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MRSA/CDI Laid Event Reporting Guidance, Flow sheets, and Case ExamplesLabID Event Report An event report must be filled out and submitted too MUCH for each case of a laboratory confirmed MRSA or CDI,
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The MRSA/CDI LabID event reporting is a process of reporting healthcare-associated infections of MRSA and C. difficile to the Centers for Disease Control and Prevention (CDC).
Healthcare facilities such as hospitals, nursing homes, and long-term care facilities are required to file MRSA/CDI LabID event reporting.
MRSA/CDI LabID event reporting can be filled out electronically through the National Healthcare Safety Network (NHSN) platform.
The purpose of MRSA/CDI LabID event reporting is to track and monitor healthcare-associated infections caused by MRSA and C. difficile in healthcare facilities.
Information such as patient demographics, laboratory test results, and infection control practices must be reported on MRSA/CDI LabID event reporting.
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