The British Journal of Rheumatology, Vol 36, 86-90, Copyright © 1997 by British Society for Rheumatology
RA Hamilton and JM Kremer
In order to compare the relative bioavailability of orally administered
methotrexate (MTX) with i.m. administration in patients with rheumatoid
arthritis, we compared the pharmacokinetics of MTX at both the usual
starting dose of 7.5 mg and at higher established maintenance dosages in 21
patients. Pharmacokinetic measures were repeated approximately 6 and 18
months after baseline while patients consumed their usual maintenance doses
of MTX (17.0 +/- 3.8 mg). The relative bioavailability of the usual
maintenance dose of MTX was reduced by 13.5% compared with the initial dose
of 7.5 mg (P = 0.026). Area under the serum concentration vs time curve
(AUC) was significantly reduced with oral vs i.m. administration at usual
maintenance doses (decrease of 0.729 mumol.h/l by oral administration, P =
0.027), but not at a 7.5 mg dose of MTX. Clinicians using MTX should not
assume constant and complete bioavailability across the dose range used to
treat patients with rheumatoid arthritis. Our observations explain the
reported clinical success of switching from an oral to a parenteral route
of administration in patients receiving maintenance doses of MTX.
ORIGINAL PAPERS
Why intramuscular methotrexate may be more efficacious than oral dosing in patients with rheumatoid arthritis
Albany College of Pharmacy, NY 12208, USA.
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