2010, Vol. 5 No. 1, Article 58
Ivermectin Toxicity in Pomeranian Pup – A Case Study
Rajneesh Pathania*1 and Vinay Kant2
1Veterinary Officer, Tihra, Himachal Pradesh
*Corresponding Author; e-mail address: email@example.com
A Pomeranian pup aged one month developing symptoms of depression, hind limb ataxia, in -coordination, tremors, behavioral disturbances, weakness, recumbency and hypersalivation about 6 hours after subcutaneous administration of 0.6 ml ivermectin (Ivomec). Administration of neostigmine 0.2 ml intravenous and dexamethasone 1ml intramuscular twice a day with infusion of dextrose saline (5%) 200 ml i/v cured the pup completely.
Ivermectin, Pomerian, Toxicity.
CASE HISTORY and clinical signs
A Pomeranian pup aged one month was presented to Veterinary hospital at Tihra, Mandi (H.P.), with the complaint of developing symptoms of depression, hind limb ataxia, in-coordination,
tremors, behavioral disturbances, weakness, recumbency and hypersalivation (drooling saliva).
The animal had been injected 0.6 ml of ivermectin (Ivomec)
subcutaneously about 6 hours earlier, to treat ectoparasites.
DIAGNOSIS AND TREATMENT
On the basis of the history and clinical signs the case was diagnosed to be of ivermectin toxicity. There is no specific antidote for ivermectin toxicity and only managemental care, supportive and symptomatic treatments are effective. The pup was administered a 0.2 ml intravenous injection of neostigmine and 1ml intramuscular injection of dexamethasone twice in a day. Additionally, dextrose saline (5%) 200 ml i/v over a period of 1 hour was also administered. Within 8 hours of therapy, the hypersalivation disappeared and there was moderate improvement in the depression and tremors. The pup recovered fully after 2 days.
Collie breed of dogs are more susceptible to ivermectin and tolerate only up to 0.1 mg/kg dose rate of ivermectin (Paul 1987). The margin of safety for ivermectin in most breeds of dog is well over 100 times the recommended dose but in Collies it is about 16 times the usual dose. Clinical signs of toxicity were reported in two Australian shepherds receiving ivermectin at oral dosage of 0.17 mg/kg and 0.34 mg/kg respectively (Hadrick et al., 1995). Occurrence of toxicity in selective breeds, may be due to the reason that these breeds have comparatively more permeable blood brain barrier to the drug (Houston et al; 1987) or due to an autosomal recessive trait (MDR-1) gene that causes a defect in the p-glycoprotein, which is a multidrug transporter in the blood brain barrier and this leads to passage of ivermectin in to the brain at low dosages thus causing toxicity (Kant, 2007). In present case, the animal was young and the blood brain barrier might not have been fully developed leading to toxicity.
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