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Tailored eradication strategy vs concomitant therapy for Helicobacter pylori eradication treatment in Korean patients

BACKGROUND: Antibiotic resistance to Helicobacter pylori (H. pylori) infection, which ultimately results in eradication failure, has been an emerging issue in the clinical field. Recently, to overcome this problem, an antibiotic sensitivity-based tailored therapy (TT) for H. pylori infection has rec...

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Autores principales: Choi, Youn I, Chung, Jun-Won, Kim, Kyoung Oh, Kwon, Kwang An, Kim, Yoon Jae, Kim, Jung Ho, Seo, Ja Young, Park, Dong Kyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8384750/
https://www.ncbi.nlm.nih.gov/pubmed/34497448
http://dx.doi.org/10.3748/wjg.v27.i31.5247
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author Choi, Youn I
Chung, Jun-Won
Kim, Kyoung Oh
Kwon, Kwang An
Kim, Yoon Jae
Kim, Jung Ho
Seo, Ja Young
Park, Dong Kyun
author_facet Choi, Youn I
Chung, Jun-Won
Kim, Kyoung Oh
Kwon, Kwang An
Kim, Yoon Jae
Kim, Jung Ho
Seo, Ja Young
Park, Dong Kyun
author_sort Choi, Youn I
collection PubMed
description BACKGROUND: Antibiotic resistance to Helicobacter pylori (H. pylori) infection, which ultimately results in eradication failure, has been an emerging issue in the clinical field. Recently, to overcome this problem, an antibiotic sensitivity-based tailored therapy (TT) for H. pylori infection has received attention. AIM: To investigate the efficacy and safety profiles of TT for H. pylori infection treatment compared to a non-bismuth quadruple therapy, concomitant therapy (CT) regimen. METHODS: We included patients (> 18 years) with an H. pylori infection and without a history of Helicobacter eradication who visited the Gil Medical Center between March 2016 and October 2020. After being randomly assigned to either the TT or CT treatment group in 1 to 1 manner, patient compliance, eradication success rate (ESR), and patient-reported side effects profiles were assessed and compared between the two groups. H. pylori infection was diagnosed using a rapid urease test, Giemsa stain, or dual priming oligonucleotide polymerase chain reaction (DPO-PCR). Tailored eradication strategy based through the presence of a 23S ribosomal RNA point mutation. For the TT group, a DPO-PCR test, which detected A2142G and/or A2143G point mutations, and a clarithromycin resistance test were performed. Patients in the clarithromycin-resistant group were treated with a bismuth-containing quadruple combination therapy, while those with sensitive results were treated with the standard triple regimen. RESULTS: Of the 217 patients with a treatment naive H. pylori infection, 110 patients [mean age: 58.66 ± 13.03, men, n = 55 (50%)] were treated with TT, and 107 patients [mean age: 56.67 ± 10.88, men, n = 52 (48.60%)] were treated with CT. The compliance (TT vs CT, 100% vs 98.13%, P = 0.30), and follow-up loss rates (8.18% vs 9.35%, P = 0.95) were not significantly different between the groups. The ESR after treatment was also not statistically different between the groups (TT vs CT, 82.73% vs 82.24%, P = 0.95). However, the treatment-related and patient-reported side effects were significantly lower in the TT group than in the CT group (22.77% vs 50.52%, P < 0.001). CONCLUSION: The DPO-based TT regimen shows promising results in efficacy and safety profiles as a first-line Helicobacter eradication regimen in Korea, especially when physicians are confronted with increased antibiotic resistance rates.
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spelling pubmed-83847502021-09-07 Tailored eradication strategy vs concomitant therapy for Helicobacter pylori eradication treatment in Korean patients Choi, Youn I Chung, Jun-Won Kim, Kyoung Oh Kwon, Kwang An Kim, Yoon Jae Kim, Jung Ho Seo, Ja Young Park, Dong Kyun World J Gastroenterol Case Control Study BACKGROUND: Antibiotic resistance to Helicobacter pylori (H. pylori) infection, which ultimately results in eradication failure, has been an emerging issue in the clinical field. Recently, to overcome this problem, an antibiotic sensitivity-based tailored therapy (TT) for H. pylori infection has received attention. AIM: To investigate the efficacy and safety profiles of TT for H. pylori infection treatment compared to a non-bismuth quadruple therapy, concomitant therapy (CT) regimen. METHODS: We included patients (> 18 years) with an H. pylori infection and without a history of Helicobacter eradication who visited the Gil Medical Center between March 2016 and October 2020. After being randomly assigned to either the TT or CT treatment group in 1 to 1 manner, patient compliance, eradication success rate (ESR), and patient-reported side effects profiles were assessed and compared between the two groups. H. pylori infection was diagnosed using a rapid urease test, Giemsa stain, or dual priming oligonucleotide polymerase chain reaction (DPO-PCR). Tailored eradication strategy based through the presence of a 23S ribosomal RNA point mutation. For the TT group, a DPO-PCR test, which detected A2142G and/or A2143G point mutations, and a clarithromycin resistance test were performed. Patients in the clarithromycin-resistant group were treated with a bismuth-containing quadruple combination therapy, while those with sensitive results were treated with the standard triple regimen. RESULTS: Of the 217 patients with a treatment naive H. pylori infection, 110 patients [mean age: 58.66 ± 13.03, men, n = 55 (50%)] were treated with TT, and 107 patients [mean age: 56.67 ± 10.88, men, n = 52 (48.60%)] were treated with CT. The compliance (TT vs CT, 100% vs 98.13%, P = 0.30), and follow-up loss rates (8.18% vs 9.35%, P = 0.95) were not significantly different between the groups. The ESR after treatment was also not statistically different between the groups (TT vs CT, 82.73% vs 82.24%, P = 0.95). However, the treatment-related and patient-reported side effects were significantly lower in the TT group than in the CT group (22.77% vs 50.52%, P < 0.001). CONCLUSION: The DPO-based TT regimen shows promising results in efficacy and safety profiles as a first-line Helicobacter eradication regimen in Korea, especially when physicians are confronted with increased antibiotic resistance rates. Baishideng Publishing Group Inc 2021-08-21 2021-08-21 /pmc/articles/PMC8384750/ /pubmed/34497448 http://dx.doi.org/10.3748/wjg.v27.i31.5247 Text en ©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/Licenses/by-nc/4.0/
spellingShingle Case Control Study
Choi, Youn I
Chung, Jun-Won
Kim, Kyoung Oh
Kwon, Kwang An
Kim, Yoon Jae
Kim, Jung Ho
Seo, Ja Young
Park, Dong Kyun
Tailored eradication strategy vs concomitant therapy for Helicobacter pylori eradication treatment in Korean patients
title Tailored eradication strategy vs concomitant therapy for Helicobacter pylori eradication treatment in Korean patients
title_full Tailored eradication strategy vs concomitant therapy for Helicobacter pylori eradication treatment in Korean patients
title_fullStr Tailored eradication strategy vs concomitant therapy for Helicobacter pylori eradication treatment in Korean patients
title_full_unstemmed Tailored eradication strategy vs concomitant therapy for Helicobacter pylori eradication treatment in Korean patients
title_short Tailored eradication strategy vs concomitant therapy for Helicobacter pylori eradication treatment in Korean patients
title_sort tailored eradication strategy vs concomitant therapy for helicobacter pylori eradication treatment in korean patients
topic Case Control Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8384750/
https://www.ncbi.nlm.nih.gov/pubmed/34497448
http://dx.doi.org/10.3748/wjg.v27.i31.5247
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