Doppler echocardiographic evaluation of midventricular obstruction in cats with hypertrophic cardiomyopathy

H B MacLea1, J A Boon, J M Bright

  • 1Department of Clinical Sciences, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Fort Collins, CO.

Insights

Hypertrophic cardiomyopathy (HCM) in cats can present with midventricular obstruction. This study documents its Doppler echocardiographic features, aiding diagnosis in cats with murmurs.

Area of Science:

  • Veterinary Cardiology
  • Feline Medicine
  • Cardiovascular Imaging

Background:

  • Hypertrophic cardiomyopathy (HCM) exhibits significant heterogeneity in feline patients.
  • Variability exists in hypertrophy distribution, hemodynamics, and echocardiographic findings in cats with HCM.

Purpose of the Study:

  • To characterize the Doppler echocardiographic features of midventricular obstruction in cats with HCM.
  • To identify a specific variant of feline HCM.

Main Methods:

  • Retrospective case series of eight cats with confirmed HCM.
  • Analysis of transthoracic two-dimensional, M-mode, and Doppler echocardiography.
  • Exclusion of cats with systemic hypertension (systolic blood pressure > 170 mmHg).

Main Results:

  • All cats displayed left ventricular hypertrophy at the papillary muscle level and midventricular hypertrophy.
  • Doppler echocardiography revealed turbulent midventricular flow in all cases.
  • Increased flow velocities and late-peaking flow profiles were observed at the left midventricle.

Conclusions:

  • A distinct variant of feline HCM involves hypertrophy at the papillary muscle level causing midventricular obstruction.
  • Recognizing this variant is crucial for diagnosing HCM in cats presenting with murmurs and atypical echocardiographic findings.
Abstract

Related Concept Videos

Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
Mitral Stenosis II: Clinical features and Diagnostic Tests01:23

Mitral Stenosis II: Clinical features and Diagnostic Tests

Mitral stenosis is a heart condition in which the mitral valve, which allows blood to flow from the left atrium to the left ventricle, becomes narrowed or stenotic. This narrowing hinders blood flow and leads to clinical symptoms requiring specific medical evaluations and management strategies. The following overview outlines the clinical symptoms, assessments, diagnostic findings, prevention methods, and treatments for mitral stenosis.Clinical ManifestationsDyspnea (shortness of breath): This...
Cardiomyopathy II: Dilated Cardiomyopathy01:30

Cardiomyopathy II: Dilated Cardiomyopathy

Dilated cardiomyopathy, or DCM, is a progressive myocardial disorder characterized by ventricular chamber dilation and contractile dysfunction.EtiologyVarious factors can cause DCM, including hypertension and heavy alcohol intake, which contribute to the weakening and enlargement of the heart muscle. Viral infections, such as Coxsackievirus B, adenoviruses, and influenza, can lead to DCM by causing inflammation and damage to heart tissue. Certain chemotherapeutic agents, including daunorubicin,...