Experience of JACIE in a Large BMT Unit - PowerPoint PPT Presentation

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Experience of JACIE in a Large BMT Unit

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... transplants / yr (40% allogeneic) Apheresis unit. 270 PBSC aphereses ... New SOP to cover transportation from apheresis unit to laboratory. Stem Cell Laboratory ... – PowerPoint PPT presentation

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Title: Experience of JACIE in a Large BMT Unit


1
Experience of JACIE in a Large BMT Unit
  • Dr Jenny Byrne
  • Nottingham City Hospital, UK

2
Nottingham BMT Programme
  • Programme Director
  • Prof NH Russell
  • Transplant Consultants
  • Dr J Byrne
  • Dr EP Das-Gupta
  • Dr AP Haynes / Dr AK McMillan (lymphoma PBSCT)
  • Clinical Programme
  • approx 130 transplants / yr (40 allogeneic)
  • Apheresis unit
  • 270 PBSC aphereses / yr
  • Stem Cell Processing Laboratory
  • gt 300 products processed / yr

3
Rationale for Early JACIE Accreditation
  • Prof NH Russell attended JACIE inspector training
    course in March 2001
  • Quality Management structure set up in April 2001
  • Successful stem cell laboratory MHRA inspection
    in 2002
  • Dr J Byrne attended JACIE Training course Sept
    2002
  • Inspections to roll out in UK in 2004
  • Aim to get it over with
  • Cheaper! (EU grant in 2004)

4
Quality Management Programme
  • Essential component for JACIE accreditation
  • Need evidence to show operational for at least 12
    months prior to inspection
  • Designated quality Manager required to
  • Write Quality Management Plan
  • Monitor quality of transplant programme eg
    audits, outcome parameters
  • Coordinating actions required to implement the
    system
  • Report progress and current situation regularly
  • Detecting, evaluating and reporting errors and
    implementing corrective actions
  • Document control and ensuring SOPs updated

5
Objectives of the Quality Management Programme
  • Ultimate goal of quality assurance is to control
    processes so that quality is built into the
    service that is delivered
  • Primary objective of the Quality Management
    Programme is to ensure that all aspects of the
    Transplant Programme conform to established
    standards
  • Provide evidence that all systems and procedures
    that influence quality are working as expected
    with the aim of preventing errors

6
Requirements Of The Quality Management Programme
  • Each Transplant Unit must have a Quality
    Management Plan outlining how it will implement
    its quality assurance activities
  • Must be a designated person to oversee the
    quality programme
  • may be an external quality manager or a member of
    the Transplant team (need sufficient knowledge to
    identify problems in the processes under review)
  • Must include all aspects of the transplantation
    service including stem cell collection
    processing

7
Nottingham Quality Management Team
  • No funding available for dedicated Quality
    Manager
  • Quality Management duties written into job
    descriptions of selected staff members
  • Overall Quality Manager
  • Dr JL Byrne
  • Delegated Quality Officers
  • Stem cell laboratory quality officer
  • Stem cell collection quality officer
  • Clinical transplantation service quality officer
  • Ownership of transplant programme and QM
    culture developed

8
Duties Of The Quality Management Team
  • Maintain and review SOPs / protocols for all
    routine procedures and ensure that these comply
    with established standards
  • Carry out quality audits to ensure that protocols
    and SOPs are adhered to
  • Report and investigate any adverse events or
    near-miss errors on Variance Forms including
    adverse reactions to progenitor cells
  • Ensure that staff are adequately trained in all
    procedures and that their competency and
    proficiency is tested
  • Ensure that research protocols are approved and
    monitored

9
Quality Management Meetings
  • Monthly meetings
  • Chaired by Dr JL Byrne
  • Membership
  • Quality officers from all 3 areas
  • Programme Director
  • Transplant physicians
  • Pharmacist
  • Blood Bank Chief
  • Infection control officer
  • Hospital Clinical Governance representative

10
Quality Management Agenda
  • Stem Cell Laboratory Issues
  • Variance forms / adverse events
  • SOPs, staffing training issues, activity,
    facilities
  • Stem Cell Collection Issues
  • Adverse events / deviation from SOPs
  • Staffing, facilities, SOPs, pt information
    feedback
  • Clinical Issues
  • Staffing issues, facilities, activity rates,
    infection rates, pharmacy issues, blood
    transfusion issues
  • Clinical guidelines / protocols, pt information
  • Incident forms, TRMs, Grade 3-4 toxicities
  • Audits / Outcome Data

