HCM could be waiting to strike

Subclinical hypertrophic cardiomyopathy (HCM) is a deadly disease that affects 1 in 7 cats.1,2 HCM causes a cat’s heart muscle to thicken, reducing the heart’s pumping efficiency and can lead to serious health complications, including sudden death.

HCM develops silently with little to no warning

In the early stages (the best time to intervene) your cat may:

Act completely normal
Have regular energy levels
Eat and play as usual

Annual checkups are the ONLY way to catch HCM early

The only way to know if your cat has HCM is through veterinary testing. If your cat receives an HCM diagnosis, ask your veterinarian about Felycin®-CA1 (sirolimus delayed-release tablets).

If left untreated, HCM can lead to:

Congestive heart failure

Fluid builds up in or around the lungs, making breathing difficult.

Aortic Thromboembolism

Causes blood clots, which can travel to the legs and cause paralysis.

Abnormal heart rhythms

These can sometimes lead to fainting or even sudden death.

of cats with HCM suffer cardiovascular mortality within 5 years of diagnosis.1,3

Cat breeds with a higher incidence of HCM

Cats of any age, sex or breed can develop HCM.1,2 However older male cats tend to be predisposed and it is more common in certain breeds including Maine Coons, Ragdolls and Sphynxes.1

When was your cat’s last checkup?

Knowing if your cat has HCM can help you make the best decisions for their care. 
If your cat is diagnosed with HCM, ask your veterinarian about Felycin-CA1.

References
1 Fuentes VL, Abbott J, Chetboul V, et al. ACVIM consensus statement guidelines for the classification, diagnosis, and management of cardiomyopathies in cats. JVIM 2020;34:1062-1077. 
2 Kittleson MD, Cote E. The feline cardiomyopathies: Hypertrophic cardiomyopathy. JFMS 2021;23:1028-1051. 
3 Fox PR, Keene BW, Lamb K, et al. International collaborative study to assess cardiovascular risk and evaluate long-term health in cats with 
 preclinical hypertrophic cardiomyopathy and apparently healthy cats: The REVEAL Study. JVIM 2018;32:930-943.