Abstract

Methotrexate (MTX) toxicity can affect multiple organ systems, manifesting as nephrotoxicity, myelosuppression, hepatotoxicity, mucositis, and gastrointestinal upset. Serious adverse events are rare in patients prescribed low-dose methotrexate. We present a case of an 86-year-old female on a weekly dose of oral MTX 12.5 mg for rheumatoid arthritis presenting with painful gingiva and oral bleeding during outpatient antimicrobial therapy (OPAT) for osteomyelitis with vancomycin and piperacillin-tazobactam. She had acute kidney injury (AKI), elevated serum MTX levels, thrombocytopenia, neutropenia, and a vancomycin level three times therapeutic concentration. MTX toxicity was suspected to have been triggered by vancomycin and piperacillin-tazobactam causing AKI and impaired renal clearance of MTX which itself is nephrotoxic. The patient was managed with leucovorin, alkalinized intravenous fluids, and filgrastim injections over a 2-week period. Her renal function continued to be reduced at 5-week outpatient follow-up, far after other markers of toxicity normalized. This case demonstrates the importance of considering potential drug-drug interactions and the need for robust monitoring for OPAT in select groups.

Highlights

  • Outpatient parenteral antimicrobial therapy (OPAT) is a cost-saving alternative to hospitalization in the management of stable patients with infections that require prolonged antibiotic therapy [1]

  • Besides the direct effect on renal function, an additional consideration in using nephrotoxic agents in OPAT is the effect on the serum concentration of medications that depend on renal clearance

  • We here present a case of severe MTX toxicity occurring in an elderly patient receiving concomitantly low-dose methotrexate (LDM) for rheumatoid arthritis (RA), and intravenous vancomycin and TZP for osteomyelitis

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Summary

Introduction

Outpatient parenteral antimicrobial therapy (OPAT) is a cost-saving alternative to hospitalization in the management of stable patients with infections that require prolonged antibiotic therapy [1]. The Infectious Diseases Society of America (IDSA) published updated recommendations in 2018 regarding patient selection, monitoring, and integration into antimicrobial stewardship [3]. Certain populations such as intravenous drug users and the elderly are recognized as high risk for complications or failure of OPAT [4,5]. The IDSA recommends regularly monitoring vancomycin levels and renal function during OPAT, though frequency is not specified and this guideline is based on “very low-quality evidence” [3]. We here present a case of severe MTX toxicity occurring in an elderly patient receiving concomitantly low-dose methotrexate (LDM) for rheumatoid arthritis (RA), and intravenous vancomycin and TZP for osteomyelitis

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