Characteristics of an effective bedside glucose monitoring (BGM) quality-control program
| Characteristic |
|---|
| • A specifically designated responsible individual, preferably a laboratory professional, is involved in the administration and quality assurance of the BGM program. |
| • A written procedure for the BGM program. |
| • An organized training program that involves laboratory personnel and nursing staff. |
| • Defined frequencies and requirements for maintenance and cleaning of BGM instruments. |
| • Regular performance of quality control testing on each instrument (daily or by shift), depending on the frequency of patient testing. |
| • A policy to regularly compare the BGM results from each operator and instrument with results from a corresponding sample tested in the clinical laboratory. Suggest that all BGM results are, at least, within ±15% variation from the clinical laboratory results. |
| • Participation in an external proficiency testing program. |
| • Acknowledgment of the limitations of BGM and requirement of a clinical laboratory glucose determination when a BGM result is outside a defined range. |
| • Acknowledgment of the effect of hematocrit value variation on BGM results and establishment of hematocrit value limitations for the instrument in use. |
| • Determination of the bias of the instrument in use and communication of this information to the physicians and the institutional quality assurance program. |
Adapted from Jones et al. (443).