Extended reports
Effect of resumption of second line drugs in patients with
rheumatoid arthritis that flared up after treatment discontinuation
a Departments of Rheumatology
, b and
Medical Statistics , c University
Hospital Leiden, the NetherlandsDepartment of
Rheumatology of Free University Hospital Amsterdam, the Netherlands
Correspondence to: Dr S ten Wolde, Department of Rheumatology, University Hospital Leiden, Building 1, C4R, PO Box 9600, 2300 RC Leiden, the Netherlands.
Accepted for publication 14 January 1997
OBJECTIVE
To assess the effect of resumption of
second line drugs in patients with rheumatoid arthritis (RA) that
flared after treatment discontinuation.
METHODS
RA patients were studied whose RA flared
up after discontinuation of second line treatment while being in
remission and who received a second course of the drug. Disease
activity parameters were prospectively assessed at the time of
treatment discontinuation, during the period when the disease flared
up, and three months thereafter. Furthermore the medical charts were
reviewed at 12 months after treatment resumption.
RESULTS
There were 51 patients included in the
study: 25 patients treated with antimalarial drugs, 10 with parenteral
gold, four with d-penicillamine, eight with sulphasalazine, two with
azathioprine, and two with methotrexate. Disease activity parameters
showed significant improvement within three months of treatment
resumption, but remained significantly worse when compared with that
measured before treatment discontinuation. Within three months 47% of
the patients fulfilled 20% response criteria. Disease activity 12 months after treatment resumption was considered to be absent in 35%,
mild in 43%, and moderate or active in 22% of the patients. In four
(8%) patients the resumed treatment was stopped because of lack of
efficacy. Side effects were recorded in four patients, which did not
result in treatment discontinuation.
CONCLUSIONS
Resumption of second line drugs in
RA patients whose disease flared up after discontinuation of treatment
is effective and safe in most patients. Half of the patients responded
within three months after resumption of the second line drug.
© 1997 by Annals of the Rheumatic Diseases
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