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Tuberculosis care cascade in Zambia - identifying the gaps in order to improve outcomes: a population-based analysis
OBJECTIVE: Tuberculosis (TB) remains a leading cause of morbidity and mortality in Zambia, especially for people living with HIV (PLHIV). We undertook a care cascade analysis to quantify gaps in care and align programme improvement measures with areas of need. DESIGN: Retrospective, population-based...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8356169/ https://www.ncbi.nlm.nih.gov/pubmed/34376439 http://dx.doi.org/10.1136/bmjopen-2020-044867 |
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author | Lungu, Patrick Kerkhoff, Andrew D Kasapo, Clara C Mzyece, Judith Nyimbili, Sulani Chimzizi, Rhehab Silumesii, Andrew Kagujje, Mary Subbaraman, Ramnath Muyoyeta, Monde Malama, Kennedy |
author_facet | Lungu, Patrick Kerkhoff, Andrew D Kasapo, Clara C Mzyece, Judith Nyimbili, Sulani Chimzizi, Rhehab Silumesii, Andrew Kagujje, Mary Subbaraman, Ramnath Muyoyeta, Monde Malama, Kennedy |
author_sort | Lungu, Patrick |
collection | PubMed |
description | OBJECTIVE: Tuberculosis (TB) remains a leading cause of morbidity and mortality in Zambia, especially for people living with HIV (PLHIV). We undertook a care cascade analysis to quantify gaps in care and align programme improvement measures with areas of need. DESIGN: Retrospective, population-based analysis. SETTING: We derived national-level estimates for each step of the TB care cascade in Zambia. Estimates were informed by WHO incidence estimates, nationally aggregated laboratory and notification registers, and individual-level programme data from four provinces. PARTICIPANTS: Participants included all individuals with active TB disease in Zambia in 2018. We characterised the overall TB cascade and disaggregated by drug susceptibility results and HIV status. RESULTS: In 2018, the total burden of TB in Zambia was estimated to be 72 495 (range, 40 495–111 495) cases. Of these, 43 387 (59.8%) accessed TB testing, 40 176 (55.4%) were diagnosed with TB, 36 431 (50.3%) were started on treatment and 32 700 (45.1%) completed treatment. Among all persons with TB lost at any step along the care cascade (n=39 795), 29 108 (73.1%) were lost prior to accessing diagnostic services, 3211 (8.1%) prior to diagnosis, 3745 (9.4%) prior to initiating treatment and 3731 (9.4%) prior to treatment completion. PLHIV were less likely than HIV-negative individuals to successfully complete the care cascade (42.8% vs 50.2%, p<0.001). Among those with rifampicin-resistant TB, there was substantial attrition at each step of the cascade and only 22.8% were estimated to have successfully completed treatment. CONCLUSIONS: Losses throughout the care cascade resulted in a large proportion of individuals with TB not completing treatment. Ongoing health systems strengthening and patient-centred engagement strategies are needed at every step of the care cascade; however, scale-up of active case finding strategies is particularly critical to ensure individuals with TB in the population reach initial stages of care. Additionally, a renewed focus on PLHIV and individuals with drug-resistant TB is urgently needed to improve TB-related outcomes in Zambia. |
format | Online Article Text |
id | pubmed-8356169 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-83561692021-08-24 Tuberculosis care cascade in Zambia - identifying the gaps in order to improve outcomes: a population-based analysis Lungu, Patrick Kerkhoff, Andrew D Kasapo, Clara C Mzyece, Judith Nyimbili, Sulani Chimzizi, Rhehab Silumesii, Andrew Kagujje, Mary Subbaraman, Ramnath Muyoyeta, Monde Malama, Kennedy BMJ Open Infectious Diseases OBJECTIVE: Tuberculosis (TB) remains a leading cause of morbidity and mortality in Zambia, especially for people living with HIV (PLHIV). We undertook a care cascade analysis to quantify gaps in care and align programme improvement measures with areas of need. DESIGN: Retrospective, population-based analysis. SETTING: We derived national-level estimates for each step of the TB care cascade in Zambia. Estimates were informed by WHO incidence estimates, nationally aggregated laboratory and notification registers, and individual-level programme data from four provinces. PARTICIPANTS: Participants included all individuals with active TB disease in Zambia in 2018. We characterised the overall TB cascade and disaggregated by drug susceptibility results and HIV status. RESULTS: In 2018, the total burden of TB in Zambia was estimated to be 72 495 (range, 40 495–111 495) cases. Of these, 43 387 (59.8%) accessed TB testing, 40 176 (55.4%) were diagnosed with TB, 36 431 (50.3%) were started on treatment and 32 700 (45.1%) completed treatment. Among all persons with TB lost at any step along the care cascade (n=39 795), 29 108 (73.1%) were lost prior to accessing diagnostic services, 3211 (8.1%) prior to diagnosis, 3745 (9.4%) prior to initiating treatment and 3731 (9.4%) prior to treatment completion. PLHIV were less likely than HIV-negative individuals to successfully complete the care cascade (42.8% vs 50.2%, p<0.001). Among those with rifampicin-resistant TB, there was substantial attrition at each step of the cascade and only 22.8% were estimated to have successfully completed treatment. CONCLUSIONS: Losses throughout the care cascade resulted in a large proportion of individuals with TB not completing treatment. Ongoing health systems strengthening and patient-centred engagement strategies are needed at every step of the care cascade; however, scale-up of active case finding strategies is particularly critical to ensure individuals with TB in the population reach initial stages of care. Additionally, a renewed focus on PLHIV and individuals with drug-resistant TB is urgently needed to improve TB-related outcomes in Zambia. BMJ Publishing Group 2021-08-10 /pmc/articles/PMC8356169/ /pubmed/34376439 http://dx.doi.org/10.1136/bmjopen-2020-044867 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Infectious Diseases Lungu, Patrick Kerkhoff, Andrew D Kasapo, Clara C Mzyece, Judith Nyimbili, Sulani Chimzizi, Rhehab Silumesii, Andrew Kagujje, Mary Subbaraman, Ramnath Muyoyeta, Monde Malama, Kennedy Tuberculosis care cascade in Zambia - identifying the gaps in order to improve outcomes: a population-based analysis |
title | Tuberculosis care cascade in Zambia - identifying the gaps in order to improve outcomes: a population-based analysis |
title_full | Tuberculosis care cascade in Zambia - identifying the gaps in order to improve outcomes: a population-based analysis |
title_fullStr | Tuberculosis care cascade in Zambia - identifying the gaps in order to improve outcomes: a population-based analysis |
title_full_unstemmed | Tuberculosis care cascade in Zambia - identifying the gaps in order to improve outcomes: a population-based analysis |
title_short | Tuberculosis care cascade in Zambia - identifying the gaps in order to improve outcomes: a population-based analysis |
title_sort | tuberculosis care cascade in zambia - identifying the gaps in order to improve outcomes: a population-based analysis |
topic | Infectious Diseases |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8356169/ https://www.ncbi.nlm.nih.gov/pubmed/34376439 http://dx.doi.org/10.1136/bmjopen-2020-044867 |
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