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Cost-effectiveness analysis of non-invasive vagus nerve stimulation for the treatment of chronic cluster headache

BACKGROUND: Cluster headache (CH) is a debilitating condition that is generally associated with substantial health care costs. Few therapies are approved for abortive or prophylactic treatment. Results from the prospective, randomised, open-label PREVA study suggested that adjunctive treatment with...

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Autores principales: Morris, James, Straube, Andreas, Diener, Hans-Christoph, Ahmed, Fayyaz, Silver, Nicholas, Walker, Simon, Liebler, Eric, Gaul, Charly
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Milan 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4840129/
https://www.ncbi.nlm.nih.gov/pubmed/27102120
http://dx.doi.org/10.1186/s10194-016-0633-x
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author Morris, James
Straube, Andreas
Diener, Hans-Christoph
Ahmed, Fayyaz
Silver, Nicholas
Walker, Simon
Liebler, Eric
Gaul, Charly
author_facet Morris, James
Straube, Andreas
Diener, Hans-Christoph
Ahmed, Fayyaz
Silver, Nicholas
Walker, Simon
Liebler, Eric
Gaul, Charly
author_sort Morris, James
collection PubMed
description BACKGROUND: Cluster headache (CH) is a debilitating condition that is generally associated with substantial health care costs. Few therapies are approved for abortive or prophylactic treatment. Results from the prospective, randomised, open-label PREVA study suggested that adjunctive treatment with a novel non-invasive vagus nerve stimulation (nVNS) device led to decreased attack frequency and abortive medication use in patients with chronic CH (cCH). Herein, we evaluate whether nVNS is cost-effective compared with the current standard of care (SoC) for cCH. METHODS: A pharmacoeconomic model from the German statutory health insurance perspective was developed to estimate the 1-year cost-effectiveness of nVNS + SoC (versus SoC alone) using data from PREVA. Short-term treatment response data were taken from the clinical trial; longer-term response was modelled under scenarios of response maintenance, constant rate of response loss, and diminishing rate of response loss. Health-related quality of life was estimated by modelling EQ-5D™ data from PREVA; benefits were defined as quality-adjusted life-years (QALY). Abortive medication use data from PREVA, along with costs for the nVNS device and abortive therapies (i.e. intranasal zolmitriptan, subcutaneous sumatriptan, and inhaled oxygen), were used to assess health care costs in the German setting. RESULTS: The analysis resulted in mean expected yearly costs of €7096.69 for nVNS + SoC and €7511.35 for SoC alone and mean QALY of 0.607 for nVNS + SoC and 0.522 for SoC alone, suggesting that nVNS generates greater health benefits for lower overall cost. Abortive medication costs were 23 % lower with nVNS + SoC than with SoC alone. In the alternative scenarios (i.e. constant rate of response loss and diminishing rate of response loss), nVNS + SoC was more effective and cost saving than SoC alone. CONCLUSIONS: In all scenarios modelled from a German perspective, nVNS was cost-effective compared with current SoC, which suggests that adjunctive nVNS therapy provides economic benefits in the treatment of cCH. Notably, the current analysis included only costs associated with abortive treatments. Treatment with nVNS will likely promote further economic benefit when other potential sources of cost savings (e.g. reduced frequency of clinic visits) are considered. TRIAL REGISTRATION: Clinicaltrials.gov identifier NCT01701245, 03OCT2012.
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spelling pubmed-48401292016-05-16 Cost-effectiveness analysis of non-invasive vagus nerve stimulation for the treatment of chronic cluster headache Morris, James Straube, Andreas Diener, Hans-Christoph Ahmed, Fayyaz Silver, Nicholas Walker, Simon Liebler, Eric Gaul, Charly J Headache Pain Research Article BACKGROUND: Cluster headache (CH) is a debilitating condition that is generally associated with substantial health care costs. Few therapies are approved for abortive or prophylactic treatment. Results from the prospective, randomised, open-label PREVA study suggested that adjunctive treatment with a novel non-invasive vagus nerve stimulation (nVNS) device led to decreased attack frequency and abortive medication use in patients with chronic CH (cCH). Herein, we evaluate whether nVNS is cost-effective compared with the current standard of care (SoC) for cCH. METHODS: A pharmacoeconomic model from the German statutory health insurance perspective was developed to estimate the 1-year cost-effectiveness of nVNS + SoC (versus SoC alone) using data from PREVA. Short-term treatment response data were taken from the clinical trial; longer-term response was modelled under scenarios of response maintenance, constant rate of response loss, and diminishing rate of response loss. Health-related quality of life was estimated by modelling EQ-5D™ data from PREVA; benefits were defined as quality-adjusted life-years (QALY). Abortive medication use data from PREVA, along with costs for the nVNS device and abortive therapies (i.e. intranasal zolmitriptan, subcutaneous sumatriptan, and inhaled oxygen), were used to assess health care costs in the German setting. RESULTS: The analysis resulted in mean expected yearly costs of €7096.69 for nVNS + SoC and €7511.35 for SoC alone and mean QALY of 0.607 for nVNS + SoC and 0.522 for SoC alone, suggesting that nVNS generates greater health benefits for lower overall cost. Abortive medication costs were 23 % lower with nVNS + SoC than with SoC alone. In the alternative scenarios (i.e. constant rate of response loss and diminishing rate of response loss), nVNS + SoC was more effective and cost saving than SoC alone. CONCLUSIONS: In all scenarios modelled from a German perspective, nVNS was cost-effective compared with current SoC, which suggests that adjunctive nVNS therapy provides economic benefits in the treatment of cCH. Notably, the current analysis included only costs associated with abortive treatments. Treatment with nVNS will likely promote further economic benefit when other potential sources of cost savings (e.g. reduced frequency of clinic visits) are considered. TRIAL REGISTRATION: Clinicaltrials.gov identifier NCT01701245, 03OCT2012. Springer Milan 2016-04-22 /pmc/articles/PMC4840129/ /pubmed/27102120 http://dx.doi.org/10.1186/s10194-016-0633-x Text en © Morris et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Research Article
Morris, James
Straube, Andreas
Diener, Hans-Christoph
Ahmed, Fayyaz
Silver, Nicholas
Walker, Simon
Liebler, Eric
Gaul, Charly
Cost-effectiveness analysis of non-invasive vagus nerve stimulation for the treatment of chronic cluster headache
title Cost-effectiveness analysis of non-invasive vagus nerve stimulation for the treatment of chronic cluster headache
title_full Cost-effectiveness analysis of non-invasive vagus nerve stimulation for the treatment of chronic cluster headache
title_fullStr Cost-effectiveness analysis of non-invasive vagus nerve stimulation for the treatment of chronic cluster headache
title_full_unstemmed Cost-effectiveness analysis of non-invasive vagus nerve stimulation for the treatment of chronic cluster headache
title_short Cost-effectiveness analysis of non-invasive vagus nerve stimulation for the treatment of chronic cluster headache
title_sort cost-effectiveness analysis of non-invasive vagus nerve stimulation for the treatment of chronic cluster headache
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4840129/
https://www.ncbi.nlm.nih.gov/pubmed/27102120
http://dx.doi.org/10.1186/s10194-016-0633-x
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