structural heart disease Flashcards

1
Q

what is coarctation of aorta

A

part of aorta is narrower than usual

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2
Q

what is it called when there is a hole between left and right atria chambers

A

patent foramen ovale (PFO)

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3
Q

fetal blood vessel fails to close after birth, leading to abnormal blood flow between the aorta and the pulmonary artery- what is this condition

A

patent ductus arteriosus (PDA)

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4
Q

what are the defects seen in Tetralogy of Fallot (TOF)

A

pulmonary stenosis,
ventricular septal defect,
overriding aorta,
right ventricular hypertrophy

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5
Q

most common to least common valve disease

A
  1. all
  2. mitral
  3. aortic

specifics:
1. mild MR
2.mild AR
3.Moderate MR
4. moderate AR

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6
Q

as Risk factor and cause

A

RF
-hypertension
-LDL levels and smoking

cause
rheumatic heart disease
-congenital heart disease
-calcium build up

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7
Q

AS pathophysiology

A
  1. valve damage from age/untreated URTI (strep)
  2. fibrosis/calcification of aortic valve
  3. disrupt blood flow
  4. LV contract harder to pump through stenotic valve
  5. concentric LV myocardial hypertrophy
  6. LV becomes stiff + harder to fill. decrease CO. Diastolic dysfunction
  7. pressure overload in LV backs up to LA causing it to dilate-> pulmonary congestion
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8
Q

sound of pulmonary congestion

A

diffused crackles

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9
Q

what are these a sign of
Exertional dyspnoea and fatigue
Chest pain, Angina
Syncope
Heart failure
Ejection systolic murmur
H/O Rheumatic fever, High lipoprotein, high LDL, CKD, age >65

A

AS

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10
Q

investigation to confirm AS

A

doppler echo

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11
Q

AS management

A

Aortic Valve replacement (AVR)
for severe aortic stenosis

-Transcatheter valve replacement
-Surgical valve prosthesis

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12
Q

AR (congenital/acquired cause) vs (aortic root dilation cause)

A

(congenital/acquired cause)
-rheumatic heart disease
-infective endocarditis

(aortic root dilation cause)
-marfan’s syndrome
-connective tissue disease/collagen vascular disease

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13
Q

AR pathophysiology

A
  1. valve leaflet close poorly due to inflammation/aortic root dilation in diastole.
  2. back flow from A->LV
  3. volume+pressure overload in LV. Increase LV pre+afterload
  4. a) acute dilatation-increase SV (frank starling law)
    4.b) chronic dilation-eccentric hypertrophy
  5. weakens myocardium. Can’t contract properly. systolic heart failure
  6. back pressure in LV to atria- > congestion
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14
Q

AR clinical finding

A

bounding/Corrigan/collapsing pulse

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15
Q

what is this a sign of :
Wide pulse pressure
Corrigan (wate hammer pulse)

A

CHRONIC AR

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16
Q

what is this a sign of: Cardiogenic shock
Tachycardia
Cyanosis
Pulmonary oedema
Diastolic murmur

A

Acute AR

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17
Q

investigation to diagnose and grade severity of AR

A

echocardiography

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18
Q

management for AR: Acute AR vs Asymptomatic patients with chronic severe AR:

A

Aortic Valve Replacement

Acute AR: medical emergency, sudden onset of pulmonary oedema and hypotension or cardiogenic shock.

Asymptomatic patients with chronic severe AR:
Vasodilator therapy improves haemodynamic and delays the need for aortic valve replacement/repair (AVR)

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19
Q

how to prevent AR

A

treat rheumatic fever and infective endocarditis

20
Q

MS cause

A

-rheumatic fever
-carcinoid syndrome
-RA
-Amyloidosis

21
Q

MS pathophysiology

A
  1. recurrent inflammation
  2. fibrous + calcification of mitral valve leaflets + chordae tendineae
    3.stiff leaflet
    4.obstruct blood flow
  3. impaired LA emptying
    6a) increase LA pressure-> back pressure in LA-> congestion
    6b) impaired filling LV. decrease SV +CO =congestive heart failure–>RV hypertrophy (right sided heart failure)
22
Q

clinical findings of MS

A

-afibrillation

-pulmonary oedema-> dyspnoea

-right sided heart failure

23
Q

what is this a sign of: H/0 of Rheumatic fever
Dyspnoea
Mid Diastolic murmur
Opening snap / loud S1 in early stages
Dysphagia
Atrial afibrillation
Haemoptysis

