The purpose of the data collection is to assess the safety of angioplasty procedures in the cardiology department of the hospital in la Rochelle. Consecutive cases over one year were enrolled.
Clinical and procedural data were collected at inclusion to describe the study population. One and three-year follow-up data were collected to determine the number of major adverse cardiac events (MACE) (all-cause death, non-fatal myocardial infarction, non-fatal stroke and revascularization of target lesion).
Categorical data were used for inclusion/exclusion criteria, gender, clinical history, clinical indication, procedural data, lesion data, type of follow-up, treatment, and MACE. Continuous data were collected for age, body mass index, biological data, radiation data, duration, diameter and length of treated lesions.
Clinical and procedural data were retrieved from CardioReport™ (MediReport).
Follow-up data were obtained after patient phone call, consultation, or hospital admission.