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Recent
Reports
All Parliamentary Groups on AIDS. Migration
and HIV: Improving Lives in Britain All-Party Parliamentary Group on AIDS,
2003. ISBN 0 9534418 2
In May 2003, the All-Party Parliamentary Group on AIDS
held a parliamentary inquiry into the Impact of the UK Nationality and
Immigration System on People Living with HIV. The Inquiry set out to address
the issues in detail as well as communicate the actual experience of migrants
living with HIV in the UK, through written and verbal testimony. They
heard evidence from a range of sources including, academics, doctors,
lawyers, NGO’s, Charities those living with HIV. This report details
their findings and sets out their conclusions and recommendations to the
UK government. The Report and the Transcript of Evidence are available
electronically at www.appg-aids.org.uk/
Chime, O. Voices for the future. Brighton Body
Positive, 2003
This report provides findings and recommendations based on needs assessment
and gap analysis of HIV prevention, support, treatment and care services
for people from Black and Minority Ethnic (BEM) Communities in Brighton
& Hove and East Sussex. The many recommendations include establishing
support services targeted at BEM communities and recruiting more BEM staff.
The report is available electronically at www.ahrf.org.uk/articles.htm
West African HIV/AIDS Prevention & Sexual
Health Project: Final report of a project undertaken by Focus Consultancy/EU
Health Partneriat, WANI, AWWG & Neovenator. Lambeth, Southwark &
Lewisham Health Commission, 2003
The aim of the project was to raise awareness and increase knowledge of
HIV/AIDS amongst the West African communities in Lewisham, Southwark and
Lewisham, (South London). The report outlines the key outputs of the project,
(workshops, seminars, outreach and capacity building), the principle findings
and recommendations of the project.
Doyal, L & Anderson, J. My heart is Loaded:
African women with HIV Surviving in London. Report of a qualitative study.
A group of 62 black women with HIV from 11 different African countries
was recruited to the study from outpatients clinics in London. The women
completed a written questionnaire before immediately taking part in a
semi-structured interview about their experiences with HIV and how it
has affected their lives. This report gives the findings of the study
and explores the circumstances of a group of African women with HIV living
in London. The report is available electronically at: http://www.tht.org.uk
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Books
Community-Based Participatory Research for Health
Edited by Meredith Minkler & Nina Wallerstein.
Forward by Budd Hall
Publishers Blurb: Meredith Minkler and Nina Wallerstein
have brought together, in one important volume, a stellar panel of contributors
who offer a comprehensive resource on the theory and application of community
based participatory research. Community Based Participatory Research for
Health contains information on a wide variety of topics including planning
and conducting research, working with communities, promoting social change,
and core research methods. The book also contains a helpful appendix of
tools, guides, checklists, sample protocols, and much more.
Jossey-Bass, November 2002 • 512 pages •
ISBN: 0-7879-6457-3
Making Sense of Research
Second Edition
Gill Hek, Pamela Moule & Maggie Judd
Publishers Blurb (Abridged): Research is now a crucial
function of health and social care practice. All professionals in these
fields need to understand research and be able to apply it in their daily
care. Making Sense of Research aims to demystify research by introducing
the relevant and essential elements. The authors provide a foundation
of research knowledge by explaining the role of research in health and
social care, giving an overview of the research process and presenting
a range of approaches both quantitative and qualitative. This completely
revised and updated Second Edition is an invaluable introductory text
for students and qualified practitioners in the health and social care
professions who have no prior training or experience in the area.
Sage Publications, September 2003 • ISBN: 1412900883
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| Papers
The following papers were published in peer-reviewed journals between
1st June 2003 and 1st September 2003.
Dougan, S. & Harris, J. P. (2003). Overcounting
of black Africans in the UK: the problem of undetected record duplication.
Commun.Dis.Public Health, 6, 147-151.
Difficulties in recording unfamiliar African names, leading to inconsistent
reporting of ‘surname’ code of the same individual, has raised
concern that there is overcounting of newly diagnosed HIV-positive black
Africans in the UK. Date of birth was used as a proxy indicator for duplication
of entries of black Africans in the national HIV/AIDS patient database.
Significantly more black Africans (59%) than whites (56%) share the same
date of birth (p = 0.0023), and among black Africans certain birthdays
occur at a very high frequency. Although this investigation provided evidence
of selective failure to detect duplicated reports of the same individual
among reports of HIV-positive black Africans, in practical terms, the
relatively small proportion (2.4%) of remaining excess duplicates is equivalent
to 141 black African individuals on the database, and would not impact
on the overall picture of the HIV epidemic in the UK
Rain-Taljaard, R. et al (2003). Potential
for an intervention based on male circumcision in a South African town
with high levels of HIV infection. AIDS Care, 15, 315-327.
The authors investigate the potential for an intervention based on male
circumcision in a South African town with a high level of HIV infection.
Among men aged 25-59 years, 36% reported being circumcised. The median
reported age at circumcision was 20. A total of 42% of 14-24-year-old
circumcised men reported having been circumcised in a medical setting.
Circumcised and uncircumcised men did not differ in their sexual behaviour
or in sociodemographic characteristics, apart from their age and ethnic
group. An intervention that would include male circumcision seems feasible
in communities such as the one where this study was conducted but needs
to be carefully planned in order to ensure that participants understand
that circumcision probably reduces, but certainly does not eliminate,
the risk of HIV infection
Potts, M. & Walsh, J. (2003). Tackling
India’s HIV epidemic: lessons from Africa. BMJ, 326, 1389-1392.
