| |
Preanalytic |
Analytic |
Postanalytic |
Anatomic Pathology |
Clinical Pathology |
Turnaround Time |
Patient Safety |
Microbiology |
Transfusion Medicine |
Chemistry/ Hematology |
Customer Satisfaction |
| Q-PROBES |
| Antimicrobial Susceptibility Testing: Monitoring and Trend Analysis (QP211) |
|
|
✓ |
|
✓ |
|
✓ |
✓ |
|
|
✓ |
Laboratory Staffing Rarios (QP222) |
|
|
|
✓ |
✓ |
|
|
|
✓ |
✓ |
|
| Technical Competency Assessment of Peripheral Blood Smears (QPC10/QPC25) |
|
✓ |
|
|
✓ |
|
✓ |
|
|
✓ |
|
| Technical Competency Assessment of Gram Stains (QPD10/QPD25) |
|
✓ |
|
|
✓ |
|
✓ |
✓ |
|
|
|
| Q-TRACKS |
| Patient Identification Accuracy (QT1) |
✓ |
|
|
|
✓ |
|
✓ |
|
|
|
✓ |
| Blood Culture Contamination (QT2) |
✓ |
✓ |
|
|
✓ |
|
✓ |
✓ |
|
|
✓ |
| Laboratory Specimen Acceptability (QT3) |
✓ |
|
|
|
✓ |
|
|
|
|
✓ |
✓ |
| In-Date Blood Product Wastage (QT4) |
|
|
✓ |
|
✓ |
|
|
|
✓ |
|
|
| Gynecologic Cytology Outcomes: Biopsy Correlation Performance (QT5) |
✓ |
✓ |
✓ |
✓ |
|
|
✓ |
|
|
|
✓ |
| Satisfaction with Outpatient Specimen Collection (QT7) |
✓ |
|
|
|
✓ |
|
✓ |
|
|
|
✓ |
| Stat Test Turnaround Time Outliers (QT8) |
|
✓ |
|
|
✓ |
✓ |
✓ |
|
|
✓ |
✓ |
| Critical Values Reporting (QT10) |
|
|
✓ |
|
✓ |
|
✓ |
|
|
✓ |
|
| Troponin Turnaround Times (QT15) |
✓ |
✓ |
✓ |
|
✓ |
✓ |
✓ |
|
|
✓ |
✓ |
| Corrected Results (QT16) |
|
|
✓ |
|
✓ |
|
✓ |
✓ |
✓ |
✓ |
✓ |
| Outpatient Order Entry Errors (QT17) |
|
|
|
|
✓ |
|
✓ |
|
|
✓ |
✓ |
*The CAP requires accredited laboratories to have a quality management plan that covers all areas of the laboratory and includes benchmarking key measures of laboratory performance (GEN.13806, GEN.20316, COM.04000). The Joint Commission requires accredited hospitals to regularly collect and analyze performance data (PI.01.01.01, PI.02.01.01). CLIA requires laboratories to monitor, assess, and correct problems identified in preanalytic, analytic, and postanalytic systems (§493.1249, §493.1289, §493.1299).
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