4.7 Article

Adherence to first-line antiretroviral therapy affects non-virologic outcomes among patients on treatment for more than 12 months in Lusaka, Zambia

期刊

INTERNATIONAL JOURNAL OF EPIDEMIOLOGY
卷 38, 期 3, 页码 746-756

出版社

OXFORD UNIV PRESS
DOI: 10.1093/ije/dyp004

关键词

HIV; adherence; medication possession ratio; mortality; survival; antiretroviral therapy; Africa; Zambia

资金

  1. FIC NIH HHS [D43-TW001035, K01-TW06670] Funding Source: Medline
  2. NIAID NIH HHS [K23-AI01411, P30-AI027767] Funding Source: Medline
  3. PHS HHS [U62/CCU12354] Funding Source: Medline

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Background High-level adherence to antiretroviral therapy (ART) is associated with favourable patient outcomes. In resource-constrained settings, however, there are few validated measures. We examined the correlation between clinical outcomes and the medication possession ratio (MPR), a pharmacy-based measure of adherence. Methods We analysed data from a large programmatic cohort across 18 primary care centres providing ART in Lusaka, Zambia. Patients were stratified into three categories based on MPR-calculated adherence over the first 12 months: optimal (>= 95%), suboptimal (80-94%) and poor (<80%). Results Overall, 27 115 treatment-naive adults initiated and continued ART for >= 12 months: 17060 (62.9%) demonstrated optimal adherence, 7682 (28.3%) had suboptimal adherence and 2373 (8.8%) had poor adherence. When compared with those with optimal adherence, post-12-month mortality risk was similar among patients with suboptimal adherence [adjusted hazard ratio (AHR) = 1.0; 95% CI: 0.9-1.2] but higher in patients with poor adherence (AHR = 1.7; 95% CI: 1.4-2.2). Those <80% MPR also appeared to have an attenuated CD4 response at 18 months (185 cells/mu l vs 217 cells/mu l; P<0.001), 24 months (213 cells/mu l vs 246 cells/mu l; P<0.001), 30 months (226 cells/mu l vs 261 cells/mu l; P<0.001) and 36 months (245 cells/mu l vs 275 cells/mu l; P<0.01) when compared with those above this threshold. Conclusions MPR was predictive of clinical outcomes and immunologic response in this large public sector antiretroviral treatment program. This marker may have a role in guiding programmatic monitoring and clinical care in resource-constrained settings.

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