Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/219687
Title: Use of non-specific immunoglobulins in Catalonia in three third-level hospitals: a descriptive analysis of a hospital-prescribed medication registry
Author: Riera-Arnau, Judith
Ballarín, E.
Llop Rius, Roser
Montané, E.
Hereu Boher, Pilar
Vancells Lujan, Guillem
Padullés Zamora, Núria
Barriocanal Barriocanal, Ana Maria
Cardona-Peitx, Glòria
Casasnovas Pons, Carlos
Montoro Ronsano, J. Bruno
Nuñez, M.
Santacana Juncosa, Eugènia
Selva O'Callaghan, Albert
Solanich Moreno, Xavier
Sabaté Gallego, Mònica
Keywords: Immunoglobulines
Unitats de cures intensives
Prescripció de medicaments
Immunoglobulins
Intensive care units
Drug prescribing
Issue Date: 16-Dec-2024
Publisher: Frontiers Media
Abstract: Background: The increasing use of non-specific immunoglobulins (NSIGs) and their current shortage show a need for NSIGs' use prioritization. Data from a clinical perspective are necessary, mainly for pediatric patients. Objectives: The aim of the study was to assess the level of clinical evidence (LoE) of the indications that NSIGs are used for, the reasons for discontinuation, and the costs invested. Methods: A retrospective multicentric study was conducted on NSIG incident users between September 2019 and December 2021 retrieved from the Registry of Patients and Treatments (RPT) from Catalonia (Spain). LoE was categorized as A) authorized indications, B) unauthorized with scientific support, C) unauthorized without support, and D) unknown (UNK), following local and the United Kingdom's guidelines as a sensitivity analysis. We also estimated overall spending and costs per patient visit. Results: A total of 400 patients were included (17.3% pediatric), with a mean follow-up of 122.1/person-years for adults. The most frequent indications were nervous system and blood diseases. Almost all pediatric patients (56; 81.2%) were treated under A-level indications, as for 217 (65.6%) adults. In the sensitivity analysis, the A-level usage rate decreased to one-third and the B-level usage rate increased by 2-3 times. Furthermore, 37.8% (151) of individuals discontinued. This was predominantly due to remission or no response. The total costs were 868,462.6€/year, with median spending per visit amounting to 1,500€ for adults and 700€ for pediatric patients. Conclusion: NSIGs are used in clinical practice mainly for approved indications; however, non-approved indications are still an important issue. This could represent a significant economic burden on the healthcare system, focusing on the pediatric population and those at risk for discontinuation with alternative therapeutic options.
Note: Reproducció del document publicat a: https://doi.org/10.3389/fphar.2024.1420682
It is part of: Frontiers in Pharmacology, 2024, vol. 15
URI: https://hdl.handle.net/2445/219687
Related resource: https://doi.org/10.3389/fphar.2024.1420682
ISSN: 1663-9812
Appears in Collections:Articles publicats en revistes (Patologia i Terapèutica Experimental)
Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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