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Endocrinology

The document provides a comprehensive overview of various endocrine disorders, including diabetes mellitus types 1 and 2, diabetic ketoacidosis, hyperosmolar hyperglycemic state, thyroid disorders, adrenal insufficiencies, and hyperparathyroidism. Each condition includes diagnostic criteria, management strategies, and contraindications for treatment. The information is structured to assist in clinical decision-making for healthcare professionals dealing with these endocrine conditions.

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0% found this document useful (0 votes)
8 views10 pages

Endocrinology

The document provides a comprehensive overview of various endocrine disorders, including diabetes mellitus types 1 and 2, diabetic ketoacidosis, hyperosmolar hyperglycemic state, thyroid disorders, adrenal insufficiencies, and hyperparathyroidism. Each condition includes diagnostic criteria, management strategies, and contraindications for treatment. The information is structured to assist in clinical decision-making for healthcare professionals dealing with these endocrine conditions.

Uploaded by

aw063855
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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Endocrinology

1. Diabetes Mellitus Type 1


Clues in Questions:
• Patient: Child or adolescent presenting with polyuria, polydipsia, weight loss, and fatigue.
• Scenario: A young patient presenting with symptoms of hyperglycemia and possible diabetic ketoacidosis (DKA)
(e.g., fruity breath, Kussmaul breathing).
Diagnosis:
• Initial test:
o Fasting plasma glucose ≥7.0 mmol/L (≥126 mg/dL).
o Random plasma glucose ≥11.1 mmol/L (≥200 mg/dL) with symptoms.
o HbA1c ≥6.5%.
• Other tests: Autoantibodies (e.g., anti-GAD, anti-IA2) to confirm Type 1 DM.
Management:
• First-line treatment: Insulin therapy (basal-bolus regimen or continuous insulin infusion).
• DKA management:
o IV insulin.
o Fluid resuscitation with isotonic saline.
o Potassium supplementation as insulin therapy may cause hypokalemia.
Contraindications:
• Avoid using oral hypoglycemic agents (e.g., sulfonylureas) in Type 1 DM, as these are ineffective due to absolute
insulin deficiency.
• In DKA, avoid rapid correction of hyperglycemia, as this can lead to cerebral edema, especially in pediatric patients.

2. Diabetes Mellitus Type 2


Clues in Questions:
• Patient: Overweight or obese adult with polydipsia, polyuria, and blurred vision.
• Scenario: Middle-aged patient with high BMI, acanthosis nigricans, and symptoms of hyperglycemia or
asymptomatic hyperglycemia found on routine screening.
Diagnosis:
• Initial test:
o Fasting plasma glucose ≥7.0 mmol/L (≥126 mg/dL).
o HbA1c ≥6.5%.
• Other tests: Lipid panel, renal function, and urine microalbumin to assess for complications.
Management:
• First-line treatment:
o Lifestyle modifications (diet, exercise).
o Metformin as the preferred initial pharmacologic therapy.
• Second-line treatment: SGLT2 inhibitors, GLP-1 receptor agonists, or DPP-4 inhibitors depending on patient
comorbidities.
• Insulin therapy: Consider in cases of severe hyperglycemia or failure of oral agents.
Contraindications:
• Avoid Metformin in patients with eGFR <30 mL/min/1.73 m² due to the risk of lactic acidosis.
• Avoid SGLT2 inhibitors in patients with recurrent UTIs or genital mycotic infections, as they increase the risk of
infections in the genital tract.
• Sulfonylureas should be used cautiously in patients prone to hypoglycemia, particularly the elderly or those with
renal impairment.

3. Diabetic Ketoacidosis (DKA)


Clues in Questions:
• Patient: Type 1 diabetic with nausea, vomiting, abdominal pain, fruity breath, polyuria, and dehydration.
• Scenario: Diabetic patient presenting with confusion, tachycardia, Kussmaul respirations, and signs of dehydration.
Diagnosis:
• Initial test:
o Plasma glucose >13.9 mmol/L (>250 mg/dL).
o Serum ketones or β-hydroxybutyrate.
o Anion gap metabolic acidosis (arterial pH <7.3, HCO₃⁻ <15 mEq/L).
• Other tests: Serum electrolytes, blood gases, urinalysis for ketones.
Management:
• First-line treatment:
o IV fluids (normal saline initially, then switch to D5 half-normal saline when glucose <250 mg/dL).
o IV insulin infusion until ketosis resolves.
o Electrolyte replacement (e.g., potassium even if K⁺ is initially normal or low).
Contraindications:
• Avoid rapid correction of hyperglycemia, which may cause cerebral edema, especially in pediatric patients.
• Avoid insulin therapy without ensuring adequate potassium levels (K⁺ <3.3 mEq/L), as insulin drives potassium into
cells and can precipitate hypokalemia.
• Bicarbonate therapy is generally avoided unless the pH is <6.9, as it can worsen hypokalemia and delay correction
of ketosis.

