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Impact of drug-resistant tuberculosis treatment on hearing function in South African adults: Bedaquiline versus kanamycin
BACKGROUND: Ototoxicity linked to medications used to treat tuberculosis (TB) remains a global challenge. OBJECTIVES: The aim was to describe the audiological function in a group of adults with drug-resistant tuberculosis (DR-TB) on bedaquiline (G-BDQ) treatment attending a TB hospital in South Afri...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AOSIS
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7876958/ https://www.ncbi.nlm.nih.gov/pubmed/33567829 http://dx.doi.org/10.4102/sajcd.v68i1.784 |
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author | Khoza-Shangase, Katijah Prodromos, Marina |
author_facet | Khoza-Shangase, Katijah Prodromos, Marina |
author_sort | Khoza-Shangase, Katijah |
collection | PubMed |
description | BACKGROUND: Ototoxicity linked to medications used to treat tuberculosis (TB) remains a global challenge. OBJECTIVES: The aim was to describe the audiological function in a group of adults with drug-resistant tuberculosis (DR-TB) on bedaquiline (G-BDQ) treatment attending a TB hospital in South Africa and compare this with patients on kanamycin (G-KCIN). METHODS: A quantitative paradigm was adopted within a non-experimental retrospective record review design. The sample consisted of 30 records of adults with DR-TB between the ages of 18 and 50 years, recruited from a Tropical Diseases Hospital in South Africa. Data were analysed through both descriptive and inferential statistical measures. RESULTS: Clear and statistically significant differences in the audiological function were found between the two groups. The group receiving G-KCIN presented with ototoxicity that was clearly demonstrated by sensorineural hearing loss of high-frequency worsening of thresholds in over 73% of the records, which was statistically (p < 0.05) and clinically significant, over the three testing sessions, demonstrating the cumulative effects of dosage. Increased evidence of tinnitus was also found in this group. The group receiving G-BDQ presented with neither statistically (p > 0.05) nor clinically significant changes in hearing thresholds across all frequencies over the same monitoring timeframe. Additionally, only one report (7%) of tinnitus was found in this group. CONCLUSION: The results indicating that bedaquiline does not cause hearing loss when compared with G-KCIN highlight the need for increased availability of bedaquiline for the treatment of DR-TB within the South African context, to preserve both the quantity and quality of life of those infected. |
format | Online Article Text |
id | pubmed-7876958 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | AOSIS |
record_format | MEDLINE/PubMed |
spelling | pubmed-78769582021-02-17 Impact of drug-resistant tuberculosis treatment on hearing function in South African adults: Bedaquiline versus kanamycin Khoza-Shangase, Katijah Prodromos, Marina S Afr J Commun Disord Original Research BACKGROUND: Ototoxicity linked to medications used to treat tuberculosis (TB) remains a global challenge. OBJECTIVES: The aim was to describe the audiological function in a group of adults with drug-resistant tuberculosis (DR-TB) on bedaquiline (G-BDQ) treatment attending a TB hospital in South Africa and compare this with patients on kanamycin (G-KCIN). METHODS: A quantitative paradigm was adopted within a non-experimental retrospective record review design. The sample consisted of 30 records of adults with DR-TB between the ages of 18 and 50 years, recruited from a Tropical Diseases Hospital in South Africa. Data were analysed through both descriptive and inferential statistical measures. RESULTS: Clear and statistically significant differences in the audiological function were found between the two groups. The group receiving G-KCIN presented with ototoxicity that was clearly demonstrated by sensorineural hearing loss of high-frequency worsening of thresholds in over 73% of the records, which was statistically (p < 0.05) and clinically significant, over the three testing sessions, demonstrating the cumulative effects of dosage. Increased evidence of tinnitus was also found in this group. The group receiving G-BDQ presented with neither statistically (p > 0.05) nor clinically significant changes in hearing thresholds across all frequencies over the same monitoring timeframe. Additionally, only one report (7%) of tinnitus was found in this group. CONCLUSION: The results indicating that bedaquiline does not cause hearing loss when compared with G-KCIN highlight the need for increased availability of bedaquiline for the treatment of DR-TB within the South African context, to preserve both the quantity and quality of life of those infected. AOSIS 2021-01-26 /pmc/articles/PMC7876958/ /pubmed/33567829 http://dx.doi.org/10.4102/sajcd.v68i1.784 Text en © 2021. The Authors https://creativecommons.org/licenses/by/4.0/ Licensee: AOSIS. This work is licensed under the Creative Commons Attribution License. |
spellingShingle | Original Research Khoza-Shangase, Katijah Prodromos, Marina Impact of drug-resistant tuberculosis treatment on hearing function in South African adults: Bedaquiline versus kanamycin |
title | Impact of drug-resistant tuberculosis treatment on hearing function in South African adults: Bedaquiline versus kanamycin |
title_full | Impact of drug-resistant tuberculosis treatment on hearing function in South African adults: Bedaquiline versus kanamycin |
title_fullStr | Impact of drug-resistant tuberculosis treatment on hearing function in South African adults: Bedaquiline versus kanamycin |
title_full_unstemmed | Impact of drug-resistant tuberculosis treatment on hearing function in South African adults: Bedaquiline versus kanamycin |
title_short | Impact of drug-resistant tuberculosis treatment on hearing function in South African adults: Bedaquiline versus kanamycin |
title_sort | impact of drug-resistant tuberculosis treatment on hearing function in south african adults: bedaquiline versus kanamycin |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7876958/ https://www.ncbi.nlm.nih.gov/pubmed/33567829 http://dx.doi.org/10.4102/sajcd.v68i1.784 |
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