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Welcome to case presentation
A 35-year male presented with
Cyanosis & Clubbing
Dr.Seebat Masrur
D-card student
SZMCH
PARTICULARS OF
THE PATIENT
• Name of the patient :Mr Sumon Reg. no.3049/05.
• Age :35-year Ward: 03
• Sex :Male Bed-CCU9
• Marital status :Married
• Religion : Islam
• Occupation : Shopkeeper
• Address : Dhunut, Bogura
• Date of admission : 15/10/2022
• Date of examination : 15/10/2022
Presenting complaints
Severe breathlessness for 3 days.
Bluish discoloration of lips, tongue, fingers &
toes on exertion since childhood.
History of Present Illness
According to the patient’s statement, he has been
suffering from breathlessness for 3 days. His
breathlessness was less marked in earlier age, only felt
during moderate to severe activity. But it has
progressively increased even during mild exertion. He is
comfortable at rest and on lying flat. He has no history of
awakening from sleep due to breathlessness. There is no
seasonal or diurnal variation of breathlessness or any
association with exposure to dust, pollen or fume.
Continued…
He has no history of cough, chest pain, fever or wheeze
or swelling in any part of the body.
His mother mentioned bluish discoloration of fingers,
nails, toes and lips since his childhood which was more
marked on exertion. It gradually progressed and became
more marked on mild exertion which partially relieved by
squatting. It was not associated with exposure to cold.
Continued…
On query he admitted to being fatigue during
competitive activities since childhood.
His mother also mentioned that he used to become
bluish and breathless while feeding or crying. She also
complained that his growth is less than other children of
same age.
He gave no history of dizziness, headache, loss of
consciousness, blurring of vision, weakness of any part of
the body.
History of past illness
He had been suffering from repeated cough, fever &
breathlessness since childhood.
He had a history of same type of attack during exertion
and playing games.
Patient is nondiabetic and normotensive.
Family history
• His father and mother are alive and healthy
• No family history of Hypertension, Diabetes mellitus,
heart disease, bronchial asthma.
Socioeconomic History
He belongs to a Lower socioeconomic family. He lives in a
tinshed house, drinks tubewell water and uses sanitary
latrine.
Treatment history
He frequently visited local village doctor for his illness.
He was treated with nebulization and other drugs which
he could not mention except for Tab Propranolol 10mg
twice daily with some relief.
He had no history of prior hospitalization.
Personal history
He is a nonsmoker, non-beetle nut chewer, nonalcoholic
and no history of drug abuse.
Immunization Hisotry
• He was Immunized as per EPI schedule.
• He took 2 doses of Covid vaccination.
General examination
• Appearance : Ill-looking
• Body built : Average
• Nutritional status : Below average
• Anemia : Absent
• Conjunctiva: Suffused
• Jaundice : Absent
• Cyanosis : Present
General examination
• Edema : Absent
• Dehydration : Absent
• Clubbing : Bilateral symmetrical both fingers & toes
• Koilonychia : Absent
• Leukonychia: Absent
• Lymphadenopathy: Absent
• Thyroid Gland: Not palpable
• Pulse : 76 beats/min
• Blood Pressure : 100/60mmHg(Sitting)
• Respiratory rate: 22 breaths / min
• Temperature : 980 F
• JVP : Not raised
SYSTEMIC EXAMINATION
Cardiovascular Examination
Pulse : 76 beats/min, regular, normal in volume and
character, condition of vessel wall normal, no radio-radial
and radio-femoral delay, all other peripheral pulses are
present and palpable.
Blood Pressure : 100/60mmHg(Sitting)
JVP : Not raised
PRECORDIUM
Inspection-No visible apical impulse
-No suprasternal or supraclavicular pulsation
-No other pulsation in precordium
-No scar mark
Palpation-
-Apex beat is located in left 5th intercostal space
just medial to midclavicular line, normal in character.
-No palpable P2
-No parasternal heave
-No thrill
Auscultation
• First heart sound is normally audible in all areas.
