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The Impact of Opioid Treatment on Regional Gastrointestinal Transit
BACKGROUND/AIMS: To employ an experimental model of opioid-induced bowel dysfunction in healthy human volunteers, and evaluate the impact of opioid treatment compared to placebo on gastrointestinal (GI) symptoms and motility assessed by questionnaires and regional GI transit times using the 3-dimens...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society of Neurogastroenterology and Motility
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4819867/ https://www.ncbi.nlm.nih.gov/pubmed/26811503 http://dx.doi.org/10.5056/jnm15175 |
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author | Poulsen, Jakob L Nilsson, Matias Brock, Christina Sandberg, Thomas H Krogh, Klaus Drewes, Asbjørn M |
author_facet | Poulsen, Jakob L Nilsson, Matias Brock, Christina Sandberg, Thomas H Krogh, Klaus Drewes, Asbjørn M |
author_sort | Poulsen, Jakob L |
collection | PubMed |
description | BACKGROUND/AIMS: To employ an experimental model of opioid-induced bowel dysfunction in healthy human volunteers, and evaluate the impact of opioid treatment compared to placebo on gastrointestinal (GI) symptoms and motility assessed by questionnaires and regional GI transit times using the 3-dimensional (3D)-Transit system. METHODS: Twenty-five healthy males were randomly assigned to oxycodone or placebo for 5 days in a double blind, crossover design. Adverse GI effects were measured with the bowel function index, gastrointestinal symptom rating scale, patient assessment of constipation symptom questionnaire, and Bristol stool form scale. Regional GI transit times were determined using the 3D-Transit system, and segmental transit times in the colon were determined using a custom Matlab(®) graphical user interface. RESULTS: GI symptom scores increased significantly across all applied GI questionnaires during opioid treatment. Oxycodone increased median total GI transit time from 22.2 to 43.9 hours (P < 0.001), segmental transit times in the cecum and ascending colon from 5.7 to 9.9 hours (P = 0.012), rectosigmoid colon transit from 2.7 to 9.0 hours (P = 0.044), and colorectal transit time from 18.6 to 38.6 hours (P = 0.001). No associations between questionnaire scores and segmental transit times were detected. CONCLUSIONS: Self-assessed GI adverse effects and increased GI transit times in different segments were induced during oxycodone treatment. This detailed information about segmental changes in motility has great potential for future interventional head-to-head trials of different laxative regimes for prevention and treatment of constipation. |
format | Online Article Text |
id | pubmed-4819867 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Korean Society of Neurogastroenterology and Motility |
record_format | MEDLINE/PubMed |
spelling | pubmed-48198672016-04-08 The Impact of Opioid Treatment on Regional Gastrointestinal Transit Poulsen, Jakob L Nilsson, Matias Brock, Christina Sandberg, Thomas H Krogh, Klaus Drewes, Asbjørn M J Neurogastroenterol Motil Original Article BACKGROUND/AIMS: To employ an experimental model of opioid-induced bowel dysfunction in healthy human volunteers, and evaluate the impact of opioid treatment compared to placebo on gastrointestinal (GI) symptoms and motility assessed by questionnaires and regional GI transit times using the 3-dimensional (3D)-Transit system. METHODS: Twenty-five healthy males were randomly assigned to oxycodone or placebo for 5 days in a double blind, crossover design. Adverse GI effects were measured with the bowel function index, gastrointestinal symptom rating scale, patient assessment of constipation symptom questionnaire, and Bristol stool form scale. Regional GI transit times were determined using the 3D-Transit system, and segmental transit times in the colon were determined using a custom Matlab(®) graphical user interface. RESULTS: GI symptom scores increased significantly across all applied GI questionnaires during opioid treatment. Oxycodone increased median total GI transit time from 22.2 to 43.9 hours (P < 0.001), segmental transit times in the cecum and ascending colon from 5.7 to 9.9 hours (P = 0.012), rectosigmoid colon transit from 2.7 to 9.0 hours (P = 0.044), and colorectal transit time from 18.6 to 38.6 hours (P = 0.001). No associations between questionnaire scores and segmental transit times were detected. CONCLUSIONS: Self-assessed GI adverse effects and increased GI transit times in different segments were induced during oxycodone treatment. This detailed information about segmental changes in motility has great potential for future interventional head-to-head trials of different laxative regimes for prevention and treatment of constipation. Korean Society of Neurogastroenterology and Motility 2016-04 2016-04-30 /pmc/articles/PMC4819867/ /pubmed/26811503 http://dx.doi.org/10.5056/jnm15175 Text en © 2016 The Korean Society of Neurogastroenterology and Motility This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://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 Poulsen, Jakob L Nilsson, Matias Brock, Christina Sandberg, Thomas H Krogh, Klaus Drewes, Asbjørn M The Impact of Opioid Treatment on Regional Gastrointestinal Transit |
title | The Impact of Opioid Treatment on Regional Gastrointestinal Transit |
title_full | The Impact of Opioid Treatment on Regional Gastrointestinal Transit |
title_fullStr | The Impact of Opioid Treatment on Regional Gastrointestinal Transit |
title_full_unstemmed | The Impact of Opioid Treatment on Regional Gastrointestinal Transit |
title_short | The Impact of Opioid Treatment on Regional Gastrointestinal Transit |
title_sort | impact of opioid treatment on regional gastrointestinal transit |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4819867/ https://www.ncbi.nlm.nih.gov/pubmed/26811503 http://dx.doi.org/10.5056/jnm15175 |
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