Complex, spanning the spectrum from congenital defects that may present at birth to acquired heart disease or late-onset inherited disorders
Risk management for CONGENITAL HEART DISEASE
Cause is idiopathic, but associations of CHD are seen with familial patterns of inheritance
Pregnant/entering pregnancy need to be fully immunized to prevent infection during pregnancy
Parents with a personal or family history of CHD need to be aware that other children born to them need to be carefully screened prenatally and at birth for a similar disorder
Risk management for ACQUIRED HEART DISEASE
Know the cause
Risk Factors: Rheumatic fever - an autoimmune response that follows a group A beta-hemolytic streptococcal infection
Management of Rheumatic fever
Ensure that all children who have a streptococcal infection such as streptococcal pharyngitis receive adequate antibiotic therapy to prevent rheumatic fever
Hypertension
Elevated blood pressure
Risk factors for hypertension
Genetic predisposition
High intake of sodium
Lack of exercise
Obesity
Increase the chances that a susceptible child will develop hypertension by late childhood (Flynn et al., 2017)
Management of hypertension
1. Reduce intake of processed foods and snacks
2. Monitor food intake
3. Advocate more nutritious menus at schools
Hyperlipidemia
High cholesterol or too many lipids in the blood
Causes of hyperlipidemia
Inherited
Diet high in saturated fat (school age and over)
Infants & toddlers - no restriction of fat intake since it's needed for brain development
School-aged children & adolescents (also adults) - reduced to 30% of total calories
Management of hyperlipidemia
1. Diet modification to low/no saturated fats
2. Participate in routine aerobic physical activity with daily limits on screen time, including television, phone, computer, social media and/or games
FETAL CIRCULATION
PLACENTA
Fetal circulation shunts
Foramen ovale - bypasses the lungs, blood from the RA to the LA
Ductusarteriosus - moves blood from the pulmonary artery to the aorta
Ductusvenosus - bypasses the liver, highly oxygenated blood bypass the liver to the inferior vena cava & then to the RA of the heart
Fetal circulation
Blood from the RA flows to the LV, then to the aorta, blood is sent to the heart muscle itself and to the brain & arms, blood returns to RA thru SVC, blood enters the umbilical arteries, flows into the placenta
Normal heart circulation
Blood from SVC& IVC enters RA, through tricuspid valve to RV, through pulmonary valve to PA, to lungs, oxygenated blood returns to LA through pulmonaryveins, through mitral valve to LV, through aortic valve to aorta
1. Inspect distal extremities for color & measure capillary refill time
2. Inspect mucous membranes of the mouth (buccal membranes & lips) to assess cyanosis
Assignment
How to perform the physical examination to child/children in assessing their cardiovascular system?
What are the different sites for cardiac auscultation?
What are the four heart sounds?
What is a heart murmur and the Levine grading scale for systolic murmurs?
Cardiac output
The volume of blood pumped by the ventricles each minute
Factors affecting stroke volume
Preload - the volume of blood in the ventricles at the point just before contraction
Contractility - ability to modulate the rate and force of fiber shortening
Afterload - the amount of resistance met by the ventricles upon ejection
Heart failure
The inability of the heart to supply adequate oxygenated blood to meet the metabolic demands of the body
Types of heart failure
Right sided failure
Left sided failure
Signs and symptoms of right-sided heart failure
Periorbital edema (infants)
Enlarged liver
Weight gain
Edema
Signs and symptoms of left-sided heart failure
Tachycardia
Dyspnea & rales
Tachypnea
Fatigue
Left sided HF can ultimately lead to right-sided failure, as excessive pressure in the pulmonary system prevents blood from leaving the right ventricle
4. If HF is due to congenital heart defect - short-term treatment to stabilize the infant's medical status until safe intervention of the CHD is performed
5. Use digoxin as the drug of choice
Classification of congenital heart defects
Embryologic formation
Structure
Physiology - "increasing pulmonary blood flow", "decreasing pulmonary blood flow", "obstruction to systemic blood flow", single ventricle defects (hypoplastic left heart syndrome)
Cyanotic heart disease
Venous blood from the right side of the heart mixes with blood on the left side, this is a "right-to-left" shunt that delivers deoxygenated blood to the body
Acyanotic heart disease
Blood shunts "left to right" then oxygenated blood from the left side mixes with blood in the right side of the heart and goes back to the lungs again
Defects that "increase pulmonary blood flow"
Patent Ductus Arteriosus
Atrial Septal Defect
Ventricular Septal Defect
Atrioventricular Septal Defect
Transposition of the Great Arteries
Anomalous Pulmonary Venous Return and Truncus Arteriosus
Patent Ductus Arteriosus
Occurs when this fetal shunt fails to close after several days of life, allowing blood to flow from the aorta (area of high pressure) through the PDA & into the main pulmonary artery (area of low pressure)
Management of Patent Ductus Arteriosus
1. Use diuretics (furosemide) if blood flow is significant
2. Increase caloric concentration of the infant's feed to gain weight if low weight
3. With heart dilatation = PDA closure
4. In premature infants with HF due to PDA = use indomethacin to facilitate closure
5. In older children = can be closed in the cardiac catheterization lab with a device placed in the duct to occlude flow
Atrial septal defect
Occurs when a portion of the atrial septal tissue does not completely form
Types of atrial septal defects
Secundum type - most common, located in the center of the atrial septum
Primum defect - located low in the atrial septum near the IVC
Sinus venosus defects - located high in the septum where the pulmonary veins enter the left atrium and allow communication of one or more of the pulmonary veins with the right atrium
Management of atrial septal defect
1. If incidentally noted, is small & is producing no clinical symptoms = it will not be closed
2. For clinically significant defects = management will be based on the child's age & the size of the defect
3. Defects that fail to close with persistent shunting after an observation period = refer for closure to prevent the incidence of supraventricular dysrhythmias & prevent pulmonary vascular disease
4. If the defect is larger with evidence of pulmonary blood flow = refer for closure
Ventricular septal defect
Occurs when a portion of the ventricular septum does not completely close
Management of ventricular septal defect
1. Medically manage to allow for spontaneous closure of the defect as the child grows
2. Use diuretics if child exhibit signs of pulmonary overload
3. Increase caloric density of the child's formula or human milk if poor weight gain
4. If small = no need to be closed
5. If large = refer for closure
6. Use digoxin to slow & strengthen the heartbeat, helping to prevent fluid from accumulating in the lungs
Atrioventricular septal defect
May comprise several defects, most common type of CHD in children with trisomy 21, varying degrees of abnormality occur with this lesion, from mild septal defects to a complete lack of central septa with incompetent valves on both sides