Endocrine ER
Here's the question-answer format for T1DM:
T1DM (Type 1 Diabetes Mellitus)
1. What is Type 1 Diabetes Mellitus (T1DM)?
Answer: T1DM is an insulin-dependent form of diabetes mellitus, where 90% of cases are autoimmune (AI) with the destruction of beta cells, leading to insulin deficiency.
2. What are the different types of autoimmune mechanisms associated with T1DM?
Answer:
T1DM A: Autoantibodies to beta cells (HLA-DR3/4).
T1DM B: Zinc autoantibodies positive.
LADA: Latent Autoimmune Diabetes in Adults.
3. What are the three initial symptoms of T1DM?
Answer:
Polydipsia (excessive thirst)
Polyuria (excessive urination)
Weight loss with hyperglycemia and ketonemia.
4. What are other common symptoms associated with T1DM?
Answer:
Perineal candidiasis
Visual disturbances.
5. What are the symptoms of Diabetic Ketoacidosis (DKA)?
Answer:
Acute dehydration
Polyuria, polydipsia
Fatigue, headache, altered mental status (AMS)
Nausea, vomiting, abdominal pain.
6. What physical examination findings are common in DKA?
Answer:
Tachycardia, tachypnea
Hypotension
Decreased skin turgor
Fruity (acetone) breath
Kussmaul respirations (deep, labored breathing).
7. What is the Dawn Phenomenon?
Answer: A glucose spike between 2-8 am.
8. What is the Somogyi Effect?
Answer: Nocturnal hypoglycemia followed by hyperglycemia.
9. What is Insulin Waning?
Answer: A progressive rise in glucose levels during the night.
10. What are the diagnostic criteria for T1DM?
Answer: One of the following:
Fasting plasma glucose ≥126 mg/dL on more than one occasion.
Random plasma glucose ≥200 mg/dL with symptoms.
OGTT: Plasma glucose ≥200 mg/dL after 2 hours.
HbA1c ≥6.5%, confirmed by repeat testing.
11. What are some autoantibodies commonly seen in T1DM?
Answer:
Zinc autoantibodies
Tyrosine kinase autoantibodies (Tyr-K)
Islet cell antibodies (ICA)
GAD65 (glutamic acid decarboxylase)
IA-2 (Insulinoma-associated antigen 2)
Insulin autoantibodies.
12. What lab value is important to monitor in T1DM?
Answer: C-peptide levels (indicates endogenous insulin production).
13. What is the potassium shift in DKA?
Answer: Potassium is depleted as it shifts from intracellular to extracellular space.
14. What is the blood glucose level range in DKA?
Answer: Blood glucose levels typically range between 250-500 mg/dL.
15. What is the general treatment for T1DM?
Answer: Insulin therapy, which can be:
a) Multiple daily injections (MDI)
b) Insulin pump therapy.
16. What is the management protocol for DKA (SIPS)?
Answer:
S: Saline (fluid resuscitation)
I: Insulin (to lower glucose)
P: Potassium (to correct potassium levels)
S: Search for the underlying cause.
17. How should potassium be managed in DKA?
Answer:
Potassium < 3.3: Hold insulin therapy.
Potassium 3.3-5.3: Continue insulin and maintain potassium levels.
Potassium > 5.3: Hold potassium.
18. When is sodium bicarbonate indicated in DKA treatment?
Answer: If the pH is less than 6.9.
Here's the question-answer format for the provided conditions:
T2DM (Type 2 Diabetes Mellitus)
1. What is Type 2 Diabetes Mellitus (T2DM)?
Answer: T2DM involves insulin insensitivity and insulin resistance. The body becomes less responsive to insulin, leading to increased blood glucose levels.
2. What are the risk factors for T2DM?
Answer:
Obesity
Decreased physical exercise
Family history (genetics)
Metabolic syndrome.
3. What are the three "P"s commonly seen in T2DM?
Answer:
Polyuria (excessive urination)
Polydipsia (excessive thirst)
Polyphagia (excessive hunger).
4. What are some other symptoms of T2DM?
Answer:
Poor wound healing
Increased infections.
5. What is Hyperosmolar Hyperglycemic State (HHS)?
Answer: HHS develops more insidiously and is characterized by:
Polyuria, polydipsia, weight loss, profound dehydration
Neuro symptoms like mental obtundation, coma, and seizures
Fatigue, weakness, nausea, and vomiting.
6. What physical examination findings are associated with HHS?
Answer:
Tachycardia
Hypotension
Decreased skin turgor
Increased capillary refill time.
