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The document outlines the purpose, procedure, materials, safety measures, and limitations related to the OneStep+ Strep A Dipstick Test for the rapid detection of Group A Streptococcal antigen.
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How to fill out onestep+ strep a dipstick test

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How to fill out onestep+ strep a dipstick test

01
Gather all necessary materials: onestep+ strep A dipstick test kit, timer, sterile swabs, and a specimen container.
02
Collect a throat swab sample using a sterile swab, ensuring to swab both tonsils and the back of the throat.
03
Place the swab in the specimen container and follow the kit instructions to prepare the sample.
04
Open the onestep+ strep A dipstick test and dip it into the processed sample for the recommended amount of time.
05
Remove the dipstick and place it on a clean, dry surface.
06
Wait for the specified time according to the kit instructions for the results to develop.
07
Read the results: compare the test line and control line according to the provided interpretation guide.

Who needs onestep+ strep a dipstick test?

01
Individuals displaying symptoms of strep throat, such as a sore throat, fever, or swollen lymph nodes.
02
Patients in environments where group infections can occur, such as schools or camps.
03
Individuals who have had close contact with someone diagnosed with strep throat.

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The onestep+ strep a dipstick test is a rapid diagnostic test used to detect the presence of Group A Streptococcus bacteria, which cause strep throat.
Healthcare providers, such as doctors or nurse practitioners, are required to perform and file results from the onestep+ strep a dipstick test.
To fill out the onestep+ strep a dipstick test, follow the manufacturer's instructions for sample collection, testing, and result recording, ensuring that all necessary patient information is accurately documented.
The purpose of the onestep+ strep a dipstick test is to quickly and accurately diagnose strep throat infection, facilitating timely treatment.
The information that must be reported includes the test results (positive or negative), patient identification details, date and time of the test, and the healthcare provider's name.
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