Feline chaphamaparvovirus (FeChPV) in cats with enteritis and upper respiratory tract disease (URTD)

Author(s):  
Federica Di Profio ◽  
Vittorio Sarchese ◽  
Andrea Palombieri ◽  
Paola Fruci ◽  
Ivano Massirio ◽  
...  
2012 ◽  
pp. 536-557 ◽  
Author(s):  
Eric J. Parente ◽  
Samantha H. Franklin ◽  
Frederik J. Derksen ◽  
Michael A. Weishaupt ◽  
Heather J. Chalmers ◽  
...  

2019 ◽  
Vol 22 (6) ◽  
pp. 492-499
Author(s):  
Lucy Kopecny ◽  
David J Maggs ◽  
Christian M Leutenegger ◽  
Lynelle R Johnson

Objectives The aim of this study was to assess the effects of famciclovir administration in cats with spontaneously acquired acute upper respiratory tract disease. Methods Twenty-four kittens with clinical signs of acute upper respiratory tract disease were randomly allocated to receive doxycycline (5 mg/kg PO q12h) alone (group D; n = 12) or with famciclovir (90 mg/kg PO q12h; group DF; n = 12) for up to 3 weeks. Clinical disease severity was scored at study entry and daily thereafter. Oculo-oropharyngeal swabs collected at study entry and exit were assessed using quantitative PCR for nucleic acids of feline herpesvirus type 1 (FHV-1), feline calicivirus (FCV), Chlamydia felis, Bordetella bronchiseptica and Mycoplasma felis. Results The median (range) age of cats was 1.5 (1–6) months in group D vs 1.6 (1–5) months in group DF ( P = 0.54). Pathogens detected in oculo-oropharyngeal swabs at study entry included FCV (n = 13/24; 54%), M felis (n = 8/24; 33%), FHV-1 (n = 7/24; 29 %), C felis (n = 7/24; 29%) and B bronchiseptica (n = 3/24; 12%). Median (range) duration of clinical signs was 11.5 (3–21) days in group DF and 11 (3–21) days in group D ( P = 0.75). Median (range) total disease score at the end of the study did not differ between groups (group D 1 [1–1] vs group DF 1 [1–3]; P = 0.08). Conclusions and relevance This study revealed no significant difference in response to therapy between cats treated with doxycycline alone or with famciclovir; cats improved rapidly in both groups. However, identification of FHV-1 DNA was relatively uncommon in this study and clinical trials focused on FHV-1-infected cats are warranted to better evaluate famciclovir efficacy.


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