Combination Therapy With Nicardipine and Isosorbide Dinitrate to Prevent Spasm in Transradial Percutaneous Coronary Intervention (from the NISTRA Multicenter Double-Blind Randomized Controlled Trial).


Journal

The American journal of cardiology
ISSN: 1879-1913
Titre abrégé: Am J Cardiol
Pays: United States
ID NLM: 0207277

Informations de publication

Date de publication:
01 02 2023
Historique:
received: 10 08 2022
revised: 27 09 2022
accepted: 08 11 2022
pubmed: 9 12 2022
medline: 28 12 2022
entrez: 8 12 2022
Statut: ppublish

Résumé

Verapamil and nitroglycerin are widely used to prevent radial artery spasm (RAS) during percutaneous cardiovascular procedures. However, these agents are not typically available in most African countries and consequently, isosorbide dinitrate is often the only spasmolytic treatment. Our aim was to compare the efficacy of isosorbide dinitrate alone versus isosorbide dinitrate used together with nicardipine to prevent RAS during transradial coronary procedures. This was a randomized controlled double-blind multicenter trial. Patients (n = 1,523) were randomized to receive either a sole therapy of isosorbide dinitrate (n = 760) or the combination of isosorbide dinitrate and nicardipine (n = 763). Our primary end point was the occurrence of RAS; defined as considerable perceived hindrance of catheter advancement. Our secondary end points were severe RAS; defined as (1) severe arm pain, (2) the need for either morphine or midazolam treatment, and (3) necessity for crossover to the contralateral radial or femoral artery. RAS incidence was reduced with the combination therapy versus isosorbide dinitrate alone (15% vs 25%, p <0.001), with a number needed to treat of 10 patients. There was also a significant reduction in the incidence of the secondary end points with combination therapy (3.6% vs 8.2%, p <0.001), with a number needed to treat of 22 patients. This result was driven by reductions in both femoral crossover (0.5% vs 2.4%, p = 0.003) and the use of morphine or midazolam injections (1.6% vs 3.5%, p = 0.02) with combination therapy. In conclusion, we demonstrated the superiority of the combination therapy of isosorbide dinitrate and nicardipine over isosorbide dinitrate alone in reducing the incidence of RAS.

Identifiants

pubmed: 36481522
pii: S0002-9149(22)01193-6
doi: 10.1016/j.amjcard.2022.11.005
pii:
doi:

Substances chimiques

Isosorbide Dinitrate IA7306519N
Nicardipine CZ5312222S
Midazolam R60L0SM5BC
Morphine Derivatives 0

Types de publication

Randomized Controlled Trial Multicenter Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

89-94

Informations de copyright

Copyright © 2022 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Disclosures The authors have no conflicts of interest to declare.

Auteurs

Nidhal Bouchahda (N)

Cardiology A Department, University of Monastir, Research Laboratory LR12 SP 16, Fattouma Bourguiba University Hospital, Rue du 1er juin, Monastir, Tunisia. Electronic address: nidhalbouchahda@gmail.com.

Mohamed Aymen Ben Abdessalem (MA)

Cardiology Department, Université de Sousse, Laboratoire de Recherche: interactions cardiopulmonaires LR14ES05, Farhat Hached University Hospital, Tunisia.

Najeh Ben Hlima (N)

Cardiology Department,Université de Sousse, Kairouen Ibn el Jazzar University Hospital, Tunisia.

Mejdi Ben Messaoud (M)

Cardiology A Department, University of Monastir, Research Laboratory LR12 SP 16, Fattouma Bourguiba University Hospital, Rue du 1er juin, Monastir, Tunisia.

Hichem Denguir (H)

Cardiology Department, University of Monastir, Gabes University Hospital, Tunisia.

Mohamed Mehdi Boussaada (MM)

Cardiology A Department, University of Monastir, Research Laboratory LR12 SP 16, Fattouma Bourguiba University Hospital, Rue du 1er juin, Monastir, Tunisia.

Wassim Saoudi (W)

Cardiology Department, Université de Sousse, Laboratoire de Recherche: interactions cardiopulmonaires LR14ES05, Farhat Hached University Hospital, Tunisia.

Ahmed Jamel (A)

Cardiology Department,Université de Sousse, Kairouen Ibn el Jazzar University Hospital, Tunisia.

Majed Hassine (M)

Cardiology A Department, University of Monastir, Research Laboratory LR12 SP 16, Fattouma Bourguiba University Hospital, Rue du 1er juin, Monastir, Tunisia.

Hatem Bouraoui (H)

Cardiology Department, Université de Sousse, Laboratoire de Recherche: interactions cardiopulmonaires LR14ES05, Farhat Hached University Hospital, Tunisia.

Marwen Mahjoub (M)

Cardiology A Department, University of Monastir, Research Laboratory LR12 SP 16, Fattouma Bourguiba University Hospital, Rue du 1er juin, Monastir, Tunisia.

Abdallah Mahdhaoui (A)

Cardiology Department, Université de Sousse, Laboratoire de Recherche: interactions cardiopulmonaires LR14ES05, Farhat Hached University Hospital, Tunisia.

Gouider Jeridi (G)

Cardiology Department, Université de Sousse, Laboratoire de Recherche: interactions cardiopulmonaires LR14ES05, Farhat Hached University Hospital, Tunisia.

Fethi Betbout (F)

Cardiology A Department, University of Monastir, Research Laboratory LR12 SP 16, Fattouma Bourguiba University Hospital, Rue du 1er juin, Monastir, Tunisia.

Habib Gamra (H)

Cardiology A Department, University of Monastir, Research Laboratory LR12 SP 16, Fattouma Bourguiba University Hospital, Rue du 1er juin, Monastir, Tunisia.

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Classifications MeSH