Endocrinology Flashcards

1
Q

What are the causes of hypothyroidism?

A

Hashimoto’s (elevated anti-TPO), iodine deficiency, amiodarone, lithium, 2nd phase of thyroiditis.

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2
Q

How is thyroxine dosed?

A

Full: 1.6micro/kg, partial: 25-50microg daily. Recheck 4-8 weekly. Aim 0.5-2.5 in most, more lax in elderly. High dose risks loss of bone mass, AF, cardiac ischaemia.

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3
Q

How is thyroxine taken?

A

Stored in fridge, empty stomach 30-60min before food or 2h post. Calcium, iron and bile resin interfere w absorption.

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4
Q

What are 3 thyroid antibodies and when are they used?

A

Anti-TPO present in most cases of hashimoto’s. Anti-thyroglobulin used in post cancer followup, can be in normal people. TSH receptor antibodies in graves disease (can have graves without it).

Thyroid stimulating immunoglobulin seen in graves

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5
Q

How is subclinical hypothyroidism managed?

A

Try treating if symptomatic. If TSH >10, repeat in 4-8 weeks. If TSH < 10 retest, check TPO and monitor 6-12mo.

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6
Q

What are the causes of hyperthyroidism?

A

Graves disease (diffuse goitre), toxic multinodular goitre or adenoma, painless post partum thyroiditis, painful subacute thyroiditis (post URTI), amiodarone use, factitious ingestion

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7
Q

What tests are indicated for hyperthyroidism?

A

TSH R ab and thyroid stimulating immunoglobulin for graves. If not obvious graves, do scintigraphy with tech-99 (C/I in pregnancy), for nodules/adenoma or diffuse uptake.

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8
Q

How is hyperthyroidism managed? Options, risks.

A

Endo review. Carbimazole + PTU for graves, adenoma. Risk agranulocytosis, PTU can affect liver. Use T3/4 to monitor. Symptom treatment: beta blockers for thyroiditis and may need thyroxine later. Iodine/surgery for severe/recurrent, MNG, cancer.

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9
Q

What is the workup for a thyroid nodule?

A

TSH first. If hypo, treat w thyroxine as may regress. If normal, do U/S for cancer. If hyper, do scintigraphy to see if hot nodule or graves or cold which needs U/S. Check lymph nodes and Fhx, U/S features guide F/U and aspiration.

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10
Q

How is hypo/hyperthyroidism managed in pregnancy?

A

Hypo risks miscarriage, low weight, neurodevelopment. Lower target TSH, increase thyroxine 25-30% at 6/40, monitor 4-6 weekly. If new hypo, refer and may need urgent treatment. Hyper generally ok -bHCG stimulates TSH receptor, treat if graves or severe.

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11
Q

What are general and medical risk factors for osteoporosis?

A

Smoking, alcohol, Fhx, Vit D deficiency, low calcium intake, sedentary lifestyle, early menopause, late menarche. Hyperthyroid, hyperparathyroid, RA, coeliac, CKD, liver disease, Diabetes, steroids (7.5mg 3mo), excess thyroxine, antiandrogens.

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12
Q

How is osteoporosis diagnosed? When is medication indicated?

A

T score < -2.5 (compared to healthy 30yo) OR >50yo with min trauma hip/vertebral fracture; OR 50yo min trauma fracture w T score <-1.5. OR 10 year risk of fracture elevated.

<-1.0 is osteopaenia

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13
Q

What is the non-pharm management of osteoporosis?

A

Falls risk and reduction strategies, Vit D if low or risk, 1300mg Ca daily (500-600mg supplement is diet poor), weight bearing impact loading exercise, balance training, avoid twisting if vertebral. Aim BMI 18-25.

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14
Q

How is prolia used in osteoporosis?

A

Denosumab 6mo injection, if missed risk spontaneous vertebral fracture. Check Vit D, Ca and CrCl >30 before 1st/every dose, risk hypocalcaemia. Increase turnover when stopped, can swap to alendronate if stopping.

