Model-Based Cost-Effectiveness of State-level Latent Tuberculosis Interventions in California, Florida, New York and Texas
Supporting Files
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11 02 2021
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File Language:
English
Details
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Alternative Title:Clin Infect Dis
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Personal Author:
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Description:Background:
Targeted testing and treatment (TTT) for latent tuberculosis infection (LTBI) is a recommended strategy to accelerate TB reductions and further tuberculosis elimination in the United States (US). Evidence on cost-effectiveness of TTT for key populations can help advance this goal.
Methods:
We used a model of TB transmission to estimate the numbers of individuals who could be tested by interferon-γ release assay (IGRA) and treated for LTBI with three months of self-administered rifapentine and isoniazid (3HP) under various TTT scenarios. Specifically, we considered rapidly scaling up TTT among people who are non-US-born, diabetic, HIV-positive, homeless or incarcerated in California, Florida, New York, and Texas – states where more than half of US TB cases occur. We projected costs (from the healthcare system perspective, in 2018 dollars), thirty-year reductions in TB incidence, and incremental cost effectiveness (cost per quality-adjusted life year [QALY] gained) for TTT in each modeled population.
Results:
The projected cost effectiveness of TTT differed substantially by state and population, while the health impact (number of TB cases averted) was consistently greatest among the non-US-born. TTT was most cost-effective among persons living with HIV (from $2,828/QALY gained in Florida to $11,265/QALY gained in New York) and least cost-effective among people with diabetes (from $223,041/QALY gained in California to $817,753 /QALY in New York).
Conclusions:
The modeled cost-effectiveness of TTT for LTBI varies across states but was consistently greatest among people living with HIV, moderate among people who are non-US-born, incarcerated, or homeless, and least cost-effective among people living with diabetes.
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Subjects:
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Keywords:
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Source:Clin Infect Dis. 73(9):e3476-e3482
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Pubmed ID:32584968
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Pubmed Central ID:PMC8077726
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Document Type:
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Funding:
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Place as Subject:
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Volume:73
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Issue:9
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Collection(s):
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Main Document Checksum:urn:sha256:fe8eb11726438b2440f625a6bbed29319972d928e054b6eb38a473eeb7695aa0
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Download URL:
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File Type:
Supporting Files
File Language:
English
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