Peds Cardiology -Junkins Flashcards
What is the normal respiratory rate and heart rate for a 12?
12: R 12-16, HR 60-100 (adult value)
Which of the following is NOT a described mechanism of tachycardia?
Increased phase 4 depolarization (e.g. sympathetic stimulation)
A. Acquired phase 4 depolarization
B. Prolonged action potential duration
C. Unidirectional block plus slowed conduction
D. Decreased phase 4 depolarization (e.g. parasympathetic stimulation)
D. Decreased phase 4 depolarization (e.g. parasympathetic stimulation)
*What are the differences in Peds EKGs?
- Heart rates are faster
- Conduction intervals are SHORTER due to the smaller cardiac size PR interval ( may look like a right axis deviation, dominant R wave in V1 and T-wave inversions in V1-3 (“juvenile T-wave pattern”)
*What are the differences in Peds EKGs?
- Heart rates are faster
- Conduction intervals are SHORTER due to the smaller cardiac size PR interval ( may look like a right axis deviation, dominant R wave in V1 and T-wave inversions in V1-3 (“juvenile T-wave pattern”)
- Rightward QRS axis > +90°
- RSR’ pattern in V1
- Slightly peaked P waves
- Slightly long QTc (≤490ms in infants≤6 months)
- Q waves in the inferior and left precordial leads
- Marked sinus arrhythmia
Is sinus arrhythmia normal in children?
yes –> benign
What is the most common symptomatic dysrhythmia in kids?
Supraventricular tachycardia (due to an accessory pathway –> WPW)
According to the Lilly text, the incidence of Wolff-Parkinson-White Syndrome is closest to which of the following? A. 1 in 1,000 people B. 1 in 100,000 people C. 1 in 10,000 people D. 1 in 100 people
A. 1 in 1,000 people
All are acceptable non-pharmacologic maneuvers to reverse a patient who is in clinically stable supraventricular tachycardia, EXCEPT?
A. Carotid massage
B. Coughing while sitting with the upper body bent forward
C. Momentarily plunging infant’s face into a bath of ice water
D. External cardioversion
E. External defibrillation
E. External defibrillation
*What are the 2 familial causes of Long QT Syndrome and their modes of inheritance?
-Jervell-Lange-Nielson Syndrome: Autosomal recessive
(also has bilateral sensorineural hearing loss)
-Romano-Ward syndrome: Autosomal Dominant (most common)
What is the treatment for Torsades de Pointes?
IV Magnesium
What are the dangerous symptoms associated with syncope?
- Syncope especially with EXERTION or EXCITEMENT- anger, fear, startle
- Cardiac arrest with exercise or excitement
*What are the physical findings commonly seen with Marfan’s Syndrome? What is the mode of inheritance?
- Autosomal dominant
- Hindfoot valgus
- Pneumothorax
- Dural extasia
- Pectus excavatum
- Arachnodactyly –> close hand and see thumb on the other side
- dilation of the aorta
- scoliosis
- reduced elbow extension
- skin striae
- myopia > 3 diopters
- mitral valve prolapse
*What causes the ductus arteriosus to close after a baby is born?
After birth, PGE1 levels drop as O2 tension rises -> causes the ductus arteriosus to close
**What medication can be given to close a patent ductus arteriosus?
Indomethicin
What is the most common cyanotic heart disease? What is the primary developmental defect?
Tetralogy of Fallot
-abnormal anterior and cephalad displacement of the conal septum, resulting in an enlarged aorta and obstructed pulmonary artery