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A Retrospective Medical Record Review of Laboratory Monitoring of HIV Infected Adults on the New Jersey AIDS Drug Distribution Program Warren Triano-Davis, MPA1 ... – PowerPoint PPT presentation

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Title: ABSTRACT


1
A Retrospective Medical Record Review of
Laboratory Monitoring of HIV Infected Adults on
the New Jersey AIDS Drug Distribution Program
Warren Triano-Davis, MPA1, Sindy M. Paul, MD,
MPH1, Patti Weinberg, PA, MPS2, Wendy Ferguson,
RN, DipEd2, Allison Xiong, PhD2   1New Jersey
Department of Health and Senior Services,
Division of HIV/AIDS Services 2Island Peer Review
Organization
ABSTRACT Background A retrospective medical
record review was conducted to evaluate
implementation of the Public Health Service
recommendations for laboratory monitoring of HIV
infected adults on the New Jersey AIDS Drug
Distribution Program (ADDP). Methods A
standardized data collection tool was used to
conduct a retrospective medical record review
from June 1, 2001 through May 31, 2004 of
patients on ADDP in 11of 21 counties. County
selection was based on HIV prevalence and number
of eligible physicians. Eligible physicians had
10 or more patients on ADDP. The medical
records reviewed were for a calendar year.
Sampling included an elimination factor for
charts or physicians not found. Physician
specific laboratory monitoring rates were
calculated. Poor performers were defined as the
bottom 5. A continuing medical education (CME)
intervention was conducted for poor
performers. Results 2,304 medical records were
reviewed from 128 physicians statewide. 78 of
patients had quarterly CD4and VL tests. Eleven
(8.6) physicians met the criteria for poor
performers. Conclusions Quarterly viral load
and CD4 count monitoring is essential to
determine if a patients needs to start
antiretroviral therapy, is a virologic failure
requiring a new drug regimen, or needs
prophylaxis for opportunistic infections.
Potential reasons for inadequate laboratory
monitoring include 1) patient non-compliance 2)
patient lost to follow-up 3) lab results not
sent to the provider 4) incorrect collection
tube used and 5) limited clinic hours. A CME
lecture series and conferences were held to
provide up-to-date information on laboratory
monitoring. Future plans include a post CME
intervention repeat retrospective medical record
review for poor performers. INTRODUCTION
  • 2,304 medical records were reviewed.
  • 1,797 (78) of the patients had quarterly CD4 and
    viral load tests documented on the medical
    records reviewed.
  • 11 (8.6) of physicians met the poor performer
    criteria.
  • CONCLUSIONS
  • Periodic viral load and CD 4 count monitoring are
    essential to determine if a patient needs to
    start antiretroviral therapy, is a virologic
    failure requiring a new drug regimen, or needs
    prophylaxis for opportunistic infections.
  • Potential reasons for inadequate laboratory
    monitoring include
  • patient non-compliance
  • patient lost to follow-up
  • lab results not sent to the provider
  • incorrect collection tube used and
  • limited clinic hours.
  • METHODS
  • A standardized data collection tool was developed
    which included questions on CD4 count and viral
    load testing.
  • The standardized data collection tool was used in
    a retrospective medical record review.
  • Medical records for the calendar year were
    reviewed from June 1, 2001 through May 31, 2004.
  • Based on HIV prevalence and the number of
    eligible physicians, 11 of the 21 counties in New
    Jersey were selected.
  •  
  • Eligible physicians were defined as physicians
    with 10 or more patients on ADDP.
  • Physician specific laboratory monitoring rates
    were calculated using Microsoft Access (Redmond,
    WA).
  • Poor performers were defined as physicians in the
    lowest 5 of those whose medical records were
    reviewed.
  • A continuing medical education (CME) intervention
    consisting of conferences and individual lectures
    was designed. Physicians were given a choice of
    attending these conferences/lectures or another
    AMA Category 1 CME lecture, conference, or
    enduring material that included laboratory
    monitoring for HIV infected persons.
  • The AIDS Drug Distribution Program (ADDP) is a
    federally funded, state administered, pharmacy
    benefit program for persons infected with HIV.
  • Eligibility criteria include infection with HIV
    disease, less than 500 of federal poverty level,
    and New Jersey Resident
  • ADDP serves approximately 7,000 patients
    annually.
  • ADDP is open formulary, therefore, providing
    access to all FDA approved antiretroviral agents
    and medications for the prophylaxis and treatment
    of opportunistic infections (OIs).
  • National recommendations for laboratory
    monitoring of HIV infected persons using CD4
    counts and viral load are well established. They
    call for CD4 testing every 3 to 6 months and
    viral load testing every 3 to 4 months.1
  • The CD4 count evaluates the status of the immune
    system. It is used to determine the need to
    start or ability to discontinue OI prophylaxis.
    It is also used in the decision to start or
    change antiretroviral therapy.
  •  
  • The viral load assesses the amount of virus
    present. It is used to guide treatment decisions
    to start or change antiretroviral therapy.
  •  
  • This poster describes a retrospective medical
    record review of laboratory monitoring of
    patients on ADDP.

Sussex
Sussex
Passaic
Passaic
Bergen
Warren
Warren
Morris
Morris
Essex
Essex
Hudson
Union
Somerset
Somerset
Hunterdon
Middlesex
Middlesex
Mercer
Mercer
Monmouth
Ocean
Ocean
Burlington
Burlington
Gloucester
Gloucester
Camden
Camden
Salem
Salem
Atlantic
Atlantic
Cumberland
Cumberland
Cape
Cape
May
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