Guest guest Posted November 26, 2006 Report Share Posted November 26, 2006 Need a national policy on Post Exposure Prophylaxis (PEP) in non occupational exposure to HIV Joe Director-general of the Armed Forces Medical Services, Surgeon Vice Admiral V K Singh's statement " ... If a person having unprotected sex is put on ARV drugs within 24 hours of getting infected, the virus can be killed, " (1) appears to be misleading interpretation of the scope of Antiretroviral Post Exposure Prophylaxis (PEP) policy. Such a misguided policy will have serious consequences on HIV prevention and care efforts within the uniformed services and in the general population. This statement indicates the urgency of the need for a national policy on Post Exposure Prophylaxis (PEP) in non occupational exposure to HIV (nPEP) The provision of antiretroviral drugs to prevent HIV infection after unanticipated sexual or injection-drug-use exposure might be beneficial (2). In the Indian context, PEP is mostly used to prevent HIV infection in occupational settings such as to prevent infection among a health care provider after an accidental exposure to infected blood or blood products. There is no official policy of PEP as such in India, so one has to rely on global standards and best practices to examine the merit of promoting PEP for each person having unprotected sex. Although, the benefits of a PEP regime after an exposure to HIV were known earlier, promoting the use of PEP to prevent HIV in non occupational exposure such as an protected sexual penetration is contentious. A demand for nPEP is occurring in hospital emergency departments in developing countries, but the diversity of practice patterns suggests the need for evidence-based practice guidelines (3). One of the most important aspect of CDC recommendation on PEP in non occupational exposure is, the use of Nonoccupational Postexposure Prophylaxis (nPEP) must be case by case basis under the supervision of a trained physician. The U.S. Department of Health and Human Services (DHHS) Working Group on nPEP made the following recommendations for the United States of America, " For persons seeking care <72 hours after nonoccupational exposure to blood, genital secretions, or other potentially infectious body fluids of a person known to be HIV infected, when that exposure represents a substantial risk for transmission, a 28-day course of highly active antiretroviral therapy (HAART) is recommended. Antiretroviral medications should be initiated as soon as possible after exposure. For persons seeking care <72 hours after nonoccupational exposure to blood, genital secretions, or other potentially infectious body fluids of a person of unknown HIV status, when such exposure would represent a substantial risk for transmission if the source were HIV infected, no recommendations are made for the use of nPEP. Clinicians should evaluate risks and benefits of nPEP on a case-by-case basis. For persons with exposure histories that represent no substantial risk for HIV transmission or who seek care >72 hours after exposure, DHHS does not recommend the use of nPEP. Clinicians might consider prescribing nPEP for exposures conferring a serious risk for transmission, even if the person seeks care >72 hours after exposure if, in their judgment, the diminished potential benefit of nPEP outweighs the risks for transmission and adverse events. For all exposures, other health risks resulting from the exposure should be considered and prophylaxis administered when indicated. Risk-reduction counseling and indicated intervention services should be provided to reduce the risk for recurrent exposures " . Promoting the use of PEP after each sexual exposure has possible policy and program implication which would undermine an effective HIV prevention response. Such a policy could decrease in risk-reduction behaviours resulting from a perception that `AIDS treatment' is available, like any other sexually transmitted diseases. A PEP treatment regime also could present serious adverse health effects from antiretroviral treatment in otherwise healthy persons(4), (5) (Data on the health consequences of a PEP treatment in a health person is hard to come by) and potential in crease of the pool of ARV resistant virus through poor adherence to an nPEP course. Promoting the use of PEP after each `at risk exposure' has further difficulties. Will such a facility available after each and every episode of `at risk behaviours'? A person could have a multiple episodes of at risk behaviour at any given time. " From a purely economic standpoint, PEP should be restricted to partners of infected persons (e.g., serodiscordant couples), to patients reporting unprotected receptive anal intercourse (including condom breakage), and possibly to cases where there is a substantial likelihood that the partner is infected. Providing PEP to all who request it does not appear to be an economically efficient use of limited HIV prevention and treatment resources " (6). nPEP is an important tool for prevention HIV infection. However, to maximise the effectiveness of nPEP, a concerted effort is necessary to develop a national policy on the use of PEP in non occupational exposure. Such a policy would definitely be helpful not only for `Jawans' but for women (children and men) who are sexually assaulted and at the risk of HIV infection as well. A policy vacuum is contributing to several unavoidable HIV infections in India. Health care providers must understand, there is no single `magic bullet' to deal with the challenges of HIV infection. Respecting individual rights, confidentiality and access to appropriate information and services, promoting the use of condom and safer sexual practices and creating an environment where safer sexual practices could be practiced are far more effective than promoting the use of PEP after each `at risk' behaviours. References (1) Siddhartha D Kashyap, [24 Nov, 2006. Times News Network] Report sexcapades: Army. http://timesofindia .indiatimes. com/Report_sexcapades_ Army/articleshow / 548219.cms (2) Antiretroviral Postexposure Prophylaxis After Sexual, Injection- Drug Use, or Other Nonoccupational Exposure to HIV in the United States Recommendations from the U.S. Department of Health and Human Services January 21, 2005 / 54(RR02);1-20 CDC MMWR (3) Kunches, Laureen M; Meehan, Thera M; Boutwell, C; McGuire, Flatley (2001) Survey of Nonoccupational HIV Postexposure Prophylaxis in Hospital Emergency Departments. JAIDS Journal of Acquired Immune Deficiency Syndromes. 26(3):263-265, March 1, 2001. (4) JM Parkin , M , J , S El-Gadi, G Forster and AJ Pinching (2000) Tolerability and side-effects of post- exposure prophylaxis for HIV infection. The Lancet 2000; 355:722-723. DOI:10.1016/S0140-6736(99)05005-9 (5) Christian Rabaud, Sibylle Bevilacqua, Isabelle Beguinot, Véronique Dorvaux, Hélène Schuhmacher, Thierry May, and Philippe Canton (2001) Tolerability of Postexposure Prophylaxis with Zidovudine, Lamivudine, and Nelfinavir for Human Immunodeficiency Virus Infection. Clinical Infectious Diseases 2001;32:1494-1495 (6) Pinkerton, D; Holtgrave, R Bloom, Frederick R (1998) Cost-effectiveness of post-exposure prophylaxis following sexual exposure to HIV. AIDS. 12(9):1067-1078, June 1998. Quote Link to comment Share on other sites More sharing options...
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