Leflunomide (Arava) in early rheumatoid arthritis

Objective. To assess efficacy and safety of leflunomide in the treatment of early rheumatoid arthritis (RA). Material and methods. 30 pts with RA aged 18 to 67 years were examined. 17 pts with disease duration less than 6 months (mean 3,6±2,6 months) were included in group 1 and 13 pts with disease...

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Main Authors: R V Balabanova, D E Karateev, R YKashevarov, E L Luchihina
Format: Article
Language:Russian
Published: IMA-PRESS LLC 2005-10-01
Series:Научно-практическая ревматология
Subjects:
Online Access:https://rsp.mediar-press.net/rsp/article/view/322
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spelling doaj-a9f85b5decde49d4a73311b47007197e2021-08-02T09:05:38ZrusIMA-PRESS LLCНаучно-практическая ревматология1995-44841995-44922005-10-01435313410.14412/1995-4484-2005-38262Leflunomide (Arava) in early rheumatoid arthritisR V BalabanovaD E KarateevR YKashevarovE L LuchihinaObjective. To assess efficacy and safety of leflunomide in the treatment of early rheumatoid arthritis (RA). Material and methods. 30 pts with RA aged 18 to 67 years were examined. 17 pts with disease duration less than 6 months (mean 3,6±2,6 months) were included in group 1 and 13 pts with disease duration from 6 months to 3 years (mean 1,8+1,3 years) - in group 2. DAS 28, ACR criteria, patient's general health, pain, HAQ, Keitel functional test and laboratory indices were used as outcome measures. Leflunomide was administered 20 mg/day during 12 months. Results. Significant decrease of RA activity indices was achieved during 3 months in both groups. Group 1 pts showed progressive improvement during the whole period of the treatment. Group 2 pts had the most prominent decrease of activity after 6 months of the treatment. Later some of them showed tendency to deterioration of several parameters. In 10 (58,8%) pts of group I clinical remission was achieved by the 6th month. The treatment was stopped because of adverse events in 4 pts. Serious adverse events were absent. Conclusion. Leflunomide (arava) is a highly effective and well tolerated disease modifying drug for the treatment of early RA. Leflunomide was more effective in pts with disease duration less than 6 months.https://rsp.mediar-press.net/rsp/article/view/322early rheumatoid arthritisaravaleflunomidedisease modifying therapy
collection DOAJ
language Russian
format Article
sources DOAJ
author R V Balabanova
D E Karateev
R YKashevarov
E L Luchihina
spellingShingle R V Balabanova
D E Karateev
R YKashevarov
E L Luchihina
Leflunomide (Arava) in early rheumatoid arthritis
Научно-практическая ревматология
early rheumatoid arthritis
arava
leflunomide
disease modifying therapy
author_facet R V Balabanova
D E Karateev
R YKashevarov
E L Luchihina
author_sort R V Balabanova
title Leflunomide (Arava) in early rheumatoid arthritis
title_short Leflunomide (Arava) in early rheumatoid arthritis
title_full Leflunomide (Arava) in early rheumatoid arthritis
title_fullStr Leflunomide (Arava) in early rheumatoid arthritis
title_full_unstemmed Leflunomide (Arava) in early rheumatoid arthritis
title_sort leflunomide (arava) in early rheumatoid arthritis
publisher IMA-PRESS LLC
series Научно-практическая ревматология
issn 1995-4484
1995-4492
publishDate 2005-10-01
description Objective. To assess efficacy and safety of leflunomide in the treatment of early rheumatoid arthritis (RA). Material and methods. 30 pts with RA aged 18 to 67 years were examined. 17 pts with disease duration less than 6 months (mean 3,6±2,6 months) were included in group 1 and 13 pts with disease duration from 6 months to 3 years (mean 1,8+1,3 years) - in group 2. DAS 28, ACR criteria, patient's general health, pain, HAQ, Keitel functional test and laboratory indices were used as outcome measures. Leflunomide was administered 20 mg/day during 12 months. Results. Significant decrease of RA activity indices was achieved during 3 months in both groups. Group 1 pts showed progressive improvement during the whole period of the treatment. Group 2 pts had the most prominent decrease of activity after 6 months of the treatment. Later some of them showed tendency to deterioration of several parameters. In 10 (58,8%) pts of group I clinical remission was achieved by the 6th month. The treatment was stopped because of adverse events in 4 pts. Serious adverse events were absent. Conclusion. Leflunomide (arava) is a highly effective and well tolerated disease modifying drug for the treatment of early RA. Leflunomide was more effective in pts with disease duration less than 6 months.
topic early rheumatoid arthritis
arava
leflunomide
disease modifying therapy
url https://rsp.mediar-press.net/rsp/article/view/322
work_keys_str_mv AT rvbalabanova leflunomidearavainearlyrheumatoidarthritis
AT dekarateev leflunomidearavainearlyrheumatoidarthritis
AT rykashevarov leflunomidearavainearlyrheumatoidarthritis
AT elluchihina leflunomidearavainearlyrheumatoidarthritis
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