General, Urology, Gynae Flashcards

1
Q

What are the types of bariatric surgery?

A

Restrictive eg sleeve gastrectomy or malabsorptive eg roux-en Y bypass

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2
Q

What is the adrenal medulla?

A
  • Modified sympathetic ganglion
  • 90% adrenaline secreting
  • 10% noradrenaline secreting
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3
Q

What is the adrenal cortex?

A
  • Produces cholesterol derived hormones
  • Glucocoriticoid
  • Mineralocorticoid
  • Androgens
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4
Q

What is Conn’s syndrome?

A
  • Hyperaldosteronism
  • 60% is due to excess secretion from an adenoma, 30% is due to bilateral adrenal hyperplasia and carcinoma is rare
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5
Q

How does Conn’s syndrome present?

A
  • Hypertension and fluid overload
  • Refractory hypokalaemia (Aldosterone saves water via Na reabsorption at expense of K)
  • Metabolic alkalosis (aldosterone also exchanges Na for H)
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6
Q

What is the anaesthetic management for Conn’s syndrome and adrenalectomy?

A
  • Correct hypokalameia and metabolic alkalosis pre op (usually achieved via spironolactone)
  • Manage Analgesia as large incision
  • manage haemodynamic instability due to adrenal handling
  • Consider steroid replacement
  • Careful positioning as prone and often jackknife
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7
Q

What is cushing’s syndrome and how does it present?

A

Excess glucocorticosteroid
- Can be endogenous eg Ant pituitary adenoma which is most common (increased ACTH) or adrenal adenoma/carcinoma (20-30%)
- presents with moon face, proximal muscle wasting, hypertension, LVH and osteoperosis

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8
Q

What are the anaesthetic issues with cushing’s syndrome?

A
  • Poorly controlled hypertension, assess for end organ injury eg IHD
  • Obestiy and metabolic changes such as OSA risk, impaired glucose tolerance and reflux
  • Careful positioning as fragile skin and osteoperosis
  • May need stress dosing of steroids
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9
Q

What is addisons disease and how does it present?

A
  • Decreased or absent secretion of glucocoritcoids, usually associated deficiency in mineralocorticoid activity
  • 80% is autoimmune mediated destruction of adrenal cortex, less common includes TB, bilateral adrenalectomy
  • Sx include abdo pain, vomiting, dehydration and hypotension
  • Also have hypoglycaemia, hyponatraemia and hyPER kalaemia
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10
Q

What are the issues with addison’s disease?

A
  • Need steroid replacement, in a crisis needs 200mg IV hydrocort, fluid resus and then 100mg Q6H post op
  • Need to check electrolytes
  • Needs stress dosing at induction regardless of if in a crisis
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11
Q

What is a pheochromocytoma

A
  • Catecholamine secreting tumours of the adrenal medulla
  • ~25% are extra-adrenal
  • ~25% are malignant
  • produce a variable amount of noradrenaline, adrenaline and dopamine (rarely)
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12
Q

How do you diagnose pheochromocytoma?

A

measuring urine or plasma metanephrines (metabolites of adrenaline and noradrenaline)

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13
Q

What are the preoperative goals for a patient with a pheochromocytoma

A

○ Arterial blood pressure control
○ Reversal of chronic circulating volume depletion
○ Heart rate and arrhythmia control
○ Assessment and optimization of myocardial function
○Reversal of glucose and electrolyte disturbances

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14
Q

How to do you manage BP and volume in a pre op pheochromocytoma?

A
  • Pre-operative alpha blockade to control blood pressure as well as normalise the circulating blood volume
  • Opposes the alpha 1 vasoconstriction action of noradrenaline and adrenaline
    ○ Phenoxybenzamine:
    Non-selective, non competitive long acting alpha blocker
    Should be stopped 24-48hrs before surgery due to its long half life (and risk of post op hypotension)
    Started 1-2 weeks prior to surgery
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15
Q

How do you know a preop pheo has adequate blockade?

A
  • Blockade adequacy assessed by Roizen criteria (1982):
    ○ BP <160/90
    ○ Orthostatic hypotension (15% drop standing/lying) but not less than 80mmhg
    ○ ECG free of ST or T wave changes for 2 weeks

Although current BP aims are tighter than this (~<130 sys), resting HR 60-70

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16
Q

How do you manage tachyarrhythmias preop in pheo?

A

Therefore prefer to start beta 1 selective antagonists (atenolol, metoprolol) BUT only after complete alpha blockade Otherwise have risk of unopposed alpha mediated vasoconstriction

17
Q

What common comorbidites are there with pheo?

A

Cardiomyopathies are common
○ Hypertrophic most common
IHD

18
Q

What drugs do you avoid in pheo?

A

○ Avoid drugs that cause catecholamine release
- Ketamine
- Morphine
- Atracurium
- Ephedrine
- Droperidol

19
Q

What drugs do you use to manage BP in pheo?

A

□ Phentolamine (reversible non selective alpha receptor antagonist), 1-2mg boluses
□ GTN, 10-200mcg/min infusion

○ Hypotension post tumour vascularisation:
§ Fluid boluses
§ Titration down of vasodilators
§ Direct alpha agonists
§ Noradrenaline

20
Q

What are post op considerations for a pheo?

A
  • Require ongoing invasive blood pressure monitoring for 24hrs post op
  • steroid replacement if bilateral adrenalectom
21
Q

What are carcinoid tumours?

A
  • Tumours that arise from different embryonic divisions of the gut
    ○ Foregut: Lungs, stomach
    ○ Mid gut: Small intestine, appendix, proximal large gut
    ○ Hind gut: distal colon/rectum
  • Majority is in the GI tract (68%), most commonly the small intestine, next largest is Lungs (25%)
22
Q

What do carcinoid tumours secrete?

A

Hormones:
* Serotonin (most common)
* Histamine
* Dopamine

23
Q

What are symptoms of carcinoid syndrome?

A
  • Histamine/seratonin release:
    ○ Flushing
    ○ Diarrhoea
    ○ Rhinorrhoea
    ○ Carcinoid heart disease
24
Q

What is carcinoid heart disease?

A

○ Usually right sided heart disease (rarely left)
○ Fibrous thickening of endocardium and fixation of tricuspid valve
○ Mixed tricuspid and pulm valve disease are common

25
Q

What is a carcinoid crisis?

A
  • Exaggerated forms of carcinoid syndrome
    ○ Profound flushing
    ○ Bronchospasm
    ○ Tachycardia
    Labile BP
26
Q

What are the preop goals for a patient with carcinoid syndrome?

A

○ Identify complications of carcinoid tumours (carcinoid syndrome in particular heart disease)
○ Minimise tumour secreting activity
○ Stable controlled anaesthesia without significant responses to stimulation

27
Q

What is the pre op optimisation for a patient with carcinoid syndrome?

A

Stabilising hormone secretion with octreotide infusion

Octreotide infusion should be 50 microgram/hr for at least 12 hrs prior to surgery

28
Q

What are the preferred intraop vasopressors for carcinoid syndrome?

A

○ Noradrenaline can paradoxically worsen hypotension
○ Octreotide is the best vasoconstrictor (IV boluses of 20-50 micgrograms)
○ Can also use vasopressor as alternative (longer lasting vasoconstrictor)