Use >10y hasn’t been studied. Small risk of ONJ

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15
Q

How are bisphosphonates used in osteoporosis?

A

Effects persist, avoid GFR < 35. Alendroate daily/weekly, risedronate weekly/monthly oral, empty stomach, use 5y min. Zoledronic acid IV yearly, use 3y min. Double use if high risk (>75, hip/spine fractures, fracture on treatment)

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16
Q

What are the side effects of bisphosphonates? What are 2nd line options?

A

Oral: upper GI irritation (GORD, PUD), affected by Ca, iron. Zoledronic acid: transient flu like symptoms, uveitis, hypocalcaemia. Long term: ONJ, atypical femur fracture. ONJ rare, dental review before starting, usually safe in first 6mo. 2nd line: raloxifene (SERM), tibolone, HRT.

17
Q

What is addison’s disease - symptoms, diagnosis.

A

Adrenal insufficiency - fatigue, weight loss, postural hypotension. High K, low Na. Hyperpigmentation, vitilgo, hair loss. Short synacthen test (also low serum/urinary cortisol)

18
Q

How is addison’s disease managed? What are the risks?

A

Endo - steroids. Adrenal crisis needs IV fluid + 100mg hydrocort or 40mg pred. Have emergency bracelet, increase steroids when sick, steroid script for travel.

19
Q

What are the causes of cushings syndrome? What tests are indicated?

A

Steroids, pituitary ACTH excess, adrenal hyperplasia or tumour, ectopic ACTH production (eg. lung). 1mg dex suppression test or midnight salivary cortisol w sponge, no food/stress 60minprior (twice) or 24hr urine cortisol (twice).

20
Q

Conn’s syndrome - features, test

A

Hypertension, weakness, polyuria, low potassium. High aldosterone to renin ratio. Conn’s from adenoma, otherwise bilateral hyperplasia can mimic.

21
Q

What is the workup for an adrenal mass?

A

Dedicated CT best. Test for activity: dex suppression test (cushings), 24hr urine metanephrines + catecholamines (phaeo), aldosterone renin ratio if hypertensive. If >4cm or symptomatic/diseased, consider surgery.

22
Q

What medications are required after weight loss surgery? How is diabetes tested for?

A

Multivitamin, ca, vitamin D. Avoid NSAIDs. Can’t do OGTT due to risk of dumping syndrome.

23
Q

Symptoms and causes of prolactinaemia

A

Menstrual irregularity, infertility, galactorrhoea, erectile dysfunction, reduced libido. Causes: prolactinoma, pregnancy, hypothyroidism, surgery, drugs - cannabis, OCP, antipsychotis, metoclopramide.

24
Q

What is the management of prolactinaemia?

A

If tumour >10mm can cause headache/vision change. Dopamine agonist: Cabergoline helps for function and size, 2nd line bromocriptine. OCP for galactorrhoea. Surgery/radiotherapy if large or not responding.

25
Q

Symptoms and causes of male androgen deficiency

A

Sx: low libido, less face hair, gynaecomastia, fatigue, reduced muscle bulk, small testes. Primary (high FSH/LH): klinefelter (XXY), cryptoorchidism, trauma, radiaiton/toxin to testes. Secondary/central: pituitary tumour, pituitary surgery/radiotherapy, haemochromatosis, GnRH analgoues, exogenous androgens, systemic illness.

26
Q

What are 2 disorders of ADH? Causes and treatment

A

Diabetes insipidus - post operative (common),tumour, infection. Desmopressin. SIADH - cancer, intracranial lesion, antipsychotics. Fluid restrict, treat cause.

27
Q

Carcinoid and acromegaly - features, test.

A

Flushing, diarrhoea, valve disease, telangiectasia. 24h urine 5-HIAA. A: frontal bossing, HTN, diabetes,OSA. IGF-1 for screening.

28
Q

Hyperparathyroidism - features, cause and management.

A

Commonest cause of high calcium, usually from a single adenoma. Need surgery. Monitor if >50, Asx, no stones or renal impairment, Ca < 2.90, no osteoporosis. Avoid VitD/Ca supplement, water.