Paeds - ILAs Flashcards

(177 cards)

1
Q

What is stridor?

A

harsh monophonic noise on breathing, primarily during inspiration, caused by turbulent airflow in the upper airway
from the THORACIC INLET UPWARDS

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2
Q

What are the causes of stridor

3 broad categories

A

Narrowing of airway:

  • Croup
  • Epiglottitis
  • Bacterial tracheitis
  • Anaphylaxis

Inhaled foreign body

Congenital airway abnormalities

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3
Q

What is wheeze?

A

Polyphonic expiratory whistling noise due to turbulent flow in the lower airway
(if severe it can be on inspiration too)

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4
Q

CASE:
2 year old child with coryza
Then barking cough, noisy breathing, hoarse cry
Healthy and up to date with immunisations

Diagnosis?

A

Croup

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5
Q

Diagnostic features of croup (symptoms)

A

Barking cough
Hoarse voice
Stridor
Preceded by coryzal symptoms and fever

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6
Q

What is epiglottitis

A

Intense swelling of epiglottis and surrounding tissue associated with sepsis

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7
Q

What is the causative pathogen for epiglottitis?

A

HiB - haemophilus influenzae B

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8
Q

What is the causative pathogen for croup?

A

Parainfluenza

+ can be:
Influenza
RSV
Human metapneumovirus

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9
Q

What is the typical age for a child with croup?

A

6 months to 6 years

Peak in second year of life

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10
Q

Classical presentation of a child with epiglottitis

A

Very unwell - toxic looking
Painful throat
Stridor
Unable to swallow - so drooling / dribbling
Immobile and upright - trying to keep airway open

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11
Q

Distinguishing features between croup and epiglottitis

A

Croup = days, epiglottitis = hours
Croup = coryzal prodrome
Cough - barking in croup, minimal in epiglottitis
Mouth closed in croup, drooling and dribbling in epiglottitis
Keeping upright in epiglottitis
Fever - mild in croup, high fever in epiglottitis

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12
Q

CASE:
5 year old girl
Sore throat, drooling of saliva, high fever
Increasing difficulty with breathing over 8 hours
Not up to date with immunisations

Diagnosis?

A

Acute epiglottitis

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13
Q

How do you treat epiglottitis?

General management
Medication
Prophylaxis for close contacts

A

Hospital admission
Call anaesthetist / paediatrician / ICU
Take cultures after airway secure / intubated

IV cephalosporin for 7-10 days
Cefuroxime, Ceftriaxome or Cefotaxime

+ prophylaxis for close contacts = Rifampicin

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14
Q

Why shouldn’t you examine the throat in a child with stridor?

A

Could cause a partial obstruction to become a full obstruction
If epiglottitis - due to laryngospasm

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15
Q

What is the first line treatment for croup?

+ DOSE

A

Oral dexamethasone - 0.15mg/kg stat dose
If none - prednisolone

If unable to take oral:

  • Nebulised budesonide
  • IM dexamethasone
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16
Q

How would you manage a child with croup who’s developing respiratory depression?

A

Call anaesthetist - get ready to intubate + ICU
High flow oxygen
Nebulised adrenaline

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17
Q
CASE:
Child with
Difficulty breathing
Difficulty feeding
Dry cough
Coryza
Unwell for 2 days but worse overnight

+ signs of respiratory depression
Widespread crepitations
Wheeze

DIAGNOSIS
Child who is 6 months
Child who is 2 years

A

6 months = bronchiolitis (up to 1 year)

2 years = viral induced wheeze (1 - 3.5 years)

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18
Q

What are the causative pathogens for bronchiolitis?

A
RSV most common
Parainfluenza
Influenza
Adenoviruses
Rhinoviruses
Metapneumovirus
Chlamydia
Mycoplasma pneumoniae
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19
Q

What are the risk factors for bronchiolitis?

A
Child <1 year of age
Chronic lung disease of prematurity
Congenital heart disease
Immunodeficiency
Other lung disease eg cystic fibrosis
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20
Q

What is the diagnostic investigation for bronchiolitis?

A

PCR nasal secretions

Maybe chest x ray - unsure tbh

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21
Q

How would you treat a child with bronchiolitis?

