Feasibility of intracoronary nicorandil for inducing hyperemia on fractional flow reserve measurement: Comparison with intracoronary papaverine.


Journal

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

Informations de publication

Date de publication:
01 09 2020
Historique:
received: 18 01 2020
revised: 22 03 2020
accepted: 04 05 2020
pubmed: 11 5 2020
medline: 15 5 2021
entrez: 11 5 2020
Statut: ppublish

Résumé

Adenosine and adenosine triphosphate (ATP) are widely used to induce hyperemia for fractional flow reserve (FFR) measurements. Caffeine attenuates their hyperemic effects, but not those of nicorandil and papaverine. No studies have systematically compared the hyperemic efficacies of nicorandil, papaverine, and ATP with and without caffeine abstention. FFRs were measured using nicorandil 2 mg (FFR In group 1, FFR Nicorandil 2 mg is a safe and practical alternative for patients who consume caffeine-containing products before the test or have contraindications for adenosine/ATP. Increasing the nicorandil dose to 4 mg or administering adjunctive nicorandil during ATP infusions does not offer any clinical advantages compared with administering nicorandil 2 mg alone.

Sections du résumé

BACKGROUND
Adenosine and adenosine triphosphate (ATP) are widely used to induce hyperemia for fractional flow reserve (FFR) measurements. Caffeine attenuates their hyperemic effects, but not those of nicorandil and papaverine. No studies have systematically compared the hyperemic efficacies of nicorandil, papaverine, and ATP with and without caffeine abstention.
METHODS
FFRs were measured using nicorandil 2 mg (FFR
RESULTS
In group 1, FFR
CONCLUSIONS
Nicorandil 2 mg is a safe and practical alternative for patients who consume caffeine-containing products before the test or have contraindications for adenosine/ATP. Increasing the nicorandil dose to 4 mg or administering adjunctive nicorandil during ATP infusions does not offer any clinical advantages compared with administering nicorandil 2 mg alone.

Identifiants

pubmed: 32387252
pii: S0167-5273(20)30097-8
doi: 10.1016/j.ijcard.2020.05.013
pii:
doi:

Substances chimiques

Vasodilator Agents 0
Nicorandil 260456HAM0
Papaverine DAA13NKG2Q

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-6

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors have no conflicts of interest to declare.

Auteurs

Hidenari Matsumoto (H)

Division of Cardiology, Showa University School of Medicine, Tokyo, Japan. Electronic address: matsumoto.hidenari@med.showa-u.ac.jp.

Mikiko Mikuri (M)

Department of Cardiology, Kyojinkai Komatsu Hospital, Neyagawa, Japan.

Ryota Masaki (R)

Division of Cardiology, Showa University School of Medicine, Tokyo, Japan.

Hideaki Tanaka (H)

Division of Cardiology, Showa University School of Medicine, Tokyo, Japan.

Kunihiro Ogura (K)

Division of Cardiology, Showa University School of Medicine, Tokyo, Japan.

Taitou Arai (T)

Division of Cardiology, Showa University School of Medicine, Tokyo, Japan.

Rikuo Sakai (R)

Division of Cardiology, Showa University School of Medicine, Tokyo, Japan.

Yosuke Oishi (Y)

Division of Cardiology, Showa University School of Medicine, Tokyo, Japan.

Natsumi Okada (N)

Department of Hospital Pharmaceutics, Showa University School of Pharmacy, Tokyo, Japan.

Toshiro Shinke (T)

Division of Cardiology, Showa University School of Medicine, Tokyo, Japan.

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Classifications MeSH