Hyperosmolar Hyperglycemic State (HHS): Causes, Pathophysiology, Diagnosis, and Management
Clinical Features: altered mental status, extreme dehydration, severe hyperglycemia, and neurological symptoms
Hyperosmolar Hyperglycemic State (HHS) is a serious diabetic emergency characterized by severe dehydration, extreme hyperglycemia, and neurological symptoms. Prompt management is crucial for survival.
Hyperosmolar Hyperglycemic State (HHS): Causes, Pathophysiology, Diagnosis, and Management
Hyperosmolar Hyperglycemic State (HHS) is a life-threatening complication of diabetes mellitus, predominantly affecting type 2 diabetics. It is characterized by extreme hyperglycemia, severe dehydration, altered mental status, and significant electrolyte imbalances.
Causes
- Poor diabetes management
- Infections (e.g., pneumonia, urinary tract infections)
- Medications (e.g., corticosteroids, diuretics)
- Underlying medical conditions (e.g., renal insufficiency, cardiovascular disease)
Pathophysiology
HHS develops due to a significant elevation in plasma glucose levels (>600 mg/dL), leading to osmotic diuresis and subsequent severe dehydration. Unlike diabetic ketoacidosis (DKA), there is minimal ketogenesis due to the presence of residual insulin activity, preventing excessive lipolysis.
Diagnosis
- Plasma glucose >600 mg/dL
- Serum osmolality >320 mOsm/kg
- Severe dehydration with altered mental status
- Absence or minimal ketonemia
Management
Management of HHS requires prompt medical intervention, including:
- Aggressive fluid replacement to correct dehydration
- Insulin therapy to gradually reduce blood glucose levels
- Electrolyte monitoring and correction
- Identification and treatment of underlying causes
Conclusion
Hyperosmolar Hyperglycemic State is a serious metabolic complication that necessitates rapid diagnosis and appropriate management to prevent mortality. Patients with diabetes should adhere to treatment regimens and seek medical attention promptly if symptoms arise.
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