Outcomes of treatment of cats with feline infectious peritonitis using parenterally administered remdesivir, with or without transition to orally administered GS-441524

被引:15
|
作者
Coggins, Sally J. [1 ]
Norris, Jacqui M. [1 ]
Malik, Richard [2 ,3 ]
Govendir, Merran [1 ]
Hall, Evelyn J. [1 ]
Kimble, Benjamin [1 ]
Thompson, Mary F. [1 ]
机构
[1] Univ Sydney, Sydney Sch Vet Sci, Sydney, NSW 2006, Australia
[2] Univ Sydney, Ctr Vet Educ, Sydney, NSW, Australia
[3] Charles Sturt Univ, Anim & Vet Sci, Bathurst, NSW, Australia
关键词
antiviral; clinical trial; feline coronavirus; nucleoside analog; DIRECT IMMUNOFLUORESCENCE TEST; POLYMERASE-CHAIN-REACTION; DIAGNOSIS; VIRUS; CORONAVIRUSES; EFFICACY; CULTURE; UTILITY; SAMPLES;
D O I
10.1111/jvim.16803
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
BackgroundNucleoside analog GS-441524 is effective in treating cats with feline infectious peritonitis (FIP). Investigation into the use of parent nucleotide analog remdesivir (GS-5734) is needed. ObjectivesTo assess efficacy and tolerability of remdesivir with or without transition to GS-441524 in cats with FIP and document clinical and clinicopathologic progression over 6 months. AnimalsTwenty-eight client-owned cats with FIP. MethodsCats were prospectively recruited between May 2021 and May 2022. An induction dosage of remdesivir 10 to 15 mg/kg intravenously or subcutaneously q24h was utilized for 4 doses, with a maintenance dosage of remdesivir (6-15 mg/kg SC) or GS-441524 (10-15 mg/kg per os) every 24 hours continued for at least 84 days. Laboratory testing, veterinary, and owner assessments were recorded. ResultsTwenty-four cats survived to 6 months (86%). Three cats died within 48 hours. Excluding these, survival from 48 hours to 6 months was 96% (24/25). Remission was achieved by day 84 in 56% (14/25). Three cats required secondary treatment for re-emergent FIP. Remission was achieved in all 3 after higher dosing (15-20 mg/kg). Adverse reactions were occasional site discomfort and skin irritation with remdesivir injection. Markers of treatment success included resolution of pyrexia, effusions, and presenting signs of FIP in the first half of treatment and normalization of globulin concentration, and continued body weight gains in the latter half of the treatment period. Conclusions and Clinical ImportanceParenteral administration of remdesivir and oral administration of GS-441524 are effective and well-tolerated treatments for FIP. Early emphasis on clinical, and later emphasis on clinicopathologic response, appears prudent when monitoring treatment efficacy.
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收藏
页码:1772 / 1783
页数:12
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