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Health-related quality of life of X-linked hypophosphatemia in Spain

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dc.contributor.author Luis-Yanes, M, I
dc.contributor.author Diaz-Curiel, M
dc.contributor.author Peris, P
dc.contributor.author Vicente, C
dc.contributor.author Marin, S
dc.contributor.author Ramon-Krauel, M
dc.contributor.author Hernández, J
dc.contributor.author Broseta, JJ
dc.contributor.author Espinosa, L
dc.contributor.author Mendizabal, S
dc.contributor.author Pérez-Sukia, L
dc.contributor.author Martínez, V
dc.contributor.author Palazon, C
dc.contributor.author Pinero, JA
dc.contributor.author Calleja, MA
dc.contributor.author Espin, J
dc.contributor.author Arborio-Pinel, R
dc.contributor.author Ariceta, G
dc.date.accessioned 2025-11-20T12:45:29Z
dc.date.available 2025-11-20T12:45:29Z
dc.date.issued 2022-07
dc.identifier.citation Yanes MIL, Diaz-Curiel M, Peris P, Vicente C, Marin S, Ramon-Krauel M, et al. Health-related quality of life of X-linked hypophosphatemia in Spain. Orphanet J Rare Dis. diciembre de 2022;17(1):298.
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/21649
dc.description.abstract BACKGROUND: Health-related quality of life (HRQoL) of patients with X-linked hypophosphatemia (XLH) is lower than that of both the general population and the patients with other chronic diseases, mainly due to diagnostic delay, treatment difficulties, poor psychosocial support, and problems with social integration. Early diagnosis and optimal treatment are paramount to control the disease in patients with XLH, avoid complications, and maintain or improve their HRQoL. We, therefore, analyzed the HRQoL of pediatric and adult patients with XLH treated with conventional therapy in Spain. RESULTS: We used several versions of the EuroQol-5 dimensions (EQ-5D) instrument according to the age of patients with XLH. Then we compared the HRQoL of patients to that of the general Spanish population. Children with XLH (n = 21) had moderate problems in walking about (61.9%), washing or dressing themselves (9.52%), and performing their usual activities (33.33%). They also felt moderate pain or discomfort (61.9%) and were moderately anxious or depressed (23.81%). Adults with XLH (n = 29) had lower HRQoL, with problems in walking (93%, with 3.45% unable to walk independently), some level of pain (86%, with 3.45% experiencing extreme pain), problems with their usual activities (80%) and self-care (> 50%), and reported symptoms of anxiety and/or depression (65%). There were important differences with the general Spanish population. CONCLUSIONS: XLH impacts negatively on physical functioning and HRQoL of patients. In Spanish patients with XLH, the HRQoL was reduced despite conventional treatment, clearly indicating the need to improve the therapeutic approach to this disorder.
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 Adult
dc.subject.mesh Child
dc.subject.mesh Delayed Diagnosis
dc.subject.mesh Familial Hypophosphatemic Rickets
dc.subject.mesh Humans
dc.subject.mesh Pain
dc.subject.mesh Quality of Life/psychology
dc.subject.mesh Spain
dc.title Health-related quality of life of X-linked hypophosphatemia in Spain
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 35906684
dc.relation.publisherversion https://ojrd.biomedcentral.com/articles/10.1186/s13023-022-02452-0
dc.identifier.doi 10.1186/s13023-022-02452-0
dc.journal.title Orphanet Journal of Rare Diseases
dc.identifier.essn 1750-1172


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