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Katherine Allen-Bridson, RN, BSN, MScPH, CIC,

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Title: Katherine Allen-Bridson, RN, BSN, MScPH, CIC,


1
Performing CAUTI Surveillance for Participation
in the CMS IRF Quality Reporting Program
  • Katherine Allen-Bridson, RN, BSN, MScPH, CIC,
  • Centers for Disease Control and Prevention
  • National Center for Emerging and Zoonotic
    Infectious Diseases

Training for Inpatient Rehabilitation
Facilities May 2, 2012
Nothing to Disclose
  • Division of Healthcare Quality Promotion

2
Objectives
  1. State the purposes of the Centers for Disease
    Control and Preventions (CDC) National
    Healthcare Safety Network (NHSN).
  2. Define methodology for Catheter-associated
    Urinary Tract Infection (CAUTI) surveillance.
  3. Define the CAUTI data required and method to
    report through the NHSN in order to meet
    requirements for the Centers for Medicare and
    Medicaid Services Quality Reporting Program (QRP)
    for Inpatient Rehabilitation Facilities (IRFs).
  4. Identify basic steps required for facility
    enrollment in NHSN.
  5. Identify the rehabilitation location types for
    which CAUTI surveillance can be performed.

3
What is NHSN?
www.cdc.gov/nhsn
  • Web-based system launched by CDC in 2005 for
    surveillance of healthcare-associated infections
    (HAI), other adverse events, and prevention
    practices.
  • Technical design enables manual data entry or
    electronic reporting.

4
Purposes of NHSN
  • Comply with legal requirements including but
    not limited to state or federal laws,
    regulations, or other requirements for
    mandatory reporting of healthcare
    facility-specific adverse event, prevention
    practice adherence, and other public health data.
  • Enable healthcare facilities to report HAI and
    prevention practice adherence data via NHSN to
    the U.S. Center for Medicare and Medicaid
    Services (CMS) in fulfillment of CMSs quality
    measurement reporting requirements for those
    data.
  • Provide state departments of health with
    information that identifies the healthcare
    facilities in their state that participate in
    NHSN.
  • Provide to state agencies, at their request,
    facility-specific, NHSN patient safety component
    and healthcare personnel safety component adverse
    event and prevention practice adherence data for
    surveillance, prevention, or mandatory public
    reporting.

5
Three Main NHSN Components
  • Patient Safety Component (will discuss in detail)
  • Healthcare Personnel Safety Component
  • Blood / Body Fluids Exposure Module
  • Influenza Vaccination and Exposure Management
    Module
  • Biovigilance Component
  • Hemovigilance Module (Blood Safety)

6
Patient Safety Component5 Modules
7
Device-associated Module 5 Events
  • CLABSI Central line-associated bloodstream
  • infection
  • CLIP Central line insertion practices
  • VAP Ventilator-associated pneumonia
  • CAUTI Catheter-associated urinary tract
    infection
  • DE Dialysis event

For outpatient dialysis only
8
NHSN Surveillance Methodology
  • ACTIVE vs. PASSIVE
  • ACTIVE Trained personnel use standard definitions
    and a variety of data sources to investigate and
    identify events.
  • PASSIVE Personnel, such as staff nurses, not
    trained to do surveillance may report events. No
    purposeful investigation for infections occurs.

9
NHSN Surveillance Methodology2
  • PATIENT-BASED vs. LABORATORY-BASED
  • PATIENT-BASED Monitoring patients for events,
    risk factors, and procedures and practices
    related to patient care
  • Visit patient care areas
  • Review patient charts
  • Discuss with caregivers
  • LABORATORY-BASED Case-finding based on positive
    lab findings

10
NHSN Surveillance Methodology3
  • PROSPECTIVE vs. RETROSPECTIVE
  • PROSPECTIVE Monitoring patients while still in
    the institution includes post-discharge period
    for surgical site infections (SSI)
  • RETROSPECTIVE Case-finding based solely on
    chart review after patient discharged

