J Am Vet Med Assoc. 2024 Apr 12;262(9):1188-1192. doi: 10.2460/javma.24.01.0032. Print 2024 Sep 1.
To retrospectively evaluate safety and tolerance of leflunomide for long-term treatment of canine idiopathic immune-mediated polyarthritis (IMPA).
27 dogs with clinical signs and synovial fluid cytology supportive of IMPA with ≥ 6 months' follow-up after starting leflunomide.
Medical records were reviewed to identify dogs prescribed leflunomide for treatment of IMPA from February 2012 to May 2022. Initial leflunomide doses of 2 to 4 mg/kg once daily were prescribed and were titrated to the lowest effective dose with concurrent anti-inflammatory therapy. Complete blood count, serum chemistry, and clinical signs were monitored throughout the course of treatment.
Adverse effects potentially attributable to leflunomide noted in 9 of 27 dogs (33%) included vomiting, diarrhea, lethargy, decreased or absent appetite, polyuria and polydipsia, and secondary antibiotic responsive infection and were self-limiting or resolved with outpatient therapy. Alkaline phosphatase (ALP) and alanine aminotransferase (ALT) elevation were documented in all dogs prescribed leflunomide plus prednisone, with persistent liver enzyme elevation in 6 of 9 dogs (67%) and normalization after antibiotic therapy in 3 of 9 dogs (33%). The majority of dogs prescribed leflunomide plus NSAID (11/17 [65%] dogs) did not experience liver enzyme elevation; 2 of 17 (12%) dogs developed transient antibiotic-responsive liver enzyme elevations, and 4 of 17 (23%) dogs had persistent liver enzyme elevation.
Leflunomide was well tolerated for long-term management of IMPA. A significant difference in liver enzyme elevation was identified between dogs prescribed prednisone versus NSAID in combination with leflunomide. Leflunomide with NSAID therapy resulted in less hepatotoxicity compared with leflunomide with prednisone.
回顾性评估来氟米特长期治疗犬特发性免疫介导性多关节炎(IMPA)的安全性和耐受性。
27 只具有临床症状和滑液细胞学支持的 IMPA 犬,在开始来氟米特治疗后有≥6 个月的随访。
回顾性分析 2012 年 2 月至 2022 年 5 月期间因 IMPA 而接受来氟米特治疗的犬的病历。初始剂量为 2 至 4mg/kg 每日 1 次,同时给予抗炎治疗,滴定至最低有效剂量。在整个治疗过程中监测全血细胞计数、血清化学和临床症状。
27 只犬中有 9 只(33%)出现了可能与来氟米特有关的不良反应,包括呕吐、腹泻、嗜睡、食欲减退或消失、多尿和多饮以及继发的抗生素反应性感染,这些不良反应是自限性的或通过门诊治疗得到解决。所有接受来氟米特加泼尼松治疗的犬均出现碱性磷酸酶(ALP)和丙氨酸氨基转移酶(ALT)升高,其中 6 只犬(67%)的肝酶持续升高,3 只犬(33%)在接受抗生素治疗后恢复正常。接受来氟米特加 NSAID 治疗的犬(17 只中的 11 只,65%)中大多数未出现肝酶升高;2 只犬(12%)出现短暂的抗生素反应性肝酶升高,4 只犬(23%)出现持续的肝酶升高。
来氟米特长期治疗 IMPA 的耐受性良好。接受泼尼松与 NSAID 联合来氟米特治疗的犬在肝酶升高方面存在显著差异。与来氟米特加泼尼松治疗相比,来氟米特联合 NSAID 治疗导致的肝毒性更小。