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Design of mobile and website health application devices for drug tolerability in hereditary fructose intolerance

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dc.contributor.author Izquierdo-García, Elsa
dc.contributor.author Lazaro-Cebas, Andrea
dc.contributor.author Pastor, Berta-Montero
dc.contributor.author Diaz, Ana-Such
dc.contributor.author Alvaro-Alonso, Elena-Alba
dc.contributor.author Guerra, Laura-López
dc.contributor.author Escobar-Rodríguez, Ismael
dc.date.accessioned 2025-11-20T12:45:36Z
dc.date.available 2025-11-20T12:45:36Z
dc.date.issued 2024-01-05
dc.identifier.citation Izquierdo-García E, Lázaro-Cebas A, Montero Pastor B, Such Díaz A, Álvaro-Alonso EA, López Guerra L, et al. Design of mobile and website health application devices for drug tolerability in hereditary fructose intolerance. Orphanet J Rare Dis. 5 de enero de 2024;19(1):12.
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/21659
dc.description.abstract BACKGROUND: Hereditary fructose intolerance (HFI) is a rare metabolic disease caused by aldolase B deficiency. The aim of our study was to analyse excipient tolerability in patients with HFI and other related diseases and to design mobile and website health applications to facilitate the search for drugs according to their tolerance. RESULTS: A total of 555 excipients listed in the Spanish Medicines Agency database (July 2023) were classified as suitable for HFI patients, suitable with considerations ((glucose and glucose syrup, intravenous sucrose, oral mannitol, polydextrose, gums and carrageenans, ethanol, sulfite caramel and vanilla), not recommended (intravenous mannitol) and contraindicated (fructose, oral sucrose, invert sugar, sorbitol, maltitol, lactitol, isomaltitol, fruit syrups, honey, sucrose esters and sorbitol esters). Glucose and glucose syrup were classified as suitable with considerations due to its possible fructose content and their potential endogenous fructose production. For other related intolerances, wheat starch was contraindicated and oatmeal was not recommended in celiac disease; oral lactose and lactose-based coprocessed excipient (Cellactose®) were not recommended in lactose intolerance; and glucose, invert sugar and oral sucrose were not recommended in diabetes mellitus. The applications were named IntoMed®. Results are listed in order of tolerability (suitable drugs appear first and contraindicated drugs at the end), and they are accompanied by a note detailing their classified excipients. If a drug contains excipients within different categories, the overall classification will be the most restrictive. The apps are also able to classify substances with the same criteria if they act as active ingredients. The tools exhibited good usability (82.07 ± 13.46 points on the System Usability Scale [range: 0-100]) on a sample of HFI patients, their families and health care professionals. CONCLUSIONS: IntoMed® is a tool for finding information about the tolerability of drugs according to excipients for patients with HFI and other related intolerances, with good usability. It is a fast and reliable system that covers the current excipient legislation and expands on it with other specific information: HFI patients should be alert for excipients such as mannitol (especially in intravenous drugs), fruit syrups, honey, sulfite caramel or vanilla. Glucose might contain or produce fructose, and special precaution is needed because of potential errors in their composition.
dc.language.iso eng
dc.publisher BMC
dc.rights Atribución-NoComercial-SinDerivadas 3.0 España
dc.rights.uri http://creativecommons.org/licenses/by-nc-nd/3.0/es/ *
dc.subject.mesh Humans
dc.subject.mesh Fructose Intolerance
dc.subject.mesh Excipients
dc.subject.mesh Lactose
dc.subject.mesh Fructose
dc.subject.mesh Mannitol
dc.subject.mesh Sorbitol
dc.subject.mesh Glucose
dc.subject.mesh Sucrose
dc.subject.mesh Sulfites
dc.title Design of mobile and website health application devices for drug tolerability in hereditary fructose intolerance
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 38183105
dc.relation.publisherversion https://ojrd.biomedcentral.com/articles/10.1186/s13023-023-03011-x
dc.identifier.doi 10.1186/s13023-023-03011-x
dc.journal.title Orphanet Journal of Rare Diseases
dc.identifier.essn 1750-1172


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