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Prevalence of methotrexate intolerance in rheumatoid arthritis and psoriatic arthritis

INTRODUCTION: The aim of this study was to determine the prevalence of gastrointestinal and behavioural symptoms occurring before (anticipatory/associative) and after methotrexate (MTX) administration, termed MTX intolerance, in rheumatoid (RA) and psoriatic arthritis (PsA). METHODS: Methotrexate In...

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Autores principales: Bulatović Ćalasan, Maja, van den Bosch, Oscar FC, Creemers, Marjonne CW, Custers, Martijn, Heurkens, Antonius HM, van Woerkom, Jan Maarten, Wulffraat, Nico M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3978699/
https://www.ncbi.nlm.nih.gov/pubmed/24345416
http://dx.doi.org/10.1186/ar4413
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author Bulatović Ćalasan, Maja
van den Bosch, Oscar FC
Creemers, Marjonne CW
Custers, Martijn
Heurkens, Antonius HM
van Woerkom, Jan Maarten
Wulffraat, Nico M
author_facet Bulatović Ćalasan, Maja
van den Bosch, Oscar FC
Creemers, Marjonne CW
Custers, Martijn
Heurkens, Antonius HM
van Woerkom, Jan Maarten
Wulffraat, Nico M
author_sort Bulatović Ćalasan, Maja
collection PubMed
description INTRODUCTION: The aim of this study was to determine the prevalence of gastrointestinal and behavioural symptoms occurring before (anticipatory/associative) and after methotrexate (MTX) administration, termed MTX intolerance, in rheumatoid (RA) and psoriatic arthritis (PsA). METHODS: Methotrexate Intolerance Severity Score (MISS), previously validated in juvenile idiopathic arthritis patients, was used to determine MTX intolerance prevalence in 291 RA/PsA patients. The MISS consisted of four domains: abdominal pain, nausea, vomiting and behavioural symptoms, occurring upon, prior to (anticipatory) and when thinking of MTX (associative). MTX intolerance was defined as ≥6 on the MISS with ≥1 point on anticipatory and/or associative and/or behavioural items. RESULTS: A total of 123 patients (42.3%) experienced at least one gastrointestinal adverse effect. The prevalence of MTX intolerance was 11%. MTX intolerance prevalence was higher in patients on parenteral (20.6%) than on oral MTX (6.2%) (p < 0.001). CONCLUSION: Besides well-known gastrointestinal symptoms after MTX, RA and PsA patients experienced these symptoms also before MTX intake. RA and PsA patients on MTX should be closely monitored with the MISS for early detection of MTX intolerance, in order to intervene timely and avoid discontinuation of an effective treatment.
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spelling pubmed-39786992014-04-09 Prevalence of methotrexate intolerance in rheumatoid arthritis and psoriatic arthritis Bulatović Ćalasan, Maja van den Bosch, Oscar FC Creemers, Marjonne CW Custers, Martijn Heurkens, Antonius HM van Woerkom, Jan Maarten Wulffraat, Nico M Arthritis Res Ther Research Article INTRODUCTION: The aim of this study was to determine the prevalence of gastrointestinal and behavioural symptoms occurring before (anticipatory/associative) and after methotrexate (MTX) administration, termed MTX intolerance, in rheumatoid (RA) and psoriatic arthritis (PsA). METHODS: Methotrexate Intolerance Severity Score (MISS), previously validated in juvenile idiopathic arthritis patients, was used to determine MTX intolerance prevalence in 291 RA/PsA patients. The MISS consisted of four domains: abdominal pain, nausea, vomiting and behavioural symptoms, occurring upon, prior to (anticipatory) and when thinking of MTX (associative). MTX intolerance was defined as ≥6 on the MISS with ≥1 point on anticipatory and/or associative and/or behavioural items. RESULTS: A total of 123 patients (42.3%) experienced at least one gastrointestinal adverse effect. The prevalence of MTX intolerance was 11%. MTX intolerance prevalence was higher in patients on parenteral (20.6%) than on oral MTX (6.2%) (p < 0.001). CONCLUSION: Besides well-known gastrointestinal symptoms after MTX, RA and PsA patients experienced these symptoms also before MTX intake. RA and PsA patients on MTX should be closely monitored with the MISS for early detection of MTX intolerance, in order to intervene timely and avoid discontinuation of an effective treatment. BioMed Central 2013 2013-12-18 /pmc/articles/PMC3978699/ /pubmed/24345416 http://dx.doi.org/10.1186/ar4413 Text en Copyright © 2013 Bulatović Ćalasan et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Bulatović Ćalasan, Maja
van den Bosch, Oscar FC
Creemers, Marjonne CW
Custers, Martijn
Heurkens, Antonius HM
van Woerkom, Jan Maarten
Wulffraat, Nico M
Prevalence of methotrexate intolerance in rheumatoid arthritis and psoriatic arthritis
title Prevalence of methotrexate intolerance in rheumatoid arthritis and psoriatic arthritis
title_full Prevalence of methotrexate intolerance in rheumatoid arthritis and psoriatic arthritis
title_fullStr Prevalence of methotrexate intolerance in rheumatoid arthritis and psoriatic arthritis
title_full_unstemmed Prevalence of methotrexate intolerance in rheumatoid arthritis and psoriatic arthritis
title_short Prevalence of methotrexate intolerance in rheumatoid arthritis and psoriatic arthritis
title_sort prevalence of methotrexate intolerance in rheumatoid arthritis and psoriatic arthritis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3978699/
https://www.ncbi.nlm.nih.gov/pubmed/24345416
http://dx.doi.org/10.1186/ar4413
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