• Second heart sound is single.
• There is an ejection systolic murmur is pulmonary area
increasing intensity with breath hold in inspiration.
• Grading of murmur 3/6.
• Lung bases are clear.
Respiratory system examination:
• Trachea centrally placed.
• Apex as mentioned above.
• Vocal fremitus is normal and symmetrical in all over both lung
fields.
• Breath sound is vesicular and no added sound.
Abdominal Examination:
• Abdomen is normal size and shape.
• Umbilicus centrally placed ,inverted .
• Soft and non tender.
• No organomegaly . No ascites.
• Bowel sound present.
Other systemic examination-
Reveals no abnormalities.
Salient feature
Mr Sumon, 35-year old normotensive, nondiabetic,
nonsmoker male, hailing from Dhunut, Bogura got
admitted in Cardiology department on 15/10/2022 with
the complaints of severe breathlessness for last 3 days. In
early age, only felt during moderate to severe activity.
But it progressively increased, now it occurs with mild
exertion.
Salient feature
There was also cyanosis in his fingers, nails, toes, lips and
tongue since childhood, which was more marked during
exertion. He gave history of cyanotic spell during feeding,
crying and playing.
There is no history of fever, cough, palpitation, joint pain
or swelling, headache, dizziness, orthopnea, paroxysmal
nocturnal dyspnea, no swelling of any part of body or
weakness, no seasonal or diurnal variation of
breathlessness. Cyanosis was not associated with
exposure to cold.
Salient feature
On examination, the patient was ill-looking, nutritional
status was below average, cyanosed and clubbing
involving all fingers and toes. There was no anemia, but
conjunctiva was suffused. His pulse was 76 b/min,
regular, normal in volume and character, condition of
vessel wall normal, no radio-radial and radio-femoral
delay.
Salient feature
BP 100/60 mm hg, respiratory rate 22 breaths/min,
temperature is 980 F, JVP not raised.
Examination of precordium, there was no visible impulse
on the precordium, apex beat was located in left 5th
intercostal space just medial to midclavicular line, normal
in character & there was no thrill and no left parasternal
heave.
Salient feature
On auscultation first heart sound was normally audible in
all areas, second heart sound was single. There was an
ejection systolic murmur in pulmonary area increasing in
intensity with breath hold in inspiration. Grading of
murmur 3/6.Lung bases were clear.
Other systemic examination revealed no abnormalities.
PROVISIONAL
DIAGNOSIS
PROVISIONAL DIAGNOSIS
So, my provisional diagnosis is-
Cyanotic Congenital Heart Disease- most likely Tetralogy
of Fallot
Differential
diagnosis
Pulmonary Stenosis with
Atrial Septal Defect
Double Outlet Right Ventricle
with Pulmonary Stenosis
Ebstein anomaly
Eisenmenger syndrome
Investigations
COMPLETE BLOOD
COUNT
results Other investigation results
Hb% 24.1 gm/dl S. creatinine 0.95 mg/dl
ESR 2 mm in 1st hour S.sodium 142.00 mmol/l
WBC 9.7x 10^9 /L S.potassium 4.10 mmol/l
RBC 9.25x 10^9 /L chloride 105.00 mmol/l
Neutrophil 60% Serum uric acid 4.91mg/dl
Lymphocyte 16% S ferritin 1756 mg/dl
Monocyte 02%
Eosinophil 02%
HCT 75.93%
MCH 30PG
ECG • Right axis deviation
• Prominent R in V1
• Predominant S wave in V6
• Tall P in lead 1 & 2
Chest X ray
• Boot shaped heart
• Oligemic lung field
• Right sided aortic arch
Echocardiography
Echocardiography
Echocardiography
-Peri membranous VSD(12mm)
-Overriding of Aorta
-Right ventricular hypertrophy
-Pulmonary valvular stenosis
Final Diagnosis
Final diagnosis
Tetralogy of Fallot
Treatment Options
Medical
management
Surgical
management
Treatment on Admission
-Oxygen inhalation( 4-6L/min)
