Test 1: lecture 18: canine Flashcards

1
Q

primary myocardial disease

A

Idiopathic or heritable disorders resulting in structural or functional abnormalities of the heart muscle
* Cardiomyopathies

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2
Q

secondary myocardial disease

A

inflammatory, metabolic, toxic or infiltrative disease of the myocardium with a known etiology or causative agent
* May or may not be reversible

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3
Q

two primary myocardial diseases

A

dilated cardiomyopathy (DCM)

Arrhythmogenic right ventricular cardiomyopathy (ARVC)

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4
Q

two secondary myocardial diseases

A

nutritional cardiomyopathy (taurine)

myocarditis

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5
Q

secondary dilated cardiomyopathy can be caused by

A

Nutritional factors – taurine, carnitine, other
* Toxins – chemotherapy
* Infection/inflammation – myocarditis
* Arrhythmias – chronic tachycardia
* Endocrine disease – hypothyroidism

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6
Q

— is Myocardial disease characterized by systolic dysfunction and secondary cardiac chamber dilation

A

dilated cardiomyopathy

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7
Q

what does heart with primary DCM look like

A

eccentric hypertrophy (thin walls- stretched out)

all four chambers but left>right

papillary muscles can be atrophies

heavy heart

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8
Q

histopath of DCM

A
  • Attenuated wavy fibers
  • Fibrofatty infiltration
  • Myocyte atrophy/necrosis
  • Minimal inflammation
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9
Q

DCM will lead to — stroke volume and — chambers

A

reduced
dilated

(impaired systolic function- reduced contractility)

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10
Q

what kind of failure will DCM cause

A

foward (poor ejection)
reduced cardiac output, hypotension → weakness and exercise intolerance

backward failure (congestion)
elevated ventricular end-diastolic pressure, high atrial pressures, high pulmonary venous pressure →CHF

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11
Q

what kind of dogs get DCM

A

large and giant male breeds

  • Doberman Pinscher
  • Boxer (ARVC)
  • Giant breeds (GD, Newfie, Irish Wolfhound)
    Exceptions: PWD, Manchester Terrier, Cocker Spaniel

Adults except PWD, Manchester Terrier (juvenile DCM)

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12
Q

clinical signs of DCM

A

from low output: weakness, lethargy, exercise intolerance, syncope, death

from congestion: cough, dyspnea, Orthopnea, insomnia, Abdominal distension, Anorexia, weight loss, Cardiac cachexia

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13
Q

why can you hear S3 with dog with DCM

A

ventricles do not fully empty (low output)

therefore when blood from atria pushed into ventricle will make a murmur

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14
Q

PE of dog with DCM

A
  • Arrhythmia
  • Pulse deficits
  • Gallop heart sound (S3)
  • Soft murmur (AV valves)
  • Weak pulses
  • Cold extremities
  • Tachypnea, dyspnea
  • Jugular distension, ascites
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15
Q

EKG of DCM

A

LV enlargement pattern
* Tall R wave
* Prolonged QRS duration (mild)

LBBB
* Prolonged QRS duration

Atrial enlargement pattern
* Increased P wave duration (P-mitrale)
* Increased P wave amplitude (P-pulmonale)

75% will get Afib

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16
Q
A

VPC
with ventricular tachycardia

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17
Q
A

Afib

75% of dogs with DCM will also have Afib

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18
Q

Xray of DCM

A

cardimegaly: left sided or generalized

left sided CHF
* distended pulmonary veins
* pulmonary edema : perihilar to caudodorsal, intersitial to alveolar

right sided CHF
* distended caudal vena vava
* pleural effusion
* ascites

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19
Q
A

DCM

large left atrium and ventricle (double opasity on VD)

