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CONGENITAL HEART DISEASES
P.THIRUNAGALINGA PANDIYAN
M.Sc.,(Child Health Nursing)
Madurai Medical College
Madurai
CONGENITAL HEART DEFECT (CHD)
Definition
A congenital heart defect (CHD) is defined
as a defect in the structure of the heart and
great vessels which is present at birth.
CAUSES
Genetics
• Genetic changes, either focal mutations or deletion or
addition of segments of DNA
Environmental
Known antenatal environmental factors include maternal
infections (Rubella), drugs (alcohol, hydantoin, lithium and
thalidomide) and maternal illness (diabetes mellitus,
phenylketonuria, and systemic lupus erythematosus).
Maternal obesity
CLASSIFICATION OF CONGENITAL HEART DISEASES
• Cyanotic heart disease, is a condition that
deoxygenated blood moves from the right side of
the heart to the left side through abnormal
openings or defects.
CLASSIFICATION OF CONGENITAL HEART DISEASES
Acyanotic heart disease is a condition that
oxygenated blood moves from the left side
of the heart to the right side and then to the
lungs.
CLASSIFICATION OF CONGENITAL HEART DISEASES
ACYANOTIC HEART DISEASE
• Blood is shunted (flows) from the left side of the heart to
the right side of the heart
• Child retain normal levels of oxyhemoglobin saturation
in systemic circulation.
CommonAcyanotic heart diseases are
• Atrial septal defect, or ASD
• Ventricular septal defect, orVSD
• Patent ductus arteriosus
• Co arctation of the aorta
• Aortic valve stenosis
• Pulmonary valve stenosis
ATRIAL SEPTAL DEFECT
• Atrial septal defect (ASD) is a form of congenital heart
defect that enables blood flow between the left and right
atria via the interatrial septum.
• The interatrial septum is the tissue that divides the right
and left atrium.
ATRIAL SEPTAL DEFECT
Types of Atrial Septal Defects
1.Ostium Secundum – defect located in the center of the
atrial septum (most common type)
2.Ostium Primum – defect located near the lower portion
of the atrial septum, may be associated with defects in
the mitral and tricuspid valve (second most common
type)
3.SinusVenosus – defect located near the top of the atrial
septum and frequently associated with abnormal
connection of the right pulmonary vein(s) to the right
atrium instead to the left atrium (least common type)
ASD TYPES
Clinical manifestations of ASD
• Asymptomatic
• Systolic murmur with fixed split second heart
sound
• May also be a diastolic murmur
• Risk for developing dysrhythmias
DIAGNOSIS OF ASD
• Ultrasonography
• Auscultation:
• Echocardiography
• Transesophageal Doppler (TCD) Bubble study
• Electrocardiogram
TREATMENT FOR ASD
• Surgical Patch Closure-open repair
• PercutaneousASD closure is currently only indicated for
the closure of secundumASD
VENTRICULAR SEPTAL DEFECT
• A ventricular septal defect (VSD) is a defect in the
ventricular septum, the wall dividing the left and right
ventricles of the heart.
VSD
Signs and symptoms of VSD
• Pansystolic (Holosystolic) murmur
• Fail to thrive
• Sweaty
• Tachypnoeic (breathe faster) .
TREATMENT
MedicalTreatment
• Cardiac glycosides (e.g., Digoxin 10-20mcg/kg per day)
• Loop diuretics (e.g., Furosemide 1–3 mg/kg per day)
• ACE inhibitors (e.g., Captopril 0.5–2 mg/kg per day).
SurgicalTreatment forVSD
• Surgical treatment: -Surgical patch closure.
PATENT DUCTUS ARTERIOSUS
• Patent ductus arteriosus (PDA) is a congenital
disorder in the heart wherein a neonate's ductus
arteriosus(connection between Pulmonary artery
and Descending aorta ) fails to close after birth.
PDA
Signs and symptoms of PDA
• Tachycardia
• Respiratory problems
• Dyspnea - shortness of breath
• Continuous machine-like heart murmur
• Cardiomegaly - enlarged heart
• Left subclavicular thrill
• Bounding pulse
Diagnosis of PDA
• Echocardiography
• Electrocardiography (ECG)
• A chest X-ray
Treatment of PDA
• Medical treatment: Indomethacin 0.1 to 0.25 mg /kg
• Surgical treatment:
Surgical division or ligation of the patent vessel is
performed.
