paeds endo Flashcards

1
Q

Signs and symptoms of DKA

A

Presentation:
- N+V
- abdo pain
- reduced GCS

on questioning:
- polyuria, enuresis and nocturia + polydipsia
- weight loss
- failure to thrive

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2
Q

Investigations and immediate management

A

ON ARRIVAL
Height and weight
vital signs
urinalysis
BM and ketones
VBG

ON DIAGNOSIS
- A-E approach, call senior and admit with 1-1 nursing

  • fluid BOLUS 10ml/kg or 10ml/kg if shocked over 30 mins
  • calculate fluid DEFICIT
    mild-mod DKA (pH 7.1-7.29)- 5% x body wieght
    severe DKA (pH <7.1) - 10% x BW
    not shocked: deficit - bolus over 48hrs
    shocked: deficit over 48hrs
  • MAINTENANCE
    1000ml first 10kg
    500ml second 10kg
    20ml for every remaining Kg
    over 24hrs

ALL FLUIDS WITH 400mmol/L KCl (unles anuric or hyperK+)

  • INSULIN (after 1-2hrs fluids)
    0.05U/Kg/hr - incrase to 0.1U/Kg/kr if unresponsive after 6hrs
  • add 5% dextose when BM <14mmol/L

MONITOR
- 2hrly: BM, ketones, U&Es, VBG
- continuous: ECG, GCS, urine output (catheter), vital signs

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3
Q

Managament/counselling of newly diagnosed T1DM

A

MDT approach: endocrinologist, paediatrician, diabetic nurse, dietician

what is it:
-T1DM is a type of diabetes diagnosed commonly at a young age
- it is when the body doesnt produce a vital hormone (called insulin) which enables our cells to use glucose
- this is because there is damage to the organ that makes this hormone by our immune system
- it is a life long condition and requires injections to replace this hormone

RISKS:
- if left untreated it can have very serious consequences on the body- most importantly the brain wont be able to use glucose –> death

what to do now:
- same day referral to an endocrinologist
- referral to diabetic nurse
- check BM, ketones –> A&E if signs of DKA
EDUCATION: diet and exercise, SN for DKA and hypo symptoms, diabetes UK support groups

What this means in the future:
- insulin injections life long
- 4x/year clinics
- screening for organ damage and other autoimmune conditions
-

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4
Q

Causes of precocious puberty

A

gonadal dependent:
- brain tumour
- brain trauma
- idiopathic

gonadal independent:
- McCune albright syndrome
- CAH (21-OH/ 11b-OH def)
- tumours (leydig- sertoli, theca cell)
- exogenous hormones eg COCP

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5
Q

investigations for precocious puberty

A
  1. bone age scan
  2. LH/FH levels
  3. GnRH stimulation test
  4. genitalia examination
  5. 21-OH/ 11bOH levels
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6
Q

Mx of precocious puberty

A
  • reassure if idiopathic
  • treat any cause
  • gonadotrophin dependent: GnRH agonist and GH agonist
  • independent: specialist referral
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7
Q

causes of delayed puberty

A

idiopathic

hypogonadotrophic hypogonadism:
- brain trauma
- brain tumour
- Kallmans syndrome

hypergonadotrophic hypogonadism
- Turners
- 17xOH def CAH
- hypothyroidism
- gonadal damage

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8
Q

causes of short stature

A

short parents
genetic: turners, downs, PWS, noonans
endocrine: GH deficiency, hypothyroidism, cushings
dispropotionalte: rickets, spinal dysplasia
chronic illness: IBD, coeliac, CF, anorexia

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