Long-term survival of methotrexate in psoriatic arthritis
Objective. The purpose of this study was to evaluate the long-term survival rate of Methotrexate (MTX) in the peripheral joint involvement of psoriatic arthritis (PsA) in a setting of everyday clinical practice. Methods. This was an observational restrospective study performed using the data from a...
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2011-06-01T00:00:00Z.
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LEADER | 00000 am a22000003u 4500 | ||
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001 | doaj_0c243911f1e64d2f95ff5bd78e0139b0 | ||
042 | |a dc | ||
100 | 1 | 0 | |a N. Battafarano |e author |
700 | 1 | 0 | |a L. Rotunno |e author |
700 | 1 | 0 | |a D. Mazzocchi |e author |
700 | 1 | 0 | |a F. Desiati |e author |
700 | 1 | 0 | |a G. De Marco |e author |
700 | 1 | 0 | |a M. Ricci |e author |
700 | 1 | 0 | |a A. Marchesoni |e author |
245 | 0 | 0 | |a Long-term survival of methotrexate in psoriatic arthritis |
260 | |b PAGEPress Publications, |c 2011-06-01T00:00:00Z. | ||
500 | |a 10.4081/reumatismo.2009.125 | ||
500 | |a 0048-7449 | ||
500 | |a 2240-2683 | ||
520 | |a Objective. The purpose of this study was to evaluate the long-term survival rate of Methotrexate (MTX) in the peripheral joint involvement of psoriatic arthritis (PsA) in a setting of everyday clinical practice. Methods. This was an observational restrospective study performed using the data from a dermatological-rheumatological PsA clinic. All of the patients evaluated at this clinic from March 1997 to December 2007 who were started on MTX alone, had a three-year follow-up time or had discontinued the therapy were included into the survey. Results. Of the 174 evaluable patients, 104 (59.8%) were still taking MTX after three years of treament. The reasons of therapy discontinuation in the remaining 70 (40.2%) patients were: 34 (19.5%) lost-to-follow-up, 18 (10.3%) adverse events, 14 (8%) inefficacies, and 4 (2.3%) deaths (none related to the therapy). MTX was effective in controlling joint inflammation but not in preventing their deterioration. Overall, adverse events were recorded in 43 patients (36.4% of the 114 patients with a three-year follow-up). No serious side effect occurred in the study population. Conclusions. The results of this study showed that, in a setting of clinical pratice, MTX had a good three-year performance in patients with peripheral PsA. Almost 60% of them were still taking this drug at the end of the study period and the toxicity was more than acceptable. In our opinion, MTX might be considered the non-biological DMARD of choice for the treatment of this condition. However it should be used earlier and at higher doses. | ||
546 | |a EN | ||
546 | |a IT | ||
690 | |a Medicine | ||
690 | |a R | ||
690 | |a Internal medicine | ||
690 | |a RC31-1245 | ||
655 | 7 | |a article |2 local | |
786 | 0 | |n Reumatismo, Vol 61, Iss 2, Pp 125-131 (2011) | |
787 | 0 | |n http://www.reumatismo.org/index.php/reuma/article/view/426 | |
787 | 0 | |n https://doaj.org/toc/0048-7449 | |
787 | 0 | |n https://doaj.org/toc/2240-2683 | |
856 | 4 | 1 | |u https://doaj.org/article/0c243911f1e64d2f95ff5bd78e0139b0 |z Connect to this object online. |