Paeds Flashcards
APGAR score
score: 2,1,0
Appearance - colour: pick, blue extremities, blue all over
Pulse: >100, <100, nil
Grimace (reflex irritability): cries/sneezes/coughs, grimace, nill
Activity - muscle tone: active, flexed, floppy
Resp effort: strong/cries, weak/irregular, nil
1, and 5 minutes of age. If low repeat at 10 mins
0-3 is very low score,
4-6 is moderate low
7-10 means the baby is in a good state
Asthma mx in children <5
- SABA
- SABA & Moderate dose ICS 8wks. Resolution & recurrence in 4 weeks-> low dose ICS. Resolution & recurrence after
4 weeks-> anther 8ks of mod dose ICS. No resolution-> alternate dx - SABA + paediatric low-dose ICS + leukotriene receptor antagonist (LTRA)
- stop LTRA & refer
Asthma mx in children 5-17
- SABA
- SABA & low dose ICS
- SABA & low dose ICS & LTRA
- SABA + paediatric low-dose ICS + LABA
- SABA + MART (low-dose ICS)
- SABA + MART (mod-dose ICS) OR #4 w mod dose ICS
- SABA + MART (high-dose ICS) OR #4 w mod dose ICS OR ++ theophylline OR referral
autosomal dominant conditions
Autosomal recessive - usually ‘metabolic’ (except G6PD - x linked recessive)
autosomal dominant conditions being ‘structural’ (except ataxia telangiectasia and Friedreich’s ataxia- AR)
Achondroplasia
Acute intermittent porphyria
Adult polycystic disease
Antithrombin III deficiency
Ehlers-Danlos syndrome
Familial adenomatous polyposis
Hereditary haemorrhagic telangiectasia
Hereditary spherocytosis
Hereditary non-polyposis colorectal carcinoma
Huntington’s disease
Hyperlipidaemia type II
Hypokalaemic periodic paralysis
Malignant hyperthermia
Marfan’s syndromes
Myotonic dystrophy
Neurofibromatosis
Noonan syndrome
Osteogenesis imperfecta
Peutz-Jeghers syndrome
Retinoblastoma
Romano-Ward syndrome
tuberous sclerosis
Von Hippel-Lindau syndrome
Von Willebrand’s disease
autosomal recessive conditions
Cystic fibrosis
Albinism
Ataxic telangiectasia
Friedreich’s ataxia
Congenital adrenal hyperplasia
Cystinuria
Fanconi anaemia
Gilbert’s syndrome
Haemochromatosis
Wilson’s disease
Sickle cell anaemia
Chickenpox features & mx
infectivity = 4 days before rash, until 5 days after the rash first appeared
incubation period = 10-21 days
school exclusion: 5 days after the onset of the rash).
keep cool, trim nails
calamine lotion
to prevent secondary bacterial infection
- avoid NSAIs
Patau syndrome (trisomy 13)
Microcephalic, small eyes
Cleft lip/palate
Polydactyly
Scalp lesions
Edward’s syndrome (trisomy 18)
Micrognathia
Low-set ears
Rocker bottom feet
Overlapping of fingers
Fragile X
Learning difficulties
Macrocephaly
Long face
Large ears
Macro-orchidism
Noonan syndrome
Webbed neck
Pectus excavatum
Short stature
Pulmonary stenosis
Pierre-Robin syndrome
Micrognathia
Posterior displacement of the tongue (may result in upper airway obstruction)
Cleft palate
Prader-Willi syndrome
Hypotonia
Hypogonadism
Obesity
William’s syndrome
Short stature
Learning difficulties
Friendly, extrovert personality
Transient neonatal hypercalcaemia
Supravalvular aortic stenosis
Cri du chat syndrome (chromosome 5p deletion syndrome)
Characteristic cry (hence the name) due to larynx and neurological problems
Feeding difficulties and poor weight gain
Learning difficulties
Microcephaly and micrognathism
Hypertelorism
congenital Rubella
Sensorineural deafness
Congenital cataracts
Congenital heart disease (e.g. patent ductus arteriosus)
Glaucoma
congenital Cytomegalovirus
Low birth weight
Purpuric skin lesions
Sensorineural deafness
Microcephaly
congenital Toxoplasmosis
Cerebral calcification
Chorioretinitis
Hydrocephalus
Constipation in children mx
-1. polyethylene glycol 3350 + electrolytes (Movicol Paediatric Plain)
2. add a stimulant laxative
do not use dietary interventions alone as first-line treatment although ensure the child is having adequate fluid and fibre intake
Infants not yet weaned (usually < 6 months)
- bottle-fed infants: give extra water in between feeds. Try gentle abdominal massage and bicycling the infant’s legs
- breast-fed infants: constipation is unusual and organic causes should be considered
Cow’s milk protein intolerance/allergy (CMPI/CMPA) mx
If formula fed
- extensive hydrolysed formula (eHF) milk
- amino acid-based formula (AAF)
if breathed
- continue breastfeeding
- eliminate cow’s milk protein from maternal diet & calcium supplements for mum
Initial management of suspected cyanotic congenital heart disease
supportive care until defensive surgical correction
- prostaglandin E1 e.g. alprostadil
developmental delay Referral points
doesn’t smile at 10 weeks
cannot sit unsupported at 12 months
cannot walk unsupportedat 18 months
Fine motor skill problems
- hand preference before 12 months
Gastro-oesophageal reflux in children mx
advise regarding position during feeds - 30 degree head-up
trial of smaller and more frequent feeds
thickened formula OR alginate therapy e.g. Gaviscon.
proton pump inhibitor (PPI) as last resort
Gastroschisis & exomphalos mx
Gastroscisis
vaginal delivery may be attempted
newborns should go to theatre asap
Exomphalos (omphalocoele)
caesarean section is indicated to reduce the risk of sac rupture
staged repair
Immune (or idiopathic) thrombocytopenic purpura mx in children
bone marrow examinations is only required if there are atypical features
mx
usually, no treatment is required
advice to avoid activities that may result in trauma (e.g. team sports)
if the platelet count is very low (e.g. < 10 * 109/L) or there is significant bleeding. Options include:
oral/IV corticosteroid
IV immunoglobulins
platelet transfusions can be used in an emergency (e.g. active bleeding)