vtx logo

request clinical advice

vtx logo sticky

scott@vtx-cpd.com

Forum Replies Created

Viewing 15 posts - 1,216 through 1,230 (of 1,885 total)
  • Author
    Posts
  • scott@vtx-cpd.com
    Keymaster

    Replying to Jen Williams 13/05/2022 - 15:30

    Hey Jen.

    Lovely to hear from you! I always keep my PDSA in mind. I still think they were the happies days of my career to date!

    Thanks for supporting the course.

    Scott 🙂

    scott@vtx-cpd.com
    Keymaster

    Replying to Hannah R. 11/05/2022 - 09:47

    Hello Hannah.

    Really lovely to hear from you. Thank you so much for supporting the course, we are so glad to have you on board!

    Let me know if you have any questions at anytime!

    Scott 🙂

    scott@vtx-cpd.com
    Keymaster

    Replying to Alison Lambert 11/05/2022 - 08:13

    Hello Alison.

    I hope you are well. Thank you so much for your kind words.

    Yes, there is no evidence to say that prophylactic use of a PPI is necessary when administering higher doses of steroids.

    Hope that helps.

    Scott 🙂

    scott@vtx-cpd.com
    Keymaster

    Replying to Alison Lambert 11/05/2022 - 08:13

    Hello Alison.

    I hope you are well. Thank you so much for your kind words.

    Yes, there is no evidence to say that prophylactic use of a PPI is necessary when administering higher doses of steroids.

    Hope that helps.

    Scott 🙂

    scott@vtx-cpd.com
    Keymaster

    Replying to Rosemary S. 10/05/2022 - 09:33

    HAHA!

    Please do not get up at 5am for journal club.

    We will record this and make available.

    Scott 🙂

    scott@vtx-cpd.com
    Keymaster

    Replying to Gillian Gordon 07/05/2022 - 13:44

    Thank you so much Gillian.

    We are so pleased you have enjoyed the course and really appreciate your support.

    Much love.

    Scott 🙂

    scott@vtx-cpd.com
    Keymaster

    Hello.

    Lovely to hear from you. I normally use this product:

    https://www.protexinvet.com/pro-enzorb/p6243

    This would normally be a capsule a day for cats. I hope that helps.

    Scott 🙂

    scott@vtx-cpd.com
    Keymaster

    Replying to Belinda Lum 04/05/2022 - 15:24

    This is all really interesting!

    I think it would be worth reporting these cases to Elanco and seeing if they have collected any similar data.

    Thanks again for sharing.

    Scott 🙂

    scott@vtx-cpd.com
    Keymaster

    Replying to Belinda Lum 04/05/2022 - 09:51

    Hey.

    This is a brilliant question. Was this in dogs or cats?

    Generally the worst side effect we see in dogs is hypersalivation. Capromorelin is dosed at 3 mg/kg PO q24h, which has been shown to increase food intake and weight gain in both inappetent client-owned dogs and healthy laboratory dogs. The pivotal field safety and effectiveness study evaluated 177 inappetent dogs (121 treated with capromorelin for 4 days, 56 with placebo). Treatment with capromorelin significantly improved appetite (68.6% versus 44.6%, respectively, P = 0.008) as well as mean body weight compared with placebo (1.8% versus 0.1%, respectively, P <0.001). The most commonly observed adverse clinical signs included diarrhea (7.0%), vomiting (6.4%), polydipsia (4.1%), and hypersalivation (2.3%).

    There are some reports coming through with concerns with the clinical use of capromorelin in cats. The authors of the 2011 study of capromorelin in cats did note lethargy and depression, but cardiovascular parameters – such as heart rate and blood pressure – were not reported. There are unpublished reports of some cats become profoundly bradycardic and hypotensive within one hour of being given capromorelin at a dose of 3 mg/kg. It is likely there will be enough data for one or several institutions to publish data describing in more detail the incidence of adverse events in cats, and ideally identify at-risk populations. It might be enough evidence to use capromorelin in cats at a lower dose (2mg/kg).

    I hope that helps.

    Scott 🙂

    scott@vtx-cpd.com
    Keymaster

    Replying to Liz Bode 03/05/2022 - 16:44

    That is really useful Liz.

    Thank you so much for sharing!

    Scott 🙂

    scott@vtx-cpd.com
    Keymaster

    Hello.

    I hope you are well.

    The mechanism causing hypercalcaemic pancreatitis may be calcium deposition in the pancreatic duct and calcium activation of trypsinogen in the pancreas.

    I hope that helps.

    Scott 🙂

    scott@vtx-cpd.com
    Keymaster

    Hello.

    It is a great question. I think the honest answer is that we don’t often definitively know and often presume an immune pathogenesis if they respond to appropriate treatment.

    Little research is available on the treatment of chronic pancreatitis in cats, and most recommendations are based on case reports or personal opinion rather than peer-reviewed literature. Chronic pancreatitis in cats often occurs concurrently with other diseases, and diagnosis and treatment of these conditions usually takes clinical priority. Targeted management of chronic pancreatitis often is not required. However, if chronic pancreatitis occurs as an isolated condition or appears to be a complicating factor that worsens the prognosis of comorbidities, particularly diabetes mellitus, then targeted management is indicated.

