Cost-Effectiveness of Low-Dose Compared to Standard-Dose Alteplase for Acute Ischemic Stroke in China : A Within-Trial Economic Evaluation of the ENCHANTED Study

© 2022 The Author(s). Published by S. Karger AG, Basel..

INTRODUCTION: The Enhanced Control of Hypertension and Thrombolysis Stroke Study (ENCHANTED) showed that a low-dose alteplase was safe but not clearly non-inferior to standard-dose alteplase in acute ischemic stroke (AIS). Given the significant cost of this medicine, we undertook a cost-effectiveness analysis to determine the probability that low-dose is cost-effective relative to standard-dose alteplase in China.

METHODS: For ENCHANTED participants in China with available health cost data, cost-effectiveness and cost-utility analyses were undertaken in which death or disability (modified Rankin scale scores 2-6) at 90 days and quality-adjusted life-years (QALYs) were used as outcome measures, respectively. There was adherence to standard guidelines for health economic evaluations alongside non-inferiority trials and according to a health-care payer's perspective. The equivalence margin for cost and effectiveness was set at USD 691 and -0.025 QALYs, respectively, for the base-case analysis. Probabilistic sensitivity analyses were used to evaluate the probability of low-dose alteplase being non-inferior.

RESULTS: While the mean cost of alteplase was lower in the low-dose group (USD 1,569 vs. USD 2,154 in the standard-dose group), the total cost was USD 56 (95% confidence interval [CI]: -1,000-1,113) higher compared to the standard-dose group due to higher hospitalization costs in the low-dose group. There were 462 (95% CI: 415-509) and 410 (95% CI: 363-457) patients with death or disability per 1,000 patients in the low-dose and standard-dose groups, respectively. The low-dose group had marginally lower (0.008, 95% CI: -0.016-0.001) QALYs compared to their standard-dose counterparts. The low-dose group was found to have an 88% probability of being non-inferior based on cost-effectiveness versus the standard-dose group.

CONCLUSIONS: This health economic evaluation alongside the ENCHANTED indicates that the use of low-dose alteplase does not save overall healthcare costs nor lead to a gain in QALYs in the management of Chinese patients with AIS compared to the use of standard dose. There is little justification on economic grounds to shift from standard-of-care thrombolysis in AIS.

Medienart:

E-Artikel

Erscheinungsjahr:

2023

Erschienen:

2023

Enthalten in:

Zur Gesamtaufnahme - volume:52

Enthalten in:

Cerebrovascular diseases (Basel, Switzerland) - 52(2023), 2 vom: 08., Seite 145-152

Sprache:

Englisch

Beteiligte Personen:

Si, Lei [VerfasserIn]
Chen, Xiaoying [VerfasserIn]
Ouyang, Menglu [VerfasserIn]
Wang, Xia [VerfasserIn]
Chen, Guofang [VerfasserIn]
Cao, Yong-Jun [VerfasserIn]
Wu, Guojun [VerfasserIn]
Zhang, Jinli [VerfasserIn]
Zhang, Jingfen [VerfasserIn]
Liu, YuKai [VerfasserIn]
Zhang, Shihong [VerfasserIn]
Song, Lili [VerfasserIn]
Delcourt, Candice [VerfasserIn]
Arima, Hisatomi [VerfasserIn]
Wang, Lidan [VerfasserIn]
Lung, Thomas [VerfasserIn]
Chen, Mingsheng [VerfasserIn]
Anderson, Craig S [VerfasserIn]
Jan, Stephen [VerfasserIn]
ENCHANTED Investigators [VerfasserIn]

Links:

Volltext

Themen:

Acute ischemic stroke
Alteplase
Clinical trial
Cost-effectiveness
EC 3.4.21.68
Fibrinolytic Agents
Health economics
Journal Article
Tissue Plasminogen Activator

Anmerkungen:

Date Completed 26.04.2023

Date Revised 07.05.2023

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1159/000525869

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM34562176X