Baseline characteristics of patients with psoriasis enrolled in the British Association of Dermatologists' Biologic Interventions Register. — Ireny Iskandar (2014) | RDL Network
Baseline characteristics of patients with psoriasis enrolled in the British Association of Dermatologists' Biologic Interventions Register.
Article 2014 en
Authors
II
Ireny Iskandar
RW
Richard B. Warren
ZY
Zenas Z N Yiu
Abstract
1 min read
ABSTRACT BODY: The British Association of Dermatologists' Biologic Interventions Register (BADBIR) is a large prospective observational cohort designed to assess the long-term safety of biologic and conventional systemic therapies for severe psoriasis. The aim was to analyse baseline demographics, disease severity, current & previous systemic therapies, and co-morbidities. Baseline data were collected from 146 Dermatology departments in the UK & Ireland. From Sept 2007 - Oct 2013, 7110 patients were registered with 4283 (60%) receiving biologics of whom 51% were on adalimumab, 27% etanercept, 17% ustekinumab & 5% infliximab. In the comparator cohort 44% were on methotrexate, 23% ciclosporin,18% acitretin & 8% fumaric acid esters. 4192 (59%) were male. Mean (±SD) age & disease duration of patients on biologics were 46±13 years & 23±13 years respectively, while patients on conventional therapies had a lower age (44±14 years) & shorter disease duration (19±13 years). Mean BMI for patients on biologics (31±7 Kg/m2) was higher than those on conventional systemic therapies (30±7 Kg/m2). Mean baseline PASI and DLQI scores were higher in patients on biologics compared to those on conventional systemics (17±8 vs 16±8 & 18±8 vs 15±7, respectively). 68% of all patients had co-morbidities & 41% had more than one. The most frequent co-morbidities were hypertension (26%), depression (22%) & psoriatic arthritis (16%). BADBIR is an invaluable resource to study the safety & effectiveness of biologic and conventional systemic therapies in routine clinical practice for severe psoriasis. Understanding differences in baseline characteristics between cohorts will be crucial in undertaking future pharmacovigilance studies.
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