Paediatrics Flashcards

1
Q

What questions should be asked about the presenting illness?

A
When and how did it start?
Was he/she well before?
How did it develop?
What aggravates or alleviates it?
Has there been contact with infections?
Has the child been overseas recently?
Have the carers sought medical attention before now?
Which treatments have been tried?
Especially in infants, wet and dirty nappies, alertness and weight gain
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2
Q

What questions should be asked around PMH?

A

In utero: Any problems (abnormal bleeding, infections, Rh disease), medications, alcohol, drug use, US normal?
At birth: Gestation, mode of delivery, birth weight, resuscitation required, birth injury, malformations
As a neonate: Jaundice, fits, fevers, bleeding, special care baby unit? - How long? Later illnesses, operations, accidents, screening tests, drugs, allergies, immunisations, travel. Check red book.

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3
Q

What are the 6 week developmental milestones?

A

smiles

follows eyes past midline

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4
Q

What are the 4-6 month milestones?

A

sits with support
rolls
reaches out for objects
starts babbling

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5
Q

What are the 6-9 month milestones?

A
crawls
sits without support
pulls to stand
gives toy on request
turns head to name
responds to 'bye bye'
gestures with babbling
first tooth
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6
Q

What are the 7-12 month milestones?

A

develops pincer grasp
plays ‘peek-a-boo’
walks with a hand held
waves goodbye

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7
Q

What are the 12-15 month milestones?

A

single words
listens to stories
drinks from cup

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8
Q

What are the 18 month milestones?

A
speaks 6 words
able to walk up steps
names pictures
walks independently
scribbles
builds with blocks
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9
Q

What are the 1.5-2 year milestones?

A
kicks/throws a ball
runs
2 word sentences
follows a 2 step command
stacks 5-6 blocks
turns pages
uses a spoon
helps with dressing
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10
Q

What are the steps in the physical examination?

A
General health
Vital signs
Respiratory system
Cardiovascular system
GI system
GU system
MSK system
ENT
Anything else parents would like to be checked?
Height, weight and head circumference
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11
Q

What information can be gained in physical examination surrounding general health?

A

Is the child well or ill? Alert, lethargic, or uncomfortable / in pain? Playing is a good sign. If crying, is it high pitched or normal? Behaving normally and interacting with the parents? Any jaundice, cyanosis, rashes, anaemia, or dehydration? Neck stiffness is a rare sign in infants

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12
Q

What do you look for during the respiratory examination?

A

Is the shape of the chest normal?
Any intercostal, subcostal or sternal recession, or nasal flaring?
Use of accessory muscles?
Is there grunting or any other audible noise breathing in (stridor) or breathing out (wheeze)?
Percuss the chest for dullness
Auscultate the chest, listening for breath sounds, fine crackles, rhonchi, wheeze and pleural rub

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13
Q

What do you look for during the CV examination?

A

Check for peripheral and central cyanosis
Look for clubbing and peripheral oedema
Compare strength of femoral and right brachial pulse
Is the apex beat displaced?
Auscultate the heart with the child sitting and lying down
Listen over the apex, 2nd intercostal space left of stermum (pulmonary valve), and right of sternum (aortic valve), 4th intercostal space over the sternum (tricuspic)

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14
Q

What is fixed splitting of the second heart sound indicative of?

A

Atrial septal defect

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15
Q

What is a galloping rhythm suggestive of?

A

Congestive cardiac failure

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16
Q

What do you look for during the GI examination?

A

Child should be supine and relaxed, with knees bent
Look for distension, visible peristalsis, and hernias
Listen for bowel sounds and percuss for hepatosplenomegaly and ascites
Palpate looking for tenderness and masses (during inspiration and deep expiration)
If relevant look for anal patency, fissures and prolapse

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17
Q

What do you look for during the GU examination?

A

If relevant, examine external genitalia for evidence of ambiguity, congenital abnormality and size
Examine once only using a chaperone

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18
Q

What do you look for during MSK examination?

A

Watch the child walk and play
Examine all limbs and digits for congenital anomaly
Symmetrical skin creases on both thighs?
If <6 months check for congenital hip dislocation
Inspect the spine for dimples, hair tufts, masses or cysts at the base
Is there any abnormal curvature or posture?

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19
Q

What do you look for during ENT examination?

