Lecture 5: Cardiology Flashcards
chest pain
- frequent pediatric complaint
- most pediatric chest pain is musculoskeletal in origin
- older children are more likely to have psychogenic reasons
- younger children are more likely to have a cause related to respiratory disease
chest pain etiologies
- etiologies
- musculoskeletal (>20% prevalence)
- idiopathic (>20% prevalence)
- psychogenic/psychiatric (<30% prevalence)
- respiratory disorders (<10% prevalence)
- gastrointestinal (<8% prevalence)
- cardiac (<6% prevalence)
- breast (<5% prevalence)
- pulmonary vascular disorders
- toxic exposure
approach to chest pain
- distinguish acute vs. chronic
- distinguish pleuritic from non-pleuritic
- identify co-morbid risk factors
- herald signs of serious causes (red flags)
- chest pain with exertion
- exertional syncope
- acute pain that is acutely worsening
- acute onset of fever with chest pain
- findings on history or exam referable to cardiac or respiratory systems
- rule out severe distress
- chest tenderness is very reassuring against a cardiac source
- initial workup typically starts with EKG and chest plain film
musculoskeletal source of chest pain
- chest tenderness with or without movement
- overuse injury or strain of chest wall muscle
- direct trauma
- rib fracture
- contusion of chest wall
- precordial catch (Texidor’s twinge)
- sharp pain at the left sternal border, lasts less than 3 minutes, associated bubble or popping sensation
- costochondritis
- pain at sites of costal cartilage reproduced by eliciting tenderness over the costochondral junctions or with AP compression of the chest
respiratory source of chest pain
- illnesses with persistent or forceful cough
- pneumonia +/- pleural effusion
- asthma +/- pneumomediastinum
- spontaneous pneumothorax
- asthma
- cystic fibrosis
- Marfan’s syndrome
- pleurisy
pulmonary vascular disorder source of chest pain
- pulmonary embolism
- rare in children but can occur in those with risk factors
- oral contraceptives
- termination of pregnancy
- trauma, particularly of lower extremities
- classic presentation
- acute onset of pleuritic chest pain, dyspnea, hypoxia
- presentation is not always classic
- rare in children but can occur in those with risk factors
- pulmonary hypertension
- pain typically related to underlying heart or lung disease
- acute chest syndrome
- chest source crisis in patients with sickle cell disease
psychogenic source of chest pain
- anxiety disorder or conversion disorder
- relative or friend with cardiac disease
- family history of depression, somatization
- triggered by stress
- hyperventilation
GI source chest pain
- reflux esophagitis
- burning, substernal pain
- worse with reclining or certain foods
- may be associated with esophageal spasm (mimicks angina)
- severe cases complicated by esophageal candidiasis
- burning, substernal pain
- intrathoracic foreign body
mammary source chest pain
- females
- mastitis
- pregnancy
- fibrocystic disease
- males
- gynecomastia
cardiac source chest pain
- Rare cause of chest pain in children
- Co-morbid risk factors raise likelihood of cardiac-source chest pain
- diabetes mellitus
- Kawasaki’s disease
- stimulant use
- cocaine
- amphetamines
- cardiac ischemia
- may result from
- anomalous coronary arteries
- left ventricular outflow tract obstruction (LVOTO)
- cardiac infection - endocarditis
- embolic phenomena
- Vasculitis
- pulmonary hypertension
- valvular disease (congenital or acquired)
- cardiomyopathy
- subaortic stenosis
- arrhythmia
- may result from
- myocardial infarction
- rare in children
- herald sign – pain with exertion
- mitral valve prolapse
- pericarditis and myocarditis may cause chest pain without ischemia
- hypertrophic obstructive cardiomyopathy (HOCM)
- autosomal dominant inheritance
- systolic murmur worsening with change from lying to standing or with squat to standing or Valsalva
- procedures that reduce blood return to ventricles (reduce preload).
- pain with exertion
cardiac infections: pericarditis
- inflammation of the pericardium
- fever
- respiratory distress
- sharp, stabbing substernal chest pain
- often unable to lie flat
- pain improves with sitting up or leaning forward
- friction rub, distant heart sounds
- jugular venous distension
- pulsus paradoxus
- Abnormal EKG – Diffuse ST elevations
cardiac infections: myocarditis
- inflammation of the heart muscle
- pain develops over a few days
- fever
- systemic symptoms consistent with CHF
- vomiting, lightheadedness, etc.
