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Objective Interpretation of the Rapid Urease Test for Helicobacter pylori Infection Using Colorimetry

BACKGROUND: The rapid urease test (RUT) is a major diagnostic tool for detecting Helicobacter pylori infection. This study aimed to establish an objective method for measuring the color changes in the RUT kit to improve the test’s diagnostic accuracy. METHODS: A UV-visible spectrophotometer was sele...

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Autores principales: Pih, Gyu Young, Noh, Jin Hee, Ahn, Ji Yong, Han, Gill Sang, Jung, Hyun Suk, Jung, Hwoon-Yong, Kim, Jung Mogg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9313973/
https://www.ncbi.nlm.nih.gov/pubmed/35880503
http://dx.doi.org/10.3346/jkms.2022.37.e227
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author Pih, Gyu Young
Noh, Jin Hee
Ahn, Ji Yong
Han, Gill Sang
Jung, Hyun Suk
Jung, Hwoon-Yong
Kim, Jung Mogg
author_facet Pih, Gyu Young
Noh, Jin Hee
Ahn, Ji Yong
Han, Gill Sang
Jung, Hyun Suk
Jung, Hwoon-Yong
Kim, Jung Mogg
author_sort Pih, Gyu Young
collection PubMed
description BACKGROUND: The rapid urease test (RUT) is a major diagnostic tool for detecting Helicobacter pylori infection. This study aimed to establish an objective method for measuring the color changes in the RUT kit to improve the test’s diagnostic accuracy. METHODS: A UV-visible spectrophotometer was selected as the colorimeter; experiments were conducted in three stages to objectively identify the color changes in the RUT kit. RESULTS: First, the urea broth solution showed an identifiable color change from yellow to red as the pH increased by 0.2. The largest transmittance difference detected using the UV-visible spectrophotometer was observed at a 590-nm wavelength. Second, the commercialized RUT kit also showed a gradual color change according to the pH change detected using the UV-visible spectrophotometer. Third, 13 cases of negative RUT results with a biopsy specimen and 16 of positive RUT results were collected. The transmittance detected using the UV-visible spectrophotometer showed a clear division between the positive and negative RUT groups; the largest difference was observed at a 559-nm wavelength. The lowest transmittance in the negative RUT group was 64, while the highest in the positive RUT group was 56, at the 559-nm wavelength. The UV-visible spectrophotometry reading showed a consistency of 92.7% compared with that of manual reading. CONCLUSION: A transmittance of 60 at a 559-nm wavelength detected using UV-visible spectrophotometer can be used as a cutoff value for interpreting RUT results; this will help develop an automatic RUT kit reader with a high accuracy.
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spelling pubmed-93139732022-07-29 Objective Interpretation of the Rapid Urease Test for Helicobacter pylori Infection Using Colorimetry Pih, Gyu Young Noh, Jin Hee Ahn, Ji Yong Han, Gill Sang Jung, Hyun Suk Jung, Hwoon-Yong Kim, Jung Mogg J Korean Med Sci Original Article BACKGROUND: The rapid urease test (RUT) is a major diagnostic tool for detecting Helicobacter pylori infection. This study aimed to establish an objective method for measuring the color changes in the RUT kit to improve the test’s diagnostic accuracy. METHODS: A UV-visible spectrophotometer was selected as the colorimeter; experiments were conducted in three stages to objectively identify the color changes in the RUT kit. RESULTS: First, the urea broth solution showed an identifiable color change from yellow to red as the pH increased by 0.2. The largest transmittance difference detected using the UV-visible spectrophotometer was observed at a 590-nm wavelength. Second, the commercialized RUT kit also showed a gradual color change according to the pH change detected using the UV-visible spectrophotometer. Third, 13 cases of negative RUT results with a biopsy specimen and 16 of positive RUT results were collected. The transmittance detected using the UV-visible spectrophotometer showed a clear division between the positive and negative RUT groups; the largest difference was observed at a 559-nm wavelength. The lowest transmittance in the negative RUT group was 64, while the highest in the positive RUT group was 56, at the 559-nm wavelength. The UV-visible spectrophotometry reading showed a consistency of 92.7% compared with that of manual reading. CONCLUSION: A transmittance of 60 at a 559-nm wavelength detected using UV-visible spectrophotometer can be used as a cutoff value for interpreting RUT results; this will help develop an automatic RUT kit reader with a high accuracy. The Korean Academy of Medical Sciences 2022-07-15 /pmc/articles/PMC9313973/ /pubmed/35880503 http://dx.doi.org/10.3346/jkms.2022.37.e227 Text en © 2022 The Korean Academy of Medical Sciences. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Pih, Gyu Young
Noh, Jin Hee
Ahn, Ji Yong
Han, Gill Sang
Jung, Hyun Suk
Jung, Hwoon-Yong
Kim, Jung Mogg
Objective Interpretation of the Rapid Urease Test for Helicobacter pylori Infection Using Colorimetry
title Objective Interpretation of the Rapid Urease Test for Helicobacter pylori Infection Using Colorimetry
title_full Objective Interpretation of the Rapid Urease Test for Helicobacter pylori Infection Using Colorimetry
title_fullStr Objective Interpretation of the Rapid Urease Test for Helicobacter pylori Infection Using Colorimetry
title_full_unstemmed Objective Interpretation of the Rapid Urease Test for Helicobacter pylori Infection Using Colorimetry
title_short Objective Interpretation of the Rapid Urease Test for Helicobacter pylori Infection Using Colorimetry
title_sort objective interpretation of the rapid urease test for helicobacter pylori infection using colorimetry
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9313973/
https://www.ncbi.nlm.nih.gov/pubmed/35880503
http://dx.doi.org/10.3346/jkms.2022.37.e227
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