Safety of low dose methotrexate in elderly patients with rheumatoid arthritis
Boaz Hirshberga, Mordechi Muszkatb, Ora Schlesingerc, Alan Rubinowc
a Department of
Internal Medicine, Hadassah University Hospital, PO Box 12000, Jerusalem 91120, Israel, b Department of Clinical Pharmacology, Hadassah
University Hospital, c Rheumatology Unit, Hadassah University Hospital
Correspondence to: Dr Rubinow rubinov{at}cc.huji.ac.il
Submitted 20 December
1999;
Accepted 9 May 2000
Weekly low dose methotrexate is an established treatment for
rheumatoid arthritis, but its use in elderly people has not been adequately examined. The aim of this study was to evaluate its safety
in elderly patients with rheumatoid arthritis. A retrospective review
of the clinical records of rheumatoid arthritis patients over the age
of 65 attending a rheumatology unit was conducted. Eligible patients
were followed for at least two years and treated with methotrexate in a
dose of 7.5 mg/week while being maintained on concurrent treatment.
Thirty three patients were studied. Their mean age was 78.8 years; 32 were female and one was male. Treatment was discontinued in four
patients, two because of raised serum liver enzymes and two because of
gastrointestinal irritation. No serious adverse events were reported.
After two years, haemoglobin levels increased from a mean (SD) of 12.4 (1.3) g/dl to 13.0 (1.1) g/dl (r = 0.226, p < 0.005). The white blood count was significantly reduced from 7.9 (1.8) × 109/l to 6.8 (1.7) × 109/l
(r = 0.184, p < 0.05). No episodes of
neutropenia or agranulocytosis were observed. There was a
non-significant decrease in platelet count. The erythrocyte
sedimentation rate decreased from 56.8 (30.8) to 35.2 (24.6) mm/h
(r = 0.246, p < 0.01). In conclusion, low
methotrexate treatment in elderly patients appears to be safe. Routine
determination of serum liver enzymes and renal function may reduce
individual risk.
Keywords: methotrexate; elderly; safety
© 2000 by The Fellowship of Postgraduate Medicine
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