1998
DOI: 10.1002/1529-0131(199803)41:3<381::aid-art2>3.3.co;2-v
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The use of methotrexate in childhood rheumatic diseases

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Cited by 10 publications
(12 citation statements)
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“…Nine of them achieved inflammation control on MMF without concomitant corticosteroids or other IMTs for a median of 15 months (range: [3][4][5][6][7][8][9][10][11][12][13][14][15][16][17][18][19][20][21][22]. During this follow-up period, 8 out of the 9 patients experienced no uveitis relapse; 1 patient experienced one relapse that was treated with 4 weeks of topical corticosteroids.…”
Section: Treatment Outcomesmentioning
confidence: 99%
See 1 more Smart Citation
“…Nine of them achieved inflammation control on MMF without concomitant corticosteroids or other IMTs for a median of 15 months (range: [3][4][5][6][7][8][9][10][11][12][13][14][15][16][17][18][19][20][21][22]. During this follow-up period, 8 out of the 9 patients experienced no uveitis relapse; 1 patient experienced one relapse that was treated with 4 weeks of topical corticosteroids.…”
Section: Treatment Outcomesmentioning
confidence: 99%
“…Because of its relative ease of use, effectiveness, and safety profile in a variety of ocular and systemic autoimmune diseases, it is frequently used as the first-line steroid-sparing treatment in paediatric uveitis, particularly those associated with juvenile idiopathic arthritis. [4][5][6][7][8] Nevertheless, MTX is not tolerated well by all …”
Section: Introductionmentioning
confidence: 99%
“…14,15 MTX hücre içine hızlıca girer ve hepatositler, fibroblastlar, kemik iliği myeloid hücreleri ve diğer hücrelerce poliglutamatlanır. 16 Her ne kadar böbrekler tarafından hızlıca elimine edilse de, poliglutamatlanmış metotreksat intraselüler alanda birikebilir, bu durum tedaviden yıllar sonra ortaya çıkan bulantı ve kusmayı açıklayabilir.…”
Section: Metotreksatunclassified
“…16 Aç karnına alındığında emilimi daha iyidir. Subkutan uygulamada absorbsiyonun çok daha iyi olduğu gösterilmiştir.…”
Section: Metotreksatunclassified
“…Il MTX si è imposto come DMARD di prima scelta per le forme ad evoluzione poliarticolare (7,8). Tuttavia, alcuni bambini non hanno un'adeguata risposta, pur incrementando le dosi (9,10), e molti sviluppano un'intolleranza, con nausea, vomito e malessere successivi all'assunzione, che rendono impossibile la prosecuzione del trattamento (11,12). Per altri DMARDs, o non esiste l'evidenza della loro efficacia, mancando studi clinici controllati, come per i sali d'oro iniettabili e la ciclosporina (13)(14), oppure, in studi controllati, si sono dimostrati inefficaci come la penicillamina, l'idrossiclorochina (15), i sali d'oro per os (16) e le immunoglobuline umane endovenose ad alte dosi (17).…”
unclassified