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Removing non-recommended tests like gamma-glutamyltransferase and uric acid from pre-eclampsia order sets significantly reduced lab requests and calls. This improved efficiency and saved resources without impacting patient care.

Keywords:
cost-effectivenesselectronic health recordshealthcare quality improvementinformation technologyobstetrics and gynaecology

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Area of Science:

  • Clinical Chemistry
  • Obstetrics and Gynecology
  • Healthcare Management

Background:

  • Current pre-eclampsia electronic order sets include gamma-glutamyltransferase (GGT) and uric acid, despite guidelines not recommending them.
  • These markers are poor predictors of maternal and neonatal outcomes in pre-eclampsia management.
  • Clinical staff confirmed non-use of these markers in patient assessment.

Purpose of the Study:

  • To evaluate the impact of removing GGT and uric acid from electronic laboratory order sets for suspected pre-eclampsia.
  • To assess the effect on laboratory request numbers and clinical workflow efficiency.

Main Methods:

  • Stakeholder engagement to confirm non-use of GGT and uric acid in clinical practice.
  • Quantified baseline GGT and uric acid requests over two months.
  • Removed GGT and uric acid from the electronic order set.
  • Quantified post-intervention requests over two months and assessed sustainability at eight months.

Main Results:

  • Significant reduction in GGT and uric acid laboratory requests from the maternity department.
  • Substantial decrease in laboratory phone calls escalating abnormal results.
  • Project demonstrated sustainability eight months post-intervention.

Conclusions:

  • Removing non-recommended tests from electronic order sets is effective in reducing unnecessary laboratory utilization.
  • This intervention streamlines clinical workflow, saves resources, and reduces staff time.
  • Optimizing laboratory order sets aligns with evidence-based practice and improves healthcare efficiency.