The rapid spread of HIV in sub-Saharan Africa is one of the greatest failures
in the history of public health. Given our detailed understanding of HIV
and the natural course of AIDS, the virus should have been controllable.
Yet in some African countries 20% of people aged over 15 are HIV positive
and 70% of them will eventually die from AIDS. By 2010 the number of HIV
infections in India is predicted to rise from 4 million to 20-25 million.
The authors discuss 10 important lessons from Africa that could limit
the spread of HIV in India
Orrell, C., Bangsberg, D. R., Badri, M., &
Wood, R. (2003). Adherence is not a barrier to successful antiretroviral
therapy in South Africa. AIDS, 17, 1369-1375.
The authors aimed to determine adherence of an indigent African HIV-infected
cohort initiating antiretroviral therapy (ART)
and to identify predictors of incomplete adherence (< 95%) and virologic
failure (> 400 HIV RNA copies/ml). They found that the proportion of
individuals achieving viral suppression matched results from the developing
world. Speaking the same language as site staff and simplified dosing
frequency were beneficial. Socio-economic status had no impact on adherence
and should not be used as a limitation to ART access
Kebaabetswe, P., etal (2003). Male circumcision:
an acceptable strategy for HIV prevention in Botswana. Sex Transm.Infect.,
79, 214-219.
The authors conducted a cross sectional survey in nine geographically
representative locations in Botswana to determine the acceptability of
male circumcision in the country, as well as the preferred age and setting
for male circumcision. Male circumcision appears to be highly acceptable
in Botswana and the option for safe male circumcision should be made available
to parents in Botswana.
Booysen, F. R. & Arntz, T. (2003). The
methodology of HIV/AIDS impact studies: a review of current practices.
Soc.Sci.Med., 56, 2391-2405.
This review of studies on the socio-economic impact of HIV/AIDS shows
that diversity in methodological design, which often is a result of practical
considerations and resource constraints rather than of poor design, is
the norm. This limits the comparability of research findings. More detailed
reporting on method, which is not the norm, can go some way towards facilitating
such comparison. The review underlines the importance of exploring intervention
issues in more detail. More longitudinal studies are required to explore
the long-term impacts of HIV/AIDS.
Mocroft, A., et al (2003). Decline in the
AIDS and death rates in the EuroSIDA study: an observational study. Lancet,
362, 22-29.
Since the introduction of highly active antiretroviral therapy (HAART),
little is known about whether changes in HIV-1 mortality and morbidity
rates have been sustained. The authors assessed possible changes in these
rates across Europe. They found that the initial drop in mortality and
morbidity after the introduction of HAART has been sustained. Potential
long-term adverse effects associated with HAART have not altered its effectiveness
in treating AIDS.
Carne, C. A., et al. (2003). Variation in clinical practice in
genitourinary medicine clinics in the United Kingdom. Sex Transm.Infect.,
79, 240-242.
This study was conducted to examine the variation in clinical practice
in genitourinary medicine clinics in the United Kingdom in early 2002.
It found that the test for infection least likely to be offered to heterosexuals
is an HIV test (71% and 70% of clinics routinely offer this to male and
female heterosexuals respectively). The practice of permitting “low
risk” patients to telephone for their HIV results now extends to
24% of clinics. Other significant variations in clinical practice were
documented. The findings indicate the need for further evidence to guide
clinical practice and a wider knowledge and debate of national guidelines.
Sinka, K. et al. (2003). Impact of the HIV epidemic in sub-Saharan Africa
on the pattern of HIV in the UK. AIDS, 17, 1683-1690.
The authors describe the epidemiology of HIV infection acquired in Africa
and among African communities in the United Kingdom. Of all reported HIV
infections diagnosed in the United Kingdom by the end of 2001, 21% (9993
of 48,226) were probably acquired in Africa and 90% of these infections
were heterosexually acquired. Infections acquired in Africa and among
Africans are making an increasing contribution to HIV infection in the
United Kingdom.. Improvement in early diagnosis of HIV continues to be
an important component of intervention to prevent onward vertical and
sexual transmission and to promote access to treatment and care.
McMichael, A. J. & Hanke, T. (2003). HIV
vaccines 1983-2003. Nature Medicine., 9, 874-880.
Twenty years after the discovery of HIV, there is still no vaccine. This
year, an envelope vaccine aimed at stimulating neutralizing antibodies
was unable to protect against infection in phase 3 trials. But more than
20 HIV vaccines designed to stimulate T-cell responses are being developed.
Will any of them work?
Weston, H. J. (2003). Public honour, private
shame and HIV: issues affecting sexual health service delivery in London’s
South Asian communities. Health Place., 9, 109-117.
Within a wider discussion of health service provision for black and minority
ethnic (BME) groups, this paper considers how socio-cultural factors affect
the provision of HIV and sexual health services to South Asians in London.
It argues that communally held concepts of honour and shame within South
Asian communities create a framework of social control with significant
implications for HIV/AIDS transmission. It examines the provision of culturally
sensitive services to BME communities by ethnically specific and generic
service providers through a case study of the Naz Project London. Finally,
it proposes an agenda for future research into BME sexual health service
provision
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