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Targeted therapies for psoriatic arthritis: an update for the dermatologist
被引:5
|作者:
Elman, Scott A.
[1
,2
]
Weinblatt, Michael E.
[3
]
Merola, Joseph F.
[1
,2
,3
]
机构:
[1] Harvard Med Sch, Brigham & Womens Hosp, Dept Dermatol, Boston, MA 02115 USA
[2] Harvard Med Sch, Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
[3] Harvard Med Sch, Brigham & Womens Hosp, Div Rheumatol Immunol & Allergy, Boston, MA 02115 USA
关键词:
PLACEBO-CONTROLLED TRIAL;
INTERLEUKIN-12/23;
MONOCLONAL-ANTIBODY;
ORAL PHOSPHODIESTERASE-4 INHIBITOR;
RANDOMIZED CONTROLLED-TRIAL;
PERIPHERAL JOINT DISEASE;
SEVERE PLAQUE PSORIASIS;
DOUBLE-BLIND;
PHASE-III;
PHARMACOLOGICAL THERAPIES;
CLINICAL-TRIALS;
D O I:
10.12788/j.sder.2018.045
中图分类号:
R75 [皮肤病学与性病学];
学科分类号:
100206 ;
摘要:
Dermatologists are on the front line to identify psoriatic arthritis (PsA) in their patients with psoriasis. PsA is a prevalent and underdiagnosed disease with potential long-term complications and sequelae for patients. Targeted biologics have transformed the landscape of psoriasis and PsA therapy. These medications variably treat clinical manifestations of psoriatic disease: skin psoriasis, peripheral and axial arthritis, enthesitis, and nail disease. With many new medications either on the market or currently being evaluated by the Food and Drug Administration, the purpose of this article is to review PsA for the dermatologist, to identify the current therapies that are available, and to help select which patients may benefit from these medications. Overall, it is important to decide therapy for patients based on the active domains of their disease, their comorbidities, and the safety profiles of these medications, as well as patient preference for route of administration, frequency, and tolerability. (C) 2018 Frontline Medical Communications
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页码:173 / 181
页数:9
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