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Design of an Impedance-Controlled Hot Snare Polypectomy Device

This paper goes through the process of first designing a feedback system that allows for the measuring of impedance while using the hot snare polypectomy method. The electrosurgical unit used in this study was the Olympus PSD-30. After the impedance-controlled feedback system was completed, the devi...

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Detalles Bibliográficos
Autores principales: Thornton, CurtisLee, Choi, JungHun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6982696/
https://www.ncbi.nlm.nih.gov/pubmed/31878285
http://dx.doi.org/10.3390/s20010142
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author Thornton, CurtisLee
Choi, JungHun
author_facet Thornton, CurtisLee
Choi, JungHun
author_sort Thornton, CurtisLee
collection PubMed
description This paper goes through the process of first designing a feedback system that allows for the measuring of impedance while using the hot snare polypectomy method. The electrosurgical unit used in this study was the Olympus PSD-30. After the impedance-controlled feedback system was completed, the device was tested under a range of power settings from 10 W–50 W. The test was performed ex vivo using porcine colon samples. Using the information gathered from these tests, a technique of determining the threshold of perforation and implementing a system to automatically stop the applied current from the PSD-30 was developed. The data showed that after an increase in impedance of 25% from that of the initially measured impedance, perforation ensued in the tissue samples. Using this information, the device was programmed to interrupt the PSD-30 at this threshold point. This final design was tested and proved able to automatically prevent the event of perforation from occurring, resulting in the ability to prevent serious complications.
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spelling pubmed-69826962020-02-28 Design of an Impedance-Controlled Hot Snare Polypectomy Device Thornton, CurtisLee Choi, JungHun Sensors (Basel) Concept Paper This paper goes through the process of first designing a feedback system that allows for the measuring of impedance while using the hot snare polypectomy method. The electrosurgical unit used in this study was the Olympus PSD-30. After the impedance-controlled feedback system was completed, the device was tested under a range of power settings from 10 W–50 W. The test was performed ex vivo using porcine colon samples. Using the information gathered from these tests, a technique of determining the threshold of perforation and implementing a system to automatically stop the applied current from the PSD-30 was developed. The data showed that after an increase in impedance of 25% from that of the initially measured impedance, perforation ensued in the tissue samples. Using this information, the device was programmed to interrupt the PSD-30 at this threshold point. This final design was tested and proved able to automatically prevent the event of perforation from occurring, resulting in the ability to prevent serious complications. MDPI 2019-12-24 /pmc/articles/PMC6982696/ /pubmed/31878285 http://dx.doi.org/10.3390/s20010142 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Concept Paper
Thornton, CurtisLee
Choi, JungHun
Design of an Impedance-Controlled Hot Snare Polypectomy Device
title Design of an Impedance-Controlled Hot Snare Polypectomy Device
title_full Design of an Impedance-Controlled Hot Snare Polypectomy Device
title_fullStr Design of an Impedance-Controlled Hot Snare Polypectomy Device
title_full_unstemmed Design of an Impedance-Controlled Hot Snare Polypectomy Device
title_short Design of an Impedance-Controlled Hot Snare Polypectomy Device
title_sort design of an impedance-controlled hot snare polypectomy device
topic Concept Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6982696/
https://www.ncbi.nlm.nih.gov/pubmed/31878285
http://dx.doi.org/10.3390/s20010142
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