Mid-term outcome of de novo lesions vs. in stent restenosis treated by intravascular lithotripsy procedures: Insights from the French Shock Initiative.


Journal

International journal of cardiology
ISSN: 1874-1754
Titre abrégé: Int J Cardiol
Pays: Netherlands
ID NLM: 8200291

Informations de publication

Date de publication:
15 10 2022
Historique:
received: 17 02 2022
revised: 11 07 2022
accepted: 12 07 2022
pubmed: 24 7 2022
medline: 30 8 2022
entrez: 23 7 2022
Statut: ppublish

Résumé

Intravascular lithotripsy (IVL) is a promising new technology for disrupting de-novo calcified coronary lesions (DNL) before percutaneous coronary intervention (PCI). We assessed 12-month outcomes of IVL in patients undergoing PCI for DNL or intra stent restenosis (ISR) lesions related to device underexpansion. Prospective analysis of patients in the multicentre all-comers French Shock Initiative IVL registry. The primary safety endpoints in this analysis were in-hospital and 12-month major adverse cardiovascular events (MACE: cardiac death, myocardial infarction or target vessel revascularization). The primary effectiveness endpoint was procedural success, defined as <30% residual stenosis without severe angiographic complications. Event rates were analysed for the cohort and for DNL and ISR procedures separately. A total of 220 lesions were treated (76.7% DNL and 23.3% ISR) in 202 patients. Procedural success was achieved in 95.5% of patients (DNL group: 96.5%; ISR group: 92.0%). In-hospital MACE occurred in 6.4% of cases, mainly driven by periprocedural infarctions. The rate of MACE-free survival at 1 year was 86.6% in the overall cohort. Rates of target vessel (TVR) and lesion (TLR) revascularisation were 6.4% and 2.5%, respectively. The 1-year MACE rate was 91.5% in DNL group and 83.8% in ISR group. In this large all-comers IVL cohort, rates of in-hospital and 1-year MACE were moderate. The safety and efficiency of IVL was comparable in DNL and ISR lesions. A comparative study of the impact of IVL on outcomes appears warranted.

Sections du résumé

BACKGROUND
Intravascular lithotripsy (IVL) is a promising new technology for disrupting de-novo calcified coronary lesions (DNL) before percutaneous coronary intervention (PCI). We assessed 12-month outcomes of IVL in patients undergoing PCI for DNL or intra stent restenosis (ISR) lesions related to device underexpansion.
METHODS
Prospective analysis of patients in the multicentre all-comers French Shock Initiative IVL registry. The primary safety endpoints in this analysis were in-hospital and 12-month major adverse cardiovascular events (MACE: cardiac death, myocardial infarction or target vessel revascularization). The primary effectiveness endpoint was procedural success, defined as <30% residual stenosis without severe angiographic complications. Event rates were analysed for the cohort and for DNL and ISR procedures separately.
RESULTS
A total of 220 lesions were treated (76.7% DNL and 23.3% ISR) in 202 patients. Procedural success was achieved in 95.5% of patients (DNL group: 96.5%; ISR group: 92.0%). In-hospital MACE occurred in 6.4% of cases, mainly driven by periprocedural infarctions. The rate of MACE-free survival at 1 year was 86.6% in the overall cohort. Rates of target vessel (TVR) and lesion (TLR) revascularisation were 6.4% and 2.5%, respectively. The 1-year MACE rate was 91.5% in DNL group and 83.8% in ISR group.
CONCLUSIONS
In this large all-comers IVL cohort, rates of in-hospital and 1-year MACE were moderate. The safety and efficiency of IVL was comparable in DNL and ISR lesions. A comparative study of the impact of IVL on outcomes appears warranted.

Identifiants

pubmed: 35870637
pii: S0167-5273(22)01091-9
doi: 10.1016/j.ijcard.2022.07.023
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

106-111

Informations de copyright

Copyright © 2022 Elsevier B.V. All rights reserved.

Auteurs

Benjamin Honton (B)

Department of Interventional Cardiology, Clinique Pasteur, Toulouse, France. Electronic address: bhonton@clinique-pasteur.com.

Janusz Lipiecki (J)

Department of Interventional Cardiology, Pole Santé République, Clermont-Ferrand, France.

Jacques Monségu (J)

Department of Interventional Cardiology, Institut Cardio Vasculaire, Groupe Hospitalier Mutualiste, Grenoble, France.

Fabrice Leroy (F)

Department of Interventional Cardiology, Clinique La Louviere, Lille, France.

Hakim Benamer (H)

Department of Interventional Cardiology, Hôpital La Roseraie, Aubervilliers, France.

Philippe Commeau (P)

Department of Interventional Cardiology, Polyclinique Les Fleurs, Ollioules, France.

Pascal Motreff (P)

Department of Interventional Cardiology, Gabriel Montpied University Hospital, Clermont-Ferrand, France.

Guillaume Cayla (G)

Department of Interventional Cardiology, Nimes University Hospital, University of Montpellier-Nimes, France.

Jean Luc Banos (JL)

Department of Interventional Cardiology, Centre cardiologique du Pays Basque, Bayonne, France.

Gael Bouchou (G)

Department of Interventional Cardiology, Saint Etienne University Hospital, Saint Etienne, France.

Clémence Laperche (C)

Department of Interventional Cardiology, Clinique Pasteur, Toulouse, France.

Bruno Farah (B)

Department of Interventional Cardiology, Clinique Pasteur, Toulouse, France.

Grégoire Rangé (G)

Department of Interventional Cardiology, Centre Hospitalier, Chartres, France.

Thierry Lefèvre (T)

Department of Interventional Cardiology, Institut Cardio-Vasculaire Paris Sud, Ramsay Générale de Santé, Massy, France.

Nicolas Amabile (N)

Department of Interventional Cardiology, Institut Mutualiste Montsouris, Paris, France.

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