24
Q

Investigations for MS

A

ECG,
Chest x-ray
transthoracic echocardiography

25
MS management for: Progressive asymptomatic, Severe asymptomatic, Severe symptomatic
Progressive asymptomatic=No therapy required Severe asymptomatic=no therapy generally required/ adjuvant balloon valvotomy Severe symptomatic= diuretic, balloon valvotomy, valve replacement & repair adjunct b- blockers
26
MR- acute vs chronic cause
acute Mitral valve prolapse, rheumatic heart disease, infective endocarditis chronic -rheumatic heart disease, SLE, Scleroderma
27
MR pathophysiology
1. impaired valve closure 2. backflow LV->LA 3.increase LA volume + pressure 4. LV dilation-> remodelling-> decrease LV systolic function 5a) back pressure in LA-> congestion 5b) decrease SV +CO = congestive heart failure
28
MR clinical findings
holosystolic murmur radiating to axilla, -increase serum creatinine -peripheral oedema -frothy sputum
29
what is this a sign of: Dyspnoea Holosystolic murmur S3 heart sound Signs of congestive heart failure
MR
30
investigation for MR
Transthoracic echocardiography, ECG Chestxray
31
MR management -Acute severe MR vs Chronic severe MR asymptomatic vs Chronic symptomatic
Acute severe MR = repair/replace the supporting valve structures. Prosthetic ring inserted to reshape the valve. Chronic severe MR asymptomatic = watchful waiting/surgery Chronic symptomatic= 1st surgery plus medical treatment
32
dilated cardiomyopathy cause- priamry vs secondary
primary: without fam fx-idiopathic secondary -myocardial ischemia/heart valve disease -myocarditis -alcohol -thyroid disease
33
Dilated Cardiomyopathy- Pathophysiology
1.myocyte damage 2. eccentric fibrosis /volume increase 3. enlarged LV without myocardial mass increase 4. over time-> systolic dysfunction 5. decreased CO. increased EDV/EDP 6. volume overload-> congestive heart failure
34
what is this a sign of? -dyspnoea, cold clammy extremities - displaced apex beat -fatigue -angina -pulmonary congestion -peripheral oedema -sudden cardiac death
Dilated Cardiomyopathy
35
Investigation for Dilated Cardiomyopathy
ECG Chest x-ray
36
management for Dilated Cardiomyopathy
-counselling -symptomatic treatment -diet modification- fluid/Na restriction -treat underlying disease -treat symptoms of heart failure -treat arrhythmias -treat thrombotic events
37
how to treat arrhythmias
amiodarone
38
treatment for heart failure symptoms
ACEi, b-blocker -diuretic/ARB
39
hypertrophic cardiomyopathy- pathophysiology
1. thickening of LV myocardium 2. often interventricular septum thickens-> block flow 3.disorganised myocytes disrupts signal conduction 4. ventricular arrhythmias 5. sudden cardiac death
40
what is this a sign of: -S4, syncope -fatigue -angina -pulmonary congestion and oedema -systolic murmur -sudden cardiac death
hypertrophic cardiomyopathy
41
investigation for hypertrophic cardiomyopathy
echocardiography
42
hypertrophic cardiomyopathy management
HCM with Symptoms -Beta blockers –If contraindicated B=Verapamil If drugs fail-> Mechanical Therapy with Pacemaker or Surgery (septal myectomy or ablation)
43
Restrictive Cardiomyopathy-cause
-idiopathic/associated with carious systemic disorders
44
Restrictive Cardiomyopathy- pathophysiology
1. infiltration- deposit fibrosis-> ventricle walls stiffening. Diastolic dysfunction. 2. Atrial enlarges (ventricle thickness normal) 3. conduction abnormalities 4. adverse remodelling-> systolic dysfunction 5. reduced ventricular filling= decreased CO
45
What is this a sign of? -ascites/pitting oedema in peripheries -hepatomegaly -S4 heart sound -increased jugular venous pressure -easy bruising, weight loss
Restrictive Cardiomyopathy-
46
investigations for Restrictive Cardiomyopathy-
complete blood count
47
Restrictive Cardiomyopathy- management
Heart failure medication -ACEi/angiotensin receptor II blockers, diuretics and aldosterone inhibitors should be initiated in patients with reduced LV -Antiarrhythmic Therapy -Immunosuppression- Steroids -Pacemaker -Cardiac transplantation -