Egyszerű nézet

dc.contributor.author Robert L Boggs
dc.contributor.author Kárpáti Sarolta
dc.contributor.author Wenzhi Li
dc.contributor.author Theresa Williams
dc.contributor.author Ronald Pedersen
dc.contributor.author Lotus Mallbris
dc.contributor.author Robert Gniadecki
dc.date.accessioned 2015-04-09T08:57:09Z
dc.date.available 2015-04-09T08:57:09Z
dc.date.issued 2014
dc.identifier 84906832735
dc.identifier.citation pagination=14; journalVolume=14; journalTitle=BMC DERMATOLOGY;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/1677
dc.identifier.uri doi:10.1186/1471-5945-14-14
dc.description.abstract BACKGROUND: Psoriasis and psoriatic arthritis (PsA) impair quality of life, including reduction in employment or job duties. The PRESTA (Psoriasis Randomized Etanercept STudy in Patients with Psoriatic Arthritis) study, a randomized, double-blind, two-dose trial, examined the efficacy of etanercept treatment in patients with moderate-to-severe plaque psoriasis and PsA and the main results have been presented previously. This analysis examined employment status, job duties and sick days, pre-defined endpoints in PRESTA, among this patient population. METHODS: Participants (N = 752) were randomized to receive etanercept 50 mg twice weekly (BIW; n = 379) or 50 mg once weekly (QW; n = 373) for 12 weeks by subcutaneous injection. All participants then received open-label etanercept 50 mg QW for 12 additional weeks, while remaining blinded to the randomization. A pharmacoeconomic questionnaire was administered at baseline, week 12 and week 24 of treatment. The questionnaire included employment status and changing job responsibilities and sick time taken due to psoriasis or PsA. The statistical methods included analysis of covariance, t-test, Fisher's exact test and McNemar's test. Last-observation-carried-forward imputation was used for missing data. RESULTS: Employment was at least maintained from baseline to week 24 in both dose groups (56% [BIW/QW] and 60% [QW/QW] at baseline, 61% and 60%, respectively, at week 24). Among employed participants, the proportion of patients whose job responsibilities changed due to PsA decreased significantly from baseline to week 24 (17-23% to 5-8%; p < 0.01). Similar results were seen with job responsibility changes due to psoriasis (11-14% to 4%; p < 0.01). The number of monthly sick days also decreased from baseline to week 24 (2.4 days for both treatment groups to 0.7 (BIW/QW) and 1.1 (QW/QW); p </= 0.03 for each). No significant differences between the treatment groups were observed for any economic endpoint at any time point. CONCLUSIONS: For patients with moderate-to-severe plaque psoriasis and PsA, etanercept treatment resulted in reducing job responsibility changes due to disease and in reducing sick time. Effective treatment of psoriasis and PsA may reduce missed work days.
dc.relation.ispartof urn:issn:1471-5945
dc.title Employment is maintained and sick days decreased in psoriasis/psoriatic arthritis patients with etanercept treatment
dc.type Journal Article
dc.date.updated 2015-04-09T08:56:36Z
dc.language.rfc3066 en
dc.identifier.mtmt 2727890
dc.identifier.pubmed 25091090
dc.contributor.department SE/AOK/K/Bőr-, Nemikórtani és Bőronkológiai Klinika
dc.contributor.institution Semmelweis Egyetem


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