A pilot study to determine the prevalence of HIV in individuals presenting for care with selected conditions: Preliminary results: the HIV in Europe Indicator.

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Presentation transcript:

A pilot study to determine the prevalence of HIV in individuals presenting for care with selected conditions: Preliminary results: the HIV in Europe Indicator Diseases Across Europe Study 10th International Congress on Drug Therapy in HIV Infection, Glasgow, November 2010 Anders Sönnerborg on behalf of the Indicator Diseases Across Europe Study Group

Background Of the estimated 2.3 million PLHIV in the European Region, 1 in 3 remain undiagnosed Undiagnosed HIV is  harmful to the person infected as appropriate health interventions are delayed  detrimental to society, as persons unaware of their HIV infection may transmit to others more frequently  late presentation associated with higher medical cost Need for innovative approaches to better target testing for those at risk of being infected

Purpose of the study ‘HIV in Europe’ Conference (2007)  recommended focused HIV testing in patients presenting with certain clinical conditions and/or diseases  estimates that testing is cost-effective if done in populations with an HIV-prevalence > 0.1% A pilot study, initiated Autumn 2009 to  develop and evaluate best methods to estimate HIV prevalence of a condition handled by the health care system  estimate which of 8 conditions have an HIV prevalence of >0.1 % in different settings across Europe

What do we mean by indicator condition ?

Methods (1) Units of care across Europe were included if they – as part of their routine care function –handled one or more of 8 conditions Sexually transmitted disease (STD) Malignant lymphoma (LYM) Cervical or anal cancer/dysplasia (CAN) Herpes zoster (HER) Hepatitis B or C (HEP) Ongoing mononucleosis-like illness (MON) Unexplained leukocytopenia/thrombocytopenia lasting >4 weeks (CYT) Seborrheic dermatitis/exanthema (SEB)

Methods (2) Consecutive patients were enrolled if: they presented with the condition in question were not already known to be HIV+ One survey=one condition at one site A detailed questionnaire was completed incl. the HIV test Data was transmitted to coordinating centre for data entry and analysis

38 surveys of 8 conditions in 14 countries % of enrollment for each condition by country as of 15 June 2010 Proportion from each country N STD Lymphoma Anal/Cervical Herpes zoster Hepatitis Mononucleosis Cytopenia Dermatitis Spain Germany Ukraine Denmark UK Croatia Belgium Belarus Austria SwedenNetherlandsPoland Bosnia Italy 100% 75% 50% 25% 0%

Demographics of 1,482 individuals enrolled Median Age: %Male%White%Heterosexual %

Results – preliminary Similar frequency of prior testing independent on the history of HIV-related symptoms If prior HIV-related symptoms: 38/104 (36,5%) If no prior HIV-related symptoms: 482/1250 (38,6%) Of 1482 patients tested, 26 (1.8%) were HIV+ STD accounted for 21/26 (21/192 = 10,9%) If prior HIV-test: 16/113 (14,2%) If no prior HIV-test: 5/79 (6,3%) Several of the surveys have been difficult to implement due to reluctance by colleagues in other medical specialties to offer the HIV test as part of routine care

Conclusions Surveys aimed at estimating HIV prevalence for various conditions managed by the health care system are possible to implement across Europe The result of such surveys can provide evidence for and inform testing guidelines Physicians in some specialities appear reluctant to adopt HIV testing as part of routine care Clinicians barriers to HIV testing needs further analysis

Preliminary Specific Conclusions A significant proportion of persons had previously had HIV-associated symptoms without being tested for HIV Many missed opportunities for earlier diagnosis exist Routine HIV testing of the conditions surveyed appears to fulfil the requirement of having an overall HIV prevalence of > 0.1% The observed overall prevalence was 1.8% STD appears to be an indicator for routine HIV testing It is not at present possible to determine which of the 7 other conditions that are also indicator(s) for routine HIV testing

Plans for finalisation of the pilot surveys and next steps The pilot surveys will end 1 March October 2010 a total of 2,600 persons have been enrolled Projected total number: 4,000 Results will be available in May 2011 Based on findings, additional surveys for other conditions and for the pilot conditions in other settings will be implemented Audits aimed at determining the extend of routine testing of AIDS conditions (= automatically defined conditions for routine HIV testing) will be implemented A panel incl. representatives from other medical specialities will be convened to develop guidelines for indicator-condition guided HIV testing

The HIV Indicator Diseases Across Europe Study Group Advisory Group: Nathan Clumeck, CHU Saint-Pierre, Brussels, Belgium, Jose Gatell, Hospital Clínic de Barcelona, Barcelona, Spain, Brian Gazzard, Chelsea and Westminster Hospital, London, England, Jens Lundgren, University of Copenhagen and Rigshospitalet, Copenhagen, Denmark, Antonella d’Arminio Monforte, Clinica delle Malattie Infettive, Milan, Italy, Jürgen Rockstroh, Department of Medicine, University of Bonn, Germany, Amanda Mocroft, University College London Medical School, UK. Centres: Austria: R Zangerle, University Hospital Innsbruck, Department of Dermatology and Venereology, Innsbruck. Belarus: A Vassilenko, Minsk Municipal Infectious Diseases Hospital, Minsk. Belgium: A Libois, S Clinic, J André, Department of Dermatology, P Kirkove, Saint-Pierre University Hospital, Brussels. Bosnia: V Hadziosmanovic, Clinical Center, University of Sarajevo, Infectious Diseases Clinic, Sarajevo. Croatia: J Begovac, University Hospital of Infectious Diseases, Zagreb. Denmark: H Sørensen, Bispebjerg Hospital, København. S Fangel, Infektionsmedicinsk Afdeling, CESOIRS/Skejby Sygehus; Århus. Germany: U Spengler, Outpatient Clinic for Hepatology, Department of Medicine, University of Bonn. I Schmidt-Wolf, Outpatient Clinic for Hepatology Department of Medicine, University of Bonn. S Esser, Uniklinikum Essen, Hautklinik, Essen. Italy: M Zuin, Liver Unit, Dept. of Medicine, San Paolo Hospital, Milan. G Podda, Hermathology Unit, Dept. of Medicine, San Paolo Hospital, Milan. M Cusini, STD Centre, Dermatology department, Milan. Netherlands: K Brinkman, Onze Lieve Vrouwe Gasthuis, Internal Medicine, Amsterdam. Poland: A Grzeszczuk, Medical University of Bialystok, Department of Infectious Diseases and Hepatology, Bialystok. Spain: F Garcia, A Leon, Hospital Clinic Barcelona, Infectious Diseases Unit, Barcelona. I Menacho, Primary Center of les Corts, M Muns, Primary Center of Raval Sur, Barcelona Spain. Sweden: A Sönnerborg, Department of Infectious Diseases, Karolinska University Hospital, Stockholm. United Kingdom: A Sullivan, Michael Rayment, ChelseaWestminster Hospital, London. Ukraine: M Krasnov, Kharkov Regional Clinic of Infectious Diseases, Kharkov. Coordinating Centre Staff: D Raben, M Ellefson, R S Brandt

For more information about the initiative and projects Financial support of the initiative has been provided by Gilead Sciences, Merck, Tibotec, Pfizer, Schering-Plough, Abbott, Boehringer Ingelheim, Bristol-Myers Squibb, GlaxoSmithKline, ViiV Healthcare and the Swedish Research Council.