Safety and Efficacy of PCSK9 Inhibitors in Patients with Acute Coronary Syndrome Who Underwent Coronary Artery Bypass Grafts: A Comparative Retrospective Analysis

Author:

Nasso Giuseppe1ORCID,Larosa Claudio2,Bartolomucci Francesco2,Brigiani Mario Siro1,Contegiacomo Gaetano1,Demola Maria Antonietta1,Vignaroli Walter1ORCID,Tripoli Alessandra1,Girasoli Cataldo1,Lisco Rosanna1,Trivigno Marialisa1,Tunzi Roberto Michele1,Loizzo Tommaso1,Hila Dritan1,Franchino Rosalba1,Amodeo Vincenzo3,Ventra Simone1,Diaferia Giuseppe4,Schinco Giacomo5,Agrò Felice Eugenio6,Zingaro Maddalena2,Rosa Isabella2,Lorusso Roberto7,Del Prete Armando8,Santarpino Giuseppe910,Speziale Giuseppe1

Affiliation:

1. Department of Cardiac Surgery, Anthea Hospital, GVM Care & Research, 70124 Bari, Italy

2. Department of Cardiology, Hospital of Andria, 76123 Andria, Italy

3. Department of Cardiology, Hospital of Polistena, 89024 Polistena, Italy

4. Department of Cardiology, “M. Di Miccoli” Hospital, 70051 Barletta, Italy

5. Health Management, Anthea Hospital, GVM Care & Research, 70124 Bari, Italy

6. Department of Anesthesiology, University Campus Bio Medico, 00128 Rome, Italy

7. Cardio-Thoracic Surgery Department, Heart and Vascular Centre, Maastricht University, 6229 Maastricht, The Netherlands

8. Department of Cardiology, Santa Maria Goretti Hospital, 04100 Latina, Italy

9. Department of Clinical and Experimental Medicine, Magna Graecia University, 88100 Catanzaro, Italy

10. Department of Cardiac Surgery, Città di Lecce Hospital, GVM Care & Research, 73100 Lecce, Italy

Abstract

Background. The in-hospital reduction in low-density lipoprotein cholesterol (LDL-C) levels following acute coronary syndrome (ACS) is recommended in the current clinical guidelines. However, the efficacy of proprotein convertase subtilisin–kexin type 9 (PCSK9) inhibitors in those patients undergoing coronary artery bypass graft (CABG) has never been demonstrated. Methods. From January 2022 to July 2023, we retrospectively analyzed 74 ACS patients characterized by higher LDL-C levels than guideline targets and who underwent coronary bypass surgery. In the first period (January 2022–January 2023), the patients increased their statin dosage and/or added Ezetimibe (Group STEZE, 43 patients). At a later time (February 2023–July 2023), the patients received not only statins and Ezetimibe but also Evolocumab 140 mg every 2 weeks starting as early as possible (Group STEVO, 31 patients). After one and three months post-discharge, the patients underwent clinical and laboratory controls with an evaluation of the efficacy lipid measurements and every adverse event. Results. The two groups did not differ in terms of preoperative risk factors and Euroscore II (STEVO: 2.14 ± 0.75 vs. STEZE: 2.05 ± 0.6, p = 0.29). Also, there was no difference between the groups in terms of ACS (ST-, Instable angina, or NSTE) and time of symptoms onset regarding total cholesterol, LDL-C, and HDL-C trends from the preprocedural period to 3-month follow-up, but there was a more significant reduction in LDL-C and total cholesterol in the STEVO group (p = 0.01 and p = 0.04, respectively) and no difference in HDL-C rise (p = 0.12). No deaths were reported. In three STEZE group patients, angina recurrence posed the need for percutaneous re-revascularization. No STEVO patients developed significant adverse events. The statistical difference in these serious events, 7% in STEZE vs. 0% in STEVO, was not significant (p = 0.26). Conclusions. Evolocumab initiated “as soon as possible” in ACS patients submitted to CABG with high-intensity statin therapy and Ezetimibe was well tolerated and resulted in a substantial and significant reduction in LDL-C levels at discharge, 1 month, and 3 months. This result is associated with a reduction but without a statistical difference between groups.

Publisher

MDPI AG

Subject

General Medicine

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