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Determinants of adverse reactions to first-line antitubercular medicines: a prospective cohort study

BACKGROUND: The success of tuberculosis treatment relies on patients adhering to their medication regimen consistently. However, adherence levels tend to decrease among patients who experience adverse drug reactions to antitubercular medications, leading to suboptimal treatment outcomes. Hence, this...

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Autores principales: Djochie, Richard Delali Agbeko, Anto, Berko Panyin, Opare-Addo, Mercy Naa Aduele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10249546/
https://www.ncbi.nlm.nih.gov/pubmed/37291618
http://dx.doi.org/10.1186/s40545-023-00577-6
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author Djochie, Richard Delali Agbeko
Anto, Berko Panyin
Opare-Addo, Mercy Naa Aduele
author_facet Djochie, Richard Delali Agbeko
Anto, Berko Panyin
Opare-Addo, Mercy Naa Aduele
author_sort Djochie, Richard Delali Agbeko
collection PubMed
description BACKGROUND: The success of tuberculosis treatment relies on patients adhering to their medication regimen consistently. However, adherence levels tend to decrease among patients who experience adverse drug reactions to antitubercular medications, leading to suboptimal treatment outcomes. Hence, this study aimed to examine the types, incidence rates, and severity of adverse reactions caused by first-line antitubercular drugs. Additionally, it aimed to identify factors associated with the development of these reactions. By doing so, the study aimed to facilitate the provision of personalized and effective treatment to patients, ultimately improving treatment outcomes. METHODS: Newly diagnosed patients with active tuberculosis were monitored from the start of their treatment until the completion of therapy. Any adverse reactions to anti-TB drugs that they encountered were carefully recorded. The collected data were analyzed using appropriate statistical methods such as analysis of variance, Chi-squared test, Fisher's exact test, and independent t-tests. Logistic regression was employed to assess the association between adverse drug reactions and various socio-demographic and clinical factors of the patients, using odds ratios as a measure of association. RESULTS: Among the 378 patients included in the study, 181 individuals (47.9%) reported experiencing at least one adverse drug reaction, with an incidence rate of 1.75 events per 100-person months. The majority of these reactions occurred during the intensive phase of treatment. The gastrointestinal tract was the most commonly affected system, followed by the nervous system and skin. Patients aged over 45 years (OR = 1.55, 95% CI 1.01–2.39, p = 0.046) and those with extrapulmonary tuberculosis (OR = 2.41, 95% CI 1.03–5.64) were more likely to develop gastrointestinal reactions. Female gender was a significant predictor of both skin (OR = 1.78, 95% CI 1.05–3.02, p = 0.032) and nervous system (OR = 1.65, 95% CI 1.07–2.55, p = 0.024) reactions. Additionally, alcohol use and HIV infection were identified as independent predictors of adverse drug reactions affecting all three systems. CONCLUSION: Significant risk factors for developing antitubercular drug adverse reactions include alcohol consumption, cigarette smoking, being HIV positive, female gender and extrapulmonary tuberculosis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40545-023-00577-6.
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spelling pubmed-102495462023-06-10 Determinants of adverse reactions to first-line antitubercular medicines: a prospective cohort study Djochie, Richard Delali Agbeko Anto, Berko Panyin Opare-Addo, Mercy Naa Aduele J Pharm Policy Pract Research BACKGROUND: The success of tuberculosis treatment relies on patients adhering to their medication regimen consistently. However, adherence levels tend to decrease among patients who experience adverse drug reactions to antitubercular medications, leading to suboptimal treatment outcomes. Hence, this study aimed to examine the types, incidence rates, and severity of adverse reactions caused by first-line antitubercular drugs. Additionally, it aimed to identify factors associated with the development of these reactions. By doing so, the study aimed to facilitate the provision of personalized and effective treatment to patients, ultimately improving treatment outcomes. METHODS: Newly diagnosed patients with active tuberculosis were monitored from the start of their treatment until the completion of therapy. Any adverse reactions to anti-TB drugs that they encountered were carefully recorded. The collected data were analyzed using appropriate statistical methods such as analysis of variance, Chi-squared test, Fisher's exact test, and independent t-tests. Logistic regression was employed to assess the association between adverse drug reactions and various socio-demographic and clinical factors of the patients, using odds ratios as a measure of association. RESULTS: Among the 378 patients included in the study, 181 individuals (47.9%) reported experiencing at least one adverse drug reaction, with an incidence rate of 1.75 events per 100-person months. The majority of these reactions occurred during the intensive phase of treatment. The gastrointestinal tract was the most commonly affected system, followed by the nervous system and skin. Patients aged over 45 years (OR = 1.55, 95% CI 1.01–2.39, p = 0.046) and those with extrapulmonary tuberculosis (OR = 2.41, 95% CI 1.03–5.64) were more likely to develop gastrointestinal reactions. Female gender was a significant predictor of both skin (OR = 1.78, 95% CI 1.05–3.02, p = 0.032) and nervous system (OR = 1.65, 95% CI 1.07–2.55, p = 0.024) reactions. Additionally, alcohol use and HIV infection were identified as independent predictors of adverse drug reactions affecting all three systems. CONCLUSION: Significant risk factors for developing antitubercular drug adverse reactions include alcohol consumption, cigarette smoking, being HIV positive, female gender and extrapulmonary tuberculosis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40545-023-00577-6. BioMed Central 2023-06-08 /pmc/articles/PMC10249546/ /pubmed/37291618 http://dx.doi.org/10.1186/s40545-023-00577-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Djochie, Richard Delali Agbeko
Anto, Berko Panyin
Opare-Addo, Mercy Naa Aduele
Determinants of adverse reactions to first-line antitubercular medicines: a prospective cohort study
title Determinants of adverse reactions to first-line antitubercular medicines: a prospective cohort study
title_full Determinants of adverse reactions to first-line antitubercular medicines: a prospective cohort study
title_fullStr Determinants of adverse reactions to first-line antitubercular medicines: a prospective cohort study
title_full_unstemmed Determinants of adverse reactions to first-line antitubercular medicines: a prospective cohort study
title_short Determinants of adverse reactions to first-line antitubercular medicines: a prospective cohort study
title_sort determinants of adverse reactions to first-line antitubercular medicines: a prospective cohort study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10249546/
https://www.ncbi.nlm.nih.gov/pubmed/37291618
http://dx.doi.org/10.1186/s40545-023-00577-6
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