Publication Date

10-2019

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Abstract

Background: Intravenous immune globulin (IVIG) is a plasma-derived product from pooled donors. It has six FDA approved indications. It is also considered standard of care for a few other conditions in specific populations. Additionally, there is growing non-evidence-based use. Due to a global shortage, IVIG has become increasing difficult to obtain.

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Conclusions: Development, implementation, and promotion of adherence to an evidence-based criterion allowed our scarce IVIG supply to be sustained. Further refinement of the criteria for use is ongoing, as is an evaluation of IVIG utilization by indication, pre- and post-implementation. This process can be applied to other situations of scarce resources

MeSH Keywords

Immunoglobulins, Intravenous; Evidence-Based Practice; Resource Allocation; Quality Improvement

Keywords

IVIG

Disciplines

Health and Medical Administration | Pharmacy and Pharmaceutical Sciences

Development and Implementation of an Evidence-Based Process for Scarce Resource Allocation

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