Validation of the BCIS CHIP Score in chronic total occlusion percutaneous coronary intervention.

CHIP score chronic total occlusion major adverse cardiac or cerebrovascular events percutaneous coronary intervention

Journal

Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions
ISSN: 1522-726X
Titre abrégé: Catheter Cardiovasc Interv
Pays: United States
ID NLM: 100884139

Informations de publication

Date de publication:
17 Apr 2024
Historique:
revised: 25 03 2024
received: 08 01 2024
accepted: 31 03 2024
medline: 17 4 2024
pubmed: 17 4 2024
entrez: 17 4 2024
Statut: aheadofprint

Résumé

The complex high-risk indicated percutaneous coronary intervention (CHIP) score is a tool developed using the British Cardiovascular Intervention Society (BCIS) database to define CHIP cases and predict in-hospital major adverse cardiac or cerebrovascular events (MACCE). To assess the validity of the CHIP score in chronic total occlusion (CTO) percutaneous coronary intervention (PCI). We evaluated the performance of the CHIP score on 8341 CTO PCIs from the Prospective Global Registry for the Study of Chronic Total Occlusion Intervention (PROGRESS-CTO) performed at 44 centers between 2012 and 2023. In our cohort, 7.8% (n = 647) of patients had a CHIP score of 0, 50.2% (n = 4192) had a CHIP score of 1-2, 26.2% (n = 2187) had a CHIP score of 3-4, 11.7% (n = 972) had a CHIP score of 5-6, 3.3% (n = 276) had a CHIP score of 7-8, and 0.8% (n = 67) had a CHIP score of 9+. The incidence of MACCE for a CHIP score of 0 was 0.6%, reaching as high as 8.7% for a CHIP score of 9+, confirming that a higher CHIP score is associated with a higher risk of MACCE. The estimated increase in the risk of MACCE per one score unit increase was 100% (95% confidence interval [CI]: 65%-141%). The AUC of the CHIP score model for predicting MACCE in our cohort was 0.63 (95% CI: 0.58-0.67). There was a positive correlation between the CHIP score and the PROGRESS-CTO MACE score (Spearman's correlation: 0.37; 95% CI: 0.35-0.39; p < 0.001). The CHIP score has modest predictive capacity for MACCE in CTO PCI.

Sections du résumé

BACKGROUND BACKGROUND
The complex high-risk indicated percutaneous coronary intervention (CHIP) score is a tool developed using the British Cardiovascular Intervention Society (BCIS) database to define CHIP cases and predict in-hospital major adverse cardiac or cerebrovascular events (MACCE).
AIM OBJECTIVE
To assess the validity of the CHIP score in chronic total occlusion (CTO) percutaneous coronary intervention (PCI).
METHODS METHODS
We evaluated the performance of the CHIP score on 8341 CTO PCIs from the Prospective Global Registry for the Study of Chronic Total Occlusion Intervention (PROGRESS-CTO) performed at 44 centers between 2012 and 2023.
RESULTS RESULTS
In our cohort, 7.8% (n = 647) of patients had a CHIP score of 0, 50.2% (n = 4192) had a CHIP score of 1-2, 26.2% (n = 2187) had a CHIP score of 3-4, 11.7% (n = 972) had a CHIP score of 5-6, 3.3% (n = 276) had a CHIP score of 7-8, and 0.8% (n = 67) had a CHIP score of 9+. The incidence of MACCE for a CHIP score of 0 was 0.6%, reaching as high as 8.7% for a CHIP score of 9+, confirming that a higher CHIP score is associated with a higher risk of MACCE. The estimated increase in the risk of MACCE per one score unit increase was 100% (95% confidence interval [CI]: 65%-141%). The AUC of the CHIP score model for predicting MACCE in our cohort was 0.63 (95% CI: 0.58-0.67). There was a positive correlation between the CHIP score and the PROGRESS-CTO MACE score (Spearman's correlation: 0.37; 95% CI: 0.35-0.39; p < 0.001).
CONCLUSIONS CONCLUSIONS
The CHIP score has modest predictive capacity for MACCE in CTO PCI.

