Myocardial disease in dogs and cats Flashcards
Types of myocardial disease
Primary myocardial dz
1. dilated cardiomyopathy (DCM)
2. arrhythmogenic right ventricular cardiomyopathy (ARVC)
3. hypertrophic cardiomyopathy (common in cats)
4. restrictive cardiomyopathy (common in cats)
Secondary myocardial dz
1. infective myocarditis
2. deficiency dz
3. toxic causes
What is the most common form of myocardial dz in dogs?
- DCM
Prevalence of DCM in cats
- rare
How is DCM characterised?
- impaired myocardial contractility with dilation of LV (± RV)
What is common with DCM?
- tachyarrhythmias
– supraventricular ± ventricular
DCM pathophysiology
- eccentric hypertrophy of the LV
- systolic failure (forward failure)
– heart doesn’t contract enough so not enough oxygen gets to the system as not enough blood moves forwards - diastolic failure (backward failure - congestion)
– every time the ventricle tries to fill and contract it doesn’t completely empty, so you get congestion and blood backs up in the system - LA dilation and increased LAP
- right side can also be affected
DCM histopathology
2 distinct types of HP are reported, these are thought to relate to the underlying mechanism of the dz
- narrow (attenuated) myocardial cells with a wavy appearance (Newfoundlands)
- myofibre degeneration, myocyte atrophy and lysis, fatty infiltration and fibrosis (Boxers, some Dobermans)
Otherwise often non-specific and include:
- scattered areas of myocardial necrosis
– myocardial degeneration and fibrosis
– inflammatory cell infiltrates are inconsistent but an active myocarditis is rare
DCM signalment
- breed predispositions (genetic basis)
– Doberman, Newfoundland, IWH, St Bernards, Labs, Great Dane, Cocker spaniels, Boxers (ARVC), GSD
– Boxers autosomal dominance inheritance pattern
– but different breeds have very different prognosis with the same dz
– Cocker spaniels - 2y with appropriate tx
– Doberman - often a few weeks - usually middle aged dogs (has been reported in puppies as young as 6m)
- usually dogs >12kg
- males tend to be more severely affected but no gender predilection
DCM - how does this condition cause dz?
- loss of systolic function results in low cardiac output (loss of contraction)
- low cardiac output results in forward failure
- sympathetic, hormonal and renal compensatory mechanisms activated therefore -> maintain cardiac output by increasing HR, peripheral vasoconstriction and volume expansion
- ventricle fails to empty, which results in increased ventricular diastolic pressure
- this in turn results in compromised coronary perfusion, worsening myocardial function further and resulting in arrhythmias
DCM - how do they present?
Occult phase
- can be prolonged
- screening programmes of specific breeds to identify this phase
– 24h holter monitor (>50VPCs/24h)
– echocardiography
- non-symptomatic
Symptomatic phase
- usually present in CHF
- CS: weight loss, sudden death, soft murmur, atrial fibrillation, lethargy, exercise intolerance, dyspnoea (signs of left sided failure)
Why use a Holter monitor?
- to monitor for HR control
- unexplained syncope or collapse
- arrhythmias
- monitoring therapy
DCM - clinical examination
Variable depending on the degree of myocardial dysfunction
- tachycardia ± arrhythmias -> AF, VPCs, VT
- variable pulses ± pulse deficits if dysrhythmic
- signs of LCHF ± RCHF
- gallop sounds - if in sinus rhythm
- soft MR/TR murmurs
If forward failure (often bad news)
- pale mm
- sluggish crt
- cool extremities
DCM investigations
- CE: usually in CHF
- echocardiography: definitive diagnosis
- clinical pathology: complications/co-existing dz
- radiography: confirms CHF
- ECG if dysrhythmic
- blood pressure esp once on tx
- 24h Holter monitor: more for screening
DCM echocardiograph findings
- large, round, poorly contractile LV
- poor systolic function (poor contractility)
- dilated, round LA
- ± mitral regurgitation small/moderate due to dilation
- ± right sided changes
- m mode confirms dilated, hypomotile LV
DCM electrocardiography
- findings are very variable
– normal
– wide ± tall complexes (occasionally small complexes - many DCM dogs have ventricular arrhythmias
- treat heart failure
- treat arrhythmias if haemodynamically unstable
Arrhythmogenic right ventricular cardiomyopathy - what is it? breed? histopath findings?
- rhythm disturbance caused by the cardiac muscle in the right ventricle
- usually Boxers
- myofibre atrophy, fibrosis and fatty infiltration
3 stages of ARVC
- asymptomatic with ventricular arrhythmias
- symptomatic - normal heart size and LV function but dogs are syncopal/weak from ventricular arrhythmias
- CHF - poor myocardial function, CHF and ventricular arrhythmias
ARVC CS
- can appear any age, mean age 8y
- ventricular arrhythmias
- supra-ventricular arrhythmias
- > 500 VPCs/24h
- but spontaneous variation of up to 80%
- syncope
- sudden death
Diagnosis and tx of ARVC
- investigations as for DCM but 24h Holter monitor is necessary
- may need further physiological monitoring -> refer these cases
- but never underestimate a syncopal/collapsing Boxer
Tx
- treat any heart failure
- anti-arrhythmic medication -> soltalol
Causes of secondary myocardial dz
- myocarditis -> infectious/non-infectious
- doxorubicin -> acute and chronic cardiotoxicity
- metabolic / nutritional toxicities
– L-carnitine deficiency
– Taurine deficiency -> grain free diets? - ischaemic heart disease
- tachycardia-induced cardiomyopathy -> most commonly seen with SVT
Feline cardiomyopathies - prevalence
- myocardial disease is most common in cats
Feline cardiomyopathies - types
- HCM: most common in literature
- RCM: restrictive cardiomyopathy
- DCM
- ARVC
- FUCM: feline unclassified cardiomyopathy
Feline cardiomyopathies - cause
- exact cause unknown but a genetic bases is thought to underlie many cases of HCM
What is HCM
= hypertrophic cardiomyopathy
- inappropriate myocardial hypertrophy of a non-dilated left ventricle, occurring in the absence of an identifiable stimulus