Laboratory Tests for Patients Presenting with Arrhythmias
For patients presenting with arrhythmias, a comprehensive laboratory workup should include thyroid function tests, electrolytes, and cardiac biomarkers as the essential initial evaluation. 1
Initial Laboratory Assessment
12-lead ECG: The cornerstone diagnostic test for all patients with suspected arrhythmias to document the rhythm disturbance and identify underlying structural abnormalities 1
Basic metabolic panel: Essential to identify electrolyte abnormalities that may trigger or worsen arrhythmias, particularly:
Thyroid function tests: Particularly important for patients with atrial fibrillation, atrial flutter, or sinus tachycardia as hyperthyroidism can trigger or exacerbate these arrhythmias 1, 2
Cardiac biomarkers: Troponin and CK/CK-MB to assess for myocardial injury that may be associated with arrhythmias 1, 2
Complete blood count: To evaluate for anemia or infection that may contribute to arrhythmias 2
Renal function tests: BUN and creatinine to assess kidney function, which impacts medication choices and dosing 2
Cardiac Imaging
Echocardiography: Recommended for all patients with suspected or known ventricular arrhythmias to evaluate cardiac structure and function, including:
- Left ventricular size and function
- Valvular heart disease
- Left and right atrial size
- Presence of left ventricular hypertrophy
- Regional wall motion abnormalities
- Evidence of cardiomyopathy 1
Chest radiograph: To evaluate lung parenchyma and pulmonary vasculature when clinical findings suggest abnormalities 1
Advanced Testing Based on Clinical Suspicion
Ambulatory ECG monitoring: For patients with intermittent symptoms to document arrhythmias:
- 24-hour Holter monitor for frequent episodes
- Event recorder for infrequent episodes
- Implantable cardiac monitor for very infrequent episodes 1
Exercise stress testing: To reproduce exercise-induced arrhythmias or evaluate rate control in permanent atrial fibrillation 1
Advanced cardiac imaging: Cardiac MRI or CT when structural heart disease is suspected but not confirmed by echocardiography 1
Electrophysiological study: For diagnostic evaluation of patients with symptoms suggestive of ventricular tachyarrhythmias, to clarify mechanisms of wide-QRS-complex tachycardias, or to identify predisposing arrhythmias 1
Special Considerations
Genetic testing: Consider in patients with suspected inherited arrhythmia syndromes or when there is a family history of sudden cardiac death 1
Natriuretic peptides (BNP or NT-proBNP): Can provide prognostic information for predicting sudden cardiac death or arrest in patients with structural heart disease 1
Transesophageal echocardiography: To identify left atrial thrombus before cardioversion in atrial fibrillation patients 1
Common Pitfalls to Avoid
Failing to check thyroid function in patients with new-onset atrial fibrillation or unexplained tachyarrhythmias 1
Overlooking electrolyte abnormalities, particularly potassium and magnesium, which can trigger or worsen arrhythmias 2
Relying solely on a single ECG when symptoms are intermittent; extended monitoring is often necessary 1, 3
Not correlating symptoms with documented arrhythmias, which may lead to misdiagnosis 4
Neglecting to evaluate for structural heart disease in patients with ventricular arrhythmias, as this significantly impacts prognosis and management 1