Paeds Flashcards
most common tumour in posterior brain and cerebellum
medulloblastoma
Red flags febrile seizure
> 5 minutes
2 in 24 hours
Not resolve within an hour
Focal symptoms: weakness in left arm
Febrile seizures and epilepsy
1% normal lifetime risk
2% simple seizures
5% complex
LD criteria
IQ <70
Onset in early childhood
Reduced life/adaptation skills
Mx of infants >3 months with lower URTI
3 days Abx
Complications of sickle cell
- Aplastic crisis (parvovirus, EBV)
- Acute stroke
- Infections (encapsulated due to hyposplenism)
Mx of new diagnosis of asthma
Give a SABA inhaler, consider a very low dose corticosteroid inhaler in new Dx
Role of health visitor
Health visitors work with parents who have new babies, offering support and informed advice from the ante-natal period until the child starts school at 5 years.
erythema nodosum and sore throat
group A strep
Complications of DM in children
- Growth and puberty delay if poor control
- Hypertension
- Nephropathy
- Infections
- DKA
most common causes of erythema multiforme
herpes
Mx of anaphylaxis?
ABCDE.
Give intramuscular (IM) adrenaline 1:1000 - repeat the dose after 5 mins
Give oxygen at the highest concentration possible.
Obtain IV access and give a rapid fluid challenge (with Hartmann’s or normal saline) using 20 mL/kg in a child.
Monitor the ECG and pulse oximetry continuously, and the blood pressure and pulse every 5 minutes.
Following initial resuscitation: Give slow IM or IV chlorphenamine. Give slow IM or IV hydrocortisone Consider nebulized salbutamol or ipratropium if the person is wheezy All children under 16 should be admitted
Long term Mx of sickle cell
Education; warning signs of crisis (e.g. tummy ache and splenic sequestration) Immunise as normal PCV every 5 years, influenza annually Life long antibiotics Folic acid
Hydroxycarbamide in repeated crises to prevent chest crises
pansystolic murmur at lower left sternal edge
VSD
Acute Mx of sickle cell crisis
- Analgesia (strong opioids +/- anti emetics and laxatives) - - Fluids
- Reassess often
inability to smell [anosmia], decrease in gonadotrophin-releasing hormone, developmental delay
Kallman syndrome
epileptic drug with side effects: transient hair loss, weight gain, liver damage and blood dyscrasias
sodium valproate
Regular screens in children with DM
- Growth and development; BMI
- BP
- Renal disease
- Feet
- Annual flu jab
single best investigation for osteomyelitis
blood culture
Harmony test
analyses cell free DNA in maternal blood
Microcephalic, small eyes
Cleft lip/palate
Polydactyly
Scalp lesions
Patau syndrome (trisomy 13)
Mx of newly diagnosed T1DM
- Education re injecting, BMs, diet, etc
- Basal-bolus regime or pump
- Aim for BM between 4 and 7, blood glucose diary
- Carbohydrate counting
- HbA1c checked 4x per year, <48mmol
- Bio psycho social
physical features of Down syndrome
My CHILD HAS a PROBLEM
Congenital heart disease / Cataracts Hypotonia / Hyperthyroidism Increased sandal gap Leukaemia Duodenal atresia / Delayed development
Hirshsprung’s disease
Alzheimer’s disease / Alantoaxial instability
Short neck / Squint
Protruding tongue / Palmar crease Roung face Oblique eye fissure / Occiput flat Behavioural difficulties Low nasal bridge Epicanthic folds Mental retardation
tetralogy of fallot
large ventricular septal defect (VSD)
pulmonary stenosis
overriding aorta
right ventricular hypertrophy
Pattern in GH deficiency
Normal growth rate until 6-12 months of age, then growth velocity falls. Associated with neonatal hypoglycaemia and jaundice
By WHAT AGE would you refer the following kids if they haven’t achieve the following milestones
a. Sit without support
b. Walk
c. Hops on one leg
d. Pincer grip
e. Smiles
Sit without support – normally by 7-8m, refer by 8m
b. Walk – normally by 15m, refer by 18m
c. Hops on one leg – normally by 4y, refer by 5y
d. Pincer grip – normally by 12m, refer by 12m
e. Smiles – normally by 6w, refer by 8w