-Volume expansion with Inf Normal saline
-Tab. Propranolol 10mg 1+0+1
-Venesection Twice
Surgical Management
Palliative Surgery
• Classic BT shunt
• Modified BT shunt
• Waterstone shunt
• Potts shunts
• Glenn shunt
Total Correction
-VSD closure
-PS correction
-RVOT widening
Tetralogy of Fallot
Commonest form of cyanotic
Congenital heart disease
Components
• Large, perimembranous, nonrestrictive, Malaligned
VSD
• Pulmonary stenosis
• Overriding of Aorta
• Right ventricular hypertrophy
Primary component
• VSD
• PS
Secondary Component
• RVH
• Overriding of Aorta
Associated defects
• Right sided Aortic arch(25%)
• Persistent left superior venacava(25%)
• Abnormal origin of coronary arteries(5%)
• LAD originate from right coronary artery and over the
RVOT
• Complete Av canal defect
• MAPCA
• ASD Secundum
• PDA
Development
Due to unequal separation of conus cordis
Presentation of TOF
• Central Cyanosis with digital Clubbing
• Effort Intolerance
-Breathlessness is associated with squatting
-Increase with exertion
• Hypoxic attacks/Cyanotic spells
• Angina on Effort
Precipitating
Factors of
Cyanotic
Spell
• Infection
• Exertion-playing,feeding,crying
• Excitement
• Emotion
• Stress
• Drug-Digitalis
Regarding Cyanosis
• 1/3rd patient cyanosed at birth
• Many patient do not cyanose until 1 year
• Both cyanosis and clubbing increase gradually with age due
to increase severity of Pulmonary stenosis
• 3/4th are cyanosed over the age of 2
Why cyanosis develop after 6
month?
• Sympathetic nervous system develops after 6 month.
• TOF is associated with sympathetic overactivity.
Mechanism of effort intolerance
• Exertion causes increase demand of tissue for oxygen
• Exertion also associate with sympathetic overactivity
So, more infundibular stenosis occurs that lead to Right to left
shunt.
Deoxygenated blood goes to systemic circulation and
Anaerobic glycolysis occurs.
More production of metabolic acids that stimulates
respiratory center.
Hyperventilation occurs.
How squatting relieves Dyspnea
So, decreases the right to left shunt
Pressure in inferior venacava reduces the amount of acid
metabolites reaching the brain.
Compression of abdominal aorta and femoral artery
raising systemic vascular resistance.
How squatting relieves Dyspnea
General Examination
• Growth retardation
• Suffused conjunctiva
• Central cyanosis
• Bilateral symmetrical clubbing
• BP low
• JVP normal
• Pulse-normal(asymmetrical if BT shunt done)
Precordium examination
• Precordium usually silent or cardiac impulse is quiet
• No left parasternal lift
• No palpable P2
• No thrill
• 2nd heart sound is single
• Ejection systolic murmur
-in pulmonary area
-murmur disappears during cyanotic spell
Investigation
• For diagnosis
ECG
Chest x ray
Echocardiogram
Cardiac catheterization
• For treatment
CBC
PCV
Iron profile
S.uric acid
ABG
ECG findings
• RVH
• RAD
• RVH with strain(if RV pressure>systemic pressure)
• RA enlargement-p pulmonale(in adult TOF)
• LAD(if AV canal defect)
X ray findings
Boot shape heart
-combination of RVH lifting the Apex
-pulmonary bay is deep due to hypoplastic pulmonary
artery
Oligemic lung field
Echocardiogram
• PLAX view
VSD
Overriding of aorta
Aorto mitral continuity present
Aorto septal discontinuity
Dilated coronary sinus(PLSVC)
Echocardiogram
• PSAX view
VSD peri membranous(10” O clock)
• Apical 4c view
VSD type
VSD pressure gradient
• Suprasternal view
Right sided aortic arch
Cardiac Catheterization
• Trajectory
• Oximetry
• Pressure study
• Root Aortogram
• Ventriculography
Complication of TOF
• Cyanotic spell
• Cerebral abscess
• Cerebrovascular accident
• Subacute infective endocarditis
• Congestive Heart Failure
• Iron deficient anemia
