Ane Urkiola, Salvador Cervantes, Isaac Carrasco, Annabel Dalmau, Mar Bardagí
{"title":"长期服用奥拉西替尼控制猫过敏性瘙痒:对14只客户养猫的回顾性研究。","authors":"Ane Urkiola, Salvador Cervantes, Isaac Carrasco, Annabel Dalmau, Mar Bardagí","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Our objective was to provide preliminary clinical and laboratory data and the minimum effective dose for long-term (≥ 7 mo) treatment of feline allergic pruritus with oclacitinib. We studied 14 privately owned cats with pruritic allergic dermatitis controlled with oclacitinib treatment. Clinical data and results of blood testing (at the onset and at least once thereafter) during treatment were retrospectively evaluated. The median initial dosage of oclacitinib was 1.1 mg/kg q12h. In 7 animals, the maintenance dose could be reduced by ≥ 50%, usually after 15 d of treatment. The median duration of treatment was 15.5 mo. An FeLV-FIV test was conducted in 10 cats and all were negative. During treatment, 4 cats had non-dermatologic disorders that resolved without changing the oclacitinib dosing schedule. Alterations in blood tests during treatment were mild and frequently transient and included hypercholesterolemia, increased alanine aminotransferase and/or creatinine, and hyperglycemia. Limited and transitory disruptions in platelets and white cell lineage numbers were identified in some cats but none required specific treatment or discontinuation of oclacitinib. Alterations observed in the 14 cats treated with oclacitinib for a median of 15.5 mo were few and mild. No direct relationships were apparent between laboratory abnormalities or clinical signs and the dosing schedule of oclacitinib. A reduction of the daily dose to control allergic pruritus was feasible in 7/14 cats. Key clinical message: Based on the 14 cases included, long-term treatment with oclacitinib appeared to be well-tolerated and effective for managing feline allergic pruritus. However, close monitoring is recommended, and prospective studies with larger samples are needed to confirm these results.</p>","PeriodicalId":9429,"journal":{"name":"Canadian Veterinary Journal-revue Veterinaire Canadienne","volume":"66 8","pages":"835-842"},"PeriodicalIF":1.0000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12330796/pdf/","citationCount":"0","resultStr":"{\"title\":\"Long-term oclacitinib administration for the control of feline allergic pruritus: A retrospective study of 14 client-owned cats.\",\"authors\":\"Ane Urkiola, Salvador Cervantes, Isaac Carrasco, Annabel Dalmau, Mar Bardagí\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Our objective was to provide preliminary clinical and laboratory data and the minimum effective dose for long-term (≥ 7 mo) treatment of feline allergic pruritus with oclacitinib. We studied 14 privately owned cats with pruritic allergic dermatitis controlled with oclacitinib treatment. Clinical data and results of blood testing (at the onset and at least once thereafter) during treatment were retrospectively evaluated. The median initial dosage of oclacitinib was 1.1 mg/kg q12h. In 7 animals, the maintenance dose could be reduced by ≥ 50%, usually after 15 d of treatment. The median duration of treatment was 15.5 mo. An FeLV-FIV test was conducted in 10 cats and all were negative. During treatment, 4 cats had non-dermatologic disorders that resolved without changing the oclacitinib dosing schedule. Alterations in blood tests during treatment were mild and frequently transient and included hypercholesterolemia, increased alanine aminotransferase and/or creatinine, and hyperglycemia. Limited and transitory disruptions in platelets and white cell lineage numbers were identified in some cats but none required specific treatment or discontinuation of oclacitinib. Alterations observed in the 14 cats treated with oclacitinib for a median of 15.5 mo were few and mild. No direct relationships were apparent between laboratory abnormalities or clinical signs and the dosing schedule of oclacitinib. A reduction of the daily dose to control allergic pruritus was feasible in 7/14 cats. Key clinical message: Based on the 14 cases included, long-term treatment with oclacitinib appeared to be well-tolerated and effective for managing feline allergic pruritus. 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Long-term oclacitinib administration for the control of feline allergic pruritus: A retrospective study of 14 client-owned cats.
Our objective was to provide preliminary clinical and laboratory data and the minimum effective dose for long-term (≥ 7 mo) treatment of feline allergic pruritus with oclacitinib. We studied 14 privately owned cats with pruritic allergic dermatitis controlled with oclacitinib treatment. Clinical data and results of blood testing (at the onset and at least once thereafter) during treatment were retrospectively evaluated. The median initial dosage of oclacitinib was 1.1 mg/kg q12h. In 7 animals, the maintenance dose could be reduced by ≥ 50%, usually after 15 d of treatment. The median duration of treatment was 15.5 mo. An FeLV-FIV test was conducted in 10 cats and all were negative. During treatment, 4 cats had non-dermatologic disorders that resolved without changing the oclacitinib dosing schedule. Alterations in blood tests during treatment were mild and frequently transient and included hypercholesterolemia, increased alanine aminotransferase and/or creatinine, and hyperglycemia. Limited and transitory disruptions in platelets and white cell lineage numbers were identified in some cats but none required specific treatment or discontinuation of oclacitinib. Alterations observed in the 14 cats treated with oclacitinib for a median of 15.5 mo were few and mild. No direct relationships were apparent between laboratory abnormalities or clinical signs and the dosing schedule of oclacitinib. A reduction of the daily dose to control allergic pruritus was feasible in 7/14 cats. Key clinical message: Based on the 14 cases included, long-term treatment with oclacitinib appeared to be well-tolerated and effective for managing feline allergic pruritus. However, close monitoring is recommended, and prospective studies with larger samples are needed to confirm these results.
期刊介绍:
The Canadian Veterinary Journal (CVJ) provides a forum for the discussion of all matters relevant to the veterinary profession. The mission of the Journal is to educate by informing readers of progress in clinical veterinary medicine, clinical veterinary research, and related fields of endeavor. The key objective of The CVJ is to promote the art and science of veterinary medicine and the betterment of animal health.
A report suggesting that animals have been unnecessarily subjected to adverse, stressful, or harsh conditions or treatments will not be processed for publication. Experimental studies using animals will only be considered for publication if the studies have been approved by an institutional animal care committee, or equivalent, and the guidelines of the Canadian Council on Animal Care, or equivalent, have been followed by the author(s).