What disorder are pathological waves on an electrocardiogram (EKG) most commonly associated with?

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Pathological Q Waves on EKG Are Most Commonly Associated with Myocardial Infarction

Pathological Q waves on an electrocardiogram (EKG) are most commonly associated with myocardial infarction, representing areas of myocardial necrosis and fibrosis. 1

Definition and Characteristics of Pathological Q Waves

  • Pathological Q waves are defined as a Q/R ratio ≥ 0.25 or Q waves ≥ 40 ms in duration in two or more contiguous leads (except III and aVR) 1
  • According to classic criteria, pathological Q waves appear as:
    • Any Q wave ≥ 0.02 sec or QS complex in leads V2–V3 1
    • Q wave ≥ 0.03 sec and ≥ 0.1 mV deep or QS complex in leads I, II, aVL, aVF or V1–V6 in any two leads of a contiguous lead grouping 1
  • These abnormal Q waves typically develop as a result of transmural myocardial necrosis, representing electrically inert myocardium that is incapable of depolarization 2

Pathophysiology of Q Waves in Myocardial Infarction

  • Q waves represent the absence of electrical activity in necrotic myocardial tissue 2
  • In myocardial infarction, Q waves typically develop after myocardial necrosis has occurred, indicating irreversible myocardial damage 1, 3
  • Patients with Q-wave MI have larger infarct size and lower left ventricular ejection fraction (LVEF) compared to non-Q-wave MI patients 3
  • Q waves can appear early in the course of acute myocardial infarction, with studies showing that up to 53% of patients admitted within 1 hour of symptom onset already have abnormal Q waves on their initial ECG 4

Clinical Significance and Prognosis

  • The presence of pathological Q waves at presentation in anterior ST-segment elevation myocardial infarction (STEMI) is associated with:
    • Higher peak creatine kinase levels 5
    • Greater incidence of heart failure during hospitalization 5
    • Higher in-hospital mortality 5
    • Shorter time to heart failure development within the first year 6
  • Q-wave regression may occur in approximately 40% of patients with initial Q-wave MI within 24 months of follow-up 3
  • Patients with Q-wave regression show significantly larger LVEF improvement (9% ± 11%) compared to those with persistent Q waves (2% ± 8%) 3

Other Conditions Associated with Pathological Q Waves

While myocardial infarction is the most common cause, pathological Q waves can also be seen in:

  • Hypertrophic cardiomyopathy (HCM) 1
  • Arrhythmogenic right ventricular cardiomyopathy (ARVC) 1
  • Infiltrative myocardial diseases 1
  • Accessory pathways 1
  • Myocardial fibrosis in the absence of coronary artery disease 1

Evaluation of Pathological Q Waves

  • An ECG with abnormal Q waves should be carefully examined for the possibility of an accessory pathway 1
  • If pathological Q waves are isolated to leads V1-V2, the ECG should be repeated with careful attention to lead placement, as high lead placement can cause a pseudo-septal infarct pattern 1
  • Persistence of pathological Q waves in two or more contiguous leads warrants further investigation with echocardiography to exclude cardiomyopathy 1
  • In patients ≥30 years with suspicion of prior myocardial infarction or risk factors for coronary artery disease, stress testing may be warranted 1

Common Pitfalls in Interpretation

  • Not all Q waves are pathological - normal septal Q waves are small (<0.03 sec and <25% of the R-wave amplitude) in leads I, aVL, aVF, and V4–V6 1
  • A QS complex in lead V1 is normal 1
  • A Q wave <0.03 sec and <25% of the R wave amplitude in lead III is normal if the frontal QRS axis is between 30° and 0° 1
  • A Q wave may also be normal in aVL if the frontal QRS axis is between 60° and 90° 1
  • Lead misplacement can cause pseudo-infarct patterns, particularly high placement of precordial leads causing Q waves in V1-V2 1

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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