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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 effectiveness of educational and pratical experiences policies and procedures dedicated to the laboratory's effors in maintaining technologists 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 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 technologists' performance on WBC differential counts and moprphology assessment. Each technologist will receive their own kit. Technologists 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

  • Individual technologist score (%) based on a standardized competency assessment method to determine a technologist's 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 technologist performance(s)

Program Information

To meet your staff technical competency assessment requirements:

  • Result forms for up to 10 technologists (QPC10)
  • Result forms for up to 25 technologists (QPC25)
  • Multiple kits may be purchased to accommodate quantity needed.
  • Preliminary study reports are provided at institution and technologists levels.

Shipping Schedule

C Mailing: June 2, 2025

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)
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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