Parncutt John, Johnson Lynelle R, Subharat Supatsak, Oke Bronwyn, Hill Kate E
Royal Society for the Prevention of Cruelty to Animals, Burwood East, VIC, Australia.
Department of Veterinary Medicine and Epidemiology, University of California, Davis, CA, USA.
J Feline Med Surg. 2025 Feb;27(2):1098612X241309826. doi: 10.1177/1098612X241309826.
The aim of this study was to test the hypothesis that intranasally administered maropitant citrate would reduce the severity of clinical signs of feline upper respiratory disease (FURD) in shelter cats with naturally acquired disease.
Shelter cats with clinical signs of FURD were randomly assigned to receive either intranasal maropitant diluted in saline (maropitant citrate 10 mg/ml q12h, diluted 1:10 with sterile 0.9% saline) or intranasal 0.9% saline q12h for 7 days. Clinical disease severity was measured at entry into the study and again after completion of 7 days of treatment using a visual analogue scale to assess four separate clinical signs: conjunctivitis, blepharospasm, ocular discharge and nasal discharge. Total disease severity was also calculated. Cats received other medications for FURD as per standard shelter protocols, and all investigators were masked to group assignments. A Mann-Whitney U-test was performed to compare the clinical improvement score (CIS) between the treatment and control groups.
There were 34 cats in the maropitant treatment group; 27 cats served as placebo controls. Groups did not differ in age, sex distribution, nature of disease, administration of other medications for FURD or baseline clinical disease severity. There was no significant difference in CIS between the maropitant treatment and control groups for conjunctivitis, blepharospasm, ocular discharge, nasal discharge or total disease severity after 7 days.
This study found no significant difference in outcomes for cats with FURD when treated with intranasal maropitant compared with treatment with intranasal saline. Further investigations would be required before intranasal maropitant could be recommended as the standard of care for FURD.
本研究旨在验证以下假设:对于自然感染疾病的收容所猫,经鼻给予枸橼酸马罗匹坦可减轻猫上呼吸道疾病(FURD)临床症状的严重程度。
将出现FURD临床症状的收容所猫随机分为两组,一组经鼻给予用生理盐水稀释的马罗匹坦(枸橼酸马罗匹坦10 mg/ml,每12小时一次,用无菌0.9%生理盐水按1:10稀释),另一组经鼻给予0.9%生理盐水,每12小时一次,持续7天。在研究开始时以及治疗7天结束后,使用视觉模拟量表评估四个独立的临床症状(结膜炎、眼睑痉挛、眼部分泌物和鼻部分泌物)来测量临床疾病严重程度。还计算了总疾病严重程度。根据收容所标准方案,猫接受FURD的其他药物治疗,所有研究人员均对分组情况不知情。采用Mann-Whitney U检验比较治疗组和对照组之间的临床改善评分(CIS)。
马罗匹坦治疗组有34只猫;27只猫作为安慰剂对照。两组在年龄、性别分布、疾病性质、FURD其他药物的使用情况或基线临床疾病严重程度方面无差异。7天后,马罗匹坦治疗组和对照组在结膜炎、眼睑痉挛、眼部分泌物、鼻部分泌物或总疾病严重程度的CIS方面无显著差异。
本研究发现,与经鼻给予生理盐水治疗相比,经鼻给予马罗匹坦治疗FURD猫的结果无显著差异。在将经鼻给予马罗匹坦推荐为FURD的标准治疗方法之前,还需要进一步研究。