What is the purpose of the Negative HIV Test form?
The Negative HIV Test form serves to document the results of an HIV antibody screening test. It provides essential information about the client, including their name, date of birth, race, and the testing location. The form is crucial for tracking test results and ensuring appropriate follow-up care.
What information is required on the form?
The form requires several key pieces of information. This includes the client's name, date of birth, race, the date of the test, and the testing location. Additionally, it documents the HIV antibody screening test result, which can be either reactive or negative/non-reactive. Follow-up appointment details and signatures from both the client and counselor are also necessary.
How is the test result categorized?
The test result is categorized as either reactive or negative/non-reactive. A reactive result indicates that the test detected HIV antibodies, while a negative/non-reactive result suggests that no antibodies were found. It is important to note that all reactive results require confirmation through additional testing.
What should be done if the test result is reactive?
If the test result is reactive, it is essential to schedule a follow-up appointment for confirmatory testing. The form will typically indicate the date, time, and location for this follow-up. Clients should be informed about the next steps and provided with support resources.
What is the significance of the CLIA number on the form?
The CLIA number, or Clinical Laboratory Improvement Amendments number, identifies the testing facility. It ensures that the laboratory meets federal standards for laboratory testing. This number is crucial for maintaining compliance and ensuring the reliability of test results.
How are storage temperatures monitored for test devices?
Storage temperatures for test devices are monitored through a daily log. The acceptable temperature range for the Clearview® COMPLETE test is between 8 to 30°C (46 to 86°F). Any deviations from this range must be documented, along with corrective actions taken to ensure the integrity of the tests.
What should be done if the storage temperature is out of range?
If the storage temperature is out of range, corrective actions must be taken immediately. This includes documenting the temperature, the date and time of the incident, and any actions taken to rectify the situation. Ensuring proper storage conditions is vital for maintaining the accuracy of test results.
Who is responsible for reviewing and signing the test results?
The test results must be reviewed and signed by a qualified individual, typically a counselor or healthcare provider. This review process ensures that the results are accurate and that clients receive appropriate information and follow-up care based on their results.
How is the test wait time recorded?
The test wait time is recorded as the duration from the start of the test to the reading of the test results. This information is crucial for ensuring that tests are conducted according to the manufacturer's instructions and that results are reported promptly to clients.