Ivermectin is an avermectin and a fermentation product of Streptomyces avermitilis (also see Macrocyclic Lactones). It acts as a GABA agonist, causing paralysis in susceptible arthropods and nematodes. It is used in small animals for treatment of Sarcoptes scabeii, Otodectes cynotis, Cheyletiella blakei, C yasguri, and Demodex canis; in cattle for psoroptic mange, lice, and Hypoderma larvae; in horses for equine filarial dermatitis from Onchocerca cervicalis; and in swine for Sarcoptes scabeii.
In small animals, all use for skin conditions is extra-label in the USA. For Demodex, the dosage is 0.3–0.6 mg/kg, PO, sid until 2 negative skin scrapings 1 mo apart. For Sarcoptes, Otodectes, and Cheyletiella, the dosage is 0.3 mg/kg, PO, repeated in 2 wk. In cattle, 0.2 mg/kg is given as a single SC injection for Psoroptes and lice. In horses, 0.2 mg/kg, PO, kills microfilariae but not adult Onchocerca cervicalis, so relapse may be noted within 2 mo of treatment. In swine, the dosage is 0.3 mg/kg, SC, repeated in 2 wk, or 0.1–0.2 mg/kg in feed for 7 days.
In mammals, GABA is found only in the CNS and does not readily cross the blood-brain barrier. At least 10 times the normal dose of ivermectin is needed for toxic reactions. Ataxia, depression, and visual impairment develop in horses given 2 mg/kg, PO. In cattle, 4 mg/kg by drench or 8 mg/kg, SC, leads to listlessness and ataxia; 30 mg/kg induces ataxia in swine.
Some dog breeds (Collies, Shetland Sheepdogs, Old English Sheepdogs, Australian Collies, and their crosses) have an abnormality in the blood-brain barrier associated with a mutation of multiple drug resistance gene MDR1, permitting increased ivermectin into the CNS and therefore toxicity. Dogs that are homozygous for the mutation produce a severely truncated P-glycoprotein (<10% of the normal amino acid sequence) and will develop ivermectin toxicity at any of the dosages used to treat demodicosis. The critical point seems to be 120–150 μg/kg, at which transient, nonfatal clinical signs (mydriasis, ataxia, tremors) are seen. At higher doses, collapse, coma, and respiratory collapse may develop. Similar idiosyncratic reactions may develop in any breed, so a gradually increasing dose (daily progression of 50, 100, 150, 200, then 300 μg/kg) should be given to identify susceptible individuals. Administration should be stopped if any side effects are seen. One cat treated with 4 mg of the oral paste (∼70 μg/kg) showed ataxia, blindness, tremors, and mydriasis, with retinal atrophy in one eye 10 hr later.
Milbemycin is derived from fermentation products of Streptomyces hygroscopicus and, like ivermectin, acts as a GABA agonist but with a wider spectrum of activity against intestinal parasites. It has been used extra-label in dogs to treat nasal mites, scabies, and generalized demodicosis. No adverse effects have been seen in ivermectin-sensitive breeds. The dosage in dogs is 1–2 mg/kg every 7 days for 3–5 treatments for nasal mites and scabies and 1–2 mg/kg, sid for Demodex.
Moxidectin belongs to the milbemycin class of compounds. It is registered for heartworm control (Dirofilaria immitis) but has also been used extra-label for treatment of Otodectes and demodi-cosis in dogs. In cattle, it is used to treat lice (Linognathus vituli, Solenopotes capillatus, Bovicola bovis), mites (Psoroptes, Chorioptes bovis), ticks (Boophilus microplus), and fly warbles and grubs (Hypoderma bovis, H lineatum). In sheep, it is used for Psorergates ovis infestation. The dosage is 0.2–0.4 mg/kg, PO, sid in dogs and 0.2 mg/kg in cattle and sheep.
This semisynthetic macrocyclic lactone is applied topically, but acts systemically. It is effective against Ctenocephalides spp (both adults and larvae), Sarcoptes scabeii, Otodectes cynotis, and Dermacentor variabilis. The dosage in dogs and cats is 6 mg/kg, applied topically.
Lufenuron is an insect growth regulator that inhibits the synthesis of chitin—a critical component of insect exoskeletons. It is taken up by adult fleas while feeding. While it has no effect on adult fleas, it prevents development of the intermediate stages of the flea life cycle (ie, eggs, larvae, pupae). It is effective against Ctenocephalides spp in dogs and cats at a dosage of 10 mg/kg, PO, once a month. Chitin is also a component in the fungal cell wall of dermatophytes. An initial study showed efficacy of lufenuron in treating small animal dermatophytosis; however, additional studies have failed to show efficacy.
Nitenpyram inhibits the nicotinic acetylcholine receptor. It is used to treat Ctenocephalides spp in dogs and cats at a dosage of 1 mg/kg, PO. Nitenpyram has a short half-life and kills fleas on the animal within 30 min of administration. It is toxic to fleas for only 24–48 hr and is normally used in combination with an insect growth regulator to provide continuous flea control.
Cythioate is an organophosphate that kills via anticholinesterase activity. It is indicated for Ctenocephalides spp infestations at a dosage of 3 mg/kg, PO, twice weekly (dogs) or 1.5 mg/kg, PO, twice weekly (cats). Although effective blood levels are maintained for <12 hr, serum cholinesterase activity may be decreased for >1 mo after dosing.
Last full review/revision March 2012 by Michael Shipstone, BVSc, FACVSc, DACVD