Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 4 de 4
Filter
1.
Clin Exp Dermatol ; 49(8): 875-878, 2024 Jul 19.
Article in English | MEDLINE | ID: mdl-38270233

ABSTRACT

Baricitinib is a Janus kinase inhibitor that has been approved by the US Food and Drugs Administration for the treatment of severe alopecia areata (AA) in adults. However, the clinical trials that demonstrated the efficacy of baricitinib in the treatment of severe AA did not include men aged > 60 years or women aged > 70 years. We retrospectively assessed the efficacy and safety of baricitinib in 14 patients aged ≥ 65 years with moderate-to-severe AA. After a mean (SD) duration of 18.5 (11.9) months, a 72% reduction in mean Severity of Alopecia Tool score from baseline was observed. Partial or complete eyebrow and eyelash hair was observed in 57% and 43% of patients, respectively. The adverse effects of baricitinib were mild. No cases of venous thromboembolism, major adverse cardiovascular events or malignancy were reported.


Subject(s)
Alopecia Areata , Azetidines , Purines , Pyrazoles , Severity of Illness Index , Sulfonamides , Humans , Azetidines/therapeutic use , Azetidines/adverse effects , Sulfonamides/therapeutic use , Sulfonamides/adverse effects , Alopecia Areata/drug therapy , Purines/therapeutic use , Purines/adverse effects , Pyrazoles/therapeutic use , Pyrazoles/adverse effects , Male , Female , Aged , Retrospective Studies , Treatment Outcome , Janus Kinase Inhibitors/therapeutic use , Janus Kinase Inhibitors/adverse effects , Aged, 80 and over
2.
Australas J Dermatol ; 60(2): 163-170, 2019 May.
Article in English | MEDLINE | ID: mdl-30411329

ABSTRACT

Alopecia areata (AA) severity varies from a single small patch to complete loss of scalp hair, body hair, eyelashes and eyebrows. While 40% of all affected individuals only ever get one patch and will achieve a spontaneous complete durable remission within 6 months, 27% will develop additional patches but still achieve complete durable remission within 12 months and 33% will develop chronic AA. Without systemic treatment, 55% of individuals with chronic AA will have persistent multifocal relapsing and remitting disease, 30% will ultimately develop alopecia totalis and 15% will develop alopecia universalis. The unpredictable course and psychological distress attributable to AA contributes to the illness associated with AA. Numerous topical, intralesional and systemic agents are currently used to treat AA; however, there is a paucity of data evaluating their use, effectiveness and tolerability. Topical therapy, including topical glucocorticosteroids, minoxidil and immunotherapy, can be used in cases of limited disease. There are no universally agreed indications for initiating systemic treatment for AA. Possible indications for systemic treatment include rapid hair loss, extensive disease (≥50% hair loss), chronic disease, severe distress or a combination of these factors. Currently available systemic treatments include glucocorticosteroids, methotrexate, ciclosporin, azathioprine, dapsone, mycophenolate mofetil, tacrolimus and sulfasalazine. The optimal treatment algorithm has not yet been described. The purpose of this consensus statement is to outline a treatment algorithm for AA, including the indications for systemic treatment, appropriate choice of systemic treatment, satisfactory outcome measures and when to discontinue successful or unsuccessful treatment.


Subject(s)
Alopecia Areata/therapy , Alopecia Areata/diagnosis , Autoimmune Diseases/complications , Disease Progression , Down Syndrome/complications , Glucocorticoids/therapeutic use , Humans , Immunosuppressive Agents/therapeutic use , Immunotherapy , Minoxidil/therapeutic use , Nail Diseases/complications , Prognosis , Vasodilator Agents/therapeutic use
SELECTION OF CITATIONS
SEARCH DETAIL