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Exploring the iceberg of errors in laboratory medicine
1Department of Laboratory Medicine, University-Hospital of Padova, Italy. mario.plebani@unipd.it
Clinical laboratory errors have decreased, but pre- and post-analytical steps, often outside lab control, remain error-prone. Improving the total testing process (TTP) is crucial for patient safety and accurate diagnostics.
Area of Science:
- Clinical Laboratory Science
- Healthcare Quality Improvement
- Diagnostic Medicine
Background:
- Analytical errors in clinical laboratories have significantly decreased over recent decades.
- Pre- and post-analytical phases of the total testing process (TTP) are more prone to errors than the analytical phase.
- Many errors occur outside the laboratory's direct control, in pre-pre-analytic and post-post analytic steps.
Purpose of the Study:
- To investigate defects in the total testing process (TTP) that negatively impact patient care.
- To consider all consequences of laboratory testing errors, regardless of the phase or responsible party.
- To highlight the need for evidence-based quality indicators for laboratory medicine.
Main Methods:
- Review of existing evidence on analytical errors in clinical laboratories.
- Analysis of diagnostic errors in primary care and emergency departments.
- Identification of common and specific faults affecting diagnostic errors.
Main Results:
- Inappropriate test requesting and incorrect interpretation are major contributors to diagnostic errors across disciplines.
- Patient misidentification and result communication issues are key areas for quality improvement.
- Errors in laboratory medicine require specific preventive and corrective actions.
Conclusions:
- A patient-centered approach necessitates examining the entire total testing process (TTP) for potential defects.
- Developing, implementing, and monitoring evidence-based quality indicators is essential for laboratory error reduction.
- Practices must proactively identify weaknesses in their TTP and implement appropriate remedies.
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