2020
An observational study demonstrating the adherence and ease of use of the injector device, RebiSmart (R)
VALIS, Martin, Jana SARLAKOVA, Simona HALUSKOVA, Blanka KLIMOVA, Pavel POTUZNIK et. al.Základní údaje
Originální název
An observational study demonstrating the adherence and ease of use of the injector device, RebiSmart (R)
Autoři
VALIS, Martin (203 Česká republika), Jana SARLAKOVA (203 Česká republika), Simona HALUSKOVA (203 Česká republika), Blanka KLIMOVA (203 Česká republika), Pavel POTUZNIK (203 Česká republika), Marek PETERKA (203 Česká republika), Kamil KUCA (203 Česká republika), Pavel ŠTOURAČ (203 Česká republika, domácí), Jan MARES (203 Česká republika) a Zbysek PAVELEK (203 Česká republika)
Vydání
EXPERT OPINION ON DRUG DELIVERY, ABINGDON, TAYLOR & FRANCIS LTD, 2020, 1742-5247
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30104 Pharmacology and pharmacy
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 6.648
Kód RIV
RIV/00216224:14110/20:00116023
Organizační jednotka
Lékařská fakulta
UT WoS
000528167500001
Klíčová slova anglicky
Multiple Sclerosis; patients; adherence; treatment; use; RebiSmart
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 17. 7. 2020 09:05, Mgr. Tereza Miškechová
Anotace
V originále
Background: Adherence to Multiple Sclerosis (MS) treatment is considered one of the crucial factors for ensuring optimal clinical outcomes. Research has shown that the use of self-injector devices improves patient compliance with treatment. Therefore, the main purpose of this study is to evaluate the ease of use of RebiSmart (R) 2.0 in clinically isolated syndrome/relapsing-remitting MS patients during 12 months treatment period. Methods: A total number of 290 subjects entered into data collection; 249 (86%) of them completed the whole 12 months study period. The primary endpoints and the secondary endpoints were assessed by the User Study Questionnaire. Adherence data were retrieved from RebiSmart (R) 2.0 (Menu - Dose History) on the respective patient's visit. Outcome measures also included Expanded Disability Status Score, Kurtzke Functional Systems, and Modified Social Support Survey, Modified Social Support Survey-5. Results: This study demonstrated a very high proportion (>95%) of patients with a positive rating of the overall ease of use and the overall convenience of RebiSmart (R). The proportion of patients with a positive rating of the ease of use by individual domains and the functions of RebiSmart (R) were also high (>80%). Conclusion: The findings demonstrate a very good perception of the usability of the device by patients overall and in its individual functions.