A

(best left until the end)
Evidence of otitis externa?
Post-auricular rash is a sign of measles, rubella and eczema
Look at the tympanic membrane - noting colour and lucency - is it perforated?
Use a spatula to check the tonsils, as well as inspecting the teeth and oral mucosa (plaques, white patches, spots, ulcers)
Can the child breathe through both nostrils
Is there a runny nose?
Check for neck lumps and lymphadenopathy

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20
Q

What is makes up ‘red’ on the traffic light system?

A

Pale, mottled, ashen blue. Doesn’t stay awake when roused. Reduced consciousness (not engaging, apathy, coma), reduced skin turgor. Any GRUNTING signs?

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21
Q

What are GRUNTING signs?

A

Grunting; weak or continuous high pitched cry; tachypnoea
Rib recession; Retraction of sternomastoid, nasal flaring, wheeze, stridor
Unequal or Unresponsive pupils; focal CNS signs, fits, marked hypotonia
Not using limbs / lying still; odd or rigid posture decorticate (flexed arms, extended legs); or decerebrate (arms and legs extended)
Temperature > or = 38 if < 6 months or >/=39 especially if cold or shutdown peripheries
I have a bad feeling about this baby
Neck rigidity, non-blanching rash, meningism, bulging fontanelle, etc.
Green bile in vomit (may = bowel obstruction, e.g. atresia, volvulus, intussusception)

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22
Q

What are common symptoms in infancy?

A
Crying
Colic
Cows' milk protein allergy
Nappy rash/diaper dermatitis
Sleep problems
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23
Q

What is the definition of colic?

A

Paroxysmal crying with pulling up of the legs, for >3h on >/= 3days/week. There is an association with feeding difficulties.

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24
Q

What advice would you give to parents with a baby with colic?

A

Movement (carry-cot on wheels) is often tried and may help
Let the baby finish the first breast first (hindmilk is easier to digest)
If breastfeeding, a low allergen diet may help, as may probiotics
Reassure strongly, reduce stress, grandparent involvement

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25
Q

How might Cows’ milk protein allergy present?

A

Separate entity to colic - IgE or non-IgE mediated.

It causes colic symptoms, but also GORD, blood/mucus in the stools, and may result in faltering growth

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26
Q

What are the four types of nappy rash?

A
  1. Common ‘ammonia dermatitis’. Red desquamating rash, sparing skin folds.
  2. Candida / thrush. Satellite spots beyond the main rash
  3. Seborrhoeic dermatitis. Diffuse, red, shiny rash extends into skin folds (occiput - cradle cap)
  4. Isolated, psoriasis-like scaly plaques
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27
Q

What are the differential diagnoses for vomiting?

A
Posseting
Vomiting between feeds (ask about carpets)
GORD, Gastritis
Over-feeding
Pyloric stenosis (projectile, at ~8 weeks old)
Any infection e.g. UTI
Adverse food reaction
Infective gastroenteritis
Rarer causes:
Pharyngeal pouch
Poisoning
Raised ICP
Metabolic conditions i.e. DKA
Almost all other conditions
Bilious (green) vomiting: get urgent help
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28
Q

What are the differentials for an ill and feverish child?

A

Self-limiting viral infection
Pneumonia
UTI
Meningitis

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29
Q

What are some problems facing babies on NICU?

A
Hypothermia
Hypoxia
Hypoglycaemia
Respiratory distress syndrome
Infection
IVH (25% of = 1500g birthweight - delayed cord clamping may reduce risk)
Apnoea
Necrotizing enterocolitis
Retinopathy of prematurity (screen)
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30
Q

Describe what happens with the first breath, and what can go wrong

A

Pulmonary vascular resistance falls, and there is a rush of blood to the lungs. Partly mediated by endogenous NO. Initiates changes from fetal to adult circulation. Process may be interrupted in various conditions e.g. meconium aspiration, pneumonia, respiratory distress syndrome, diaphragmatic hernia, group B strep infection, pulmonary hyperplasia. Pulmonary hypertension results as a consequences of these adverse events may also be primary (hypertrophy of muscular layer of pulmonary arteries.

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31
Q

What are some types of non-invasive ventilation for neonates?

A

CPAP (continuous positive airways pressure)
NIPPV (nasal intermittent positive pressure ventilation)
HFNC (high-flow nasal cannula)

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32
Q

What are some types of invasive ventilation for neonates?

A

TCPL (time cycled pressure limited ventilation)
PTV (patient-triggered ventilation)
HFV (high-frequency ventilation)

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33
Q

What might be the presentation of neonatal sepsis?

A

Signs may be non-specific and subtle. Labile temperature, lethargy, poor feeding, respiratory distress, collapse, DIC.

