# Long-Term Clinical Outcomes of PCI Versus Medical Therapy in NSTEMI Patients with Prior CABG

**Authors:** Onur Altınkaya, Selim Aydemir, Murat Özmen, Mustafa Özkoç, Rauf Macit, Abuzer Ocak, Emrah Aksakal

PMC · DOI: 10.3390/medicina62020315 · 2026-02-03

## TL;DR

This study found no long-term benefit of PCI over medical therapy for NSTEMI patients with prior CABG, highlighting the role of comorbidities in outcomes.

## Contribution

The study provides new evidence on the lack of PCI advantage in a high-risk NSTEMI subgroup with prior CABG.

## Key findings

- MACE rates were similar between PCI and medical therapy (14.3% vs. 18.9%).
- All-cause mortality was comparable in both groups (9.8% vs. 10.3%).
- Hypoalbuminemia, CKD, and HF were key predictors of poor outcomes.

## Abstract

Background and Objectives: Patients with a prior history of coronary artery bypass grafting (CABG) who present with non-ST-segment elevation myocardial infarction (NSTEMI) represent a complex, high-risk subgroup due to advanced comorbidity burden and challenging coronary anatomy. Whether an invasive strategy offers meaningful benefit over conservative management in this population remains unclear. Therefore, this study aimed to compare long-term outcomes of percutaneous coronary intervention (PCI) versus medical therapy in NSTEMI patients with previous CABG and to identify independent predictors of major adverse cardiovascular events (MACE) and all-cause mortality. Materials and Methods: This retrospective cohort study included 286 NSTEMI patients with prior CABG (PCI: 112; medical therapy: 174). Baseline demographic, clinical, laboratory, and angiographic characteristics were assessed. The primary endpoint was MACE, while the secondary endpoint was all-cause mortality. Kaplan–Meier analysis evaluated survival differences, and multivariable Cox regression identified independent predictors. Results: During follow-up, MACE rates were comparable between PCI and medical therapy (14.3% vs. 18.9%; p = 0.305). All-cause mortality was likewise similar (9.8% vs. 10.3%; p = 0.541). Kaplan–Meier analysis showed no survival benefit with PCI (log-rank p = 0.334). Hypoalbuminemia independently predicted both MACE and mortality, while CKD and HF were major determinants of long-term mortality. Conclusions: In NSTEMI patients with prior CABG, no long-term superiority of PCI over medical therapy was observed with respect to MACE or mortality. Prognosis appears more closely linked to hypoalbuminemia, CKD, and HF than to the chosen management strategy. These findings underscore the importance of individualized and risk-adapted clinical decision-making in this complex population.

## Linked entities

- **Diseases:** chronic kidney disease (MONDO:0005300), heart failure (MONDO:0005252)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** coronary artery disease (MESH:D003324), TIA (MESH:D002546), HF (MESH:D006333), sepsis (MESH:D018805), death (MESH:D003643), malnutrition (MESH:D044342), HT (MESH:D006973), occlusion (MESH:D001157), atherosclerosis (MESH:D050197), ACS (MESH:D000168), cerebrovascular disease (MESH:D002561), infection (MESH:D007239), CKD (MESH:D012080), MACE (MESH:D002318), myocardial infarction (MESH:D009203), ischemic stroke (MESH:D002544), Atrial fibrillation (MESH:D001281), Hypoalbuminemia (MESH:D034141), stroke (MESH:D020521), NSTEMI (MESH:D000072657), frailty (MESH:D000073496), ischemia (MESH:D007511), acute coronary syndrome (MESH:D054058), chronic inflammation (MESH:D007249), injury to (MESH:D014947), CKD (MESH:D051436), cardiogenic shock (MESH:D012770), three-vessel disease (MESH:C536223), malignancy (MESH:D009369), DM (MESH:D003920), ischemic (MESH:D002545), endothelial dysfunction (MESH:D014652)
- **Chemicals:** glucose (MESH:D005947), ACEI (-), ASA (MESH:D001241), insulin (MESH:D007328), MRA (MESH:C502936)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12942241/full.md

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Source: https://tomesphere.com/paper/PMC12942241