ABIM Endocrinology flashcards
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- A1c diagnostic threshold
- An A1c of 6.5% or higher meets a diabetes diagnostic criterion, but it should be confirmed on a separate sample unless hyperglycemia is unequivocal.
- Euglycemic DKA
- Diabetic ketoacidosis can occur with glucose below 250 mg/dL, especially with SGLT2 inhibitors or pregnancy; diagnosis still requires ketosis and metabolic acidosis.
- Metformin renal precautions
- Do not start metformin when eGFR is below 45 mL/min/1.73 m2; stop it when eGFR falls below 30, and hold it during acute illness or contrast exposure when AKI risk is high.
- SGLT2 inhibitor indications
- In type 2 diabetes with heart failure, chronic kidney disease, or atherosclerotic cardiovascular disease, an SGLT2 inhibitor with proven benefit is recommended independent of A1c and metformin use.
- Hypoglycemia level 2
- Level 2 hypoglycemia is a glucose concentration below 54 mg/dL. It is clinically important because it increases risk of severe events and usually requires immediate carbohydrate treatment.
- HHS diagnostic features
- Hyperosmolar hyperglycemic state shows glucose above 600 mg/dL, effective osmolality above 320 mOsm/kg, minimal ketosis, and often profound dehydration with altered consciousness.
- BMI obesity classes
- Obesity begins at a BMI of 30 kg/m2: class 1 is 30 to 34.9, class 2 is 35 to 39.9, and class 3 is 40 or higher.
- Weight loss threshold
- A 5% to 10% weight loss improves glycemia, blood pressure, and lipids; weight loss of 10% or more can produce remission of type 2 diabetes in some patients.
- Friedewald LDL validity
- The Friedewald equation estimates LDL cholesterol as total cholesterol minus HDL cholesterol minus triglycerides divided by five, and it is unreliable when triglycerides exceed 400 mg/dL.
- Statin intensity
- High-intensity statin therapy lowers LDL cholesterol by at least 50%, whereas moderate-intensity therapy lowers it by 30% to 49%; very-high-risk patients often need additional nonstatin therapy.
- GLP-1 RA contraindication
- Liraglutide and semaglutide are contraindicated in patients with a personal or family history of medullary thyroid carcinoma or multiple endocrine neoplasia type 2.
- Overt hypothyroidism
- Overt hypothyroidism is diagnosed by an elevated TSH with a low free T4. Levothyroxine is indicated, and TSH is rechecked about six to eight weeks after dose changes.
- Subclinical hypothyroidism
- Subclinical hypothyroidism has an elevated TSH with a normal free T4. Treatment is usually considered when TSH exceeds 10 mIU/L, or with symptoms, pregnancy, or cardiovascular risk.
- Thyroid storm treatment
- Thyroid storm is treated with a beta blocker, a thionamide, iodine given after the thionamide, glucocorticoids, and supportive care for fever, dehydration, and arrhythmia.
- Medullary thyroid cancer
- Medullary thyroid carcinoma arises from parafollicular C cells, secretes calcitonin, and is associated with RET mutations and multiple endocrine neoplasia type 2.
- Amiodarone thyroid types
- Amiodarone-associated thyrotoxicosis type 1 is iodine-induced excess synthesis, while type 2 is destructive thyroiditis; type 2 often responds to glucocorticoids rather than antithyroid drugs.
- Adrenal crisis treatment
- Adrenal crisis requires immediate hydrocortisone 100 mg intravenously, followed by about 50 mg every six hours, plus saline and glucose resuscitation; do not delay steroids for testing.
- Primary aldosteronism screen
- Primary aldosteronism is screened with the aldosterone-to-renin ratio in patients with resistant hypertension, hypokalemia, or an adrenal incidentaloma; confirmatory testing follows an elevated ratio.
- Pheochromocytoma biochemical test
- Pheochromocytoma is best screened with plasma free metanephrines or 24-hour urine fractionated metanephrines; alpha blockade must precede beta blockade to avoid unopposed vasoconstriction.
- Cushing screening tests
- Cushing syndrome screening uses a 1 mg overnight dexamethasone suppression test, late-night salivary cortisol, or 24-hour urinary free cortisol; abnormal results require confirmatory and subtype testing.
- Pituitary apoplexy
- Pituitary apoplexy causes sudden headache, visual loss, ophthalmoplegia, and hypotension from acute pituitary hemorrhage or infarction; urgent glucocorticoids and neurosurgical evaluation are required.
- PCOS Rotterdam criteria
- PCOS requires two of three findings: oligo-ovulation or anovulation, clinical or biochemical hyperandrogenism, and polycystic ovaries, after excluding thyroid, prolactin, and adrenal disorders.
- Menopause diagnosis
- Menopause is diagnosed clinically after 12 months of amenorrhea in a woman over 45; FSH is high and estradiol low, but testing is not required when symptoms are typical.
- Male hypogonadism diagnosis
- Male hypogonadism requires low morning total testosterone on at least two occasions; LH and FSH distinguish primary testicular failure from secondary hypothalamic-pituitary failure.
- Klinefelter syndrome
- Klinefelter syndrome is 47,XXY and causes small firm testes, gynecomastia, infertility, elevated gonadotropins, and often low testosterone; testosterone replacement supports virilization and bone health.
- Letrozole ovulation induction
- Letrozole is first-line ovulation induction for anovulatory PCOS and often produces higher live-birth rates than clomiphene; it is also used in unexplained infertility.
- Corrected calcium formula
- Corrected calcium equals measured calcium plus 0.8 times (4.0 minus albumin in g/dL); this adjustment estimates calcium when albumin is low but is less reliable in critical illness.
- Primary hyperparathyroidism
- Primary hyperparathyroidism shows high or inappropriately normal PTH with hypercalcemia and usually low phosphate; surgery is indicated for symptoms, young age, marked hypercalcemia, kidney stones, or osteoporosis.
- Hypercalcemia of malignancy
- Malignancy-associated hypercalcemia usually has a suppressed PTH; PTHrP mediates many solid tumors, while myeloma and lymphoma may cause hypercalcemia through other mechanisms.
- Osteoporosis T-score
- Osteoporosis is defined by a DXA T-score of -2.5 or lower at the hip or spine; a T-score between -1.0 and -2.5 defines osteopenia or low bone mass.
- Denosumab discontinuation
- Stopping denosumab without a follow-on antiresorptive can cause rapid rebound bone loss and vertebral fractures; transition to a bisphosphonate or continue therapy is often needed.
- Paget disease features
- Paget disease of bone causes elevated alkaline phosphatase, bone pain, deformity, skull enlargement, and hearing loss; bisphosphonates are used for symptoms and complications.