Evidence map›Paper›PMID 31297736›Full record

ArticleCanadian journal of public health = Revue canadienne de sante publique2019

Latent tuberculosis treatment completion rates from prescription drug administrative data.

Pierre J Plourde, Christopher A Basham, Shelley Derksen, Jennifer Schultz, Scott McCulloch, Linda Larcombe, Kathi Avery Kinew, Lisa M Lix

Open access · bronzeAbstract read
In one paragraph

Article in Canadian journal of public health = Revue canadienne de sante publique, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 37% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 5 institutions in 1 country.

Pierre J PlourdeDepartment of Community Health Sciences, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Canada. pplourde@wrha.mb.ca.ORCID 0000-0003-3089-4335
Christopher A BashamBritish Columbia Centre for Disease Control and School of Population and Public Health, University of British Columbia, Vancouver, Canada.
Shelley DerksenManitoba Centre for Health Policy, Winnipeg, Canada.
Jennifer SchultzManitoba Centre for Health Policy, Winnipeg, Canada.
Scott McCullochManitoba Centre for Health Policy, Winnipeg, Canada.
Linda LarcombeDepartment of Community Health Sciences, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Canada.
Kathi Avery KinewNanaandawewigamig, First Nations Health and Social Secretariat of Manitoba, Winnipeg, Canada.
Lisa M LixDepartment of Community Health Sciences, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Canada.
Manitoba Health · CAFirst Nations Health and Social Secretariat of Manitoba · CAUniversity of British Columbia · CAUniversity of Manitoba · CAWinnipeg Regional Health Authority · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveIn 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.

methodsPrescription 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.

resultsThe 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.

conclusionsBenchmark 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.

Indexed as

AdolescentAdultAgedAge FactorsAntitubercular AgentsChildChild, PreschoolDatabases, FactualFemaleHumansInfantInfant, NewbornIsoniazidLatent TuberculosisMaleManitobaAntitubercular AgentsIsoniazidPrescription DrugsRifampinrifapentineCanadaCohort studiesEnglishHumansPublic health practice

Identifiers

PMID31297736
PMCPMC6964601
OpenAlexW2957954880

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.