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Pharmacist-Driven Therapeutic Infliximab Monitoring at the Point of Care Using Rapidly Assessed Drug Levels in Patients with Inflammatory Bowel Disease

英夫利昔单抗 医学 治疗药物监测 槽水位 炎症性肠病 内科学 药品 维持剂量 毒品假日 维持疗法 治疗指标 疾病 药代动力学 药理学 化疗 免疫学 他克莫司 移植 人类免疫缺陷病毒(HIV)
作者
Clarissa Rentsch,Mark G. Ward,Raphael P. Luber,Kirstin M. Taylor,David Gibson,Belinda Headon,Ourania Rosella,Heidi Y. Su,Antony B. Friedman,Michael Dooley,Miles Sparrow,Peter R. Gibson
出处
期刊:Therapeutic Drug Monitoring [Lippincott Williams & Wilkins]
卷期号:45 (3): 383-391 被引量:3
标识
DOI:10.1097/ftd.0000000000001044
摘要

Therapeutic monitoring of infliximab is limited by the time lag between drug-level measurement and dose adjustment, along with the cost of dose escalation. Strategies for dose reduction in stable patients on maintenance infliximab at supratherapeutic levels are uncertain. This study determined the feasibility of a pharmacist-driven strategy for immediate dose adjustment using a sliding scale at the point of care in stable patients with inflammatory bowel disease on maintenance therapy.Adult patients with stable disease undergoing maintenance therapy with infliximab infusions, 5 mg/kg every 8 weeks, were prospectively studied. Trough drug levels were assessed by a rapid assay (and later by ELISA) at all infusions for up to 12 months with immediate but quantitatively small dose adjustment according to a sliding scale targeting a therapeutic range of 3-7 mcg/mL. Disease activity was assessed both clinically and biochemically.The rapid assay and ELISA detected similar infliximab levels, and the strategy added approximately 30 minutes to the duration of infusion events. Only 20% of 48 patients (77% with Crohn disease) had baseline trough infliximab concentrations within the therapeutic range. This value increased 3-fold after 24 and 48 weeks of interventions. One in 2 patients had baseline supratherapeutic levels, and most were brought into the therapeutic range without a discernible impact on disease activity by 1 dose adjustment, but 2 or 3 adjustments were generally needed for 29% of patients with subtherapeutic levels. Overall, drug costs were reduced by 4%.Immediate dose adjustment after infliximab rapid assay performed by a pharmacist using a sliding scale is a feasible strategy. Supratherapeutic infliximab levels can be safely and quickly brought into the therapeutic range using small dose adjustments without affecting disease activity, offsetting (at least partly) costs associated with dose escalation.
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