Endocrine Flashcards

(53 cards)

1
Q

What is the proposed mechanism for PU/PD in feline hyperthyroidism?

A

Altered renal blood flow
Electrolyte abnormalities
Thyroid hormone excess causing primary polydipsia
Concurrent renal dz?

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2
Q

Methimazole/carbimazole toxicity

A

Vomiting
Pruritis
Peripheral LN enlargement
Lymphocytosis, eosinophilia, leukopaenia, <5% agranulocytosis, thrombocytopaenia, IMHA
Hepatic toxicity
Increase in ANAs, acquired MG, coagulopathy with normal platelet count

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3
Q

Prognosis hyperthyroidism

Medical management vs I131 tx

A

MST 2 years vs 2-4 years

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4
Q

Gold standard test for hypothyroidism

A

TSH response test

No recombinant canine TSH available so have to use human

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5
Q

Hypothyroidism clinical signs

A

Lethargy
Weight gain
Bradycardia, May worsen DCM
Skin/ coat changes most common (recurrent OE, malassezia, symmetrical slope is)
Reproductive problems
Neurological (diffuse neuropathy, laryngeal paralysis and megaoesophagus - often do not resolve on tx and may be assoc with more generalise myopathy/m.gravis
Dry eye
Lipidosis corneal and retina
Corneal ulceration, uveitis and 2ndary glaucoma
Assoc with Cushings, DM and Addison’s

Congenital: disproportionate growth and puppy coat. Mental retardation

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6
Q

Calcitonin actions

A

Limits post-prandial hypercalcaemia

Primarily inhibits osteoclasts activity

High doses promote urinary calcium excretion

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7
Q

Calcitriol actions

A

G-I calcium and phosphorous absorption
Tubular calcium and phosphorous reabsorption
Inhibits further calcitriol production in the kidney
Inhibits PTH

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8
Q

When to use bicarbonate in DKA cases

A

When pH is less than 7.2 and HCO3 is <12mmol/l despite aggressive fluid therapy and insulin admin
MEq = BW (kg) x 0.4 x (12-HCO3) x 0.5
Five slowly over 6h then check again

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9
Q

Insulin tx in DKA i/m route

A

0.2mg/kg im once
Continue with 0.1mg/kg im every hour
When bg < 15mmol/l give 0.1mg/kg im q 4 hourly in order to maintain bg stable and avoid hypos
Switch to longer acting when patient stable bright and eating

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10
Q

Insulin for DKA I/v protocol

A

Prepare 2.2mg/kg soluble insulin in 250mls NaCl 0.9%
Discharge 50ml of this to allow insulin binding to the giving set tubing
Administer solution at 10ml/hr until until Bg <15 then 7ml/hr until bg < 12 then 2-5ml/hr to maintain stable bg

Switch to longer acting when patient stable and eating

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11
Q

Hypoglycaemia Ddx

A
Lab error
Insulinoma
Addison’s
Sepsis
Tumours (hepatocellular carcinoma, mammary carcinoma, haemangiosarc etc)
End stage hepatic failure
PSS
Toy breed and neonate hypoglycaemia
Glycogen storage dz
Excessive exercise
Starvation
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12
Q

Hypoglycaemic crisis - what to do?

A

Glucose 0.5g/kg IV diluted 1:3 in saline as a slow iv bolus
Continue with CRI or 2.5-5% glucose saline
(Always start low as insulinomad retain the ability to secrete more insulin in response to glucose)
Monitor for hypoxia, cerebral oedema, hyperthermia, lung atelectasis from prolonged recumbency

If failing to respond administer dexamethasone 0.1mg/kg IV

May need sedation w diazepam/pentobarbital in severe cases

In one study a dog was treated with a glucagon CRI and signs resolved in 20mins

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13
Q

Insulinoma medical tx

A

Prednisolone (start low and work up)
Diazoxide (benzothiazine derivative inhibits insulin secretion and gluconeogenesis) (70% success)
Ocreotide (long acting somatostatin analogue - also inhibits GH and glucagon so can worsen hypoglycaemia)
Streptozocin (nitrosurea antibiotic - toxic to pancreas and metastatic sites but highly nephrotoxic - MSTs similar to controls)

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14
Q

Insulinoma prognosis

A

785d surgery alone (stage I, stage II 547 and III 217d)
1316d partial pancreatectomy abd preds
12-14months with young dogs having a worse prognosis and clinical stage I having a longer dz-free interval

Stage I - just pancreas
II - pancreas plus node
iii - pancreas plus node and mets (or without node)

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15
Q

Where do insulinomas metastasise to?

A

Mainly liver, spleen and regional LNs

Rarely lungs

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16
Q

Insulinoma diagnosis

A

Low glucose with a high or normal insulin
Need abdo ultrasound may see mass but can be nodular
CT may see pancreatic mass (MRI same as CT)
Do 3 view thoracic rads to check for mets

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17
Q

Why do we get hepatomegaly and raised liver enzymes with diabetes mellitus?