• Hyperviscosity syndrome
• Gout
Management of TOF
General management
• Avoid dehydration
• Plenty of fluid intake to prevent hyperviscosity
• Treatment of infection
• Correction of anemia
• Prophylaxis of Infective Endocarditis
Management of Cyanotic spell
• Knee chest position
• Oxygen inhalation
• Morphine 1microgram per kg intravenously
• Propranolol 1 to 3 mg/kg IV
• Sodibicurb IV if acidosis
• Adequate hydration
• Convulsions/epileptic fits
IV phenytoin/phenobarbitone
Surgical Management
• Palliative surgery
• Definitive corrective surgery
Palliative indication
• Very small infant(<5kg) with recurrent spells
• Pulmonary artery anatomy unsuitable for corrective
surgery
• TOF with Pulmonary Atresia
• Unfavorable coronary artery anatomy
Palliative surgery option
• Classic BT shunt
• Modified BT shunt
• Waterstone shunt
• Potts shunts
• Glenn shunt
Cause of death
• Cyanotic spell
• Malignant Ventricular Arrhythmias
• Congestive Heart failure
• Cerebral abscess
• Infective endocarditis
Prognosis
Ref https://jamanetwork.com/journals/jamacardiology/fullarticle/2718499
Without surgery
• 33% die within 1 year
• 50% die by 4-5 years
• 75% die by 10 years
• 5% survive beyond 30 years
With Surgery(Complete repair)
• 1-year survival 98.6%
• 5-year survival 97.8%
• 10-year survival 97.1%
• 20-year survival 95.5%
• 25-year survival 94.5%
Take Home
message
• Tetralogy of Fallot is a common
cyanotic congenital heart
disease in childhood.
• Typical cyanotic spell, repeated
chest infections & clubbing
should be considered as
Tetralogy of Fallot.
• A simple Echocardiography can
confirm the diagnosis.
• A patient with Tetralogy of
Fallot can survive like a normal
person after corrective surgery.
Tetralogy of Fallot.pptx

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Tetralogy of Fallot.pptx

  • 1. Welcome to case presentation A 35-year male presented with Cyanosis & Clubbing Dr.Seebat Masrur D-card student SZMCH
  • 2. PARTICULARS OF THE PATIENT • Name of the patient :Mr Sumon Reg. no.3049/05. • Age :35-year Ward: 03 • Sex :Male Bed-CCU9 • Marital status :Married • Religion : Islam • Occupation : Shopkeeper • Address : Dhunut, Bogura • Date of admission : 15/10/2022 • Date of examination : 15/10/2022
  • 3. Presenting complaints Severe breathlessness for 3 days. Bluish discoloration of lips, tongue, fingers & toes on exertion since childhood.
  • 4. History of Present Illness According to the patient’s statement, he has been suffering from breathlessness for 3 days. His breathlessness was less marked in earlier age, only felt during moderate to severe activity. But it has progressively increased even during mild exertion. He is comfortable at rest and on lying flat. He has no history of awakening from sleep due to breathlessness. There is no seasonal or diurnal variation of breathlessness or any association with exposure to dust, pollen or fume.
  • 5. Continued… He has no history of cough, chest pain, fever or wheeze or swelling in any part of the body. His mother mentioned bluish discoloration of fingers, nails, toes and lips since his childhood which was more marked on exertion. It gradually progressed and became more marked on mild exertion which partially relieved by squatting. It was not associated with exposure to cold.
  • 6. Continued… On query he admitted to being fatigue during competitive activities since childhood. His mother also mentioned that he used to become bluish and breathless while feeding or crying. She also complained that his growth is less than other children of same age. He gave no history of dizziness, headache, loss of consciousness, blurring of vision, weakness of any part of the body.
