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Equine atypical myopathy in the UK : Epidemiological characteristics of cases reported from 2011 to 2015 and factors associated with survival
Author(s) -
GonzálezMedina S.,
Ireland J. L.,
Piercy R. J.,
Newton J. R.,
Votion D. M.
Publication year - 2017
Publication title -
equine veterinary journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.82
H-Index - 87
eISSN - 2042-3306
pISSN - 0425-1644
DOI - 10.1111/evj.12694
Subject(s) - epidemiology , myopathy , medicine , oncology
Summary Background Equine atypical myopathy ( AM ) is a toxic rhabdomyolysis associated with ingestion of hypoglycin A, derived typically in Europe, from Acer pseudoplatanus tree. Despite the wide distribution of this tree species in the UK , the number of cases reported annually varies, and there has been an apparent increase in prevalence in recent years. Although AM was first recognised in the UK , epidemiological studies have never been conducted focused solely on this country. Objectives To describe the spatiotemporal distribution, presentation, treatment and outcome of AM cases reported in the UK . Study design Retrospective case series. Methods British AM cases reported to the atypical myopathy alert website, between 2011 and 2015 were included (n = 224). Data were obtained via standardised epidemiological questionnaires from owners and veterinarians. Factors associated with survival were assessed using logistic regression. Results Most cases reported were from England (87.9%). Survival was 38.6% (n = 73/189). Clinical factors associated with reduced odds of survival included, hypothermia (odds ratio [ OR ] 0.18; 95% confidence interval [ CI ] 0.06–0.57; P = 0.01), bladder distension ( OR 0.11; CI 0.02–0.59; P = 0.01), tachycardia ( OR 0.97; CI 0.94–0.99; P = 0.04) and serum creatine kinase activity >100,000 IU/L ( OR 0.17; CI 0.04–0.68; P = 0.01) in the univariable analysis as well as recumbency. The latter was the only sign retained in multivariable analysis ( OR = 0.19; CI 0.06–0.62; P = 0.006). Administration of vitamins during the disease was associated with survival ( OR 3.75; CI 1.21–11.57; P = 0.02). Main limitations Reporting cases to the Atypical Myopathy Alert Group is voluntary; therefore, under‐reporting will result in underestimation of AM cases; furthermore, direct owner‐reporting could have introduced misdiagnosis bias. Conclusion Some areas of the UK reported AM cases more commonly. Clinical signs such as recumbency, rectal temperature, distended bladder and serum creatine kinase activity might be useful prognostic indicators though should be considered in the context of the clinical picture. Treatment with vitamins increases odds of survival.