7. What are the stages of Diabetic Retinopathy?
Answer:
Non-proliferative: Microaneurysms, cotton wool spots, hard exudates, blot & dot hemorrhages, flame-shaped hemorrhages.
Proliferative: Neovascularization (growth of new vessels that can cause hemorrhages).
Maculopathy: Macular edema or exudate leading to blurred vision.
8. How is T2DM diagnosed?
Answer: Diagnosis is similar to T1DM, with additional findings:
High insulin levels
C-peptide levels.
9. What are the lab findings in HHS?
Answer:
Blood glucose >600 mg/dL, often >1000 mg/dL
Plasma osmolality >320
pH >7.3, bicarbonate >18
Small ketones.
10. What is the initial treatment approach for T2DM?
Answer:
Lifestyle changes: Diet, exercise, weight management.
Pharmacological treatment:
Asymptomatic: Metformin is the most common initial therapy.
If intolerant/contraindicated: GLP-1 receptor agonists, SGLT2 inhibitors.
11. How is HHS treated?
Answer:
Primary: IV fluids (0.9% NaCl at 1L/h).
Once glucose reaches 300 mg/dL, switch to 5% dextrose with 0.45% NaCl.
Insulin: Initial bolus of 0.1 units/kg, then continuous infusion at 0.1 units/kg/h.
Potassium: Managed according to the same guidelines as in T1DM.
12. What is the treatment for diabetic retinopathy?
Answer:
Bevacizumab (anti-VEGF therapy)
Laser therapy.
Hypoglycemia
1. What is hypoglycemia?
Answer: Hypoglycemia is when blood sugar levels drop too low, impairing brain function, which requires glucose for normal activity.
2. What is the Whipple triad for hypoglycemia?
Answer:
Plasma glucose <50 mg/dL (fasting).
Symptoms of hypoglycemia.
Symptoms resolve after glucose administration.
3. How is hypoglycemia monitored?
Answer:
Fingerstick glucose measurement 4 times per day.
A1C target: <7%, measured every 3 months.
Blood glucose goals:
Before meals: 80-130 mg/dL
Bedtime: 80-140 mg/dL.
Hyperparathyroidism
1. What is the most common cause of hyperparathyroidism?
Answer: Parathyroid adenoma.
2. What are the symptoms of hyperparathyroidism?
Answer:
Hypercalcemia: Nephrolithiasis (kidney stones), bone pain, fractures, ileus, nausea, vomiting, constipation
Decreased deep tendon reflexes (DTR).
3. What is the diagnostic triad for hyperparathyroidism?
Answer:
High calcium levels
High parathyroid hormone (PTH) levels
Low phosphate levels.
4. What is the treatment for hyperparathyroidism?
Answer:
Parathyroidectomy (surgical removal of the parathyroid gland)
Cinacalcet (used when surgery is not an option).
If calcium is very high: IV fluids and furosemide.
Hypoparathyroidism
1. What is the most common cause of hypoparathyroidism?
Answer: Neck surgery (e.g., thyroidectomy) and autoimmune conditions.
2. What are the symptoms of hypoparathyroidism?
Answer:
Hypocalcemia: Carpopedal spasm, perioral numbness.
Increased deep tendon reflexes (DTR).
Special tests:
Trousseau sign (biceps contraction when inflating BP cuff).
Chvostek sign (twitching of facial muscles when tapping the facial nerve).
3. What is the diagnostic triad for hypoparathyroidism?
Answer:
Low calcium levels
Low PTH levels
High phosphate levels.
4. What is the treatment for hypoparathyroidism?
Answer:
Calcium supplements
IV calcium gluconate if severe.
Cushing Syndrome
1. What are the causes of Cushing syndrome?
Answer:
Exogenous: Steroid use.
Endogenous:
Cushing disease (high ACTH from pituitary)
Ectopic ACTH production (e.g., from lung tumors)
Adrenal tumors (e.g., cortisol-producing).
2. What are the common symptoms of Cushing syndrome?
Answer:
Moon face
Buffalo hump
Thin extremities
Striae (skin marks)
Acanthosis nigricans
Androgen excess symptoms
Hypertension.
3. What are the 3 screening tests for Cushing syndrome?
Answer:
24-hour urine free cortisol
Nighttime salivary cortisol
Low-dose overnight dexamethasone suppression test.
4. How is Cushing syndrome diagnosed?
Answer:
Cushing’s disease: High ACTH with suppression of cortisol
Ectopic ACTH-producing tumor: High ACTH with no suppression
Adrenal tumors/steroids: Low ACTH with no suppression
Syndrome: Cortisol with no suppression.
