Outcomes Associated with Reducing the Urine Alkalinization Threshold in Patients Receiving High-Dose Methotrexate

Pharmacotherapy. 2017 Jun;37(6):684-691. doi: 10.1002/phar.1935. Epub 2017 May 12.

Abstract

Study objectives: Urine alkalinization increases methotrexate (MTX) solubility and reduces the risk of nephrotoxicity. The objectives of this study were to determine whether a reduction in the urine pH threshold from 8 to 7 in patients receiving high-dose methotrexate (HDMTX) results in a shorter length of hospital stay, delayed MTX clearance, or higher rates of nephrotoxicity; and to determine whether specific factors were associated with prolonged MTX clearance.

Design: Retrospective cohort study.

Setting: Hematology service of a large university-affiliated teaching hospital in Ottawa, Canada.

Patients: Sixty-five adults with 150 HDMTX exposures who had elective admissions for HDMTX between September 1, 2014, and December 18, 2015, were included. Thirty-four patients (with 79 HDMTX exposures) had their urine alkalinized to a pH of 8 or higher, and 31 patients (with 71 HDMTX exposures) had their urine alkalinized to a pH of 7 or higher, after an institutional change in the urine pH threshold from 8 to 7 was implemented on May 1, 2015.

Measurements and main results: Data related to patient demographics, urine alkalinization, MTX serum concentration monitoring, hospital length of stay, and renal function were collected retrospectively from patients' electronic health records. Lowering the urine pH threshold from 8 to 7 did not significantly affect hospital length of stay (absolute difference 3.5 hrs, 95% confidence interval -4.0 to 10.9) or clearance of MTX (elimination rate constant 0.058 in the pH of 7 or higher group vs 0.064 in the pH of 8 or higher group, p=0.233). Nephrotoxicity rates were similar between groups (15.5% in the pH of 7 or higher group vs 10.1% in the pH of 8 or higher group, p=0.34). Higher MTX dose and interacting medications (e.g., proton pump inhibitors and sulfonamide antibiotics) were significantly associated with delayed MTX elimination.

Conclusion: No significant differences in HDMTX-associated hospital length of stay, MTX clearance, or rates of nephrotoxicity were noted between patients in the urine pH of 7 or higher and 8 or higher groups. Interacting medications and higher MTX dose were associated with delayed MTX elimination, suggesting that a closer review of interacting medications before HDMTX administration may be warranted.

Keywords: adverse drug reactions; drug safety; hematology; pharmacokinetics.

MeSH terms

  • Acute Kidney Injury / chemically induced*
  • Acute Kidney Injury / prevention & control
  • Acute Kidney Injury / urine*
  • Adult
  • Aged
  • Antacids / pharmacology
  • Antacids / therapeutic use*
  • Antimetabolites, Antineoplastic / adverse effects
  • Antimetabolites, Antineoplastic / urine
  • Cohort Studies
  • Female
  • Humans
  • Hydrogen-Ion Concentration
  • Length of Stay / trends
  • Male
  • Metabolic Clearance Rate / drug effects
  • Metabolic Clearance Rate / physiology
  • Methotrexate / adverse effects*
  • Methotrexate / urine*
  • Middle Aged
  • Retrospective Studies
  • Sodium Bicarbonate / pharmacology
  • Sodium Bicarbonate / therapeutic use
  • Treatment Outcome
  • Urine / parasitology
  • Urine / physiology

Substances

  • Antacids
  • Antimetabolites, Antineoplastic
  • Sodium Bicarbonate
  • Methotrexate