CLIA Flashcards
What is Clinical Laboratory Improvement Amendments (CLIA)?
- federal regulation (law)
- regulates all laboratory testing (except research) on human samples
- established quality standards
T/F Only some labs need CLIA licenses.
FALSE
ALL labs must have CLIA license to do business of laboratory testing (except research) on human specimens
CLIA regulations are site _________.
Neutral
All regulations are the same no matter the location, size of location or type of laboratory.
Are CLIA licenses facility or personnel based?
Facility
The laboratory is issued a certificate in which categories (4)?
Waived PPM Moderate High categories are based on complexity of testing method/instrument and how complex it is for the person to perform the test.
T/F testing personnel are responsible for all aspects of the lab operation.
FALSE
Director: responsible for all aspects of lab operation (MD, CLS)
Testing personnel: education, on-site training, yearly competency assessment
Procedure Manual Requirements are:
A) Specific guidelines for each test performed
B) Must be approved and signed/dated by lab director initially, then yearly, and with each change
C) Available to all testing personnel
D) Provide procedural steps to perform the test
E) All of the above
E) All of the above
It also provides information about:
- specimen collection, handling, processing
- instrumentation calibration, verification, maintenance
- quality control requirements, frequency, evaluation
What are quality control requirements? How long are records maintained?
How often must quality control must be tested and how to determine the validity.
Must be maintained for at least 2 years.
-5years immunohematology
-10 years pathology
Accuracy, Precision, Sensitivity, Specificity, Linearity, Reportable Range, and Reference Range are examples of:
Method Verification Requirements
T/F In order to maintain CLIA certification (moderate-high complexity) proficiency testing is performed periodically.
True
Lab enrolls in a approved testing program. The PT program sends lab ‘unknown’ specimen, lab runs the tests, sends the results back, and must PASS to maintain certification.
Quality assurance program evaluates the ongoing and overall of the total testing process through: A) Error detection B) Corrective actions C) Incorporating future improvements D) all of the above
D) All of the above
Patient test management requirements: Lab must define specific policies to ensure maintaining sample integrity and _______ _________ identification throughout the testing process.
Positive patient
T/F laboratories must be accredited once every 10 years.
FALSE - every 2 years by: CMS or CMS approved organization JCAHO, CAP, COLA
What is waived testing?
simple laboratory examinations and procedures, little risk of error
pose no reasonable risk of harm to the patient if the test is performed inaccurately
Which of the following is NOT an example of waived testing? A) Dipstick UA B) Hemoglobin (hemacue) C) Complete Blood Count D) Strep A E) Blood Glucose F) Fecal occult blood G) Urine pregnancy H) Non-automated ESR I) Spun hematocrit
C) Complete Blood Count is NOT waived testing
others include:
FDA approved for home use: glucose self-monitoring, pregnancy, ovulation
Fecal occult blood
Urine pregnancy
Non-automated ESR
Spun hematocrit