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Evaluation of adherence measures of antiretroviral prophylaxis in HIV exposed infants in the first 6 weeks of life
BACKGROUND: Adherence to an antiretroviral regimen is imperative for treatment success in both HIV infected adults and children. Likewise, adherence to antiretroviral prophylaxis is critical in HIV prevention. Studies on pediatric adherence are limited, particularly the prophylactic use of antiretro...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4381484/ https://www.ncbi.nlm.nih.gov/pubmed/25885678 http://dx.doi.org/10.1186/s12887-015-0340-9 |
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author | Desmond, Alicia Catherine Moodley, Dhayendre Conolly, Catherine A Castel, Sandra A Coovadia, Hoosen M |
author_facet | Desmond, Alicia Catherine Moodley, Dhayendre Conolly, Catherine A Castel, Sandra A Coovadia, Hoosen M |
author_sort | Desmond, Alicia Catherine |
collection | PubMed |
description | BACKGROUND: Adherence to an antiretroviral regimen is imperative for treatment success in both HIV infected adults and children. Likewise, adherence to antiretroviral prophylaxis is critical in HIV prevention. Studies on pediatric adherence are limited, particularly the prophylactic use of antiretroviral drugs and treatment adherence in very young infants. The HIV Prevention Trials Network (HPTN) 046 study (Clinical Trial Registration NCT00074412) determined the safety and efficacy of an extended regimen of nevirapine suspension in infants born to HIV-1 infected women for the prevention of vertical HIV transmission during breastfeeding. As per protocol, adherence to nevirapine prophylaxis was measured by maternal verbal reports. In addition, the pharmacy assessed the unused returned suspension. The aim of this sub-study was to determine the reliability of maternal verbal reports in measuring adherence to antiretroviral prophylaxis in infants in the first 6 weeks of life and evaluating the unused returned nevirapine as an alternative method of measuring adherence. METHODS: Maternal verbal reports and pharmacy returns indicative of “missed < 2 doses” were evaluated against a plasma nevirapine concentration of >100 ng/ml in a subgroup of infants at 2, 5 and 6 weeks of age. Plasma nevirapine concentration of >100 ng/ml was used as a marker of adherence (10 times the in vitro IC(50) against HIV). RESULTS: Adherence was 87.7% (maternal verbal report) and 71.3% (unused returned medication), as compared to 85.6% by plasma nevirapine concentration. Evaluated against plasma nevirapine concentration <100 ng/ml, the sensitivity and specificity of maternal verbal reports to detect a missed dose in the last 3 days were 75% and 78% (p = 0.03) respectively. Overall, among infants who were classified as adherent based on missed doses by maternal verbal reports and unused returned medication, 88.4% and 87.4% of infants attained a nevirapine concentration above 100 ng/ml respectively. CONCLUSION: Maternal verbal reports are a reliable measure of adherence to infant antiretroviral prophylaxis in the first 6 weeks of life and could be useful in assessing adherence to antiretroviral treatment in infants younger than 6 weeks. In the absence of resources or expertise to determine plasma drug concentration, we would recommend random assessments of unused returned medication. |
format | Online Article Text |
id | pubmed-4381484 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43814842015-04-02 Evaluation of adherence measures of antiretroviral prophylaxis in HIV exposed infants in the first 6 weeks of life Desmond, Alicia Catherine Moodley, Dhayendre Conolly, Catherine A Castel, Sandra A Coovadia, Hoosen M BMC Pediatr Research Article BACKGROUND: Adherence to an antiretroviral regimen is imperative for treatment success in both HIV infected adults and children. Likewise, adherence to antiretroviral prophylaxis is critical in HIV prevention. Studies on pediatric adherence are limited, particularly the prophylactic use of antiretroviral drugs and treatment adherence in very young infants. The HIV Prevention Trials Network (HPTN) 046 study (Clinical Trial Registration NCT00074412) determined the safety and efficacy of an extended regimen of nevirapine suspension in infants born to HIV-1 infected women for the prevention of vertical HIV transmission during breastfeeding. As per protocol, adherence to nevirapine prophylaxis was measured by maternal verbal reports. In addition, the pharmacy assessed the unused returned suspension. The aim of this sub-study was to determine the reliability of maternal verbal reports in measuring adherence to antiretroviral prophylaxis in infants in the first 6 weeks of life and evaluating the unused returned nevirapine as an alternative method of measuring adherence. METHODS: Maternal verbal reports and pharmacy returns indicative of “missed < 2 doses” were evaluated against a plasma nevirapine concentration of >100 ng/ml in a subgroup of infants at 2, 5 and 6 weeks of age. Plasma nevirapine concentration of >100 ng/ml was used as a marker of adherence (10 times the in vitro IC(50) against HIV). RESULTS: Adherence was 87.7% (maternal verbal report) and 71.3% (unused returned medication), as compared to 85.6% by plasma nevirapine concentration. Evaluated against plasma nevirapine concentration <100 ng/ml, the sensitivity and specificity of maternal verbal reports to detect a missed dose in the last 3 days were 75% and 78% (p = 0.03) respectively. Overall, among infants who were classified as adherent based on missed doses by maternal verbal reports and unused returned medication, 88.4% and 87.4% of infants attained a nevirapine concentration above 100 ng/ml respectively. CONCLUSION: Maternal verbal reports are a reliable measure of adherence to infant antiretroviral prophylaxis in the first 6 weeks of life and could be useful in assessing adherence to antiretroviral treatment in infants younger than 6 weeks. In the absence of resources or expertise to determine plasma drug concentration, we would recommend random assessments of unused returned medication. BioMed Central 2015-03-19 /pmc/articles/PMC4381484/ /pubmed/25885678 http://dx.doi.org/10.1186/s12887-015-0340-9 Text en © Desmond et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Desmond, Alicia Catherine Moodley, Dhayendre Conolly, Catherine A Castel, Sandra A Coovadia, Hoosen M Evaluation of adherence measures of antiretroviral prophylaxis in HIV exposed infants in the first 6 weeks of life |
title | Evaluation of adherence measures of antiretroviral prophylaxis in HIV exposed infants in the first 6 weeks of life |
title_full | Evaluation of adherence measures of antiretroviral prophylaxis in HIV exposed infants in the first 6 weeks of life |
title_fullStr | Evaluation of adherence measures of antiretroviral prophylaxis in HIV exposed infants in the first 6 weeks of life |
title_full_unstemmed | Evaluation of adherence measures of antiretroviral prophylaxis in HIV exposed infants in the first 6 weeks of life |
title_short | Evaluation of adherence measures of antiretroviral prophylaxis in HIV exposed infants in the first 6 weeks of life |
title_sort | evaluation of adherence measures of antiretroviral prophylaxis in hiv exposed infants in the first 6 weeks of life |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4381484/ https://www.ncbi.nlm.nih.gov/pubmed/25885678 http://dx.doi.org/10.1186/s12887-015-0340-9 |
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