4. Hyperosmolar Hyperglycemic State (HHS)


Clues in Questions:
• Patient: Elderly patient with poorly controlled Type 2 diabetes, presenting with extreme hyperglycemia,
dehydration, altered mental status, but no significant ketosis.
• Scenario: Diabetic patient with symptoms of profound dehydration, confusion, and serum glucose >33.3 mmol/L
(>600 mg/dL).
Diagnosis:
• Initial test:
o Plasma glucose >33.3 mmol/L (>600 mg/dL).
o Serum osmolality >320 mOsm/kg.
o Minimal or no ketones.
o pH >7.3 and HCO₃⁻ >18 mEq/L.
• Other tests: Electrolytes, blood gases, urinalysis.
Management:
• First-line treatment:
o IV fluids (initially isotonic saline).
o IV insulin (after adequate fluid resuscitation).
o Electrolyte management (particularly potassium).
Contraindications:
• Avoid rapid correction of serum glucose and sodium, as this may cause cerebral edema.
• Avoid insulin administration without sufficient fluid resuscitation, as this can worsen hypovolemia.
• Be cautious with diuretics in HHS, as patients are already profoundly dehydrated.

5. Hypothyroidism
Clues in Questions:
• Patient: Adult with fatigue, weight gain, cold intolerance, constipation, and dry skin.
• Scenario: Patient presenting with symptoms of slowed metabolism, bradycardia, and delayed reflexes.
Diagnosis:
• Initial test:
o Elevated TSH with low free T4 (primary hypothyroidism).
• Other tests: Anti-TPO antibodies to diagnose Hashimoto’s thyroiditis.
Management:
• First-line treatment: Levothyroxine (synthetic T4).
o Adjust dose based on TSH levels (goal: normalize TSH).
Contraindications:
• Avoid overtreatment with Levothyroxine, especially in elderly patients, as this can lead to atrial fibrillation and
osteoporosis.
• In patients with adrenal insufficiency, correct this before initiating levothyroxine to avoid adrenal crisis.
• Avoid abrupt dose changes in pregnancy, as hypothyroidism needs closer monitoring due to the increased demand
for thyroid hormone.

6. Hyperthyroidism (Graves' Disease)


Clues in Questions:
• Patient: Adult with weight loss, heat intolerance, tremor, palpitations, and exophthalmos.
• Scenario: Patient presenting with symptoms of thyrotoxicosis (e.g., weight loss, tachycardia) and enlarged thyroid.
Diagnosis:
• Initial test:
o Low TSH, elevated free T4 and/or T3.
• Other tests:
o Thyroid-stimulating immunoglobulins (TSI) to confirm Graves' disease.
o Radioactive iodine uptake (RAIU) to differentiate causes of hyperthyroidism.
Management:
• First-line treatment:
o Methimazole or Propylthiouracil (PTU) to block thyroid hormone synthesis.
o Beta-blockers (e.g., Propranolol) for symptom control.
• Definitive therapy: Radioactive iodine ablation or thyroidectomy in refractory cases.
Contraindications:
• Avoid Methimazole in the first trimester of pregnancy due to teratogenic effects; PTU is preferred during early
pregnancy.
• Avoid radioactive iodine therapy in pregnant or breastfeeding women.
• Use caution with radioactive iodine in patients with ophthalmopathy, as it can worsen eye symptoms; steroid
prophylaxis may be needed.

