paeds endo Flashcards
Signs and symptoms of DKA
Presentation:
- N+V
- abdo pain
- reduced GCS
on questioning:
- polyuria, enuresis and nocturia + polydipsia
- weight loss
- failure to thrive
Investigations and immediate management
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
Managament/counselling of newly diagnosed T1DM
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
-
Causes of precocious puberty
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
investigations for precocious puberty
- bone age scan
- LH/FH levels
- GnRH stimulation test
- genitalia examination
- 21-OH/ 11bOH levels
Mx of precocious puberty
- reassure if idiopathic
- treat any cause
- gonadotrophin dependent: GnRH agonist and GH agonist
- independent: specialist referral
causes of delayed puberty
idiopathic
hypogonadotrophic hypogonadism:
- brain trauma
- brain tumour
- Kallmans syndrome
hypergonadotrophic hypogonadism
- Turners
- 17xOH def CAH
- hypothyroidism
- gonadal damage
causes of short stature
short parents
genetic: turners, downs, PWS, noonans
endocrine: GH deficiency, hypothyroidism, cushings
dispropotionalte: rickets, spinal dysplasia
chronic illness: IBD, coeliac, CF, anorexia