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Intimate Partner Violence: A Retrospective Review of Records in Primary Care Settings

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to gather data regarding the documentation of disclosure of IPV in primary ... at four primary care health centers in diverse communities on the island of Oahu. ... – PowerPoint PPT presentation

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Title: Intimate Partner Violence: A Retrospective Review of Records in Primary Care Settings


1
Intimate Partner ViolenceA Retrospective Review
of Records in Primary Care Settings
  • Lois Magnussen Ed.D.
  • Jan Shoultz, DrPh
  • Mary Oneha,PhD
  • University of Hawaii at Manoa
  • School of Nursing

2
Goals of the Study
  • The goals of this study were twofold
  • to gather data regarding the documentation of
    disclosure of IPV in primary care settings
  • to collect demographic data, including ethnicity
    of women who disclose in primary care settings.

3
Significance of the Study
  • Intimate partner violence (IPV) is pervasive in
    American Society.
  • One in five US couples have experienced at least
    one episode of violence.
  • It is estimated that 1 in 3 women will be
    assaulted by a partner at some time in their
    lives.

4
Cultural Variation
  • Reported rates of IPV have a wide range of
    variation from one racial or ethnic group to
    another
  • Women of Asian/Pacific Islander background report
    a lower rate of IPV than other ethnic groups.

5
Cultural Variation (cont)
  • Researchers who work with battered Asian/ Pacific
    Islander (API) women estimate that the prevalence
    of IPV is as great in API populations as in other
    groups.
  • Disclosure of IPV may also be hidden in the
    context of other civil and criminal complaints
    such as assault.
  • IPV disclosure may also be hidden in the skewed
    proportion of emergency room visits by API
    Americans (18 of all visits) versus European
    American (12 of all visits). NAWHO, 1995.

6
IPV in Hawaii
  • In the State of Hawaii it is difficult to obtain
    accurate statistics regarding IPV.
  • Estimates are that at least 20 of all women in
    Hawaii between the ages of 18 and 64 have been
    victims of domestic violence. DVFCMP, 1996.
  • There is no correlation and crossover of data
    from health care providers, criminal justice, or
    courts.

7
The Need to Understand IPV in Hawaii
  • Few studies documenting disclosure of IPV have
    been done in Community Health Centers.
  • Given the unique factors of the multicultural
    population in Hawaii there is a need to further
    investigate disclosure of IPV.

8
The Need to Understand IPV in Hawaii (cont)
  • While people in Hawaii are influenced by their
    ethnic heritage, these cultural perspectives are
    often modified within the multi-cultural context.
  • Cultural differences in perspectives related to
    IPV may lead to barriers that prevent women from
    receiving effective screening and care.

9
Methodology
  • Study Design
  • A community-based participatory research design
    was used to gather descriptive data via a
    retrospective chart review at the four primary
    care centers.

10
Community based participatory research
  • This systematic inquiry was designed with input
    from clinicians and administrators at four
    primary care health centers in diverse
    communities on the island of Oahu.
  • The four sites were
  • Kalihi Palama Health Center
  • Kokua Kalihi Valley Health Center
  • Waianae Coast Comprehensive Health Center
  • Waikiki Health Center

11
Design of the Survey Instrument
  • The study was undertaken as a partnership to
    meet the needs of the specific health centers and
    address the purpose of the funded study.
  • The following were designed using a collaborative
    process
  • development of the survey tool
  • collection of the data
  • analysis of the data

12
Survey InstrumentData were collected on the
following variables
  • Ethnicity
  • Age of the woman
  • Report of IPV
  • Pregnancy Status
  • Year IPV was reported
  • Gender of the provider
  • Initiation of the discussion of IPV
  • Location of documentation in the chart
  • Program in clinic associated with initial
    disclosure
  • Documentation of referral

13
Data Collection
  • Personnel at the health centers participated in
    data collection
  • The research assistants assignment changed from
    data collection to data entry.

14
Training for Data Collection
  • To assure inter-rater reliability, staff who
    collected the data were guided by the the
    investigators from the University of Hawaii in
    data collection and sampling.

15
Procedures
  • The sample size was computed to determine the
    number of records needed for a descriptive pilot
    study.
  • Inclusion criteria
  • age between 19 and 64
  • seen between 1998 and 2002

16
Total Sample
  • 351 charts were reviewed
  • 14 charts did not fall within the age range or
    were less than 80 complete and were excluded
    from the data analysis.
  • 337 charts were included in the retrospective
    chart review.

17
Data Analysis
  • Data was managed using the Statistical Package
    for the Social Sciences (SPSS).
  • Health center staff were involved in the data
    analysis.

18
Findings
  • Out of a total valid sample of 337 records that
    were reviewed at the four community health
    centers, 31 or 9.1 reported IPV.
  • Four of the women who reported violence
  • were pregnant.
  • Five of these women reported either two or three
    incidents.

19
Ethnicity of Sample compared to Ethnicity of
Those Reporting IPV
20
Comparison of Age of Sample and of those
Reporting IPV
21
Year IPV Reported
22
Location of Report of IPV in Chart
23
Per Cent of Reports by Program
24
Referrals Made
25
Implications
  • Between ethnic group variation shows nearly
    double the incidence of IPV in some groups.
  • The level and depth of resources accessible and
    available to communities may be impacting
    providers interest and desire to provide
    opportunities for disclosure.

26
Implications (cont)
  • Screening for IPV and documentation within the
    chart varies between and within departments of
    the four primary care centers.
  • The ICD Code was not used to document the
    incidents of IPV.

27
Future Research
  • More specific ethnic categories need to be used
    in data collection.
  • Identification of prevalence by specific
    populations will assist community sites in
    directing appropriate resources to those
    populations with the highest prevalence
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