Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2015 May 1;10(5):e0125665.
doi: 10.1371/journal.pone.0125665. eCollection 2015.

Factors Associated with Timing of Initiation of Antiretroviral Therapy among HIV-1 Infected Adults in the Niger Delta Region of Nigeria

Affiliations

Factors Associated with Timing of Initiation of Antiretroviral Therapy among HIV-1 Infected Adults in the Niger Delta Region of Nigeria

Dimie Ogoina et al. PLoS One. .

Abstract

Introduction: Based on growing evidence mainly from countries outside Sub-Saharan Africa, the World Health Organisation (WHO) now recommends initiation of antiretroviral therapy (ART) in HIV-infected individuals in developing countries when CD4 cell count (CD4+) is ≤ 500 cells/ul. Nigeria accounts for about 14% of the estimated HIV/AIDS burden in Sub-Saharan Africa. We evaluated the factors associated with timing of initiation of ART among treatment-ineligible HIV-infected adults from Nigeria.

Methods: We retrospectively reviewed the hospital records of ART ineligible HIV-infected adults who enrolled into HIV care between January 2008 and December 2012 at two major tertiary hospitals in Bayelsa State, South-South Nigeria. Demographic, clinical and laboratories data were obtained at presentation, at each subsequent visit at 6 monthly intervals and at time of initiation of ART. Cox proportional regression and Kaplan-Meier survival analysis were used to evaluate independent predictors of time to initiation of ART.

Results: Amongst the 280 study participants, 70.6% were females, 62.6% had CD4+ ≥500 cells/ul, 48.4% had WHO HIV Stage 1 disease and 34.3% were lost to follow up. In a cohort of 180 participants followed up for ≥3 months, participants with CD4+ of 351-500 cells/ul and stage 2 disease were more likely to start ART earlier than those with CD4+ > 500 cells/ul (Hazard ratio [HR]-1.7, 95% confidence interval [CI] of 1.0-2.9) and stage 1 disease (HR-2.3 (95% CI-1.3-4.2) respectively. HIV-infected adults with faster CD4+ decay required earlier ART initiation, especially in the first year of follow up.

Conclusion: ART-ineligible HIV-infected adults on follow up in South-South Nigeria are more likely to require earlier initiation of ART if they have stage 2 HIV disease or CD4+ ≤500 cells/ul at presentation. Our findings suggest faster progression of HIV-disease in these groups of individuals and corroborate the growing evidence in support for earlier initiation of ART.

PubMed Disclaimer

Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

Figures

Fig 1
Fig 1. Kaplan-Meier curves of time to initiation of ART in relation to CD4 cell count group.
The median time to ART initiation was significantly shorter in participants with CD4 cell count of 351-500cells/ul than those (16months) with CD4 count >500cells/ul (23months).
Fig 2
Fig 2. Kaplan-Meier curves of time to initiation of ART in relation to WHO HIV stage.
The median time to ART initiation was significantly shorter in participants with stage 2 disease (15months) than participants with stage 1 disease (23months).
Fig 3
Fig 3. Temporal 6monthly median CD4 cell counts according to ART status.
At each individual time points, the observed median CD4 cell counts were significantly higher in participants who were yet to start ART (p<0.0001 at each indivudal time points of 0, 6, 12 and 24 months and p = 0.0001 at 18months; Mann Whitnet test). Among study participants who started ART, the graph shows a steep and progressive drop in median CD4 cell counts in the first year of follow up.

Similar articles

Cited by

References

    1. World Health Organization. Consolidated guidelines on the use of antiretroviral drugs for treating and preventing HIV infection: recommendation for a public health approach 2013:1–272. www.who.int (accessed May 24, 2014). - PubMed
    1. Anglemyer A, Rutherford GW, Easterbrook PJ, Horvath T, Vitória M, Jan M, et al. Early initiation of antiretroviral therapy in HIV-infected adults and adolescents: a systematic review. AIDS 2014;28 Suppl 2:S105–18. 10.1097/QAD.0000000000000232 - DOI - PubMed
    1. Siegfried N, Uthman OA, Rutherford GW. Optimal time for initiation of antiretroviral therapy in asymptomatic, HIV-infected, treatment-naive adults. Cochrane Database Syst Rev 2010:CD008272. 10.1002/14651858.CD008272.pub2 - DOI - PMC - PubMed
    1. Cohen MS, Chen YQ, McCauley M, Gamble T, Hosseinipour MC, Kumarasamy N, et al. Prevention of HIV-1 Infection with Early Antiretroviral Therapy. N Engl J Med 2011;365:493–505. 10.1056/NEJMoa1105243 - DOI - PMC - PubMed
    1. Le T, Wright EJ, Smith DM, He W, Catano G, Okulicz JF, et al. Enhanced CD4+ T-cell recovery with earlier HIV-1 antiretroviral therapy. N Engl J Med 2013;368:218–30. 10.1056/NEJMoa1110187 - DOI - PMC - PubMed

MeSH terms

Substances