Flat feet in children usually resolve at what age?
Children’s gait is constantly developing, and it is important to recognise normal variations in gait patterns. Flat feet are usually painless and most will resolve by the age of 6 years.
Current UK immunisation schedule
At birth: BCG if risk factors
2 months: ‘6-1 vaccine’ (Diphtheria, Tetanus, Whooping cough, Polio, Hib and Hepatitis B)
Oral rotavirus vaccine
Men B
3 months: ‘6-1 vaccine’ (diphtheria, tetanus, whooping cough, polio, Hib and hepatitis B)
Oral rotavirus vaccine
PCV
4 months: ‘6-1 vaccine’ (diphtheria, tetanus, whooping cough, polio, Hib and hepatitis B)
Men B
12-13 month:
Hib/Men C
MMR
PCV
Men B
3-4 years: ‘4-in-1 pre-school booster’ (diphtheria, tetanus, whooping cough and polio)
MMR
13-18 years: ‘3-in-1 teenage booster’ (tetanus, diphtheria and polio)
Men ACWY
Infantile Colic
Infantile colic describes a relatively common and benign set of symptoms seen in young infants. It typically occurs in infants less than 3 months old and is characterised by bouts of excessive crying and pulling-up of the legs, often worse in the evening.
Infantile colic occurs in up to 20% of infants. The cause of infantile colic is unknown.
NICE do not recommend the use of simeticone (such as Infacolµ) or lactase (such as Colief) drops.
Cows milk protein intolerance/allergy
Cow’s milk protein intolerance/allergy (CMPI/CMPA) occurs in around 3-6% of all children and typically presents in the first 3 months of life in formula-fed infants, although rarely it is seen in exclusively breastfed infants.
Both immediate (IgE mediated) and delayed (non-IgE mediated) reactions are seen. The term CMPA is usually used for immediate reactions and CMPI for mild-moderate delayed reactions.
Features:
- Regurgitation and vomiting
- Diarrhoea
- Urticaria, atopic eczema
- ‘colic’ symptoms: irritability, crying
- wheeze, chronic cough
- rarely angioedema and anaphylaxis may occur
Diagnosis is often clinical (e.g. improvement with cow’s milk protein elimination). Investigations include:
skin prick/patch testing
total IgE and specific IgE (RAST) for cow’s milk protein
Mx for CMPI/CMPA?
If the symptoms are severe (e.g. failure to thrive) refer to a paediatrician.
Management if formula-fed:
- Extensive hydrolysed formula (eHF) milk is the first-line replacement formula for infants with mild-moderate symptoms.
- Amino acid-based formula (AAF) in infants with severe CMPA or if no response to eHF
- around 10% of infants are also intolerant to soya milk
Management if breastfed:
- continue breastfeeding
- Eliminate cow’s milk protein from maternal diet. Consider prescribing calcium supplements for breastfeeding mothers whose babies have, or are suspected to have, CMPI, to prevent deficiency whilst they exclude dairy from their diet.
- Use eHF milk when breastfeeding stops, until 12 months of age and at least for 6 months
Immunisation for premature babies?
Premature neonates should be immunised according to the vaccination schedule, regardless of how premature they are.
The first vaccine should thus be given eight weeks after birth and continue in line with the schedule based on birthday, not on corrected gestation.
When to send bronchiolitis to hospital?
Immediately refer children with bronchiolitis for emergency hospital care if they have any of the following:
Consider referring children with bronchiolitis to hospital if they have any of the following:
If otherwise deemed suitable to cover how to recognise developing ‘red flag’ symptoms:
Bronchiolitis virus?
Respiratory syncytial virus (RSV) is the pathogen in 75-80% of cases.
Most common cause of a serious lower respiratory tract infection in < 1yr olds (90% are 1-9 months with a peak incidence of 3-6 months). Higher incidence in winter.
Coryzal symptoms (including mild fever) precede:
- dry cough
- increasing breathlessness
- wheezing, fine inspiratory crackles (not always present)
- feeding difficulties associated with increasing dyspnoea are often the reason for hospital admission
Management is largely supportive:
- humidified oxygen is given via a head box and is typically recommended if the oxygen saturations are persistently < 92%
- nasogastric feeding may be needed if children cannot take enough fluid/feed by mouth
- suction is sometimes used for excessive upper airway secretions
Newborn blood spot programme
The newborn blood spot screening enables early identification, referral and treatment of babies with 9 conditions. These are sickle cell disease, cystic fibrosis, congenital hypothyroidism, phenylketonuria, medium-chain acyl-CoA dehydrogenase deficiency, maple syrup urine disease, isovaleric acidaemia, glutaric aciduria type 1 and homocystinuria. Testing is done usually on day 5 via a heel prick by the health visitor or the midwife. There are some variations across the UK home nations with regards to what tests are included within the blood spot test.