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34
Q

How would you manage suspected neonatal sepsis?

A

ABC
Supportive (ventilation, volume expansion, inotropes)
Bloods for FBC, CRP, glucose
Blood cultures (results take 48h)
CXR
Lumbar puncture for culture, glucose, protein count, WCC and Gram stain
Failure to responsd within 24h investigate further with stool sample for virology, throat swab, serology for herpes virus, urine CMV culture, VDRL (syphyllis)

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35
Q

What antibiotics would you give in early-onset neonatal infection?

A

Broad spectrum i.e. benzylpenicillin + gentamicin until culture results are available. Stop if well and cultures negative. Continue treatment for 7 days if +ve cultures.
In meningitis suspected then give cefotaxime

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36
Q

What antibiotics would you give in late-onset neonatal infection?

A

Broad spectrum e.g. flucloxacillin + gentamicin until cultures available
Cefotaxime if meningitis is likely
Coagulase -ve Staph is more likely in a preterm infant with CVP line - give vancomycin + discuss removal of line

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37
Q

What are the risk factors for early onset neonatal sepsis

A

Prolonged rupture of membranes >18h
Maternal infection; maternal pyrexia, chorioamnionitis, UTI
Mother carrier of Group B strep (GBS) from vagina or urine, or previous infant affected by it
Preterm labour
Fetal distress
Breaks in neonatal skin or mucosa
(caused by organisms acquired from the mother)

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38
Q

What are the risk factors for late-onset neonatal sepsis?

A

Central lines and catheters
Congenital malformations e.g. spina bifida
Severe illness
Malnutrition
Immunodeficiency
(tends to be caused by environmental organisms)

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39
Q

How common are neonatal seizures?

A

~4/1000 births - most occur 12-48h after birth. May be generalised or focal, tonic, clonic or myoclonic

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40
Q

What are the causes for neonatal seizures?

A

Hypoxic-ischaemic encephalopathy (due to antenatal or intrapartum hypoxia/ respiratory distress)
Infection (meningitis/encephalitis)
Intracranial haemorrhage / infarction
Structural CNS lesions (focal cortical dysplasia/tuberous sclerosis)
Metabolic disturbance (hypoglycaemia, hypocalcaemia, hypo/hypernatraemia, hypomagnesium)
Metabolic disorders (urea cycle disorders / amino acid metabolism)
Neonatal withdrawal from maternal drugs or substance abuse
Kernicterus (hyperbilirubinaemia)
Idiopathic seizures e.g. benign 5th day fits

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41
Q

How would you treat a neonatal seizure?

A

ABC - Help
Rule out and treat reversible causes i.e. hypoglycaemia
Start empirical antibiotics
IV access and take blood for FBC, U+E, LFTs, calcium, magnesium, glucose and blood gas
If available, start CFAM
Consider cranial US and MRI
Specialist tests include toxicology screening, serum ammonia, urine organic acids, serum amino acids, karyotype and TORCH screen.
Treat cause

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42
Q

What is hypoxic-ischaemic encephalopathy (HIE)?

A

A clinical syndrome of brain injury secondary to a hypoxic-ischaemic insult

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43
Q

What are the causes of HIE?

A

Antenatal, intrapartum up postpartum causes e.g. cord prolapse, placental abruption, maternal hypoxia (any cause) or inadequate postnatal cardiopulmonary circulation.

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44
Q

What are the causes of shock in a neonate?

A
Blood loss (placental haemorrhage, twin-twin transfusion, IVH, lung haemorrhage)
Capillary plasma leaks (sepsis, hypoxia, acidosis, necrotizing enterocolitis)
Fluid loss (D&amp;V, inappropriate diuresis)
Cardiac causes (hypoxia, left to right shunts, valve disease, coarctation)
45
Q

What should you ask before examining a neonate if not taking a history?

A

Birthweight normal?
Birth and pregnancy normal?
Mother Rh-ve?
Enlist mothers help, explain aims and listen if mother talks

46
Q

What do you look for when examining the head of a neonate?

A

Circumference
Shape (odd shapes from a difficult labour quickly resolve)
Fontanelles (tense or sunken)
Eyes - red reflex, corneal opacities, conjunctivitis
Ears - shape, position, low set? tip of the nose in white babies when pressed will be jaundiced. Shut the mouth to test breathing through the nose (choanal atresia). Oto-acoustic screening done?
Complexion - cyanosed, pale, jaundiced, or ruddy (polycythaemia)?
Mouth - Look inside, insert a finger: palate intact? suck good? does baby’s face look normal?

