The podcast discusses the approach to syncope in children, including initial workup similarities for children and adults, the rule of 50s for dextrose administration, and the importance of ECG analysis for diagnosing dysrhythmias. Topics covered include long QT syndrome, Brugada syndrome, and Wolff-Parkinson-White syndrome, emphasizing the need for a comprehensive evaluation and management in pediatric syncope cases.
Immediate assessment for syncope in children includes checking for hypoglycemia and performing an EKG to detect cardiac rhythm abnormalities.
Recognizing breath-holding spells triggered by emotions in children is crucial for proper evaluation and understanding their typical resolution by age 8.
Deep dives
Initial Assessment and Management:
When a child presents with syncope, immediate assessments should include checking for hypoglycemia and performing an EKG to detect any cardiac rhythm abnormalities. The rule of 50s is applied to determine the appropriate dextrose solution for hypoglycemic children. EKG findings should be closely monitored for serious conditions like long QT syndrome, brugada syndrome, and other rhythm abnormalities that can be life-threatening.
History and Breath-Holding Spells:
During history-taking, symptoms such as exertional syncope or prolonged unconsciousness are crucial, as they can indicate cardiac issues or seizure disorders. Breath-holding spells, often triggered by emotions like anger or fear, involve forced exhalation followed by apnea and typically resolve by the age of 8 without long-term complications. Recognizing these spells and their characteristics is essential for proper evaluation.
Cardiac Evaluation and Differential Diagnosis:
On examination, prioritizing the cardiac evaluation is crucial, particularly for signs of conditions like hypertrophic cardiomyopathy, indicated by murmurs that intensify with increased venous return. Emergency medicine practitioners must maintain a broad differential diagnosis for less common causes of syncope in children, avoiding premature closure in diagnosis and focusing on a detailed history and physical examination for appropriate patient workup.
Similar initial workup for children and adults: checking glucose levels for hypoglycemia and conducting an EKG.
The history and physical exam are crucial.
Dextrose Administration in Children:
Explanation of the ‘rule of 50s’ for determining the appropriate dextrose solution and dosage for children.
ECG Analysis:
Importance of ECG in diagnosing dysrhythmias like long QT syndrome, Brugada syndrome, catecholamine polymorphic V tach, ARVD, ALCAPA, and Wolff-Parkinson-White syndrome.
Younger children’s dependency on heart rate for cardiac output and the risk of arrhythmias in kids with congenital heart disease.
Narrow QRS complexes, Absence of P waves, Tachycardia
Congenital/Acquired
Ventricular Tachycardia
Wide QRS complexes, Tachycardia
Congenital/Acquired
Arrhythmogenic Right Ventricular Dysplasia (ARVD/C)
Epsilon waves, V1-V3 T wave inversions, Right bundle branch block
Congenital
Hypertrophic Cardiomyopathy (HCM)
Left ventricular hypertrophy, Deep Q waves
Congenital
Pulmonary Hypertension
Right ventricular hypertrophy, Right axis deviation
Acquired
Athlete’s Heart
Sinus bradycardia, Voltage criteria for left ventricular hypertrophy
Acquired
Catecholaminergic Polymorphic VT (CPVT)
Bidirectional or polymorphic VT, typically normal at rest
Congenital
Anomalous Origin of Left Coronary Artery from Pulmonary Artery (ALCAPA)
May be normal, signs of ischemia or infarction in severe cases
Congenital
History Taking:
Key aspects include asking about syncope with exertion, syncope after being startled, and syncope after pain or emotional stress.
Prolonged loss of consciousness may indicate seizures, and emotional stress and pain can trigger breath-holding spells.
Breath-Holding Spells:
Clarification of misconceptions about breath-holding spells, discussing their causes and characteristics, like cyanotic and pallid types.
Association with iron deficiency and the fact that most children outgrow these spells by age 8.
Physical Examination and History:
A cardiac exam is vital, with specific signs to look for, like murmurs in hypertrophic cardiomyopathy.
History can help identify the etiology of syncope, such as vasovagal responses or orthostatic hypotension.
Vasovagal Syncope:
Common in kids, especially teenagers, typically presenting with a prodrome of lightheadedness, diaphoresis, and pallor.
Normal glucose and EKG are expected in these cases.
Additional Lab Tests:
Pregnancy tests in reproductive-age women, and checking for less common causes like pulmonary embolism, subarachnoid hemorrhage, and toxic exposures.
Take Home Points:
Immediate assessments for syncope in children should include a FS to evaluate for hypoglycemia and an ECG to evaluate any cardiac rhythm or conduction abnormalities.
Apply the “Rule of 50s” for hypoglycemic patients to suggest which fluids should be used.
Refer to our table for ECG findings to look out for when reviewing ECG tracings for these patients.
Pay particular attention to clues in the history that would suggested HCOM or seizures.
Breath-holding spells usually resolve by eight
HCOM murmurs will increase with Valsalva maneuver
Always keep your differential broad when approaching these patients given the heterogeneity of potential pathology that could lead to this chief complaint