Publication:
The time course of gastric methotrexate intolerance in patients with rheumatoid arthritis and psoriatic arthritis

dc.contributor.buuauthorDalkılıç, Ediz
dc.contributor.buuauthorŞahbazlar, Mustafa
dc.contributor.buuauthorGüllülü, Mustafa
dc.contributor.buuauthorYavuz, Mahmut
dc.contributor.buuauthorDilek, Kamil
dc.contributor.buuauthorErsoy, Alparslan
dc.contributor.buuauthorÖzkaya, Güven
dc.contributor.buuauthorYurtkuran, Mustafa Abbas
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentİç Hastalıkları Ana Bilim Dalı
dc.contributor.orcid0000-0002-0710-0923
dc.contributor.orcid0000-0003-0297-846X
dc.contributor.researcheridAAH-5054-2021
dc.contributor.researcheridA-4421-2016
dc.contributor.scopusid6506739457
dc.contributor.scopusid55260646400
dc.contributor.scopusid6602684544
dc.contributor.scopusid7006244754
dc.contributor.scopusid56005080200
dc.contributor.scopusid16316866500
dc.contributor.scopusid35612977100
dc.contributor.scopusid7003389525
dc.date.accessioned2022-08-11T05:49:01Z
dc.date.available2022-08-11T05:49:01Z
dc.date.issued2013-05
dc.description.abstractThis study aimed to evaluate the incidence and the time course of methotrexate (MTX)-associated gastric intolerance in patients with rheumatoid arthritis and psoriatic arthritis. Four hundred twenty subjects undergoing MTX treatment for rheumatoid arthritis (n = 346) and psoriatic arthritis (n = 74) were retrospectively assessed. The incidence and time course of gastric MTX intolerance resulting in treatment discontinuation were investigated. In addition, the relations between gastric intolerance and patient characteristics, including gender, age, diagnosis, and rheumatoid factor (RF) positivity, were examined. Overall, oral MTX discontinuation rate due to gastric intolerance was 28.6 %. The time to discontinuation for oral MTX was 8.1 +/- A 11.5 months on average, with more than half of the discontinuations occurring within the first three months of treatment. Discontinuation was not associated with gender, age, diagnosis, or RF positivity. More than half of the patients that switched to a parenteral treatment regimen (52.6 %, 20/38) could tolerate the agent. Gastric MTX intolerance usually develops within the first year of treatment and presents a major obstacle to long-term treatment retention in patients with rheumatologic disease. However, parenteral MTX appears to be a good alternative for patients intolerant of oral MTX.
dc.identifier.citationDalkılıç, E. vd. (2013). "The time course of gastric methotrexate intolerance in patients with rheumatoid arthritis and psoriatic arthritis". Modern Rheumatology, 23(3), 525-528.
dc.identifier.endpage528
dc.identifier.issn1439-7595
dc.identifier.issue3
dc.identifier.pubmed22752502
dc.identifier.scopus2-s2.0-84877732637
dc.identifier.startpage525
dc.identifier.urihttps://doi.org/10.1007/s10165-012-0685-y
dc.identifier.urihttps://academic.oup.com/mr/article-abstract/23/3/525/6313445?redirectedFrom=fulltext&login=true
dc.identifier.urihttp://hdl.handle.net/11452/28165
dc.identifier.volume23
dc.identifier.wos000318847500014
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherTaylor & Francis
dc.relation.journalModern Rheumatology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectRheumatology
dc.subjectMethotrexate
dc.subjectIntolerance
dc.subjectTime course
dc.subjectRheumatoid arthritis
dc.subjectPsoriatic arthritis
dc.subjectFolate supplementation
dc.subjectEfficacy
dc.subjectMortality
dc.subjectTherapy
dc.subjectUpdate
dc.subjectDrugs
dc.subject.emtreeCreatinine
dc.subject.emtreeFolic acid
dc.subject.emtreeMethotrexate
dc.subject.emtreeRheumatoid factor
dc.subject.emtreeAdult
dc.subject.emtreeArticle
dc.subject.emtreeBlood cell count
dc.subject.emtreeClinical examination
dc.subject.emtreeDrowsiness
dc.subject.emtreeDrug hypersensitivity
dc.subject.emtreeDrug safety
dc.subject.emtreeDrug withdrawal
dc.subject.emtreeFemale
dc.subject.emtreeFollow up
dc.subject.emtreeGastrointestinal symptom
dc.subject.emtreeHuman
dc.subject.emtreeIncidence
dc.subject.emtreeLeukopenia
dc.subject.emtreeLiver function test
dc.subject.emtreeMajor clinical study
dc.subject.emtreeMale
dc.subject.emtreeMouth ulcer
dc.subject.emtreeNausea
dc.subject.emtreePriority journal
dc.subject.emtreePsoriatic arthritis
dc.subject.emtreeRheumatoid arthritis
dc.subject.emtreeSide effect
dc.subject.emtreeTime
dc.subject.emtreeUrea nitrogen blood level
dc.subject.emtreeVomiting
dc.subject.meshAdult
dc.subject.meshAged
dc.subject.meshAntirheumatic agents
dc.subject.meshArthritis, psoriatic
dc.subject.meshArthritis, rheumatoid
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshMale
dc.subject.meshMethotrexate
dc.subject.meshMiddle aged
dc.subject.meshNausea
dc.subject.meshRetrospective studies
dc.subject.meshTime factors
dc.subject.meshTreatment outcome
dc.subject.meshVomiting
dc.subject.scopusMethotrexate; Rheumatoid Arthritis; Pustulosis Palmoplantaris
dc.subject.wosRheumatology
dc.titleThe time course of gastric methotrexate intolerance in patients with rheumatoid arthritis and psoriatic arthritis
dc.typeArticle
dc.wos.quartileQ3
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/İç Hastalıkları Ana Bilim Dalı
local.indexed.atScopus
local.indexed.atWOS

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