Stent Underexpansion Is an Underestimated Cause of Intrastent Restenosis: Insights From RESTO Registry.

in‐stent restenosis optical coherence tomography underexpansion

Journal

Journal of the American Heart Association
ISSN: 2047-9980
Titre abrégé: J Am Heart Assoc
Pays: England
ID NLM: 101580524

Informations de publication

Date de publication:
25 Oct 2024
Historique:
medline: 25 10 2024
pubmed: 25 10 2024
entrez: 25 10 2024
Statut: aheadofprint

Résumé

Despite improvement in devices, in-stent restenosis remains a frequent and challenging complication of percutaneous coronary interventions. The RESTO (Morphological Parameters of In-Stent Restenosis Assessed and Identified by OCT [Optical Coherence Tomography]; study NCT04268875) was a prospective multicenter registry including patients presenting with coronary syndromes related to in-stent restenosis. All patients underwent preintervention OCT analysis, which led to analysis of in-stent restenosis phenotype, number of strut layers, and presence of stent underexpansion. The primary end point was the in-stent restenosis type according to the OCT morphological classification. The 1-year incidence of target vessel failure (a composite of death from cardiac causes, target-vessel myocardial infarction, or ischemia-driven target-vessel revascularization) was assessed. The study included 297 patients. The culprit stent was a drug-eluting stent in 74.2% of cases. OCT analysis revealed the presence of neoatherosclerosis in 57% (52% calcified), neointimal hyperplasia in 43% (58% homogeneous), stent underexpansion (minimal stent area <4.5 mm OCT identified neoatherosclerosis and neointimal hyperplasia in comparable proportions. Stent underexpansion was frequent and favored subsequent adverse clinical outcomes.

Sections du résumé

BACKGROUND BACKGROUND
Despite improvement in devices, in-stent restenosis remains a frequent and challenging complication of percutaneous coronary interventions.
METHODS AND RESULTS RESULTS
The RESTO (Morphological Parameters of In-Stent Restenosis Assessed and Identified by OCT [Optical Coherence Tomography]; study NCT04268875) was a prospective multicenter registry including patients presenting with coronary syndromes related to in-stent restenosis. All patients underwent preintervention OCT analysis, which led to analysis of in-stent restenosis phenotype, number of strut layers, and presence of stent underexpansion. The primary end point was the in-stent restenosis type according to the OCT morphological classification. The 1-year incidence of target vessel failure (a composite of death from cardiac causes, target-vessel myocardial infarction, or ischemia-driven target-vessel revascularization) was assessed. The study included 297 patients. The culprit stent was a drug-eluting stent in 74.2% of cases. OCT analysis revealed the presence of neoatherosclerosis in 57% (52% calcified), neointimal hyperplasia in 43% (58% homogeneous), stent underexpansion (minimal stent area <4.5 mm
CONCLUSIONS CONCLUSIONS
OCT identified neoatherosclerosis and neointimal hyperplasia in comparable proportions. Stent underexpansion was frequent and favored subsequent adverse clinical outcomes.

Identifiants

pubmed: 39450717
doi: 10.1161/JAHA.124.036065
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e036065

Auteurs

Géraud Souteyrand (G)

Institut Pascal, Thérapies Guidées par l'Image, CNRS SIGMA UCA UMR 6602 University Hospital Gabriel Montpied Clermont-Ferrand France.

Thomas Mouyen (T)

Jacques Lacarin Vichy Hospital Centre Vichy Cedex France.

Benjamin Honton (B)

Clinique Pasteur Toulouse France.

Aurélien Mulliez (A)

Institut Pascal, Thérapies Guidées par l'Image, CNRS SIGMA UCA UMR 6602 University Hospital Gabriel Montpied Clermont-Ferrand France.

Benoit Lattuca (B)

University Hospital of Nimes Nimes France.

Jean-Guillaume Dilinger (JG)

Université Paris-Cité, Assistance Publique-Hôpitaux de Paris, Hôpital Lariboisière, and Inserm U-942 Paris France.

Sébastien Levesque (S)

Centre Hospitalier Universitaire de Poitiers Poitiers France.

Grégoire Range (G)

Les hôpitaux de Chartres Chartres France.

Nicolas Combaret (N)

Institut Pascal, Thérapies Guidées par l'Image, CNRS SIGMA UCA UMR 6602 University Hospital Gabriel Montpied Clermont-Ferrand France.

Stéphanie Marliere (S)

CHU Grenoble Grenoble France.

Ouarda Lamallem (O)

Institut Pascal, Thérapies Guidées par l'Image, CNRS SIGMA UCA UMR 6602 University Hospital Gabriel Montpied Clermont-Ferrand France.

Marine Quillot (M)

Centre Hospitalier Henri Duffaut Avignon France.

Edouard Gerbaud (E)

CHU Bordeaux Bordeaux France.

Pascal Motreff (P)

Institut Pascal, Thérapies Guidées par l'Image, CNRS SIGMA UCA UMR 6602 University Hospital Gabriel Montpied Clermont-Ferrand France.

Nicolas Amabile (N)

Institut Cardiovasculaire Paris Sud Massy France.

Classifications MeSH