# Drug-Coated Balloons in Coronary Bifurcation Disease: A State-of-the-Art Review

**Authors:** Saad M. Ezad, Natasha Khullar, Peter O’Kane, Jonathan Hinton

PMC · DOI: 10.3390/jpm16020075 · 2026-01-31

## TL;DR

Drug-coated balloons offer a new way to treat complex heart artery issues without permanent implants.

## Contribution

This review highlights the emerging role of drug-coated balloons in managing coronary bifurcation disease.

## Key findings

- Drug-coated balloons deliver medication directly to vessel walls, promoting healing.
- They simplify procedures and avoid permanent metallic implants in bifurcation treatments.

## Abstract

Coronary bifurcation disease remains one of the more challenging lesion subsets to treat with percutaneous coronary intervention due to bifurcation geometry and increased risk of target lesion failure. Whilst a provisional approach is preferred in most bifurcations, two-stent techniques may be required where there is a high risk of side branch compromise or a bailout; however, this further increases procedure complexity. Drug-coated balloons (DCBs) are emerging as a promising alternative that allow vessel healing without leaving behind a permanent metallic implant by delivering antiproliferative medication directly to the vessel wall and simplifying procedures. This state-of-the-art review summarises the current evidence and the evolving role of DCBs in the management of coronary bifurcation lesions with a focus on patient- and lesion-specific factors that might influence the treatment strategy choice.

## Full-text entities

- **Genes:** MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, FKBP1AP4 (FKBP prolyl isomerase 1A pseudogene 4) [NCBI Gene 2285] {aka FKBP12, FKBP1P4}
- **Diseases:** stent thrombosis (MESH:D013927), ISR (MESH:D023903), DEFINITION II (MESH:C537730), atherosclerosis (MESH:D050197), CV death (MESH:D003643), cardiovascular death (MESH:D002318), myocardial infarction (MESH:D009203), renal dysfunction (MESH:D007674), side (MESH:D006333), coronary artery lesions (MESH:D003324), necrosis (MESH:D009336), neointimal hyperplasia (MESH:D006965), crush (MESH:D003444), calcified (MESH:D018333), bifurcation disease (MESH:C537283), SB disease (MESH:D000069584), inflammation (MESH:D007249), injury to (MESH:D014947), disease (MESH:D004194), Coronary Bifurcation Disease (MESH:D003327), acute coronary syndromes (MESH:D054058), vessel disease (MESH:C536223), calcification (MESH:D002114), diabetes (MESH:D003920), TLF (MESH:D051437), anxiety (MESH:D001007), impaired ventricular function (MESH:D018754), bleeding (MESH:D006470), TLR (MESH:D009059), LMS (MESH:C537878), DCB (MESH:D058456), small vessel disease (MESH:D059345), ischaemia (MESH:D007511), stenoses (MESH:D003251), CBL (OMIM:613563)
- **Chemicals:** DCB (-), Everolimus (MESH:D000068338), Urea (MESH:D014508), lipid (MESH:D008055), BTHC (MESH:C033729), PLGA (MESH:D000077182), calcium (MESH:D002118), biolimus (MESH:C518022), OCT (MESH:C051883), DEB (MESH:C007366), zotarolimus (MESH:C489443), Paclitaxel (MESH:D017239), sirolimus (MESH:D020123), phospholipids (MESH:D010743), iopromide (MESH:C038192)
- **Species:** Homo sapiens (human, species) [taxon 9606], Sus scrofa (pig, species) [taxon 9823]
- **Cell lines:** muscle — Rattus norvegicus (Rat), Finite cell line (CVCL_XB60)

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12941830/full.md

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Source: https://tomesphere.com/paper/PMC12941830