Peer-reviewed veterinary case report
Cat diabetes caused by prednisolone and cyclosporine toxicity goes
By Cha, Sijin et al.·Published in Veterinary medicine and science·2024·College of Veterinary Medicine, South Korea·View original on PubMed →
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Original publication title: Remission of diabetes mellitus induced by prednisolone in combination with cyclosporine toxicity in a cat.
- Species:
- cat
Plain-English summary
A 6-year-old female domestic short-hair cat was brought in because she was not eating and seemed very tired. She had been on cyclosporine and prednisolone for skin and digestive issues, but after stopping the prednisolone, she developed serious problems like high blood sugar and diabetic ketoacidosis (DKA). The vet treated her with insulin and fluids, and found that she had too much cyclosporine in her system, which was stopped immediately. After a week, her condition improved, and she was switched to a different insulin that was eventually stopped because her blood sugar stayed normal for 28 days. This case highlights the risks of using prednisolone with cyclosporine and shows that diabetic cats can go into remission after careful management.
People also search for: cat not eating lethargic · diabetic ketoacidosis treatment cat · cyclosporine toxicity in cats · insulin treatment for cat diabetes · cat diabetes remission after DKA
Abstract
A 6-year-old spayed female domestic short-hair cat was presented for primary complaints of anorexia and lethargy. The cat was being treated with cyclosporine (25 mg/cat, PO q24h) and prednisolone (1 mg/kg, PO q12h) for feline hypersensitivity dermatitis and inflammatory bowel disease for 1 year, wherein prednisolone was withdrawn 2 weeks prior to presentation. At presentation, dehydration, hyperglycaemia, ketonaemia, increased fructosamine, glucosuria, ketonuria and metabolic acidosis were observed. The cat was diagnosed with diabetic ketoacidosis (DKA). Immediate treatments with insulin continuous-rate infusion and intravenous fluid therapy were initiated. A serum cyclosporine concentration was >2100 ng/mL, indicating cyclosporine toxicity. Cyclosporine was discontinued immediately. The cat's acidosis and ketonaemia were resolved within a week, allowing a switch from insulin continuous-rate infusion to subcutaneous glargine (1 IU/cat), which was eventually discontinued due to persistent normoglycaemia 12 days after initial presentation. Hyperglycaemia was not observed for 28 days thereafter without insulin, indicating remission of diabetes mellitus. This report suggests that using prednisolone, particularly immune suppressive doses, could be problematic in cats receiving long-term cyclosporine therapy. Additionally, diabetic cats receiving immune-suppressive agents can possibly achieve diabetic remission after surviving DKA through regular monitoring of blood glucose concentration, elimination of prednisolone and intensive blood glucose management.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/39042703/