Renner Kelsey Ann, Cattin Ryan, Kimble Benjamin, Munday John, White Alex, Coggins Sally
Animal Referral Centre, Auckland, New Zealand.
Sydney School of Veterinary Science, The University of Sydney, NSW, Australia.
J Feline Med Surg. 2025 May;27(5):1098612X251335189. doi: 10.1177/1098612X251335189. Epub 2025 May 27.
ObjectivesThe primary aim of this prospective observational study was to document clinical progression, survival, remission and relapse in New Zealand cats with feline infectious peritonitis (FIP) that were treated with compounded oral remdesivir with or without initial parenteral remdesivir therapy. The secondary aims were to determine the optimal monitoring protocols and report the adverse effects of treatment and complications associated with FIP.MethodsA total of 29 client-owned cats with a clinical diagnosis of FIP were prospectively recruited. Cats were administered oral remdesivir (30 mg/kg q24h), rounded up to the nearest capsule size as the sole treatment, or after initial parenteral remdesivir (15-30 mg/kg q24h). Rechecks were recommended at weeks 1, 2, 4, 8 and 12 during treatment, and at 2 and 12 weeks after treatment. A full physical examination (including neurological and ophthalmic examination) and point-of-care ultrasound were performed at each recheck. A complete blood count and biochemistry panel were performed at weeks 4, 8, 12 and 24. Molnupiravir was offered as a rescue therapy for cats that relapsed.ResultsIn total, 25 (86%) cats entered remission and survived beyond 6 months (range 6-27). A total of 22 (75%) cats achieved remission within 84 days while receiving oral remdesivir. Three cats received subsequent molnupiravir rescue therapy to achieve remission. Five cats (20%) experienced relapse: four with non-effusive disease and one with effusive disease. Notably, 4/8 (50%) non-effusive cases relapsed, compared with only 1/20 (5%) with effusive disease.Conclusions and relevanceThis study demonstrates that oral remdesivir at a dose rate of 30 mg/kg q24h is an effective treatment for effusive FIP. The survival rate in non-effusive cats was significantly lower; therefore, an increased dose rate or frequency of administration should be considered in these cats. Oral remdesivir is a viable antiviral option where GS-441524 is unavailable.
目的
这项前瞻性观察性研究的主要目的是记录接受口服瑞德西韦复方制剂治疗(无论是否联合初始肠外瑞德西韦治疗)的新西兰猫传染性腹膜炎(FIP)的临床进展、生存情况、缓解和复发情况。次要目的是确定最佳监测方案,并报告治疗的不良反应以及与FIP相关的并发症。
方法
前瞻性招募了总共29只临床诊断为FIP的宠物猫。猫接受口服瑞德西韦(30mg/kg,每24小时一次),向上取整至最接近的胶囊规格,作为唯一治疗方法,或在初始肠外给予瑞德西韦(15 - 30mg/kg,每24小时一次)之后使用。建议在治疗期间的第1、2、4、8和12周以及治疗后2周和12周进行复查。每次复查时进行全面体格检查(包括神经和眼科检查)以及即时超声检查。在第4、8、12和24周进行全血细胞计数和生化检测。对于复发的猫,提供莫努匹拉韦作为挽救治疗。
结果
总共有25只(86%)猫进入缓解期并存活超过6个月(范围为6 - 27个月)。共有22只(75%)猫在接受口服瑞德西韦治疗的84天内实现缓解。3只猫接受了后续的莫努匹拉韦挽救治疗以实现缓解。5只猫(20%)复发:4只患有非渗出性疾病,1只患有渗出性疾病。值得注意的是,4/8(50%)的非渗出性病例复发,而渗出性疾病的复发率仅为1/20(5%)。
结论及意义
本研究表明,以30mg/kg每24小时一次的剂量口服瑞德西韦是治疗渗出性FIP的有效方法。非渗出性猫的存活率显著较低;因此,对于这些猫应考虑增加给药剂量或频率。在无法获得GS - 441524的情况下,口服瑞德西韦是一种可行的抗病毒选择。