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2SPD-009 Cost minimisation study of the biological treatment of inflammatory bowel disease: ustekinumab versus vedolizumab
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  1. L Cantarelli,
  2. F Gutierrez Nicolas,
  3. B Del Rosario Garcia,
  4. J Ramos Rodriguez,
  5. J Garcia Cairos,
  6. JA Morales Barrios,
  7. S Garcia Gil,
  8. GA Gonzalez De La Fuente,
  9. J Gonzalez Garcia,
  10. GJ Nazco Casariego
  1. Complejo Hospitalario Universitario De Canarias, Pharmacy, Santa Cruz De Tenerife, Spain

Abstract

Background and importance Therapy for inflammatory bowel disease (IBD) has included ustekinumab and vedolizumab in cases where antitumour necrosis factor-alpha (TNFα) drugs or conventional therapy has failed. Currently, both drugs constitute a high economic impact at the hospital level.

Aim and objectives This was a cost minimisation analysis between vedolizumab and ustekinumab in IBD to determine the economic impact in a third level hospital.

Material and methods A 2 year, unicentre, retrospective study (January 2017–December 2019) was carried out in all IBD patients treated with vedolizumab and ustekinumab. The following variables were collected: patient weight, type of treatment and cost from the start of biological therapy.

The price of each drug was obtained from official data from the computer programme BOTPlus. The cost of each treatment was estimated taking into account: the posological regimen described in the technical data sheet, costs derived from the day hospital and costs related to dispensing of the drug in the ambulatory pharmacy service of the centre. To carry out the study, both therapies were considered equivalent in terms of efficacy.

Results The cost of treatment per year with vedolizumab was 13 765.05€ patient/year. The cost of treatment with ustekinumab was variable, depending on patient weight: 16 086.78€ patient/year in patients <55 kg (savings of 14.5% compared with vedolizumab), 17 868.87€ patient/year in patients 55–85 kg (savings of 23%) and 19 650.96€/patient/year in patients >85 kg (savings of 30%).

A total of 63 patients were treated with ustekinumab and vedolizumab in our hospital during the study and 34.9% received ustekinumab (n=22). Of these, 36.4% (n=8) weighed <55 kg, 59.1% (n=13) 55–85 kg and 9.1% (n=2) >85 kg. The total expenditure for ustekinumab on IBD during the study period was 388 911.39€. Application of the pharmacoeconomic model described in the present work, in our population, would have meant a saving of 76 814.24€.

Conclusion and relevance The results of this study show that vedolizumab is the most efficient alternative in all scenarios, with savings of up to 30% over the use of ustekinumab. Further cost effectiveness studies are necessary to corroborate the validity of these results.

References and/or acknowledgements No conflict of interest.

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