PACES - Diabetes/Endo Flashcards

1
Q
A

Thyroid acropachy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Thyroid history qs

A

Sweating/heat or cold intolerance

Appetite/weight change

Anxious/irritable or depressed/tired

Visual problems, eye pain, change in bowel habit

Oligomenorrhoea or menorrhagia

Compression Sx: dysphagia, SoB, neck discomfort, change of voice

Triggers - hyper: childbirth, stress, infection, hypo: radioiodine, drugs, surgery

Other AI disease, previous thyroid surgery

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Complications of thyroid surgery

A

Early
Reactionary haemorrhage
RLNP
Hypocalcaemia
Thyroid storm

Late
Hypothyroidism
Hypoparathyroidism
Recurrence of disease
Keloid scar

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Hyperthyroidism management

A

Medical
Propranolol
Carbimazole, titreated to TFTs or block and replace
Treat for 12-18m
Radioiodine
CI: pregnancy, around children
May worsen eye disease
Most patients become hypothyroid

Thyroidectomy
Eye disease
Stop smoking, artificial tears, dark glasses
Severe: high dose steroids, surgical decompression

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Describe the cortisol feedback system

A

Hypothalamus -> CRH -> Ant. Pituitary -> ACTH -> Adrenal Cortex -> Cortisol

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

How does cushing’s present?

A

Headache, visual disturbance
Weight gain
Bruising
DM/AI disease e.g. pigmentation Sxs
Cause → RhA, fibrosis, COPD = LT steroid use

Moon face, easy bruising, large body habitus, stretch marks

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What are the main causes of Cushing’s

A

ACTH independent
Steroids
Adrenal adenoma
Carney complex

ACTH dependent
Cushing’s disease
SCLC

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Qs to ask in acromegaly history

A

Headache/visual disturbance
Voice deepened
Ring size/shoe size/hat size changed
Pain/numbness in hands → CTS
DM and OSA Sxs
Anyone noticed appearance has changed?
Old photographs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

How is acromegaly managed

A

Transsphenoidal resection
Complications: meningitis, diabetes insipidus, panhypopituitarism

Medical therapy
Somatostatin analogue: octreotide
GH antagonist: pegvisomant
Da agonist: cabergoline

Radiotherapy
Yearly FU with bloods, visual fields, ECG +/- MRI head

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Qs to ask in an addison’s history

A

Weight loss, anorexia
Postural hypotension/dizziness/faints
Hyperpigmentation
Lethargy, depression
AI disease Sxs e.g. DM, vitiligo
TB Sxs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

How would you investigate addisons

A

Bloods - U&Es (low Na, high K), low glucose, 21-hydroxylase Ab
SynACTHen test
8am cortisol low
8am ACTH high
Test leads to no increase in cortisol
CXR for TB
AXR for adrenal calcification

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

How would you investigate acromegaly?

A

BP, urine dipstick or CBG (GH normally suppressed by glucose)
Formal perimetry
Bloods - IGF-1, GH, baseline pituitary function tests
OGTT - no suppression of GH
CXR - cardiomegaly, can lead to HF = leading cause of death
MRI pituitary fossa

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

How would you manage addison’s

A

Acute
0.9% NS IV rehydration
100 mg hydrocortisone IV
Treat cause e.g. infection

Chronic
Replace hydrocortisone and fludrocortisone
Pt education
Don’t stop steroids suddenly
Increase dose during illness/stress
Wear bracelet
Carry steroid card

How well did you know this?
1
Not at all
2
3
4
5
Perfectly