7. Thyroid Storm
Clues in Questions:
• Patient: Known or suspected hyperthyroid patient presenting with fever, tachycardia, delirium, agitation, or coma.
• Scenario: Patient with a history of Graves' disease or untreated hyperthyroidism presenting with acute
decompensation following stress (e.g., surgery, infection).
Diagnosis:
• Initial test: Clinical diagnosis based on severe thyrotoxicosis (e.g., hyperpyrexia, tachycardia, altered mental status).
• Other tests: TSH, free T4/T3 (usually markedly elevated).
Management:
• First-line treatment:
o Beta-blockers (e.g., Propranolol) to control heart rate.
o Antithyroid drugs (e.g., PTU to block new hormone synthesis).
o Iodine (after PTU) to block hormone release.
o Steroids to prevent peripheral conversion of T4 to T3.
• Supportive care: Cooling, IV fluids, treatment of precipitating cause (e.g., infection).
Contraindications:
• Avoid Methimazole in thyroid storm, as PTU is preferred due to its additional effect of inhibiting peripheral
conversion of T4 to T3.
• Avoid delaying treatment, as thyroid storm is a life-threatening condition with high mortality if not managed
aggressively.

8. Primary Hyperparathyroidism
Clues in Questions:
• Patient: Middle-aged or older adult presenting with bone pain, fractures, kidney stones, abdominal pain, and
depression.
• Scenario: A patient with hypercalcemia and symptoms related to "stones, bones, groans, and psychiatric
overtones".
Diagnosis:
• Initial test:
o Elevated serum calcium with elevated PTH.
• Other tests: 24-hour urine calcium to differentiate from familial hypocalciuric hypercalcemia.
Management:
• First-line treatment: Parathyroidectomy for symptomatic patients or those with complications (e.g., osteoporosis,
kidney stones).
• Medical management:
o Bisphosphonates or Cinacalcet for patients who are not surgical candidates.
o Hydration to prevent kidney stones.
Contraindications:
• Avoid delaying surgical intervention in symptomatic patients, as untreated hyperparathyroidism can lead to
osteoporosis and renal damage.
• Be cautious using thiazide diuretics in hyperparathyroidism, as they can increase calcium reabsorption and
exacerbate hypercalcemia.

9. Addison’s Disease (Primary Adrenal Insufficiency)


Clues in Questions:
• Patient: Adult with fatigue, weight loss, hyperpigmentation, hypotension, and salt craving.
• Scenario: A patient presenting with chronic fatigue, orthostatic hypotension, and hyperkalemia.
Diagnosis:
• Initial test:
o Low cortisol with high ACTH (primary adrenal insufficiency).
• Other tests:
o ACTH stimulation test (cortisol fails to rise in response to ACTH).
o Electrolytes (hyponatremia, hyperkalemia).
Management:
• First-line treatment: Glucocorticoid replacement (e.g., Hydrocortisone) and mineralocorticoid replacement (e.g.,
Fludrocortisone) for primary adrenal insufficiency.
Contraindications:
• Avoid delaying steroid replacement, as untreated adrenal insufficiency can lead to an adrenal crisis, which is life-
threatening.
• Use caution in patients with active infections, as glucocorticoid therapy can suppress the immune response.
10. Cushing’s Syndrome (Hypercortisolism)
Clues in Questions:
• Patient: Adult with weight gain, central obesity, moon facies, purple striae, muscle weakness, and hypertension.
• Scenario: A patient presenting with features of cortisol excess, such as easy bruising, proximal muscle weakness,
and hirsutism.
Diagnosis:
• Initial test:
o 24-hour urinary free cortisol (elevated).
o Low-dose dexamethasone suppression test (no suppression of cortisol).
• Other tests: ACTH levels to differentiate between ACTH-dependent (e.g., Cushing's disease, ectopic ACTH) and
ACTH-independent (e.g., adrenal adenoma) causes.
Management:
• First-line treatment:
o Surgical resection of the underlying cause (e.g., pituitary adenoma, adrenal tumor).
o Ketoconazole or Metyrapone to reduce cortisol production in cases where surgery is delayed or not
possible.
Contraindications:
• Avoid long-term glucocorticoid use, as this is the most common cause of exogenous Cushing's syndrome. Careful
tapering of steroids is required to avoid adrenal insufficiency.
• In patients with adrenal adenomas, avoid delaying surgical resection, as untreated Cushing’s syndrome can lead to
complications such as diabetes, osteoporosis, and hypertension.

