Cardiac exam Flashcards

(54 cards)

1
Q

Still’s mumur

A

prevalence: age 2-6yrs and resolves at adolescence

location: left lower sternal border

intensity: grade 1/2

quality: musical/vibratory

radiation: minimal

position: louder supine than sitting

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2
Q

Innocent mumurs

A

duration: short systolic

quality: musical or vibrational

radiation: minimal

intensity: grade 2 or less

position: louder supine than sitting

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3
Q

Pathological mumurs

A

intensity: grade 3 or higher with maximum at LUSB

timing: holosystolic or diastolic

quality: harsh or blowing, click

position: increased sitting

S2: abnormal with wide or fixed split

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4
Q

Systolic mumurs

A

early systolic: small muscular VSD

mid-systolic/ejection systolic: aortic stenosis

pansystolic: moderate/large VSD, mitral regurgitation

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5
Q

Diastolic mumurs

A

early distolic: aortic regurgitation, ASD with tricuspid stenosis

late diastolic: mitral stenosis

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6
Q

Mumurs

Right upper stenal border

A

pathogenesis: left ventricular outflow obstruction eg. aortic stenosis

radiation: usually to carotid region

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7
Q

Mumurs

Left upper sternal border

A

SYSTOLIC

cause: right ventricular outflow tract obstruction eg. pulmonary stenosis, benign flow mumurs

radiation: to axilla/back

DIASTOLIC

cause: aortic regurgitation or pulmonary regurgitation

radiation: left sternal border

CONTINUOUS

cause: PDA, cervical venous hum

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8
Q

Mumurs

Left lower sternal border

A

SYSTOLIC

cause: VSDs, tricuspid regurgitation, subvalvular AS, HCM, Still’s

DIASTOLIC

cause: semilunar valve regurgitation, tricuspid stenosis

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9
Q

Mumurs

Apex

A

SYSTOLIC

cause: mitral regurgitation

radiation: axilla

DIASTOLIC

cause: mitral stenosis

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10
Q

Cardiac failure

causes

A

congenital heart disease:

- volume overload: VSD, PDA, ASD, single ventricle

- pressure overload: AS, coarctation, PS

structurally normal heart:

  • cardiomyopathy, myocarditis, MI, arrhythmias (CHB, SVT, VT), drugs/toxins

non-cardiac:

  • sepsis, ESRF, HIV, SLE
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11
Q

Cardiac failure

clinical

A

cyanosis

tachycardia

hypertension

gallop rhythm (S3)

respiratory distress

hepatomegaly

jugular venous distension

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12
Q

Pulsus alternans

A

definition: varied pulse amplitude with alternate beats

causes:

  • hypertrophic CM
  • tachypnoea
  • severe arotic regurgitation
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13
Q

Pulses paradoxus

A

definition: drop >10mmHg with inspiration

causes:

  • cardiac tamponade
  • restrictive CM/pericarditis
  • hypovolaemic shock
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14
Q

Pulses bisferiens

A

definition: 2 systolic pulse peaks

causes:

  • AR
  • AS
  • HCM
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15
Q

Water hammer pulse

A

definition: abrupt rapid upstroke of pulse with collapse

cause: rapid LV volume against low resistance system

  • AR
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16
Q

Bounding pulse

A

definition: widened pulse pressue

cause: increased stroke volume

  • PDA
  • large AV fistula
  • hyperkinetic state
  • thyrotoxicosis
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17
Q

Chest wall scars

A
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18
Q

Fontan procedure

A

Single functional ventricles:

  • HLHS
  • tricuspid/mitral atresia
  • complex CHD

Stage I (Norwood): BT shunt

  • connecting brachiocephalic artery to right pulmonary artery

Stage II (Bidirectional Glenn): cavopulmonary shunt

  • BT removed
  • SVC anastomosed to PA

Stage III (Fontan): total cavopulmonary connection

  • IVC joined to PA

Issues

  • decreased exercise tolerance
  • decreased neurodevelopmental outcome
  • poor growth
  • thromboses
  • arrhythmias (SVT)