- gallop rhythm (S3, S4 sounds)
- Tachycardia, hepatomegaly
- orthostatic hypotension
- CXR - cardiomegaly
- abnormal EKG, elevated CK and troponins
pediatric arrhythmias
- sinus arrhythmia can be very pronounced in children
- HR slows with expiration
- most common pediatric dysrhythmia is supraventricular tachycardia
- mechanisms include
- intra-atrial reentry
- AV nodal reentrant tachycardia
- AV accessory conduction
- Wolff-Parkinson-White syndrome
- slurred upstroke of the QRS (delta wave) à
- Babies normal heartrates when they’re born are 130-160, a 2-3yo is around 100 etc. so tachycardia for younger ones is different than tachy in an adult
approach to chest pain
- distinguish acute vs. chronic
- distinguish pleuritic from non-pleuritic
- identify co-morbid risk factors
- herald signs of serious causes (red flags)
- chest pain with exertion
- acute pain that is acutely worsening
- acute onset of fever with chest pain
- findings on history or exam referable to cardiac or respiratory systems
- rule out severe distress
- chest tenderness is very reassuring against a cardiac source
- initial workup typically starts with EKG and chest plain film
describing a murmur
- intensity (grade I-VI)
- quality
- timing
- relationship to cardiac cycle
- Duration
- “shape”
- location
- variation with position
qualities of an innocent heart murmur
- Early Systolic Ejection
- Short Duration
- Soft - Low intensity (Grade 1 or 2)
- Vibrating or musical quality
qualities of a pathologic murmur (one or more)
- Pansystolic
- Diastolic(except venous hum)
- Long loud systolic murmurs
innocent murmurs
- roughly 80% of kids have a murmur at some time in their lives
- “innocent” is synonymous with terms functional, benign, & flow
- peripheral pulmonic stenosis
- Still’s (vibratory) murmur
- venous hum
- carotid bruit
- “innocent” is synonymous with terms functional, benign, & flow
innocent murmurs: peripheral pulmonic stenosis (PPS)
- peripheral pulmonic stenosis (PPS)
- caused by turbulence in the branches of the pulmonary artery in neonates
- grade I-II
- soft, short, high-pitched
- loudest over LUSB
- radiates to back & axillae
- Resolves by 3 to 6 months
- With a VSD, even the process of breast feeding is something that will make the baby SUPER tired
innocent murmurs: still’s (vibratory) murmur
- heard from age 2 and up
- grade I-III
- musical, vibratory, short
- LLSB to apex
- loudest when patient is in the supine position; diminishes when the patient sits or stands
innocent murmurs: venous hum
- heard after age 2
- continuous musical hum
- located at the upper right and left sternal borders
- usually louder on the right
- intensity changes with turning of the neck
- Goes away when the patient lays down
innocent murmurs: carotid bruit
- any age
- more common in the older child and adolescent
- grade II-III
- long, systolic ejection murmur
- heard in right supraclavicular area
- radiates to neck
congenital heart disease
- Shunts
- systemic (left) and pulmonary (right) circuits generally operate in series
- a shunt implies a connection that allows communication between the two systems
- shunting proceeds down gradient in pressure
- right-to-left shunts cause cyanosis
acyanotic congenital heart disease
- ASD, VSD, PDA
- semilunar valvular defects
- coarctation of the aorta
- VSD accounts for about 25% of all CHD
- ASD or PFO places patients at risk for systemic embolism
- PDA covered in neonatal lecture
- aortic stenosis and pulmonic stenosis are uncommon
- AS 5% of all CHD, PS 10% of all CHD
- both at risk for endocarditis
ventricular septal defect
-
Small VSD
- 80-85% of VSDs
- asymptomatic
- generally close on their own without surgery
-
Moderate VSD
- serially monitored by cardiologists
- Large VSD with normal pulmonary vascular resistance
- left-to-right shunting as pulmonary vascular resistance naturally decreases (2-8 weeks of life)
- infant develops congestive heart failure
- failure to thrive
- difficulty feeding
- labored breathing/pulmonary edema
Eisenmenger’s syndrome
- an untreated large VSD will cause pulmonary overcirculation
- overcirculation of pulmonary system causes pulmonary hypertension
- normal left-to-right shunt reverses to right-to-left shunt as pulmonary system pressures surpass systemic pressures
- prolonged cyanosis
- causes organ and vascular damage
- platelet dysfunction
- treatable only with heart transplant
coarctation of the aorta
- main artery to body stenotic or interrupted
- causes upper extremity hypertension and reduced flow to abdominal organs and lower extremities (SBP different by 20 should raise concern)