11
Healthcare-associated Infection (HAI)
  • A localized or systemic condition resulting from
    an adverse reaction to the presence of an
    infectious agent(s) or its toxin(s) that
  • Occurs in a patient in a healthcare setting
  • And
  • Was not present or incubating at the time of
    admission, unless the infection was related to a
    previous admission

12
NHSN and CMSQuality Reporting Program
13
Healthcare Facility HAI Reporting to CMS via NHSN
Current and Proposed Requirements DRAFT
(11/14/2011)
HAI Event Facility Type Reporting Start Date
CLABSI Acute Care Hospitals Adult, Pediatric, and Neonatal ICUs January 2011
CAUTI Acute Care Hospitals Adult and Pediatric ICUs January 2012
SSI Acute Care Hospitals Colon and abdominal hysterectomy January 2012
I.V. antimicrobial start Dialysis Facilities January 2012
Positive blood culture Dialysis Facilities January 2012
Signs of vascular access infection Dialysis Facilities January 2012
CLABSI Long Term Care Hospitals October 2012
CAUTI Long Term Care Hospitals October 2012
CAUTI Inpatient Rehabilitation Facilities October 2012
MRSA Bacteremia LabID Event Acute Care Hospitals January 2013
C. difficile LabID Event Acute Care Hospitals January 2013
HCW Influenza Vaccination Acute Care Hospitals January 2013
HCW Influenza Vaccination ASCs October 2014
SSI (future proposal) Outpatient Surgery/ASCs TBD
Long Term Care Hospitals are called Long Term Acute Care Hospitals in NHSN Long Term Care Hospitals are called Long Term Acute Care Hospitals in NHSN Long Term Care Hospitals are called Long Term Acute Care Hospitals in NHSN
14
NHSN and CMS
  • CMS Final Rules in Federal Register published
    August 18, 2011.
  • Must follow NHSN CAUTI protocol exactly and
    report complete and accurate data.
  • Data must be reported to NHSN by means of manual
    data entry into NHSN web-based application or via
    file imports using the Clinical Document
    Architecture (CDA) file format.
  • Pass quality control acceptance checks that
    assess the data for completeness and accuracy.

15
NHSN and CMS, contd
  • NHSN requires data to be submitted monthly
    (within 30 days of the end of the month in which
    it is collected) so it has the greatest impact on
    infection prevention activities.
  • Data must be entered into NHSN no later than 4 ½
    months after the end of the quarter to be shared
    with CMS.
  • E.g. Q1 (January-March) data must be entered into
    NHSN by August 15 Q2 by November 15 Q 3 by
    February 15 and Q4 by May 15
  • Does not preempt any state mandates for CAUTI
    reporting to NHSN.

16
NHSN and the CMS Annual Payment Update (APU)
Hospital/IRF Inpatient Quality Reporting (IQR)
Program
  • Hospitals/IRFs enter quarterly HAI data into NHSN
  • lt 4 ½ months following the end of the reporting
    quarter
  • CDC prepares facility-specific HAI summary
    statistics that are submitted in monthly and
    quarterly files to CMS using a secure QualityNet
    exchange account
  • Hospitals/IRFs can view their own HAI summary
    statistics at a secure CMS website where the APU
    Dashboard is posted (for more information see
    http//www.qualitynet.org/dcs/ContentServer?cPage
    pagenameQnetPublic2FPage2FQnetBasiccid122869
    4346716)

17
ENROLLMENT INTO NHSN
  • http//www.cdc.gov/nhsn/enroll.html

18
Facility Administrators Usersshould complete
allrequired NHSN Trainingsbefore beginning
Enrollment
  • http//www.cdc.gov/nhsn/training.html

19
NHSN Facility AdministratorEnrollment Guide
  • http//www.cdc.gov/nhsn/PDFs/FacilityAdminEnrollme
    ntGuideCurrent.pdf

20
NHSN Facility Administrator
  • Only one Facility Administrator per facility
  • Only person who can enroll a facility
  • Responsible for initial set-up
  • Adding locations
  • Adding users and assigning user rights
  • Joining and conferring rights to groups

