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102 - Prophylaxis of opportunistic infections in HIV disease

from Part XII - HIV

Published online by Cambridge University Press:  05 April 2015

Amy S. Baranoski
Affiliation:
Drexel University College of Medicine
Jeffrey M. Jacobson
Affiliation:
Drexel University College of Medicine
David Schlossberg
Affiliation:
Temple University, Philadelphia
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Summary

Prior to the introduction of antiretroviral therapy (ART), treatment and prevention of opportunistic infections (OIs) were the main-stays of reducing morbidity and mortality in people living with human immunodeficiency virus (HIV). While the widespread use of ART has greatly decreased the frequency of OIs, a sizeable number of HIV-infected individuals are either not taking ART or do not have an adequate immune response to ART. Thus OIs continue to cause a significant burden of disease in people living with HIV, and prophylaxis against OIs remains a major component in the management of HIV. The guidelines for OI prophylaxis in HIV-infected individuals are published by the Centers for Disease Control and Prevention, National Institutes of Health, and HIV Medicine Association of the Infectious Disease Society of America. The newest version of the guidelines was published in 2013 and includes revisions on the vaccination strategies for HIV-infected people.

Primary prophylaxis refers to treatment given to prevent development of infection. The most influential example of primary prophylaxis in HIV is the use of trimethoprim–sulfamethoxazole (TMP–SMX) in immune compromised individuals to prevent development of Pneumocystis jirovecii (carinii) pneumonia (PCP).

Secondary prophylaxis refers to continued treatment given after the acute course of treatment is complete in order to decrease the risk of relapse. Depending on the infection, secondary prophylaxis is sometimes referred to as maintenance or chronic suppressive therapy for difficult-to-treat OIs. The timing of primary prophylaxis and recommended vaccinations is summarized in Table 102.1. The preferred and alternative agents and dosages for primary and secondary prophylaxis are summarized in Tables 102.2 and 102.3.

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Publisher: Cambridge University Press
Print publication year: 2015

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References

Aberg, JA, Kaplan, JE, Libman, H, et al. Primary care guidelines of the management of persons infected with human immunodeficiency virus: 2009 update by the HIV Medicine Association of the Infectious Diseases Society. Clin Infect Dis. 2009;49:651–681.CrossRefGoogle ScholarPubMed
ACIP Adult Immunization Work Group, Bridges, CB, Woods, L, Coyne-Beasley, T, Centers for Disease Control and Prevention (CDC). Advisory Committee on Immunization Practices (ACIP) recommended immunization schedule for adults aged 19 years and older – United States, 2013. MMWR Surveill Summ. 2013;62(Suppl 1):9–19.Google Scholar
Mazurek, GH, Jereb, J, Vernon, A, et al.; IGRA Expert Committee; Centers for Disease Control and Prevention (CDC). Updated guidelines for using Interferon Gamma Release Assays to detect Mycobacterium tuberculosis infection – United States, 2010. MMWR Recomm Rep. 2010;59(RR-5):1–25.Google ScholarPubMed
Panel on Opportunistic Infections in HIV-Infected Adults and Adolescents. Guidelines for the prevention and treatment of opportunistic infections in HIV-infected adults and adolescents: recommendations from the Centers for Disease Control and Prevention, the National Institutes of Health, and the HIV Medical Association of the Infectious Diseases Society of America. Available at: .

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