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Treatment Modifications in Acute Coronary Syndrome Patients Treated with Ticagrelor: Insights from the FORCE-ACS
Niels M R van der Sangen1, Jaouad Azzahhafi2, Dean R P P Chan Pin Yin2
1Department of Cardiology, Amsterdam UMC, University of Amsterdam, Amsterdam Cardiovascular Sciences, Amsterdam, The Netherlands.
Insights
Treatment modifications like interruption or disruption of ticagrelor in acute coronary syndrome patients are common. These specific changes, unlike discontinuation, significantly increase the risk of ischemic events.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Medicine
Background:
- Acute coronary syndrome (ACS) patients often receive ticagrelor, a P2Y12-inhibitor.
- Premature discontinuation of ticagrelor is observed, but its reasons and clinical impact are not well understood.
Purpose of the Study:
- To determine the incidence, reasons, and clinical implications of ticagrelor treatment modifications in ACS patients.
- To investigate the association between different types of ticagrelor modification and ischemic events.
Main Methods:
- Analysis of data from 4,278 ACS patients in the FORCE-ACS registry (2015-2020).
- Categorization of treatment modifications: discontinuation, alteration, interruption, disruption.
- Cox regression analysis to assess the risk of ischemic events (death, myocardial infarction, stroke) within 12 months.
Main Results:
- Treatment modifications occurred in 26.7% (discontinuation), 20.1% (alteration), 2.8% (interruption), and 3.1% (disruption) within 12 months.
- Treatment interruption (aHR 2.93) and disruption (aHR 2.33) were significantly associated with increased ischemic event risk.
- Discontinuation and alteration were not linked to a higher risk of ischemic events.
Conclusions:
- Ticagrelor treatment modifications are frequent in ACS patients, with varied reasons and types.
- Treatment interruption and disruption are linked to increased cardiovascular risk.
- Clinical practice requires careful consideration of ticagrelor modification types to mitigate ischemic event risk.
Abstract:
Patients presenting with acute coronary syndrome (ACS) are frequently treated with the P2Y12-inhibitor ticagrelor. Some patients prematurely discontinue ticagrelor, but the incidence of reasons for and clinical implications of treatment modification are relatively unknown.Data from 4,278 ACS patients (mean age: 63.6 years, 26.1% women) who were discharged on ticagrelor and enrolled in the FORCE-ACS registry between 2015 and 2020 were used. Treatment modifications were categorized as physician-recommended discontinuation, alteration, interruption, or disruption and occurred in 26.7, 20.1, 2.8, and 3.1% of patients within 12 months of follow-up (VISUAL SUMMARY: ). Underlying reasons for treatment modification differed per type of modification. Overall, the rate of ischemic events defined as all-cause death, myocardial infarction, or stroke was 6.6% at 12 months of follow-up. Cox regression analysis using time-updated modification variables as independent variables showed that treatment interruption (adjusted hazard ratio [HR]: 2.93, 95% confidence interval [CI]: 1.48-5.79, p < 0.01) and disruption (adjusted HR: 2.33, 95% CI: 1.07-5.07, p = 0.03) were associated with an increased risk of ischemic events even after adjustment for relevant confounders. Discontinuation and alteration were not associated with increased ischemic risk.In clinical practice, treatment modifications in ACS patients discharged on ticagrelor are common, although type and reasons for modification are heterogeneous. Treatment interruption and disruption are associated with excess cardiovascular risk.
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