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DEVICE SAFETY

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DEVICE SAFETY – PowerPoint PPT presentation

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Title: DEVICE SAFETY


1
DEVICE SAFETY STANDARDIZATION COMMITTEE
2
DEVELOPMENT
  • Infusion Device Task Force/CPI Team August,
    2000
  • Institute of Medicine Report
  • National publicity
  • Sponsored by PT Committee

3
RECOMMENDATIONS
  • Infusion device standardization
  • Multidisciplinary committee with representation
    from all areas to address safety issues
  • Training and competency validations
  • Policy development and revision Role of Health
    Care Safety Task Force

4
  • Device Safety Standardization Committee (DSSC)
    formed in February 2002
  • All recommendations from CPI Team transitioned to
    this committee

5
RESPONSIBILITIES
  • Complete the infusion device transition
  • Provide recommendations regarding safety and
    standardization of devices to include evaluation
    of new devices and review of current devices
  • Develop and maintain a formulary of approved
    devices
  • Provide consultation of device safety and
    standardization
  • Oversee the education and compliance components
    of device safety in conjunction with the
    Equipment Safety Committee

6
MEMBERSHIP COMPOSITION
  • Patient care areas
  • Education
  • Pharmacy
  • Clinical Equipment Service
  • Risk Management
  • Quality Management
  • Anesthesia Faculty
  • Hospital Administration
  • Value Analysis Coordinating Committee member
  • Equipment Safety Sub-committee member
  • Safety Management Sub-committee member

7
REPORTING
  • UTMB Network of Quality of Care Committee
  • ( direct report quarterly)
  • Information sharing through joint committee
    membership
  • Health Care Safety Task Force
  • Value Analysis Coordinating Committee
  • Environment of Care Equipment Safety
  • Safety Management Sub-committee

8
REQUEST PROCESS
  • UTMB Product Request Form
  • UTMB Capitol Equipment Questionnaire
  • Consultation request to DSSC chair

9
Recent Device Selection Process
  • Identification of need to replace large volume
    infusion device
  • Potential devices identified by DSSC through
    review of
  • ECRI Reporting
  • MD Buyline
  • Two potential devices were identified for
    demonstration to the committee

10
Recent Device Selection Process (contd)
  • Eligibility for pilot determined by
  • Previously established criteria determined by
    DSSC
  • Maude Search
  • UHC inquiries
  • Updated reports from ERCI and MD Buyline
  • One pump identified for pilot and was reviewed
    and pilot supported by the Pharmacy Nursing
    Committee.
  • Pilot completed
  • Pilot evaluations reviewed by DSSC
  • DSSC recommends purchase

11
Progress
  • Infusion device standardization completed
  • Program for of education and competency
    validation in progress
  • Formulary of approved safety devices under
    development
  • Vital sign machines
  • Defibrillators

12
For additional information contactrjensen_at_utmb.e
du
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