The effectiveness of methotrexate for the escape by salazosulfapyridine

Yoichi Kawasaki, Masahiro Moriyama, Kazuhiko Shibata, Yutaka Gomita

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

Although disease modifying anti-rheumatic drugs (DMARDs) are used in the treatment of rheumatoid arthritis (RA), the selection of agents in the case of relapse (escape phenomenon) lacks clear-cut standards. We compared the effectiveness in a salazosulfapyridine and then methotrexate (SASP→MTX) group with that in the mothotrexate (SASP + MTX) group after escape phenomenon expression in C-reactive protein (CRP) and erythrocyte sedimentation rate (ESR) data. Outpatients of the Matsubara Mayflower Hospital with a history of DMARD administration during the 4 years prior to May 2003 were studied. The CRP level in the SASP→MTX group (n=8) after the escape phenomenon expression showed a decline after 3 months, but no decline was seen even after 3 months the two in the CRP level in the SASP + MTX group (n=10). However, the difference between groups was not significant. The fluctuation in ESR was similar to that in CRP. However, ESR was significantly lower in the SASP→MTX group 20 weeks after escape phenomenon expression. In evaluating treatment effectiveness after escape phenomenon expression in each group, SASP →MTX was effective in 10 and SASP + MTX in 7 patients. Side effects necessitated cessation of treatment in 1 patient in the SASP→MTX group. Treatment continued in 4 patients in the SASP→MTX group and 2 in the SASP + MTX group, even though side effects occurred. It should be borne in mind that combination therapy often has greater clinical benefit than single agent therapy but not always.

Original languageEnglish
Pages (from-to)579-582
Number of pages4
JournalYakugaku Zasshi
Volume125
Issue number7
DOIs
Publication statusPublished - Jul 1 2005

    Fingerprint

Keywords

  • Disease modifying anti-rheumatic drugs
  • Escape phenomenon
  • Methotrexate
  • Rheumatoid arthritis
  • Salazosulfapyridine

ASJC Scopus subject areas

  • Pharmacology
  • Pharmaceutical Science

Cite this