A

Hepatic lipidosis

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18
Q

Supplementation if fluids in DKA

A

Potassium
Phosphorous if low (can cause haemolysis) - half of potassium can be given as potassium phosphate
Magnesium
Possibly bicarbonate but unlikely

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19
Q

Treatment of acromegaly

A

Radiotherapy
Transphenoidal hypophysectomy
Ocreotide (somatostatin analogue) - moderately successful in cats
Long acting insulin with short acting insulin around meal times for insulin resistant DM

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20
Q

Diagnosis of acromegaly

A

CT showing pituitary mass

High ilgf-1 can support a diagnosis

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21
Q

Causes of central diabetes insipidus

A
Intracranial tumours
Metastatic neoplasia
Inflammatory dz
Parasites
Pituitary surgery
Severe head trauma
Idiopathic (rare)
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22
Q

Causes of acquired nephrogenic diabetes insipidus

And pathophysiology of these

A

Metabolic (hypokalaemia - downregulates aquaporin 2), hypercalcaemia)
Drugs (lithium, chemotherapy)
Urethral obstruction
Kidney failure
Paraneoplastic syndrome (only leiomyosarcoma)

Hyperthyroidism - increased blood flow to kidney
Pyelonephritis
Addison’s - sodium depleted so can’t generate concentrated renal medullary interstitium
Liver failure - reduced urea
Pyometra
Cushings - reduced release and Action of ADH
Acromegaly - DM or glomerulopathy
Hypercalcaemia - interferes with proper functioning of renal tubular cells that normally respond to ADH

23
Q

When to stop phase 2 of a water deprivation test

A

If the patient is

  • dull or clinically dehydrated
  • has lost >5% BW
  • is azotaemic
  • is hypernatraemic
  • USG >1.030

Then obtain urine, bloods, measure USG and urine osmolality

24
Q

Phase 1 of modified water deprivation test

A

Determine water intake at home
Gradually decrease water intake at home over 3-5 days until having 100mlKg/day or becoming lethargic or aggressively seeking water
Divide daily water portions into multiple small portions
Withhold food for 12 hours before phase 2

