Final answer:
For a glucose monitor quality control record, important information to include is the date of the battery change and the time that control values were recorded, ensuring the accuracy and reliability of the device's performance.
Step-by-step explanation:
When completing a glucose monitor quality control record, it is essential to include details that ensure the accuracy and reliability of the glucose monitoring system. This does not include daily patient test results or the physician's NPI number, as these are not related to the quality control of the device. Instead, the correct information to record is the date of battery change and the time that values were recorded.
Recording the date of battery change is crucial because a low or depleted battery can cause inaccurate readings. The time that the control values were recorded helps to establish a reliable record for identifying any patterns or issues with the device's performance over time. Quality control records are fundamental in ensuring that the device is functioning correctly and providing reliable data for patient management.
In clinical settings, a nurse may review a number of items with the team, such as the name of the procedure as recorded, sponge and instrument counts, specimen labeling, and any equipment issues. Despite this, for glucose monitor quality control, the main concerns are device-specific factors like battery change dates and timing of quality control checks.
Learn more about Glucose Monitor Quality Control Record