COARCTATION OFTHE AORTA
• Coarctation of the aorta is a congenital condition
whereby the aorta narrows in the area where the
ductus arteriosus
• This results in increased pressure proximal to the
defect and decreased pressure distal to the
obstruction.
COARCTATION OFTHE AORTA
Signs and symptoms of
Coarctation of aorta
• Difficulty breathing,
• Poor appetite
• Trouble feeding,
• Failure to thrive.
• Dizziness or shortness of breath,
• Faint or near-fainting episodes
• Chest pain,
• Fatigue,
• Headaches, or nosebleeds
Imaging and diagnosis
• A classic 'figure E sign' on x-ray
• Magnetic resonanceAngiography.
• Echocardiograms
• MR, CT
• Angiography
Treatment
Surgical treatment:
• Surgical repair is by resection of the coarcted portion with
an end-to-end anastomosis of the aorta
• Enlargement of the constricted section using a graft of
prosthetic material or a portion of the lift subclavian
artery.
Non surgical treatment:
• Baloon angioplasty
AORTICVALVE STENOSIS
•Aortic valve stenosis (AS) is a disease of the
heart valves in which the opening of the
aortic valve is narrowed.
Signs and symptoms
• Mild to moderate aortic stenosis do not have symptoms.
• Shortness of breath on exertion
• Syncope
• Chest Pain
Diagnosis
• Electrocardiogram
• Heart catheterization
• Echocardiogram.
• Chest X-ray
Management
Aortic valve replacement
Percutaneous (Transcatheter)AorticValve Replacement
Balloon valvuloplasty
PULMONIC STENOSIS
• Pulmonic stenosis is a condition of narrowing of
Pulmonary valve
PULMONIC STENOSIS
Symptoms
• Jugular vein distension
• Cyanosis
• Right ventricular hypertrophy
• Sudden fainting.
• An enlarged liver (hepatomegaly)
• Swelling in the legs (edema)
Treatment
• Valve replacement
• BalloonValvuloplasty
CYANOTIC HEART DISEASE
• Tetralogy of Fallot
• Transposition of the great vessels
• Tricuspid atresia
• Hypoplastic left heart syndrome
TETRALOGY OF FALLOT
• Tetralogy of Fallot (TOF) is a congenital heart defect
which has four anatomical abnormalities
Four defects are
• Pulmonary Stenosis
• Overriding aorta
• Ventricular Septal Defect (VSD)
• Right ventricular hypertrophy
TETRALOGY OF FALLOT
Signs and symptoms
• Low blood oxygen saturation causes cyanosis
• Heart murmur
• Difficulty in feeding,
• Failure to gain weight,
• Retarded growth and physical development,
• Dyspnea on exertion,
• Clubbing of the fingers and toes, and Polycythemia.
Diagnosis
•Chest X ray-The abnormal " (Boot-like)
appearance of a heart
•Echocardiogram
Management
• There are also simple procedures such as Squatting and
the Knee Chest Position
Management
• Beta-blockers such as propranolol,
• Morphine to reduce ventilatory drive
• Vasopressor such as epinephrine, phenylephrine, or
norepinephrine to increase blood pressure.
• Oxygen (100%)
Surgical procedures
Palliative surgery
• Blalock-Thomas-Taussig shunts
• The Potts shunt and the Waterston-Cooley shunt
Total surgical repair
TRANSPOSITION OFTHE GREATVESSEL
• The aorta is present at Right ventricle ( usually Left
Ventrilcle) and Pulmonary artery is present at Left
ventricle ( usually rightVentrilcle)
• The condition is also called dextro-transposition of the
great arteries.
TRANSPOSITION OFTHE GREATVESSEL
TRANSPOSITION OFTHE GREATVESSEL
Clinical manifestations
• Cyanotic
• Growth failure
• Abnormal Heart sounds
• Cardiomegaly
TRANSPOSITION OFTHE GREATVESSEL
Management :
Prostaglandin E1, digoxin,Lasix
Surgical treatment
• An Arterial switch procedure.
• Intra Artial baffle repairs, Rastelli procedure also
performed.
TRICUSPID ATRESIA
• Tricuspid atresia is a form of congenital heart disease
whereby there is a complete narrowing of the tricuspid
valve.
