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. 2015 Feb 22;15:11. doi: 10.1186/s12911-015-0137-7

Table 2.

Changes to electronic medical record affecting laboratory test ordering

Variable Intervention Date(s) of intervention
Allowable frequencies for repetitive ordering of laboratory tests Customized to tests July 2012
Review of electronic order sets All order sets with laboratory tests reviewed by pathology (pathology informatics and medical director) prior to release to production environment September 2009
Duplicate ordering of tests • Expanded duplicate checking to catch overlap of testing (e.g., glucose ordered individually at same time as basic metabolic panel that also included glucose order) • October 2009
• Instituted Best Practice Alert warning for attempt at duplicate orders of germline genetic tests • January 2011
Send-out test warnings • Removed generic send-out test prompt May to July 2012
• Instituted specific warnings with hard-stops customized to tests to include one or more of the following:
  - High cost and very high cost warnings
  - Long turnaround time warnings
  - Genetic counseling prompt
  - Reflex testing warning (if applicable)
Restriction of tests requiring approval (formulary) Instituted restrictions on 170 tests that required pathologist or clinical specialist approval prior to ordering July 2012
  - 164 tests required pathologist approval
  - 4 tests required infectious disease attending approval
  - 2 tests required neurology attending approval
Interventions targeting specific tests Instituted based on review (see Table 3) Various times 2009-2012
Laboratory test charges Posted in EMR for most tests (either as discrete charges or range of possible charges) July 2012