Can terofundin be given subcutaneously to a cat?

Can terofundin be given subcutaneously to a cat? - briefly

Terofundin is not typically administered subcutaneously in cats due to its potential for causing local tissue irritation and necrosis. Intravenous administration is generally preferred for this medication.

Can terofundin be given subcutaneously to a cat? - in detail

Terofundin, also known as enalapril maleate, is an angiotensin-converting enzyme (ACE) inhibitor commonly used in veterinary medicine for the treatment of hypertension and heart failure in cats. The primary route of administration for this medication is oral, as it is designed to be taken by mouth and absorbed through the gastrointestinal tract. However, when considering subcutaneous administration, several factors must be evaluated.

Subcutaneous injection involves the delivery of a drug into the layer of tissue beneath the skin, typically in the form of a slow-release suspension or solution. While this method can be effective for certain medications, it is not commonly recommended for terofundin due to its pharmacokinetic properties and potential adverse effects.

The bioavailability of oral enalapril maleate is relatively low, with only about 10-20% of the drug being absorbed systemically after ingestion. This is because a significant portion of the medication is metabolized in the liver before it can exert its effect on the cardiovascular system. When administered subcutaneously, the absorption rate and bioavailability may vary significantly, leading to unpredictable blood levels and therapeutic outcomes.

Moreover, enalapril maleate is a prodrug that requires hepatic conversion to its active metabolite, enalaprilat, for its pharmacological effects. Subcutaneous administration might bypass the first-pass hepatic metabolism, potentially resulting in higher and more variable blood concentrations of enalaprilat. This could increase the risk of adverse reactions such as hypotension, bradycardia, and hyperkalemia, which are known side effects of ACE inhibitors.

In addition to these pharmacokinetic considerations, the formulation of terofundin is not designed for subcutaneous use. The drug is typically presented in tablet or capsule form, which is not suitable for injection. Attempting to administer it subcutaneously could lead to local irritation, inflammation, or even abscess formation at the injection site.

In conclusion, while subcutaneous administration of terofundin may seem like an alternative route in specific cases where oral administration is difficult or impossible, it is generally not recommended due to potential variability in drug absorption and increased risk of adverse effects. Veterinarians should carefully consider the risks and benefits before deviating from the established oral route of administration for this medication. If a cat requires parenteral therapy, alternative medications specifically formulated for injection may be more appropriate.