Paeds Flashcards
Which infants should routinely be referred for US for DDH?
Child hip problem in 1st-deg relative
Breech >= 36 wk
Multiple pregnancy
Barlow and Ortolani tests done when?
Newborn check
6-8 week check
Investigation of suspected DDH with US hips at age
<4.5 months old
Investigation of suspected DDH with Xray at age:
> 4.5 months old
Management of DDH with Pavlov harness at age:
<5 months old
Management of DDH with surgery at age:
> 5 months old
Neonatal blood spot screening (‘Guthrie’/’heel-prick’) is performed at..
Day 5-9 of life
Neonatal blood spot screens for..
Congenital hypothyroidism
Cystic fibrosis
Sickle cell disease
Phenylketonuria
Medium chain acyl-CoA dehydrogenase deficiency (MCADD)
Maple syrup urine disease (MSUD)
Isovaleric acidaemia (IVA)
Glutaric aciduria type 1 (GA1)
Homocystinuria (HCU)
Precocious puberty in females
Secondary sexual characteristics <8 yrs
Precocious puberty in males
Secondary sexual characteristics <9yrs
5-16y asthma - Newly-diagnosed with symptoms <3/week + no nocturnal waking
SABA reliever therapy alone
(salbutamol)
5-16y asthma - Newly-diagnosed with symptoms >=3/week +/- nocturnal waking
SABA + paediatric low-dose ICS
(<=200 mcg budesonide/equiv)
5-16y asthma -
Not controlled on:
SABA alone
SABA + paediatric low-dose ICS
(<=200 mcg budesonide/equiv)
5-16y asthma -
Not controlled on:
SABA + paediatric low dose ICS
SABA + paediatric low-dose ICS + LTRA
5-16y asthma -
Not controlled on:
SABA + paediatric low dose ICS + LTRA
Stop LTRA
SABA + paediatric low-dose ICS + LABA
5-16y asthma -
Not controlled on:
SABA + paediatric low-dose ICS + LABA
SABA + MART [paediatric low-dose ICS + LABA]
5-16y asthma -
Not controlled on:
SABA + MART [paediatric low-dose ICS + LABA]
SABA + MART [paediatric moderate-dose ICS + LABA]
or
SABA + paediatric moderate-dose ICS + LABA
5-16y asthma -
Not controlled on:
SABA + moderate-dose ICS + LABA
(fixed-dose or MART)
Paediatric high-dose ICS (MART/separate)
or
Theophylline/Expert advice
Refer for unilateral undescended testes - at what age?
3 months
Management of bilateral undescended testes
Same-day paediatrician review
Occurrence of undescended testis in newborn term male
2-3%
Croup - features prompting admission
Moderate/severe
<6m
Known upper airway abnormality
Uncertain diagnosis
Management of mild croup
Stat dose PO dexamethasone 150mcg/kg
Management of scarlet fever
PO Penicillin V QDS for 10/7
Notify PHE
Management of Scarlet Fever (pen-allergic)
Azithromycin OD for 5/7
Management of impetigo
Fusidic acid 2% TDS 5 days
Presentation of Measles
Irritable febrile prodrome
Conjunctivitis
Koplik spots
Rash behind ears > confluent
Classic presentation of Rubella
Maculopapular rash, from face -> whole body
Postauricular + suboccipital LN
Classic presentation of Mumps
Fever
Earache + pain on eating (unilateral -> bilateral)
Presentation of Erythema Infectiousum
(Fifth-disease/Slapped-cheek/Parvovirus B19)
Fever
Headache + lethargy
Rash from cheeks -> upper arms.
Scarlet fever - features
(Group A haemolytic strep toxins)
Fever
Tonsillitis
Strawberry tongue
Sandpaper rash + Circumoral pallor
HFM disease presentation
(Cocksackie A16 virus)
Vesicles in mouth + palms + soles
Fever, sore throat
Bed-wetting is considered normal up to age.
