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Device-associated Module CLABSI Central Line-Associated Bloodstream Infection CLABSI Event Introduction An estimated 41 000 central line-associated bloodstream infections CLABSI occur in U*S* hospitals each year. 1 These infections are usually serious infections typically causing a prolongation of hospital stay and increased cost and risk of mortality. CLABSI can be prevented through proper insertion techniques and management of the central line. These techniques are addressed in the CDC s...

How to fill out device-associated module clabsi

How to fill out Device-associated Module CLABSI

1. Access the Device-associated Module CLABSI form from the designated health data system.
2. Read the instructions provided at the beginning of the form for context.
3. Identify the specific patient and their associated devices for the reporting period.
4. Document the dates of device insertion and removal accurately.
5. Record any relevant clinical data, including infection signs or laboratory results.
6. Fill in sections related to the type of device and duration of use.
7. Ensure all mandatory fields are completed as indicated by asterisks.
8. Review the information entered for errors or omissions.
9. Submit the completed form according to the facility's protocols.

Who needs Device-associated Module CLABSI?

1. Healthcare professionals managing patients with central lines, catheters, or ventilators.
2. Infection preventionists who monitor and report CLABSI rates.
3. Quality assurance personnel for data collection and hospital accreditation needs.
4. Regulatory agencies requiring infection data for public health monitoring.

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What is an eligible BSI organism?

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What is the function of the NHSN group?

What are NHSN Groups? A Group is a collection of facilities that have joined together within the NHSN framework to share some or all of their data at a single (Group) level for a mutual purpose (e.g., performance improvement, state and/or public reporting).

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What is Device-associated Module CLABSI?

The Device-associated Module CLABSI refers to a specific reporting framework used to track and manage central line-associated bloodstream infections (CLABSIs) that are associated with the use of central venous catheters.

Who is required to file Device-associated Module CLABSI?

Healthcare facilities that provide inpatient care and are engaged in monitoring and reporting CLABSI cases as part of their infection prevention and control programs are required to file the Device-associated Module CLABSI.

How to fill out Device-associated Module CLABSI?

To fill out the Device-associated Module CLABSI, healthcare facilities must collect data related to CLABSI cases, including patient demographics, clinical information, device utilization, and laboratory results, and accurately enter this data into the reporting system as per the guidelines.

What is the purpose of Device-associated Module CLABSI?

The purpose of the Device-associated Module CLABSI is to standardize the collection and reporting of CLABSI cases to improve patient safety, inform infection prevention strategies, and enhance the overall quality of healthcare.

What information must be reported on Device-associated Module CLABSI?

The information that must be reported on the Device-associated Module CLABSI includes the date of infection, patient identifiers, central line details, organism identification, and any other relevant clinical data required for accurate tracking and analysis of CLABSIs.