A
Supportive treatment
Oxygen to get sats above 92%
Fluids
CPAP / mechanical ventilation
Infection control
Bronchodilator for wheeze
Antivirals if immunodeficient / underlying heart or lung disease
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22
Q

How would you prevent bronchiolitis?

+ what groups of people would you do this for

A

Pavilizumab
IM injection for 5 months starting October

Preterm babies
Oxygen dependent infants at risk of RSV infection
Chronic lung disease eg cystic fibrosis

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23
Q

What is used in newborns to diagnose cystic fibrosis?

A

Heel prick test - Guthrie

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24
Q

What conditions are picked up on the newborn heel prick screening test?

A
Many Children Can Present More Severely
Maple syrup urine disease
Cystic fibrosis
Congenital hypothyroidism
Phenylketonuria
MCADD
Sickle cell disease
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25
What is the pattern of inheritance for cystic fibrosis?
Autosomal recessive
26
Which gene is affected in Cystic fibrosis and what chromosome is this gene on?
CFTR - cystic fibrosis transmembrane regulator | Chromosome 7
27
Which organ systems are affected in cystic fibrosis? (6)
``` Lungs Liver Skin Pancreas GI Reproductive ```
28
How would an infant present with cystic fibrosis? (5)
``` Delayed passage of meconium Prolonged jaundice Failure to thrive Recurrent infections Malabsorption and steatorrhoea ```
29
How would a young child present with cystic fibrosis? (4)
Bronchiectasis Rectal prolapse Nasal polyps Sinusitis
30
How would an older child present with cystic fibrosis? (6)
``` ABPA (allergic bronchopulmonary aspergillosis) Diabetes mellitus Cirrhosis / portal hypertension Distal intestinal obstruction Pneumothorax / recurrent haemoptysis Sterility in males ```
31
CASE 6 week old 3 week history of progressive wheeze, poor feeding, poor weight gain Now appears short of breath, especially at end of feeds Born at term with no difficulties Neonatal exam normal Differential diagnoses?
``` Heart failure Bronchiolitis Pneumonia Cystic fibrosis GORD Foreign body ```
32
How would you investigate a child with wheeze, poor feeding, poor weight gain, respiratory distress, harsh pansystolic murmur loudest at left sternal edge, palpable liver, creps in lungs?
ECG - upright T wave = pulmonary hypertension CXR - for cardiomegaly and pulmonary vascular markings ECHO - to look for congenital heart disease Blood pressure in limbs - for coarctation of aorta Pre and post ductal sats - for PDA
33
What medications would you give to a baby with heart failure?
Diuretics - furosemide | ACE inhibitor
34
How would you treat a baby with heart failure?
Medications - diuretics and ACE inhibitors Surgical repair of VSD - at 3 months Additional calorie input to make them bigger for surgery
35
What are the causes of heart failure in neonates? (4)
Hypoplastic left heart syndrome Critical aortic stenosis Severe coarctation of the aorta Interruption of the aortic arch
36
What are the causes of heart failure in infants? (3)
VSD AVSD Large persistent ductus arteriosus
37
What are the causes of heart failure in older children? (3)
Rheumatic heart disease Eisenmengers Cardiomyopathy
38
What are the components of the septic screen?
Bloods - FBC - U&E - CRP - Cultures - PCR (viral cause) Urine - Dipstick - Microscopy - Culture - Virology ``` CXR Sputum culture Stool culture Lumbar puncture Rapid antigen test ```
39
What does the rapid antigen test identify?
Group A strep
40
What would you look for on a lumbar puncture in a septic child? (4)
Appearance WBC Glucose Protein
41
What are the contraindications for a lumbar puncture in a septic child? (6)
``` Signs of raised ICP Reduced conscious level Local infection at site of LP Thrombocytopaenia Focal neurological signs Cardiac instability ```
42
``` Lumbar puncture results: Turbid appearance Increased polymorphs Increased protein Decreased glucose ``` Likely diagnosis?
Bacterial meningitis
43
What are the signs of raised ICP in a child? (5)
``` Coma High BP Low heart rate Papilloedema Bulging fontanelle ```
44
