Cooper Ann E, Thomasy Sara M, Drazenovich Tracy L, Kass Philip H, Potnis Sanskruti S, Leutenegger Christian M, Maggs David J
1 Veterinary Medical Teaching Hospital, School of Veterinary Medicine, University of California, Davis, Davis, CA, USA.
2 Department of Surgical and Radiological Sciences, School of Veterinary Medicine, University of California, Davis, Davis, CA, USA.
J Feline Med Surg. 2019 Jun;21(6):544-552. doi: 10.1177/1098612X18789719. Epub 2018 Aug 13.
In humans with herpetic disease, early or pre-emptive famciclovir therapy reduces disease duration and severity. This prospective, masked, placebo-controlled study tested therapeutic and prophylactic effects of two famciclovir doses given to cats for 7 days following shelter entry.
Cats were assigned to prophylactic or therapeutic study arms based on clinical evidence of herpetic disease at study entry. Cats in the therapeutic arm received no treatment (n = 19), placebo (lactose; n = 18) or famciclovir at ~30 (n = 21) or ~90 mg/kg (n = 20) PO q12h for 7 days. Cats in the prophylactic arm received no treatment (n = 25) or famciclovir at ~30 (n = 28) or ~90 mg/kg (n = 27) PO q12h for 7 days. Disease scores, body weight, conjunctival feline herpesvirus 1 (FHV-1) shedding, and adoption rates were recorded on days 1 (admission), 8 (end of therapy) and 15 (1 week after cessation of therapy).
No significant differences in clinical scores were observed among groups in the prophylactic or therapeutic arms at any of the three time points. However, within the therapeutic arm, viral shedding on day 8 was significantly higher in cats receiving no treatment than in those receiving ~30 or ~90 mg/kg famciclovir, and this effect persisted 1 week after famciclovir was stopped (day 15) only in cats receiving ~30 mg/kg, although this approached significance in cats receiving ~90 mg/kg. No significant differences in adoption rates were detected among groups in either arm throughout the study.
Although we did not demonstrate a statistically or clinically significant effect of famciclovir administration upon clinical signs of infectious upper respiratory disease or adoption, when it was administered at ~30 or ~90 mg/kg q12h for 1 week famciclovir reduced conjunctival FHV-1 shedding. This suggests a potential role in interrupting the infectious cycle within a shelter population; however, cost in time and resources, and stress and pathogen transmission induced by oral administration should be considered.
在患有疱疹性疾病的人类中,早期或抢先使用泛昔洛韦治疗可缩短疾病持续时间并减轻疾病严重程度。这项前瞻性、双盲、安慰剂对照研究测试了在猫进入庇护所后7天内给予两种泛昔洛韦剂量的治疗和预防效果。
根据研究开始时疱疹性疾病的临床证据,将猫分配到预防或治疗研究组。治疗组的猫不接受治疗(n = 19)、接受安慰剂(乳糖;n = 18)或口服泛昔洛韦,剂量约为30(n = 21)或90 mg/kg(n = 20),每12小时一次,共7天。预防组的猫不接受治疗(n = 25)或口服泛昔洛韦,剂量约为30(n = 28)或90 mg/kg(n = 27),每12小时一次,共7天。在第1天(入院)、第8天(治疗结束)和第15天(治疗停止后1周)记录疾病评分、体重、结膜猫疱疹病毒1型(FHV-1)脱落情况和领养率。
在三个时间点的任何一个时间点,预防组或治疗组的各亚组之间在临床评分上均未观察到显著差异。然而,在治疗组中,未接受治疗的猫在第8天的病毒脱落率显著高于接受约30或90 mg/kg泛昔洛韦的猫,并且这种影响仅在接受约30 mg/kg泛昔洛韦的猫中在泛昔洛韦停药后1周(第15天)仍然存在,尽管在接受约90 mg/kg泛昔洛韦的猫中这种差异接近显著水平。在整个研究过程中,两个组的各亚组之间在领养率上均未检测到显著差异。
尽管我们没有证明泛昔洛韦给药对传染性上呼吸道疾病的临床症状或领养有统计学或临床显著影响,但当以约30或90 mg/kg每12小时一次的剂量给药1周时,泛昔洛韦可减少结膜FHV-1脱落。这表明其在中断庇护所猫群中的感染循环方面可能具有潜在作用;然而,应考虑到时间和资源成本以及口服给药引起的应激和病原体传播。