Pediatric HIV Disclosure Intervention Improves Immunologic Outcome at 48 Weeks: The Sankofa Trial Experience

Author:

Shabanova Veronika1,Emuren Leonard1ORCID,Gan Geliang2,Antwi Sampson3,Renner Lorna4,Amissah Kofi3,Kusah Jonas Tettey4,Lartey Margaret5,Reynolds Nancy R.6,Paintsil Elijah1,

Affiliation:

1. Department of Pediatrics, Yale School of Medicine, New Haven, CT;

2. Department of Biostatistics, Yale School of Public Health, New Haven, CT;

3. Department of Child Health, School of Medical Sciences, Kwame Nkrumah University of Science and Technology and Komfo Anokye Teaching Hospital, Kumasi, Ghana;

4. Department of Child Health, University of Ghana Medical School and Korle-Bu Teaching Hospital Accra, Ghana;

5. Department of Medicine, University of Ghana Medical School and Korle-Bu Teaching Hospital Accra, Ghana; and

6. Johns Hopkins School of Nursing, Baltimore, MD.

Abstract

Background: The World Health Organization recommends disclosure of HIV status to children and adolescents living with HIV (CALWH). HIV disclosure improves adherence to antiretroviral therapy and immunologic and virologic outcomes. However, the prevalence of HIV disclosure is low in sub-Saharan Africa. We assessed the longitudinal effect of the Sankofa Pediatric HIV disclosure intervention on immunologic and virologic outcomes among CALWH in Ghana. Methods: We conducted a secondary analysis of a two-arm site-randomized clinical trial among CALWH aged 7–18 years. Data were collected at baseline, 24, and 48 weeks. Generalized linear mixed models were used to compare immunologic (CD4) and virologic (viral load) outcomes as both continuous and categorical variables by disclosure status and by intervention group. Results: Among participants who had their HIV status disclosed during this study, the proportion with CD4 percent >25% increased from 56.5% at baseline to 75.4% at week 48 (P = 0.03), with a slight increase in the undisclosed group (69.5% vs. 74.3%, P = 0.56). In the intervention arm, there was a steady increase in proportion with CD4 percent >25% from 47.1% at baseline to 67.8% at week 48 (P = 0.01) while it remained unchanged in the control arm (80.5% vs. 81.3% [P = 0.89]). Concurrently, declines in detectable viral load were observed in both disclosed (63.3% vs. 51.5%, P = 0.16) and undisclosed (69.9% vs. 62.0%, P = 0.17) groups while the intervention group experienced a meaningful drop from 72.9% to 57.6% at 24 weeks (P = 0.04), which was maintained at 48 weeks. Conclusions: A structured, culturally relevant disclosure intervention can improve clinical outcomes.

Funder

National Institute of Child Health and Human Development

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Pharmacology (medical),Infectious Diseases

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