Otitis media features?
Possible otoscopy findings:
- bulging tympanic membrane → loss of light reflex
- opacification or erythema of the tympanic membrane
- perforation with purulent otorrhoea
- decreased mobility if using a pneumatic otoscope
Mx for acute otitis media?
Acute otitis media is generally a self-limiting condition that does not require an antibiotic prescription. Parents should be advised to seek medical help if the symptoms worsen or do not improve after 3 days.
Antibiotics should be prescribed immediately if:
- Symptoms lasting more than 4 days or not improving
- Systemically unwell but not requiring admission
- Immunocompromise or high risk of complications secondary to significant heart, lung, kidney, liver, or neuromuscular disease
- Younger than 2 years with bilateral otitis media
- Otitis media with perforation and/or discharge in the canal
If an antibiotic is given, a 5-7 day course of Amoxicillin is first-line. In patients with penicillin allergy, Erythromycin or Clarithromycin should be given.
Mx for constipation in children?
If faecal impaction is present:
polyethylene glycol 3350 + electrolytes (Movicol Paediatric Plain) - using an escalating dose regimen as the first-line treatment
- add a stimulant laxative if Movicol Paediatric Plain does not lead to disimpaction after 2 weeks
- substitute a stimulant laxative singly or in combination with an osmotic laxative such as lactulose if Movicol Paediatric Plain is not tolerated
- inform families that disimpaction treatment can initially increase symptoms of soiling and abdominal pain
Maintenance therapy:
very similar to the above regime, with obvious adjustments to the starting dose, i.e.
- first-line: Movicol Paediatric Plain
- add a stimulant laxative if no response
- substitute a stimulant laxative if Movicol Paediatric Plain is not tolerated. Add another laxative such as lactulose or docusate if stools are hard.
- continue medication at maintenance dose for several weeks after regular bowel habit is established, then reduce the dose gradually
Red and Amber flag feature in children temp of what in which age group?
Amber:
- Age 3-6 months, temperature >=39ºC
* Fever for >=5 days
* Rigors
* Swelling of a limb or joint
* Non-weight bearing limb/not using an extremity
RED:
* Age <3 months, temperature >=38°C
* Non-blanching rash
* Bulging fontanelle
* Neck stiffness
* Status epilepticus
* Focal neurological signs
* Focal seizures
Coeliac disease testing in children?
Patients should be advised not to start a gluten‑free diet until diagnosis is confirmed by a specialist, and to continue on a normal diet (containing gluten) with some gluten in more than one meal every day for at least six weeks before testing.
Measles features?
Mx:
- mainly supportive
- notifiable disease → inform public health!!
Mx of contacts:
- If a child not immunized against measles comes into contact with measles then MMR should be offered. (vaccine-induced measles antibody develops more rapidly than that following natural infection).
This should be given within 72 hours
Features of HSP?
Henoch-Schonlein purpura (HSP) is an IgA mediated small vessel vasculitis. HSP is usually seen in children following an infection.
Features:
- Palpable purpuric rash (with localized oedema) over buttocks and extensor surfaces of arms and legs.
- Abdominal pain
- Polyarthritis
- Features of IgA nephropathy may occur e.g. haematuria, renal failure
Treatment:
- Analgesia for arthralgia
- Treatment of nephropathy is generally supportive. There is inconsistent evidence for the use of steroids and immunosuppressants.
Prognosis:
- usually excellent, HSP is a self-limiting condition, especially in children without renal involvement.
- blood pressure and urinanalysis should be monitored to detect progressive renal involvement.
- Around 1/3rd of patients have a relapse
GORD in children?
Gastro-oesophageal reflux is the commonest cause of vomiting in infancy. Around 40% of infants regurgitate their feeds to a certain extent so there is a degree of overlap with normal physiological processes.
