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The Null technique as a novel, potential first-line method of device delivery for complicated lesions during percutaneous coronary intervention

AIM: During percutaneous coronary intervention (PCI), complicated lesions in the target coronary artery often hinder device delivery. Fluid lubricants have commonly been used to reduce friction between adjacent solid materials in manufacturing, thus achieving smoother action. This ex vivo experiment...

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Detalles Bibliográficos
Autores principales: Akima, Takashi, Sakurai, Yasuo, Nakajima, Kazuaki, Koyama, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10422662/
https://www.ncbi.nlm.nih.gov/pubmed/37576084
http://dx.doi.org/10.1016/j.ijcha.2023.101241
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author Akima, Takashi
Sakurai, Yasuo
Nakajima, Kazuaki
Koyama, Takashi
author_facet Akima, Takashi
Sakurai, Yasuo
Nakajima, Kazuaki
Koyama, Takashi
author_sort Akima, Takashi
collection PubMed
description AIM: During percutaneous coronary intervention (PCI), complicated lesions in the target coronary artery often hinder device delivery. Fluid lubricants have commonly been used to reduce friction between adjacent solid materials in manufacturing, thus achieving smoother action. This ex vivo experimental study examined whether a contrast medium could function as a fluid lubricant during PCI. METHODS AND RESULTS: We used two different coronary artery lesion models with distinct complexities made from silicon. Each model was fit into the ex vivo PCI-simulation system. This ex vivo laboratory equipment consisted of ordinary PCI instruments and an aorta model from the Valsalva sinus to the descending aorta. A Wolverine™ cutting balloon catheter was advanced through each lesion model via a guide catheter set into the system. The maximum force required to push the catheter through the lesion models was measured while the vessel system was filled with either normal saline or contrast medium. The maximum force required was significantly lower with the contrast medium (1.38 ± 0.21 N in the normal-saline condition vs. 0.92 ± 0.05 N in the contrast-medium condition in the lesion model A, p < 0.001; 1.30 ± 0.07 N in the normal-saline condition vs. 1.14 ± 0.04 N in the contrast-medium condition in the lesion model B, p < 0.001). CONCLUSIONS: The contrast medium for vessel system filling reduced the force required to push the devices through the lesion models. This contrast medium represents a potential candidate for a liquid lubricant to facilitate device delivery for complicated coronary lesions.
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spelling pubmed-104226622023-08-13 The Null technique as a novel, potential first-line method of device delivery for complicated lesions during percutaneous coronary intervention Akima, Takashi Sakurai, Yasuo Nakajima, Kazuaki Koyama, Takashi Int J Cardiol Heart Vasc Original Paper AIM: During percutaneous coronary intervention (PCI), complicated lesions in the target coronary artery often hinder device delivery. Fluid lubricants have commonly been used to reduce friction between adjacent solid materials in manufacturing, thus achieving smoother action. This ex vivo experimental study examined whether a contrast medium could function as a fluid lubricant during PCI. METHODS AND RESULTS: We used two different coronary artery lesion models with distinct complexities made from silicon. Each model was fit into the ex vivo PCI-simulation system. This ex vivo laboratory equipment consisted of ordinary PCI instruments and an aorta model from the Valsalva sinus to the descending aorta. A Wolverine™ cutting balloon catheter was advanced through each lesion model via a guide catheter set into the system. The maximum force required to push the catheter through the lesion models was measured while the vessel system was filled with either normal saline or contrast medium. The maximum force required was significantly lower with the contrast medium (1.38 ± 0.21 N in the normal-saline condition vs. 0.92 ± 0.05 N in the contrast-medium condition in the lesion model A, p < 0.001; 1.30 ± 0.07 N in the normal-saline condition vs. 1.14 ± 0.04 N in the contrast-medium condition in the lesion model B, p < 0.001). CONCLUSIONS: The contrast medium for vessel system filling reduced the force required to push the devices through the lesion models. This contrast medium represents a potential candidate for a liquid lubricant to facilitate device delivery for complicated coronary lesions. Elsevier 2023-07-08 /pmc/articles/PMC10422662/ /pubmed/37576084 http://dx.doi.org/10.1016/j.ijcha.2023.101241 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Paper
Akima, Takashi
Sakurai, Yasuo
Nakajima, Kazuaki
Koyama, Takashi
The Null technique as a novel, potential first-line method of device delivery for complicated lesions during percutaneous coronary intervention
title The Null technique as a novel, potential first-line method of device delivery for complicated lesions during percutaneous coronary intervention
title_full The Null technique as a novel, potential first-line method of device delivery for complicated lesions during percutaneous coronary intervention
title_fullStr The Null technique as a novel, potential first-line method of device delivery for complicated lesions during percutaneous coronary intervention
title_full_unstemmed The Null technique as a novel, potential first-line method of device delivery for complicated lesions during percutaneous coronary intervention
title_short The Null technique as a novel, potential first-line method of device delivery for complicated lesions during percutaneous coronary intervention
title_sort null technique as a novel, potential first-line method of device delivery for complicated lesions during percutaneous coronary intervention
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10422662/
https://www.ncbi.nlm.nih.gov/pubmed/37576084
http://dx.doi.org/10.1016/j.ijcha.2023.101241
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