The Feline Cardiomyopathies: 1. General concepts
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Published on: August 8, 2022
Mark D Kittleson1, Etienne Côté2
1School of Veterinary Medicine, Department of Medicine and Epidemiology, University of California, Davis, and Veterinary Information Network, 777 West Covell Boulevard, Davis, CA 95616, USA.
Insights
Feline cardiomyopathies are common cat heart diseases, often indistinguishable clinically. Early diagnosis and understanding disease progression are crucial for prognosis, even if treatment options are limited.
Area of Science:
- Veterinary Cardiology
- Feline Medicine
- Cardiovascular Diseases
Background:
- Feline cardiomyopathies are the most common heart disease in adult cats.
- Hypertrophic cardiomyopathy (HCM) is the most prevalent form.
- Clinical presentation can range from subclinical to severe heart failure or systemic arterial thromboembolism (ATE).
Purpose of the Study:
- To review the practical relevance, patient groups, diagnostics, key findings, and conclusions regarding feline cardiomyopathies.
- To highlight the importance of understanding pathophysiological mechanisms for diagnosis and management.
- To discuss the limitations of current diagnostic tests and the need for further investigation.
Main Methods:
- Review of existing literature on feline cardiomyopathies.
- Discussion of clinical signs, diagnostic tools (echocardiography, radiography, biomarkers), and treatment approaches.
- Analysis of disease progression from subclinical to clinical phases.
Main Results:
- Feline cardiomyopathies are often clinically indistinguishable, making diagnosis challenging.
- Echocardiography is the definitive diagnostic test, but other methods like point-of-care ultrasound and NT-proBNP testing can be useful.
- Heart failure and ATE are common manifestations of severe disease, with guarded prognoses.
Conclusions:
- Differentiating cardiomyopathy from normal variation is important for prognosis.
- While definitive treatments are often unavailable, understanding disease evolution is critical.
- Further research is needed for cases with nonspecific phenotypes.
Practical Relevance:
The feline cardiomyopathies are the most prevalent type of heart disease in adult domestic cats. Several forms have been identified (see Parts 2 and 3), with hypertrophic cardiomyopathy (HCM) being the most common. Clinically the cardiomyopathies are often indistinguishable. Cats with subclinical cardiomyopathy may or may not have characteristic physical examination findings (eg, heart murmur, gallop sound), or radiographic cardiomegaly. Cats with severe disease may develop signs of heart failure (eg, dyspnea, tachypnea) or systemic arterial thromboembolism (ATE; eg, pain and paralysis). Sudden death is possible. Treatment usually does not alter the progression from subclinical to clinical disease and often the treatment approach, once clinical signs are apparent, is the same regardless of the type of cardiomyopathy. However, differentiating cardiomyopathy from normal variation may be important prognostically.
Patient Group:
Domestic cats of any age from 3 months upward, of either sex and of any breed, can be affected. Mixed-breed cats are most commonly affected but certain breeds are disproportionately prone to developing HCM.
Diagnostics:
Subclinical feline cardiomyopathies may be suspected based on physical examination findings, thoracic radiographs and cardiac biomarker results but often the disease is clinically silent. The definitive clinical confirmatory test is echocardiography. Left heart failure (pulmonary edema and/or pleural effusion) is most commonly diagnosed radiographically, but point-of-care ultrasound and amino terminal pro-B-type natriuretic peptide (NT-proBNP) biomarker testing can also be useful, especially when the stress of taking radiographs is best avoided.
Key Findings:
Knowledge of pathophysiological mechanisms helps the practitioner identify the feline cardiomyopathies and understand how these diseases progress and how they manifest clinically (heart failure, ATE). Existing diagnostic tests have strengths and limitations, and being aware of these can help a practitioner deliver optimal recommendations regarding referral.
Conclusions:
Several types of feline cardiomyopathies exist in both subclinical (mild to severe disease) and clinical (severe disease) phases. Heart failure and ATE are the most common clinical manifestations of severe cardiomyopathy and are therapeutic targets regardless of the type of cardiomyopathy. The long-term prognosis is often guarded or poor once overt clinical manifestations are present.
Areas Of Uncertainty:
Some cats with presumed cardiomyopathy do not have echocardiographic features that fit the classic cardiomyopathies (cardiomyopathy - nonspecific phenotype). Although no definitive treatment is usually available, understanding how cardiomyopathies evolve remains worthy of investigation.
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Cardiomyopathy I: Introduction and Classification
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Cardiomyopathy V: Interprofessional Care
Cardiomyopathy II: Dilated Cardiomyopathy
Pathophysiology of Heart Failure
Cardiomyopathy IV: Restrictive Cardiomyopathy