Post operative mumur

  • AV regurgitation
  • subaortic stenosis
  • VSD

Associated conditions: PLE, plastic bronchitis

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19
Q

Continuous mumurs

A

Aneurysm

ASD

AV malformation

Blalock-Taussig Shunt

Collateral Vessels

pDA

vEnous hum

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20
Q

Mumur timing

A
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21
Q

Mumur site of intensity

A
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22
Q

Complex cyanotic heart disease

5 T’s

A
  1. Transposition Great Arteries (TGA)
  2. Truncus Arteriosus (TA)
  3. Tetralogy of Fallot (ToF)
  4. TAPVD
  5. Tricuspid valve anomalies

OTHER: HLHS, DORV, pulmonary atresia

23
Q

Eisenmenger’s syndrome

A

Triad

  1. pulmonary to systemic shunt
  2. pulmonary artery disease
  3. cyanosis

associated defects: VSD 33%, ASD 30%, PDA 14%

clinical:

  • cyanosis, clubbing
  • RV impulse, palpable P2
  • elevated JVP, oedema
  • tricuspid/pulmonary regurgitation
24
Q

Pulmonary flow mumur

A

prevalence: very common

timing: brief in mid-systole

position: loudest lying down

associated: hyperdynamic states

25
Venous hum
**prevalence:** ages 2-6yrs **timing:** diastolic component loudest **location:** supraclavicular fossa on the right and may radiate **quality:** associated thrill **position:** disappears when flat
26
VSDs
**inspection:** no cyanosis/clubbing **clinical:** - pansystolic mumur maximal at left sternal edge - loud S2 - active praecordium - thrill at left sternal edge - no radiation but heard all over chest wall - diastolic rumble at apex **haemodynamically significant if:** - symptoms including tachypnoea - mumur may be softer - hyperactive praecordium - loud S2 - displaced apex - diastolic mumur - growth decreased **treatment:** **- medical:** diuretics, ACEi **- surgical (age 4yrs or shunt\>2:1):** pulmonary artery banding 1st if complication, VSD repair
27
ASD
**haemodynamic:** RV overload during diastole with an increased pulmonary blood flow secondary to shunt **complications:** atrial arrhythmias, pulmonary HTN, heart failure **clinical:** - parasternal heave - ejection systolic mumur left sternal edge - S2 widely split - diastolic mumur due to flow across tricuspid valve **ECG:** - ostium secundum: RAD, partial RBBB - ostium primum: LAD, partial RBBB **treatment:** surgical closure 4th/5th decade
28
AVSD
**pathophysiology:** left to right shunt through ASD/VSD **clinical:** hyperdynamic apex beat, RV heave, palpable thrill LLSE - loud pansystolic mumur LLSE, MR at apex **complications:** atrial dilation, arrhythmias, volume loaded ventricles, pulmonary HTN **ECG:** superior axis (-40 to -150), RVH **CXR:** cardiomegaly, pulmonary plethora **Treatment:** repair 4 to 6 months, diuretics - delaying treatment increases the risk of pulmonary hypertension
29
Sign of cardiac failure
30
Cardiac lesions T21
31
Aortic regurgitation
**congenital:** Ehlers-Danlos, Marfan syndrome, Turner syndrome **acquired:** rheumatic fever, post operative, infective endocarditis **pathophysiology:** LV overload, pulmonary oedema **clinical:** - collapsing pulse - decrescendo diastolic mumur LSE - increased sitting forward in expiration - associated thrill **ECG:** LVH **CXR:** cardiomegaly
32
Pulmonary stenosis
associated syndromes: Noonan's, Williams **pathophysiology:** RV overload **clinical:** - thrill over pulmonary area - RV heave - ejection systolic mumur LUSE - radiation to back - widely split S2 **ECG:** RVH, tall p waves **CXR:** normal **treatment:** surgery depending on pressure gradient p**ost repair:** residual systolic and diastolic mumur
