Clinical Appropriateness Review
Whether a facility is converting to a Baxter product or is reevaluating their current product portfolio, the Clinical Appropriateness Review provides clinically relevant product recommendations for I.V. administration sets, components and needlestick prevention devices. If a product conversion will be taking place, it also prepares the facility's staff for a seamless transition to Baxter's broad portfolio of I.V. products.
Objectives
- Identify clinically equivalent Baxter I.V. administration sets, components, and needlestick prevention devices that meet a facility's patient care I.V. therapy requirements.
- Enhance staff's understanding and use of Baxter I.V. administration sets and components.
Methodology
IV therapy practice and product utilization are monitored throughout the facility. An analysis of product mix, clinical procedures and protocols and product usage is performed. Data are collected through staff interviews and product utilization report data.
Customer Benefits
- A customized report that delivers a high level overview of the facility's infusion systems portfolio, including infusion pumps, I.V. needleless administration sets and components.
- Potential inventory and clinical efficiencies
