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By setting up a national database of all cases and entering patients into trials
| The first 150 words of the full text of this article appear below. |
Systemic sclerosis is a rare disease (about 10 cases/1 000 000/year) with a substantially higher mortality than
other autoimmune rheumatic diseases.1 This, and an even
greater morbidity, make it an unwelcome diagnosis for clinicians and a
fearful one for patients. No cure exists, though much can be done to
alleviate the organ based complications of the condition, and many
different agents are used in an attempt to modify disease progression.
Unfortunately, few drugs have been properly evaluated in clinical
trials and even the standard treatments are not of proved
efficacy.2 More aggressive therapies are now being tried
in some centres
for example, immunoablation with autologous
peripheral stem cell rescue3
and there is an urgent need
to compare these novel regimens with standard treatments. How can we
improve the management of this condition and ensure that management is
based on the best possible evidence?
Research over the past 20 years has led to a clearer
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