Cost-effectiveness of stent-retriever thrombectomy in large vessel occlusion strokes of the anterior circulation: Analysis from the French societal perspective.


Journal

Revue neurologique
ISSN: 0035-3787
Titre abrégé: Rev Neurol (Paris)
Pays: France
ID NLM: 2984779R

Informations de publication

Date de publication:
Mar 2020
Historique:
received: 05 11 2018
revised: 05 02 2019
accepted: 06 06 2019
pubmed: 19 9 2019
medline: 18 12 2020
entrez: 19 9 2019
Statut: ppublish

Résumé

To determine the cost-effectiveness of stent retriever thrombectomy (SRT) added to standard of care (SOC) in large vessel occlusion (LVO) strokes, adopting the French societal perspective given the lack of published studies with such perspective. We developed an hybrid model (decision tree until one year post-stroke followed by a Markov model from one year onward). The time horizon was 20 years. We calculated transition probabilities across the modified Rankin Scale (mRS) based on a published meta-analysis. The main outcome measure was quality adjusted life-years (QALYs) gained. Resources and input costs were derived from a literature search. We calculated the incremental cost-effectiveness ratio (ICER) expressed as cost/QALY. We used 1-way deterministic and probabilistic sensitivity analysis (PSA) to evaluate the model uncertainty. In the base-case, adding SRT to SOC resulted in increased effectiveness of 0.73 QALY while total costs were reduced by 3,874€ (ICER of -5,400€/QALY). In the scenario analysis adopting the French healthcare system perspective, the ICER was 4,901€/QALY. Parameters the most influential were the relative risks of SRT over SOC for 90-days mortality and for 90-days mRS 0-2, and the time horizon. PSA showed the 95% confidence interval of the ICER was -21,324 to 4,591€/QALY, with SRT having 85.5% chance to be dominant and 100% to be cost-effective at a threshold of 50,000€/QALY. SRT was dominant from a French societal perspective, from 9 years post-stroke onwards. Cost-effectiveness of SRT added to SOC becomes undisputable with evidences from payer and societal viewpoints.

Identifiants

pubmed: 31526554
pii: S0035-3787(18)30896-8
doi: 10.1016/j.neurol.2019.06.007
pii:
doi:

Substances chimiques

Tissue Plasminogen Activator EC 3.4.21.68

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

180-188

Informations de copyright

Copyright © 2019 Elsevier Masson SAS. All rights reserved.

Auteurs

M Barral (M)

Hospices civils de Lyon, pôle de santé publique, Lyon, 69003, France; University Lyon, University Claude Bernard Lyon 1, HESPER EA 7425, 69008 Lyon, France. Electronic address: marine.barral@outlook.com.

X Armoiry (X)

Division of Health Sciences, Warwick medical school, University of Warwick, Gibbet Hill road, CV47AL Coventry, England, UK; Hospices Civils de Lyon, UMR-CNRS 5510, MATEIS, 69500 Bron, France.

S Boudour (S)

Department of Pharmacy, Hospital of Voiron, 38500 Voiron, France.

G Aulagner (G)

Hospices Civils de Lyon, UMR-CNRS 5510, MATEIS, 69500 Bron, France.

A-M Schott (AM)

Hospices civils de Lyon, pôle de santé publique, Lyon, 69003, France.

F Turjman (F)

Department of Interventional Neuroradiology, Neurologic Hospital Pierre Wertheimer, Hospices Civils de Lyon/FHU IRIS, 69500 Bron, France.

B Gory (B)

Department of Diagnostic and Therapeutic, Neuroradiology, University Hospital of Nancy, Nancy, France/University of Lorraine, Inserm U1254, IADI, 54000, Nancy, France.

M Viprey (M)

Hospices civils de Lyon, pôle de santé publique, Lyon, 69003, France.

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