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Global patterns of prescription pain medication usage in disorders of gut–brain interactions

BACKGROUND: Forty percent of individuals globally meet Rome IV criteria for a disorder of gut–brain interaction (DGBI). The global burden of pain across these disorders has not been characterized. METHODS: Our study included 54,127 respondents from the 26 Internet survey countries. Prescription pain...

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Autores principales: Luo, Yuying, Camey, Suzi A., Bangdiwala, Shrikant I., Palsson, Olafur S., Sperber, Ami D., Keefer, Laurie A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10078418/
https://www.ncbi.nlm.nih.gov/pubmed/36111642
http://dx.doi.org/10.1111/nmo.14457
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author Luo, Yuying
Camey, Suzi A.
Bangdiwala, Shrikant I.
Palsson, Olafur S.
Sperber, Ami D.
Keefer, Laurie A.
author_facet Luo, Yuying
Camey, Suzi A.
Bangdiwala, Shrikant I.
Palsson, Olafur S.
Sperber, Ami D.
Keefer, Laurie A.
author_sort Luo, Yuying
collection PubMed
description BACKGROUND: Forty percent of individuals globally meet Rome IV criteria for a disorder of gut–brain interaction (DGBI). The global burden of pain across these disorders has not been characterized. METHODS: Our study included 54,127 respondents from the 26 Internet survey countries. Prescription pain medication usage was selected as the proxy for pain. The associations between prescription pain medications and the environmental, sociodemographic, psychosocial, and DGBI diagnosis variables were investigated using the multivariate generalized robust Poisson regression model. KEY RESULTS: Respondents with DGBI used prescription pain medications at higher rates than those without a DGBI diagnosis with pooled prevalence rate of 14.8% (95% confidence interval [CI], 14.4–15.3%), varying by country from 6.8% to 25.7%. The pooled prevalence ratio of prescription pain medication usage in respondents with and without DGBI was 2.2 (95% CI: 2.1–2.4). Factors associated with higher prevalence of pain medication usage among respondents with a DGBI diagnosis included living in a small community, increased anxiety, depression or somatization, increased stress concern or embarrassment about bowel functioning and having more than one anatomic DGBI diagnosis. CONCLUSION: 14.8% of patients globally with at least one diagnosis of DGBI were on prescription pain medications with wide geographic variation, about twice as many as their counterparts without a diagnosis of DGBI. Environmental, sociodemographic, and individual factors may influence clinicians to consider personalized, multimodal approaches to address pain in patients with DGBI.
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spelling pubmed-100784182023-04-07 Global patterns of prescription pain medication usage in disorders of gut–brain interactions Luo, Yuying Camey, Suzi A. Bangdiwala, Shrikant I. Palsson, Olafur S. Sperber, Ami D. Keefer, Laurie A. Neurogastroenterol Motil Original Articles BACKGROUND: Forty percent of individuals globally meet Rome IV criteria for a disorder of gut–brain interaction (DGBI). The global burden of pain across these disorders has not been characterized. METHODS: Our study included 54,127 respondents from the 26 Internet survey countries. Prescription pain medication usage was selected as the proxy for pain. The associations between prescription pain medications and the environmental, sociodemographic, psychosocial, and DGBI diagnosis variables were investigated using the multivariate generalized robust Poisson regression model. KEY RESULTS: Respondents with DGBI used prescription pain medications at higher rates than those without a DGBI diagnosis with pooled prevalence rate of 14.8% (95% confidence interval [CI], 14.4–15.3%), varying by country from 6.8% to 25.7%. The pooled prevalence ratio of prescription pain medication usage in respondents with and without DGBI was 2.2 (95% CI: 2.1–2.4). Factors associated with higher prevalence of pain medication usage among respondents with a DGBI diagnosis included living in a small community, increased anxiety, depression or somatization, increased stress concern or embarrassment about bowel functioning and having more than one anatomic DGBI diagnosis. CONCLUSION: 14.8% of patients globally with at least one diagnosis of DGBI were on prescription pain medications with wide geographic variation, about twice as many as their counterparts without a diagnosis of DGBI. Environmental, sociodemographic, and individual factors may influence clinicians to consider personalized, multimodal approaches to address pain in patients with DGBI. John Wiley and Sons Inc. 2022-09-16 2023-01 /pmc/articles/PMC10078418/ /pubmed/36111642 http://dx.doi.org/10.1111/nmo.14457 Text en © 2022 The Authors. Neurogastroenterology & Motility published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Luo, Yuying
Camey, Suzi A.
Bangdiwala, Shrikant I.
Palsson, Olafur S.
Sperber, Ami D.
Keefer, Laurie A.
Global patterns of prescription pain medication usage in disorders of gut–brain interactions
title Global patterns of prescription pain medication usage in disorders of gut–brain interactions
title_full Global patterns of prescription pain medication usage in disorders of gut–brain interactions
title_fullStr Global patterns of prescription pain medication usage in disorders of gut–brain interactions
title_full_unstemmed Global patterns of prescription pain medication usage in disorders of gut–brain interactions
title_short Global patterns of prescription pain medication usage in disorders of gut–brain interactions
title_sort global patterns of prescription pain medication usage in disorders of gut–brain interactions
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10078418/
https://www.ncbi.nlm.nih.gov/pubmed/36111642
http://dx.doi.org/10.1111/nmo.14457
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