A Patient of Recurrent Syncope 97-2003 Ppt

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    WELCOME

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    A PATIENTOF

    RECURRENTSYNCOPE

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    SALIENTFEATURES:

    Mr . Abdul Mazid, 30 yrs old male, healing from

    Saidullahpur, Gaibandha, presented with complains

    several attacks of syncope in last 3 years, wasassociated with dyspnoea on effort, exertional

    tirdness and intermittent mild chest pain. He had

    recovered completely from syncope within 2 minutes

    on each occasion without neurological sequelae or

    transient confusion. He had no notable past medical

    history, was not taking any medications, and had nofamily historyof either syncope or sudden death.

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    SALIENTFEATURES(CONT.)

    On examination , his pulsewas 96beats per minute

    (Regular), BP was 110/60 mm Hg with no postural

    drop, pallor was absent, he was non-icteric and

    non-cyanosed. Finger clubbing was absent , JVP-

    Not raised and Ankle oedema was absent. His

    neurological examination was unremarkable andcardiovascular examination revealed , visible

    apical pulsation. Thrusting apical impulse on

    palpation with double impulse and slight shifting

    towards left.

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    SALIENTFEATURES(CONT.)

    There was no palpable thrills or RV heave. On

    auscultation, Heart sound s1 and s2 were audiblein all four areas , with a pan-systolic murmer heard

    over mitral and tricuspid area and radiates towards

    axila. All ther systemic examination revealed

    nothing abnormal.

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    DIFFERENTIALDOAGNOSIS:

    1. VSD

    2. Aortic Stenosis

    3. Hypertrophic

    Cardiomyopathy(HCM)

    4. Mitral Vulvular Diseases

    (MVD).

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    INVESTIGATION: CBC

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    INVESTIGATIONS: CXR P/A VIEW

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    INVESTIGATION: ECG

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    ECHOCARDIOGRAPHY

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    ECHOCARDIOGRAPHY(REPORT)

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    CONFIRMATORYDIAGNOSIS:

    HyopertrophicCardiomyopathy

    (HCM)

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    HYPERTROPHICCARDIOMYOPATHY

    The most common form of cardiomyopathy.

    Prevalence of 100 per 100 000 population.

    Hypertrophic cardiomyopathy (HCM) is a primary

    disease of the myocardium(the muscleof

    the heart) in which a portion of the myocardium

    ishypertrophied(thickened) without any obvious

    cause.

    http://en.wikipedia.org/wiki/Myocardiumhttp://en.wikipedia.org/wiki/Musclehttp://en.wikipedia.org/wiki/Hearthttp://en.wikipedia.org/wiki/Left_ventricular_hypertrophyhttp://en.wikipedia.org/wiki/Left_ventricular_hypertrophyhttp://en.wikipedia.org/wiki/Hearthttp://en.wikipedia.org/wiki/Musclehttp://en.wikipedia.org/wiki/Myocardium
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    HCM

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    PATHOPHYSIOLOGYInappropriate and elaborate left ventricular hypertrophy

    with malalignment of the myocardial fibers.

    The hypertrophy may be generalized or confined largely

    to the interventricular septum (asymmetric septal

    hypertrophy) or other regions (apical hypertrophic

    cardiomyopathy).

    Heart failure may develop because the stiff non-

    compliant ventricles impede diastolic filling.

    Septal hypertrophy may also cause dynamic left

    ventricular outflow obstruction (HypertrophicObstructive cardiomyopathy or HOCM ).

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    PATHOPYSIOLOGY(CONT)

    HCM has genetic prevalence, genemutation causes ventricular hypertrophy,

    Troponin mutation associated with

    myocardial fibre mal-alignement and

    Myosine-binding protein c mutationassociated with hypertension and

    arrythmia.

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    CLINICALFEATURESSymptoms

    Angina on effort

    Dyspnoea on effort

    SyncopeSudden death

    Signs

    Jerky pulse

    Palpable left ventricular hypertrophy

    Double impulse at the apex

    Pansystolic murmur at apex ( due to MR )

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    DIAGNOSIS: .

    ECG : Shows LVH , T-wave

    inversion.

    Echocardiography : is diagnostic .

    Genetic testing.

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    TREATMENT

    Asymptomatic: Avoid physical work, regular

    screening.

    Medical treatment : beta-blockers, rate-

    limiting calcium antagonist ( Verapamil

    ),disopyramides and anti-arrythmics to treatarrythmias.

    Surgical: Outflow tract obstruction can be

    improved by partial surgical resection ( eg.

    Myomectomy, septal ablation )ICD: should be considered in patients with

    clinical risk of sudden death.

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    THANKYOU