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Cardiomyopathy

Cardiomyopathies are a group of heart disorders characterized by structural abnormalities limited to the myocardium, often resulting in heart failure. The main types are dilated, hypertrophic, and restrictive cardiomyopathy. Dilated cardiomyopathy involves dilation of all four heart chambers and impaired systolic function. Causes include viral infections, alcohol toxicity, and genetic factors. Symptoms include heart failure and arrhythmias. Hypertrophic cardiomyopathy is characterized by thickened myocardium and impaired diastolic function. It is usually genetic and can cause outflow tract obstruction. Symptoms include chest pain, syncope, and sudden death. Restrictive cardiomyopathy involves stiffened myocardium and impaired di

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100% found this document useful (1 vote)
243 views45 pages

Cardiomyopathy

Cardiomyopathies are a group of heart disorders characterized by structural abnormalities limited to the myocardium, often resulting in heart failure. The main types are dilated, hypertrophic, and restrictive cardiomyopathy. Dilated cardiomyopathy involves dilation of all four heart chambers and impaired systolic function. Causes include viral infections, alcohol toxicity, and genetic factors. Symptoms include heart failure and arrhythmias. Hypertrophic cardiomyopathy is characterized by thickened myocardium and impaired diastolic function. It is usually genetic and can cause outflow tract obstruction. Symptoms include chest pain, syncope, and sudden death. Restrictive cardiomyopathy involves stiffened myocardium and impaired di

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HiLmy Zakiyah
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CARDIOMYOPATHY

Rizki Amalia Gumilang


CARDIOMYOPATHIES

A group of heart disorders, major


structural abnormality is limited to the
myocardium
Often result Heart failure
etiology frequently unknown
Hyperthrophic
Dilated CM Restrictive CM
CM

Ventricular Thickened Stiffened


enlargement myocardium myocardium
Impaired systolic Abnormal diastolic Impaired diastolic
function function function
3
DILATED CARDIOMYOPATHY

Dilated all 4 chamber (typical DCM)


Decrease contractile function (systolic)
Low CO
MR or TR or both
Arrythmia

4
Etiology
Idiopathic
Inflammatory
Infection : Viral, bacterial, parasit
Noninfection : Sarcoidosis, peripartum CM
Toxic
Alkohol
Chemotherapeutic agent
Metabolic
Hypothyroidism
Chronic hypoCa or HypoPO4
Neuromuscular
Muscular or myotonic dystrophy

5
PATHOLOGY
Four chamber dilatation
Mild to moderate ventricular
hypertrophy
Varying degrees of interstitial
fibrosis and myocyte
hypertrophy
Functional atrioventricular
regurgitation is common
Normal epicardial coronary
arteries
6
PATHOPHYSIOLOGY
MYOCYTE INJURY

Contractility
Pulmonary congestion
Dyspneu, orthopneu, rales
Fatigue
Systemic congestion Weakness
Edema, ascites, JVD
SV

Ventricular filling
LV Dilatation Forward CO
pressure

Mitral Regurgitasi
Lilly L.S, 2007, Pathophysiology of Heart Disease
7
NEUROHUMORAL ACTIVATION

8
CLINICAL PRESENTATIONS

Heart failure symptoms

Anginal chest pain

Emboli (systemic or pulmonary)

Syncope

Sudden cardiac death

9
INVESTIGATION
CXR : enlargement of cardiac silhoutte
ECG : evidence of old MCI, conduction abnormalities e.g LBBB,
LV hypertrophy, AF or VT
24-hour ambulatory ECG (Holter)
lightheadedness, palpitation, syncope
Two-dimensional echocardiogram or Radionuclide
ventriculography to assess : LV ejection fraction, end-diastolic
volume, diastolic function
Cardiac catheterization
age >40, ischemic history, high risk profile, abnormal ECG

10
echocardiography

11
treatment
THE GOAL THERAPY :
Treatment of underlying disease
Relieve
Treatment symptom
of heart failure
Prevent complication
Relief vascular congestion
Augmentation of low CO
Improve
Prevention long term survival
& treatment of arrhythmias
Prevention of thromboembolic event
Cardiac transplantation

12
Hyperthrophic CARDIOMYOPATHY

LV hyperthrophy
Cardiac cause (-)
Systemic cause (-)
Small LV cavity
Contractile function is
vigorous
Impaired ventricular
relaxation
High diastolic pressure
13
14
etiology
HCM is the most common genetic cardiovascular
disease.
Mutations of the cardiac sarcomere myofilaments
Affected genes :
-myosin heavy chain,
myosin-binding protein C
cardiac troponin T and I
-tropomyosin
actin
titin
myosin light chains.

inherited in an autosomal dominant


15
pathology
Pathological changes are muscular
hyperthrophy associated with fibrosis
Muscle fiber hyperthrophy
Myocardial disarray some part of heart

16
pathology

Normal muscle structure Myocardial disarray

17
18
Types of hcm
HCM or HOCM
Asymmetric septal (ASH) - without obstruction
Asymmetric septal (ASH) - with obstruction
Symmetric hypertrophy - concentric
Apical hypertrophy

