Workup for Patient with Dizziness, Hypoglycemic Episodes, and Elevated Insulin Level
The patient with dizziness, hypoglycemic episodes, and markedly elevated insulin level (72.8) requires immediate evaluation for insulinoma or other causes of hyperinsulinemic hypoglycemia, including measurement of proinsulin, C-peptide, and a 72-hour supervised fast.
Initial Diagnostic Approach
Laboratory Evaluation
- Fasting blood tests:
- Glucose, insulin, proinsulin, and C-peptide levels simultaneously during a hypoglycemic episode
- Confirm insulin level is inappropriately elevated relative to glucose level
- Check proinsulin levels (elevated in insulinoma and proinsulinoma) 1
- Measure C-peptide (elevated in endogenous hyperinsulinism, normal/high in insulinoma)
- Screen for sulfonylurea and meglitinide drugs in blood/urine (to rule out surreptitious use)
Specialized Testing
72-hour supervised fast (gold standard for diagnosis of insulinoma)
- Monitor glucose, insulin, C-peptide, and proinsulin levels
- Document Whipple's triad: hypoglycemia, symptoms of hypoglycemia, and resolution with glucose administration
- Test is positive if patient develops hypoglycemia with inappropriately elevated insulin/C-peptide 2
Continuous glucose monitoring (CGM)
- Recommended for patients with recurrent hypoglycemia to identify patterns 3
- Helps distinguish between fasting and postprandial hypoglycemia
- Can identify overnight hypoglycemia that may be missed with spot checks
Imaging Studies (if hyperinsulinemic hypoglycemia is confirmed)
- Abdominal CT with contrast - first-line imaging for insulinoma
- Endoscopic ultrasound - high sensitivity for pancreatic lesions
- MRI of abdomen - if CT is negative but clinical suspicion remains high
- Somatostatin receptor scintigraphy (Octreoscan) - for detection of neuroendocrine tumors
- 68Ga-DOTATATE PET/CT - higher sensitivity than Octreoscan for neuroendocrine tumors
Additional Workup Considerations
Autoimmune evaluation:
- Anti-insulin antibodies to rule out insulin autoimmune syndrome 4
- Other autoimmune markers (may be associated with autoimmune hypoglycemia)
Genetic testing if clinically indicated:
- Multiple endocrine neoplasia type 1 (MEN1) gene
- Consider testing for congenital hyperinsulinism genes if history suggests
Management During Workup
- Document all hypoglycemic episodes with corresponding symptoms 5
- Provide glucagon prescription and education on its use for severe hypoglycemia 5
- Consider temporary adjustment of glycemic targets to avoid hypoglycemia 5
- Implement dietary modifications:
- Small, frequent meals
- Complex carbohydrates
- Bedtime snack containing protein and carbohydrate 3
Potential Pharmacologic Management
Diazoxide may be considered as a temporizing measure while completing diagnostic workup:
Octreotide (somatostatin analog) may be considered if diazoxide is ineffective:
- Helps manage hypoglycemia in some cases of hyperinsulinemic hypoglycemia 8
- Monitor for side effects including gallbladder abnormalities
Common Pitfalls to Avoid
- Failing to recognize insulinoma presenting with postprandial hypoglycemia (occurs in approximately 6% of cases) 1
- Misdiagnosing proinsulinoma when insulin levels are low despite clinical picture of insulinoma 2
- Not considering insulin autoimmune syndrome in differential diagnosis 4
- Failing to adjust treatment after hypoglycemic episodes, which can lead to recurrent events 3
- Not recognizing that 84% of patients with severe hypoglycemia had a preceding episode during the same period 3
This comprehensive workup will help identify the underlying cause of the patient's hypoglycemic episodes and elevated insulin level, allowing for appropriate targeted therapy.