Initial Laboratory Investigations for Patient Evaluation
The initial laboratory investigations recommended for a patient should include complete blood count, comprehensive metabolic panel (including electrolytes, renal function, and liver function tests), urinalysis, and electrocardiogram, with additional specialized tests based on clinical presentation. 1, 2
Core Laboratory Tests for Initial Patient Evaluation
- Complete blood count (CBC) is essential to assess for infection, anemia, or other hematologic abnormalities 1, 2
- Comprehensive metabolic panel including:
- Lipid profile to assess cardiovascular risk 1
- Thyroid-stimulating hormone (TSH) to screen for thyroid dysfunction 1
- Urinalysis to evaluate for renal, metabolic, or systemic disorders 1, 2
- 12-lead electrocardiogram to assess cardiac rhythm and identify structural heart disease 1
Additional Tests Based on Clinical Presentation
For Patients with Suspected Stroke or Neurological Issues
- Coagulation studies (aPTT, INR) to assess bleeding risk and anticoagulation status 1
- Brain imaging (CT or MRI) to evaluate for structural abnormalities 1
- Vascular imaging (CTA or MRA) if cerebrovascular disease is suspected 1
- Extended ECG monitoring (>24 hours) if embolic stroke is suspected 1
For Patients with Suspected Heart Failure
- Troponin to assess for myocardial injury 1
- Two-dimensional echocardiography with Doppler to assess left ventricular function, size, wall thickness, and valve function 1
- Chest radiograph (PA and lateral) to evaluate cardiac size and pulmonary congestion 1
For Patients with Gastrointestinal Symptoms
- C-reactive protein (CRP) to assess for inflammatory processes 2, 1
- Blood gas analysis for base excess and lactate levels to evaluate acid-base status and tissue perfusion 2, 1
- Stool studies (culture, C. difficile testing, parasite examination) if infectious etiology is suspected 1
For Patients on Specific Medications
- For patients taking aripiprazole or other antipsychotics:
Special Considerations
- For patients with suspected metabolic disorders, consider specialized testing such as plasma amino acids, acylcarnitine profile, and urine organic acids 1
- For patients with neurodevelopmental disorders, genetic testing may be indicated, including chromosomal microarray (CMA) and specific gene testing based on clinical presentation 1
- Laboratory tests should be interpreted in the context of the patient's clinical presentation, as results can be affected by various factors including medications, timing of collection, and pre-existing conditions 4
Common Pitfalls to Avoid
- Ordering unnecessary tests without clear clinical indications can lead to increased costs and potential harm from false positives 5
- Failure to consider pre-analytical variables (such as timing of collection, fasting status) can affect test interpretation 6
- Not accounting for disease prevalence when interpreting test results can lead to misinterpretation of positive and negative predictive values 7
- Over-reliance on laboratory tests without proper clinical correlation can lead to diagnostic errors 8
- Failing to repeat abnormal results to confirm findings before initiating treatment 6
By following this structured approach to laboratory investigations, clinicians can efficiently evaluate patients while avoiding unnecessary testing and ensuring appropriate interpretation of results.