25
Phase 2 of the MWDT
Withhold food and water, empty bladder, check USG and urine osmolality, weigh patient, check BUN/crea and electrolytes Check clinical signs, weigh and check urine every 1-2 hours Bloods every 2-6 hours
26
Phase 3 MWDT
Administer exogenous ADH if Urine has not yet concentrated IM - monitor USG every 30 mins for up to two hours Conjunctival - monitor every 1-2 hours for 8-12 hours SQ - every 1-2 hours for 8-12 hours
27
Phase four MDWT
Offer small amounts of food and water every 20-30 mins for 2 hours Monitor signs and return to free choice water when patient clinically normal
28
Interpretation of MDWT
USG >1.030 after phase 1 or 2= primary polydipsia <1.008 after phase 2 = complete CDI or congenital NDI USG after phase 3 >1.015 = CDI <1.008 after phase 3 = congenital NDI USG 1.008-1.020 after phase 2 = acquired NDI or partial CDI progress to phase three and if osmolality increases by 10-15% = CDI Osmolality = 36 x USG (1.010 = 360)
29
Treatment of diabetes insipidus
One drop DDAVP in conjunctival sac If NDI - hydrochlorthiazide and low sodium diet (reduced stimulation of thirst centre and water intake - reducing urine volume)
30
DDx PUPD
``` Central DI/ nephrogenic DI renal failure Cushings Addison’s Liver failure Hypercalcaemia Pyometra Septicaemia Hypercalcaemia Hyperthyroidism Hypokalaemia Acromegaly Very low protein diet Primary hyperaldosteronism fanconis syndrome Primary renal glycosuria Diabetes mellitus Post-obstructive diuresis Glucocorticoids Diuretics Phenobarbitone High salt diet Levothyroxine Vitamin D Primary polydipsia Renal medullary washout Bacterial pyelonephritis ```
31
Osmotic diuresis causes of PUPD
``` DM Fanconis Primary renal glucosuria Renal failure Post obstructive diuresis ```
32
DDx hypercalcaemia
``` Primary hyperparathyroidism Renal secondary hyperparathyroidism Nutritional secondary hyperparathyroidism Vitamin D toxicity Malignancy (lymphoma, AGA, myeloma) Addison’s Young growing animal Granulomatous dz Non-malignant skeletal dz Lab error (Hyperalbuminaemia) Hyperthyroidism Grape toxicity ```
33
Treatment of primary polydipsia
Reduce water intake by 10% each week Increase exercise, add another pet, increase human contact, provide a distraction eg radio
34
Most common cause of feline hypercortisolism (Cushings)
Pituitary corticotropin secreting tumour (80%) Rest are cortisol secreting adrenal tumours (50% malignant)
35
Preferred tests for Cushings in cats
LDDST | UCCR
36
Treatment of feline primary hyperaldosteronism
Adrenalectomy Medical management: Potassium gluconate Spironolactone Amlodipine
37
Treatment of pituitary dwarfism
Porcine growth hormone injections Medroxyprogesterone acetate to stimulate mammary GH production as well as proligestone (should spay before to prevent pyometra) If concurrent hypothyroidism May need levothyroxine
38
Hypocalcaemia clinical signs
Tetany, seizures, tremors, fasciculations, weakness/ataxia(less common), Earlier signs: facial pawing, anxiety, aggression due to muscle pain, Cataracts: immature, cortical, punctate and diffuse (characteristic of hypoparathyroidism hypocalcaemia)
39
Treatment of hypoparathyroidism
Calcium and vitamin D supplement (needed for GI absorption Ca) Can eventually stop calcium and only give vitamin D (calcitriol and alfacidiol as these are hydroxylated forms) In emergency iv calcium gluconate 0.5-1.5mlKg IV over 10-30 minutes. Must monitor ECG for bradycardia, shortened QT interval. Risk for cardiac arrest. If vomiting stop or slow infusion Maintenance 60-90mg/kg/day do not add to lactate containing fluids as it can precipitate and don’t mix calcium and bicarbonate Can give calcium gluconate 1:1 w saline s/c q6-8 hours too after tetany has resolved and this may be easier whilst awaiting oral vitamin D to take effect Should check magnesium levels because if low hypocalcaemia can be refractory to tx
40
DDx for Na:K < 27
``` Renal/ urinary Tract dz Addison’s Severe GI disease Parasites Hepatic failure Effusions Pregnancy DM Drug induced Other - repercussion injury/haemolysis ``` If <24 highly specific for Addison’s
41
Tx acute Addisonian crisis
Fluids 20-30ml/kg/hr saline Give Dex if in shock Perform ACTH stim If not yet had dex now give dex or hydrocortisone Once fluid balance improved give hyrocortisone sodium succinate (dex has no mineralocorticoid activity) 0.5-0.625mg/kg/h CRI If acidotic and PH <7.2 May require bicarbonate
42
Tx of hyperkalaemia in acute addisonian crisis
Most important tx is IV fluids Glucose IV 0.2iu/kg soluble insulin IV and dextrose 2g/unit of insulin (always measure BG after administration) Calcium gluconate 10% slowly IV monitoring ECG
43
Prognosis of hyperaldosteronism (Conns)
Medical tx - 7 months - 984 days Post-adrenalectomy - good 50% Alive one year post-op but surgical mortality is high Protracted survival post-op if tumour is a carcinoma cf Adenoma
44
Best test for discriminating PDH from ADH (cushings) in cats
Measure ACTH levels - very sensitive and specific but difficult to do Better than high dose dex
45
Differences between canine and feline HAC
Cats don’t have low urine specific gravity despite PU/PD ALP is often low
46
Clinical signs of hypercalcaemia
``` PUPD Anorexia Dehydration Lethargy Weakness Vomiting Pre-renal azotaemia Chronic renal failure (mineralisation likely if phos x tCa = > 5) ``` ``` Constipation Cardiac arrhythmia Seizures or twitching Death Acute renal failure Calcium urolithiasis ```
47
Treatment of hypercalcaemia in an emergency
``` Saline 3x maintenance Furosemide once rehydrated Calcitonin (acts for around two days) Bisphosphonates Glucocorticoids (once diagnosis is reached) Bicarbonate if acidotic ``` If idiopathic often responds to high fibre diet +/- steroids
48
Hypocalcaemia DDx
Parathyroid disorders: Primary hypoparathyroidism Or secondary to trauma/surgery Vitamin D disorders: Acute/chronic renal, Nutritional secondary hyperparathyroidism ``` Redistribution disorders: Puerperal tetany (eclampsia) Feline urt obstruction Sodium phosphate enemas Alkalinizing therapy Massive blood transfusion (excess of citrate products) Furosemide Ethylene glycol intoxication Pancreatitis ``` Acute renal failure - massive increase in phosphate lowering calcium
49
Side effects of bisphosphonates
``` Nausea Vomiting Reflux and oesophagitis Abdominal pain Dyspesia Hypocalcaemia Hypophosphataemia Hypomagnesaemia Hypokalaemia Cost and availability ```
50
Thyroid carcinoma complications and MSTs
Megaoesophagus, laryngeal paralysis, haemorrhage, horners syndrome MST 3 years if mobile and 6-12 months if fixed
51
When to use chemo for thyroid carcinoma
Animals with documented mets or tumours greater than 27cm^3
52
What level are fructosamines if there is a somogyi effect
They are usually high
53
Complications with surgical treatment of insulinoma
Pancreatitis, thromboembolic dz and arrhythmias