Percutaneous Left Ventricular Unloading During High-Risk Coronary Intervention: Rationale and Design of the CHIP-BCIS3 Randomized Controlled Trial.

coronary artery disease heart-assist devices left ventricular systolic dysfunction percutaneous coronary intervention randomized controlled trial

Journal

Circulation. Cardiovascular interventions
ISSN: 1941-7632
Titre abrégé: Circ Cardiovasc Interv
Pays: United States
ID NLM: 101499602

Informations de publication

Date de publication:
Mar 2024
Historique:
pubmed: 27 2 2024
medline: 27 2 2024
entrez: 27 2 2024
Statut: ppublish

Résumé

Percutaneous coronary intervention for complex coronary disease is associated with a high risk of cardiogenic shock. This can cause harm and limit the quality of revascularization achieved, especially when left ventricular function is impaired at the outset. Elective percutaneous left ventricular unloading is increasingly used to mitigate adverse events in patients undergoing high-risk percutaneous coronary intervention, but this strategy has fiscal and clinical costs and is not supported by robust evidence. CHIP-BCIS3 (Controlled Trial of High-Risk Coronary Intervention With Percutaneous Left Ventricular Unloading) is a prospective, multicenter, open-label randomized controlled trial that aims to determine whether a strategy of elective percutaneous left ventricular unloading is superior to standard care (no planned mechanical circulatory support) in patients undergoing nonemergent high-risk percutaneous coronary intervention. Patients are eligible for recruitment if they have severe left ventricular systolic dysfunction, extensive coronary artery disease, and are due to undergo complex percutaneous coronary intervention (to the left main stem with calcium modification or to a chronic total occlusion with a retrograde approach). Cardiogenic shock and acute ST-segment-elevation myocardial infarction are exclusions. The primary outcome is a hierarchical composite of all-cause death, stroke, spontaneous myocardial infarction, cardiovascular hospitalization, and periprocedural myocardial infarction, analyzed using the win ratio. Secondary outcomes include completeness of revascularization, major bleeding, vascular complications, health economic analyses, and health-related quality of life. A sample size of 250 patients will have in excess of 80% power to detect a hazard ratio of 0.62 at a minimum of 12 months, assuming 150 patients experience an event across all follow-up. To date, 169 patients have been recruited from 21 National Health Service hospitals in the United Kingdom, with recruitment expected to complete in 2024. URL: https://www.clinicaltrials.gov; Unique identifier: NCT05003817.

Identifiants

pubmed: 38410944
doi: 10.1161/CIRCINTERVENTIONS.123.013367
pmc: PMC10942170
doi:

Banques de données

ClinicalTrials.gov
['NCT05003817']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e013367

Subventions

Organisme : British Heart Foundation
ID : FS/CRTF/21/24118
Pays : United Kingdom

Déclaration de conflit d'intérêts

None.

Auteurs

Matthew Ryan (M)

School of Cardiovascular and Metabolic Medicine & Sciences at the British Heart Foundation Centre of Research Excellence, King's College London, United Kingdom (M.R., S.M.E., H.R., D.P.).

Saad M Ezad (SM)

School of Cardiovascular and Metabolic Medicine & Sciences at the British Heart Foundation Centre of Research Excellence, King's College London, United Kingdom (M.R., S.M.E., H.R., D.P.).

Ian Webb (I)

King's College Hospital National Health Service (NHS) Foundation Trust, London, United Kingdom (I.W.).

Peter D O'Kane (PD)

University Hospitals Dorset NHS Foundation Trust, Bournemouth, United Kingdom (P.D.O.).

Matthew Dodd (M)

Clinical Trials Unit, London School of Hygiene & Tropical Medicine, United Kingdom (M.D., R.E., T.C.).

Richard Evans (R)

Clinical Trials Unit, London School of Hygiene & Tropical Medicine, United Kingdom (M.D., R.E., T.C.).

Lynn Laidlaw (L)

Patient and Public Contributor, London School of Hygiene & Tropical Medicine, United Kingdom (L.L.).

Sohail Q Khan (SQ)

University Hospitals Birmingham NHS Foundation Trust, United Kingdom (S.Q.K.).

Roshan Weerackody (R)

Bart's Health NHS Foundation Trust, London, United Kingdom (R.W.).

Alan Bagnall (A)

Newcastle Hospitals NHS Foundation Trust (A.B.).

Vasileios F Panoulas (VF)

Harefield Hospital, London, United Kingdom (V.F.P.).

Haseeb Rahman (H)

School of Cardiovascular and Metabolic Medicine & Sciences at the British Heart Foundation Centre of Research Excellence, King's College London, United Kingdom (M.R., S.M.E., H.R., D.P.).

Julian W Strange (JW)

University Hospitals Bristol NHS Foundation Trust, United Kingdom (J.W.S.).

Farzin Fath-Ordoubadi (F)

Manchester University Hospitals NHS Foundation Trust, United Kingdom (F.F.-O.).

Stephen P Hoole (SP)

Royal Papworth Hospital NHS Foundation Trust, Cambridge, United Kingdom (S.P.H.).

Rod H Stables (RH)

University of Liverpool, United Kingdom (R.H.S.).

Nick Curzen (N)

University of Southampton, United Kingdom (N.C.).

Tim Clayton (T)

Clinical Trials Unit, London School of Hygiene & Tropical Medicine, United Kingdom (M.D., R.E., T.C.).

Divaka Perera (D)

School of Cardiovascular and Metabolic Medicine & Sciences at the British Heart Foundation Centre of Research Excellence, King's College London, United Kingdom (M.R., S.M.E., H.R., D.P.).
Guy's and St Thomas' NHS Foundation Trust, London, United Kingdom (D.P.).

Classifications MeSH