Cholestech Ldx System Certification Quiz

The optics check should be run each day before patient samples are tested to ensure accurate and reliable results. By performing this check daily, any potential issues or malfunctions with the optics system can be identified and addressed promptly, reducing the risk of erroneous test results. Regularly monitoring the optics before testing patient samples is crucial in maintaining the quality and integrity of the laboratory's analytical processes.

Good fingerstick technique involves obtaining a free flowing drop of blood, wiping the first drop of blood off the finger, and cleaning the finger well with alcohol. Allowing air bubbles into the capillary tube is not a part of good fingerstick technique as it can interfere with the accuracy of the blood sample and may cause inaccurate results. Air bubbles can affect the volume of blood in the capillary tube, leading to incorrect measurements. Therefore, it is important to avoid introducing air bubbles into the capillary tube during the fingerstick procedure.

The correct answer is "Immediately" because the sentence states that after the blood has been dispensed into the sample well of the cassette, the next step is to place the cassette in the drawer and press RUN. Therefore, there is no waiting time mentioned in the sentence, indicating that the action should be done without delay.

Quality control is a process that ensures the system or product meets the required standards. In this case, running quality control helps to verify that the system is functioning properly. It ensures that all components and functions of the system are working as intended, identifying any potential issues or errors. By conducting quality control, any problems can be addressed and resolved, ensuring the system's reliability and accuracy. The other options mentioned, such as using cassettes, checking pipette function, and complying with state requirements, may be part of the quality control process, but ultimately the main purpose is to verify the system's proper functioning.

The DATA button allows the user to view the last reported results. This means that when the user presses the DATA button, they will be able to access and review the most recent test results. It provides a convenient way for the user to retrieve and analyze the data from previous tests.

The LDX does not require a room with 25% humidity. The other requirements listed, such as room temperature, a stable work surface, and no direct sunlight, are necessary for the LDX. However, the humidity level is not specified as a requirement for the LDX.

The correct answer is to call Cholestech Technical Service. This is the most appropriate option as it directly relates to any questions or issues regarding the operation of the Cholestech LDX System. Cholestech Technical Service is likely to have the necessary expertise and knowledge to provide assistance and guidance in resolving any technical problems or concerns.

Before testing, the cassette should warm up, unopened, at room temperature for 10 minutes. This is because allowing the cassette to warm up helps to ensure accurate and reliable test results. The warming up process allows the cassette to reach the same temperature as the testing environment, reducing the potential for temperature variations to affect the test outcome. Waiting for 10 minutes provides enough time for the cassette to equilibrate with the room temperature, ensuring optimal testing conditions.

It is important to disconnect the analyzer from the power source before removing the replaceable ROM pack to ensure safety and prevent any damage to the equipment. Removing the power source reduces the risk of electrical shock and allows for a safe removal of the ROM pack.

The correct answer suggests using a Cholestech Mini-Pet™ and pipette tips to place the quality control sample into the cassette. This implies that the Cholestech Mini-Pet™ and pipette tips are the appropriate tools for accurately and precisely transferring the control sample into the cassette.

Serum samples should not be tested using the "Whole B." type. The "Whole B." type is typically used for fingerstick samples, quality control samples, and venous whole blood samples. Serum samples are obtained by allowing the blood to clot and then removing the clot and the blood cells, leaving only the liquid portion (serum). This liquid portion is then used for testing. Therefore, serum samples should be tested using a different type of sample, not the "Whole B." type.

If an optics check reading is outside the range, it indicates that there is an issue with the analyzer. This means that the analyzer will not function properly and may not provide accurate results. Therefore, it is not advisable to run patient samples or record the results on the optics check log. Instead, it is recommended to run the quality control material to ensure the accuracy and reliability of the analyzer.

not-available-via-ai

The sample in the capillary tube should be dispensed into the cassette in less than 5 minutes because after a certain amount of time, the sample may start to degrade or undergo changes that could affect the accuracy of the test results. It is important to transfer the sample as quickly as possible to ensure the most reliable and accurate results.

To perform a CHD Risk assessment, one should select "Risk = CHD Risk" in the configuration menu. This step is necessary to set up the device for assessing the risk. Running a cassette with total cholesterol and HDL cholesterol is also required as it provides the necessary data for the assessment. Pushing the DATA button twice after the results appear on the screen is not mentioned as a step in the process. Running a TC•GLU cassette is not mentioned as a step either, so it is not necessary for the CHD Risk assessment.