TRICUSPID ATRESIA
Clinical manifestations
• Progressive cyanosis
• Poor feeding
• Tachypnea over the first 2 weeks of life
• Holosystolic murmur due to theVSD
• Left ventricular hypertrophy
Treatment
• Prostoglandins to maintain Patent Ductus Arteriosus
• Modified Blalock-Taussig shunt to maintain pulmonary
blood flow
• Cavopulmonary anastomosis to provide stable pulmonary
flow
• Fontan procedure to redirect inferior vena cava and
hepatic vein flow into the pulmonary circulation
HYPOPLASTIC LEFT HEART SYNDROME
• Hypoplastic left heart syndrome (HLHS) is a birth defect
that affects normal blood flow through the heart.
• The left side of the heart does not form correctly.
HYPOPLASTIC LEFT HEART SYNDROME
Signs and symptoms
• Cyanosis
• Heart failure
• Decreased cardiac output
Treatment
• Multiple stage approach surgery - Norwood procedure
Anastamosis of the main pulmonary artery to the aorta
• Heart transplantation
Nursing Interventions
A. Provide adequate nutritional and fluid intake to maintain the
growth and developmental needs of the child
• Feed in semi-erect position
• Provide small frequent feedings
• Provide foods with high nutritional value
• Determine child’s likes and dislikes
• Strict input and output
• Daily weight
Nursing Interventions
B. Prevent infection
• Prevent exposure to communicable diseases
• Immunizations should be up-to-date
• Handwashing should be observed
• Be certain that the child receives prophylactic medication
for infective endocarditis
Nursing Interventions
• Reduce the workload of the heart since decreased activity
and expenditure of energy will decrease oxygen
requirements
• Adequate rest
• Avoid unnecessary activities
• Prevent excessive crying
• Provide diversional activities
• Relieve the respiratory distress associated with increased
pulmonary blood flow or oxygen deprivation
NURSING MANAGEMENT OFTHE CHILDWITH A
CONGENITAL HEART DEFECT
Nursing Diagnoses
• Impaired gas exchange related to altered pulmonary
blood flow or oxygen deprivation
• Altered cardiac output related to specific anatomic defect
• Activity intolerance related to decreased oxygenation in
blood and tissues
• Altered Nutrition: less than body requirements related to
the excessive energy demands required by increased
cardiac workload
NURSING MANAGEMENT OFTHE CHILD WITH A
CONGENITAL HEART DEFECT
• Increased potential for infection related to poor
nutritional status
• Anxiety related to diagnostic procedures and
hospitalization
• Developmental delay related to decreased energy,
inadequate nutrition, physical limitations and social
isolation
• Alteration in parenting related to parental perception of
the child as vulnerable
CONGENITAL HEART DISEASES   PPT

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CONGENITAL HEART DISEASES PPT

  • 1. CONGENITAL HEART DISEASES P.THIRUNAGALINGA PANDIYAN M.Sc.,(Child Health Nursing) Madurai Medical College Madurai
  • 2. CONGENITAL HEART DEFECT (CHD) Definition A congenital heart defect (CHD) is defined as a defect in the structure of the heart and great vessels which is present at birth.
  • 3. CAUSES Genetics • Genetic changes, either focal mutations or deletion or addition of segments of DNA Environmental Known antenatal environmental factors include maternal infections (Rubella), drugs (alcohol, hydantoin, lithium and thalidomide) and maternal illness (diabetes mellitus, phenylketonuria, and systemic lupus erythematosus). Maternal obesity
  • 4. CLASSIFICATION OF CONGENITAL HEART DISEASES • Cyanotic heart disease, is a condition that deoxygenated blood moves from the right side of the heart to the left side through abnormal openings or defects.
  • 5. CLASSIFICATION OF CONGENITAL HEART DISEASES Acyanotic heart disease is a condition that oxygenated blood moves from the left side of the heart to the right side and then to the lungs.
  • 7. ACYANOTIC HEART DISEASE • Blood is shunted (flows) from the left side of the heart to the right side of the heart • Child retain normal levels of oxyhemoglobin saturation in systemic circulation. CommonAcyanotic heart diseases are • Atrial septal defect, or ASD • Ventricular septal defect, orVSD • Patent ductus arteriosus • Co arctation of the aorta • Aortic valve stenosis • Pulmonary valve stenosis
  • 8. ATRIAL SEPTAL DEFECT • Atrial septal defect (ASD) is a form of congenital heart defect that enables blood flow between the left and right atria via the interatrial septum. • The interatrial septum is the tissue that divides the right and left atrium.