``` Lumbar puncture results: Clear appearance Increased lymphocytes Normal glucose Normal protein ``` Likely diagnosis?
Viral meningitis
45
``` Lumbar puncture results: Viscous appearance Increased lymphocytes Increased protein Decreased glucose ``` Likely diagnosis?
TB meningitis
46
``` Lumbar puncture results: Clear appearance Normal WCC Increased protein Decreased glucose ``` Likely diagnosis?
Encephalitis
47
What does the rash look like for meningococcal septicaemia?
Purpuric | Non-blanching
48
What is the likely diagnosis in a child with purpuric rash and fever?
Meningococcal sepsis
49
How would you immediately manage a child with meningococcal sepsis?
``` ABCDE Protect the airway Give high flow O2 Set up IVI If in shock give boluses of 0.9% saline (20ml/kg) If shock persists - intubate ```
50
What medical treatment would you give to child with suspected meningococcal sepsis if you were in primary care? + dose + route
IM benpen 300mg up to 1 year 600mg 1-9 years 1.2g >10 years
51
What medical treatment would you give to a child with suspected meningococcal sepsis in secondary care? + dose + route
Ceftriaxone 50-80mg/kg/day IV infusion If <3 months cefotaxime + amoxicillin 50mg/kg qds
52
What measures would you use to monitor a child with meningococcal sepsis?
``` Pulse BP Resp rate Consciousness level WCC Platelets ```
53
How is N. Meningitidis carried?
Carried in the throat
54
How is N. Meningitidis passed on? | And who to?
Person-to-person through droplets of respiratory or throat secretions Close and prolonged contact (kissing, sneezing, coughing) or living in close quarters
55
What is the definition of a close contact?
Household member or 8 or more hours of contact
56
What is the prophylactic treatment for meningococcal sepsis? | + dose and how many
``` Rifampicin 4 doses orally, 12 hourly 5mg/kg <1 year 10mg/kg 1-12 years 600mg >12 years ```
57
What are the contraindications for Rifampicin? (4)
Liver disease Diabetes Porphyria On antiretrovirals
58
What are the side effects for Rifampicin to warn people about? (4)
Turns urine red Can stain contact lenses Flu-like symptoms Interacts with OCP + other P450 drugs eg Warfarin
59
CASE 3 year old with 7 day history of high fevers, red eyes, diffuse maculopapular rash, sore mouth and throat, cervical swelling, swollen palms Differential diagnoses?
Kawasaki disease Scarlet fever Staph scalded skin Toxic shock syndrome
60
What are the diagnostic criteria for Kawasaki disease?
Fever for >5 days with no other explanation + 4/5 of: Conjunctivitis Changes of mucous membranes of mouth - cracked lips, strawberry tongue Swollen hands and feet --> peeling Diffuse maculopapular rash (polymorphous exanthem) Cervical lymphadenopathy >1.5cm (non-suppurative)
61
What would you see in the bloods of a child with Kawasaki disease? (8)
``` FBC - leucocytosis initially - thrombocytosis - normocytic, normochomic anaemia Increased coagulability Raised ESR (mainly, beyond fever) / CRP Raised LFTs Hypoalbminaemia B cell / circulating monocyte and macrophage activation ```
62
What is the first line management for Kawasaki disease? | + doses
High dose IVIG 2g/kg over 12 hours single infusion Aspirin 30-50mg/kg/day When fever resolves - 3-5mg/kg/day for 6 weeks
63
How would you follow up a child with Kawasaki disease?
Serial ECHO from 6 weeks | If aneurysm --> warfarin
64
What are the complications with first line treatments for Kawasaki disease?
``` Infections from IVIG eg Hep C Reyes syndrome - aspirin Anaphylaxis / allergic reaction Acute renal failure Thrombosis Aseptic meningitis ```
65
What is the initial drug treatment for JIA?
NSAIDs - ibuprofen, diclofenac, naproxen
66
Other than NSAIDs, what types of medication can be used in the treatment of JIA? (4)
Methotrexate Etanercept (anti-TNF) Tocilizumab (anti-IL6) Intra-articular steroid injections - Triamcinolone
67
What should be included in the follow up for a patient with JIA?
Regular screening for uveitis | Measuring growth
68
CASE Child with weight loss, drinking and weeing a lot, unresponsive, stomach ache GCS 8 Dehydrated Diagnosis?
DKA
69
How would you immediately resuscitate a child in DKA?
``` ABCDE IV access Intubate if GCS 8 or below Boluses of 0.9% saline 10ml/kg - NOT TWENTY AS DKA ```