  • 7. History of past illness He had been suffering from repeated cough, fever & breathlessness since childhood. He had a history of same type of attack during exertion and playing games. Patient is nondiabetic and normotensive.
  • 8. Family history • His father and mother are alive and healthy • No family history of Hypertension, Diabetes mellitus, heart disease, bronchial asthma.
  • 9. Socioeconomic History He belongs to a Lower socioeconomic family. He lives in a tinshed house, drinks tubewell water and uses sanitary latrine.
  • 10. Treatment history He frequently visited local village doctor for his illness. He was treated with nebulization and other drugs which he could not mention except for Tab Propranolol 10mg twice daily with some relief. He had no history of prior hospitalization.
  • 11. Personal history He is a nonsmoker, non-beetle nut chewer, nonalcoholic and no history of drug abuse.
  • 12. Immunization Hisotry • He was Immunized as per EPI schedule. • He took 2 doses of Covid vaccination.
  • 13. General examination • Appearance : Ill-looking • Body built : Average • Nutritional status : Below average • Anemia : Absent • Conjunctiva: Suffused • Jaundice : Absent • Cyanosis : Present
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  • 16. General examination • Edema : Absent • Dehydration : Absent • Clubbing : Bilateral symmetrical both fingers & toes • Koilonychia : Absent • Leukonychia: Absent • Lymphadenopathy: Absent • Thyroid Gland: Not palpable
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  • 19. • Pulse : 76 beats/min • Blood Pressure : 100/60mmHg(Sitting) • Respiratory rate: 22 breaths / min • Temperature : 980 F • JVP : Not raised
  • 21. Cardiovascular Examination Pulse : 76 beats/min, regular, normal in volume and character, condition of vessel wall normal, no radio-radial and radio-femoral delay, all other peripheral pulses are present and palpable. Blood Pressure : 100/60mmHg(Sitting) JVP : Not raised
  • 22. PRECORDIUM Inspection-No visible apical impulse -No suprasternal or supraclavicular pulsation -No other pulsation in precordium -No scar mark Palpation- -Apex beat is located in left 5th intercostal space just medial to midclavicular line, normal in character. -No palpable P2 -No parasternal heave -No thrill
  • 23. Auscultation • First heart sound is normally audible in all areas. • Second heart sound is single. • There is an ejection systolic murmur is pulmonary area increasing intensity with breath hold in inspiration. • Grading of murmur 3/6. • Lung bases are clear.
  • 24. Respiratory system examination: • Trachea centrally placed. • Apex as mentioned above. • Vocal fremitus is normal and symmetrical in all over both lung fields. • Breath sound is vesicular and no added sound.
  • 25. Abdominal Examination: • Abdomen is normal size and shape. • Umbilicus centrally placed ,inverted . • Soft and non tender. • No organomegaly . No ascites. • Bowel sound present. Other systemic examination- Reveals no abnormalities.
  • 26. Salient feature Mr Sumon, 35-year old normotensive, nondiabetic, nonsmoker male, hailing from Dhunut, Bogura got admitted in Cardiology department on 15/10/2022 with the complaints of severe breathlessness for last 3 days. In early age, only felt during moderate to severe activity. But it progressively increased, now it occurs with mild exertion.
  • 27. Salient feature There was also cyanosis in his fingers, nails, toes, lips and tongue since childhood, which was more marked during exertion. He gave history of cyanotic spell during feeding, crying and playing. There is no history of fever, cough, palpitation, joint pain or swelling, headache, dizziness, orthopnea, paroxysmal nocturnal dyspnea, no swelling of any part of body or weakness, no seasonal or diurnal variation of breathlessness. Cyanosis was not associated with exposure to cold.
  • 28. Salient feature On examination, the patient was ill-looking, nutritional status was below average, cyanosed and clubbing involving all fingers and toes. There was no anemia, but conjunctiva was suffused. His pulse was 76 b/min, regular, normal in volume and character, condition of vessel wall normal, no radio-radial and radio-femoral delay.
