Psoriasis therapy in real life : the need for registries

• The introduction of new therapeutic options for the management of psoriasis is a challenge for the dermatology community, and new tools are needed to face this challenge. This article argues for the establishment of profession-based registries to collect solid, long-term data on the safety and effectiveness of different psoriasis treatment regimens. Managed by health care professionals, registries will be most successful if they enroll patients based on indications for treatment rather than on drugs given. This protects the evaluation process from commercial influences and allows a fair comparison of old- versus new-generation psoriasis treatments. In contrast to the patients in a registry who receive care in the natural clinical setting, subjects in randomized clinical trials (RCTs) are selected according to study criteria and may therefore not reflect the experience of patients in clinical practice. It is possible that particular risks and opportunities in the real patient population may therefore go undetected in RCTs.Copyright © 2006 S. Karger AG, Basel

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Dermatologi och venereologi (hsv//swe)

MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Dermatology and Venereal Diseases (hsv//eng)

Keyword

Adverse Drug Reaction Reporting Systems

Clinical Medicine

Dermatologic Agents/adverse effects/contraindications/*therapeutic use

Humans

Longitudinal Studies

Psoriasis/*drug therapy

Quality Assurance; Health Care

Randomized Controlled Trials as Topic

Registries

Risk Assessment

Safety

Treatment Outcome

Publication and Content Type

ref (subject category)

art (subject category)