47
Q

What do you look for when examining the arms and hands of a neonate?

A

Single palmar creases? (normal or trisomy 21)
Does baby look like the parents?
Waiter’s tip sign of Erb’s palsy of C5 and 6 trunks
Number of fingers
Clinodactyly (5th finger curved towards ring finger (normal or trisomy 21)

48
Q

What do you look for when examining the thorax of a neonate?

A
Watch respirations
Not grunting, recessions
Palpate the precordium and apex beat
Listen to the heart and lungs
Inspect the vertebral column for neural tube defects
49
Q

What do you look for when examining the abdomen of a neonate?

A

Expect to feel the liver. Any other masses?
Inspect the umbilicus, is it healthy?
Assess skin turgor
Inspect genitalia and anus, are the orifices patent?
Ensure in the first 24hr baby passes urine (if not consider posterior urethral valves in boys) and stool (if not consider Hirschprung’s, CF, Hypothyroidism)
Is the urinary meatus misplaced, are both testes descended?
Neonatal clitoris looks large, if very large consider CAH Bleeding PV may be a normal variant following maternal oestrogen withdrawal

50
Q

What do you look for when examining the legs of a neonate?

A

Test for development dysplasia of the hip
Avoid repeated tests as it hurts, and may induce dislocation
Feel femoral pulses to ‘rule out’ coarctation
Note talipes
Toes - too many, too few, too blue?

51
Q

What do you look for when examining the buttocks/sacrum of a neonate?

A

Is there an anus?
Are there ‘mongolian spots’?
Tufts of hair +/- dimples suggest bifida occulta - if you can’t see the bottom of a dimple, arrange US
Any pilonidal sinus?

52
Q

What do you look for when assessing the CNS of a neonate?

A

Assess posture and handle the baby
Intuition can be most helpful in deciding if the baby is ill or well
Is he jittery (hypoxia, ischaemia, encephalopathy, hypoglycaemia, infection, hypocalcaemia)?
There should be some control of the head
Do limbs move normally?
Is the tone floppy, or spastic?
Are responses absent on one side (hemiplegia)?
Moro reflex
Stroke palm to elicit grasp reflex
Is the baby post-mature, small for dates, or premature?

53
Q

What are the signs of pneumonia?

A

Raised temperature
Malaise
Poor feeding
Respiratory distress:
tachypnoea, cyanosis, grunting, intercostal recession, use of accessory muscles
(older children may have typical lobar signs - pleural pain, crackles, bronchial breathing)

54
Q

When should you admit for pneumonia?

A

If SpO2 is <92%; signs of respiratory distress

55
Q

What tests should you order when suspecting pneumonia?

A

CXR
Bloods: FBC/ blood and sputum cultures if severe
Not required in community acquired pneumonia if a child is going home

56
Q

How would you treat pneumonia?

A

Amoxicillin is 1st line

Alternatives: co-amoxiclav, axithromycin, clarithromycin

57
Q

Which bacteria typically cause pneumonia?

A

Pneumococcus, Mycoplasma, Haemophilus, Staphlycoccus, (Tb, Viral)

58
Q

What are the signs of croup?

A

Stridor, Barking cough, Hoarseness from obstruction in the region of the larynx

59
Q

What is the typical epidemiology of croup?

A

<6yrs but can be recurrent in older, atopic children

Autumn

60
Q

What are the causes of croup?

A

Parainfluenza virus (1, 2, 3)
Respiratory syncitial virus
Measles (rare)

61
Q

What is the pathology of croup?

A

Subglottic oedema, inflammation and exudate

62
Q

What is mild croup?

A

Minimal recession / stridor, no cyanosis, alert child, good air entry
Can be sent home if settles w/ Tx

63
Q

How would you treat mild croup?

A

Dexamethasone (0.15mg/kg PO) or prednisolone 1-2mg/kg

64
Q

If there is a poor response to treatment in a child with croup, what should you do?

A

Adrenaline via nebuliser 1:1000 (400mcg/kg up to 5ml)

If poor response again, repeat and take to ITU

65
Q

If there is failure to improve with steroids/nebulised adrenaline in croup what should you consider?

A

Bacterial tracheitis

66
Q

How would you manage epiglottitis?

A

Avoid approaching child, don’t examine throat, don’t cannulate. Senior help.
Inhalation induction and EUA if necessary
Cause may be Haemophilus influenzae type B (Hib) - treat with cefotaxime, 25-50mg/kg/8h IV

67
Q

What is the differential for stridor in babies?

