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The effect of tuberculosis on immune reconstitution among HIV patients on highly active antiretroviral therapy in Adigrat general hospital, eastern Tigrai, Ethiopia; 2019: a retrospective follow up study

BACKGROUND: Ethiopia initiated antiretroviral therapy early in 2005. Managing and detecting antiretroviral treatment response is important to monitor the effectiveness of medication and possible drug switching for low immune reconstitution. There is less recovery of CD4+ T cells among human immunode...

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Autores principales: Negash, Hadush, Legese, Haftom, Tefera, Mebrahtu, Mardu, Fitsum, Tesfay, Kebede, Gebresilasie, Senait, Fseha, Berhane, Kahsay, Tsega, Gebrewahd, Aderajew, Berhe, Brhane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6896417/
https://www.ncbi.nlm.nih.gov/pubmed/31805857
http://dx.doi.org/10.1186/s12865-019-0327-7
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author Negash, Hadush
Legese, Haftom
Tefera, Mebrahtu
Mardu, Fitsum
Tesfay, Kebede
Gebresilasie, Senait
Fseha, Berhane
Kahsay, Tsega
Gebrewahd, Aderajew
Berhe, Brhane
author_facet Negash, Hadush
Legese, Haftom
Tefera, Mebrahtu
Mardu, Fitsum
Tesfay, Kebede
Gebresilasie, Senait
Fseha, Berhane
Kahsay, Tsega
Gebrewahd, Aderajew
Berhe, Brhane
author_sort Negash, Hadush
collection PubMed
description BACKGROUND: Ethiopia initiated antiretroviral therapy early in 2005. Managing and detecting antiretroviral treatment response is important to monitor the effectiveness of medication and possible drug switching for low immune reconstitution. There is less recovery of CD4+ T cells among human immunodeficiency virus patients infected with tuberculosis. Hence, we aimed to assess the effect of tuberculosis and other determinant factors of immunological response among human immunodeficiency virus patients on highly active antiretroviral therapy. A retrospective follow up study was conducted from October to July 2019. A total of 393 participants were enrolled. An interviewer based questionnaire was used for data collection. Patient charts were used to extract clinical data and follow up results of the CD4+ T cell. Current CD4+ T cell counts of patients were performed. STATA 13 software was used to analyze the data. A p-value ≤0.05 was considered a statistically significant association. RESULTS: The mean age of study participants was 39.2 years (SD: + 12.2 years) with 8.32 mean years of follow up. The overall prevalence of immune reconstitution failure was 24.7% (97/393). Highest failure rate occurred within the first year of follow up time, 15.7 per 100 Person-year. Failure of CD4+ T cells reconstitution was higher among tuberculosis coinfected patients (48.8%) than mono-infected patients (13.7%). Living in an urban residence, baseline CD4+ T cell count ≤250 cells/mm(3), poor treatment adherence and tuberculosis infection were significantly associated with the immunological failure. CONCLUSIONS: There was a high rate of CD4+ T cells reconstitution failure among our study participants. Tuberculosis infection increased the rate of failure. Factors like low CD4+ T cell baseline count, poor adherence and urban residence were associated with the immunological failure. There should be strict monitoring of CD4+ T cell counts among individuals with tuberculosis coinfection.
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spelling pubmed-68964172019-12-11 The effect of tuberculosis on immune reconstitution among HIV patients on highly active antiretroviral therapy in Adigrat general hospital, eastern Tigrai, Ethiopia; 2019: a retrospective follow up study Negash, Hadush Legese, Haftom Tefera, Mebrahtu Mardu, Fitsum Tesfay, Kebede Gebresilasie, Senait Fseha, Berhane Kahsay, Tsega Gebrewahd, Aderajew Berhe, Brhane BMC Immunol Research Article BACKGROUND: Ethiopia initiated antiretroviral therapy early in 2005. Managing and detecting antiretroviral treatment response is important to monitor the effectiveness of medication and possible drug switching for low immune reconstitution. There is less recovery of CD4+ T cells among human immunodeficiency virus patients infected with tuberculosis. Hence, we aimed to assess the effect of tuberculosis and other determinant factors of immunological response among human immunodeficiency virus patients on highly active antiretroviral therapy. A retrospective follow up study was conducted from October to July 2019. A total of 393 participants were enrolled. An interviewer based questionnaire was used for data collection. Patient charts were used to extract clinical data and follow up results of the CD4+ T cell. Current CD4+ T cell counts of patients were performed. STATA 13 software was used to analyze the data. A p-value ≤0.05 was considered a statistically significant association. RESULTS: The mean age of study participants was 39.2 years (SD: + 12.2 years) with 8.32 mean years of follow up. The overall prevalence of immune reconstitution failure was 24.7% (97/393). Highest failure rate occurred within the first year of follow up time, 15.7 per 100 Person-year. Failure of CD4+ T cells reconstitution was higher among tuberculosis coinfected patients (48.8%) than mono-infected patients (13.7%). Living in an urban residence, baseline CD4+ T cell count ≤250 cells/mm(3), poor treatment adherence and tuberculosis infection were significantly associated with the immunological failure. CONCLUSIONS: There was a high rate of CD4+ T cells reconstitution failure among our study participants. Tuberculosis infection increased the rate of failure. Factors like low CD4+ T cell baseline count, poor adherence and urban residence were associated with the immunological failure. There should be strict monitoring of CD4+ T cell counts among individuals with tuberculosis coinfection. BioMed Central 2019-12-05 /pmc/articles/PMC6896417/ /pubmed/31805857 http://dx.doi.org/10.1186/s12865-019-0327-7 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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
Negash, Hadush
Legese, Haftom
Tefera, Mebrahtu
Mardu, Fitsum
Tesfay, Kebede
Gebresilasie, Senait
Fseha, Berhane
Kahsay, Tsega
Gebrewahd, Aderajew
Berhe, Brhane
The effect of tuberculosis on immune reconstitution among HIV patients on highly active antiretroviral therapy in Adigrat general hospital, eastern Tigrai, Ethiopia; 2019: a retrospective follow up study
title The effect of tuberculosis on immune reconstitution among HIV patients on highly active antiretroviral therapy in Adigrat general hospital, eastern Tigrai, Ethiopia; 2019: a retrospective follow up study
title_full The effect of tuberculosis on immune reconstitution among HIV patients on highly active antiretroviral therapy in Adigrat general hospital, eastern Tigrai, Ethiopia; 2019: a retrospective follow up study
title_fullStr The effect of tuberculosis on immune reconstitution among HIV patients on highly active antiretroviral therapy in Adigrat general hospital, eastern Tigrai, Ethiopia; 2019: a retrospective follow up study
title_full_unstemmed The effect of tuberculosis on immune reconstitution among HIV patients on highly active antiretroviral therapy in Adigrat general hospital, eastern Tigrai, Ethiopia; 2019: a retrospective follow up study
title_short The effect of tuberculosis on immune reconstitution among HIV patients on highly active antiretroviral therapy in Adigrat general hospital, eastern Tigrai, Ethiopia; 2019: a retrospective follow up study
title_sort effect of tuberculosis on immune reconstitution among hiv patients on highly active antiretroviral therapy in adigrat general hospital, eastern tigrai, ethiopia; 2019: a retrospective follow up study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6896417/
https://www.ncbi.nlm.nih.gov/pubmed/31805857
http://dx.doi.org/10.1186/s12865-019-0327-7
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