Features:
- Typically develops before 8 weeks
- Vomiting/regurgitation
- Milky vomits after feeds
- May occur after being laid flat
- Excessive crying, especially while feeding
Mx:
- Advise regarding position during feeds - 30 degree head-up.
NICE do not recommend a proton pump inhibitor (PPI) to treat overt regurgitation in infants and children occurring as an isolated symptom.
A trial of one of these agents should be considered if 1 or more of the following apply:
- unexplained feeding difficulties (for example, refusing feeds, gagging or choking)
- distressed behaviour
- faltering growth
Prokinetic agents e.g. metoclopramide should only be used with specialist advice.
Kawasaki disease features?
Kawasaki disease is a type of vasculitis which is predominately seen in children.
Features:
- High-grade fever which lasts for > 5 days. Fever is characteristically resistant to antipyretics.
- Conjunctival injection
- Bright red, cracked lips
- Strawberry tongue
- Cervical lymphadenopathy
- Red palms of the hands and the soles of the feet which later peel
Mx:
- High-dose aspirin
- Kawasaki disease is one of the few indications for the use of aspirin in children. Due to the risk of Reye’s syndrome aspirin is normally contraindicated in children.
intravenous immunoglobulin
echocardiogram (rather than angiography) is used as the initial screening test for coronary artery aneurysms.
CRASH BURN
C – Conjunctivitis
R – Rash
A – Adenopathy Cervical lymphadenopathy (usually unilateral, >1.5 cm)
S – Strawberry tongue. Plus red, cracked lips and oral mucositis
H – Hands and feet changes Redness, swelling, later peeling (desquamation)
and
BURN – Fever, persistent fever ≥ 5 days (often resistant to antipyretics)
Hand, foot and mouth disease caused by which virus?
Hand, foot and mouth disease is a self-limiting condition affecting children. It is caused by the intestinal viruses of the Picornaviridae family (most commonly coxsackie A16 and enterovirus 71). It is very contagious and typically occurs in outbreaks at nursery.
Symptomatic treatment only: general advice about hydration and analgesia
children do not need to be excluded from school.
Duration of Abx for UTI in children? Mx for UTI?
Infants less than 3 months old should be referred immediately to a paediatrician.
Children aged more than 3 months old with an upper UTI should be considered for admission to hospital. If not admitted oral antibiotics such as cephalosporin or co-amoxiclav should be given for 7-10 days.
Children aged more than 3 months old with a lower UTI should be treated with oral antibiotics for 3 days according to local guidelines, usually trimethoprim, nitrofurantoin, cephalosporin or amoxicillin.
Mx for undescended testis?
***Unilateral undescended testis:
Referral should be considered from around 3 months of age, with the baby ideally seeing a urological surgeon before 6 months of age.
orchidopexy: Surgical practices vary although the majority of procedures are performed at around 1 year of age.
Bilateral undescended testes:
Should be reviewed by a senior paediatrician within 24hours as the child may need urgent endocrine or genetic investigation.
Referral before 3m: referral sooner than this may be unnecessary in a proportion of cases that may eventually descend naturally.
Still undescended at 3 months:(corrected for gestational age) Refer to paediatric surgery / urology — do not wait beyond this!
Acquired / ascending testis (previously in scrotum, now not palpable): Refer promptly — same urgency as congenital case
Infant dyschezia
Infant dyschezia is a benign, self-limiting condition that typically presents in infants aged under 9 months. It is caused by immature coordination of abdominal muscles and the anal sphincter, leading to straining and crying before passing soft stools. Key features include:
UTI in children, imaging?
NICE suggests that a child under six months with a first-time UTI would need an ultrasound scan carried out within six weeks, looking for structural abnormality.
In line with NICE, if a child over the age of six months has responded to antibiotic treatment within 48 hours, then they do not need any further investigations.
For children aged six months and older with first-time UTI that responds to treatment, without any atypical signs and symptoms, routine ultrasound is not recommended.
CMPI/CMPA
This child has non-IgE mediated cow’s milk allergy with a delayed rather than immediate reaction, which is often mislabelled as ‘lactose intolerance’. (Lactose intolerance would only cause gut symptoms).
Infants with allergy symptoms occurring immediately after milk ingestion require specific IgE milk antibody testing - either blood testing, or skin prick testing in secondary care.
Infants with delayed symptoms do not need testing and dietary management involves removing the allergenic protein from his diet. If the child is breast-fed then all dairy products must also be removed from the mother’s diet.