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1.
Aust Vet J ; 88(6): 222-4, 2010 Jun.
Article in English | MEDLINE | ID: mdl-20553570

ABSTRACT

OBJECTIVE: To determine the specificity of a snake venom detection kit in urine samples from dogs and cats presenting to a referral centre for diseases unrelated to snake envenomation. DESIGN: Urine was collected from 50 dog and 25 cats presented for investigation and treatment of diseases unrelated to snake envenomation. Urine was collected as a voided sample, by cystocentesis or by catheterisation, and routine urinanalysis was performed. Snake venom testing was performed within 2 h of collection using a commercially available snake venom detection kit, which was observed continuously during the 10-min colour reaction phase for evidence of a visible colour indicating a positive test. RESULTS: No false-positive reactions occurred in any sample analysed. CONCLUSION: The snake venom detection kit appears to have 100% specificity for using urine as a test sample.


Subject(s)
Cats/urine , Dogs/urine , Reagent Kits, Diagnostic/veterinary , Snake Venoms/isolation & purification , Animals , False Positive Reactions , Sensitivity and Specificity
2.
Aust Vet J ; 87(4): 152-6, 2009 Apr.
Article in English | MEDLINE | ID: mdl-19335471

ABSTRACT

A 4-year-old Siberian Husky dog was treated with brown snake antivenom by his regular veterinarian after a witnessed episode of brown snake envenomation. The dog was discharged 5 hours post presentation despite an ongoing coagulopathy. The dog was presented to the emergency centre 2 hours later because the owner believed the dog to be in pain. Initial examination revealed an ambulatory but neurologically normal patient with thoracolumbar pain and laboratory evidence of a coagulopathy. Despite correction of the coagulopathy, the signs progressed to bilateral hind limb paresis after approximately 3 hours of hospitalisation, and continued to deteriorate over the next 56 hours to loss of deep pain perception in the right hind limb. Computed tomography imaging identified the presence of an extradural haematoma which was subsequently removed via a hemilaminectomy. Surgical decompression was successful in treating the spinal compression and the dog recovered with minimal complications. To our knowledge this is the first report of extradural haematoma secondary to coagulopathy induced by brown snake envenomation.


Subject(s)
Disseminated Intravascular Coagulation/veterinary , Dog Diseases/etiology , Elapid Venoms/adverse effects , Elapidae , Hematoma, Epidural, Spinal/veterinary , Snake Bites/veterinary , Animals , Antivenins/administration & dosage , Decompression, Surgical/veterinary , Disseminated Intravascular Coagulation/drug therapy , Disseminated Intravascular Coagulation/etiology , Dog Diseases/diagnostic imaging , Dog Diseases/surgery , Dogs , Hematoma, Epidural, Spinal/etiology , Hematoma, Epidural, Spinal/surgery , Lumbar Vertebrae/diagnostic imaging , Male , Paresis/etiology , Paresis/veterinary , Snake Bites/complications , Tomography, X-Ray Computed/veterinary , Treatment Outcome
3.
Chest ; 113(6): 1673-9, 1998 Jun.
Article in English | MEDLINE | ID: mdl-9631810

ABSTRACT

Tropical pulmonary eosinophilia (TPE) usually affects people living in the tropics, especially those in Southeast Asia, India, and certain parts of China and Africa. However, owing to the rising frequency of world-wide travel and the migration between continents, this disease is increasingly seen in the West, where the diagnosis can be easily missed since it is rarely encountered and can mimic many other conditions. Cases of TPE have typically been reported to masquerade as acute or refractory bronchial asthma. TPE results from a hypersensitivity reaction to lymphatic filarial parasites found in endemic regions. There is evidence that it is more likely to occur in nonimmune individuals, ie, visitors to endemic regions, than in individuals of endemic populations who have developed immunity to filarial infections. Clinical features include paroxysmal cough, wheezing and dyspnea, and systemic manifestations such as fever and weight loss. A history of residence in a filarial endemic region and a finding of peripheral eosinophilia >3,000/mm3 should initiate a consideration of this disease. Other criteria for the diagnosis of TPE include absence of microfilariae in the blood, high titers of antifilarial antibodies, raised serum total IgE >1,000 U/mL, and a favorable response to the antifilarial, diethylcarbamazine, which is the recommended treatment. This disease, if left untreated or treated late, may lead to long-term sequelae of pulmonary fibrosis or chronic bronchitis with chronic respiratory failure. Herein lies the importance of early diagnosis and treatment of TPE.


Subject(s)
Filariasis/complications , Pulmonary Eosinophilia , Animals , Diagnosis, Differential , Humans , Microfilariae/immunology , Pulmonary Eosinophilia/diagnosis , Pulmonary Eosinophilia/epidemiology , Pulmonary Eosinophilia/etiology , Pulmonary Eosinophilia/therapy , Tropical Climate
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