21
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22
Enrollment into NHSN
  • NHSN Registration http//nhsn.cdc.gov/Registration
    Form/index.jsp

23
2 IRF Enrollment Options
  • Freestanding, separately licensed facility
  • Location within an Acute Care Facility

24
Enrollment RequirementsIRFs Requiring Unique
NHSN orgID
  • Enroll in NHSN as a separate facility if
  • Free standing licensed IRF with a CCN (CMS
    Certification Number) with the last four digits
    between 3025-3099
  • Identify as HOSP-REHAB facility type

25
Enrollment RequirementsIRFs Requiring Unique
NHSN orgID
  • Annual survey required
  • Complete new, rehabilitation specific annual
    survey for calendar year 2011
  • Use whole numbers without decimal points
  • Two locations Adult and Pediatric IRF

26
Rehabilitation Facility Locations
CDC Definitions
Page 15-13 of NHSN Patient Safety Component Manual
27
Enrollment Requirements IRF Units Within a
Hospital
  • Set-up as Inpatient Rehabilitation Ward location
    within an enrolled acute care or critical access
    facility type if
  • IRF unit within a hospital and 3rd character of
    CCN is either a T or an R
  • Additional questions are required for licensed
    IRF units within hospitals to be identified for
    CMS reporting.

28
Rehabilitation Locations Within Hospital
CDC Definitions
Page 15-8 of NHSN Patient Safety Component Manual
29
Beyond Enrollment
30
Annual Survey IRF
  • Annual survey required for HOSP REHAB facility
    type
  • Must complete a new IRF-specific annual survey
    for calendar year 2011.
  • Use whole numbers without decimal points.

31
Monthly Reporting Plan
  • CAUTI must be included in Monthly Reporting Plan
    for data to be reported on behalf of the facility
    to CMS.
  • Locations Inpatient Adult and Pediatric
    Rehabilitation Wards

Example for freestanding IRF
AddLocations
32
Monthly Reporting Plan, contd
  • The Monthly Reporting Plan informs CDC which
    modules a facility is following during a given
    month.
  • A facility must enter a Plan for every month of
    the year, even those in which no modules are
    followed.
  • A facility may enter data only for months in
    which Plans are on file.

Reminder!
33
Reporting Numerator and Denominator Data
  • Report each CAUTI detected or indicate that no
    CAUTI occurred for reporting locations. (Found
    on Denominator screen).
  • Report total device days and total patient days
    for reporting locations, including months in
    which no CAUTIs were identified and/or no patient
    days or urinary catheter days occurred.

34
RESOURCES
35
Resources for NHSN
http//www.cdc.gov/nhsn/index.html
36
Resources for Surveillance
  • NHSN Patient Safety Component Manual, January
    2012
  • Ch 3 Monthly Reporting Plan
  • Ch 7 CAUTI Protocol (January 2012)
  • Ch 14 Tables of Instructions
  • Ch 16 Key Terms

http//www.cdc.gov/nhsn/TOC_PSCManual.html
37
Resources for Surveillance, contd
  • NHSN Forms (June 2011)
  • 57.106 Monthly Reporting Plan
  • 57.114 Urinary Tract Infection
  • 57.118 Denominators for Intensive Care Unit
    (ICU)/ Other locations (not NICU or SCA)

http//www.cdc.gov/nhsn/forms/Patient-Safety-forms
.html
38
Available Training
  • Training
  • Device Associated Module
  • Pre-recorded Webinars
  • Lectoras

http//www.cdc.gov/nhsn/training/
39
Available Training, contd
  • NHSN Enrollment Facility Set-up (Slidesets
    PDFs)
  • Overview of the Patient Safety Component,
    Device-associated module (Slideset PDF)
  • Data Entry, Surveillance, Analysis, Data Entry,
    Import, and Customization (Slideset PDF)
  • Introduction to the Device-associated Module
    (Training Course with quiz)
  • Catheter-associated Urinary Tract Infection
    (CAUTI) (Training Course with quiz)

http//www.cdc.gov/nhsn/training/
40
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