Prevalence, Management and Outcomes of Percutaneous Coronary Intervention for Coronary In-Stent Restenosis: Insights From the France PCI Registry.


Journal

Cardiovascular revascularization medicine : including molecular interventions
ISSN: 1878-0938
Titre abrégé: Cardiovasc Revasc Med
Pays: United States
ID NLM: 101238551

Informations de publication

Date de publication:
07 2023
Historique:
received: 08 01 2023
accepted: 10 02 2023
medline: 3 7 2023
pubmed: 23 2 2023
entrez: 22 2 2023
Statut: ppublish

Résumé

Despite the evolution of stent technology, there is a non-negligible risk of in-stent restenosis (ISR) after Percutaneous coronary intervention (PCI). Large-scale registry data on the prevalence and clinical management of ISR is lacking. The aim was to describe the epidemiology and management of patients with ≥1 ISR lesions treated with PCI (ISR PCI). Data on characteristics, management and clinical outcomes were analyzed for patients undergoing ISR PCI in the France-PCI all-comers registry. Between January 2014 and December 2018, 31,892 lesions were treated in 22,592 patients, 7.3 % of whom underwent ISR PCI. Patients undergoing ISR PCI were older (68.5 vs 67.8; p < 0.001), and more likely to have diabetes (32.7 % vs 25.4 %, p < 0.001), chronic coronary syndrome or multivessel disease. ISR PCI concerned drug eluting stents (DES) ISR in 48.8 % of cases. Patients with ISR lesions were more frequently treated with DES than drug eluting balloon or balloon angioplasty (74.2 %, 11.6 % and 12.9 %, respectively). Intravascular imaging was rarely used. At 1 year, patients with ISR had higher target lesion revascularization rates (4.3 % vs. 1.6 %; HR 2.24 [1.64-3.06]; p < 0.001). In a large all-comers registry, ISR PCI was not infrequent and associated with worse prognosis than non-ISR PCI. Further studies and technical improvements are warranted to improve the outcomes of ISR PCI.

Sections du résumé

BACKGROUND
Despite the evolution of stent technology, there is a non-negligible risk of in-stent restenosis (ISR) after Percutaneous coronary intervention (PCI). Large-scale registry data on the prevalence and clinical management of ISR is lacking.
METHODS
The aim was to describe the epidemiology and management of patients with ≥1 ISR lesions treated with PCI (ISR PCI). Data on characteristics, management and clinical outcomes were analyzed for patients undergoing ISR PCI in the France-PCI all-comers registry.
RESULTS
Between January 2014 and December 2018, 31,892 lesions were treated in 22,592 patients, 7.3 % of whom underwent ISR PCI. Patients undergoing ISR PCI were older (68.5 vs 67.8; p < 0.001), and more likely to have diabetes (32.7 % vs 25.4 %, p < 0.001), chronic coronary syndrome or multivessel disease. ISR PCI concerned drug eluting stents (DES) ISR in 48.8 % of cases. Patients with ISR lesions were more frequently treated with DES than drug eluting balloon or balloon angioplasty (74.2 %, 11.6 % and 12.9 %, respectively). Intravascular imaging was rarely used. At 1 year, patients with ISR had higher target lesion revascularization rates (4.3 % vs. 1.6 %; HR 2.24 [1.64-3.06]; p < 0.001).
CONCLUSIONS
In a large all-comers registry, ISR PCI was not infrequent and associated with worse prognosis than non-ISR PCI. Further studies and technical improvements are warranted to improve the outcomes of ISR PCI.

Identifiants

pubmed: 36813696
pii: S1553-8389(23)00062-3
doi: 10.1016/j.carrev.2023.02.006
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

39-46

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest GS and PM declare consulting fees for Terumo and Abbott. BD declares lecture fees for Organon and Amgen. JPC declares research funding or fees from Astrazeneca, Boston Scientific, Bristol-Myers Squibb, Cor2ed, Lead-Up, Medtronic, WebMD. GC declare research funding or fees from Abbot, Amgen, Astrazeneca, Bayer, Biotronik, Bristol-Myers Squibb, Medtronic, Microport, Pfizer, Sanofi-Aventis. PC declares consulting fees for Terumo, Bsci, Abbott, Edwards.

Auteurs

Benjamin Duband (B)

Cardiology Department, Centre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, France. Electronic address: bduband@chu-clermontferrand.fr.

Géraud Souteyrand (G)

Cardiology Department, Centre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, France.

Jean Michel Clerc (JM)

Cardiology Department, Centre Hospitalier Universitaire de Tours, Tours, France.

Stephan Chassaing (S)

Cardiology Department, Clinique Saint Gatien, Tours, France.

Olivier Fichaux (O)

Cardiology Department, Centre Hospitalo-Régional d'Orléans, Orléans, France.

Pierre Marcollet (P)

Cardiology Department, Centre Hospitalier Jacques Cœur, Bourges, France.

Ronan Deballon (R)

Cardiology Department, Clinique Oréliance, France.

Laurent Roussel (L)

Cardiology Department, Les Hôpitaux de Chartres, Chartres, France.

Bruno Pereira (B)

Biostatistics Unit, Direction de la Recherche Clinique, Centre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, France.

Jean-Philippe Collet (JP)

Cardiolgy Department, Groupe Hospitalier Pitié-Salpêtrière, Paris, France.

Philippe Commeau (P)

Cardiology Department, Polyclinique Les Fleurs, Groupe ELSAN, Ollioules, France.

Guillaume Cayla (G)

Cardiology Department, Centre Hospitalier Universitaire de Nîmes, Nîmes, France.

Rene Koning (R)

Cardiology Department, Clinique Saint-Hilaire, Rouen, France.

Pascal Motreff (P)

Cardiology Department, Centre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, France.

Hakim Benamer (H)

Cardiology Department, Clinique de la Roseraie, Soissons, France.

Gregoire Rangé (G)

Cardiology Department, Les Hôpitaux de Chartres, Chartres, France.

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