11. Pheochromocytoma
Clues in Questions:
• Patient: Adult presenting with paroxysmal episodes of headache, palpitations, sweating, and hypertension.
• Scenario: A patient with episodic hypertension and symptoms of sympathetic overactivity (e.g., tachycardia,
diaphoresis).
Diagnosis:
• Initial test:
o 24-hour urinary metanephrines or plasma free metanephrines (elevated).
• Other tests:
o CT/MRI of the abdomen to localize the tumor.
o MIBG scan if there is suspicion of metastatic or extra-adrenal pheochromocytoma.
Management:
• First-line treatment:
o Alpha-blockade (e.g., Phenoxybenzamine) to control hypertension.
o Beta-blockers after adequate alpha-blockade to control tachycardia.
o Surgical resection of the tumor is the definitive treatment.
Contraindications:
• Avoid beta-blockers alone without prior alpha-blockade, as unopposed alpha stimulation can worsen hypertension.
• Avoid delaying surgery once the tumor is adequately blocked, as untreated pheochromocytomas can lead to
hypertensive crises and life-threatening complications.

12. Hyperaldosteronism (Conn’s Syndrome)


Clues in Questions:
• Patient: Adult with hypertension, hypokalemia, muscle cramps, and fatigue.
• Scenario: A hypertensive patient with unexplained hypokalemia and metabolic alkalosis, despite not being on
diuretics.
Diagnosis:
• Initial test:
o Plasma aldosterone-to-renin ratio (elevated aldosterone, suppressed renin).
• Accurate test:
o Adrenal CT to locate an adrenal adenoma.
o Adrenal vein sampling to differentiate unilateral from bilateral disease.
Management:
• First-line treatment:
o Unilateral adrenal adenoma: Surgical resection.
o Bilateral adrenal hyperplasia: Spironolactone or Eplerenone (aldosterone antagonists).
Contraindications:
• Avoid unnecessary diuretic use in patients with primary hyperaldosteronism, as this can exacerbate hypokalemia.
• In patients with bilateral adrenal hyperplasia, avoid surgery, as it is only indicated for unilateral causes.

13. Hypocalcemia
Clues in Questions:
• Patient: Adult or child with muscle cramps, tetany, paresthesias, and a history of thyroid or parathyroid surgery.
• Scenario: A patient presenting with Chvostek's sign, Trousseau's sign, and symptoms of hypocalcemia (e.g.,
perioral numbness, muscle cramps).
Diagnosis:
• Initial test:
o Low serum calcium with elevated phosphate and low PTH (primary hypoparathyroidism).
• Other tests:
o Vitamin D levels (to assess for vitamin D deficiency).
o Magnesium levels (hypomagnesemia can contribute to hypocalcemia).
Management:
• First-line treatment:
o Calcium supplementation (oral or IV depending on severity).
o Vitamin D supplementation (e.g., calcitriol) for long-term management in chronic hypoparathyroidism.
Contraindications:
• Avoid delayed calcium replacement, especially in patients with acute symptomatic hypocalcemia, as this can lead
to seizures or cardiac arrhythmias.
• In patients with renal failure, avoid high-dose calcium supplementation without monitoring, as it can lead to
hyperphosphatemia and vascular calcifications.

14. Hypercalcemia (Primary Hyperparathyroidism or Malignancy-Related)


Clues in Questions:
• Patient: Adult with polyuria, constipation, bone pain, kidney stones, and mental status changes.
• Scenario: A patient presenting with hypercalcemia and related symptoms (e.g., "stones, bones, moans, and
groans").
Diagnosis:
• Initial test:
o Elevated serum calcium.
o PTH level: Elevated in primary hyperparathyroidism, low in malignancy-related hypercalcemia.
• Other tests:
o Chest X-ray or serum protein electrophoresis to rule out malignancy.
o 24-hour urine calcium to differentiate from familial hypocalciuric hypercalcemia.
Management:
• First-line treatment:
o IV fluids and bisphosphonates for symptomatic hypercalcemia.
o Calcitonin for rapid calcium reduction in severe cases.
o Surgical resection for parathyroid adenoma (primary hyperparathyroidism).
Contraindications:
• Avoid thiazide diuretics in hypercalcemia, as they increase calcium reabsorption and worsen the condition.
• In patients with malignancy-related hypercalcemia, avoid delaying treatment with bisphosphonates, as rapid
calcium reduction is needed to prevent cardiac arrhythmias and coma.

15. Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH)


Clues in Questions:
• Patient: Adult presenting with hyponatremia, nausea, headache, confusion, and a history of lung disease (e.g.,
small cell lung cancer).
• Scenario: A patient with euvolemic hyponatremia and low serum osmolality, often with a history of malignancy or
CNS trauma.
Diagnosis:
• Initial test:
o Low serum sodium (<135 mmol/L).
o Low serum osmolality with high urine osmolality and elevated urine sodium.
• Other tests:
o Chest X-ray to look for underlying malignancy.
o CT/MRI of the brain if CNS cause is suspected.
Management:
• First-line treatment:
o Fluid restriction.
o IV hypertonic saline for severe hyponatremia (e.g., seizures).
o Demeclocycline or vasopressin receptor antagonists (e.g., Tolvaptan) for chronic management.
Contraindications:
• Avoid rapid correction of hyponatremia, as this can lead to osmotic demyelination syndrome (central pontine
myelinolysis).
• Be cautious using loop diuretics in patients with SIADH, as they can cause further electrolyte imbalances.

16. Diabetes Insipidus (DI)


Clues in Questions:
• Patient: Adult presenting with polyuria, polydipsia, and hypernatremia following head trauma or pituitary surgery.
• Scenario: A patient with excessive thirst, high-volume dilute urine output, and hypernatremia, with a history of CNS
disease or trauma.
Diagnosis:
• Initial test:
o Water deprivation test showing inability to concentrate urine (continued dilute urine).
• Other tests:
o Serum sodium (elevated) and serum osmolality (elevated).
o Desmopressin (ADH) challenge to differentiate between central and nephrogenic DI.
Management:
• First-line treatment:
o Central DI: Desmopressin (DDAVP).
o Nephrogenic DI: Thiazide diuretics, indomethacin, or amiloride.
Contraindications:
• Avoid delayed administration of desmopressin in central DI, as untreated DI can lead to severe dehydration and
hypernatremia.
• In patients with nephrogenic DI, avoid NSAIDs in those with compromised kidney function, as they may worsen
renal disease.

17. Adrenal Crisis


Clues in Questions:
• Patient: Known patient with Addison’s disease or chronic glucocorticoid use presenting with shock, hypotension,
vomiting, abdominal pain, and fever.
• Scenario: A patient with a history of adrenal insufficiency presenting with acute hypotension, dehydration, and
altered mental status following a stressor (e.g., infection, surgery).
Diagnosis:
• Initial test:
o Clinical diagnosis based on acute hypotension, hyponatremia, and hyperkalemia.
• Other tests:
o Serum cortisol (low), ACTH (high in primary adrenal insufficiency).
Management:
• First-line treatment:
o IV fluids (normal saline).
o IV hydrocortisone or dexamethasone immediately.
o Correct electrolyte imbalances (e.g., hypoglycemia, hyperkalemia).
Contraindications:
• Avoid delaying steroid replacement, as adrenal crisis can lead to shock and death if not treated promptly.
• Use caution with vasopressors in adrenal crisis; they may not be effective until cortisol levels are corrected.
18. Hyperkalemia
Clues in Questions:
• Patient: Adult with renal failure, on potassium-sparing diuretics, ACE inhibitors, or with adrenal insufficiency,
presenting with muscle weakness, fatigue, or palpitations.
• Scenario: A patient with chronic kidney disease, heart failure, or adrenal insufficiency, presenting with symptoms
of weakness, paresthesias, and arrhythmias.
Diagnosis:
• Initial test:
o Serum potassium >5.5 mmol/L.
o ECG changes: Peaked T waves, prolonged PR interval, widened QRS, sine wave pattern in severe cases.
• Other tests:
o Serum creatinine to assess kidney function.
o Urine potassium and aldosterone levels to assess renal and adrenal function.
Management:
• First-line treatment (for ECG changes or severe hyperkalemia):
o Calcium gluconate (to stabilize cardiac membrane).
o Insulin with glucose (to drive potassium into cells).
o Beta-agonists (e.g., albuterol) to shift potassium intracellularly.
o Sodium bicarbonate (in metabolic acidosis).
o Loop diuretics (e.g., furosemide) to promote potassium excretion if renal function allows.
o Hemodialysis in patients with severe renal impairment or refractory hyperkalemia.
• Chronic management: Potassium binders (e.g., patiromer, sodium polystyrene sulfonate) for patients with chronic
hyperkalemia.
Contraindications:
• Avoid calcium administration in patients taking digitalis (digoxin), as it can precipitate digoxin toxicity and worsen
cardiac arrhythmias.
• Avoid using potassium-sparing diuretics (e.g., spironolactone, eplerenone) in patients with severe hyperkalemia,
as they may further increase serum potassium.
• Be cautious with ACE inhibitors and ARBs in patients with renal failure or hyperkalemia, as they reduce aldosterone
secretion and impair potassium excretion.

