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DOI 10.1111/ddg.12233

Медицинская библиотека · Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG · 2014

German psoriasis registry PsoBest: objectives, methodology and baseline data.

Augustin Matthias, Spehr Christina, Radtke Marc A, Boehncke Wolf-Henning, Luger Thomas, Mrowietz Ulrich, Reusch Michael, Strömer Klaus, Wozel Gottfried, von Kiedrowski Ralph, Rustenbach Stephan J, Purwins Sandra, Reich Kristian

СтатьяМногоцентровое исследованиеПеревод в очереди

Аннотация

BACKGROUND

The German psoriasis registry PsoBest records the long-term efficacy, safety, patient benefit and treatment regimens of psoriasis.

PATIENTS AND

METHODS

Patients with moderate or severe psoriasis are included in PsoBest when treatment with a conventional systemic agent or biologic is started for the first time. Observation time is five years. Standardized physician and patient case report forms are obtained every three to six months. Baseline data of patients included by 31 December 2012 are presented and compared to the national health care study PsoHealth 2007 (n = 2,009).

RESULTS

602 dermatology practices and clinics have been registered and 199 have recruited n = 2,556 patients (63 % by practices, 37 % by clinics). Initially, n = 808 received biologics (316 adalimumab, 34 efalizumab, 209 etanercept, 75 infliximab, 22 golimumab, 152 ustekinumab) and n = 1,651 conventional systemic therapy (928 fumaric acid esters, 518 methotrexate, 161 cyclosporine A, 191 other drugs or UV treatment). Compared to PsoHealth, patients in PsoBest had on average a higher disease severity (PASI 14.7 vs. 10.1; DLQI 11.0 vs. 7.5; EQ-5D VAS 54.0 vs. 64.5), shorter disease duration (18.2 vs. 21.3 yrs.), lower age (47.3 vs. 51.5), higher rates of psoriatic arthritis (20.5 vs. 19.1 %) and nail psoriasis (55.0 vs. 35.6 %). On average patients receiving biologics were younger, more often male and had higher disease severity and comorbidity.

CONCLUSIONS

Patients in PsoBest represent patients with a high burden of disease.

Для цитирования: Augustin Matthias, Spehr Christina, Radtke Marc A, Boehncke Wolf-Henning, Luger Thomas, Mrowietz Ulrich, Reusch Michael, Strömer Klaus, Wozel Gottfried, von Kiedrowski Ralph, Rustenbach Stephan J, Purwins Sandra, Reich Kristian. German psoriasis registry PsoBest: objectives, methodology and baseline data.. Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG. 2014. DOI: 10.1111/ddg.12233.

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