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133rd Annual Meeting & Exposition December 10-14, 2005 Philadelphia, PA |
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Maria Isabel Tavarez, MD1, Talía Flores, MD2, Arelis Batista, MD3, Jose Gonzalez Carpio, MD2, Virginia Salcedo, MPH1, Consuelo Beck-Sague, MD4, and Toye Brewer, MD5. (1) Unidad Central de Atención Integral, Secretaría de Salud Pública y Asistencia Social, Programa Nacional de Atención Integral a Personas que Viven con VIH/SIDA, Av. San Cristobal esq. Tiradentes, Santo Dominigo, Dominican Republic, 809-541-3121, isabelmaria06@yahoo.es, (2) Centro de Dia, Hospital Luis E Aybar, Calle Federico Velásquez # 1 Urb. Maria Auxiliadora, Santo Domingo, Dominican Republic, (3) Clinica Rural Sabana Perdida Lotes y Servicio, Calle 12 esq. Flor del Sol # 35, lotes y servicios, Santo Domingo Norte, Dominican Republic, (4) International Family AIDS Program, Columbia University, Casa de Paz Complejo Micaeliano, Calle Gastón F. Deligne # 168 esq. Gregorio Luperón, La Romana, Dominican Republic, (5) Mailman School of Public Health, International Center for AIDS Care and Treatment Programs-, Columbia University, Torre Piantini, Esq. Gustavo Mejia Ricart con Abraham Lincoln, Ofc 405, Santo Domingo, Dominican Republic
Background: HIV is an important cause of death among 18-44 year-olds in the DR, the highest HIV-prevalence-country in the Spanish-speaking world. In 2004, the number of persons receiving HAART in the DR soared due to distribution of free antiretrovirals by the Dominican government. Through January 14, 2005,-HAART was initiated in 1,053 patients (928 adults [88.1%], 125 children [11.9%]). Methods: Data were abstracted from medical records of 184 (20%) adult patients initiating HAART in three of 16 facilities and analyzed using Chi-square or ANOVA. Results: At HAART initiation, adults ranged in age from 21-78 years (median=38); 95 (51.6%) were female. CD4+T-cell counts ranged from 2-464 (median=94), and were lower among men than women (median=73 vs. 98, p=.06). Most patients' initial regimen (105 [57%]) consisted of generic zidovudine-lamivudine and nevirapine formulations; 11.9% received stavudine instead of zidovudine due to anemia. Efavirenz in combination with other antiretrovirals was prescribed initially to 36 (19.6%) patients, largely because of hepatic dysfunction. Women were less likely to receive efavirenz-containing regimens than men (10.5% vs. 29.9%; p=.001). Twelve adverse reactions, one fatal, were reported in 11 (6.4%) of patients; 11 were nevirapine-related hepatic or dermatologic reactions. Thirty patients (16.3%) receiving HAART were known to have died by January 2005. Initial median CD4-count of those who died was lower than that of patients still alive in 2005 (30 versus 99; p=.007). Marked clinical improvement was noted in most patients within weeks of HAART initiation. Conclusions: HAART in adults, despite high adverse reaction rate, was associated with considerable improvement.
Learning Objectives: At the conclusion of this session, participants will be able to
Keywords: Antiretroviral Combination Therapy, Developing Countries
Presenting author's disclosure statement:
I wish to disclose that I have NO financial interests or other relationship with the manufactures of commercial products, suppliers of commercial services or commercial supporters.
The 133rd Annual Meeting & Exposition (December 10-14, 2005) of APHA