  • 10. Types of Atrial Septal Defects 1.Ostium Secundum – defect located in the center of the atrial septum (most common type) 2.Ostium Primum – defect located near the lower portion of the atrial septum, may be associated with defects in the mitral and tricuspid valve (second most common type) 3.SinusVenosus – defect located near the top of the atrial septum and frequently associated with abnormal connection of the right pulmonary vein(s) to the right atrium instead to the left atrium (least common type)
  • 12. Clinical manifestations of ASD • Asymptomatic • Systolic murmur with fixed split second heart sound • May also be a diastolic murmur • Risk for developing dysrhythmias
  • 13. DIAGNOSIS OF ASD • Ultrasonography • Auscultation: • Echocardiography • Transesophageal Doppler (TCD) Bubble study • Electrocardiogram
  • 14. TREATMENT FOR ASD • Surgical Patch Closure-open repair • PercutaneousASD closure is currently only indicated for the closure of secundumASD
  • 15. VENTRICULAR SEPTAL DEFECT • A ventricular septal defect (VSD) is a defect in the ventricular septum, the wall dividing the left and right ventricles of the heart.
  • 16. VSD
  • 17. Signs and symptoms of VSD • Pansystolic (Holosystolic) murmur • Fail to thrive • Sweaty • Tachypnoeic (breathe faster) .
  • 18. TREATMENT MedicalTreatment • Cardiac glycosides (e.g., Digoxin 10-20mcg/kg per day) • Loop diuretics (e.g., Furosemide 1–3 mg/kg per day) • ACE inhibitors (e.g., Captopril 0.5–2 mg/kg per day).
  • 19. SurgicalTreatment forVSD • Surgical treatment: -Surgical patch closure.
  • 20. PATENT DUCTUS ARTERIOSUS • Patent ductus arteriosus (PDA) is a congenital disorder in the heart wherein a neonate's ductus arteriosus(connection between Pulmonary artery and Descending aorta ) fails to close after birth.
  • 21. PDA
  • 22. Signs and symptoms of PDA • Tachycardia • Respiratory problems • Dyspnea - shortness of breath • Continuous machine-like heart murmur • Cardiomegaly - enlarged heart • Left subclavicular thrill • Bounding pulse
  • 23. Diagnosis of PDA • Echocardiography • Electrocardiography (ECG) • A chest X-ray
  • 24. Treatment of PDA • Medical treatment: Indomethacin 0.1 to 0.25 mg /kg • Surgical treatment: Surgical division or ligation of the patent vessel is performed.
  • 25. COARCTATION OFTHE AORTA • Coarctation of the aorta is a congenital condition whereby the aorta narrows in the area where the ductus arteriosus • This results in increased pressure proximal to the defect and decreased pressure distal to the obstruction.
  • 27. Signs and symptoms of Coarctation of aorta • Difficulty breathing, • Poor appetite • Trouble feeding, • Failure to thrive. • Dizziness or shortness of breath, • Faint or near-fainting episodes • Chest pain, • Fatigue, • Headaches, or nosebleeds
  • 28. Imaging and diagnosis • A classic 'figure E sign' on x-ray • Magnetic resonanceAngiography. • Echocardiograms • MR, CT • Angiography
  • 29. Treatment Surgical treatment: • Surgical repair is by resection of the coarcted portion with an end-to-end anastomosis of the aorta • Enlargement of the constricted section using a graft of prosthetic material or a portion of the lift subclavian artery. Non surgical treatment: • Baloon angioplasty
  • 30. AORTICVALVE STENOSIS •Aortic valve stenosis (AS) is a disease of the heart valves in which the opening of the aortic valve is narrowed.
  • 31. Signs and symptoms • Mild to moderate aortic stenosis do not have symptoms. • Shortness of breath on exertion • Syncope • Chest Pain
  • 32. Diagnosis • Electrocardiogram • Heart catheterization • Echocardiogram. • Chest X-ray
  • 33. Management Aortic valve replacement Percutaneous (Transcatheter)AorticValve Replacement Balloon valvuloplasty
  • 34. PULMONIC STENOSIS • Pulmonic stenosis is a condition of narrowing of Pulmonary valve
  • 36. Symptoms • Jugular vein distension • Cyanosis • Right ventricular hypertrophy • Sudden fainting. • An enlarged liver (hepatomegaly) • Swelling in the legs (edema)
  • 37. Treatment • Valve replacement • BalloonValvuloplasty
  • 38. CYANOTIC HEART DISEASE • Tetralogy of Fallot • Transposition of the great vessels • Tricuspid atresia • Hypoplastic left heart syndrome
  • 39. TETRALOGY OF FALLOT • Tetralogy of Fallot (TOF) is a congenital heart defect which has four anatomical abnormalities Four defects are • Pulmonary Stenosis • Overriding aorta • Ventricular Septal Defect (VSD) • Right ventricular hypertrophy
  • 41. Signs and symptoms • Low blood oxygen saturation causes cyanosis • Heart murmur • Difficulty in feeding, • Failure to gain weight, • Retarded growth and physical development, • Dyspnea on exertion, • Clubbing of the fingers and toes, and Polycythemia.
