Coronary lithotripsy for the treatment of underexpanded stents: the international & multicentre CRUNCH registry.


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:
20 Sep 2022
Historique:
pubmed: 24 3 2022
medline: 24 9 2022
entrez: 23 3 2022
Statut: ppublish

Résumé

Stent underexpansion increases the risk of cardiac adverse events. At present, there are limited options to treat refractory stent underexpansion. In this context, the intravascular lithotripsy (IVL) system might be a safe and effective strategy. We aimed to evaluate the safety and efficacy of IVL in addressing resistant stent underexpansion due to heavy underlying calcification. This was an international multicentre registry including patients receiving IVL therapy to treat stent underexpansion from December 2017 to August 2020. Angiographic and intracoronary imaging data were collected. The efficacy endpoint was device success (technical success with a final percentage diameter stenosis <50%). The safety endpoint was in-hospital major adverse cardiac events (MACE). Seventy patients were included, the mean age was 73±9.2 years and 76% were male. The median time from stent implantation to IVL therapy was 49 days (0-2,537). Adjuvant treatment with non-compliant balloon dilatations pre- and post-IVL was performed in 72.3% and 76.8% of patients, respectively, and additional stenting was performed in 22.4%. Device success was 92.3%. Minimum lumen diameter increased from 1.49±0.73 mm to 2.41±0.67 mm (p<0.001) and stent expansion increased by 124.93±138.19% (p=0.016). No IVL-related procedural complications or MACE were observed. The use of bailout IVL therapy directly after stenting and the presence of ostial underexpanded lesions negatively predicted lumen diameter gain. Coronary lithotripsy is safe and effective in increasing lumen and stent dimensions in underexpanded stents secondary to heavily calcified lesions.

Sections du résumé

BACKGROUND BACKGROUND
Stent underexpansion increases the risk of cardiac adverse events. At present, there are limited options to treat refractory stent underexpansion. In this context, the intravascular lithotripsy (IVL) system might be a safe and effective strategy.
AIMS OBJECTIVE
We aimed to evaluate the safety and efficacy of IVL in addressing resistant stent underexpansion due to heavy underlying calcification.
METHODS METHODS
This was an international multicentre registry including patients receiving IVL therapy to treat stent underexpansion from December 2017 to August 2020. Angiographic and intracoronary imaging data were collected. The efficacy endpoint was device success (technical success with a final percentage diameter stenosis <50%). The safety endpoint was in-hospital major adverse cardiac events (MACE).
RESULTS RESULTS
Seventy patients were included, the mean age was 73±9.2 years and 76% were male. The median time from stent implantation to IVL therapy was 49 days (0-2,537). Adjuvant treatment with non-compliant balloon dilatations pre- and post-IVL was performed in 72.3% and 76.8% of patients, respectively, and additional stenting was performed in 22.4%. Device success was 92.3%. Minimum lumen diameter increased from 1.49±0.73 mm to 2.41±0.67 mm (p<0.001) and stent expansion increased by 124.93±138.19% (p=0.016). No IVL-related procedural complications or MACE were observed. The use of bailout IVL therapy directly after stenting and the presence of ostial underexpanded lesions negatively predicted lumen diameter gain.
CONCLUSIONS CONCLUSIONS
Coronary lithotripsy is safe and effective in increasing lumen and stent dimensions in underexpanded stents secondary to heavily calcified lesions.

Identifiants

pubmed: 35318955
pii: EIJ-D-21-00545
doi: 10.4244/EIJ-D-21-00545
pmc: PMC10241293
pii:
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

574-581

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Auteurs

Maria Natalia Tovar Forero (MN)

Erasmus University Medical Center, Rotterdam, the Netherlands.

Gennaro Sardella (G)

Policlinico Umberto I' "Sapienza" University of Rome, Rome, Italy.

Nicolò Salvi (N)

Policlinico Umberto I' "Sapienza" University of Rome, Rome, Italy.

Bernardo Cortese (B)

Cardiovascular Research Team, Clinica San Carlo, Milano, Italy and Fondazione Ricerca e Innovazione Cardiovascolare, Milano, Italy.

Gaetano di Palma (G)

Cardiovascular Research Team, Clinica San Carlo, Milano, Italy and Fondazione Ricerca e Innovazione Cardiovascolare, Milano, Italy.

Nikos Werner (N)

Heart Center, Trier, Germany.
Heart Center Bonn, University Hospital, Bonn, Germany.

Adem Aksoy (A)

Heart Center Bonn, University Hospital, Bonn, Germany.

Javier Escaned (J)

Hospital Clinico San Carlos IdISSC, Complutense University of Madrid, Madrid, Spain.

Carlos H Salazar (CH)

Hospital Clinico San Carlos IdISSC, Complutense University of Madrid, Madrid, Spain.

Nieves Gonzalo (N)

Hospital Clinico San Carlos IdISSC, Complutense University of Madrid, Madrid, Spain.

Fabrizio Ugo (F)

Sant'Andrea Hospital, Vercelli, Italy.

Chiara Cavallino (C)

Sant'Andrea Hospital, Vercelli, Italy.

Tej N Sheth (TN)

McMaster University, Hamilton, Ontario, Canada.

Isabella Kardys (I)

Erasmus University Medical Center, Rotterdam, the Netherlands.

Nicolas M Van Mieghem (NM)

Erasmus University Medical Center, Rotterdam, the Netherlands.

Joost Daemen (J)

Erasmus University Medical Center, Rotterdam, the Netherlands.

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