70
How do you calculate fluid requirements? (equation)
Overall fluid requirement = maintenance + deficit + ongoing losses
71
How do you calculate maintenance fluids?
First 10kg = 100ml/kg daily 11-20kg = 50ml/kg daily Over 20kg = 20mg/kg daily So 100/50/20 per day Or 4/2/1 per hour
72
How do you calculate fluid deficit?
Fluid deficit = current weight (kg) x % deficit x 10
73
How long is fluid deficit given over?
Normally = 24 hours | In DKA = 48 hours
74
How do you treat shock? (fluids)
Normal child = 20ml/kg boluses of 0.9% saline | DKA = 10ml/kg boluses of 0.9% saline
75
Outline the management of a child in DKA
First 12 hours = 0.9% saline + 40mmol/L KCL + insulin infusion 0.1 units/kg/hour after 1 hour + when glucose is <14mmol/L add 5% glucose After 12 hours - if plasma sodium stable - 0.45% saline + 5% glucose + 40mmol/L KCL + treat precipitating cause
76
What would you monitor while treating a child in DKA? (8)
``` Fluid input/output Blood glucose (hourly) Blood ketones (1-2 hourly) Electrolytes - sodium, potassium, calcium (2-4 hourly) Creatinine (dehydration) (2-4 hourly) Acid base status (2-4 hourly) + continuous cardiac monitoring until potassium stable + neurological state ```
77
When should you stop the insulin infusion when treating a child in DKA?
1 hour after first subcut insulin given
78
Why should you give the correction of fluid deficit over 48 hours in a child with DKA?
To prevent cerebral oedema
79
How do you make a diagnosis of DKA - from the bloods? (5)
Hyperglycaemia Blood gas: - Low pH - Low HCO3 - METABOLIC - Low pCO2 - respiratory compensation Ketones
80
CASE A neonate with high TSH on screening Diagnosis?
Congenital hypothyroidism
81
Which axis is involved in the production of thyroid hormones?
Hypothalamo-pituitary-thyroid axis
82
What is the most common cause of hypothyroidism worldwide?
Iodine deficiency - poor intake
83
What is the most likely cause of hypothyroidism in a child in the UK?
Thyroid dysgenesis: - Aplasia - Hypoplasia - Ectopic thyroid
84
What is the biosynthetic cause of hypothyroidism in children?
Consanguineous pedigree - thyroid hormone biosynthetic defect (truncated TSH)
85
Clinically, how would you differentiate between thyroid dysgenesis and a biosynthetic thyroid defect and what are you looking for?
Thyroid imaging - USS to see aplasia / hypoplasia Radionucleotide scanning - for location of thyroid as - Dysgnesis is anatomical - Biosynthetic would appear normal
86
What is the treatment for congenital hypothyroidism? + route + dose
Levothyroxine Oral 10-15mcg/kg/day
87
What are the symptoms of hypothyroidism? (10)
``` Prolonged jaundice Umbilical hernia Pallor Hypothermia Macroglossia Hypotonia Dry skin Constipation Goitre Cretinism ```
88
CASE 10 day old baby Collapsed and shocked Differential diagnoses? (7)
``` Hypovolaemia - dehydration, sepsis, DKA, blood loss Infection - meningitis, GBS, septicaemia Thyrotoxicosis Congenital heart defects Hypoglycaemia / other metabolic NAI NEC ```
89
What is your immediate management for a shocked and collapsed neonate? (7)
``` ABCDE Neonatal unit Vascular access Bolus 0.9% saline 10-20ml/kg if circulatory compromise Bloods Septic screen Start broad spectrum abx ```
90
Which blood tests would you do for a collapsed and shocked neonate and what are you looking for? (4)
Glucose - hypoglycaemia FBC - anaemia / blood loss / infection U&E - metabolic shit / dehydration Blood gas - self explanatory
91
What do the bloods show in a child in salt losing crisis (congenital adrenal hyperplasia)?
``` Hyponatraemia Hyperkalaemia Hyperuraemia Decreased bicarb Low pH Low CO2 if respiratory compensation Hypoglycaemia ``` (metabolic acidosis)
92
How would you initially manage a child with salt losing crisis / congenital adrenal hyperplasia?
ABCDE Fluid resuscitation Glucose etc IV: - Hydrocortisone - Saline - Glucose
93
What enzyme are children with congenital adrenal hyperplasia deficient in?
21-hydroxylase
94
Describe the pathophysiology of why children with 21-hydroxylase deficiency present the way they do
Less progesterone can turn into aldosterone and cortisol as 21-hydroxylase is the enzyme needed for this So more is turned into 17-hydroxyprogesterone and then adrenal androgens
