6. ECGs in children
• Heart rate >100 beats/min
• Rightward QRS axis > +90°
• T wave inversions in V1-3 (“juvenile T-wave pattern”)
• Dominant R wave in V1
• RSR’ pattern in V1
• Marked sinus arrhythmia
• Short PR interval (< 120ms) and QRS duration
(<80ms)
• Slightly peaked P waves
• Q waves in the inferior and left precordial leads.
7. The normal ECG
• QRS variable with age - Newborn 50-80ms, at 16
years 75-115ms
• cQTC under 6/12: 490ms, 440ms otherwise
• Notched t waves; may be normal in V2&3
• Transient Wenckebach during sleep
8. The normal ECG
• Parameters vary through age
• Right ventricular dominance owing to high
pulmonary pressures, normalise at ~6/12
• T waves; usually upright in most leads for first 7/7,
then downwards in most leads until adolescence.
•Upright t waves in childhood may reflect RVH.
10. Chest pain
Common but usually benign presentation
4436 presentations age < 19 yrs over 3 1/2 year period
in a tertiary PED in USA
•0.6% deemed cardiac
•37% arrhythmia
•29% pericardial
•17% myocarditis
•13% AMI
•4% PE
American Journal of Emergency Medicine Volume 29, Issue 6 , Pages 632-638, July 2011)
11. Non cardiac chest pain
• 56% musculoskeletal
• 12% asthma/ wheeze
• 8% infection
• 6% GI – gastritis and GORD
• 4% sickle cell disease
12. Texidor’s twinge
• Precordial catch syndrome:
• acute, non-radiating left sided chest pain in an
adolescent
• occurs suddenly, exacerbated during inspiration and
resolves in a few minutes
14. Syncope
• 15-20% all children will have an episode
Neurally mediated
Vasovagal
Reflex anoxic seizures
Orthostatic
Cardiac
Structural
Cardiomyopathy
Arrythmias
Non CVS
Psychogenic
Factitious
Neurological non syncope e.g. Seizure
15. Syncope Red Flags
• History of cardiac disease
• Family history of SCD
• Recurrent episodes
• Exertional
• Prolonged LoC
• Associated chest pain / palpitations
• Medications that can alter cardiac conduction
18. Cardiac arrhythmias in children
• Likely to be the result rather than the cause of
acute illness
• Often preceded by hypoxia, acidosis and / or
hypotension
• Primary cardiac arrhythmias are uncommon
21. Bradycardia - causes
• Bradyarrythmias rare in structurally normal
hearts
• Usually pre-terminal following hypoxia and
ischaemia
• Vagal stimulation
• Raised ICP
• Poisoning with digoxin/ beta-blockers
• Congenital CHB seen in infants of mothers
with anti ro and la antibodies
27. Supraventricular Tachycardia
• Most common primary cardiac arrhythmia in
children
• Paroxysmal, regular, narrow QRS complexes
• Caused by re-entry mechanism through an accessory
pathway or AV conduction system
• HR > 220 bpm in infants or > 180 bpm in children
33. Long QT - congenital
Normal QTc < 400ms, > 460 ms abnormal
Easiest to reproducibly measure in II & V5
Channelopathy
Genetic mutations identifies in 90% familial cases
Subtypes 1-14
Risk of torsades and VF
May present with syncope (VT), risk greatest with QT > 500ms
Ask about family history of syncope, sudden death and epilepsy
European registry 1993; 8% 5 yr mortality
Treatment with BB
36. Atrial Flutter and Fibrillation
• Rare
• Underlying CHD, status post-open heart surgery
• Cardioversion in decompensated
• In haemodynamically stable children,
amiodarone or elective cardioversion
37. Pre-excitation syndromes
• Commonest WPW
• Ventricular Pre-excitation in SR,
short PR and delta wave
• Commonest arrhythmia is
orthodromic AV re-entry
tachycardia
• Antidromic less common
39. The collapsed infant
• Wide differential
• Always cover for sepsis
Congenital heart disease
• May present as lethargy, poor feeding, "not right",
cyanosis to complete cardiovascular collapse
40. Congenital heart disease
Foetal PVR>SVR; blood
bypasses lungs through
ductus arteriosus and
foramen ovale
DA usually closes 24-36hrs
post birth – may be much
longer
FO closes when left atrium
volume increases
41. Congenital heart disease
• Failure of normal development or
• Persistence of foetal circulation
• 7-9% live births
• Acyanotic or Cyanotic heart disease
42. Acyanotic Heart Disease
VSD (25%)
ASD
PDA
PV stenosis
CoA
AS
Hypoplastic left heart
HOCM
Dextrocardia
Cyanotic Heart Disease
Tetralogy
Transposition
Tricuspid atresia
TAPVD
46. Innocent murmurs
• Common in children
• Never diastolic
• Soft, Short, midsystolic,
low intensity
• Localised
• Often vibratory or
musical
• Increase with output,
(fever)
• No thrill/ heave or
radiation
• Asymptomatic
• May resolve in few
months
• Commonest at lower left
sternal edge
• Venous hum
47. Evaluation
• Pre-natal (USS)
• Family history
• Birth history (birth state, trauma, risk infection)
• Is this cardiac? (murmur + cyanosis + absent pulses)
Pre- and post ductal oxygen saturations
ABG
4 limb BP (>10mmHg difference suggests coarctation)
ECG
CXR
Echo
48. ED management
• ABC – sats 75-85%
• Correct metabolic acidosis and shock with fluid and
bicarb
• 2 lines/ UVC if possible
• Antibiotics anyway!
• Gentle handling
• Keep warm
• Prostoglandin – ductal patency
• Inotropes
• Ventilate – in air if possible, PEEP 4-6cmH2O
49. Prostaglandin
• PGE2 infusion (dinoprostone)
• In duct dependent lesion
• Hyperoxia test suggestive, femoral pulses
diminished, metabolic acidosis persistent after
volume and inotropes
• Ensure antibiotics given!
• Beware of apnoea. May cause hypotension,
jitteriness and jerks
• No absolute contraindications
53. • 18 month old girl
6 days of high fever
Miserable
Swollen hands and feet with pain and redness
Immediate action?
Investigations?
Working diagnosis?
Further management?
55. Kawasaki Disease
• Commonest cause of acquired heart disease in
children in the UK
• Febrile, exanthematous, multi-system vasculitis in
children <5y
• Coronary arteritis with aneurysm formation in 20-
30% in untreated patients
56. Diagnosing Kawasaki disease
• Fever of 5 days plus any 4 physical exam findings:
Rash
Cervical lymphadenopathy (at least 1.5 cm in
diameter)
Bilateral conjunctival injection
Oral mucosal changes
Peripheral extremity changes
57. Kawasaki disease
• Admission as in-patient
• ECG, ECHO
• IV immunoglobulins
• Aspirin high dose
• Paediatric/Cardiology F/U (repeat ECHO at 6
weeks)