Cardiology Flashcards

1
Q

Antenatal history for cardiac long cases

A
  • Morphology scans, foetal echocardiograms, amniocentesis for genetic diagnoses
  • Maternal infections
    • CHD: Rubella
    • Congenital cardiomyopathy: CMV, HSV, coxsackie, parvovirus B19, HHV6, toxoplasmosis and possibly HIV
  • Maternal medications
    • Anticonvulsants, ACE inhibitors, Lithium, Retinoic acid, Valproic acid, warfarin
  • Maternal drugs/alcohol/smoking
  • Maternal conditions
    • CHD: DM, HTN, obesity, phenylketonuria, thyroid disorders, systemic connective tissue disorders, and epilepsy
    • CCHB: SLE/Sjogren’s
  • Fertility treatment
    • Has been linked to increased risk of septal defects and cyanotic CHD
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2
Q

Screening questions for cardiac cases

A
  • Weight gain
  • Cyanosis
  • Tachypnoea
  • Periorbital oedema
  • Frequency of respiratory infections
  • Exercise intolerance
  • Chest pain
  • Syncope
  • Dizziness
  • Palpitations
  • Joint symptoms
  • Neurological symptoms
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3
Q

Complications to screen for in cardiac cases

A

Complications:

  • Stroke
  • Global hypoxic insult
  • Infective endocarditis
  • Arrhythmias + blocks

Often affected:

  • Neurodevelopment: increased risk if on bypass or cyanotic
  • Increased risk of ADHD
  • Growth / nutrition
  • Immunisations: ensure up to date including fluvax +/- RSV prophylaxis
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4
Q

Risk of recurrence in siblings for congenital heart disease

A

Baseline risk = 1%

In close relatives of patient with CHD risk increases to 3-7%

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5
Q

Infectious endocarditis prophylaxis

A
  • Endocarditis after dental/other procedures is infrequent, so prophylaxis prevents very few cases
  • More likely to result from bacteraemia associated with daily activities, so the maintenance of good oral health and hygiene is more important than periprocedural antibiotics
  • NICE guidelines don’t recommend prophylaxis for anyone
  • eTG recommends for a restricted group:
    • Prosthetic valve or material used for valve repair
    • Previous infective endocarditi
    • Congenital heart disease if:

Unrepaired cyanotic defects including palliative shunts/conduits

Repaired defects with residual defects

RHD in high risk patients

Consider post heart transplant

  • In the exam say you would check with the patient’s cardiologist
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6
Q

When do patients need IE prophylaxis?

A

Dental proceduresonly those involving manipulation of the gingival or periapical tissue or perforation of the oral mucosa (e.g. extraction, implant placement, biopsy, removal of soft tissue or bone, subgingival scaling and root planing, replanting avulsed teeth).

Dermatological or musculoskeletal proceduresonly those involving infected skin, skin structures or musculoskeletal tissues.

Respiratory tract or ear, nose and throat proceduresonly for tonsillectomy or adenoidectomy, or invasive respiratory tract or ear, nose and throat procedures to treat an established infection (e.g. drainage of abscess).

Genitourinary and gastrointestinal tract procedures—only if surgical antibiotic prophylaxis is required or for patients with an established infection.

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7
Q

Intercurrent illness management in cardiac disease

A
  • Taking documentation of child’s condition when travelling
  • Risk from increased PVR during respiratory infections
  • Dehydration may predispose to thrombosis in polycythaemic patients or lead to hypokalaemia in patients of diuretics or cause toxicity in patients taking digoxin
  • Febrile illness = increased metabolic demand
  • Fever = increases risk of arrhythmia in Brugada syndrome
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8
Q

Exercise restriction in cardiac disease

A

ALL sports

  • Insignificant left to right shunts (ASD / VSD / PDA ) can engage in all sports
    • Wait 3-6 months until post repair
  • Mild PS / AS
  • Coarct without aortic arch dilatation or BP difference
  • Normal or near normal funtion (EF >50%)

Low intensity only

  • Significant left to right shunts (ASD / VSD / PDA) with pulmonary HTN (>25mmHg) have decreased capacity for exercise and may develop chest pain, arrhythmias + syncope or SCD
  • > moderate PS / AS
  • Severe PR
  • Coarctation with aortic arch dilatation or BP difference
  • Ventricular dysfunction (EF <40-50%)

Restrict if;

  • Ventricular dysfunction
  • Outflow obstruction
  • Recurrent or uncontrolled arrhythmias
  • Exercise intolerance
  • Exercise induced ischaemia
  • Fontan circulation
  • ALCAPA pending repair
  • LQTS
  • CPVT
  • Anticoagulated: avoid spots with body impacts*
  • Pacemaker: avoid sports with direct blows to chest*
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9
Q

Cardiac disease

  • Pregnancy + contraception considerations
A

Pregnancy

  • Contraindicated in Eisenmenger’s or severe PHTN of any cause
  • Relative CI: severe CCF, severe cyanosis (spO2 < 80%)

