Program Supplement [International Conference on AIDS (14th: 2002: Barcelona, Spain)]

Late Breaker Abstracts Oral Sessions iBOR0oAI Management of post-exposure prophylaxis after occupational exposure to HIV in healthcare workers in Europe Cicalini, Stefania1, Antunes, Francisco2, Balslev, Ulla3, Bernasconi, Enos4, Boaventura, Jos Luis2, Campins, Magdas, Evans, Barry6, Francioli, Patrick4, Genasi, Fiona6, Larsen, Christine7, Lot, Florence7, Lunding, Suzanne3, Marcus, Ulrich8, Pereira, Alvaro2, Schonwald, SlavkO9, Thomas, Tania6, De Carli, Gabriella, Ippolito, Giuseppe', Puro, Vincenzo' (ltaly; 2Portugal; 3Denmark; 4Switzerland; sSpain; 6United Kingdom; 7France; 8Germany; 9Croatia) Background: Occupational post-exposure prophylaxis (OPEP) against H IV represents the standard of care in exposed healthcare workers (HCW), but no general consensus exists on some issues. Methods: On September 2001, the European Commission funded a project co-ordinated by Italy (I), to evaluate and standardize the management of OPEP in Europe. Croatia (C), Denmark (DK), United Kingdom (UK), France (F), Germany (D), Portugal (P), Spain (E), Switzerland (CH), participate in the project. Existing guidelines (GL) were collected; policies, procedures and data regarding OPEP were investigated through a questionnaire and discussed with representatives of participating Countries. Results: All Countries have National or hospital (P, C) GL that recommend starting 4-week PEP as soon as possible, with 3 drugs regardless of risk assessment in UK, CH, F, D, DK, or only in high risk exposure in C, E, I, P. The interval after which PEP is discouraged ranges from 24 h (I, DK) to 72 h (CH, D, E, P), allowing 14d for high risk exposures (UK, P). HIV testing schedule differs in timing, with HIV-Ag/RNA performed only in F. PEP is available in all (F, UK) or larger (P, E, CH, C) hospitals, or in hospitals with an infectious diseases department (D, DK, I). PEP collected cases approximate looo/year [data from the National Registry (CH, DK, F, I, UK); from a network of hospitals (E), or a University hospital (C); not available (P, D)]. Acceptance rates varied from 28% (E) to 73% (UK); the proportion of HCW who completed PEP ranged between 25% (UK) to 84% (F). A significant number of PEP is started after exposure to a source who later tested HIV negative, lasting a mean of 1-4 days. Rapid HIV testing is rarely used. Conclusions: OPEP is widely prescribed in EU Countries, though differing in several aspects. Uniform GL should be developed to implement a rapid risk assessment, optimize availability and management, and minimize unnecessary treatments and related toxicity and costs. Corresponding author: Cicalini, Stefania, Dipartimento di Epidemiologia, INMI Spallanzani, Via Portuense 292, Rome, Italy, Tel: +39 0655170930, Fax: +39 065582825, Email: [email protected] SLBOROIB I Proposed European Recommendations for Post-Exposure Prophylaxis against HIV infection in Health Care Workers Puro, Vincenzo', Cicalini, Stefanial, Schonwald, Slavko2, Balslev, U//a3, Lot, Florence4, Marcus, Ulrichs, Boaventura, lose Luis6, Campins, Magda7, Bernasconi, Enos8, Thomas, Tania9, De Carli, Gabriella, Ippolito on behalf of the EuROPEP Study Group, Giuseppe' (/taly; 2Croatia; 3Denmark; 4France; 5Germany; 6Portugal; 7Spain; 8Switzerland; 9United Kingdom) Background: Management of occupational H IV post-exposure prophylaxis (PEP) varies among European countries, and several issues remain controversial. Methods: In September 2001, the European Commission funded a project to standardise the management of occupational HIV PEP in,irope. During a 2-day consensus meeting, expert representatives from Italy, Croatia, Denmark, United Kingdom, France, Germany, Portugal, Spain, Switzerland reviewed and discussed available National recommendations and policies, data from local surveillance programs and current literature, thus issuing a consensus document. Results: The consensus document recommends that all efforts should be made to prevent occupational exposures. PEP prescription should be based on the type of exposure, body material involved and source patient's evaluation. After the source patient's consent to H IV testing, "immediate" results should be obtained in order to prevent unnecessary PEP, also by using rapid HIV-antiFody tests. PEP should be initiated as soon as possible and is discouraged after 72 hours from exposure. A 4-week course of any combination of antiretrovirals approved for the treatment of HIV patients could be used in a PEP regimen. Triple therapy (i.e. 2 NRTI + 1 PI or 1 NNRTI) is recommended as a first line PEP regimen. The source patient's history about previous and current antiretroviral treatments may be important in the choice of PEP regimen. HIV testing should be performed shortly after exposure and thereafter at 6 weeks, 3 and 6 months. The routine use of direct virus assays (HIVp24Ag, HIV-RNA) in an exposed healthcare worker is not recommended. Drug adherence and tolerability should be monitored. Conclusions: A standardized management of PEP in EU countries could effectively improve occupational safety in the healthcare setting, in increasing our understanding of efficacy and toxicity of antiretroviral drugs and optimising the use of available resources to reduce the risk of HIV infection. Corresponding author: Puro, Vincenzo, Dipartimento di Epidemiologia, INMI Spallanzani, Via Portuense 292, Rome, Italy, Tel: +39 0655170902, Fax: +39 065582825, Email: [email protected] XIV International AIDS Conference BARCELONA - JULY 7-12 19

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Program Supplement [International Conference on AIDS (14th: 2002: Barcelona, Spain)]
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International AIDS Society
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Prous Science
2002
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programs
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