Changes in coronary collateral function after successful chronic total occlusion percutaneous coronary intervention.


Journal

EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology
ISSN: 1969-6213
Titre abrégé: EuroIntervention
Pays: France
ID NLM: 101251040

Informations de publication

Date de publication:
02 Dec 2022
Historique:
pubmed: 23 8 2022
medline: 23 2 2023
entrez: 22 8 2022
Statut: epublish

Résumé

Contemporary chronic total occlusion (CTO) percutaneous coronary intervention (PCI) incorporates wire escalation and dissection/re-entry recanalisation strategies. The purpose of the study was to investigate changes in collateral function after CTO PCI and to identify whether the mode of successful recanalisation influences collateral function regression. Patients scheduled for elective CTO PCI with evidence of viability in the CTO territory by noninvasive imaging were included in this study. After successful CTO PCI, the aortic pressure (Pa) and distal coronary artery wedge pressure (Pw) during balloon occlusion were measured, both in a resting state and during infusion of intravenous adenosine, allowing the calculation of the pressure-derived collateral pressure index at rest and hyperaemia (CPI Eighty-one patients had physiological measurements at baseline and follow-up. In the final cohort the mean age was 64 years and 82% were male. The mean maximal stent diameter and total stent length were 3.2±0.5 mm and 68±31 mm, respectively. Successful strategies were antegrade wiring (64.2%), antegrade dissection re-entry (8.6%), and retrograde dissection re-entry (27.1%). Between the index procedure and follow-up, wedge pressure decreased from 34±11 mmHg to 21±8.5 mmHg (p<0.01), respectively. FFR There was a significant reduction in collateral flow over time, independent of the recanalisation technique.

Sections du résumé

BACKGROUND BACKGROUND
Contemporary chronic total occlusion (CTO) percutaneous coronary intervention (PCI) incorporates wire escalation and dissection/re-entry recanalisation strategies.
AIMS OBJECTIVE
The purpose of the study was to investigate changes in collateral function after CTO PCI and to identify whether the mode of successful recanalisation influences collateral function regression.
METHODS METHODS
Patients scheduled for elective CTO PCI with evidence of viability in the CTO territory by noninvasive imaging were included in this study. After successful CTO PCI, the aortic pressure (Pa) and distal coronary artery wedge pressure (Pw) during balloon occlusion were measured, both in a resting state and during infusion of intravenous adenosine, allowing the calculation of the pressure-derived collateral pressure index at rest and hyperaemia (CPI
RESULTS RESULTS
Eighty-one patients had physiological measurements at baseline and follow-up. In the final cohort the mean age was 64 years and 82% were male. The mean maximal stent diameter and total stent length were 3.2±0.5 mm and 68±31 mm, respectively. Successful strategies were antegrade wiring (64.2%), antegrade dissection re-entry (8.6%), and retrograde dissection re-entry (27.1%). Between the index procedure and follow-up, wedge pressure decreased from 34±11 mmHg to 21±8.5 mmHg (p<0.01), respectively. FFR
CONCLUSIONS CONCLUSIONS
There was a significant reduction in collateral flow over time, independent of the recanalisation technique.

Identifiants

pubmed: 35994015
pii: EIJ-D-22-00118
doi: 10.4244/EIJ-D-22-00118
pmc: PMC9743238
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e920-e928

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Auteurs

Danielle C J Keulards (DCJ)

Cardiology Department, Catharina Hospital Eindhoven, Eindhoven, the Netherlands.

Osama Alsanjari (O)

Cardiology Department, The Essex Cardiothoracic Centre, Mid and South Essex NHS Foundation Trust, Basildon, United Kingdom.
Anglia Ruskin University School of Medicine, Chelmsford, United Kingdom.
Cardiology Department, Sussex Cardiac Centre, Brighton and Sussex University Hospitals, Brighton, United Kingdom.

Thomas R Keeble (TR)

Cardiology Department, The Essex Cardiothoracic Centre, Mid and South Essex NHS Foundation Trust, Basildon, United Kingdom.
Anglia Ruskin University School of Medicine, Chelmsford, United Kingdom.

Pieter-Jan Vlaar (PJ)

Cardiology Department, Catharina Hospital Eindhoven, Eindhoven, the Netherlands.

Paul A Kelly (PA)

Cardiology Department, The Essex Cardiothoracic Centre, Mid and South Essex NHS Foundation Trust, Basildon, United Kingdom.

Kare H Tang (KH)

Cardiology Department, The Essex Cardiothoracic Centre, Mid and South Essex NHS Foundation Trust, Basildon, United Kingdom.

Sarosh Khan (S)

Cardiology Department, The Essex Cardiothoracic Centre, Mid and South Essex NHS Foundation Trust, Basildon, United Kingdom.
Anglia Ruskin University School of Medicine, Chelmsford, United Kingdom.

James Cockburn (J)

Cardiology Department, Sussex Cardiac Centre, Brighton and Sussex University Hospitals, Brighton, United Kingdom.

Nico H J Pijls (NHJ)

Cardiology Department, Catharina Hospital Eindhoven, Eindhoven, the Netherlands.

David Hildick-Smith (D)

Cardiology Department, Sussex Cardiac Centre, Brighton and Sussex University Hospitals, Brighton, United Kingdom.

Koen Teeuwen (K)

Cardiology Department, Catharina Hospital Eindhoven, Eindhoven, the Netherlands.

John Davies (J)

Cardiology Department, The Essex Cardiothoracic Centre, Mid and South Essex NHS Foundation Trust, Basildon, United Kingdom.
Anglia Ruskin University School of Medicine, Chelmsford, United Kingdom.

Grigoris V Karamasis (GV)

Cardiology Department, The Essex Cardiothoracic Centre, Mid and South Essex NHS Foundation Trust, Basildon, United Kingdom.
Anglia Ruskin University School of Medicine, Chelmsford, United Kingdom.

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Classifications MeSH