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Small Animal Clinical Pharmacology - CYF MEDICAL DISTRIBUTION

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10<br />

Antiparasitic drugs<br />

Stephen W Page<br />

INTRODUCTION<br />

Helminth, arthropod and protozoal infections of companion<br />

animals continue to cause significant morbidity<br />

and mortality in dogs and cats and frequently present a<br />

zoonotic hazard with public health implications. Infection<br />

occurs frequently despite the availability and use of<br />

a number of very potent and selective antiparasitic<br />

drugs (Table 10.1). This highlights the fact that, in addition<br />

to the type of drug selected, the way in which drugs<br />

are used and integrated with other approaches to parasite<br />

control is critical to successful and sustained management<br />

of parasite infection. This chapter provides<br />

information on the clinical pharmacology of the major<br />

antiparasitic drugs together with a summary of the most<br />

important epidemiological and public health considerations<br />

associated with the parasites of dogs and cats.<br />

PUBLIC HEALTH CONSIDERATIONS<br />

Close contact of humans with dogs and cats as true<br />

companions in an aging and increasingly immunocompromised<br />

human population has increased the<br />

importance and likelihood of transmission of parasitic<br />

infections with zoonotic potential. As well as direct<br />

transmission of parasitic diseases from dogs and cats to<br />

humans, the diagnosis of a specific parasitosis in dogs<br />

and cats is frequently a warning or signal that humans<br />

too may be exposed to a common source of infection.<br />

The list of parasitoses is growing in size and many<br />

known associations with human disease are identified<br />

in the Appendix to this chapter (p. 245). Veterinarians<br />

should include discussion of public health implications<br />

of diagnosed parasite infections with clients wherever<br />

appropriate, providing advice concerning measures to<br />

minimize or exclude the possibility of transmission.<br />

Antiparasitic drug use in dogs and cats has the potential<br />

to select resistant parasites. If resistant parasites can be<br />

transmitted to humans then treatment of infected<br />

humans may be jeopardized. Dogs are the major reservoir<br />

of Leishmania infantum and the public health<br />

implications of use of pentavalent antimonial drugs and<br />

other agents that are also used in humans have been<br />

raised as an issue for consideration when selecting the<br />

most appropriate therapy of leishmaniosis in dogs.<br />

APPARENT INEFFICACY<br />

When interventions to treat parasite infections do not<br />

meet the therapeutic objective it is important to investigate<br />

and find the cause, rather than to simply assume<br />

drug failure and change to an alternative drug. Common<br />

causes of apparent inefficacy include:<br />

● incorrect diagnosis<br />

● inappropriate or unrealistic therapeutic objective<br />

(e.g. the animal may have had a lethal infection and<br />

could not have been expected to respond to treatment;<br />

control of clinical signs may be possible when<br />

eradication of infection is unlikely)<br />

● inappropriate drug prescribed (target disease agent<br />

resistant or not inherently susceptible)<br />

● incorrect dose regimen recommended or implemented<br />

(inadequate dose rate, frequency or duration of<br />

treatment)<br />

● compliance failure (a large category that includes<br />

insufficient mixing of suspensions, inadequate application<br />

of externally applied products, incorrect<br />

dosing frequency and many more)<br />

● reinfection by continuous or intermittent exposure<br />

(very common with many parasites such as fleas,<br />

Trichuris and Giardia)<br />

● insufficient supplementary specific or supportive<br />

treatment (e.g. with Babesia infection, Toxoplasma<br />

uveitis, tick paralysis, flea allergy dermatitis, adult<br />

heartworm infection)<br />

● multiple infection (e.g. concurrent infection with<br />

ticks, Babesia and Ehrlichia spp)<br />

● physiological or pathological conditions (e.g. gut<br />

stasis and piperazine may allow ascarids to recover<br />

from drug exposure, increased gut motility may not<br />

allow sufficient time for drug absorption)<br />

● underlying disease (e.g. immunodeficiency and infections<br />

with Pneumocystis or Demodex spp)<br />

● drug interactions (e.g. corticosteroids and praziquantel,<br />

piperazine and pyrantel)<br />

● drug resistance<br />

● out-of-date or incorrectly stored product.<br />

Knowledge of the actual cause of apparent inefficacy<br />

permits appropriate revisions to the therapeutic plan to<br />

be made, elevating the chances of future success.<br />

198

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