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The Use of Oral Herbal Medicine (Hange-Shashin-To) in Patients with Pouchitis: A Pilot Study

Objectives: Hange-Shashin-To (HST), which is a combination of seven herbs, has previously been used in the treatment of inflammatory or ulcerative gut disease. The aim of this study was to evaluate the safety and efficacy of HST for the treatment of chronic pouchitis. Methods: Nineteen patients with...

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Autores principales: Matsuoka, Hiroki, Uchino, Motoi, Horio, Yuki, Sasaki, Hirofumi, Chohno, Teruhiro, Hirata, Akihiro, Bando, Toshihiro, Ito, Takashi, Yamaguchi, Toshimasa, Ikeuchi, Hiroki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japan Society of Coloproctology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6768822/
https://www.ncbi.nlm.nih.gov/pubmed/31583317
http://dx.doi.org/10.23922/jarc.2017-015
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author Matsuoka, Hiroki
Uchino, Motoi
Horio, Yuki
Sasaki, Hirofumi
Chohno, Teruhiro
Hirata, Akihiro
Bando, Toshihiro
Ito, Takashi
Yamaguchi, Toshimasa
Ikeuchi, Hiroki
author_facet Matsuoka, Hiroki
Uchino, Motoi
Horio, Yuki
Sasaki, Hirofumi
Chohno, Teruhiro
Hirata, Akihiro
Bando, Toshihiro
Ito, Takashi
Yamaguchi, Toshimasa
Ikeuchi, Hiroki
author_sort Matsuoka, Hiroki
collection PubMed
description Objectives: Hange-Shashin-To (HST), which is a combination of seven herbs, has previously been used in the treatment of inflammatory or ulcerative gut disease. The aim of this study was to evaluate the safety and efficacy of HST for the treatment of chronic pouchitis. Methods: Nineteen patients with chronic pouchitis, defined as either frequent episodes (≥ three episodes per six months) of pouchitis or persistent symptoms that required continuous antibiotic therapies, were selected and treated with ciprofloxacin (CPFX) 600 mg/day for 2 weeks (week 0~2) and HST 3,750 mg/day for 32 weeks (week 0~32). The Pouchitis Disease Activity Index (PDAI) score was measured at week 0 and 6 for short-term evaluation. For long-term evaluation, total CPFX dose in the 26-week period prior to study entry (from 30 weeks before study entry to 5 weeks before study entry) was compared with the total CPFX dose during the 26-week study period (week 7~32). Although no concomitant administration of CPFX was permitted from week 2-6, patients whose condition deteriorated were prescribed CPFX from week 7 to week 32. Results: Fourteen patients completed this 32-week study. The PDAI scores of eight patients decreased below seven. The mean total PDAI scores decreased significantly from 11 ± 2.5 to 6.5 ± 2.5 (P < 0.001). The mean value of total CPFX dose decreased significantly from 491.6 ± 182.4 mg/kg to 392.5 ± 184.0 mg/kg (P < 0.05). No severe adverse events were noted. Conclusions: Our data suggest that HST has a positive effect on chronic pouchitis with no adverse effects.
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spelling pubmed-67688222019-10-03 The Use of Oral Herbal Medicine (Hange-Shashin-To) in Patients with Pouchitis: A Pilot Study Matsuoka, Hiroki Uchino, Motoi Horio, Yuki Sasaki, Hirofumi Chohno, Teruhiro Hirata, Akihiro Bando, Toshihiro Ito, Takashi Yamaguchi, Toshimasa Ikeuchi, Hiroki J Anus Rectum Colon Original Research Article Objectives: Hange-Shashin-To (HST), which is a combination of seven herbs, has previously been used in the treatment of inflammatory or ulcerative gut disease. The aim of this study was to evaluate the safety and efficacy of HST for the treatment of chronic pouchitis. Methods: Nineteen patients with chronic pouchitis, defined as either frequent episodes (≥ three episodes per six months) of pouchitis or persistent symptoms that required continuous antibiotic therapies, were selected and treated with ciprofloxacin (CPFX) 600 mg/day for 2 weeks (week 0~2) and HST 3,750 mg/day for 32 weeks (week 0~32). The Pouchitis Disease Activity Index (PDAI) score was measured at week 0 and 6 for short-term evaluation. For long-term evaluation, total CPFX dose in the 26-week period prior to study entry (from 30 weeks before study entry to 5 weeks before study entry) was compared with the total CPFX dose during the 26-week study period (week 7~32). Although no concomitant administration of CPFX was permitted from week 2-6, patients whose condition deteriorated were prescribed CPFX from week 7 to week 32. Results: Fourteen patients completed this 32-week study. The PDAI scores of eight patients decreased below seven. The mean total PDAI scores decreased significantly from 11 ± 2.5 to 6.5 ± 2.5 (P < 0.001). The mean value of total CPFX dose decreased significantly from 491.6 ± 182.4 mg/kg to 392.5 ± 184.0 mg/kg (P < 0.05). No severe adverse events were noted. Conclusions: Our data suggest that HST has a positive effect on chronic pouchitis with no adverse effects. The Japan Society of Coloproctology 2018-03-09 /pmc/articles/PMC6768822/ /pubmed/31583317 http://dx.doi.org/10.23922/jarc.2017-015 Text en Copyright © 2018 by The Japan Society of Coloproctology https://creativecommons.org/licenses/by-nc-nd/4.0/ Journal of the Anus, Rectum and Colon is an Open Access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research Article
Matsuoka, Hiroki
Uchino, Motoi
Horio, Yuki
Sasaki, Hirofumi
Chohno, Teruhiro
Hirata, Akihiro
Bando, Toshihiro
Ito, Takashi
Yamaguchi, Toshimasa
Ikeuchi, Hiroki
The Use of Oral Herbal Medicine (Hange-Shashin-To) in Patients with Pouchitis: A Pilot Study
title The Use of Oral Herbal Medicine (Hange-Shashin-To) in Patients with Pouchitis: A Pilot Study
title_full The Use of Oral Herbal Medicine (Hange-Shashin-To) in Patients with Pouchitis: A Pilot Study
title_fullStr The Use of Oral Herbal Medicine (Hange-Shashin-To) in Patients with Pouchitis: A Pilot Study
title_full_unstemmed The Use of Oral Herbal Medicine (Hange-Shashin-To) in Patients with Pouchitis: A Pilot Study
title_short The Use of Oral Herbal Medicine (Hange-Shashin-To) in Patients with Pouchitis: A Pilot Study
title_sort use of oral herbal medicine (hange-shashin-to) in patients with pouchitis: a pilot study
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6768822/
https://www.ncbi.nlm.nih.gov/pubmed/31583317
http://dx.doi.org/10.23922/jarc.2017-015
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