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Procedure: Neogene GBS Procedure and revision number: SN134763 REV. 09/19Catalog # 410200Institution:Address: Department:Prepared By: Date Adopted Supersedes procedure #:Distributed To: # of Copies Distributed
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Revogene gbs lb rapid is typically used by healthcare professionals, specifically those involved in the screening and diagnosis of Group B Streptococcus (GBS) infections.
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Revogene GBS LB Rapid is a molecular diagnostic test used for the rapid detection of Group B Streptococcus (GBS) and Listeria monocytogenes (LB) in pregnant women and newborns.
Healthcare providers and laboratories that conduct the Revogene GBS LB Rapid test are typically required to file the results to ensure proper patient management and public health recordkeeping.
The Revogene GBS LB Rapid test form should be filled out with patient identification information, test details, results, and clinician information as per the guidelines provided by the testing laboratory.
The purpose of the Revogene GBS LB Rapid test is to quickly identify the presence of Group B Streptococcus and Listeria monocytogenes to prevent serious infections in newborns during delivery.
The information that must be reported includes patient demographics, test results, the method of testing, the date of the test, and interpretations as necessary.
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