Cargando…

Acceptability, feasibility, and likelihood of stakeholders implementing the novel BPaL regimen to treat extensively drug-resistant tuberculosis patients

BACKGROUND: BPaL, a 6 month oral regimen composed of bedaquiline, pretomanid, and linezolid for treating extensively drug-resistant tuberculosis (XDR-TB) is a potential alternative for at least 20 months of individualized treatment regimens (ITR). The ITR has low tolerability, treatment adherence, a...

Descripción completa

Detalles Bibliográficos
Autores principales: van de Berg, S. E. J., Pelzer, P. T., van der Land, A. J., Abdrakhmanova, E., Ozi, A. Muhammad, Arias, M., Cook-Scalise, S., Dravniece, G., Gebhard, A., Juneja, S., Handayani, R., Kappel, D., Kimerling, M., Koppelaar, I., Malhotra, S., Myrzaliev, B., Nsa, B., Sugiharto, J., Engel, N., Mulder, C., van den Hof, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8284025/
https://www.ncbi.nlm.nih.gov/pubmed/34271884
http://dx.doi.org/10.1186/s12889-021-11427-y
_version_ 1783723315223855104
author van de Berg, S. E. J.
Pelzer, P. T.
van der Land, A. J.
Abdrakhmanova, E.
Ozi, A. Muhammad
Arias, M.
Cook-Scalise, S.
Dravniece, G.
Gebhard, A.
Juneja, S.
Handayani, R.
Kappel, D.
Kimerling, M.
Koppelaar, I.
Malhotra, S.
Myrzaliev, B.
Nsa, B.
Sugiharto, J.
Engel, N.
Mulder, C.
van den Hof, S.
author_facet van de Berg, S. E. J.
Pelzer, P. T.
van der Land, A. J.
Abdrakhmanova, E.
Ozi, A. Muhammad
Arias, M.
Cook-Scalise, S.
Dravniece, G.
Gebhard, A.
Juneja, S.
Handayani, R.
Kappel, D.
Kimerling, M.
Koppelaar, I.
Malhotra, S.
Myrzaliev, B.
Nsa, B.
Sugiharto, J.
Engel, N.
Mulder, C.
van den Hof, S.
author_sort van de Berg, S. E. J.
collection PubMed
description BACKGROUND: BPaL, a 6 month oral regimen composed of bedaquiline, pretomanid, and linezolid for treating extensively drug-resistant tuberculosis (XDR-TB) is a potential alternative for at least 20 months of individualized treatment regimens (ITR). The ITR has low tolerability, treatment adherence, and success rates, and hence to limit patient burden, loss to follow-up and the emergence of resistance it is essential to implement new DR-TB regimens. The objective of this study was to assess the acceptability, feasibility, and likelihood of implementing BPaL in Indonesia, Kyrgyzstan, and Nigeria. METHODS: We conducted a concurrent mixed-methods study among a cross-section of health care workers, programmatic and laboratory stakeholders between May 2018 and May 2019. We conducted semi-structured interviews and focus group discussions to assess perceptions on acceptability and feasibility of implementing BPaL. We determined the proportions of a recoded 3-point Likert scale (acceptable; neutral; unacceptable), as well as the overall likelihood of implementing BPaL (likely; neutral; unlikely) that participants graded per regimen, pre-defined aspect and country. We analysed the qualitative results using a deductive framework analysis. RESULTS: In total 188 stakeholders participated in this study: 63 from Kyrgyzstan, 51 from Indonesia, and 74 from Nigeria The majority were health care workers (110). Overall, 88% (146/166) of the stakeholders would likely implement BPaL once available. Overall acceptability for BPaL was high, especially patient friendliness was often rated as acceptable (93%, 124/133). In contrast, patient friendliness of the ITR was rated as acceptable by 45%. Stakeholders appreciated that BPaL would reduce workload and financial burden on the health care system. However, several stakeholders expressed concerns regarding BPaL safety (monitoring), long-term efficacy, and national regulatory requirements regarding introduction of the regimen. Stakeholders stressed the importance of addressing current health systems constraints as well, especially in treatment and safety monitoring systems. CONCLUSIONS: Acceptability and feasibility of the BPaL regimen is high among TB stakeholders in Indonesia, Kyrgyzstan, and Nigeria. The majority is willing to start using BPaL as the standard of care for eligible patients despite country-specific health system constraints. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12889-021-11427-y.