A
Viral croup
Bacterial tracheitis
Epiglottitis
Inhaled foreign body
Laryngomalacia
68
Q

Define asthma

A

Reversible airway obstruction (peak flows vary by >20%)
+/- wheeze, dyspnoea or cough
(10% of the population is affected)

69
Q

What risk factors exist for asthma?

A
Low birthweight
FHx
Bottle fed
Atopy
Male
Pollution
Past lung disease
70
Q

What gene causes susceptibility to asthma?

A

ADAM33

71
Q

What are some triggers for asthma?

A
Pollen
House dust mite
Feathers
Fur
Exercise
Viruses
Chemicals
Smoke
Traffic
72
Q

What is the differential diagnosis of asthma?

A
Foreign body
Pertussis
Croup
Pneumonia / TB (do CXR)
Hyperventilation
Aspiration
CF (wet cough, starting at birth, failure to thrive)
73
Q

How should you treat asthma exacerbations?

A

Treat early - rescue prednisolone 30-40mg/day if >5yrs or 20mg/day if 2-5 years for 5 days

74
Q

What should be the general management of a child with asthma?

A

Annual review of symptoms, exacerbations, oral steroid use, and time off school or nursery, check inhaler technique and medication adherence, make a personalised self-management action plan, advice regarding tobacco smoke exposure, record height and weight on centile charts

75
Q

What is the first line drug therapy for asthma?

A

Occasional Beta-agonist via pMDI e.g. salbutamol 100mcg - use spacer

76
Q

What is the second step in drug therapy for asthma?

A

Add inhaled steroid e.g. beclometasone - 50mcg use up to 200mcg / 12hr (i.e. 4 times in 12 hrs)

77
Q

When should you add the second step of treatment to a patient with asthma?

A

If beta-agonist is needed >3 times per week (also if >5yrs and many exacerbations, or asthma wakes from sleep >once per week)

78
Q

If first two steps of asthma treatment are not working, what should you do next?

A

Review diagnosis. Check inhaler use/concordance. Eliminate triggers. Monitor height.
If <5yrs: Add 1 evening dose of Montelukast 4mg
If >5yrs: Consider respiratory review. Can try salmeterol (LABA). If symptomatic then increased inhaled steroid and try motelukast 5my or theophylline

79
Q

How should you treat severe asthma acutely?

A

Sit up - high flow 100% oxygen
Salbutamol: 5mg O2 nebulised in 4ml saline with ipratropium bromide 0.25mg
Hydrocortisone or prednisolone
Consider one IV dose of magnesium sulphate 40mg/kg over 20 mins
Aminophylline 5mg/kg IV over 20 mins

80
Q

What is classed as a near fatal / life threatening acute asthma exacerbation?

A
Respiratory acidosis and/or requiring mechanical ventilation with increased ventilation pressures
Any one of the following: 
PEFR <33% predicted
Sats < 92%
Silent chest
Cyanosis
Feeble respiratory effort
Bradycardia, dysrhythmia, hypotension
Exhaustion, confusion, coma
81
Q

What is classed as an acute severe asthma exacerbation?

A
Any one of:
PEFR 33-50% predicted
RR: 2-5yrs > 40/min  ;   5-12 yrs >30/min   ;   >12yrs >25/min
Pulse: >140bpm, >125, >110
Inability to complete sentences
Use of accessory muscles
82
Q

What is classed as a moderate asthma exacerbation?

A

Increasing symptoms
PEFR 50-70% best or predicted
No features of severe asthma

83
Q

What is classed as brittle asthma?

A

Type 1: wide variability in PEFR despite intensive therapy

Type 2: sudden severe attacks despite apparently well controlled asthma

84
Q

What is the commonest lung infection in infants?

A

Acute bronchiolitis

85
Q

What are the features of acute bronchiolitis?

A
Coryza preceds cough
Fever (sometimes)
Tachypnoea
Wheeze
Inspiratory crackles
Apnoea
Intercostal recession +/- cyanosis +/- fever
86
Q

What are the causes of acute bronchiolitis?

A

Typically - Respiratory syncytial virus (RSV)

Others - Mycoplasma, parainfluenza, adenoviruses.

87
Q

Who is most at risk in acute bronchiolitis?

A

<6 months old

underlying conditions

88
Q

What signs in acute bronchiolitis should prompt admission?

