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ASSESS PERIPH BLD MORPHOLOGY CONSISTENCY - QPC10
QPC10/QPC25
The widespread use of automated white blood cell (WBC) differential counts and computer-generated whole slide imaging has decreased the time that the medical laboratory scientist/technologist staff dedicated to morphological assessment of blood cells. However, these staff must maintain their morphological skills. Laboratories have an annual requirement to do a morphologic comparison of their technical staff's peripheral blood smear results, assess their competency on peripheral blood smears, and provide apppropriate education.
Objectives
This study will help assess the educational and pratical experiences policies and procedures dedicated to the laboratory's effors in maintaining medical laboratory scientis skills in the performance of accurate WBC differential counts and other peripheral blood smear morphological assessments. The evaluation provided will assist in the construction of individual educational programs for the technical staff and show areas that need focused review and improvement. The study will help laboratories meet requirements for consistency of reporting morphology among staff and personnel competency requirements (testing previously analyzed specimens).*
Data Collection
A series of online whole slide imagies of Wright or Wright-Giemsa-stained peripheral blood smears using DigitalScope® technology will be available to each participating institution to assess medical laboratory scientists performance on WBC differential counts and moprphology assessment. Each medical laboratory scientists will receive their own kit. Medical laboratory scientists will provide information about their continuing education and professional background. Information will be collected from each site regarding their institution's minimum continuing education requirements for their technologists in hematology and relevant procedures and policies related to peripheral blood smear assessment.
Performance Indicators
An individual medical laboratory scientist score are based on a standardized competency assessment method to determine a medical laboratory scientist ability to identify various WBC types, red blood cell morphology, and platelet morphology in normal and abnormal cases
Overall laboratory score based on the facility's individual medical laboratory scientist’s performance(s).
Program Information
Your Reports – What to Expect:
A Participant Summary Report explaining the grading criteria for each case, how to read the reports, annotated images, and case descriptions.
An institution report with your facility’s score summary with comparison to other institutions and a technologist score summary by case for each participant.
An individual report for each participant listing their responses and score for each case.
To meet your staff comparative morphology and technical competency assessment requirements:
Result forms for up to 10 medical laboratory scientists (QPC10)
Result forms for up to 25 medical laboratory scientists (QPC25)
Multiple kits may be purchased to accommodate quantity needed.
Shipping Schedule
C Mailing: June 2, 2027
Additional Information
*Participation in this study helps laboratories meet applicable requirements:
CLIA personnel requirements (Subpart M, 42 CFR §493.1)
CAP Laboratory Accreditation Program Checklist statements HEM.34400,consistency of morphologic observation among personnel performing blood cell microscopy at least annually; GEN.55500, element 5, Competency Assessment of Testing Personnel; GEN.55525, Performance Assessment of Supervisors/Consultants; DRA.11425, functions or responsibilities are properly performed by a qualified individual
The Joint Commission Standards HR.01.05.03,01.06.01 (EPs 3, 18, 19), HR.01.07.01, PI.03.01.01(EPs 3-5), and LD.04.05.01, 04.05.03 (EPs 1-6) regarding in-service training, continuing education, competency, and evaluation of staff members.
This is a one-time study conducted in the third quarter.
Select Q-PROBES and Q-TRACKS studies to support your quality improvement initiatives.
Preanalytic
Analytic
Postanalytic
Anatomic Pathology
Clinical Pathology
Turnaround Time
Patient Safety
Microbiology
Transfusion Medicine
Chemistry/ Hematology
Customer Satisfaction
Q-PROBES
Non-Physician Care Team Satisfaction With Clinical Laboratory Services (QP231)
✓
✓
✓
✓
✓
✓
Technical Competency Assessment of Body Fluid Review (QPB10)
✓
✓
✓
✓
Technical Competency Assessment of Peripheral Blood Smears (QPC10/QPC25)
✓
✓
✓
✓
Technical Competency Assessment of Gram Stains (QPD10/QPD25)
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).