| Literature DB >> 31714427 |
Sara Domínguez-Rodríguez1,2,3, Alfredo Tagarro1,2,3, Paolo Palma4, Caroline Foster5, Thanyawee Puthanakit6,7, Thidarat Jupimai6,7, Nicola Cotugno4, Jintanat Ananworanich8,9,10, Paola Zangari4, Eleni Nastouli11, María Ángeles Muñoz-Fernández12, María Luisa Navarro2,13, Carlo Giaquinto14, Paolo Rossi4, Louise Kuhn15, Pablo Rojo1,2.
Abstract
There are limited data on infants with HIV starting antiretroviral therapy (ART) in the neonatal period. We investigated the association between the timing of ART initiation and time-to-suppression among infants who tested HIV-positive and initiated ART within the first 28 days of life. The effect was estimated using cumulative probability flexible parametric spline models and a multivariable generalized additive mixed model was performed to test nonlinear associations. Forty-four neonates were included. Nineteen (43.2%) initiated ART within 7 days of life and 25 (56.8%) from 8 to 28 days. Infants treated within 7 days were 4-fold more likely to suppress earlier than those treated after 7 days [Hazard ratio (HR) 4.01 (1.7-9.5)]. For each week the ART initiation was delayed, the probability of suppression decreased by 35% (HR 0.65 [0.46-0.92]). Age at ART start was linearly associated with time-to-suppression. However, a linear association with normally distributed residuals was not found between baseline viral load and time-to-suppression, with no association found when baseline viral loads were ≤5 log(10) copies/mL, but with exponential increase in time-to-suppression with > log5 copies/mL at baseline. Starting ART within 7 days of life led to 4-fold faster time to viral suppression, in comparison to initiation from 8 to 28 days.Entities:
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Year: 2019 PMID: 31714427 PMCID: PMC6857716 DOI: 10.1097/QAI.0000000000002188
Source DB: PubMed Journal: J Acquir Immune Defic Syndr ISSN: 1525-4135 Impact factor: 3.731