95
What is the long term management for congenital adrenal hyperplasia?
Glucocorticoids - hydrocortisone (suppresses ACTH and so testosterone) Mineralocorticoids - fludrocortisone (salt loss) Referral to endocrinologist
96
How may females present with congenital adrenal hyperplasia?
``` Ambiguous genitalia (giant clit) (less likely to get salt-losing crisis) ```
97
How do you classify the causes of faltering growth?
Non-organic = not getting enough in (maternal depression, neglect, insufficient breast milk) Organic = stuff to do with the baby - Impaired suck / swallow - Bringing it up - vomiting, GORD - Chronic disease (CKD< anaemia, CF, Crohn's) - Malabsorption (CF, Crohn's) - Increased requirements (chronic infection, cancer, thyrotoxicosis) - Failure to utilise nutrients (hypothyroidism, infection, chromosomal abnormalities, IUGR)
98
How would you investigate a 4 month old baby, exclusively breast fed, who has faltering growth and is possetting more but nothing else?
Check how much the mother is expressing Bloods: - U&Es (dehydration, electrolytes) - TFTs - Coeliac antibodies - LFTs (CF) Urinalysis
99
What are the causative organisms for UTI?
E coli Klebsiella Proteus Pseudomonas
100
Which antibiotic would you prescribe for a 4 month old with a UTI (from urinalysis)?
IV cefotaxime / cefuroxime / gentamicin
101
Which oral antibiotics would you prescribe for a 4 month old with a UTI?
Trimethoprim Nitrofurantoin Co-amoxiclav
102
What further investigations would you perform on a small child who has had a UTI? + what do you look for
USS - obstruction DMSA - renal scarring / kidney function Micturating cysterourethrogram - retrograde flow of urine
103
What would increase your likelihood of investigating a child with a UTI?
Whether they respond to abx in 48 hours Previous UTI Any child under 6 months with UTI Atypical organism (non-E coli)
104
What are the possible causes of diarrhoea in children?
Toddler's diarrhoea Overflow diarrhoea Gastroenteritis Inflammatory bowel disease
105
CASE A 5 year old girl, previously continent of faeces, now soiling herself, is small amounts of loose stool, unaware that she is doing it. O/E mass in left iliac fossa Diagnosis?
Overflow diarrhoea
106
How would you explain overflow diarrhoea to the parents of a child who has it?
Explain that she is chronically constipated - this is blocking the lumen of the bowel So everything else ie water has to go round it and just comes out
107
How would you manage a child with overflow diarrhoea?
Movicol | Loads of it
108
What are the causes of proteinuria in children?
Minimal change disease Infection, exercise, orthostatic Hypertension Reduced renal mass
109
What are the specific diagnostic criteria for nephrotic syndrome?
``` Heavy proteinuria = 1g/m2/24 hours Hypoalbuminaemia <25g/L Oedema (clinical) High protein:creatinine ratio Hyperlipidaemia ```
110
What initial investigations would you do in a patient with nephrotic syndrome?
``` FBC U&E LFTs Immunoglobulins Complement levels Varicella titres ``` Hep B+C serology Consider renal USS / biopsy
111
What are the possible causes of nephrotic syndrome?
Minimal change disease Focal segmental glomerulosclerosis Membranous nephropathy Secondary to Hep B / SLE / diabetes
112
How would you manage a child with nephrotic syndrome?
Oral prednisolone 60mg/m2 for 4 weeks then 40mg/m2 on alternate days for 4 weeks then wean over 4 months
113
Why do you wean children with nephrotic syndrome off of their steroids?
To avoid adrenal crisis
114
What are children with nephrotic syndrome prone to?
Infections with capsulative organisms as depleted of IG and complement
115
What is the prognosis for nephrotic syndrome?
1/3 resolve 1/3 relapse 1/3 become steroid resistant
116
What are the clinical features of adrenal crisis / insufficiency / Addison's crisis?
Circulatory collapse Dehydration Hypertension
117
What are the features in the blood of a child in adrenal crisis?
``` Hyperkalaemia Hypercalcaemia Hyponatraemia Hypoglycaemia Hypothyroid ```
118
CASE A girl who is basically zoning out at home and school. Her work is deteriorating at school. Everything else - neuro exam, development is normal. Differentials?
