Subscriber Login Students | Administrators
Online compliance and continuing education courses for clinical laboratories

Analytic Information and Courses from MediaLab, Inc.

These are the MediaLab courses that cover Analytic and links to relevant pages within the course.

Learn more about laboratory continuing education for medical technologists to earn CE credit for AMT, ASCP, NCA, and state license renewal and recertification. Or get information about laboratory safety and compliance courses that deliver cost-effective OSHA safety training and continuing education to your laboratory's employees.

Laboratories Individuals

Introduction to Quality Control
Additional Variables

To ensure reliability of results, many other factors besides controls are monitored. These include: water quality analytic balance calibration glassware calibration centrifuge calibration thermometer calibration electric power stability heating bath temperatures refrigerator temperatures freezer temperatures expiration of reagents, standards, and controls instrument maintenance procedure manuals, including written step-by-step procedures of all tests performed by laboratory method selection, based on local population and clinician needs normal range verification based on the local population technical competencies of laboratory staff members

View Page

Medical Error Prevention (retired)
Root Causes are specific, underlying, and identifiable reasons that ________ occur.View Page
Analytic Medical Errors

Medical errors also occur in the analytic processes and systems of patient care. Analytic errors begin with problems in the transportation of medical samples for testing. These occur between the patient's location and the testing facility. They happen during the time between specimen collection and arrival in the testing facility. The possibility for analytic medical error continues through the analytic processes and procedures of medical testing. Analytic medical error also includes systems, processes, and procedures involved in the transmission and reporting of test results. These medical errors occur during the time the laboratory is directly involved in receiving, analyzing, and reporting test samples. Examples: Wrong transport storage or temperature Delay in transport Sample mixup during transport Acceptance of unacceptable samples that are insufficient, hemolyzed, or clotted Centrifugation, mixing, and other test sample preparation errors Wrong test procedures Test control errors Sample mixup during testing Outdated reagents Wrong reagents Test result mixup Transcription errors Data reporting process errors Result report delays

View Page

Quality Control
Why Run Controls?

Running controls helps monitor and control analytic error when performing a testing procedure. The bottom line: can we accept this test's results with certainty? There is no one quality control format that is appropriate or practical for every testing situation; nor will a single QC system detect every error.

View Page
Possible Corrective Action (4)

Review calibration of the test instrument.What was the date of the last calibration? Test instruments need to be calibrated according to the manufacturer’s instructions or more frequently if necessary. Federal requirements call for analytic tests to be recalibrated at least every six months to verify the accuracy of the testing procedure.

View Page

Risk Management in the Clinical Laboratory
Introduction to Patient Safety and Risk Exposures

Laboratory quality management and risk management plans that address processes in the preanalytic, analytic, and postanalytic phases of testing are key elements in ensuring patient safety. The preanalytic phase of testing includes all processes prior to the actual testing of a specimen. The analytic phase consists of all the processes involved in the testing of a specimen, and the postanalytic phase includes all the processes involved after test analysis.

View Page
Analytic Phase

Errors occur much less frequently in the analytic phase of laboratory testing than in either the preanalytic or postanalytic phases. The supposition of published studies on the error rate in this category is that the percentages remain low primarily because of: The qualifications of testing personnel Effectiveness of internal quality control programs and external assessment practices which assist in identifying analytical errors and detecting possible sources.Following is a list of examples of errors that may be encountered during the analytic testing activities. The list includes both human and instrumentation errors. While random errors (those that occur independently of the operator) may be encountered during the analytic phase, primarily listed are systematic errors. That is, errors that bias the measurement resulting from either instrument malfunctions or human mistakes. Errors in quality control and verification of performance specifications. Instrument malfunctions. Calibration errors causing a direction of bias in results. Manual pipetting errors. Reagent errors. Test interference caused by unsuspected antibodies. Specimen interference i.e. failing to visually see sample was lipemic. Math errors. Staff errors in testing preparation and processing. Inadequate staffing which may precipitate errors caused by fatigue.

View Page
The majority of all laboratory errors occur during which phase of laboratory testing?View Page


MediaLab, Inc.

http://www.MediaLabInc.net    |    (877) 776-8460 (tollfree)    |    sales@medialabinc.net