format Online
Article
Text
id pubmed-8284025
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-82840252021-07-19 Acceptability, feasibility, and likelihood of stakeholders implementing the novel BPaL regimen to treat extensively drug-resistant tuberculosis patients van de Berg, S. E. J. Pelzer, P. T. van der Land, A. J. Abdrakhmanova, E. Ozi, A. Muhammad Arias, M. Cook-Scalise, S. Dravniece, G. Gebhard, A. Juneja, S. Handayani, R. Kappel, D. Kimerling, M. Koppelaar, I. Malhotra, S. Myrzaliev, B. Nsa, B. Sugiharto, J. Engel, N. Mulder, C. van den Hof, S. BMC Public Health Research Article BACKGROUND: BPaL, a 6 month oral regimen composed of bedaquiline, pretomanid, and linezolid for treating extensively drug-resistant tuberculosis (XDR-TB) is a potential alternative for at least 20 months of individualized treatment regimens (ITR). The ITR has low tolerability, treatment adherence, and success rates, and hence to limit patient burden, loss to follow-up and the emergence of resistance it is essential to implement new DR-TB regimens. The objective of this study was to assess the acceptability, feasibility, and likelihood of implementing BPaL in Indonesia, Kyrgyzstan, and Nigeria. METHODS: We conducted a concurrent mixed-methods study among a cross-section of health care workers, programmatic and laboratory stakeholders between May 2018 and May 2019. We conducted semi-structured interviews and focus group discussions to assess perceptions on acceptability and feasibility of implementing BPaL. We determined the proportions of a recoded 3-point Likert scale (acceptable; neutral; unacceptable), as well as the overall likelihood of implementing BPaL (likely; neutral; unlikely) that participants graded per regimen, pre-defined aspect and country. We analysed the qualitative results using a deductive framework analysis. RESULTS: In total 188 stakeholders participated in this study: 63 from Kyrgyzstan, 51 from Indonesia, and 74 from Nigeria The majority were health care workers (110). Overall, 88% (146/166) of the stakeholders would likely implement BPaL once available. Overall acceptability for BPaL was high, especially patient friendliness was often rated as acceptable (93%, 124/133). In contrast, patient friendliness of the ITR was rated as acceptable by 45%. Stakeholders appreciated that BPaL would reduce workload and financial burden on the health care system. However, several stakeholders expressed concerns regarding BPaL safety (monitoring), long-term efficacy, and national regulatory requirements regarding introduction of the regimen. Stakeholders stressed the importance of addressing current health systems constraints as well, especially in treatment and safety monitoring systems. CONCLUSIONS: Acceptability and feasibility of the BPaL regimen is high among TB stakeholders in Indonesia, Kyrgyzstan, and Nigeria. The majority is willing to start using BPaL as the standard of care for eligible patients despite country-specific health system constraints. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12889-021-11427-y. BioMed Central 2021-07-16 /pmc/articles/PMC8284025/ /pubmed/34271884 http://dx.doi.org/10.1186/s12889-021-11427-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 Article
van de Berg, S. E. J.
Pelzer, P. T.
van der Land, A. J.
Abdrakhmanova, E.
Ozi, A. Muhammad
Arias, M.
Cook-Scalise, S.
Dravniece, G.
Gebhard, A.
Juneja, S.
Handayani, R.
Kappel, D.
Kimerling, M.
Koppelaar, I.
Malhotra, S.
Myrzaliev, B.
Nsa, B.
Sugiharto, J.
Engel, N.
Mulder, C.
van den Hof, S.
