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Clinical Application of Oclacitinib in Dogs with Atopic Dermatitis

  • Hong, Eun-Hyung (Veterinary Medical Center, College of Veterinary Medicine, Chungbuk National University) ;
  • Park, Seo-Jin (Veterinary Medical Center, College of Veterinary Medicine, Chungbuk National University) ;
  • Jung, Dong-In (Research Institute of Natural Science, College of Veterinary Medicine, Gyeongsang National University) ;
  • Kang, Ji-Houn (Veterinary Medical Center, College of Veterinary Medicine, Chungbuk National University) ;
  • Yang, Mhan-Pyo (Veterinary Medical Center, College of Veterinary Medicine, Chungbuk National University) ;
  • Kang, Byeong-Teck (Veterinary Medical Center, College of Veterinary Medicine, Chungbuk National University)
  • 투고 : 2017.01.13
  • 심사 : 2017.02.14
  • 발행 : 2017.02.28

초록

This study evaluated the efficacy and safety to determine the therapeutic responses of oclacitinib in canine atopic dermatitis (CAD) and identified factors related to the therapeutic response. Overall, 13 dogs with CAD were treated with oclacitinib for 56 days. Owners and veterinarians assessed visual analog scale (VAS) scores of pruritus and dermatitis. The examined dogs were grouped according to treatment success and failure based on changes in the VAS scores. To identify factors related to the therapeutic responses of oclacitinib, signalments (breed, sex, age, and body weight), mean progression time of CAD, mean Owner and Veterinarian VAS scores at day 0, and preexisting infection rate were compared between the two groups. Among the 13 dogs, 7 (53.8%) met the criteria of treatment success. In the success group, the Owner VAS scores were significantly lower from day 6 to 56 compared with the score at day 0 (P < 0.05). Additionally, the Veterinarian VAS scores were significantly decreased at days 14 and 42 compared with the score at day 0 (P < 0.05). There were no changes in hematological indices after the administration of oclacitinib. The most common abnormality reported was otitis externa (30.8%), followed by pyoderma (23.1%), and vomiting (7.7%). Factors related to responses of oclacitinib were not identified. This study demonstrated that oclacitinib was safe and moderately effective in dogs with CAD. This is the first report of the clinical application of oclacitinib in South Korea.

키워드

참고문헌

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