diffuse perihilar and caudodorsal pulmonary edema

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20
Q

how to measure systolic function on echo

A

fractional shortening
ejection fraction

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21
Q

stages of DCM

A

stage 1: normal Heart, no signs

stage 2 occult: abnormal heart, no signs

stage 3 overt: abnormal heart with clinical signs/CHF

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22
Q

—% of dobermans have DCM

A

50-60

occurs in males 4-10 years old

sudden onset with syncope and CHF

23
Q

DCM in dobermans

A

50-60% of all males 4-10 years old

sudden onset of symptoms: syncope and CHF

ventricular arrythmia more common then Afib

sudden death (VT→VF) 30-50%
CHF made worse by AFib

24
Q

what genetic mutation in dobermans with DCM

A

autosomal dominant
incomplete, age related penetrance

PDK4 (DCM1)
DCM2

both mutations = 30% increased risk

25
PDK4( DCM1) encodes for
Encodes mitochondrial protein **pyruvate dehydrogenase kinase 4** * PDK4 has an important role in cardiac energy metabolism DCM in dobermans
26
DCM2 codes for
* Encodes sarcomeric protein titin * Titin contributes to active contraction, passive stiffness 21% risk increase DCM in dobermans
27
testing in dobermans for DCM
annual echo and holter starting at 3 years old genetic testing (NCSU) for **PDK4 and DCM2**
28
boxers with advanced --- can develop DCM
ARVC
29
DCM is --- in great danes
x linked with Afib more common then Vtach
30
DCM in newfoundlands and irish wolfhounds is ---
autosomal dominant with Afib more common then Vtach
31
what causes DCM in cocker spaniels
inherited? diet? unknown
32
what two dogs get juvenile DCM
**portugese water dogs** (2-32 weeks old), autosomal recessive **Toy machester terrier** (10 weeks-1 year old), autosomal recessive, K channel, complete penetrance
33
how to treat preclinical DCM
pimobendan (inodilator)
34
how to treat clinical stage of DCM
pimobendan diuretic ACE inhibitor spironolactone
35
how to treat ventricular arrhythmias in DCM
sotalol, mexiletine, amiodarone used for VPCs or Vtach
36
how to treat supraventricular arrhythmias in dogs with DCM
AFib diltiazem, digoxin
37
what did protect study show
DCM study in dobermans **pimobendan** prolonged survival and kept dogs asymptomatic for an extra 9 months
38
outcome of DCM in different dog breeds
mean survival 6-9 months
39
ARVC is common in
boxers, english bulldogs, cats and humans ## Footnote ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY (ARVC)
40
how is ARVC inherited
autosomal dominant mutation in **Striatin (ARVC1) and ARVC 2**
41
what does ARVC do
attacks **desmosomes** that hold cardiac cells together causes mechanical and electrical uncoupling atrophy of cells and replacement by fibrofatty tissue
42
scar tissue from ARVC causes
**arrhythmias**: VPCs, Vtach → right ventricle origin systolic failure → **heart failure** →fainting and sudden death (40%)
43
ARVC will lead to --- in 40% of cases
sudden cardiac death
44
what genes for ARVC in boxers
autosomal dominant **Striatin (ARVC 1)** * Colocalizes to intercalated disk * Homozygotes - higher risk of severe disease (DCM phenotype) **ARVC 2** * SNP in a regulatory gene
45
what happens to english bulldogs with ARVC
no gene found yet but happens more often in males most will get CHF instead of arrhythmias
46
Sotalol is treatment of choice for --- arrhythmias in Boxers
ventricular ARVC (will get ventricular arrhythmias (VPC and Vtach), syncope, sudden death and CHF)
47
what are some things that cause nutritional cardiomyopathy
* Taurine deficiency * L-carnitine deficiency * Boutique, exotic ingredient, grain-free (BEG) diets **can be reversible**
48
what breeds can develop taurine deficiency?
cocker spaniel golden newfoundland dogs can make taurine, cats can not found in seafood and meat
49
how to diagnose taurine deficiency
paired (whole and plasma) taurine levels if low supplement
50
--- helps transport fatty acids into mitochondria for beta oxidation
L- carnitine found in red meat and dairy or synthesized in skeletal and cardiac muscle
51
why is diagnosis of L carnitine deficiency hard
normal levels could be false positive carnitine found in red meat, dairy or synthesized in skeletal and cardiac muscle helps transport fatty acids into mitochondria for beta oxidation
52
some causes of myocarditis
parvo trypanosoma
53
how to diagnose myocarditis
high troponin infectious disease screening echo with low EF ECG with arrhythmias post mortem