11
JACIE Preparations in Nottingham
  • Accreditation applied for Jan 04
  • January 2004, Nottingham JACIE workforce group
    established
  • Representatives from all 3 sections of transplant
    programme invited
  • Regular fortnightly meetings
  • Review of each standard and evidence of
    compliance collected
  • If necessary new documents written / updated
  • Secretary commandeered to gather evidence and
    convert to electronic format

12
JACIE Preparations (cont)
  • June 2004 all evidence collected
  • End June electronic submission of all evidence
  • Slight delay over summer period
  • Inspection date finally set for Oct 2004
  • JACIE workforce meetings continue
  • to check all SOPs in date
  • collect clinical notes and check necessary data
    filed and easy to find
  • gather together all necessary documentation
  • ensure all staff aware

13
Inspection Oct 2004
  • 2 day schedule planned
  • 3 inspectors
  • 1 clinical programme
  • 1 collection facility
  • 1 processing facility
  • (1 observer)
  • Documents required
  • Notes for 10 autografts and 10 allografts
  • SOPs for clinical / collection / processing areas
  • Staff training and competencies
  • Quality documents / audits etc

14
Timetable
  • Day 1
  • Am Welcome and Structure and Organisation of
    BMT programme
  • Introduction to key staff members
  • Document review
  • Pm Guided visits of inspectors to specific
    areas to complete checklist
  • View procedure eg cell return, apheresis,
  • freeze
  • Interview staff members, eg pharmacist
  • Request documents eg SOP for stem cell
  • infusion, consent form for trials

15
Timetable (cont)
  • Day 2
  • Am Complete document review
  • Interview staff members eg quality
  • manager, microbiology Consultant
  • LUNCH
  • Pm Meet privately with Programme Director
  • Exit Interview all staff invited
  • Summarise findings, feedback positives,
    negatives

16
Post Inspection Issues
  • Level 2 accreditation awarded
  • Few points to address
  • Clinical programme
  • Modify bone marrow harvest SOP
  • Stem Cell Collection facility
  • New SOP to cover transportation from apheresis
    unit to laboratory
  • Stem Cell Laboratory
  • Modify 1 label
  • Put in worked examples in SOPs
  • Cross reference SOPs
  • Add references to SOPs

17
Timeline
Prepare for accreditation
6-18 m
April 01
-3-6 m
Jan 04
Submit application
-3 m
Jun 04
Submit documentation
Oct 04
INSPECTION
0
Max 2 m
Jan 05
Report from JACIE
Correct deficiencies/ submit evidence
Max 12 m
Feb 05
Final JACIE Report Recommendation to Board
April 05
Max 2 m
ACCREDITATION
3 yrs
April 05
18
JACIE On Line
  • Useful web-site
  • Examples of quality management plans and
    documents available Dec 05
  • CV Template for Transplant personnel
  • List of accreditation deficiencies
  • 3rd Edition of JACIE standards available Jan 06
    (30 day public consultation)
  • Discussion forum
  • All documents available electronically
  • JACIE Surveys

19
JACIE Survey of Centres Results1 Motivation
  • What was your motivation for applying for JACIE
    Accreditation?

20
Survey of CentresResults2 Personnel
  • Was there a person responsible for day-to-day
    management of the process apart from the
    Programme Director?
  • Was this person employed full-time or part-time?
  • Was this person a trained expert in quality
    management?
  • Was this person part of your team or was it an
    external person?

21
Survey of CentresResults3 Difficulties
  • Which of the following areas presented the most
    difficulties in preparing for accreditation?
  • What were the most difficult parts of your
    preparations?

22
Survey of CentresResults4 Difficulties (cont)
  • What levels of difficulty did you experience in
    the following?

23
Survey of CentresResults5 Training
  • Did you or any member of your team attend any
    JACIE-specific training?
  • If yes, how much did this training help?

24
Survey of CentresResults6 Resources
  • What extra resources
  • were required specifically
  • to implement JACIE?
  • What financial support
  • did your programme receive,
  • if any?

25
Survey of CentresResults7 Satisfaction
  • Were you satisfied with the manner in which your
    centre was inspected?
  • Please rate the inspection team that visited your
    centre
  • Do you consider that the inspection was fair and
    objective?
  • How would you rate the quality of the inspection?

26
Survey of CentresSummary Statement
  • How satisfied are you with the overall
    accreditation process?
  • How satisfied are you with the support received
    from the JACIE Office?
  • Is accreditation worth the effort?
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