Skip to main content
. 2021 Mar 29;27(3):857–868. doi: 10.1007/s10741-021-10099-5

Table 3.

Characteristic of included studies for long-term outcome

Author and year Country Design Patients (and cohort by antiplatelet drug use) Mean age (years) Male sex (%) Outcome measured Length of follow-up Results
D’Ascenzo et al. (2019) 25 cardiovascular centers across nine countries (InterTAK Registry) Multicenter observational retrospective cohort study 1533 (aspirin at discharge: 1031; none: 502) 66.4 ± 13.1 9.8 MACCE 5 years HR 1.11 (95% CI 0.78–1.58), p = 0.58
Piackova et al. (2018) Austria Observational retrospective cohort study 99 (44 aspirin alone, 44 DAPT for 12 months than aspirin, 11 none) 67.8 18.2 All-cause and cardiovascular mortality 5.9 years CV mortality HR = 0.61; CI = 0.21–1.79, p 0.37; all-cause HR = 0.81; CI = 0.45–1.46, p = 0.49)
Abanador-Kamper et al. (2016) Germany Observational retrospective cohort study 72 (28 on monotherapy; 29 on DAPT; 2 on triple therapy; 4 on OAC + aspirin/clopidogrel; 9 none) 68.8 7 MACE 24 months and 36 months Low MACE rate compared with existing data. 1 had a stroke on OAC; 1 recurrence in DAPT, 1 MI in monotherapy
Khalighi et al. (2016) USA Observational retrospective cohort study 12 (6 patients on aspirin, 4 on DAPT; 2 patients with none) 66 0 Death, cardio- shock, SCD, recurrence, re-hospitalization 8.3 ± 3.6 years No difference
Cacciotti et al. (2012) Italy Observational retrospective cohort study 75 (19 were lost during follow-up, so 56, 83.9% on aspirin) 71.9 4 MACE 2.2 years Both death and recurrence occurred in patients on aspirin

MACCE major adverse cardiovascular and cerebrovascular events, HR hazard ratio, CI confidence interval, DAPT dual antiplatelet therapy, CV cardiovascular, OAC oral anticoagulation, MACE major adverse cardiovascular events, MI myocardial infarction, SCD sudden cardiac death