Age 5
Short-term management of bed-wetting in >7yr old (eg school trip)
Desmopression
Limit fluid 1hr pre - 8hr post
Incidence of cleft lip/palate
1 / 1000
Cleft lip usually repaired when
1 week - 3 months
Cleft palate usually repaired when
6 months - 1 year
Presentation of missed DDH in an older child
Trendelenberg gait + leg length discrepancy
1st-line management of CMPA
Formula-fed
Mild/moderate
eHF (extensive hydrolysed formula)
Management of CMPA
Formula-fed
Severe/2nd-line
AAF (amino acid-based formula)
1st-line management of CMPA- breast-fed
Maternal cows milk elimination
Calcium + vit D supplement
eHF milk after weaning
Pertussis vaccine in pregnancy
All offered 16-32 wks
Management of pertussis
>6 months old
Macrolide (if within 21 days onset)
Prophylactic antibiotics for household
Notify PHE
Complications of pertussis
Apnoea
Pneumonia, Bronchiectasis
Seizures
Subconjunctival haemorrhage, petechiae
Incidence of DDH
1 - 3%
(20% of which are bilateral)
Features of congenital Rubella
Sensorineural deafness
Congenital cataracts
Pyloric stenosis age of presentation
2wk - 6wk (rarely up to 4 months)
Definitive management of pyloric stenosis
Pyloromyotomy (Ramstedt or laparoscopic)
Presentation of pyloric stenosis
Projectile vomits 30min after feed
Upper abdominal mass
Constipation, dehydration, alkalosis
Chance of Down’s syndrome child - at maternal age 35
1 in 270
Chance of Down’s syndrome child - at maternal age 20
1 in 1,500
Chance of Down’s syndrome child - at maternal age 30
1 in 800
Chance of Down’s syndrome child - at maternal age 40
1 in 100
Chance of Down’s syndrome child - at maternal age 50
> =1 in 50
Investigation used to diagnose vesicoureteric reflux (VUR)
Micturating cystourethrogram
Investigation to look for renal scarring secondary to VUR
Radionuclide scan using dimercaptosuccinic acid (DMSA)
Complications of measles
Otitis media
Pneumonia
Encephalitis (1-2 weeks later)
Subacute sclerosing panencephalitis (5 - 10 yr later)
Keratoconjunctivitis
Myocarditis
Management of measles contacts
Offer MMR within 72hr, if not already vaccinated
6-8 week check looks for:
Undescended testes
DDH
Congenital heart disease
Congenital cataract
Diagnosis of whooping cough
Cough >14 days, and 1 of:
Paroxysmal cough
Inspiratory whoop
Post-tussive vomiting
Apnoea attacks
Hip abnormality found at 6 week check - management
Refer specialist + US <10wks
Roseola infantum - presentation
High fever, rash follows later
Features of Patau syndrome (trisomy 13)
Cleft lip/palate
Polydactyly
Scalp lesions
Features of Noonan syndrome
Webbed neck
Pulmonary stenosis
Pectus excavatum
Features of Fragile X
Macrocephaly
Macro-orchidism
Learning difficulty
Features of Pierre-Robin syndrome
Micrognathia
Posterior tongue displacement
Cleft palate
Features of Prader-Willi syndrome
Obesity
Hypotonia
Hypogonadism
Features of Edward’s syndrome (trisomy 18)
Rocker-bottom feet
Overlapping fingers
Low-set ears
Features of William’s syndrome
Friendly and extroverted
Transient neonatal hypercalcaemia
Supravalvular aortic stenosis
Cri du chat syndrome (chromosome 5p deletion)
Characteristic cry
Feeding difficulty
Hypertelorism
Suspected meningococcal septicaemia in the community - immediate antibiotic management if < 1 year old
IM benzylpenicillin 300mg
Suspected meningococcal septicaemia in the community - immediate antibiotic management if 1 - 10 years old
IM benzylpenicillin 600mg
Suspected meningococcal septicaemia in the community - immediate antibiotic management if > 10 years old
IM benzylpenicillin 1200mg
Limping child - indications for urgent assessment (admission)
< 3 years old
> 9 years + painful/restricted ROM
Unable to weight-bear
Fever / B symptoms
Severe pain / Night-awakening
Neurovascular compromise
Safeguarding concern
Develepment - hand dominance before what age is a red flag (for cerebral palsy)
18 months
Unexplained abdominal mass in a child - management
Urgent paediatric review within 48hr (possible Wilm’s tumour)
Household contacts of threadworms
Stat Mebendazole - all family members on same day
Which household members should not be treated for threadworms
Pregnant, breastfeeding,
< 2 years old
Features of Kawasaki disease
High fever > 5 days
Conjunctival injection
Cervical LN
Red cracked lips, strawberry tongue
Red palms/sole > peel
Management of Kawasaki disease
High-dose aspirin
IVIG
ECHO for coronary aneurysm
Antibiotic treatment of whooping cough in community
(onset < 21 days) -
