Economic evaluation of a designated oncology pharmacist in hemato-oncology outpatient care: A randomized clinical trial.
Abstract
11063 Background: Adverse drug reactions (ADRs) and medication errors are major contributors to morbidity and healthcare utilization in hemato-oncology. In a randomized clinical trial, we previously demonstrated that integrating a designated oncology pharmacist significantly reduced ADRs and intercepted potentially serious medication errors. The economic value of this intervention has not yet been established. Methods: We conducted a trial-based cost-effectiveness analysis alongside a single-center randomized clinical trial (n=182), in which adult patients with hematologic malignancies were randomized 1:1 to comprehensive pharmaceutical care delivered by a designated oncology pharmacist versus standard care. Patients were followed for 5 months (4-month intervention plus 1-month follow-up). The primary economic outcome was incremental cost per ADR avoided; secondary outcomes included cost per emergency department visit and hospitalization avoided. The analysis was conducted from the public healthcare system perspective and included only the pharmacist program cost, estimated at $105 per patient over the 5-month study period. Incremental cost-effectiveness ratios (ICERs) were calculated using absolute risk reduction, with uncertainty assessed by nonparametric bootstrap resampling (5,000 replications). Costs are reported in 2022 USD. Results: ADRs occurred in 47.3% of control patients compared with 23.1% of intervention patients, corresponding to an absolute risk reduction of 24.2% and a number needed to treat of 4.1. The ICER was $434 per ADR avoided (bootstrap 95% CI: $281–$956), with a >99.9% probability that the intervention reduced ADRs. Secondary outcomes also favored the intervention: emergency department visits (37.4% vs 28.6%; ICER $1,194 per visit avoided) and hospitalizations (28.6% vs 23.1%; ICER $1,911 per hospitalization avoided). In addition, the pharmacist intercepted 287 medication errors in real time, including 13 potentially severe errors, with a physician acceptance rate of 94.8%. Conclusions: This economic evaluation demonstrates that integrating a designated oncology pharmacist in hemato-oncology outpatient care is a cost-effective strategy for preventing ADRs and reducing acute healthcare utilization. These findings support broader implementation of oncology pharmacists as a high-value patient safety intervention.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (7)
Areen Khateeb Alabbasi
Clalit Health Services, Tel Aviv, Israel
Shai Cohen
Technion Israel Institute of Technology, Miami, FL
Manfred S. Green
Haifa University, Haifa, Israel
Meir Preis
Institute of Hematology, Lady Davis Carmel Medical Center, Haifa, Israel
Shmuel Klang
University of Haifa, Haifa, Israel
Mouna Ballan Haj
Clalit Health Service, Haifa, Israel
Shuli Z. Brammli-Greenberg
The Hebrew University of Jerusalem, Jerusalem, Israel