  • 29. Salient feature BP 100/60 mm hg, respiratory rate 22 breaths/min, temperature is 980 F, JVP not raised. Examination of precordium, there was no visible impulse on the precordium, apex beat was located in left 5th intercostal space just medial to midclavicular line, normal in character & there was no thrill and no left parasternal heave.
  • 30. Salient feature On auscultation first heart sound was normally audible in all areas, second heart sound was single. There was an ejection systolic murmur in pulmonary area increasing in intensity with breath hold in inspiration. Grading of murmur 3/6.Lung bases were clear. Other systemic examination revealed no abnormalities.
  • 32. PROVISIONAL DIAGNOSIS So, my provisional diagnosis is- Cyanotic Congenital Heart Disease- most likely Tetralogy of Fallot
  • 33. Differential diagnosis Pulmonary Stenosis with Atrial Septal Defect Double Outlet Right Ventricle with Pulmonary Stenosis Ebstein anomaly Eisenmenger syndrome
  • 34. Investigations COMPLETE BLOOD COUNT results Other investigation results Hb% 24.1 gm/dl S. creatinine 0.95 mg/dl ESR 2 mm in 1st hour S.sodium 142.00 mmol/l WBC 9.7x 10^9 /L S.potassium 4.10 mmol/l RBC 9.25x 10^9 /L chloride 105.00 mmol/l Neutrophil 60% Serum uric acid 4.91mg/dl Lymphocyte 16% S ferritin 1756 mg/dl Monocyte 02% Eosinophil 02% HCT 75.93% MCH 30PG
  • 35. ECG • Right axis deviation • Prominent R in V1 • Predominant S wave in V6 • Tall P in lead 1 & 2
  • 36. Chest X ray • Boot shaped heart • Oligemic lung field • Right sided aortic arch
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  • 42. Echocardiography -Peri membranous VSD(12mm) -Overriding of Aorta -Right ventricular hypertrophy -Pulmonary valvular stenosis
  • 46. Treatment on Admission -Oxygen inhalation( 4-6L/min) -Volume expansion with Inf Normal saline -Tab. Propranolol 10mg 1+0+1 -Venesection Twice
  • 47. Surgical Management Palliative Surgery • Classic BT shunt • Modified BT shunt • Waterstone shunt • Potts shunts • Glenn shunt Total Correction -VSD closure -PS correction -RVOT widening
  • 48. Tetralogy of Fallot Commonest form of cyanotic Congenital heart disease
  • 49. Components • Large, perimembranous, nonrestrictive, Malaligned VSD • Pulmonary stenosis • Overriding of Aorta • Right ventricular hypertrophy
  • 50. Primary component • VSD • PS Secondary Component • RVH • Overriding of Aorta
  • 51. Associated defects • Right sided Aortic arch(25%) • Persistent left superior venacava(25%) • Abnormal origin of coronary arteries(5%) • LAD originate from right coronary artery and over the RVOT • Complete Av canal defect • MAPCA • ASD Secundum • PDA
  • 52. Development Due to unequal separation of conus cordis
  • 53. Presentation of TOF • Central Cyanosis with digital Clubbing • Effort Intolerance -Breathlessness is associated with squatting -Increase with exertion • Hypoxic attacks/Cyanotic spells • Angina on Effort
  • 54. Precipitating Factors of Cyanotic Spell • Infection • Exertion-playing,feeding,crying • Excitement • Emotion • Stress • Drug-Digitalis
  • 55. Regarding Cyanosis • 1/3rd patient cyanosed at birth • Many patient do not cyanose until 1 year • Both cyanosis and clubbing increase gradually with age due to increase severity of Pulmonary stenosis • 3/4th are cyanosed over the age of 2
  • 56. Why cyanosis develop after 6 month? • Sympathetic nervous system develops after 6 month. • TOF is associated with sympathetic overactivity.