< 1 month old
Clarithromycin
Antibiotic treatment of whooping cough in community
(onset < 21 days) -
>= 1 month old
Azithromycin or clarithromycin
Antibiotic treatment of whooping cough in community
(onset < 21 days) -
pregnant woman
Erythromycin
Which conditions are Autosomal Recessive
Metabolic conditions
Inherited ataxias
Which conditions are Autosomal Dominant
Structural conditions
(+ Gilberts, hyperlipidaemia II)
Features of Freiberg’s disease
Mid-foot pain, swelling + stiffness
Adolescents
Pathology of Freibergs disease
Infarction > flattening of metatarsal head
Management of Freiberg’s disease
Activity limitation + analgesia
Orthotics
Surgery (rare)
Epistaxis under 2 years old
Fast-track referral to exclude haematological disorder
Hearing test done as newborn
Otoacoustic emission test
If abnormal > Auditory brainstem response test
Hearing test done at 6 - 9 months
Distraction test, by health visitor
Hearing test done at 18 months - 2.5 years
Recognition of familiar objects
Hearing test done at 2-3 years
Performance testing
Speech discrimination tests
Hearing test done at school entry
Pure tone audiometry
1st-line management of infantile spasm (non-tuberous sclerosis)
Vigabatrin or steroid (prednisolone or tetracosactide)
EEG in Infantile spasm
Hypsarrhythmia
Age of presentation - intussusception
6 - 18 months
Features of intussusception
Paroxysmal colic, knees up, pale
Vomiting
Red-currant jelly stool
Sausage-shaped mass RUQ (25%)
EEG findings with Benign Rolandic Epilepsy
Centro-temporal spikes
Features of Benign Rolandic Epilepsy seizures
At night
Partial seizure
Child otherwise normal
What age should child be competent with a spoon, and not spil with a cup
2 - 2.5 years
Developmental milestone - copies square and triangle
5 years
Developmental milestone - circular scribble
18 months
Developmental milestone - copies vertical line
2 years
Developmental milestone - copies circle
3 years
Developmental milestone - copies cross
4 years
Developmental milestone - says mama and dada
9 months
Developmental milestone - Knows and reponds to own name
9 - 12 months
Developmental milestone - knows 2-6 words
12 - 15 months
(Refer at 18 months)
Developmental milestone - vocabulary of 200 words
2.5 years
Developmental milestone - talks in short sentences
2.5 - 3 years
Management of bruising in a non-mobile infant
Refer for same day paediatric assessment
Developmental milestone - tower of 2 bricks
15 months
Developmental milestone - tower of 3 bricks
18 months
Developmental milestone - tower of 6 bricks
2 years
Developmental milestone - tower of 9 bricks
3 years
Genu valgum (knock knees) usually resolve by
8 years
Genu varum (bow legs) usually resolve by
4 - 5 years
<6m had UTI which responded to treatment - follow-up?
US within 6 weeks
Child >6m
First UTI responded to treatment - follow-up
No imaging required
(unless suggested atypical infection)
Features suggestive of an atypical urine infection
Seriously ill
Poor urine flow
Abdominal/bladder mass
Raised creatinine
Not responding to 48hr of antibiotics
Non-E.colli organism found
Infant with GORD - 2nd line after alginate
omeprazole suspension 4wk trial
Management of mild/moderate cradle cap
Baby shampoo + baby oils
Management of severe cradle cap (seborrhoeic dermatitis)
mild topical steroid (1% hydrocortisone)
Presentation of calcaneal apophysitis (Sever disease)
Bilateral heel pain in sporty child
Heel squeeze tenderness
Features of Barter syndrome
Normotensive hypokalaemia
Failure to thrive
Visible haematuria in a child
Paediatric review within 48hr (rule out Wilm’s tumour)
WADR syndrome
Wilm’s tumour
Aniridia
Genitourinary malformation
Retardation
General risk of a further febrile convulsion
1 in 3
Management of suspected UTI in <3 month old
Immediate paediatrician review
Management of lower UTI in >3 months old
3 days oral antibiotics (according to local guidelines)
Re-review if still unwell 24-48hr
Migraine - 1st line acute management
Ibuprofen
What is the average age that puberty starts in boys
12 years
Send urine MCS before antibiotics if:
<3y
Pregnant
Pyelonephritis/complicated UTI
Recurrent UTI
Leucocyte/nitrite +ve only
Management of pertussis in <6 month old
Admit
Prophylactic antibiotics for household
Notify PHE
1st line management infantile spasm - tuberous sclerosis
Vigabatrin
2nd line management infantile spasm - tuberous sclerosis
Steroid (prednisolone or tetracosactide)
Vitamin K given to
All babies (3rd dose if breast-fed)