Severe pancytopenia associated with low-dose methotrexate therapy for rheumatoid arthritis
- PMID: 11793624
- DOI: 10.1345/aph.1A052
Severe pancytopenia associated with low-dose methotrexate therapy for rheumatoid arthritis
Abstract
Objective: To report the occurrence of severe pancytopenia associated with low-dose methotrexate (MTX) therapy for rheumatoid arthritis.
Case summary: Two patients developed severe pancytopenia after 10 days (cumulative dose 15 mg) and 23 months (cumulative dose 1030 mg), respectively, of low-dose MTX therapy for rheumatoid arthritis. Both patients had renal impairment. One died and the other recovered completely.
Discussion: Pancytopenia is a rare adverse effect of low-dose oral MTX therapy. The exact mechanism for development of pancytopenia is unknown, although it is likely that several factors play a role. The most important risk factor for MTX toxicity is impaired renal function. This adverse effect may occur at any time during MTX therapy.
Conclusions: Severe pancytopenia associated with low-dose MTX therapy for rheumatoid arthritis is a potentially serious complication that may occur at any time during therapy. This adverse effect is more likely to occur in patients with renal impairment.
Comment in
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Comment: severe pancytopenia associated with methotrexate therapy for rheumatoid arthritis.Ann Pharmacother. 2002 Jul-Aug;36(7-8):1295. doi: 10.1345/aph.19113b. Ann Pharmacother. 2002. PMID: 12086573 No abstract available.
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Myelodysplastic syndrome associated with low-dose methotrexate in rheumatoid arthritis.Ann Pharmacother. 2004 Jan;38(1):172-3. doi: 10.1345/aph.1D117. Ann Pharmacother. 2004. PMID: 14742816 No abstract available.
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