5. What imaging is needed for Cushing syndrome?
Answer:
Cushing disease: Pituitary MRI
Adrenal tumors: Abdominal CT
Ectopic ACTH: Chest X-ray (lung tumors).
6. What is the treatment for Cushing syndrome?
Answer:
Resection of the pituitary or adrenal tumors
Gradual tapering of corticosteroid use.
Chronic Adrenal Insufficiency (Addison's Disease)
1. What are the causes of adrenal insufficiency?
Answer:
Primary (Addison's Disease): Autoimmune, tuberculosis, HIV.
Secondary: Due to pituitary dysfunction or steroid use.
2. What are the symptoms of Addison’s disease?
Answer:
Darkened skin
Hypotension
GI symptoms (nausea, vomiting, diarrhea)
Salt craving, low glucose
Amenorrhea in women.
3. What are the diagnostic features of Addison’s disease?
Answer:
Primary: Low cortisol, low aldosterone, high ACTH.
Secondary: Low cortisol, low ACTH.
Screening: High-dose ACTH stimulation test.
First: No cortisol response.
Second: Cortisol response indicates secondary insufficiency.
4. What is the treatment for Addison’s disease?
Answer:
Hydrocortisone (first-line treatment)
Fludrocortisone (if primary Addison's disease)
In times of stress, administer 3x the normal dose
.
Adrenal Crisis
1. What is the most common cause of adrenal crisis?
Answer: Stress events or failure to taper off steroids.
2. What are the symptoms of adrenal crisis?
Answer:
Shock
Hypotension
Hypovolemia
Abdominal pain
Peripheral vascular collapse.
3. What is the treatment for adrenal crisis?
Answer:
Isotonic fluids (e.g., normal saline)
IV hydrocortisone.
Pheochromocytoma
1. What is pheochromocytoma?
Answer: A catecholamine-secreting adrenal tumor that produces norepinephrine, epinephrine, and dopamine.
2. What are the symptoms of pheochromocytoma?
Answer:
Hypertension (most common)
Palpitations
Headache
Excessive sweating.
Chest pain, weight loss, pallor.
3. How is pheochromocytoma diagnosed?
Answer:
Urine tests: High levels of metanephrines and vanillylmandelic acid.
Imaging: MRI/CT of the abdomen and pelvis.
MIBG scanning (for detecting metastatic disease).
4. What is the treatment for pheochromocytoma?
Answer:
Surgical resection (complete adrenalectomy)
Medications: Phenoxybenzamine or phentolamine (alpha-blockers), Beta-blockers or calcium channel blockers for blood pressure control.
Diabetes Insipidus
1. What are the two types of diabetes insipidus?
Answer:
Central DI: No ADH production from the pituitary.
Nephrogenic DI: The kidneys do not respond to ADH.
2. What are the causes of nephrogenic diabetes insipidus?
Answer:
Lithium use is the most common cause.
3. What are the symptoms of diabetes insipidus?
Answer:
Polyuria
Polydipsia
High volume nocturia
Hypernatremia (leading to confusion, lethargy, seizures, and coma).
4. How is diabetes insipidus diagnosed?
Answer:
Serum osmolality: High in DI.
Urine osmolality: Low in DI.
Fluid deprivation test: Low urine osmolality indicates DI.
ADH stimulation test:
Central DI: Responds to ADH.
Nephrogenic DI: Does not respond to ADH.
5. What is the treatment for diabetes insipidus?
Answer:
Central DI: Desmopressin (DDAVP).
Nephrogenic DI: Hydrochlorothiazide, sodium restriction.
Thyroid Storm
1. What is thyroid storm?
Answer: A life-threatening exacerbation of hyperthyroidism.
2. What are the symptoms of thyroid storm?
Answer:
Fever
Cardiovascular dysfunction (e.g., tachycardia, arrhythmias)
CNS dysfunction (e.g., agitation, delirium).
3. How is thyroid storm treated?
Answer:
IV fluids
Beta-blockers (e.g., propranolol)
Antithyroid medications (e.g., PTU)
Sodium iodide for rapid reduction of thyroid hormones.
Steroids to reduce inflammation.
Aspirin should be avoided (can increase thyroid hormone release).
Myxedema Coma
1. What is myxedema coma?
Answer: An extreme form of hypothyroidism, often occurring in elderly patients during winter months.
2. What are the symptoms of myxedema coma?
Answer:
Bradycardia
Hypothermia
Hypotension.
3. How is myxedema coma treated?
Answer:
Levothyroxine (IV)
IV fluids
If adrenal involvement: corticosteroids.