Peer-reviewed veterinary case report
Azathioprine treatment for acquired myasthenia gravis in dogs
By Dewey, C W et al.·Published in Journal of the American Animal Hospital Association·1999·Department of Small Animal Medicine and Surgery, United States·View original on PubMed →
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Original publication title: Azathioprine therapy for acquired myasthenia gravis in five dogs.
- Species:
- dog
Plain-English summary
Five dogs diagnosed with acquired myasthenia gravis, a condition that causes muscle weakness, were treated with a medication called azathioprine. Four of these dogs also received another medication, pyridostigmine, to help improve their symptoms. Within three months, three of the dogs showed significant improvement, and their antibody levels decreased, indicating a positive response to treatment. Unfortunately, one dog passed away due to a severe complication before reaching the full treatment dose. The remaining dogs had varying outcomes, with two being euthanized later due to unrelated health issues, while two others were doing well at follow-up visits.
People also search for: dog muscle weakness treatment · myasthenia gravis in dogs · azathioprine for dogs · dog medication for muscle problems
Abstract
Five dogs with acquired myasthenia gravis (MG), verified via positive serum acetylcholine (ACh) receptor antibody concentrations, were treated with a drug protocol including azathioprine (AZA). Four of the five dogs were concurrently treated with pyridostigmine. Azathioprine was used as the sole immunosuppressive agent in four dogs. One dog was temporarily treated with a combination of an immunosuppressive dose of prednisone and AZA, then maintained on AZA as the sole immunosuppressive drug. Three patients experienced complete remission of clinical signs within three months of therapy. In the four dogs for which follow-up serum ACh receptor antibody concentrations were available, initial versus final concentrations decreased substantially (81%), coincident with clinical improvement. One dog died suddenly due to a suspected myasthenic crisis before attaining the target dose of AZA. Two of the four surviving dogs were euthanized approximately one and seven years after diagnosis. One of these two dogs was euthanized because of a rib osteosarcoma, and the other dog was euthanized because of paraparesis of undetermined cause. The remaining two dogs were alive and doing well at the time of final follow-up evaluation, approximately six months and one year after diagnosis. The use of AZA as a therapeutic agent for acquired canine MG has not been investigated. The cases presented in this report suggest a potentially important role for AZA in the treatment of acquired MG in dogs.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/10493415/