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scott@vtx-cpd.com

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Viewing 15 posts - 1,741 through 1,755 (of 2,413 total)
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  • scott@vtx-cpd.com
    Keymaster

    Replying to Jen Williams 31/05/2022 - 17:18

    Haha!!!

    All the good guys do seem to be in there! Thank you for sharing!

    Scott 🙂

    scott@vtx-cpd.com
    Keymaster

    Hello Austeja.

    I hope you are well. Theses are really tricky cases, so don’t beat yourself up about the outcome. You did a great job.

    I have popped some thoughts under your questions:

    1. How long do you have to wait after discontinuing pred so you can take biopsies?

    This is a great question. In an ideal world I would wait as long as possible, at least a couple of weeks. Longer if possible. Endoscopy would have maybe been a good option in this case. You could have considered endoscopic biopsies even when the albumin was lower.

    2. I gave metronidazole as immunomodulatory drug, however, now I think it was unjustified. Was it wrong to prescribe it in this case?

    The dog had very severe signs, so I understand your reasoning. I would probably not be rushing to use antibiotics in this case. I would have considered diet, probiotics and steroids before antibiotics.

    3. Was the shaking fit similar to eclampsia, because of low calcium secondary to low albumin? I assume low glucose was secondary to long standing diarrhea and not eating?

    Sounds like the shaking was due to the low calcium and I would suspect moist of this is due to the albumin. The severity of the GI disease will also contribute to issues with calcium absorption. When exactly was the low glucose documented? This could be post seizure/neurological; activity. The other possible concern for low glucose could be sepsis?

    4. Could extreme liver enzymes be caused by diazepam and other drugs being more toxic with such low albumin.

    I think there are lots of reasons for the liver to take a hit in this case (drugs/GI disease/hypoxia). I would suspect this was a secondary hepatopathy.

    5. How would you approach hypoalbuminemic crisis like this?

    These are very challenging. Treating the cause as aggressively as possible. I would also be aggressive regarding calcium supplementation (IV in a crisis) as well as considering vitamin D supplementation to help longer term. Plasma and human albumin are the only option for albumin replacement, but both options have their limitations.

    6. Do you have any more comments on how would you manage this case?

    I think the main thing I would have pushed for earlier on would have been endoscopic biopsies. I would also have considered vitamin D supplementation to help with calcium.

    I hope that helps.

    Scott 🙂

    scott@vtx-cpd.com
    Keymaster

    Hey Julie.

    Great points. I think overall the association with Helicobacter and disease is much better determined in human medicine.

    I have definitely been in a position where I have ‘treated’ the helicobacter before. I would only consider treatment if there was histopathological evidence of Helicobacter. I would tend to supplement vitamin B and change diet first and see what kind of response there was. If there was associated inflammatory change it might even be worth considering a trial of steroids too. But in some cases, more direct treatment of Helicobacter may be warranted.

    Hope that helps.

    Scott 🙂

    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 🙂

Viewing 15 posts - 1,741 through 1,755 (of 2,413 total)