  • 57. Mechanism of effort intolerance • Exertion causes increase demand of tissue for oxygen • Exertion also associate with sympathetic overactivity So, more infundibular stenosis occurs that lead to Right to left shunt. Deoxygenated blood goes to systemic circulation and Anaerobic glycolysis occurs. More production of metabolic acids that stimulates respiratory center. Hyperventilation occurs.
  • 58. How squatting relieves Dyspnea So, decreases the right to left shunt Pressure in inferior venacava reduces the amount of acid metabolites reaching the brain. Compression of abdominal aorta and femoral artery raising systemic vascular resistance.
  • 60. General Examination • Growth retardation • Suffused conjunctiva • Central cyanosis • Bilateral symmetrical clubbing • BP low • JVP normal • Pulse-normal(asymmetrical if BT shunt done)
  • 61. Precordium examination • Precordium usually silent or cardiac impulse is quiet • No left parasternal lift • No palpable P2 • No thrill • 2nd heart sound is single • Ejection systolic murmur -in pulmonary area -murmur disappears during cyanotic spell
  • 62. Investigation • For diagnosis ECG Chest x ray Echocardiogram Cardiac catheterization • For treatment CBC PCV Iron profile S.uric acid ABG
  • 63. ECG findings • RVH • RAD • RVH with strain(if RV pressure>systemic pressure) • RA enlargement-p pulmonale(in adult TOF) • LAD(if AV canal defect)
  • 64. X ray findings Boot shape heart -combination of RVH lifting the Apex -pulmonary bay is deep due to hypoplastic pulmonary artery Oligemic lung field
  • 65. Echocardiogram • PLAX view VSD Overriding of aorta Aorto mitral continuity present Aorto septal discontinuity Dilated coronary sinus(PLSVC)
  • 66. Echocardiogram • PSAX view VSD peri membranous(10” O clock) • Apical 4c view VSD type VSD pressure gradient • Suprasternal view Right sided aortic arch
  • 67. Cardiac Catheterization • Trajectory • Oximetry • Pressure study • Root Aortogram • Ventriculography
  • 68. Complication of TOF • Cyanotic spell • Cerebral abscess • Cerebrovascular accident • Subacute infective endocarditis • Congestive Heart Failure • Iron deficient anemia • Hyperviscosity syndrome • Gout
  • 70. General management • Avoid dehydration • Plenty of fluid intake to prevent hyperviscosity • Treatment of infection • Correction of anemia • Prophylaxis of Infective Endocarditis
  • 71. Management of Cyanotic spell • Knee chest position • Oxygen inhalation • Morphine 1microgram per kg intravenously • Propranolol 1 to 3 mg/kg IV • Sodibicurb IV if acidosis • Adequate hydration • Convulsions/epileptic fits IV phenytoin/phenobarbitone
  • 72. Surgical Management • Palliative surgery • Definitive corrective surgery
  • 73. Palliative indication • Very small infant(<5kg) with recurrent spells • Pulmonary artery anatomy unsuitable for corrective surgery • TOF with Pulmonary Atresia • Unfavorable coronary artery anatomy
  • 74. Palliative surgery option • Classic BT shunt • Modified BT shunt • Waterstone shunt • Potts shunts • Glenn shunt
  • 75. Cause of death • Cyanotic spell • Malignant Ventricular Arrhythmias • Congestive Heart failure • Cerebral abscess • Infective endocarditis
  • 76. Prognosis Ref https://jamanetwork.com/journals/jamacardiology/fullarticle/2718499 Without surgery • 33% die within 1 year • 50% die by 4-5 years • 75% die by 10 years • 5% survive beyond 30 years With Surgery(Complete repair) • 1-year survival 98.6% • 5-year survival 97.8% • 10-year survival 97.1% • 20-year survival 95.5% • 25-year survival 94.5%
  • 77. Take Home message • Tetralogy of Fallot is a common cyanotic congenital heart disease in childhood. • Typical cyanotic spell, repeated chest infections & clubbing should be considered as Tetralogy of Fallot. • A simple Echocardiography can confirm the diagnosis. • A patient with Tetralogy of Fallot can survive like a normal person after corrective surgery.