A

Inadequate feeding
Respiratory distress
Hypoxia

89
Q

If the acute bronchiolitis is severe, what should you do?

A

CXR to exclude pneumothorax or lobar collapse
Blood gases/ SpO2
FBC

90
Q

How would you treat acute bronchiolitis?

A

Oxygen (stop when SpO2 >/=92%)
Nasogastric feeds
5% of those need respiratory support (mostly CPAP)
(mortality roughly 1%; 33% if symptomatic congenital heart disease)

91
Q

What can be given to immunocompromised children to try and prevent bronchiolitis?

A

Ribavirin

92
Q

What is viral-induced wheeze?

A

Cough and wheeze. Too young for diagnosis of asthma to be made confidently. These infants often end up being treated with escalating bronchodilator therapy with frequent courses of antibiotics against uncultured organisms. Non-atopic disorder. RSV more often than haemophilus. Spectrum.

93
Q

What is at the lower and upper end of viral induced wheeze severity?

A

Lower end is ‘happy wheezers’ i.e. undistressed

Upper end is CF in those with loose stools and failure to thrive

94
Q

What gene mutation causes CF?

A

Mutations of the transmembrane conductance regulator gene (CFTR) on chromosome 7, which codes for a cyclic AMP-regulated sodium/chloride channel.

95
Q

Broadly, what are the problems / pathology in CF?

A

Varying severity of exocrine gland function. Meconium ileus in neonates (and its equivalent in children), lung disease akin to bronchiectasis, pancreatic exocrine insufficiency, raised Na+ sweat level - in 85% of mutations.

96
Q

How do you diagnose CF?

A

All newborns are screened looking for an abnormally raised immunoreactive trypsinogen, and 29 CFTR mutations on the Guthrie card (85% coverage).
10% present with meconium ileus as neonates
Later presentation is with:
- Recurrent pneumonia
- Failure to thrive
- Slow growth
- Fatty, oily, pale stools are reflective of steatorrhoea

97
Q

What is a positive finding in the sweat test for CF?

A

<40mmol/L is normal. >60mmol/L supports the diagnosis. Intermediate results are suggestive but not diagnostic.

98
Q

What can cause false positive results in the sweat test?

A
Up to 25% of normal newborns show a sweat sodium concentration >65mmol/L (rapidly declines on the 2nd day after birth)
Atopic eczema
Adrenal insufficiency
Ectodermal dysplasia
Some types of glycogen storage disease
Hypothyroidism
Dehydration
Malnutrition
99
Q

What can cause false negative results in the sweat test?

A

Oedema

Poor technique when testing

100
Q

What is meconium ileus and how is it managed?

A

Presents with failure to pass stool or vomiting in the first 2 days of life.
Distended loops of of bowel are seen through the abdominal wall. A plug of meconium may show in one of the loops.
NG tube drainage / washout enemas / excision of gut containing meconium

101
Q

How should you manage respiratory problems in CF?

A

Physiotherapy 3x per day
Educate parents - teach percussion and postural drainage
Older children learn forced expiration techniques

102
Q

What respiratory infections can occur in CF?

A
Staph aureus
H. influenzae (rarer)
Strep pneumoniae (younger children)
Aspergillosis (in adolescents)
Eventually >90% are chronically infection with pseudomonas aeruginosa
103
Q

What GI problems do CF patients experience?

A

Energy needs rise by ~130% due to malabsorption and chronic lung inflammation
Most need enzymes for pancreatic insufficiency
Omeprazole helps absorption by increasing duodenal pH
Vitamins needed
Diet should be high protein / high calorie

104
Q

What is the prognosis for CF patients?

A

Death from pneumonia or cor pulmonale. Most survive to adulthood.
Median survival is >31 years, and possibly >50 for those born after 2000

105
Q

How does acute otitis media present?

A

Rapid onset pain
Fever +/- irritability
Vomiting
(often after a viral URTI)

106
Q

What are some common organisms that cause otitis media?

A

Pneumoccocus
Haemophilus
Moraxella
Other streps and staphs

107
Q

What causes pain in acute otitis media?

A

Bulging tympanic membrane which is relieved if it perforates

108
Q

How should you treat acute otitis media?

A

Analgesia
Resolves in >60% within 24hours without antibiotics
Consider immediate antibiotics if systemically unwell, immunocompromised or no improvement in >4 days
Amoxicillin for 5 days if required

109
Q

What are some complications of otitis media?

A

Mastoiditis

Petrositis, labrynthitis, meningitis, abscess etc (rare)