Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/118733
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dc.contributor.authorClavo Varas, Bernardinoen_US
dc.contributor.authorRodríguez Abreu, Delvysen_US
dc.contributor.authorGalván, Sarayen_US
dc.contributor.authorFederico, Marioen_US
dc.contributor.authorMartínez-Sánchez, Gregorioen_US
dc.contributor.authorRamallo Fariña, Yolandaen_US
dc.contributor.authorAntonelli, Carlaen_US
dc.contributor.authorBenítez, Gretelen_US
dc.contributor.authorRey-Baltar, Doloresen_US
dc.contributor.authorJorge, Ignacio J.en_US
dc.contributor.authorRodríguez Esparragón, Francisco Javieren_US
dc.contributor.authorSerrano-Aguilar, Pedroen_US
dc.date.accessioned2022-10-03T13:18:55Z-
dc.date.available2022-10-03T13:18:55Z-
dc.date.issued2022en_US
dc.identifier.otherScopus-
dc.identifier.urihttp://hdl.handle.net/10553/118733-
dc.description.abstractBackground: Pain secondary to chemotherapy-induced peripheral neuropathy (CIPN) can limit the administration of chemotherapy, cancer-treatment outcomes, and the quality of life of patients. Oxidative stress and inflammation are some of the key mechanisms involved in CIPN. Successful treatments for CIPN are limited. This report shows our preliminary experience using ozone treatment as a modulator of oxidative stress in chronic pain secondary to CIPN. Methods: Ozone treatment, by rectal insufflation, was administered in seven patients suffering from pain secondary to grade II or III CIPN. Pain was assessed by the visual analog scale (VAS). Results: All patients, except one, showed clinically relevant pain improvement. Median pain score according to the VAS was 7 (range: 5–8) before ozone treatment, 4 (range: 2–6) at the end of ozone treatment (p = 0.004), 5.5 (range: 1.8–6.3) 3 months after the end of ozone treatment (p = 0.008), and 6 (range: 2.6–6.6) 6 months after the end of ozone treatment (p = 0.008). The toxicity grade, according to the Common Terminology Criteria for Adverse Events (CTCAE v.5.0), improved in half of the patients. Conclusion: This report shows that most patients obtained clinically relevant and long-lasting improvement in chronic pain secondary to CIPN after treatment with ozone. These observed effects merit further research and support our ongoing randomized clinical trial (NCT04299893).en_US
dc.languageengen_US
dc.relation.ispartofFrontiers in Physiologyen_US
dc.sourceFrontiers in Physiology[EISSN 1664-042X],v. 13, (Agosto 2022)en_US
dc.subject32 Ciencias médicasen_US
dc.subject3201 Ciencias clínicasen_US
dc.subject2411 Fisiología humanaen_US
dc.subject.otherAntioxidantsen_US
dc.subject.otherCancer Survivorshipen_US
dc.subject.otherCancer Therapy-Induced Side Effectsen_US
dc.subject.otherChemotherapy-Induced Peripheral Neuropathyen_US
dc.subject.otherNeuropathic Painen_US
dc.subject.otherOxidative Stressen_US
dc.subject.otherOzone Therapyen_US
dc.subject.otherPainen_US
dc.titleLong-term improvement by ozone treatment in chronic pain secondary to chemotherapy-induced peripheral neuropathy: A preliminary reporten_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typeArticleen_US
dc.identifier.doi10.3389/fphys.2022.935269en_US
dc.identifier.scopus85138224075-
dc.contributor.orcidNO DATA-
dc.contributor.orcidNO DATA-
dc.contributor.orcidNO DATA-
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dc.contributor.authorscopusid57190093030-
dc.contributor.authorscopusid23989750700-
dc.contributor.authorscopusid57222392811-
dc.contributor.authorscopusid57201785606-
dc.contributor.authorscopusid6603422480-
dc.contributor.authorscopusid25823987800-
dc.contributor.authorscopusid57895552600-
dc.contributor.authorscopusid57219776100-
dc.contributor.authorscopusid6505717937-
dc.contributor.authorscopusid54580963400-
dc.contributor.authorscopusid6603262370-
dc.contributor.authorscopusid6602510866-
dc.identifier.eissn1664-042X-
dc.relation.volume13en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.utils.revisionen_US
dc.date.coverdateAgosto 2022en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.sjr1,028
dc.description.jcr4,0
dc.description.sjrqQ1
dc.description.jcrqQ2
dc.description.scieSCIE
dc.description.miaricds10,5
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.author.deptGIR IUIBS: Farmacología Molecular y Traslacional-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptGIR Nanomaterials and Corrosion-
crisitem.author.deptDepartamento de Ciencias Médicas y Quirúrgicas-
crisitem.author.deptGIR IUSA-ONEHEALTH 5: Reproducción Animal, Oncología y Anestesiología Comparadas-
crisitem.author.deptIU de Sanidad Animal y Seguridad Alimentaria-
crisitem.author.orcid0000-0003-2522-1064-
crisitem.author.orcid0000-0003-0506-1366-
crisitem.author.orcid0000-0003-1663-3673-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.parentorgDepartamento de Ingeniería Mecánica-
crisitem.author.parentorgIU de Sanidad Animal y Seguridad Alimentaria-
crisitem.author.fullNameClavo Varas,Bernardino-
crisitem.author.fullNameRodríguez Abreu, Delvys-
crisitem.author.fullNameRamallo Fariña, Yolanda-
crisitem.author.fullNameRodríguez Esparragón,Francisco Javier-
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