Identifiants

pubmed: 38629740
doi: 10.1002/ccd.31045
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Philanthropic support of our generous Anonymous donors(2), and the philanthropic support of Drs. Mary Ann and Donald A Sens; Mr. Raymond Ames and Ms. Barbara Thorndike; Frank J and Eleanor A. Maslowski Charitable Trust; Joseph F and Mary M Fleischhacker Family Foundation; Mrs. Diane and Dr. Cline Hickok; Mrs. Marilyn and Mr. William Ryerse; Mr. Greg and Mrs. Rhoda Olsen; Mrs. Wilma and Mr. Dale Johnson; Mrs. Charlotte and Mr. Jerry Golinvaux Family Fund; the Roehl Family Foundation; the Joseph Durda Foundation

Informations de copyright

© 2024 Wiley Periodicals LLC.

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Auteurs

Athanasios Rempakos (A)

Minneapolis Heart Institute and Minneapolis Heart Institute Foundation, Abbott Northwestern Hospital, Minneapolis, Minnesota, USA.

Michaella Alexandrou (M)

Minneapolis Heart Institute and Minneapolis Heart Institute Foundation, Abbott Northwestern Hospital, Minneapolis, Minnesota, USA.

Deniz Mutlu (D)

Minneapolis Heart Institute and Minneapolis Heart Institute Foundation, Abbott Northwestern Hospital, Minneapolis, Minnesota, USA.

James W Choi (JW)

Texas Health Presbyterian Hospital & Baylor Scott and White Heart and Vascular Hospital, Dallas, Texas, USA.

Paul Poommipanit (P)

University Hospitals, Case Western Reserve University, Cleveland, Ohio, USA.

Jaikirshan J Khatri (JJ)

Cleveland Clinic, Cleveland, Ohio, USA.

Laura Young (L)

Cleveland Clinic, Cleveland, Ohio, USA.

Brian Jefferson (B)

Tristar Centennial Medical Center, Nashville, Tennessee, USA.

Sevket Gorgulu (S)

Biruni University Medical School, Istanbul, Turkey.

Farouc A Jaffer (FA)

Massachusetts General Hospital, Boston, Massachusetts, USA.

Raj Chandwaney (R)

Oklahoma Heart Institute, Tulsa, Oklahoma, USA.

Rhian Davies (R)

WellSpan York Hospital, York, Pennsylvania, USA.

Stewart Benton (S)

WellSpan York Hospital, York, Pennsylvania, USA.

Khaldoon Alaswad (K)

Henry Ford Cardiovascular Division, Detroit, Michigan, USA.

Lorenzo Azzalini (L)

Department of Medicine, Division of Cardiology, University of Washington, Seattle, Washington, USA.

Kathleen E Kearney (KE)

Department of Medicine, Division of Cardiology, University of Washington, Seattle, Washington, USA.

Oleg Krestyaninov (O)

Meshalkin Novosibirsk Research Institute, Novosibirsk, Russia.

Dmitrii Khelimskii (D)

Meshalkin Novosibirsk Research Institute, Novosibirsk, Russia.

Philip Dattilo (P)

Medical Center of the Rockies, Loveland, Colorado, USA.

Niranjan Reddy (N)

Kettering Medical Center, Dayton, Ohio, USA.

Nidal Abi-Rafeh (N)

North Oaks Health System, Hammond, Louisiana, USA.

Ahmed Elguindy (A)

Aswan Heart Center, Magdi Yacoub Foundation, Cairo, Egypt.

Omer Goktekin (O)

Memorial Bahcelievler Hospital, Istanbul, Turkey.

Bavana V Rangan (BV)

Minneapolis Heart Institute and Minneapolis Heart Institute Foundation, Abbott Northwestern Hospital, Minneapolis, Minnesota, USA.

Olga C Mastrodemos (OC)

Minneapolis Heart Institute and Minneapolis Heart Institute Foundation, Abbott Northwestern Hospital, Minneapolis, Minnesota, USA.

Ahmed Al-Ogaili (A)

Minneapolis Heart Institute and Minneapolis Heart Institute Foundation, Abbott Northwestern Hospital, Minneapolis, Minnesota, USA.

Yader Sandoval (Y)

Minneapolis Heart Institute and Minneapolis Heart Institute Foundation, Abbott Northwestern Hospital, Minneapolis, Minnesota, USA.

Nicholas M Burke (NM)

Minneapolis Heart Institute and Minneapolis Heart Institute Foundation, Abbott Northwestern Hospital, Minneapolis, Minnesota, USA.

Emmanouil S Brilakis (ES)

Minneapolis Heart Institute and Minneapolis Heart Institute Foundation, Abbott Northwestern Hospital, Minneapolis, Minnesota, USA.

Mir B Basir (MB)

Henry Ford Cardiovascular Division, Detroit, Michigan, USA.

Classifications MeSH