Identificador persistente para citar o vincular este elemento: https://accedacris.ulpgc.es/handle/10553/121760
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dc.contributor.authorVera- Rosas, A.en_US
dc.contributor.authorAguiar, D.en_US
dc.contributor.authorDomínguez, A.en_US
dc.contributor.authorCabrera- Vicente, A.en_US
dc.contributor.authorMartín- Barrientos, P.en_US
dc.contributor.authorCabrera, R.en_US
dc.contributor.authorSalas-Salas, B. G.en_US
dc.contributor.authorFerrera- Alayón, L.en_US
dc.contributor.authorRibeiro, I.en_US
dc.contributor.authorChicas-Sett, R.en_US
dc.contributor.authorLara Jiménez, Pedro Carlosen_US
dc.contributor.authorLloret Sáez-Bravo, Martaen_US
dc.date.accessioned2023-04-10T15:03:02Z-
dc.date.available2023-04-10T15:03:02Z-
dc.date.issued2023en_US
dc.identifier.otherScopus-
dc.identifier.urihttps://accedacris.ulpgc.es/handle/10553/121760-
dc.description.abstractBackground/purpose: The aim of this study is to assess for the first time the immediate and long term impact on quality-of-life of HBO treatments(HBOT) at 1.45 ATA (Absolute Atmospheric Pressure) Medical Hyperbaric chamber. Methods: Patients over 18 years-old, suffering of grade 3 Common Terminology Criteria for Adverse Events (CTCAE) 4.0 radiation induced late toxicity and progressing to standard support therapy were included in this prospective study. HBOT was given daily, sixty minutes per session by a Medical Hyperbaric Chamber Biobarica System at 1.45 ATA at 100% O2. Forty sessions were prescribed for all patients given in 8 weeks. Patients reported outcomes (PROs) was assessed by the QLQ-C30 questionnaire, before starting, in the last week of the treatment, as well as during follow up. Results: Between February-2018/June-2021, 48 patients fulfilled the inclusion criteria. A total of 37 patients (77%) completed the treatment prescribed HBOT sessions. Patients with anal fibrosis (9/37) and brain necrosis (7/37) were the most frequently treated. The most common symptoms were pain (65%) and bleeding (54%). In addition, thirty out of the 37 patients who completed the pre- and post-treatment Patients Reported Outcomes (PROs) assessment also completed the follow up European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire C30 (EORTC-QLQ-C30), and were evaluated in the present study. Mean follow up was 22,10 (6–39) months. The Median score of the EORTC-QLQ-C30, at the end of HBOT and during follow-up, was improved in all assessed domains, except in the cognitive aspect (p = 0.106). Conclusions: HBOT at 1.45 ATA is a feasible and well tolerated treatment, improving long term quality of life in terms of physical function, daily activities and general health subjective state of patients suffering severe late radiation-induced toxicity.en_US
dc.languageengen_US
dc.relation.ispartofClinical and translational radiation oncologyen_US
dc.sourceClinical and Translational Radiation Oncology [EISSN 2405-6308],v. 40:100620, (Mayo 2023)en_US
dc.subject32 Ciencias médicasen_US
dc.subject320713 Oncologíaen_US
dc.subject.otherHyperbaric Chamberen_US
dc.subject.otherQlqen_US
dc.subject.otherRadiotherapyen_US
dc.subject.otherToxicityen_US
dc.titleProspective Pilot study of Quality of Life in patients with severe late-radiation-toxicity treated by Low hyperbaric-oxigen-therapyen_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.ctro.2023.100620en_US
dc.identifier.scopus85151277761-
dc.contributor.orcidNO DATA-
dc.contributor.orcidNO DATA-
dc.contributor.orcidNO DATA-
dc.contributor.orcidNO DATA-
dc.contributor.orcidNO DATA-
dc.contributor.orcidNO DATA-
dc.contributor.orcid0000-0002-4336-4045-
dc.contributor.orcidNO DATA-
dc.contributor.orcidNO DATA-
dc.contributor.orcidNO DATA-
dc.contributor.orcid0000-0003-1709-6232-
dc.contributor.orcid0000-0001-7273-4693-
dc.contributor.authorscopusid58164426200-
dc.contributor.authorscopusid58164726200-
dc.contributor.authorscopusid57417632900-
dc.contributor.authorscopusid58165022000-
dc.contributor.authorscopusid58164726300-
dc.contributor.authorscopusid57189214490-
dc.contributor.authorscopusid57209142019-
dc.contributor.authorscopusid57209144026-
dc.contributor.authorscopusid57196623600-
dc.contributor.authorscopusid57190872784-
dc.contributor.authorscopusid7004374085-
dc.contributor.authorscopusid7003855087-
dc.identifier.eissn2405-6308-
dc.relation.volume40en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.utils.revisionen_US
dc.date.coverdateMayo 2023en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.sjr0,999
dc.description.jcr2,7
dc.description.sjrqQ1
dc.description.jcrqQ2
dc.description.scieSCIE
dc.description.miaricds11,0
item.grantfulltextopen-
item.fulltextCon texto completo-
crisitem.author.deptDepartamento de Ciencias Clínicas-
crisitem.author.fullNameLara Jiménez, Pedro Carlos-
crisitem.author.fullNameLloret Sáez-Bravo, Marta-
Colección:Artículos
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