    The consensus statement demonstrates that there is a varying opinion on steroids:

    ”Although some panel members felt that prednisolone should only be used in cats that are not hyperglycemic and only at anti-inflammatory dosages (ie, 0.5-1.0 mg/kg PO q24h on a tapering schedule), other panel members felt that immunosuppressive dosages of prednisolone (eg, 2.0 mg/kg q12h for 5 days and then 1.0 mg/kg q12h for 6 weeks with a decreasing dosing schedule after that time) with close monitoring (ie, clinical re-evaluation and measurement of fPLI after 2-3 weeks) could have a beneficial effect. If hyperglycemia develops, or is pre-existing, some panel members recommend the use of cyclosporine (5 mg/kg q24h for 6 weeks) with close monitoring (ie, clinical re-evaluation and measurement fPLI after 2-3 weeks). In cats treated with either prednisolone or cyclosporine in which clinical signs have not improved and pancreatic lipase has not decreased, discontinuation of treatment should be considered. In cats that show a clinical response, continuation of treatment is indicated. Unmasking latent toxoplasmosis may be a concern with long-term use of high-dose cyclosporine.206 Toxoplasmosis may be of a greater concern in geographic locations where cats frequently hunt in the wild or consume raw meat and has been reported in renal transplant cats and a cat treated for atopy.”

    I would normally use the regime that is suggested above.

    I hope that helps.

    Scott 🙂

    scott@vtx-cpd.com
    Keymaster

    Hello.

    Thank you so much for your question. These are tricky cases!

    The presence of enteric protozoans in diarrhoea samples does not prove that disease was due to the organism. Some enteric protozoans, especially Cryptosporidium spp., live chronically in the intestinal tract of normal animals; other conditions causing GI tract disease can induce repeat shedding. Thus, animals with enteric protozoal infections that do not respond to therapy should be evaluated for underlying causes of disease.

    High-fiber diets are generally indicated if large-bowel diarrhea is occurring. However, feeding a high-fiber diet may also aid in the treatment of giardiasis due to inhibition of trophozoite attachment to duodenal epithelial cells. Use of probiotics may also have clinical benefit in some cases. A diet change may be a plan in these cases and possibly considering the Vivomixx probiotic.

    Having said all of that, if the clinical signs are persistent, diet and probiotics not working, I might consider treating the cryptosporidium. Paromomycin, tylosin (10 to 15 mg/kg PO q 12 h), azithromycin (10 mg/kg PO q 24 h), and nitazoxanide (25 mg/kg PO q 12 h) have all been used to lessen diarrhea in dogs, cats, calves or people with cryptosporidiosis, but no treatment has consistently stopped Cryptosporidium spp. oocyst shedding. The drugs are generally prescribed initially for 7 to 10 days. However, it sometimes takes as long as 4 to 6 weeks to achieve total resolution of diarrhoea. The most commonly prescribed drugs to treat Cystoisospora spp. infections of dogs and cats are trimethoprim-sulfonamide, sulfadimethoxine, furazolidone, amprolium, or amprolium-sulfadimethoxine. Quinacrine, spiramycin, toltrazuril, roxithromycin, and ponazuril have been used on a limited basis. Ponazuril appears to be safe in most puppies and kittens and can eliminate infection after one dose (50 mg/kg PO). However, administration of ponazuril daily for 3 days at 50 mg/kg was the most effective protocol in one study.

    As far as I was aware metronidazole is not helpful for Tritrichomonas foetus. Really useful information from the iCatCare website:

    ”Unfortunately, most studies on the treatment of T. foetus infection in cats have been unrewarding. The organism is resistant to most traditionally used anti-protozoal drugs such as fenbendazole and metronidazole. The use of a variety of different antimicrobial drugs has been reported to improve faecal consistency during therapy of infected cats, possibly because of interaction between T. foetus and the bacteria normally present in the intestine, and/or other concurrently carried enteric pathogens. However, such antibiotic use is not recommended as it may ultimately prolong the shedding of the organism, and does not resolve the underlying problem.

    A study by Dr Jody Gookin at the North Carolina State University (who has performed most of the work on this infection in cats) identified that ronidazole and tinadazole (antibiotics similar but not the same as metronidazole) have some efficacy against T. foetus infection in cats (JVIM, 2006;20:536; Am J Vet Res, 2007; 68:1085), and that ronidazole is more effective than tinadazole. Ronidazole appears to be relatively safe, although a small number of patients have developed neurological signs eg, twitching and seizures, which have resolved on stopping the drug. The neurological signs are similar to those seen in some kittens or cats with liver disease, when they are given standard or high doses of metronidazole. However, ronidazole is not licensed for use in cats; it should only be used with caution and with informed, signed, owner consent. Initial studies suggested that a dose of 30-50mg/kg once to twice daily for two weeks is capable of both resolving clinical signs and potentially eradicating T. foetus but it can also be associated with neurological side effects, plus occasional lethargy and/or vomiting. Therefore, we now recommend 20-30mg/kg once daily for two weeks, which should be reduced for young kittens or cats with hepatopathy to 10mg/kg once daily for two weeks. To ensure that each kitten receives the correct dose, and so reduce the risk of side effects, it is important to weigh the kittens prior to ordering the reformulated capsules. The bitterness of the powder means that it must be placed in capsules prior to administration. For the same reason it is important not to split tablets or open capsules and sprinkle the contents on food.”

    The PCR test is pretty sensitive here, but if you really still thought they had the infection you could re-test.

    I hope that helps.

    Scott 🙂

    scott@vtx-cpd.com
    Keymaster

    Replying to Vicki B. 01/05/2022 - 14:57

    Hey.

    The recording should be available now:

    Lesson 9: Live Q&A Session (Thurs 28/04/2021 @ 8pm GMT)

    Let me know if any problems.

    Scott 🙂

    scott@vtx-cpd.com
    Keymaster

    Replying to Hannah B. 25/04/2022 - 13:31

    Hello again.

    MILA 0.2 Micron Bacteria Filter (Box of 10)

    I hope that helps.

    Scott 🙂

Viewing 15 posts - 1,216 through 1,230 (of 1,885 total)