Department of Internal Medicine, Massachusetts Veterinary Referral Hospital, Woburn, MA, 01801, USA.
Department of Internal Medicine, Angell Animal Medical Center, Boston, MA, 02130, USA.
J Small Anim Pract. 2024 Apr;65(4):261-269. doi: 10.1111/jsap.13715. Epub 2024 Mar 3.
To describe leflunomide as an adjunctive therapy in the treatment of non-associative immune-mediated thrombocytopenia.
A retrospective study of dogs with a diagnosis of non-associative immune-mediated thrombocytopenia treated with leflunomide March 2008 to September 2021 was conducted. Data collected included signalment, clinical signs, physical examination findings and diagnostic testing performed. Medications administered, duration of hospital stay, time to platelet concentration >150×10/L and adverse events during leflunomide therapy were recorded. Relapses within a year of diagnosis were reported.
A total of 20 client-owned dogs met inclusion criteria. Nineteen of 20 dogs (95%) achieved a platelet concentration >150×10/L with leflunomide and prednisone combination therapy and four dogs (21.1%) relapsed during treatment or shortly after treatment. Adverse effects included diarrhoea (n=5), mild lymphopenia (n=9) and mild intermittent anaemia (n=1). A single dog developed hepatotoxicity presumed to be secondary to leflunomide therapy that resolved after drug discontinuation. One dog was treated for aspiration pneumonia during treatment. Two dogs were euthanased while receiving leflunomide.
Length of hospitalisation, time to platelet recovery, treatment response and relapse rate were comparable with alternative treatment protocols. Most adverse effects did not require leflunomide dose adjustment; however, two dogs died while undergoing leflunomide treatment and there is compelling evidence that one of these dogs experienced fatal infection secondary to immune-suppression. Hepatotoxicity remains a known complication of leflunomide treatment and serial biochemistry testing is recommended.
描述来氟米特作为辅助治疗用于治疗非关联免疫介导性血小板减少症。
对 2008 年 3 月至 2021 年 9 月期间接受来氟米特治疗的非关联免疫介导性血小板减少症犬进行回顾性研究。收集的资料包括年龄、临床症状、体格检查结果和进行的诊断性检查。记录使用的药物、住院时间、血小板浓度>150×10/L的时间以及来氟米特治疗期间的不良反应。报告了诊断后一年内的复发情况。
共有 20 只符合纳入标准的犬。20 只犬中有 19 只(95%)通过来氟米特联合泼尼松治疗达到血小板浓度>150×10/L,4 只(21.1%)在治疗期间或治疗后不久复发。不良反应包括腹泻(n=5)、轻度淋巴细胞减少(n=9)和轻度间歇性贫血(n=1)。一只狗因疑似来氟米特治疗引起的肝毒性而停药,停药后恢复。一只狗在治疗期间发生吸入性肺炎。两只狗在接受来氟米特治疗时被安乐死。
住院时间、血小板恢复时间、治疗反应和复发率与替代治疗方案相当。大多数不良反应不需要调整来氟米特剂量;然而,有两只狗在接受来氟米特治疗时死亡,有充分的证据表明其中一只狗因免疫抑制而发生致命感染。肝毒性仍然是来氟米特治疗的已知并发症,建议进行连续生化检测。