TY - JOUR
T1 - Treatment Modifications in Acute Coronary Syndrome Patients Treated with Ticagrelor
T2 - Insights from the FORCE-ACS Registry
AU - van der Sangen, Niels M. R.
AU - Azzahhafi, Jaouad
AU - Yin, Dean R. P. P. Chan Pin
AU - Zaaijer, Lucas J. G.
AU - van den Broek, Wout W. A.
AU - Walhout, Ronald J.
AU - Gin, Melvyn Tjon Joe
AU - Pisters, Ron
AU - Nicastia, Deborah M.
AU - Langerveld, Jorina
AU - Vlachojannis, Georgios J.
AU - van Bommel, Rutger J.
AU - Appelman, Yolande
AU - Henriques, Jose P. S.
AU - Kikkert, Wouter J.
AU - ten Berg, Jurrien M.
PY - 2024/10/1
Y1 - 2024/10/1
N2 - Aims 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. Methods and Results 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 ischemicevents definedas all-cause death, myocardialinfarction, or stroke was 6.6% at 12 months of follow-up. Cox regression analysis usingtime-updated modification variables as independent variables showed that treatmentinterruption (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. Conclusion 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.
AB - Aims 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. Methods and Results 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 ischemicevents definedas all-cause death, myocardialinfarction, or stroke was 6.6% at 12 months of follow-up. Cox regression analysis usingtime-updated modification variables as independent variables showed that treatmentinterruption (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. Conclusion 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.
KW - acute coronary syndrome
KW - treatment modifications
KW - ticagrelor
KW - DRUG-ELUTING STENTS
KW - MYOCARDIAL-INFARCTION
KW - NONCARDIAC SURGERY
KW - CLOPIDOGREL
KW - EVENTS
KW - RISK
KW - DISCONTINUATION
KW - THROMBOSIS
U2 - 10.1055/a-2421-8866
DO - 10.1055/a-2421-8866
M3 - Article
SN - 0340-6245
JO - Thrombosis and Haemostasis
JF - Thrombosis and Haemostasis
ER -