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MITRAL STENOSIS

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MITRAL STENOSIS Dr R Schulenburg Division of Adult Cardiac Surgery, Universitas Hospital, BFN Etiology and Essential Pathology Predominately post-inflammatory ... – PowerPoint PPT presentation

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Title: MITRAL STENOSIS


1
MITRAL STENOSIS
  • Dr R Schulenburg
  • Division of Adult Cardiac Surgery,
  • Universitas Hospital, BFN

2
Etiology and Essential Pathology
  • Predominately post-inflammatory scarring(other
    malignant carcinoid, SLE)
  • Fibroreactive transformation of the valve
  • Affecting all segments of the valvular apparatus
  • Calcifications at commisural edges lead to
    classic fish-mouth appearance
  • Only 25 have pure MS

3
Pathophysiology
  • Reduction in MVA with a rise in atrioventricular
    gradient
  • LA hypertrophy and imposes a pressure load on the
    RV through the development of pulmonary
    hypertension
  • Increases in RV end-diastolic pressure and volume
    cause RV dilatation which may result in
    funtional TVR(annular dilatation)

4
Pathophysiology
  • LV diastolic function is usually preserved
    although there may be(25) dysfunction in
    patients with severe, chronic MS(chronic preload
    reduction and/or extension of scarring from the
    valve to adjacent myocardium)
  • Systemic effects of severe TVR

5
Classification and Natural History
  • Mild(MVAgt1.5, MGlt5mmHg, PASPlt30mmHg)
  • Moderate(MVA 1-1.5, MG 5-10mmHg, PASP 30-50mmHg)
  • Severe(MVAlt1, MGgt10mmHg, PASPgt50mmHg)

6
Natural History
  • MVgt1.5 usually does not produce symptoms at rest
  • Symptoms develop when the LAP increases(Dyspnoea)
    gt5mmHg
  • Occurs when there is an increase in transmitral
    flow or a decrease in diastolic filling
    time(exercise, emotional stress, infection,
    pregnancy, AF with a rapid ventricular response)

7
Nutural History
  • MS is a continuous, progressive, life-long
    disease, usually consisting of a slow, stable
    course in the early years followed by a
    progressive acceleration in later life
  • Once symptoms develop, there is another period of
    almost a decade before symptoms become disableing
  • Asymptomatic/minimally symptomatic survival is
    80 at 10yrs but once significant limiting
    symptoms develop, there is a dismal 0-15 1-year
    survival rate

8
Natural History
  • When severe pulmonary HPT develops , mean
    survival drops to lt3yrs
  • 60-70-progressive pulmonary and systemic
    congestion
  • 20-30-systemic embolism
  • 10-pulmonary embolism
  • 1-5-infection

9
Diagnosis
  • History slow, indolent increase in dyspnoea and
    general fatigue(any sudden change in symptom
    complex should raise suspicion!)
  • ClinicalRV heave, Apex beat, Diastolic rumble,
    Opening snap
  • ECG
  • CXRCardiac chamber enlargement, Pulmonary venous
    hypertension, Pulmonary arterial hypertension
  • ECCHO/TEE
  • Cardiac cath

10
Management
  • Medical AB prophylaxis, diuretics, negetive
    chronotropic drugs, atrial fibrillation
  • Interventional Percutaneous balloon valvotomy
  • Surgical Cosed/open commissurotomy, MVR
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