19. Hypokalemia
Clues in Questions:
• Patient: Adult or child with a history of diarrhea, vomiting, diuretic use (especially loop diuretics or thiazides), or
hyperaldosteronism, presenting with muscle weakness, cramps, or arrhythmias.
• Scenario: A patient presenting with muscle cramps, fatigue, constipation, and flattened T waves on ECG, with a
history of diuretic use or gastrointestinal losses.
Diagnosis:
• Initial test:
o Serum potassium <3.5 mmol/L.
o ECG changes: Flattened T waves, U waves, ST depression, prolonged QT interval.
• Other tests:
o Serum magnesium (hypomagnesemia can exacerbate hypokalemia).
o Urine potassium to assess renal losses (high in renal causes, low in non-renal causes).
o Arterial blood gas to assess for metabolic alkalosis (often seen in hypokalemia due to vomiting or diuretics).
Management:
• First-line treatment:
o Oral potassium chloride for mild-to-moderate hypokalemia.
o IV potassium chloride for severe hypokalemia or symptomatic patients (e.g., arrhythmias, muscle
weakness). Administer slowly to avoid rapid infusion risks.
o Magnesium replacement if concurrent hypomagnesemia is present.
Contraindications:
• Avoid IV potassium bolus administration or rapid infusion rates (>10 mEq/hr) as this can lead to cardiac
arrhythmias or cardiac arrest.
• Be cautious with potassium supplementation in patients with renal impairment due to the risk of inducing
hyperkalemia.
• Avoid diuretics that can worsen potassium loss (e.g., loop or thiazide diuretics) in patients with ongoing
hypokalemia. Consider potassium-sparing diuretics (e.g., spironolactone) for these patients.

20. Hypernatremia
Clues in Questions:
• Patient: Adult or elderly patient with dehydration, diabetes insipidus, or inadequate water intake, presenting with
lethargy, confusion, or seizures.
• Scenario: A patient with hypernatremia and signs of dehydration, often with a history of diabetes insipidus,
excessive diuretic use, or inability to access water.
Diagnosis:
• Initial test:
o Serum sodium >145 mmol/L.
• Other tests:
o Urine osmolality to differentiate between causes (high in extrarenal losses, low in diabetes insipidus).
o Water deprivation test and desmopressin challenge to confirm diabetes insipidus (central vs nephrogenic).
Management:
• First-line treatment:
o Oral or IV fluids with isotonic saline to correct volume depletion.
o Hypotonic fluids (e.g., 5% dextrose in water or 0.45% saline) for slow correction of hypernatremia once
volume is restored.
o Desmopressin (DDAVP) for central diabetes insipidus.
Contraindications:
• Avoid rapid correction of hypernatremia, as this can lead to cerebral edema and herniation. The goal is to lower
serum sodium by no more than 8-10 mmol/L per day.
• In patients with diabetes insipidus, avoid delaying desmopressin treatment, as untreated DI can lead to severe
dehydration and hypernatremia.

21. Hyponatremia
Clues in Questions:
• Patient: Elderly or hospitalized patient on diuretics, or with conditions such as heart failure, SIADH, or liver
cirrhosis, presenting with lethargy, headache, or seizures.
• Scenario: A patient with altered mental status, lethargy, and symptoms of hyponatremia (e.g., nausea, confusion).
Diagnosis:
• Initial test:
o Serum sodium <135 mmol/L.
• Other tests:
o Serum osmolality and urine osmolality to differentiate causes (e.g., SIADH, volume depletion, heart
failure).
o Urine sodium (high in SIADH, low in hypovolemia).
Management:
• First-line treatment:
o Fluid restriction for SIADH and hypervolemic hyponatremia.
o IV hypertonic saline for severe symptomatic hyponatremia (e.g., seizures, coma).
o Vasopressin antagonists (e.g., tolvaptan) for chronic SIADH.
Contraindications:
• Avoid rapid correction of hyponatremia, as this can lead to osmotic demyelination syndrome (central pontine
myelinolysis). Serum sodium should not increase by more than 8-10 mmol/L per day.
• Avoid using diuretics without electrolyte monitoring in patients with hyponatremia, as this can exacerbate the
condition.

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