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Incidence and Causes for Early Ticagrelor Discontinuation: A "Real-World" Dutch Registry Experience
Thomas O Bergmeijer1, Paul W A Janssen, Mathijs van Oevelen
1Department of Cardiology, St. Antonius Hospital, Nieuwegein, The Netherlands.
Insights
Early discontinuation of ticagrelor occurred in nearly a quarter of patients, primarily due to dyspnea or bleeding. This real-world data highlights key reasons for stopping this acute coronary syndrome treatment.
Area of Science:
- Cardiology
- Pharmacology
Background:
- The PLATO trial demonstrated ticagrelor's superiority over clopidogrel for acute coronary syndrome (ACS) patients.
- However, adverse events like bleeding and dyspnea associated with ticagrelor may lead to early discontinuation (ETD).
Purpose of the Study:
- To evaluate the incidence and causes of early ticagrelor discontinuation (ETD) in a real-world setting.
- To analyze reasons for switching antiplatelet therapy in patients treated with ticagrelor.
Main Methods:
- Retrospective single-center registry analysis of patients prescribed ticagrelor.
- Screening for ETD and data collection via electronic patient records and telephone follow-up.
Main Results:
- Ticagrelor was prescribed to 354 patients; follow-up data were available for 301.
- Early discontinuation or switching occurred in 24.3% of patients within a mean follow-up of 330 days.
- The primary reasons for ETD were dyspnea (11.6%), bleeding (3.7%), and planned major surgery (2.7%).
Conclusions:
- Nearly a quarter of patients discontinued ticagrelor prematurely or switched therapy within one year.
- Dyspnea and bleeding were the most frequent causes for early ticagrelor discontinuation in this real-world cohort.
Objectives:
The PLATO trial revealed superiority of ticagrelor over clopidogrel for the prevention of atherothrombotic events in patients with acute coronary syndrome. However, adverse events such as bleeding, dyspnea, and bradycardia were frequently reported, potentially leading to excess early ticagrelor discontinuation (ETD), later confirmed in the PEGASUS trial. We here evaluated the incidence and causes for ETD in a real-world patient cohort in a high-volume nonacademic percutaneous coronary intervention center in the Netherlands.
Methods:
In a retrospective single-center registry, all patients discharged from the hospital with a new ticagrelor prescription were screened for ETD. Follow-up data were obtained using the hospital electronic patient file records and confirmed by telephone contact with the patient and/or general practitioner, if necessary, to complement the data.
Results:
Ticagrelor was prescribed in 354 patients between December 2011 and December 2012. The follow-up data were available in 301 patients with a mean follow-up duration of 330 days. ETD or switching to another antiplatelet agent occurred in 73 patients (24.3%), mostly due to dyspnea (11.6%), bleeding (3.7%), or planned major surgery (2.7%).
Conclusions:
Almost one quarter of ticagrelor patients were discontinued prematurely or switched to another antiplatelet agent within 1 year, mostly due to dyspnea or bleeding.
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