practice: Results From the Bern Percutaneous Coronary Intervention Registry.

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BORIS DOI
10.7892/boris.116567
Publisher DOI
10.1161/CIRCINTERVENTIONS.117.006132
PubMed ID
29748219
Description
BACKGROUND

Although ticagrelor has improved clinical outcomes among patients with acute coronary syndrome compared with clopidogrel, adherence to this new antiplatelet agent in real-world practice has not been fully investigated.

METHODS AND RESULTS

Between November 2011 and June 2014, 1278 of 4831 consecutive patients (26.5%) undergoing percutaneous coronary intervention at a tertiary care center were treated with ticagrelor. Premature ticagrelor cessation was categorized into (1) change, when ticagrelor was replaced by prasugrel; (2) de-escalation, when ticagrelor was replaced by clopidogrel; and (3) premature discontinuation, when ticagrelor was discontinued without P2Y12 inhibitor replacement. Of 1278 patients treated with ticagrelor, premature treatment cessation occurred in 212 patients (17%). De-escalation to clopidogrel was the most frequent scenario (57%; n=120), followed by premature discontinuation (28%; n=60) and change to prasugrel (15%; n=32). Reasons for ticagrelor cessation included adverse effects (49%), initiation of oral anticoagulation (19%), and unspecified general practitioner preference (10%). Most frequent adverse effects leading to premature ticagrelor cessation were bleeding (41%), dyspnea (29%), and gastrointestinal symptoms (18%). Premature ticagrelor cessation was not associated with an increased risk of cardiac death, myocardial infarction, or stroke (hazard ratio, 0.73; 95% confidence interval: 0.40-1.32; =0.29).

CONCLUSIONS

Premature ticagrelor cessation in routine clinical practice occurred in 1 of 6 patients and was primarily related to adverse effects among which bleeding and dyspnea were the most frequent. Although premature ticagrelor cessation was not associated with adverse cardiovascular outcomes, this finding requires careful interpretation in view of the modest sample size.

CLINICAL TRIAL REGISTRATION

URL: https://www.clinicaltrials.gov. Unique identifier: NCT02241291.
Date of Publication
2018-05
Publication Type
Article
Subject(s)
600 Technology > 610 Medicine & health
300 Social sciences, sociology & anthropology > 360 Social problems & social services
Keyword(s)
clopidogrel dyspnea percutaneous coronary intervention tertiary care centers ticagrelor
Language(s)
en
Contributor(s)
Zanchin, Thomas
Temperli, Fabrice
Karagiannis Voules, Alexios
Clinical Trials Unit Bern (CTU)
Institut für Sozial- und Präventivmedizin (ISPM)
Zanchin, Christian
Universitätsklinik für Kardiologie
Räsänen, Markus
Koskinas, Konstantinos
Universitätsklinik für Kardiologie
Stortecky, Stefan
Universitätsklinik für Kardiologie
Hunziker Munsch, Lukas Christoph
Universitätsklinik für Kardiologie
Praz, Fabien Daniel
Universitätsklinik für Kardiologie
Blöchlinger, Stefan
Universitätsklinik für Kardiologie
Moro, Christina
Moschovitis, Aris
Universitätsklinik für Kardiologie
Seiler, Christian
Universitätsklinik für Kardiologie
Billinger, Michael
Universitätsklinik für Kardiologie
Heg, Dierik Hansorcid-logo
Clinical Trials Unit Bern (CTU)
Pilgrim, Thomas
Universitätsklinik für Kardiologie
Valgimigli, Marco
Universitätsklinik für Kardiologie
Windecker, Stephan
Universitätsklinik für Kardiologie
Räber, Lorenz
Universitätsklinik für Kardiologie
Additional Credits
Clinical Trials Unit Bern (CTU)
Universitätsklinik für Kardiologie
Series
Circulation: Cardiovascular interventions
Publisher
Lippincott Williams & Wilkins
ISSN
1941-7632
Access(Rights)
restricted
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