Adverse Drug Reactions to Antiretroviral Therapy in HIV-Infected Patients at the Largest Public Hospital in Nicaragua
Author(s) -
Marco A. Lorio,
Jonathan Colasanti,
Sumaya Moreira,
Gamaliel Gutiérrez,
Carlos Quant
Publication year - 2014
Publication title -
journal of the international association of providers of aids care (jiapac)
Language(s) - English
Resource type - Journals
eISSN - 2325-9582
pISSN - 2325-9574
DOI - 10.1177/2325957414535978
Subject(s) - medicine , lamivudine , discontinuation , incidence (geometry) , zidovudine , regimen , pediatrics , emtricitabine , adverse effect , retrospective cohort study , drug reaction , adverse drug reaction , antiretroviral therapy , human immunodeficiency virus (hiv) , drug , viral load , pharmacology , viral disease , immunology , virus , hepatitis b virus , physics , optics
Objective: Adverse drug reactions (ADRs) to antiretroviral therapy (ART) are an important cause of hospitalization, treatment discontinuation, and regimen changes in both developed and developing countries. This study is the first to examine and understand ADRs in HIV-infected patients in Nicaragua.Methods: A retrospective descriptive study was conducted from May 2010 to March 2011, in a cohort of HIV-infected patients receiving ART at the largest public hospital in Managua, Nicaragua. Patients were identified based on ADRs reporting on a standardized antiretroviral pharmacotherapy form. Subsequently, chart reviews of these patients were performed in order to document the specific ADRs.Results: Six hundred ninety-two patients on ART were included. The incidence of ADRs was 6.4% (95% confidence interval [CI] 4.5-8.2). Females demonstrated a higher incidence, that is, 10.2% (95% CI 5.3-15.1, P = .020). Patients treated with combinations of zidovudine (ZDV)/lamivudine (3TC) and emtricitabine (FTC)/tenofovir (TDF) had fewer ADRs ( P < .01) than those using other combinations. Five patients were hospitalized or had a prolonged hospitalization secondary to ADRs, with no mortality attributed to ADR. The most common manifestations of ADRs were central nervous system (20 of 44), gastrointestinal (12 of 44), and dermatologic (8 of 44) reactions. Adverse drug reactions were classified as “likely ADRs” (25 of 44) and “possible ADRs” (19 of 44). No ADRs were preventable.Conclusion: Adverse drug reactions most frequently affected the central nervous system. No ADR was life threatening. The frequency of ADRs in this Nicaraguan patient population was less than that reported from other studies in resource-limited settings.
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