Contraception

  • Theoretical risk of thrombosis potentiated by oestrogens
  • IUD potential source of bacteraemia
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10
Q

Cardiac transplantation

  • General facts
A
  • Immunosuppressants
    • MMF, tacrolimus, steroids
  • Risk of rejection highest in first 6 months (most common cause of mortality for first 3 years)
  • Infections (bacterial / fungal / viral)
  • Coronary artery disease (cardiac allograft vasculopathy)
  • Neoplasia (PTLD)
  • Hypertension
  • Abnormal renal function
  • Osteoporosis
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11
Q

Causes of aortic root disease

A

Connective tissue disorders

  • Marfans
  • Loeys-Dietz
  • Ehlers-Danlos syndrome
  • Osteogenesis imperfecta
  • Familial thoracic aortic aneurysmal disease

Non-connective tissue disorders

  • Bicuspic aortic valve
  • Conotruncal abnormalities
  • Turner syndrome
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12
Q

Bicuspid aortic valve monitoring

A
  • Lifelong surveillance required
  • Screen family members
  • Exercise restrict if > moderate AS
  • Control hypertension
  • Valve replacement
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13
Q

Cyanotic heart lesions

A

6 T’s 2D’s 1 H + 1P

1: TA truncus arteriosus (1 trunk)
2: tricuspid atresia
3: tricuspid ectasia (ebsteins)
4: TOF
5: TAPVD
6: TGA

DORV
DILV

Pulmonary atresia

HLHS

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14
Q

Common cardiac conditions that are inheritable

A
  • Cardiomyopathy
  • Arrhythmia syndromes: (LQT, Brugada, CPVT, SQT)
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15
Q

What are the 3 general classess of cardiac surgery repairs?

A

Repaired

Unrepaired

Palliated

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16
Q

Common cardiac long case management issues

A
  • Development
  • Growth + nutrition
  • Infective endocarditis prophylaxis
  • Intercurrent illness management
  • Social issues
  • Exercise restriction
  • Pregnancy / contraception
  • Cardiac transplantation
  • ADHD screening
  • Aortic root disease
  • Transition
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17
Q

Transposition of the great arteries

  • Presentation + management
A

Presentation

  • Antenatal scans
  • Critically unwell + cyanotic (inadequate mixing; PFO small)
  • Cyanosis and well: VSD + PS or large ASD / PDA
  • Not very blue + CHF in first few weeks: large VSD

Management

  • Prostaglandin
  • Balloon atrial septostomy
  • Arterial switch

Complications

  • AS / PS / AR / PR
  • Aortic root dilation
  • Coronary artery obstruction
  • Ventricular dysfunction
  • Arrhythmias
18
Q

Tetralogy of Fallot

  • 4 features
A

​MOST common cyanotic heart defect ~ 10% of CHD

Associations = DiGeorge 22q11

  • VSD
  • Overriding aorta (degree < 50% otherwise classified as DORV)
  • Pulmonary stenosis (RVOT)
  • Right ventricular hypertrophy
19
Q

Tetralogy of Fallot

  • Presentation / diagnosis
  • Management
  • Complications
A

Presentation

  • Antenatally
  • Cyanosis (most)
  • No heart failure
  • Test spell peak between 2-4 months

Management

  • Tet spell: knee to chest, oxygen, morphine, propranolol
  • Repair at 6 months (close VSD + widen RVOT)
  • +/- balloon dilatation of pulmonary valve
  • +/- shunt

Complications

  • RBBB
  • Arrythmias
  • Complete heart block
  • Residual VSD / RVOTO / PS / PR
20
Q

Tetralogy of Fallot

  • Examination
  • Investigations
A

Examination

  • RV tap + thrill
  • S2 single (low PA pressure)
  • PS murmur (2-5 ESM LUSE)
  • Murmur disappears / softens during spell

Investigations

  • ECG: RVH +/- RAD +/- LVH
  • CXR
    • Acyanotic = small-mod VSD
    • Cyanotic = boot shaped
21
Q

Tricuspid Atresia

  • Presentation
  • Management
A

Presentation

  • Antenatal
  • Cyanosis from birth
  • Tachypnoea + poor feeding

Management

  • Staged palliative procedure (s) before Fontan
22
Q

Tricuspid atresia

  • Examination
  • Investigations
A

Examination

  • Cyanosis
  • +/- thrill
  • S2 single
  • 2-3/6 murmur of VSD
  • +/- PDA murmur

Investigations

  • ECG: superior axis is characeristic
  • CXR: normal or slightly increased heart size, RA + LV enlargement, decreased PBF
23
Q

