Definition
Hypoglycaemia is a clinical condition characterized by abnormally low plasma glucose concentration, typically defined as blood glucose levels below 4.0 mmol/L (72 mg/dL) in diabetic patients and below 3.0 mmol/L (54 mg/dL) in non-diabetic individuals, accompanied by autonomic and/or neuroglycopenic symptoms.
Causes
1. In People with Diabetes
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Excessive insulin administration.
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Sulfonylurea overdose (e.g., glibenclamide, gliclazide, glimepiride).
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Skipping or delaying meals after taking insulin or oral hypoglycaemic drugs.
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Increased physical activity without adequate carbohydrate intake.
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Alcohol consumption without food intake.
2. In People without Diabetes
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Severe liver disease (impaired gluconeogenesis).
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Sepsis.
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Hormonal deficiencies (e.g., adrenal insufficiency, hypopituitarism).
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Insulinoma (rare pancreatic β-cell tumor).
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Critical illness or prolonged fasting.
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Post–bariatric surgery hypoglycaemia.
Pathophysiology
Glucose homeostasis is maintained through a balance between insulin secretion, counter-regulatory hormones (glucagon, adrenaline, cortisol, growth hormone), and hepatic glucose production. Hypoglycaemia occurs when:
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Glucose utilization exceeds supply.
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Hepatic glucose output is insufficient.
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Insulin or insulin-like activity is excessive.
Clinical Features
Autonomic Symptoms (adrenergic activation)
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Sweating.
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Palpitations.
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Tremor.
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Anxiety.
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Hunger.
Neuroglycopenic Symptoms (glucose deprivation to the brain)
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Confusion.
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Drowsiness.
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Slurred speech.
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Visual disturbances.
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Seizures.
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Loss of consciousness.
Diagnosis
Whipple’s Triad
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Symptoms consistent with hypoglycaemia.
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Low plasma glucose concentration.
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Resolution of symptoms after raising blood glucose.
Investigations
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Capillary or plasma glucose measurement during symptoms.
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Serum insulin, C-peptide, proinsulin (if endogenous hyperinsulinism suspected).
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β-hydroxybutyrate (low in insulin-mediated hypoglycaemia).
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Cortisol and thyroid function tests if endocrine cause suspected.
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Imaging for insulinoma (CT, MRI, endoscopic ultrasound).
Management
Immediate Treatment
If the patient is conscious and able to swallow
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Give 15–20 g of fast-acting carbohydrate:
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Glucose tablets.
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Glucose gel.
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Sugary drinks (non-diet).
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Recheck blood glucose in 10–15 minutes; repeat if still low.
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Follow with long-acting carbohydrate (e.g., bread, biscuits) once recovered.
If the patient is unconscious or unable to swallow
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Glucagon 1 mg IM/SC (adults and children >25 kg; 0.5 mg for smaller children).
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Glucose 10% IV, 100–200 mL over 10 minutes, or glucose 50% IV, 25–50 mL slowly (hospital setting).
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Monitor closely and treat underlying cause.
Long-Term Management
1. For People with Diabetes
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Adjust insulin regimen or oral hypoglycaemic dose.
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Educate on timing of meals, carbohydrate counting, and hypoglycaemia recognition.
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Avoid skipping meals.
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Reduce alcohol consumption and always consume with food.
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Continuous glucose monitoring (CGM) for those with recurrent hypoglycaemia.
2. For Non-Diabetic Hypoglycaemia
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Treat underlying cause (e.g., surgery for insulinoma).
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Small frequent meals, complex carbohydrates, and avoidance of high-sugar foods in reactive hypoglycaemia.
Pharmacological Details – Key Medications
Glucagon
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Generic name: glucagon.
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Dose (adults): 1 mg IM/SC; repeat if necessary after 15 minutes if IV glucose unavailable.
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Dose (children): <25 kg or <8 years, 0.5 mg IM/SC.
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Used for emergency treatment of severe hypoglycaemia when IV access is not available.
Glucose (Dextrose)
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Generic name: glucose monohydrate (dextrose).
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IV dosing:
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10% glucose: 100–200 mL IV over 10 minutes.
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50% glucose: 25–50 mL slow IV bolus, followed by infusion if needed.
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Octreotide (for sulfonylurea-induced hypoglycaemia)
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Generic name: octreotide acetate.
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Dose: 50–100 mcg SC every 6–12 hours or continuous IV infusion 50–125 mcg/hour.
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Inhibits insulin secretion and prevents recurrent hypoglycaemia.
Complications
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Seizures and coma.
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Cardiac arrhythmias.
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Neurological damage with prolonged severe hypoglycaemia.
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Hypoglycaemia unawareness (loss of warning symptoms).
Prevention Strategies
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Individualized glycaemic targets for diabetic patients at risk of hypoglycaemia.
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Regular review of insulin therapy and oral hypoglycaemics.
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Patient education on recognition and early management of symptoms.
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CGM or flash glucose monitoring for high-risk individuals.
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