Improving adherence to ticagrelor in patients after acute coronary syndrome: Results from the progress trial

Autor: Felice Gragnano, Marco Di Maio, Arturo Cesaro, Elisabetta Moscarella, Plinio Cirillo, Claudia Concilio, Paolo Calabrò, Dario Di Maio, Fabio Fimiani, Mario Crisci, Vittorio Taglialatela, Ivana Pariggiano, Vincenzo Diana
Přispěvatelé: Crisci, M., Gragnano, F., Di Maio, M., Diana, V., Moscarella, E., Pariggiano, I., Di Maio, D., Concilio, C., Taglialatela, V., Fimiani, F., Cesaro, A., Cirillo, P. L., Calabro, P., Crisci, Mario, Gragnano, Felice, Di Maio, Marco, Diana, Vincenzo, Moscarella, Elisabetta, Pariggiano, Ivana, Di Maio, Dario, Concilio, Claudia, Taglialatela, Vittorio, Fimiani, Fabio, Cesaro, Arturo, Cirillo, Plinio Lorenzo, Calabrò, Paolo
Jazyk: angličtina
Rok vydání: 2020
Předmět:
Male
Acute coronary syndrome
medicine.medical_specialty
Ticagrelor
Outpatient Clinics
Hospital

Time Factors
Hemorrhage
030204 cardiovascular system & hematology
Drug Administration Schedule
law.invention
Medication Adherence
03 medical and health sciences
Appointments and Schedules
0302 clinical medicine
Percutaneous Coronary Intervention
Randomized controlled trial
law
Internal medicine
medicine
Clinical endpoint
Outpatient clinic
Humans
In patient
Prospective Studies
Aged
030203 arthritis & rheumatology
Pharmacology
Aspirin
business.industry
Dual Anti-Platelet Therapy
Bleeding
Middle Aged
medicine.disease
Discontinuation
Telephone
Treatment Outcome
Italy
Adherence
Dual antiplatelet therapy
Disruption
Female
Cardiology and Cardiovascular Medicine
business
Platelet Aggregation Inhibitors
medicine.drug
Popis: Background: Dual antiplatelet therapy (DAPT) with aspirin and ticagrelor is recommended for at least 12 months in patients after an acute coronary syndrome (ACS). However, its underuse and premature discontinuation are common in clinical practice. We aimed to investigate the impact of a dedicated follow-up strategy with clinical visits and counselling on adherence levels to ticagrelor in patients after ACS. Methods: PROGRESS (PROmotinG dual antiplatelet therapy adheREnce in the setting of acute coronary Syndromes) is a prospective, randomized trial enrolling 400 ACS patients treated with ticagrelor. Patients were randomized to be followed-up in a dedicated outpatient clinic (In-person follow-up group, [IN-FU], n=200), or with scheduled for phone interviews only (Telephone follow-up group [TEL-FU], n=200), to assess ticagrelor adherence and related complications. DAPT disruption was defined as an interruption of the administration of the drug due to complications or other reasons of non-adherence, and divided according to the duration into short (1-5 days), temporary (6-30 days) and permanent (≥30 days) disruption. The primary endpoint was the rate of DAPT disruption at 1-year follow-up. Results: The rate of ticagrelor disruption at 1 year follow-up was higher in the TEL-FU group than in the IN-FU group (19.6 vs 5.5%; p Conclusion: The PROGRESS trial showed a net reduction in DAPT disruption in patients followed-up with clinical (in-person) follow-up visits in a dedicated outpatient clinic compared with those scheduled for phone interviews only.
Databáze: OpenAIRE