Treatment interruption and variation in tablet taking behaviour result in viral failure: a case-control study from Cape Town, South Africa.
<h4>Background</h4>Understanding of the impact of non-structured treatment interruption (TI) and variation in tablet-taking on failure of first-line antiretroviral therapy (ART) is limited in a resource-poor setting.<h4>Methods</h4>A retrospective matched case-control analysi...
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oai:doaj.org-article:bbe75fae51fe4333b1de4689c4f3eab12021-11-18T06:48:28ZTreatment interruption and variation in tablet taking behaviour result in viral failure: a case-control study from Cape Town, South Africa.1932-620310.1371/journal.pone.0023088https://doaj.org/article/bbe75fae51fe4333b1de4689c4f3eab12011-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21858001/?tool=EBIhttps://doaj.org/toc/1932-6203<h4>Background</h4>Understanding of the impact of non-structured treatment interruption (TI) and variation in tablet-taking on failure of first-line antiretroviral therapy (ART) is limited in a resource-poor setting.<h4>Methods</h4>A retrospective matched case-control analysis. Individuals failing ART were matched by time on ART with 4 controls. Viral load (VL) and CD4 count were completed 4-monthly. Adherence percentages, from tablet returns, were calculated 4-monthly (interval) and from ART start (cumulative). Variation between intervals and TI (>27 days off ART) were recorded. Conditional multivariate logistic regression analysis was performed to estimate the effect of cumulative adherence <90%, at least one episode of adherence variation >10% and TI on virological failure. Age, gender, baseline log VL and CD4 were included as possible confounders in the multivariate model.<h4>Results</h4>244 patients (44 cases, 200 controls) were included. Median age was 32 years (IQR28-37), baseline CD4 108 cells/mm3 (IQR56-151), VL 4.82 log (IQR4.48-5.23). 94% (96% controls, 86% failures) had cumulative adherence >90%. The odds of failure increased 3 times (aOR 3.01, 95%CI 0.81-11.21) in individuals with cumulative adherence <90%, 2.2 times (aOR 2.20, 95%CI 1.04-4.64) in individuals with at least one episode of fluctuating adherence of >10% and 4.01 times (aOR 4.01, 95%CI 1.45-11.10) in individuals with TIs. For individuals with TI and cumulative adherence >95%, the odds of failing were 5.65 (CI 1.40-22.85).<h4>Conclusion</h4>It is well known that poor cumulative adherence increases risk of virological failure, but less well understood that TI and variations in tablet-taking also play a key role, despite otherwise excellent adherence.Lisa-Noelle NcacaKatharina KranzerCatherine OrrellPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 6, Iss 8, p e23088 (2011) |
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Medicine R Science Q Lisa-Noelle Ncaca Katharina Kranzer Catherine Orrell Treatment interruption and variation in tablet taking behaviour result in viral failure: a case-control study from Cape Town, South Africa. |
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<h4>Background</h4>Understanding of the impact of non-structured treatment interruption (TI) and variation in tablet-taking on failure of first-line antiretroviral therapy (ART) is limited in a resource-poor setting.<h4>Methods</h4>A retrospective matched case-control analysis. Individuals failing ART were matched by time on ART with 4 controls. Viral load (VL) and CD4 count were completed 4-monthly. Adherence percentages, from tablet returns, were calculated 4-monthly (interval) and from ART start (cumulative). Variation between intervals and TI (>27 days off ART) were recorded. Conditional multivariate logistic regression analysis was performed to estimate the effect of cumulative adherence <90%, at least one episode of adherence variation >10% and TI on virological failure. Age, gender, baseline log VL and CD4 were included as possible confounders in the multivariate model.<h4>Results</h4>244 patients (44 cases, 200 controls) were included. Median age was 32 years (IQR28-37), baseline CD4 108 cells/mm3 (IQR56-151), VL 4.82 log (IQR4.48-5.23). 94% (96% controls, 86% failures) had cumulative adherence >90%. The odds of failure increased 3 times (aOR 3.01, 95%CI 0.81-11.21) in individuals with cumulative adherence <90%, 2.2 times (aOR 2.20, 95%CI 1.04-4.64) in individuals with at least one episode of fluctuating adherence of >10% and 4.01 times (aOR 4.01, 95%CI 1.45-11.10) in individuals with TIs. For individuals with TI and cumulative adherence >95%, the odds of failing were 5.65 (CI 1.40-22.85).<h4>Conclusion</h4>It is well known that poor cumulative adherence increases risk of virological failure, but less well understood that TI and variations in tablet-taking also play a key role, despite otherwise excellent adherence. |
format |
article |
author |
Lisa-Noelle Ncaca Katharina Kranzer Catherine Orrell |
author_facet |
Lisa-Noelle Ncaca Katharina Kranzer Catherine Orrell |
author_sort |
Lisa-Noelle Ncaca |
title |
Treatment interruption and variation in tablet taking behaviour result in viral failure: a case-control study from Cape Town, South Africa. |
title_short |
Treatment interruption and variation in tablet taking behaviour result in viral failure: a case-control study from Cape Town, South Africa. |
title_full |
Treatment interruption and variation in tablet taking behaviour result in viral failure: a case-control study from Cape Town, South Africa. |
title_fullStr |
Treatment interruption and variation in tablet taking behaviour result in viral failure: a case-control study from Cape Town, South Africa. |
title_full_unstemmed |
Treatment interruption and variation in tablet taking behaviour result in viral failure: a case-control study from Cape Town, South Africa. |
title_sort |
treatment interruption and variation in tablet taking behaviour result in viral failure: a case-control study from cape town, south africa. |
publisher |
Public Library of Science (PLoS) |
publishDate |
2011 |
url |
https://doaj.org/article/bbe75fae51fe4333b1de4689c4f3eab1 |
work_keys_str_mv |
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