19
20
pathophysiology
Myocyte Dynamic LVO
hyperthrophy obstruction

Ventricular Systolic
LVH pressure
arrhythmia

Mitral
regurgitation
LVDEP MVO2

Failure to CO
with exertion

Sudden
Syncope Dyspneu Angina
death

21
INOTROPIC

Mitral valve
Venturi
presses against
effect
septum

22
Clinical findings
Asymptomatic
Symptomatic :
Dyspnea
Angina
Presyncope / syncope
Palpitation due to arrhythmia
Sudden death young population

23
Physical examination
Usually limited to HOCM patient
Carotid impulse
Prominent a waves of JV pulse
Palpable S4 double apical impulse
S4 can be heard
Outflow murmur
Mitral regurgitation
Atrial fibrilation
Heart Failure symptoms

24
25
Murmur of as & hcm

VALSAVA SQUATTING STANDING


HCM murmur

AS murmur

26
Diagnostic study

Electrocardiography

Chest X-ray

Echocardiography

Cardiac catheterization

27
HCM - ECG
LAD
LVH, LAE
Prominent Q waves in inferolateral leads
ST-T changes
Arrhytmia AF, VT

28
HCM - Cxr
Mild to moderate enlargement of the
cardiac silhouette
Concentric left ventricular hypertrophy
Enlargement of the left atrium and the
right

29
HCM - echocardiography
2 Dimension & M-Mode :
LV wall thickening (15 mm)
Region
Left Ventricular Outflow Tract Obstruction (LVOTO)
Abnormal motion of Anterior Mitral Leaflet (AML)
Doppler :
Outflow pressure gradient
Associated Mitral Regurgitation (MR)

30
31
32
33
Differential diagnostic
Left Ventricular Hypertrophy
Outflow obstruction secondary to valvular
heart disease e.g AS, coarctation of aorta and
infiltrative disorder of myocardium
Pattern hypertrophy in hypertension is
concentric meanwhile in HCM is distinctive

34
Treatment drugs theraphy
blocker (standart therapy)
Myocardial O2 demand angina & dyspneu <<
LV outflow gradient
Passive diastolic filling time
Frequency of ventricular ectopic beat

Ca channel blocker
Reduce ventricular stiffness
Improve exercise capacity
Reduce rhytme disturbance

35
Amiodarone and disopyramide
For arryhthmias
Reduce inotropic
Infective endocarditis prophylaxis
Diuretic
For pulmonary congestion (avoid volume depletion!!!)
Avoid !!!
Nitrates
Digitalis

36
Treatment nondrugs theraphy
Septal myectomy
Dual chamber pacing
Decrease LVOTO
Reduce symptom
Alkohol septal ablation
Newer modality
Decrease LVOTO
Lessen systolic anterior motion (SAM) of mitral valve
Reduce LVOT gradient
37
RESTRICTIVE CARDIOMYOPATHY

Restrictive filling
Normal or reduced
LV and RV volumes
Abnormal diastolic
function
Normal or nearly
normal systolic (LV
and RV) function
38
etiology

Myocardial Endomyocardial
Non infiltratif Obliterative
Idiopathic Endomyocardial fibrosis
Scleroderma Hypereosinophilic syndrome
Infiltratif Nonobliterative
Amyloidosis Carcinoid
Sarcoidosis Malignant infiltration
Iatrogenic (radiation therapy)
Storage disease
Hemochromatosis
Glycogen storage diseases

Lilly L.S, 2007, Pathophysiology of Heart Disease


39
Pathophysiology
Rigid myocard

JVD
Fatigue Hepato>>
Diastolic & Ascites
ventricular
Ventricular filling
Weakness Peripheral edema
pressure

Cardiac output Venous congestion

Lilly L.S, 2007, Pathophysiology of Heart Disease


40
Clinical findings
Fatigue
Decrease exercise tolerance
Pulmonary congestion
Systemic congestion (JVD, ascites, peripheral edema)
Kussmaul sign
S3 and S4 gallops
Arrhythmias
Various type of heart block

41
DIAGNOSTIC APPROACH
CXR
Normal size ventricles
Pulmonary congestion
Atrial enlargement
ECG
Low voltage
Poor R wave progression
Pseudoinfarction pattern in the inferior leads
Nonspecific ST-T wave abnormalies
Conduction disturbances
Atrial and ventricular arrhythmias

42
DIAGNOSTIC APPROACH cont.

Echocardiographic (nonspecific)
Exculpate other causes of HF
Abnormal diastolic function
Endomyocardial biopsy
Cardiac MRI

43
management
No satisfactory medical therapy
Drug therapy must be used with caution
diuretics for extremely high filling pressures
vasodilators may decrease filling pressure
? Calcium channel blockers to improve diastolic
compliance
digitalis and other inotropic agents are not indicated
Chronic oral anticoagulant
Antiarrhythmias

44

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