Diabetes and Pituitary Flashcards

1
Q

Cause of T1DDM?

A

pancreatic islet beta-cells desstroyed by autoimmmune

ABSOLUTE insulin sinsufficiency -> lipolysis and ketogenesis

Associated with HLADR3/4

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2
Q

Cause of T2DM?

A

Obesity, HTN, inactivity, and disturbed lipids

Reduced peripheral sensitivty to insulin and reduced insulin production over time

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3
Q

T1DM presentation?

A

5-15YO
Polyuria and polydipsia (osmotic diuresis)
Weight loss from muscle and fat breakdown

DKA: abdo pain, N&V, tachypnoea (kussmaul), coma

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4
Q

T2DM presentation?

A

Asymptomatic
RFs present, obesity, Fhx, south asian, black, age,

Fatigue, poludipsia, polyria, infections e.g. fungal, cellulitis
Acanthosis nigricans

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5
Q

Which patients should HbA1c not be used in?

A

All children/young, high risk of acutely ill, medication that can rise glucose e.g. steroids, antipsychotis, acute pancreatic damage patients

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6
Q

T1DM management?

A

Basal bolus insulin

Long = glargine subcut OD)
Short = lispro/aspart subcut pre meal
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7
Q

T2DM glycaemic Mx?

A

1) Metformin if HbA1c >48
2) Add another drug (Dpp4i, pioglitazone, SU, SGLT-2i)
3) Add further drug

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8
Q

T2DM lipid Mx?

A

Atorvastatin 20mg OD if 10year CV>10%

80mg if IHD/CVD/peripheral arter disease

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9
Q

T2DM BP Mx?

A

1)ACEi or ARB
2) Add CCB or thiazide
3) Add ccb or thiazide
4) if K+>4,5, spironolactone
if less then alpha blocker/beta blocker

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10
Q

Example of each glycaemic medication?

A

DPP4i = sitagliptin
Pioglitazone
Sulfonylurea = glicazide
SGLT = dapaglifozin

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11
Q

Platelet Mx for T2DM?

A

Aspiring 75mg for patients with IHD/CVD/perpheral artery disease

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12
Q

what are the micro/macro complications of DM?

A

Micro = retinopathy, nephropathy, neuropathy

Macro = IHD, Cerebrovascular disease, peripheral artery disease

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13
Q

Causes of hypoglycaemia?

A

Missed meals, inadequate snacks, unaccustomed exercise, alcohol, some drugs e.g. SU, SGLT2, inappropriate insulin regime

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14
Q

Signs of hypoglycaemia?

A

Palpitations, tremor, seating, pallor, anxiety, drowsiness, confusion, altered behaviour, coma

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15
Q

Tx for hypoglycaemia?

A

Conscious = oral glucose and complex carborhydrates

Impaired = PArenteral 1mgglucagon IM
2nd line = IV dextrose (10% glucosie infusion)

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16
Q

DKA triad?

A

Hyperglyaemia, ketonaemia and metabolic acidosis

Also dehydration

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17
Q

S+S and Ix DKA?

A

Collapse and confusion, dehyrated, kussmaul breathing, abdo pain, N+V

Ketones >3mmol?l, pH <7.3 (high anion gap metabolic acidosis, plasma glucose >11

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18
Q

Mx of DKA?

A

Fluids started (normal saline unless K+ <5.5. then potassium chloride)
IV insulin after fluids
Include dextrose
Treat underlying cause

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19
Q

Breakdown of diabetic retinopathy?

A

Background = blot and dot haemorrhages/hard exudates

Pre-proliferative = background + cotton wool spots

Proliferative = pre-proliferative + new vessels on disk (neovascularization)

maculopathy = Previous + hard exudates near macula

20
Q

Mx of diabetic retinopathy?

A

background = improve glycaemic control

Pre and proliferative = pan-retinal photocagulation

Maculopathy = grid of photocoagulation

21
Q

What is neovascularization associated with?

A

Retinal detachment and vitreous haemorrhage -> visual loss

22
Q

Diabetic nephropathy features and Ix?

A

Albuminuria, reduction of eGFR, associated with retinopathy

1) urinarlysis and eGFR
Biopsy gold standard and show Kimmelstiel-wilson nodules (mesangiel expansion)

23
Q

Mx for diabetic nephropathy?