  • 42. Diagnosis •Chest X ray-The abnormal " (Boot-like) appearance of a heart •Echocardiogram
  • 43. Management • There are also simple procedures such as Squatting and the Knee Chest Position
  • 44. Management • Beta-blockers such as propranolol, • Morphine to reduce ventilatory drive • Vasopressor such as epinephrine, phenylephrine, or norepinephrine to increase blood pressure. • Oxygen (100%)
  • 45. Surgical procedures Palliative surgery • Blalock-Thomas-Taussig shunts • The Potts shunt and the Waterston-Cooley shunt Total surgical repair
  • 46. TRANSPOSITION OFTHE GREATVESSEL • The aorta is present at Right ventricle ( usually Left Ventrilcle) and Pulmonary artery is present at Left ventricle ( usually rightVentrilcle) • The condition is also called dextro-transposition of the great arteries.
  • 48. TRANSPOSITION OFTHE GREATVESSEL Clinical manifestations • Cyanotic • Growth failure • Abnormal Heart sounds • Cardiomegaly
  • 49. TRANSPOSITION OFTHE GREATVESSEL Management : Prostaglandin E1, digoxin,Lasix Surgical treatment • An Arterial switch procedure. • Intra Artial baffle repairs, Rastelli procedure also performed.
  • 50. TRICUSPID ATRESIA • Tricuspid atresia is a form of congenital heart disease whereby there is a complete narrowing of the tricuspid valve.
  • 52. Clinical manifestations • Progressive cyanosis • Poor feeding • Tachypnea over the first 2 weeks of life • Holosystolic murmur due to theVSD • Left ventricular hypertrophy
  • 53. Treatment • Prostoglandins to maintain Patent Ductus Arteriosus • Modified Blalock-Taussig shunt to maintain pulmonary blood flow • Cavopulmonary anastomosis to provide stable pulmonary flow • Fontan procedure to redirect inferior vena cava and hepatic vein flow into the pulmonary circulation
  • 54. HYPOPLASTIC LEFT HEART SYNDROME • Hypoplastic left heart syndrome (HLHS) is a birth defect that affects normal blood flow through the heart. • The left side of the heart does not form correctly.
  • 56. Signs and symptoms • Cyanosis • Heart failure • Decreased cardiac output
  • 57. Treatment • Multiple stage approach surgery - Norwood procedure Anastamosis of the main pulmonary artery to the aorta • Heart transplantation
  • 58. Nursing Interventions A. Provide adequate nutritional and fluid intake to maintain the growth and developmental needs of the child • Feed in semi-erect position • Provide small frequent feedings • Provide foods with high nutritional value • Determine child’s likes and dislikes • Strict input and output • Daily weight
  • 59. Nursing Interventions B. Prevent infection • Prevent exposure to communicable diseases • Immunizations should be up-to-date • Handwashing should be observed • Be certain that the child receives prophylactic medication for infective endocarditis
  • 60. Nursing Interventions • Reduce the workload of the heart since decreased activity and expenditure of energy will decrease oxygen requirements • Adequate rest • Avoid unnecessary activities • Prevent excessive crying • Provide diversional activities • Relieve the respiratory distress associated with increased pulmonary blood flow or oxygen deprivation
  • 61. NURSING MANAGEMENT OFTHE CHILDWITH A CONGENITAL HEART DEFECT Nursing Diagnoses • Impaired gas exchange related to altered pulmonary blood flow or oxygen deprivation • Altered cardiac output related to specific anatomic defect • Activity intolerance related to decreased oxygenation in blood and tissues • Altered Nutrition: less than body requirements related to the excessive energy demands required by increased cardiac workload
  • 62. NURSING MANAGEMENT OFTHE CHILD WITH A CONGENITAL HEART DEFECT • Increased potential for infection related to poor nutritional status • Anxiety related to diagnostic procedures and hospitalization • Developmental delay related to decreased energy, inadequate nutrition, physical limitations and social isolation • Alteration in parenting related to parental perception of the child as vulnerable