170 likes | 493 Views
Laboratory Safety. Biohazard SafetyGeneral PoliciesApprovalsWaste disposalAccident reporting and follow-upSafety committee. Specimen Processing. General PoliciesApprovalPeriodic reviewSpecimen CollectionPhlebotomyTrainingDocumentationSpecimen Handling and TransportSpecimen Requisition,
E N D
1. CD4 GLP ProtocolsClinical Standard Operating Procedures for CD4 Enumeration by Flow Cytometry Using the BD FACSCount System Burt Houtz, CLS
Technical Adviser, Flow Cytometry Applications
BD Biosciences
This Get With The Flow seminar is presented by the Customer Education Services department.This Get With The Flow seminar is presented by the Customer Education Services department.
2. Laboratory Safety Biohazard Safety
General Policies
Approvals
Waste disposal
Accident reporting and follow-up
Safety committee
3. Specimen Processing General Policies
Approval
Periodic review
Specimen Collection
Phlebotomy
Training
Documentation
Specimen Handling and Transport
Specimen Requisition, Receipt and Assessment
Specimen Processing and Storage
4. Specimen Identification Log Proper Identification
Condition of the Specimen
Date and Time
Collection
Receipt
Source
Lab location
5. Immunofluorescent Labeling Preparing Controls
Preparing Samples
Vortexing
Pipetting
Incubation Times
6. FACSCount Quality Control Startup Procedure
Priming the System
Entering Control and Reagent Information
Running Controls
7. FACSCount Quality Control Report Control Run Result
Pass/Fail
CD3 Range
CD4 Range
Process Control Reporting
8. FACSCount Analysis of Specimens Startup Procedure
Priming the System
Entering Patient and Reagent Information
Running Patient Samples
Cleaning Procedure
Shutdown Procedure
9. Laboratory Reporting of CD4 Test Results Laboratory Worksheet
Recording Patient Test Results
10. FACSCount Maintenance Daily
Cleaning
Monthly
Drain / Fill Cycle
Annually
System Fluid Filter Change
11. FACSCount Maintenance Record Recording Data
About Service Visits
12. CD4 Enumeration Quality Assurance Quality Control Procedures
Internal Controls
Evaluate Patient Data
T-Sum
CD3 Consistency Check
Positive Reagent Control
Specimen Integrity
Reagent Quality Control
13. CD4 Enumeration Quality Assurance Reference Ranges
Proficiency Testing
Clerical Processing
Quality Improvement
Use of the Reagent Log
14. Data Reporting of CD4 Test Results Supervisory Review
Interpret in the Proper Context
Provide Appropriate Information
Provide Legible Results
Retain Files for a Sufficient Length of Time
Notify the Physician If Results Are Below a Critical Level
Specify a Turnaround Time
Control Patient Data
15. Proficiency Testing Formal Programs
CAP
NEQAS
Peer Review Processes
Country-Based Organizations
Specimen Concerns
16. Proficiency Testing
17. Clinical Training What is it?
Why it is Important
Know the Audience (if you can!)
Lesson Plan
Feedback