Direct and Indirect Costs of Influenza-Like Illness Treated with and Without Oseltamivir in 15 European Countries: A Descriptive Analysis Alongside the Randomised Controlled ALIC4E Trial
Li, Xiao; Bilcke, Joke; van der Velden, Alike W.; Bongard, Emily; Bruyndonckx, Robin; Sundvall, Pär Daniel; Harbin, Nicolay J.; Coenen, Samuel; Francis, Nick; Bruno, Pascale; Garcia-Sangenis, Ana; Glinz, Dominik; Kosiek, Katarzyna; Mikó-Pauer, Réka; Radzeviciene Jurgute, Ruta; Seifert, Bohumil; Tsakountakis, Nikolaos; Aabenhus, Rune; Butler, Christopher C.; Beutels, Philippe
(2021) Clinical Drug Investigation, volume 41, issue 8, pp. 685 - 699
(Article)
Abstract
Background and Objective: Influenza-like illness (ILI) leads to a substantial disease burden every winter in Europe; however, oseltamivir is not frequently prescribed to ILI patients in the primary-care setting. An open-label, multi-country, multi-season, randomised controlled trial investigated the effectiveness of oseltamivir for treating ILI in 15 European countries. We aimed
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to evaluate whether patients presenting with ILI in primary care and being managed with the addition of oseltamivir to usual care had lower average direct and indirect costs compared to patients with usual care alone. Methods: Resource use data were extracted from participants’ daily diaries. Itemised country-specific unit costs were collected through official tariffs, pharmacies or literature. Costs were converted to 2018 values. The null hypothesis was tested based on one-sided credible intervals (CrIs) obtained by bootstrapping. Base-case analysis estimated direct cost and productivity losses using itemised costed resource use and the human capital approach. Scenario analyses with self-reported spending rather than itemised costing were also performed. Results: Patients receiving oseltamivir (N = 1306) reported fewer healthcare visits, medication uses, hospital attendances and paid-work hours lost than the other patients (N = 1298). Excluding the oseltamivir cost, the average direct costs were lower in patients treated with oseltamivir from all perspectives, but these differences were not statistically significant (perspective of patient: €17 [0–95% Crl: 16–19] vs. €24 [5–100% Crl: 18–29]; healthcare provider: €37 [28–67] vs. €44 [25–55]; healthcare payers: €54 [45–85] vs. €68 [45–81]; and society: €423 [399–478] vs. €451 [390–478]). Scenario and age-group analyses confirmed these findings, but with some between-country differences. Conclusion: The average direct and indirect costs were consistently lower in patients treated with oseltamivir than in patients without from four perspectives (excluding the oseltamivir cost). However, these differences were not statistically significant.
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Keywords: Pharmacology (medical)
ISSN: 1173-2563
Publisher: Adis International Ltd
Note: Funding Information: NF reports grants from Synairgen outside the submitted work. CCB reports grants from National Institute for Health Research Health and grants from National Institute for Health Research Health Protection Research Unit on Health Care Associated Infections and Antimicrobial Resistance during the conduct of the study; personal fees from Roche Molecular Systems, grants from Roche Molecular Diagnostics, personal fees from Pfizer, personal fees from Roche diagnostics, personal fees from Janssen Pharmaceuticals, outside the submitted work. DG reports being employed since 1 June 2020 by Roche Pharma (Schweiz) AG, Basel, Switzerland. Data collections for this articlet were completed before his current employment. The current employment did not influence this article. PB reports grants from European commission IMI, outside the submitted work. XL, JB, AWV, EB, RB, SC, PS, NJH, PaB, AGS, KK, RMP, RRJ, BS, NT and RA report no conflicts of interest. Funding Information: The ALICE trial and the contributions of AWV, EB, SC, NF, PS, NJH, PaB, AGS, DG, KK, RMP, RRJ, BS, NT, RA, CCB and PB were funded by the European Commission’s Seventh Framework Programme: Platform for European Preparedness Against (Re-)emerging Epidemics (PREPARE) (grant HEALTH-F3-2013-602525). PB, XL, JB and RB acknowledge partial Methusalem funding from the VAX-IDEA and ASCID Centres of Excellence in vaccination and infectious diseases at the University of Antwerp. JB and RB were funded by their personal postdoctoral grants from the Research Foundation—Flanders (FWO). PS acknowledges that The Healthcare Committee, Region Västra Götaland, Sweden, partially funded the Swedish part of the study. 4 Publisher Copyright: © 2021, The Author(s).
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