Extra-cardiac complications of congenital cyanotic heart disease

A
  • Polycythaemia - due to persistent hypoxia - tx= phlebotomy
  • Relative anaemia - due to nutritional deficiency - tx = iron replacement
  • CNS acscesses - due to R-> L shunting - tx= antibiotics / draining
  • CNS thrombo-embolic events - due to R-> L shunting + polycythaemic - tx= anticoag
  • Gingival disease - due to polycythaemic, bleeding, gingivitis - tx = dental hygiene
  • Gout - due to polycythaemia + diuretics - tx = allopurinol
  • Arthritis / clubbing - due to hypoxia
24
Q

Ebsteins anomaly

  • Presentation
  • Management
  • Complications
  • Examination
  • Investigations
A

Downward displacement at the tricuspid valve = atrialisation of the RV = hypoplasia

Presentation

  • Antenatal
  • Severe cases = cyanosis + CHF
  • Milder cases = SOB, fatigue, cyanosis, SVT

Management

  • Depends on severity from observation –> Fontan

Complications

  • CHB
  • SV arrhythmias

Examination

  • Soft, holosystolic mumur LLSE (TR)
  • Soft scratchy mid-diastolic murmur

Investigations

  • ECG: RBBB + RAH
  • CXR: massive cardiomegaly
25
Q

Truncus arteriosus

  • Presentation
  • Management
  • Complications
  • Examination
  • Investigations
A

Presentation

  • Antenatal
  • Cyanosis not usually clinically apparent as normall > 85% SpO2
    • As PVR falls PBF increases + symptoms HF worsen

Management

  • Test for DiGeorge (33%)

Complications

  • Truncal valve insufficiency
  • Conduit stenosis
  • Arrhythmias

*Most require re-intervention*

Examination

  • Bounding pulses, wide pulse pressure, hyperactive precordium
  • Single S2
  • VSD murmur
  • Apical diastolic rumble if high PBF

Investigations

  • ECG: BVH
  • CXR: cardiomegaly
26
Q

RVH on ECG

A

Rules of thumb for RVH and LVH – the 5,4,3,2,1 rules

RVH

Look at R wave in V1 – RVH if

  • > 5 squares in < 1 month
  • > 4 squares in <1yo
  • > 3 squares in > 1yr old

Look at S wave in V6 – RVH

  • > 3 squares in < 1 month
  • > 2 squares in < 1 yr
  • >1 squares in >1yo
27
Q

LVH on ECG

Rules of thumb for RVH and LVH – the 5,4,3,2,1 rules

RVH

Look at R wave in V6 – LVH if

> 3 squares in < 1 month

> 4 squares in <1yo

> 5 squares in > 1yr old

Look at S wave in V1 – RVH

> 1 squares in < 1 month

> 2 squares in < 1 yr

> 3 squares in >1yo

A
28
Q

ECG hypertrophy key point

A

**Remember all the ECG is suggesting is that there is ‘bigness’

  • Use the CXR to help decide if the bigness is dilation (volume) or hypertrophy (pressure)

ALWAYS comment on the presence or absence of strain if you think there is hypertrophy

29
Q

Left –> R shunt lesion key points

A
  • Large ventricular or arterial L->R shunt lesions cause big trouble within 1st 6months of life and are fixed
    • So your 6yr doesn’t have a big VSD
    • Likewise a PDA- if it is an older child, is likely small- moderate, and CXR and ECG changes may be minimal
  • ASD
    • Usually well grown
    • RV heave / sternal deformity
    • PV ESM, wide + fixed split S2
    • IRBBB on ECG
    • CXR: heart big, lungs wet
30
Q

Left to right shunt lesions

A
  • ASD
  • Primum ASD = partial AVSD
  • VSD
  • PDA
  • Volume load
    • MR
    • AR
  • Stenotic valves
    • MS
    • TS
31
Q

Cyanotic patients: progression for the palliated cyanotic patients

A
  • Initial operation in first days of life (Norwood or shunt or PA band)
  • BCPC at 3-12 months; SaO2 around 80-85%
  • Fontan completion around 4-5 years; SaO2 around 90 after
32
Q

Cyanotic patients CXR

A
  • Heart should be small
  • Lungs not wet (they have less flow)
  • May have coils etc in collaterals
  • Remember to check abdominal organs
    • This is the clue for isomerism
33
Q

Williams Syndrome CHD

A
  • Supravalvular aortic stenosis
  • Peripheral pulmonary stenosis
34
Q

Turners CHD

A
  • Bicuspid aortic valve
  • Coarctation of the aorta
  • Aortic stenosis
  • HLHS
35
Q

Fetal alcohol syndrome

A
  • ASD
  • VSD
36
Q

Infant of a diabetic mother

A
  • HOCM
  • VSD
  • Conotruncal anomalies
37
Q

Alagille syndrome

A
  • Peripheral pulmonary stenosis
  • Tetralogy of fallot
  • ASD
38
Q

T21 CHD

A
  • AVSD
  • ASD
  • VSD
  • TOF
39
Q

Acute Rheumatic heart disease

A

MR is the MOST common lesion acute

Can also lead to aortic involvement (in 25%)

40
Q

Ehler’s Danlos CHD

A
  • Aortic + carotid aneurysms