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Acta Derm Venereol ; 98(3): 324-328, 2018 Mar 13.
Article in English | MEDLINE | ID: mdl-29182791

ABSTRACT

Atopic dermatitis (AD) is a chronic, itchy, inflammatory skin disorder that may worsen due to stress and anxiety. Tachykinins have been suggested to be involved in the inflammation in AD, as well as pruritus. Aprepitant is a NK-1 receptor antagonist. This open randomized trial evaluated the effect of aprepitant added to topical treatment in adult patients with moderate-severe AD. The treatment group (n = 19) received 80 mg/day aprepitant for 7 days as a supplement to standardized topical treatment with a moderately strong steroid and a moisturizer. The control group (n = 20) received topical treatment alone. Patients were monitored for the extent of the disease (using SCORing of Atopic Dermatitis; SCORAD), pruritus, and scratching movements. In both the aprepitant-treated and the control groups there was a decrease in SCORAD, pruritus and scratching movements. However, there was no significant additional improvement in any of these parameters in the aprepitant-treated group compared with the control group.


Subject(s)
Antipruritics/administration & dosage , Dermatitis, Atopic/drug therapy , Morpholines/administration & dosage , Neurokinin-1 Receptor Antagonists/administration & dosage , Pruritus/drug therapy , Skin/drug effects , Substance P/antagonists & inhibitors , Administration, Cutaneous , Adult , Antipruritics/adverse effects , Aprepitant , Dermatitis, Atopic/diagnosis , Dermatitis, Atopic/metabolism , Drug Therapy, Combination , Female , Humans , Male , Middle Aged , Morpholines/adverse effects , Neurokinin-1 Receptor Antagonists/adverse effects , Pruritus/diagnosis , Pruritus/metabolism , Severity of Illness Index , Skin/metabolism , Skin/pathology , Substance P/metabolism , Sweden , Time Factors , Treatment Outcome , Young Adult
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