A

Improve glycaemic control and ACEi/ARB

24
Q

Breakdown of diabetic neuropathy?

A

Caused by blockage of vasa nervorum

Perpheral neuropathy = loss of sensation (feet) and may not sense injury. Monofilament exam and loss of anklejerk/vibration/fractures (charcots joint)

Mononeuropathy = sudden motor loss usually e.g. wrist drp, foot drop, 3rd nerve palsy (down and out)

Autonomic neuropathy = dysphagia, delayed gastric empyting, bladder dysfunction, postural hypotension and cardiac autonomic supply

25
Mx of diabetic neuropathy?
Glycaemic control, if painful then neuropathic pain agent e.g. duloxetine, pregabalin or gabapentin
26
Causes of cranial DI?
pituitary tumour/surgery, TBI, infection e.g. meningitis, sarcoidosis, SAH
27
Causes of nephrogenic DI?
Lithium therapy, electrolyte imbalance e.g. Increase ca, decreased K, idiopahic, ureteric obstruction , Inherited AVPV2 gene
28
DI presentation?
polyuria and nocturia, polydipsia, dehydration so tachycardia, reduced tissue turgor, dry mucous membranes Cause e.g. bitemporal hemianopia
29
IX for DI?
General = U&Es, Na but increased urea, glucose to exclude DM Water deprivation test with desmopressin is diagnostic
30
Mx for DI?
1) treat the cause 2) Crnial = intranasal desmopressin (less water) 3) nephrogenic = thiazide diurteic or NSAIDs (these inhibit prostaglandin and prostaglandin inhibits AHD)
31
Causes of SIADH?
``` CNS = SAH, stroke, tumour, TBI Pulmonary = pneumonia, bronchietasis Malignancy = Small cell lung cancer Drugs = carbamazepine, SSRI Idiopathic ```
32
Features of SIADH?
expansion of ECF volume, decreased plasma osmolality and hyponatraemia, concentrated urine and increased Na excretion
33
Mx for SIADH?
Treat the cause Immediate fluid resus for hyponatraemia oral demeclocyline or IV vaptans
34
Features of volume statuses with hyponatraemia?
Hypovolaemic = tachy, reduced skin turgor, dry, low bp, postural hypotension and urine sodium low Euvolaemic = normal or cause Hypervolaemia = peripheral oedema, bibasal crackles and raised JVP
35
Causes of each volume status with hyponatraemia?
Hypo = vomiting/diarrhoea + diuretics ``` Eu = Hypothrypid (TFTs) Adrenal insufficiency (short synacthen)or SIADH (decreased plasma and increased urine osmolality ``` hyper = heart failure, cirrhosis of nephrotic syndrome
36
Mx for volume statues>
Hypo = volume replacement with 0.9% saline Other two si fluid restriction and treat underlying cause
37
What do rapid Na+ changes cause?
if seizing/reduced GCS + hyponatraemic = give hypertonic 3% saline Usually slow changes to prevent central pontine myelinlysis = quadriplegia, pseudobulbar palsy, seizures, coma and death
38
Causes of hypernatraemia?
GI losses and sweat loss, rena losses such as osmotic diuresis (HHS) or DKI Sodium Overload in Cushings, primary aldosteronism, iatrogenic
39
Mx of hypernatraemia?
Correct water deficit - 5% dectrose Correct ECF volume - 0.9% saline Measure Na every 4-6 hours
40
Examples of pituitary adenomas?
Acromegaly (GH secreting) Prolactinoma Cusings
41
Causes of hyperprolactinaemia?
Pregnancy and breast feeding Prolactinoma or other pituitary adenoma (stalk compression), oprimary hypothyroidism High prolactin suppresses GnRH pulsatility
42
S+S of hyperprolactinaemia?
Men = libido loss, erectile dysfunction, infertility, rare galactorrhoea Women = galactorrhoea, secondary amenorrhoea/oligomenorrhoea, libido loss, infertilyi Mass effect = heachache/visual field deficit
43
Ix for hyperprolactinaemia>
Pregancy test TFTs Basal serum prolactin (if >60000mU/L) = prolactinma MRI
44
Prolactinoma Mx.
Dopamine agonists e.g. oral bromocriptine and cabergoline
45
what is a hyperosmolar hyperglycaemic state (HHS)
hyperglycaemia but no ketonaemia so same presentation as DKA bar abdo pain as no ketonaemia