Estimating direct healthcare costs attributable to laboratory-confirmed Lyme disease in Ontario, Canada: A population-based matched cohort study using health administrative data.


Journal

Zoonoses and public health
ISSN: 1863-2378
Titre abrégé: Zoonoses Public Health
Pays: Germany
ID NLM: 101300786

Informations de publication

Date de publication:
06 2019
Historique:
received: 28 05 2018
revised: 29 11 2018
accepted: 15 12 2018
pubmed: 22 1 2019
medline: 8 6 2019
entrez: 22 1 2019
Statut: ppublish

Résumé

The objective of this study was to determine healthcare costs attributable to laboratory-confirmed Lyme disease (LD) from the healthcare payer perspective in Ontario, Canada. A cost-of-illness study was conducted for incident LD subjects from 1 January 2006 through 31 December 2013 ascertained from provincial laboratory and reportable disease databases, linked to health administrative data. All LD subjects included were laboratory-confirmed, according to provincial case definitions. Incident LD subjects were propensity-score matched to uninfected subjects on age, sex, comorbidities and urban/rural status. We used phase-of-care methods to calculate attributable costs for two phases of illness: initial care (≤30 days following "index date") and continuing care (>30 days after index date to the end of the follow-up period). A total of 663 incident, confirmed LD subjects were identified from 2006 through 2013. Mean age was 44.2 ± 20.1 years; 339 (51.1%) were female; and 31 (4.7%) were hospitalized ≤30 days after index date. Six hundred fifty-eight (99.2%) LD subjects were matched to uninfected subjects; mean follow-up time was 3.3 years. Mean attributable costs per case during the initial care phase and continuing care were $277 (95% CI: $197, $357) and -$5 (-$27, $17), respectively. Attributable costs per LD subject aged 5-14 years were $440 ($132, $747), greater than the costs observed for other age strata. Expected 1-year attributable costs were $832, given continuing care costs were negligible. Limitations to our study include estimating costs using a cohort of only laboratory-confirmed LD cases, introducing selection bias for diagnosed and treated patients who may have a lower risk of developing sequelae. In conclusion, the initial care phase of LD is associated with increased healthcare costs, but without significant costs attributable to LD infection after 30 days. Estimates of costs attributable to LD are important for healthcare resource prioritization and the evaluation of novel interventions.

Identifiants

pubmed: 30665259
doi: 10.1111/zph.12560
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

428-435

Subventions

Organisme : Ontario Ministry of Health and Long-Term Care (MOHLTC)
Pays : International
Organisme : Public Health Agency of Canada
Pays : International

Informations de copyright

© 2019 Her Majesty the Queen in Right of Canada Zoonoses Public Health © 2019 Blackwell Verlag GmbH Reproduced with the permission of the Minister of Public Health Ontario.

Auteurs

Emily Shing (E)

Public Health Ontario, Toronto, Ontario, Canada.

John Wang (J)

Public Health Ontario, Toronto, Ontario, Canada.
Institute for Clinical Evaluative Sciences, Toronto, Ontario, Canada.

Edwin Khoo (E)

Public Health Ontario, Toronto, Ontario, Canada.

Gerald A Evans (GA)

Public Health Ontario, Toronto, Ontario, Canada.
Queens University, Kingston, Ontario, Canada.

Stephen Moore (S)

Public Health Ontario, Toronto, Ontario, Canada.

Mark P Nelder (MP)

Public Health Ontario, Toronto, Ontario, Canada.

Samir N Patel (SN)

Public Health Ontario, Toronto, Ontario, Canada.
Public Health Ontario Laboratory, Toronto, Ontario, Canada.

Curtis Russell (C)

Public Health Ontario, Toronto, Ontario, Canada.

Doug Sider (D)

Public Health Ontario, Toronto, Ontario, Canada.

Beate Sander (B)

Public Health Ontario, Toronto, Ontario, Canada.
Institute for Clinical Evaluative Sciences, Toronto, Ontario, Canada.
Institute of Health Policy, Management and Evaluation, University of Toronto, Ontario, Canada.
University Health Network, Toronto, Ontario, Canada.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH