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dc.creatorDardiotis E., Perpati G., Borsos M., Nikolaidis I., Tzanetakos D., Deretzi G., Koutlas E., Kilidireas C., Mitsikostas D.D., Hadjigeorgiou G., Grigoriadis N., Papagiannopoulos S., Orologas A., Aggelidakis P., Antonios A., Fakas N., Papadimitriou A., Iliopoulos I., Kostadima V., Karageorgiou K., Lamprakopoulos S., Nikiforidis D., Voumvourakis K., Kaponi A., Maltezou M., Acquaviva T.P., Kerezoudi E., Balamoutsos G., Kerasnoudis A., Mitsias P., Doskas T., Maris T., Baltogiannis C., Chroni E., The AURELIO investigatorsen
dc.date.accessioned2023-01-31T07:50:54Z
dc.date.available2023-01-31T07:50:54Z
dc.date.issued2022
dc.identifier10.1007/s40120-022-00384-2
dc.identifier.issn21938253
dc.identifier.urihttp://hdl.handle.net/11615/73089
dc.description.abstractIntroduction: Multiple sclerosis (MS) is a highly heterogeneous inflammatory disease of the central nervous system. Patient-reported outcomes (PROs) in a real-world clinical setting can provide detailed information about MS from the patient's perspective. PROs were used here to assess quality of life (QoL), treatment satisfaction, clinical efficacy, and safety outcomes in a Greek cohort of relapsing remitting MS (RRMS) patients treated with oral teriflunomide (14 mg/day). Methods: AURELIO was a 2-year, prospective, observational study whose QoL primary endpoint was assessed with the Multiple Sclerosis Impact Scale (MSIS-29). Secondary endpoints included analyses of Patient Determined Disease Steps (PDDS), Treatment Satisfaction Questionnaire for Medication (TSQM), Expanded Disability Status Scale (EDSS), annualized relapse rate (ARR), adherence, and safety outcomes. Results: AURELIO enrolled 282 patients (62.8% female; mean age 44.8 [SD ± 11] years; EDSS 2.0 [SD ± 1.6]; 44.6% treatment-naïve), with 212 patients (75%) remaining on treatment at study end. MSIS-29 total scores remained stable, while the MSIS-29 psychological scale showed significant improvement (p = 0.0015) at 2 years vs. baseline. TSQM scores at 2 years showed significant improvements in effectiveness (+ 6.6, p = 0.0001), convenience (+ 1.9, p = 0.0256), and global satisfaction (+ 8.1, p = 0.0001) vs. baseline. Disease progression was stable as indicated by non-significant changes in PDDS and EDSS vs. baseline. The ARR was low at 0.065, with a slightly higher ARR in previously treated (0.070) vs. naïve patients (0.058). Adherence was high at > 90%. Overall, 91 patients (32.3%) in the study reported a total of 215 safety events (32 serious, of which 21 were classified as mild–moderate). No new safety signals were observed. Conclusions: These data highlight the importance of PROs to facilitate personalized treatment strategies in MS. In line with other teriflunomide studies, AURELIO showed stable QoL, efficacy and safety outcomes, and good treatment satisfaction both in treatment-naïve and previously treated patients in this Greek cohort of patients with RRMS. © 2022, The Author(s).en
dc.language.isoenen
dc.sourceNeurology and Therapyen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85134310426&doi=10.1007%2fs40120-022-00384-2&partnerID=40&md5=a7ad70d2a057f1635d779288d7dd55fc
dc.subjectalanine aminotransferaseen
dc.subjectaminotransferaseen
dc.subjectbeta interferonen
dc.subjectcolecalciferolen
dc.subjectfampridineen
dc.subjectgadoliniumen
dc.subjectgamma glutamyltransferaseen
dc.subjectglatirameren
dc.subjectlevothyroxineen
dc.subjectmethylprednisoloneen
dc.subjectteriflunomideen
dc.subjectadulten
dc.subjectadverse eventen
dc.subjectalopeciaen
dc.subjectArticleen
dc.subjectautoimmune hepatitisen
dc.subjectcohort analysisen
dc.subjectdepressionen
dc.subjectdiarrheaen
dc.subjectdisease activityen
dc.subjectdizzinessen
dc.subjectdrug efficacyen
dc.subjectdrug safetyen
dc.subjectdyslipidemiaen
dc.subjectExpanded Disability Status Scaleen
dc.subjectfemaleen
dc.subjectGreeceen
dc.subjecthumanen
dc.subjecthypertensionen
dc.subjectlower respiratory tract infectionen
dc.subjectmajor clinical studyen
dc.subjectmaleen
dc.subjectmiddle ageden
dc.subjectmononucleosisen
dc.subjectmulticenter studyen
dc.subjectmultiple sclerosisen
dc.subjectnauseaen
dc.subjectnuclear magnetic resonance imagingen
dc.subjectobservational studyen
dc.subjectpatient-reported outcomeen
dc.subjectprospective studyen
dc.subjectquality of lifeen
dc.subjectquality of life assessmenten
dc.subjectquestionnaireen
dc.subjectrecurrence risken
dc.subjectseptic shocken
dc.subjectAdisen
dc.titleReal-World Assessment of Quality of Life in Patients with Relapsing Remitting Multiple Sclerosis Treated with Teriflunomide for Two Years: Patient-Reported Outcomes from the AURELIO Study in Greeceen
dc.typejournalArticleen


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