Feasibility of decentralised, task-shifted hepatitis C testing and treatment services in urban Myanmar: implications for scale-up.

gastroenterology health services administration & management international health services public health

Journal

BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874

Informations de publication

Date de publication:
03 05 2022
Historique:
entrez: 3 5 2022
pubmed: 4 5 2022
medline: 6 5 2022
Statut: epublish

Résumé

To assess the feasibility considerations for a decentralised, one-stop-shop model of care implemented in Yangon, Myanmar. Two primary care level clinics in urban Yangon, Myanmar. This is a feasibility study of a highly effective care model. Using Intervention Complexity Framework by Gericke Programmatic data were collected from clinical records, GeneXpert device test and maintenance reports, national guidelines, product and device instructions and site monitoring visit reports. Healthcare providers involved in delivering care model contributed interview data. The main feasibility considerations are appropriate storage for test kits and treatments (in response to temperature and humidity requirements), installation of a continuous stable electricity supply for the GeneXpert device, air-conditioning for the laboratory room hosting GeneXpert, access to a laboratory for pretreatment assessments and clear referral pathways for specialist consultation when required. Lessons from our project implementation experiences included the extensive time requirements for patient education, the importance of regular error monitoring and stock storage reviews and that flexible appointment scheduling and robust reminder system likely contributed to high retention in care. Detailed documentation and dissemination of feasibility requirements and implementation considerations is vital to assist others to successfully implement a similar model of care elsewhere. We provide 10 recommendations for successful implementation. The trial was registered at ClinicalTrials.gov NCT03939013 on May 6, 2019. This manuscript presents post-results data on feasibility.

Identifiants

pubmed: 35504640
pii: bmjopen-2021-059639
doi: 10.1136/bmjopen-2021-059639
pmc: PMC9066562
doi:

Banques de données

ClinicalTrials.gov
['NCT03939013']

Types de publication

Clinical Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e059639

Subventions

Organisme : World Health Organization
ID : 001
Pays : International

Informations de copyright

© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: MH has received investigator-initiated grant funding from Gilead Sciences and AbbVie for unrelated work. AP has received investigator-initiated grant funding from Gilead Sciences, MSD and AbbVie and speaker fees from Gilead Sciences for unrelated work. JH has received investigator-initiated grant funding and speaker fees from Gilead Sciences for unrelated work. WLY has received Gilead Sciences Fellowship for related work. KPK has received non-financial support from Mylan, Hetero and Royal Ruby. WN has received non-financial support from Mylan and Cipla. All others declare no potential competing interests.

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Auteurs

Bridget Louise Draper (BL)

Disease Elimination, Burnet Institute, Melbourne, Victoria, Australia bridget.draper@burnet.edu.au.
School of Public Health and Preventive Medicine, Monash University, St Kilda, Victoria, Australia.

Win Lei Yee (WL)

Disease Elimination, Burnet Institute Myanmar, Yangon, Myanmar.

Anna Bowring (A)

Disease Elimination, Burnet Institute, Melbourne, Victoria, Australia.

Hla Htay (H)

Disease Elimination, Burnet Institute Myanmar, Yangon, Myanmar.

Nwe Nwe (N)

FIND, Geneva, Switzerland.

Jessica Markby (J)

FIND, Geneva, Switzerland.

Khin Pyone Kyi (KP)

Myanmar Liver Foundation, Yangon, Myanmar.

Philippa Easterbrook (P)

Department of Global HIV, Hepatitis, and STI Programmes, World Health Organization, Geneva, Switzerland.

Win Naing (W)

Myanmar Liver Foundation, Yangon, Myanmar.
Yangon Specialty Hospital, Yangon, Myanmar.

Thin Mar Win (TM)

Disease Elimination, Burnet Institute Myanmar, Yangon, Myanmar.

Khin Sanda Aung (KS)

National Hepatitis Control Program, Department of Public Health, Ministry of Health and Sports, Yangon, Myanmar.

Jessica Howell (J)

Disease Elimination, Burnet Institute, Melbourne, Victoria, Australia.
St Vincent's Hospital Melbourne, Fitzroy, Victoria, Australia.
Department of Medicine, University of Melbourne, Melbourne, Victoria, Australia.

Alisa Pedrana (A)

Disease Elimination, Burnet Institute, Melbourne, Victoria, Australia.
School of Public Health and Preventive Medicine, Monash University, St Kilda, Victoria, Australia.
Health Services Research and Implementation, Monash Partners, Melbourne, Victoria, Australia.

Margaret Hellard (M)

Disease Elimination, Burnet Institute, Melbourne, Victoria, Australia.
School of Public Health and Preventive Medicine, Monash University, St Kilda, Victoria, Australia.
Hepatitis Services, Department of Infectious Diseases, Alfred Hospital, Melbourne, Victoria, Australia.
Doherty Institute, Melbourne, Victoria, Australia.
School of Population and Global Health, University of Melbourne, Melbourne, Victoria, Australia.

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