Latent tuberculosis treatment completion rates from prescription drug administrative data.


Journal

Canadian journal of public health = Revue canadienne de sante publique
ISSN: 1920-7476
Titre abrégé: Can J Public Health
Pays: Switzerland
ID NLM: 0372714

Informations de publication

Date de publication:
12 2019
Historique:
received: 03 01 2019
accepted: 21 06 2019
pubmed: 13 7 2019
medline: 10 4 2020
entrez: 13 7 2019
Statut: ppublish

Résumé

In the province of Manitoba, Canada, given that latent tuberculosis infection (LTBI) treatment is provided at no cost to the patient, treatment completion rates should be optimal. The objective of this study was to estimate LTBI treatment completion using prescription drug administrative data and identify patient characteristics associated with completion. Prescription drug data (1999-2014) were used to identify individuals dispensed isoniazid (INH) or rifampin (RIF) monotherapy. Treatment completion was defined as being dispensed INH for ≥ 180 days (INH180) or ≥ 270 days (INH270) or RIF for ≥ 120 days (RIF120). Logistic regression models tested socio-demographic and comorbidity characteristics associated with treatment completion. The study cohort comprised 4985 (90.4%) persons dispensed INH and 529 (9.6%) RIF. Overall treatment completion was 60.2% and improved from 43.1% in 1999-2003 to 67.3% in 2009-2014. INH180 showed the highest completion (63.8%) versus INH270 (40.4%) and RIF120 (27.0%). INH180 completion was higher among those aged 0-18 years (68.5%) compared with those aged 19+ (61.0%). Sex, geography, First Nations status, income quintile, and comorbidities were not associated with completion. Benchmark 80% treatment completion rates were not achieved in Manitoba. Factors associated with non-completion were older age, INH270, and RIF120. Access to shorter LTBI treatments, such as rifapentine/INH, may improve treatment completion.

Identifiants

pubmed: 31297736
doi: 10.17269/s41997-019-00240-1
pii: 10.17269/s41997-019-00240-1
pmc: PMC6964601
doi:

Substances chimiques

Antitubercular Agents 0
Prescription Drugs 0
Isoniazid V83O1VOZ8L
Rifampin VJT6J7R4TR
rifapentine XJM390A33U

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

705-713

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Auteurs

Pierre J Plourde (PJ)

Department of Community Health Sciences, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Canada. pplourde@wrha.mb.ca.
Department of Medical Microbiology and Infectious Diseases, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Canada. pplourde@wrha.mb.ca.
Integrated Tuberculosis Services, Winnipeg Regional Health Authority, 490 Hargrave Street, Winnipeg, Manitoba, R3A 0X7, Canada. pplourde@wrha.mb.ca.

Christopher A Basham (CA)

British Columbia Centre for Disease Control and School of Population and Public Health, University of British Columbia, Vancouver, Canada.

Shelley Derksen (S)

Manitoba Centre for Health Policy, Winnipeg, Canada.

Jennifer Schultz (J)

Manitoba Centre for Health Policy, Winnipeg, Canada.

Scott McCulloch (S)

Manitoba Centre for Health Policy, Winnipeg, Canada.

Linda Larcombe (L)

Department of Community Health Sciences, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Canada.
Department of Medical Microbiology and Infectious Diseases, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Canada.
Department of Internal Medicine, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Canada.

Kathi Avery Kinew (KA)

Nanaandawewigamig, First Nations Health and Social Secretariat of Manitoba, Winnipeg, Canada.

Lisa M Lix (LM)

Department of Community Health Sciences, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Canada.
Manitoba Centre for Health Policy, Winnipeg, Canada.

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Classifications MeSH