Chest pain (peds)

This page is for pediatric patients. For adult patients, see: chest pain

Background

  • Common cause of presentation to the ED, especially in adolescents[1]
  • The vast majority (>95%) of pediatric chest pain is benign and non-cardiac in origin
  • Most common causes are musculoskeletal (costochondritis, muscle strain), idiopathic, and respiratory[2]
  • Cardiac causes are rare but must be identified: pericarditis, myocarditis, arrhythmias, coronary anomalies
  • Family history plays an important part screening for familial history of sudden death, hypertrophic cardiomyopathy, long QT syndrome, or Marfan syndrome

Red Flags for Cardiac Etiology

  • Exertional chest pain or syncope
  • Associated palpitations, syncope, or near-syncope
  • History of Kawasaki disease (coronary aneurysms)
  • Known congenital heart disease or cardiac surgery
  • Family history of sudden cardiac death at age <50, HCM, LQTS
  • Pain associated with fever (consider pericarditis, myocarditis)
  • New murmur or abnormal cardiac exam
  • Marfan syndrome habitus (consider aortic root dissection)

Clinical Features

History

  • Onset, location, duration, character, radiation, exertional vs. rest
  • Reproducibility with palpation (suggests musculoskeletal)
  • Associated symptoms: fever, dyspnea, palpitations, syncope, cough, anxiety
  • Recent illness, trauma, or strenuous activity
  • Drug/substance use in adolescents (energy drinks, stimulants, vaping)

Physical Exam

  • Vital signs including pulse oximetry
  • Chest wall palpation for tenderness (reproducible tenderness suggests musculoskeletal cause)
  • Cardiac auscultation: murmurs, rubs, gallops, muffled heart sounds
  • Lung auscultation: wheezing, crackles, decreased breath sounds
  • Assess for Marfan syndrome features: tall stature, arm span > height, arachnodactyly, pectus deformity

Differential Diagnosis

Chest pain (peds)

Evaluation

Low Risk (Typical Musculoskeletal)

  • Reproducible chest wall tenderness, no red flags
  • No further workup generally needed
  • Consider CXR if history of cough, fever, or dyspnea

Moderate to High Risk

  • ECG: evaluate for ST changes, arrhythmia, prolonged QTc, ventricular hypertrophy, Brugada pattern
  • CXR: cardiomegaly, pneumothorax, pneumonia, mediastinal widening
  • Troponin if concern for myocarditis or pericarditis with myocardial involvement
  • BNP or NT-proBNP if concern for heart failure
  • Consider echocardiography for: new murmur, abnormal ECG, suspected pericardial effusion, known cardiac disease
  • Consider CT angiography for suspected pulmonary embolism (rare in pediatrics, but consider in adolescents with risk factors)

Management

Musculoskeletal (Most Common)

  • Reassurance — this is the most important intervention
  • NSAIDs (ibuprofen) for pain control
  • Activity modification as needed

Cardiac Causes

Disposition

Admit

  • Hemodynamically unstable
  • Suspected myocarditis or large pericardial effusion
  • Significant arrhythmia
  • Pneumothorax requiring intervention

Discharge

  • Musculoskeletal chest pain with normal exam and no red flags
  • Stable patients with mild pericarditis (arrange cardiology follow-up)
  • Provide clear return precautions: worsening pain, exertional symptoms, syncope, palpitations, fever
  • Cardiology referral for: abnormal ECG, family history of sudden death, exertional symptoms

See Also

External Links

References

  1. Jindal A, Singhi S. Acute chest pain. Indian J Pediatr. 2011 Oct;78(10):1262-7. PMID 21541647
  2. Huang SW, Liu YK. Pediatric Chest Pain: A Review of Diagnostic Tools in the Pediatric Emergency Department. Diagnostics (Basel). 2024 Mar 1;14(5). PMID 38473000
  3. Pickering D. Precordial catch syndrome. Arch Dis Child. 1981;56(5):401-403. doi:10.1136/adc.56.5.401