Introduction. - The treatment of rheumatoid arthritis includes non-steroid
anti-inflammatory drugs (NSAID), low-dose steroids and drugs which modify t
he evolution of the disease (disease modifying anti-rheumatic drugs, [DMARD
]). In the last few years, the long-term efficiency of the recommended trea
tment strategies in rheumatoid arthritis has been a matter of debate and th
eir basic assumptions have been challenged. Numerous studies were undertake
n to settle the question. They tried to delineate the rules for an optimal
use of current drugs and other therapeutic means.
Current knowledge and key points, - Rheumatoid arthritis is a crippling dis
ease. It decreases life expectancy and irreversible bone and joint damage m
ay develop even in the first months of evolution. The sooner the prescripti
on of DMARD, the higher the frequency and quality of rheumatoid arthritis i
mprovement and, in the long-ten, the lesser the functional impairment. Low
dose steroids, when administered early, can slow down the development of ra
diologic lesions. Some of their effects are thus closer to those of DMARD t
han to those of symptomatic treatment. NSAID are at least as equally danger
ous as DMARD and possibly more so in terms of the potential number of sever
e side effects. The combination of several DMARD does not increase their ov
erall toxicity. An evaluation of the most efficient combinations and of the
clinical situations in which combinations show promise of improved results
is in progress.
Future prospects and projects, - At present, the tendency is to treat early
and intensively, in order to obtain complete remission, improve evolution
and reduce functional impairment. This strategy requires early diagnosis an
d early evaluation of prognosis of rheumatoid arthritis. Rheumatoid arthrit
is with benign evolution would not warrant intensive treatment. Studies are
in progress to evaluate the prognostic factors in early rheumatoid arthrit
is that would enable us to adapt the strength of initial treatment to the d
isease's putative severity. (C) 1999 Elsevier, Paris.