Acceptability, feasibility, and likelihood of stakeholders implementing the novel BPaL regimen to treat extensively drug-resistant tuberculosis patients
title Acceptability, feasibility, and likelihood of stakeholders implementing the novel BPaL regimen to treat extensively drug-resistant tuberculosis patients
title_full Acceptability, feasibility, and likelihood of stakeholders implementing the novel BPaL regimen to treat extensively drug-resistant tuberculosis patients
title_fullStr Acceptability, feasibility, and likelihood of stakeholders implementing the novel BPaL regimen to treat extensively drug-resistant tuberculosis patients
title_full_unstemmed Acceptability, feasibility, and likelihood of stakeholders implementing the novel BPaL regimen to treat extensively drug-resistant tuberculosis patients
title_short Acceptability, feasibility, and likelihood of stakeholders implementing the novel BPaL regimen to treat extensively drug-resistant tuberculosis patients
title_sort acceptability, feasibility, and likelihood of stakeholders implementing the novel bpal regimen to treat extensively drug-resistant tuberculosis patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8284025/
https://www.ncbi.nlm.nih.gov/pubmed/34271884
http://dx.doi.org/10.1186/s12889-021-11427-y
work_keys_str_mv AT vandebergsej acceptabilityfeasibilityandlikelihoodofstakeholdersimplementingthenovelbpalregimentotreatextensivelydrugresistanttuberculosispatients
AT pelzerpt acceptabilityfeasibilityandlikelihoodofstakeholdersimplementingthenovelbpalregimentotreatextensivelydrugresistanttuberculosispatients
AT vanderlandaj acceptabilityfeasibilityandlikelihoodofstakeholdersimplementingthenovelbpalregimentotreatextensivelydrugresistanttuberculosispatients
AT abdrakhmanovae acceptabilityfeasibilityandlikelihoodofstakeholdersimplementingthenovelbpalregimentotreatextensivelydrugresistanttuberculosispatients
AT oziamuhammad acceptabilityfeasibilityandlikelihoodofstakeholdersimplementingthenovelbpalregimentotreatextensivelydrugresistanttuberculosispatients
AT ariasm acceptabilityfeasibilityandlikelihoodofstakeholdersimplementingthenovelbpalregimentotreatextensivelydrugresistanttuberculosispatients
AT cookscalises acceptabilityfeasibilityandlikelihoodofstakeholdersimplementingthenovelbpalregimentotreatextensivelydrugresistanttuberculosispatients
AT dravnieceg acceptabilityfeasibilityandlikelihoodofstakeholdersimplementingthenovelbpalregimentotreatextensivelydrugresistanttuberculosispatients
AT gebharda acceptabilityfeasibilityandlikelihoodofstakeholdersimplementingthenovelbpalregimentotreatextensivelydrugresistanttuberculosispatients
AT junejas acceptabilityfeasibilityandlikelihoodofstakeholdersimplementingthenovelbpalregimentotreatextensivelydrugresistanttuberculosispatients
AT handayanir acceptabilityfeasibilityandlikelihoodofstakeholdersimplementingthenovelbpalregimentotreatextensivelydrugresistanttuberculosispatients
AT kappeld acceptabilityfeasibilityandlikelihoodofstakeholdersimplementingthenovelbpalregimentotreatextensivelydrugresistanttuberculosispatients
AT kimerlingm acceptabilityfeasibilityandlikelihoodofstakeholdersimplementingthenovelbpalregimentotreatextensivelydrugresistanttuberculosispatients
AT koppelaari acceptabilityfeasibilityandlikelihoodofstakeholdersimplementingthenovelbpalregimentotreatextensivelydrugresistanttuberculosispatients
AT malhotras acceptabilityfeasibilityandlikelihoodofstakeholdersimplementingthenovelbpalregimentotreatextensivelydrugresistanttuberculosispatients
AT myrzalievb acceptabilityfeasibilityandlikelihoodofstakeholdersimplementingthenovelbpalregimentotreatextensivelydrugresistanttuberculosispatients
AT nsab acceptabilityfeasibilityandlikelihoodofstakeholdersimplementingthenovelbpalregimentotreatextensivelydrugresistanttuberculosispatients
AT sugihartoj acceptabilityfeasibilityandlikelihoodofstakeholdersimplementingthenovelbpalregimentotreatextensivelydrugresistanttuberculosispatients
AT engeln acceptabilityfeasibilityandlikelihoodofstakeholdersimplementingthenovelbpalregimentotreatextensivelydrugresistanttuberculosispatients
AT mulderc acceptabilityfeasibilityandlikelihoodofstakeholdersimplementingthenovelbpalregimentotreatextensivelydrugresistanttuberculosispatients
AT vandenhofs acceptabilityfeasibilityandlikelihoodofstakeholdersimplementingthenovelbpalregimentotreatextensivelydrugresistanttuberculosispatients