Endocrinology - HHS Flashcards

1
Q

What is HHS? What are the 3 characteristic features?

A

Hyperosmolar hyperglycaemic state

  1. severe hyperglycaemia (>30 mmol/L) without sig. hyperketonaemia (<3 mmol/L) or acidosis (pH >7.3)
  2. hyperosmolarity (>320 mOsmol/kg)
  3. hypovolaemia
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2
Q

Why does HHS occur? Give examples.

A

Occurs in people with T2DM (typically elderly): very high blood glucose levels develop due to combination of illness, dehydration and inability to take normal diabetes medication due to effects of illness.

E.g.

1) intercurrent or co-existing illness: MI, pneumonia, stroke, AKI, hyperthyroidism, etc.
2) medication-induced: diuretics, beta-blockers, CCS, anti-psychotics, prednisolone, alcohol, cocaine, etc.
3) diabetes-related: 1st presentation of DM or poor control/non-compliance

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3
Q

what are the downstream effects of hyperglycaemia? what are the possible complications?

A

Hyperglycaemia causes an osmotic diuresis… dehydration and hyperosmolarity… osmotic shift of water into intravascular compartment… intracellular dehydration.

Complications:

  • vascular: MI, stroke, organ infarction, DVT and PE
  • DIC
  • multi-organ failure and ARDS
  • iatrogenic complications of rehydration adne electrolyte management, e.g. cerebral oedema, central pontine myelinosis
  • foot pressure ulcers (examine feet daily)
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4
Q

describe the early and late symptoms of HHS

A

Usually develops over days-wks.

Early:

  • polydipsia and polyuria
  • generalised weakness
  • leg cramps
  • visual impairment
  • +/- nausea and vomiting (occur less often than in DKA)

Late:

  • confusion, lethargy
  • focal neurological symptoms, e.g. unilateral weakness or hemisensory abnormalities
  • seizures (25%) - may be generalised, focal, mov.-inducted or myoclonic-jerk type
  • coma (rare, 10%)
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5
Q

describe the signs of HHS.

A
  • signs of dehydration, e.g. dry mucous membranes, reduced skin turgor
  • appear ill and exhausted
  • evidence of disorientation or confusion
  • cranial nn. dysfunction, e.g. visual field deficits, nystagmus
  • tachycardia, hypotension, increased resp. rate +/- decreased SaO2
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6
Q

which investigations would you perform on someone with suspected HHS?

A

Bloods:

  • plasma glucose: increased
  • serum osmolarity: increased, >320 mOsmol/kg
  • FBC and CRP
  • UandE: ?dehydration/pre-renal AKI, deranged Na+ and K+ levels
  • CK: ?rhabdomyolysis
  • troponin I and T: if MI suspected
  • blood cultures: ?sepsis

Bedside tests:

  • capillary blood glucose: >30 mmol/L
  • urine dipstick: glycosuria with normal or only slightly raised ketones
  • urine MandC: ?UTI
  • ECG: ?MI, ?arrythmias
  • CXR: ?chest infection
  • CT/MRI head: if reduced consciousness or focal neurology
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7
Q

how would you manage a pt with HHS?

A

Continuous SaO2, ECG and BP/HR monitoring. Catheterise to monitor UO and for urinalysis. Measure or calculate osmolality frequently to monitor treatment response.

  1. Fluid resuscitation with IV 0.9% saline. encourage oral fluid intake as soon as possible. Rate of plasma Na+ decrease should not exceed 10 mmol/L in 24 hrs.
  2. Low dose IV insulin (0.05 units/kg/hr) started once blood glucose no longer falling with IV fluids alone, OR immediately if significant ketonaemia.
  3. ID and treat precipitant.
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8
Q

how do you calculate serum osmolality?

A

Osmolality = 2Na + glucose + urea

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