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Paediatric Cardiology
Dr Ratna Merugumalla
Consultant in Emergency Medicine
Peterborough City Hospital
Cardiovascular presentations
• Collapse
• The blue baby
• Syncope
• Palpitations
• Chest pain
The normal Heart Rate
THE ECG
ECG in a 2 year old
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.
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
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.
CHEST PAIN
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)
Non cardiac chest pain
• 56% musculoskeletal
• 12% asthma/ wheeze
• 8% infection
• 6% GI – gastritis and GORD
• 4% sickle cell disease
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
SYNCOPE
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
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
Sudden Cardiac Death
• Myocarditis
• HOCM
• Cyanotic / Acyanotic congenital heart disease
• Valvular heart disease
• Complete heart block
• WPW, long QT syndrome
• Marfan’s syndrome
• CAD
• Anomalous coronary arteries
PALPITATIONS
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
Heart rate
Age Bradycardia Tachycardia
< 1 y < 80 min-1 > 180 min-1
> 1 y < 60 min-1 > 160 min-1
Bradycardia
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
Bradycardia Treatment
• Oxygenation
• Adrenaline – 10mcg/kg
• Atropine - Consider when vagal stimulation e.g.
airway instrumentation – 20mcg/kg
• Pacing (rarely required)
Tachycardia
rdia
Narrow QRS complex Broad QRS complex
ST VT or SVT
SVT Treat as VT
Sinus Tachycardia
ST – Treat the cause
• Physiological response:
Crying
Exercise
Anxiety/fear
Pain
• Compensatory
mechanism for:
Respiratory failure
Hypovolaemia
Sepsis
Anaemia
Supraventricular tachycardia
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
ST or SVT
SVT - Management
• Valsalva manoeuvre
• IV Adenosine
100 mcg/kg
200 mcg/kg
maximum 1st dose 6mg, 2nd dose 12mg
• Amiodarone in refractory SVT
• DC cardioversion – for decompensated children
Ventricular Tachycardia
Ventricular Tachycardia Causes
• Congenital HD & surgery
• Poisoning (TCAs, Quinidine)
• Brugada syndrome / Long QT interval
• Renal Disease / Hyperkalaemia
VT - management
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
Atrial Flutter
Atrial Fibrillation
Atrial Flutter and Fibrillation
• Rare
• Underlying CHD, status post-open heart surgery
• Cardioversion in decompensated
• In haemodynamically stable children,
amiodarone or elective cardioversion
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
COLLAPSE
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
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
Congenital heart disease
• Failure of normal development or
• Persistence of foetal circulation
• 7-9% live births
• Acyanotic or Cyanotic heart disease
Acyanotic Heart Disease
VSD (25%)
ASD
PDA
PV stenosis
CoA
AS
Hypoplastic left heart
HOCM
Dextrocardia
Cyanotic Heart Disease
Tetralogy
Transposition
Tricuspid atresia
TAPVD
Congenital heart disease
Common presentations:
• Cyanosis
• Heart failure
• Heart murmur
Cyanosis
• Cyanosis – ~4-5g/dL of deoxygenated blood
• Cardiac cause – ‘comfortably blue’, worse with crying,
minimal improvement with O2
• Primary pulmonary disease; no R-L sats diff
• Primary cardiac; 5-10 % R-L sats diff
• Sepsis; no diff
Failure
• Sweating
• Poor feeding
• Hepatomegaly
• SOB
• Creps
• Tachycardia
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
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
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
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
Prostaglandin
Possible Adverse Effects
• Apnoea
• Hypotension
• Hyperthermia (transient)
• Tachycardia
• Bradycardia
• Seizures
• Diarrhoea
• Skin flush
Administration
• Intravenous infusion
• Consider intubation
• Dose
• 0.01 – 0.1 mcg/kg/min
Hyperoxia test
• 10 mins on 100% O2
PaO2 <20 KPa, cyanotic heart disease likely
Pao2 <27KPa but >20, equivocal
PaO2 >27 KPa, respiratory disease
Caution, severe pulmonary disease
Care duct dependent lesions
ACQUIRED HEART DISEASE
• 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?
Diagnosis?
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
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
Kawasaki disease
• Admission as in-patient
• ECG, ECHO
• IV immunoglobulins
• Aspirin high dose
• Paediatric/Cardiology F/U (repeat ECHO at 6
weeks)
Any Questions?

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paediatric_cardiology3.ppt

  • 1. Paediatric Cardiology Dr Ratna Merugumalla Consultant in Emergency Medicine Peterborough City Hospital
  • 2. Cardiovascular presentations • Collapse • The blue baby • Syncope • Palpitations • Chest pain
  • 5. ECG in a 2 year old
  • 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
  • 16. Sudden Cardiac Death • Myocarditis • HOCM • Cyanotic / Acyanotic congenital heart disease • Valvular heart disease • Complete heart block • WPW, long QT syndrome • Marfan’s syndrome • CAD • Anomalous coronary arteries
  • 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
  • 19. Heart rate Age Bradycardia Tachycardia < 1 y < 80 min-1 > 180 min-1 > 1 y < 60 min-1 > 160 min-1
  • 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
  • 22. Bradycardia Treatment • Oxygenation • Adrenaline – 10mcg/kg • Atropine - Consider when vagal stimulation e.g. airway instrumentation – 20mcg/kg • Pacing (rarely required)
  • 23. Tachycardia rdia Narrow QRS complex Broad QRS complex ST VT or SVT SVT Treat as VT
  • 25. ST – Treat the cause • Physiological response: Crying Exercise Anxiety/fear Pain • Compensatory mechanism for: Respiratory failure Hypovolaemia Sepsis Anaemia
  • 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
  • 29. SVT - Management • Valsalva manoeuvre • IV Adenosine 100 mcg/kg 200 mcg/kg maximum 1st dose 6mg, 2nd dose 12mg • Amiodarone in refractory SVT • DC cardioversion – for decompensated children
  • 31. Ventricular Tachycardia Causes • Congenital HD & surgery • Poisoning (TCAs, Quinidine) • Brugada syndrome / Long QT interval • Renal Disease / Hyperkalaemia
  • 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
  • 43. Congenital heart disease Common presentations: • Cyanosis • Heart failure • Heart murmur
  • 44. Cyanosis • Cyanosis – ~4-5g/dL of deoxygenated blood • Cardiac cause – ‘comfortably blue’, worse with crying, minimal improvement with O2 • Primary pulmonary disease; no R-L sats diff • Primary cardiac; 5-10 % R-L sats diff • Sepsis; no diff
  • 45. Failure • Sweating • Poor feeding • Hepatomegaly • SOB • Creps • Tachycardia
  • 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
  • 50. Prostaglandin Possible Adverse Effects • Apnoea • Hypotension • Hyperthermia (transient) • Tachycardia • Bradycardia • Seizures • Diarrhoea • Skin flush Administration • Intravenous infusion • Consider intubation • Dose • 0.01 – 0.1 mcg/kg/min
  • 51. Hyperoxia test • 10 mins on 100% O2 PaO2 <20 KPa, cyanotic heart disease likely Pao2 <27KPa but >20, equivocal PaO2 >27 KPa, respiratory disease Caution, severe pulmonary disease Care duct dependent lesions
  • 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)