Experience of piloting BPaLM/BPaL for DR-TB care at selected sites in Pakistan

BACKGROUND: Pakistan ranks fourth globally in terms of high drug-resistant TB (DR-TB) burden, with approximately one-third of cases resistant to fluoroquinolones. Bedaquiline, pretomanid, linezolid and moxifloxacin (BPaLM/BPaL) offers an opportunity for most DR-TB patients to benefit from a shorter,...

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Main Authors: M.A. Khan, A. Ismail, A. Ghafoor, N. Khan, N. Muzaffar, F. Zafar, A. Gupta, S. Foraida, S. Juneja, R. Fatima, A.W. Khan, S. Shahid
Format: Article
Language:English
Published: International Union Against Tuberculosis and Lung Disease (The Union) 2024-11-01
Series:IJTLD Open
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Online Access:https://www.ingentaconnect.com/contentone/iuatld/ijtldo/2024/00000001/00000011/art00006
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author M.A. Khan
A. Ismail
A. Ghafoor
N. Khan
N. Muzaffar
F. Zafar
A. Gupta
S. Foraida
S. Juneja
R. Fatima
A.W. Khan
S. Shahid
M.A. Khan
author_facet M.A. Khan
A. Ismail
A. Ghafoor
N. Khan
N. Muzaffar
F. Zafar
A. Gupta
S. Foraida
S. Juneja
R. Fatima
A.W. Khan
S. Shahid
M.A. Khan
author_sort M.A. Khan
collection DOAJ
description BACKGROUND: Pakistan ranks fourth globally in terms of high drug-resistant TB (DR-TB) burden, with approximately one-third of cases resistant to fluoroquinolones. Bedaquiline, pretomanid, linezolid and moxifloxacin (BPaLM/BPaL) offers an opportunity for most DR-TB patients to benefit from a shorter, all-oral, well-tolerated and more effective treatment. METHODS: We conducted a retrospective cohort study to pilot the BPaLM/BPaL regimen at four selected sites in two provinces of Pakistan, i.e. Punjab and Khyber Pakhtunkhwa. Data were extracted and analysed using electronic medical records from the program. Descriptive statistics, survival analysis and binary logistic regression analysis were employed. RESULTS: A total of 116 patients took treatment between October 2022 and February 2023. The treatment success rate was 96%, with 3% deaths and <1% loss to follow-up. Patients typically completed treatment in 26.2–26.7 weeks for BPaLM and BPaL, respectively. No serious adverse events were observed. The most common side effects included QTcF prolongation (BPaLM: 55%, BPaL: 84%), haematological events (BPaLM: 32%, BPaL: 34%), and gastrointestinal problems (BPaLM: 36%, BPaL: 25%). CONCLUSION: The BPaLM/BPaL regimens for DR-TB are highly effective with minimal adverse events and feasible to implement in routine program circumstances.
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spelling doaj-art-f0d0871406e3404db2ebf689226b58142025-01-23T13:39:03ZengInternational Union Against Tuberculosis and Lung Disease (The Union)IJTLD Open3005-75902024-11-0111150851510.5588/ijtldopen.24.03696Experience of piloting BPaLM/BPaL for DR-TB care at selected sites in PakistanM.A. Khan0A. Ismail1A. Ghafoor2N. Khan3N. Muzaffar4F. Zafar5A. Gupta6S. Foraida7S. Juneja8R. Fatima9A.W. Khan10S. Shahid11M.A. Khan12Association for Social Development, Islamabad, Pakistan;Association for Social Development, Islamabad, Pakistan;National TB Control Programme, Islamabad, Pakistan;Association for Social Development, Islamabad, Pakistan;Association for Social Development, Islamabad, Pakistan;Association for Social Development, Islamabad, Pakistan;TB Alliance, New York, USA;TB Alliance, New York, USA;TB Alliance, New York, USA;Common Management Unit, AIDS, TB, Malaria, Ministry of National Health Services, Regulation and Coordination, Islamabad, Pakistan.National TB Control Programme, Islamabad, Pakistan;Association for Social Development, Islamabad, Pakistan;Association for Social Development, Islamabad, Pakistan;BACKGROUND: Pakistan ranks fourth globally in terms of high drug-resistant TB (DR-TB) burden, with approximately one-third of cases resistant to fluoroquinolones. Bedaquiline, pretomanid, linezolid and moxifloxacin (BPaLM/BPaL) offers an opportunity for most DR-TB patients to benefit from a shorter, all-oral, well-tolerated and more effective treatment. METHODS: We conducted a retrospective cohort study to pilot the BPaLM/BPaL regimen at four selected sites in two provinces of Pakistan, i.e. Punjab and Khyber Pakhtunkhwa. Data were extracted and analysed using electronic medical records from the program. Descriptive statistics, survival analysis and binary logistic regression analysis were employed. RESULTS: A total of 116 patients took treatment between October 2022 and February 2023. The treatment success rate was 96%, with 3% deaths and <1% loss to follow-up. Patients typically completed treatment in 26.2–26.7 weeks for BPaLM and BPaL, respectively. No serious adverse events were observed. The most common side effects included QTcF prolongation (BPaLM: 55%, BPaL: 84%), haematological events (BPaLM: 32%, BPaL: 34%), and gastrointestinal problems (BPaLM: 36%, BPaL: 25%). CONCLUSION: The BPaLM/BPaL regimens for DR-TB are highly effective with minimal adverse events and feasible to implement in routine program circumstances.https://www.ingentaconnect.com/contentone/iuatld/ijtldo/2024/00000001/00000011/art00006drug-resistant tuberculosisintegrated carebedaquilinepretomanidlinezolidpublic hospitals
spellingShingle M.A. Khan
A. Ismail
A. Ghafoor
N. Khan
N. Muzaffar
F. Zafar
A. Gupta
S. Foraida
S. Juneja
R. Fatima
A.W. Khan
S. Shahid
M.A. Khan
Experience of piloting BPaLM/BPaL for DR-TB care at selected sites in Pakistan
IJTLD Open
drug-resistant tuberculosis
integrated care
bedaquiline
pretomanid
linezolid
public hospitals
title Experience of piloting BPaLM/BPaL for DR-TB care at selected sites in Pakistan
title_full Experience of piloting BPaLM/BPaL for DR-TB care at selected sites in Pakistan
title_fullStr Experience of piloting BPaLM/BPaL for DR-TB care at selected sites in Pakistan
title_full_unstemmed Experience of piloting BPaLM/BPaL for DR-TB care at selected sites in Pakistan
title_short Experience of piloting BPaLM/BPaL for DR-TB care at selected sites in Pakistan
title_sort experience of piloting bpalm bpal for dr tb care at selected sites in pakistan
topic drug-resistant tuberculosis
integrated care
bedaquiline
pretomanid
linezolid
public hospitals
url https://www.ingentaconnect.com/contentone/iuatld/ijtldo/2024/00000001/00000011/art00006
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