acute coronary syndrome
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: This study included patients with a history of acute coronary syndrome and more than or equal to 50% coronary stenosis, who were administered PCSK9i due to LDL-C levels more than or equal to 70 mg/dl despite the administration of optimized statin therapy
Exclusion criteria
Exclusion criteria: A pregnancy or inability to provide written informed consent, Participants had already had anti-PCSK9 antibody on admission
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The maxLCBI4mm were assessed at baseline, 9 months after PCSK9i, and after cessation of PCSK9i (24 months) | — |
Secondary
| Measure | Time frame |
|---|---|
| The maxLCBI4mm,laque burden measured by IVUS, FFR, and low-density lipoprotein cholesterol (LDL-C) were assessed at baseline, 9 months after PCSK9i, and after cessation of PCSK9i (24 months) | — |
Countries
Japan
Contacts
Gifu Heart Center Department of Cardiovascular Medicine