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Estimating the population health burden of Lyme disease in Ontario, Canada: a microsimulation modelling approach
BACKGROUND: If untreated, Lyme disease can lead to long-term sequelae and post-treatment Lyme disease syndrome (PTLDS), resulting in reduced health-related quality of life. The objective of this study was to develop a microsimulation model to estimate the population-level health burden of Lyme disea...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
CMA Joule Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8598239/ https://www.ncbi.nlm.nih.gov/pubmed/34785530 http://dx.doi.org/10.9778/cmajo.20210024 |
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author | Mac, Stephen Evans, Gerald A. Patel, Samir N. Pullenayegum, Eleanor M. Sander, Beate |
author_facet | Mac, Stephen Evans, Gerald A. Patel, Samir N. Pullenayegum, Eleanor M. Sander, Beate |
author_sort | Mac, Stephen |
collection | PubMed |
description | BACKGROUND: If untreated, Lyme disease can lead to long-term sequelae and post-treatment Lyme disease syndrome (PTLDS), resulting in reduced health-related quality of life. The objective of this study was to develop a microsimulation model to estimate the population-level health burden of Lyme disease in Ontario, Canada. METHODS: We developed a Lyme disease history model using microsimulation, simulating 100 000 people (mean age 37.6 yr, 51% female) from 2017 in Ontario over a lifetime risk of infection and time horizon. We extracted the sensitivity and specificity of the 2-tier testing recommended by the Canadian Public Health Laboratory Network, probabilities and health state utility values from the published literature and health administrative data. Our reported outcomes from our stochastic analysis include diagnosed cases of Lyme disease (stratified by stage), undiagnosed infections, sequelae, individuals with PTLDS and quality-adjusted life-years (QALYs) lost. RESULTS: Our model estimated 333 (95% confidence interval [CI] 329–337) infections over the lifetime of 100 000 simulated people (mean age 37.6 yr, 51% female), with 92% (95% CI 91%–93%) of infections diagnosed. Of those 308 people with Lyme Disease diagnoses, 67 (95% CI 65–69) developed sequelae (e.g., arthritic, cardiac, neurologic sequelae), and 34 (95% CI 33–35) developed PTLDS. Lyme disease resulted in a loss of 84.5 QALYs (95% CI 82.9–86.2) over the lifetime of the simulated cohort. Sensitivity and scenario analysis showed that increasing incidence rates of Lyme disease, potential underreporting, duration of PTLDS and quality of life (health state utility) associated with PTLDS had the greatest impact on health burden. INTERPRETATION: Lyme disease contributes considerable health burden in terms of QALYs lost. Our analysis provides evidence to understand the disease burden and lays the foundation to assess the cost-effectiveness of pharmaceutical and nonpharmaceutical interventions. |
format | Online Article Text |
id | pubmed-8598239 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | CMA Joule Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85982392021-11-19 Estimating the population health burden of Lyme disease in Ontario, Canada: a microsimulation modelling approach Mac, Stephen Evans, Gerald A. Patel, Samir N. Pullenayegum, Eleanor M. Sander, Beate CMAJ Open Research BACKGROUND: If untreated, Lyme disease can lead to long-term sequelae and post-treatment Lyme disease syndrome (PTLDS), resulting in reduced health-related quality of life. The objective of this study was to develop a microsimulation model to estimate the population-level health burden of Lyme disease in Ontario, Canada. METHODS: We developed a Lyme disease history model using microsimulation, simulating 100 000 people (mean age 37.6 yr, 51% female) from 2017 in Ontario over a lifetime risk of infection and time horizon. We extracted the sensitivity and specificity of the 2-tier testing recommended by the Canadian Public Health Laboratory Network, probabilities and health state utility values from the published literature and health administrative data. Our reported outcomes from our stochastic analysis include diagnosed cases of Lyme disease (stratified by stage), undiagnosed infections, sequelae, individuals with PTLDS and quality-adjusted life-years (QALYs) lost. RESULTS: Our model estimated 333 (95% confidence interval [CI] 329–337) infections over the lifetime of 100 000 simulated people (mean age 37.6 yr, 51% female), with 92% (95% CI 91%–93%) of infections diagnosed. Of those 308 people with Lyme Disease diagnoses, 67 (95% CI 65–69) developed sequelae (e.g., arthritic, cardiac, neurologic sequelae), and 34 (95% CI 33–35) developed PTLDS. Lyme disease resulted in a loss of 84.5 QALYs (95% CI 82.9–86.2) over the lifetime of the simulated cohort. Sensitivity and scenario analysis showed that increasing incidence rates of Lyme disease, potential underreporting, duration of PTLDS and quality of life (health state utility) associated with PTLDS had the greatest impact on health burden. INTERPRETATION: Lyme disease contributes considerable health burden in terms of QALYs lost. Our analysis provides evidence to understand the disease burden and lays the foundation to assess the cost-effectiveness of pharmaceutical and nonpharmaceutical interventions. CMA Joule Inc. 2021-11-16 /pmc/articles/PMC8598239/ /pubmed/34785530 http://dx.doi.org/10.9778/cmajo.20210024 Text en © 2021 CMA Joule Inc. or its licensors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY-NC-ND 4.0) licence, which permits use, distribution and reproduction in any medium, provided that the original publication is properly cited, the use is noncommercial (i.e., research or educational use), and no modifications or adaptations are made. See: https://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Research Mac, Stephen Evans, Gerald A. Patel, Samir N. Pullenayegum, Eleanor M. Sander, Beate Estimating the population health burden of Lyme disease in Ontario, Canada: a microsimulation modelling approach |
title | Estimating the population health burden of Lyme disease in Ontario, Canada: a microsimulation modelling approach |
title_full | Estimating the population health burden of Lyme disease in Ontario, Canada: a microsimulation modelling approach |
title_fullStr | Estimating the population health burden of Lyme disease in Ontario, Canada: a microsimulation modelling approach |
title_full_unstemmed | Estimating the population health burden of Lyme disease in Ontario, Canada: a microsimulation modelling approach |
title_short | Estimating the population health burden of Lyme disease in Ontario, Canada: a microsimulation modelling approach |
title_sort | estimating the population health burden of lyme disease in ontario, canada: a microsimulation modelling approach |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8598239/ https://www.ncbi.nlm.nih.gov/pubmed/34785530 http://dx.doi.org/10.9778/cmajo.20210024 |
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