- all newborns screened for femoral pulses and saturations
- mild cases may have long-term growth problems,
- often have aortic valve abnormalities audible on exam
- may have chronic leg discomfort or lower extremity wasting
- in severe cases with pre ductal coarctation the PDA needs to be kept open to ensure survival
- if PDA closes, shock and acidosis ensue rapidly
cyanotic CHD
- five most common cyanotic CHD
- truncus arteriosus
- transposition of the great arteries
- tricuspid atresia
- tetralogy of Fallot
- total anomalous pulmonary venous return
tetralogy of fallot
- ~10% of all congenital heart disease
- four components to defect
- ventricular septal defect
- pulmonary stenosis
- right ventricular hypertrophy
- overriding aorta
- The patient may be ‘pink’ (not cyanotic) if pulmonic stenosis mild and VSD shunts left to right
- “Tet spells” where patient grows cyanotic, progressively worse with age
- infants become agitated, tachypneic and have difficulty feeding
- toddlers may squat to resolve Tet spell
- long systolic ejection murmur (from PS)
- classic CXR appearance - boot-shaped heart
- surgically repaired in infancy
- Tet spells are medical emergencies: SOB, cyanosis, loss of consciousness
- Squatting helps to fix these
rheumatic fever
- follows a previous infection with Strep pyogenes (GAβHS) – rate in untreated is approx. 3%
- typically between ages 5 and 15 years
- mortality of 2-5%
- pathophysiology
- sensitization of B lymphocytes
- formation of anti-streptococcal antibodies
- formation of Immune complexes
- myocardial & valvular inflammatory response
- major criteria JONES criteria (mnemonic J<3NES) –
- 2 major criteria make the diagnosis
- joints – migratory polyarthritis
- carditis
- as myocarditis, pericarditis or valvular disease
- nodules (subcutaneous)
- extensor surfaces of extremities
- erythema marginatum
- pink-red macules grow, then coalesce into serpiginious long patches
- Sydenham’s chorea – uncontrolled movements
- with or without psychiatric disease
- may define disease as a single criterion
- 1 major + 2 minor can also signify disease
- Minor criteria
- polyarthralgia
- fever
- elevated ESR, CRP
- prolonged PR interval
- Previous rheumatic fever
- Supportive serology of previous infection
- anti-streptolysin O is the best test
- anti-DNAse B & streptozyme also used
rheumatic fever treatment
- antibiotics
- short-term to treat indolent infection
- long-term to prevent recurrence
- often every 3-4 weeks for life
- aspirin for anti-inflammatory effects
- sometimes requires corticosteroids
- supportive
- cardiac meds (digoxin, diuretics)
- endocarditis prophylaxis for procedures
infective endocarditis
- greatest risk is to those with preexisting heart disease or cardiac foreign material
- may be acute or subacute
- viridans streptococci
- S. aureus
- less common
- enterococci
- HACEK organisms (fastidious Gram-negative rods)
- fever
- chest pain
- symptoms of heart failure
- fatigue, tachypnea, dyspnea on exertion
- changing murmur
- petechiae & embolic phenomena
- splenomegaly +/- hepatomegaly
- arthritis
- weight loss (subacute or chronic illness)
- Bacteremia with positive blood cultures
- hematuria
- markedly elevated inflammatory markers
treatment of infective endocarditis
- treatment
- long-term antibiotics
- directed therapy (based on cultures)
- surgical excision or valve repair sometimes warranted
- supportive care for sequelae
- congestive heart failure
- long-term antibiotics
- use transthoracic echos first and blood cultures, etc.
- Has to be treated for a very long time
endocarditis prevention
- cardiac risk factors that are often indications for prophylaxis
- prior history of infective endocarditis
- any valvulopathy
- prosthetic heart valves
- unrepaired cyanotic CHD
- repaired CHD with prosthetic material, device or venous pacer wires
- risk of procedure also important to determine need
- dental/oral or upper respiratory tract
- amoxicillin
- GU/GI procedures
- amoxicillin for enterococcal coverage
- aminoglycoside - for gram-negative coverage
- procedures that involved infected tissues
- clindamycin or vancomycin to cover MRSA
- dental/oral or upper respiratory tract
chest pain history
- Pain is in the center of the chest over the past 3 days.
- No history of chest pain
- Pain is worse with deep breathing
- No fever
- He has been coughing
- No history of pain with activity, some increase in symptoms while active
- No history of fainting
- No family history of cardiac disease