33
Aortic stenosis
**associations:** Turner syndrone, Williams (supravalvular), coarctation **pathophysiology:** LV overload **symptoms:** syncope, pain on exertion **clinical:** - collapsing pulse - suprasternal/carotid thrill - apex displaced - ejection click LLSE - ejection systolic mumur at LLSE radiating into the neck **ECG:** LVH (tall R waves V5/V6, inverted T in 1, aVL, V5-6) **CXR:** prominent LV **treatment:** valve replacement if gradient \>60mmHg **post repair:** mumur of aortic stenosis and regurgitation
34
Coarctation of the aorta
**associations:** Turner's, biscuspid valve (70%) **clinical:** - high BP arms, low in legs (20mmHg difference) - radiofemoral delay - systolic mumur loudest at left interscapular area - ejection click LUSE if biscuspid aortic valve **ECG:** LVH **CXR:** cardiac enlargement, rib notching **treatment:** end-end anastomoses via left thoracotomy **complications:** residual HTN, recoarctation
35
Causes cardiac cyanosis
**decreased pulmonary blood flow:** * tetralogy of fallot * pulmonary atresia * Ebstein's * tricuspid atresia **poor mixing:** * transposition great arteries **common mixing:** * truncus arteriosus * DORV * TAPVD * univentricular heart
36
Tetralogy of Fallot
**Tetrad:** 1. RVOT obstruction 2. VSD 3. Overiding aorta 4. RVH **Variations:** 25% Right sided AA **clinical:** * FTT, clubbing, cyanosis * RV impulse * systolic thrill ULSE * systolic ejection mumur ULSE **CXR:** prominent RV, small pulmonary arteries, oligaemia **ECG:** RAD, RVH, tall p wave **treatment:** - modified BT Shunt - corrective survery 4-12 months **complications:** - exertional dyspnoea - cerebral thrombosis/brain abscess - infective endocarditis - arrhythmias **tx tet spells:** morphine, beta blockers, vasoconstrictors
37
Hypertrophic cardiomyopathy
**familial:** AD 60% **HOCM:** associated with septal hypertrophy or abnormal MV movement causing LVOTO **symptoms:** angina, syncome, arrhythmias, sudden death **clinical:** * systolic ejection mumur from LVS hypertrophy or mitral regurgitation **treatment:** beta blockers, endocarditis prophylaxis, myectomy
38
Dilated cardiomyopathy
most common cardiomyopathy **cause:** usually idiopathic, toxic insult **pathophysiology:** dilation 4 chambers **clinical:** * displaced apex * MR or TR mumur * 3rd heart sound * left and right sided cardiac failure **symptoms:** weakness, pulmonary oedema **treatment:** medical, transplantation
39
Trisomy 21 cardiac
40
Turner syndrome cardiac
41
Noonan syndrome cardiac
42
William syndrome cardiac
43
22q11 cardiac
44
CHARGE cardiac
45
VACTERL cardiac
46
Marfan cardiac
47
Ehler Danlos cardiac
48
Fetal alcohol syndrome
49
LEOPARD syndrome
50
Repair procedures
* VSD * ASD * TOF: BT shunt then definitive procedure at 1 year * TGA: arterial switch
51
Pallative repairs
**Can be temporary or permanent** * BT shunt * Pulmonary banding * Atrial septostomy
52
Timing of cardiac surgery
**1st week:** * duct dependent * severe obstructive lesion **First month:** * severe pulmonary pressure: PA banding or BT shunt * obstructive lesions eg. TAPVD **Infants:** * left to right shunt to prevent pulmonary HTN * RVOTO **Children:** * staged procedures * asymptomatic lesions **Adolescence:** * surgery for acquired diseases * stent procedure eg. non duct dependent CoA * repeat procedures
53
Complications post cardiac surgery
* diaphragmatic palsy * arrhythmias * vocal cord palsy * protein losing enteropathy (post Fontan) * developmental problems
54
CXR in cardiac disease