Efficacy of ustekinumab for treatment of moderate - to - severe plaque psoriasis at 108 Military Central Hospital
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Abstract
Objective: To assess the efficacy of ustekinumab in patient with moderate-to-severe plaque psoriasis. Subject and method: A retrospective study; 14 patients (male or female) aged ≥ 18 years with moderate-to-severe chronic plaque psoriasis; to receive subcutaneous injections of ustekinumab 45mg at week 0, 4, 16 and 28. Evaluate efficacy at week 4, 16, 28 included the proportion of patients achieving at least 75%, 90%, 100% improvement from baseline in Psoriasis Area and Severity Index (PASI 75, PASI 90, PASI 100), change from baseline in Dermatology Life Quality Index (DLQI). Result: At week 16, the proportion of patients achieving PASI 75 was 50%, PASI 90 was 28.6%, 35.7% of patients achieved DLQI 0/1. Efficacy was maintained through week 28 in ustekinumab - treated patients. Serious adverse drug reaction observed was 0%. At week 28, 1 patient with < 50% improvement in Psoriasis Area and Severity Index (PASI) discontinued ustekinumab. Conclusion: Ustekinumab was efficacious and generally
well-tolerated in patients with moderate-to-severe plaque-type psoriasis through 28 weeks.
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References
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