Daydreaming Deafness Absence seizures Inattentive ADHD
119
How could you investigate a child who is zoning out a lot of the time and is otherwise normal?
ECG (arrhythmias) Connor's questionnaire (inattentive ADHD) EEG + hyperventilation (3/s spike and wave, in all 4 quadrants as generalised) MRI + CT Metabolic tests
120
How do you treat absence seizures? + side effects
``` Sodium valproate Vomiting Appetite increase Liver failure Pancreatitis Regrowth of hair curly Oedema Ataxia Thrombocytopaenia / teratogenicity / Encephalopathy ```
121
What medication would you NOT give in absence seizures?
Carbamazepine
122
CASE A child with previous absence seizures has a generalised tonic clonic a few years later and she is clumsy in the mornings Diagnosis?
Myoclonic jerks / juvenile myoclonic seizures
123
How do you treat juvenile myoclonic epilepsy?
Lamotrigine / valproate (but if approaching childbearing age then would stop valproate)
124
What is the long term prognosis of childhood absence seizures?
80% go on to remain seizure-free | 20% develop either juvenile absence epilepsy or juvenile myoclonic epilepsy
125
What are the four fields of development?
Gross motor Fine motor Speech, language, hearing Social
126
What developmental milestones would you expect a 6 month old child to have achieved?
Gross motor - hold head up, sit without support (with round back) Fine motor - grip with whole palm, hold objects with both hands and bang together, transfer objects between hands - Newborn - fix and follow - 6 weeks - turn head 90 degrees to follow object - 3-4 months spend time watching hands Speech and language - use consonant monosyllables, turns to sounds out of sight - Newborn - quieten to voices and startle to loud noises - 6 weeks - respond to mothers voice - 12 weeks - vocalise when spoken to, coo and laugh Social - smile, become more socially responsive, put food in mouth
127
What developmental milestones would you expect a child to have reached by 12 months?
Gross motor - cruising round edge of furniture or walking Fine motor - pincer grip using thumb and index finger, use index finger to point to objects Speech and language - non-specific two syllable babble (mama, dada), maybe use two syllable words appropriately and understanding of other single words (drink, no) Social - separation anxiety, wave goodbye, feed self using fingers and drink from a cup
128
What is the Moro reflex?
STARTLE REFLEX sudden extension of head causing symmetrical extension then flexion of the arms
129
What is the significance of abnormal persistence of primitive reflexes?
Abnormal development of the brain | UMN lesion
130
What are the primitive reflexes? (6)
``` Moro Sucking reflex Grasp reflex Rooting reflex (turn head to nipple) Stepping response Asymmetrical tonic neck reflex (look out to one side and throw the arm out) ```
131
What is cerebral palsy?
Umbrella term for a permanent disorder of movement and/or posture and of motor function due to a non-progressive abnormality in the brain before 2 years of age
132
What happens if a child get a non-progressing abnormality of the brain after 2 years of age? ie what is it called
Acquired brain injury
133
What causes cerebral palsy?
``` Antenatal (80%) - Cerebrovascular haemorrhage - Ischaemia - Cortical migration disorder - Structural maldevelopment of the brain Perinatal - Hypoxic ischaemic injury Postnatal (10%) - Meningitis / encephalitis - Head trauma - NAI - Symptomatic hypoglycaemia - Hydrocephalus - Hyperbilirubinaemia ```
134
What predisposes children to the causes of cerebral palsy?
Prematurity
135
Why do the clinical signs of cerebral palsy change over time?
When peers are developing normally, they aren't acquiring the same skills so looks like more are forming progressive motor dysfunction
136
What are the types of cerebral palsy?
Spastic (90%) - unilateral or bilateral (bilateral = diplegia / quadriplegia) Dyskinetic (floppy, chorea, dystonia) Ataxic (cerebellar - genetically determined)
137
What are the features of a spastic cerebral palsy?
UMN Hypertonia Brisk deep tendon reflexes Clasp knife shit
138
What investigations would you perform to confirm a diagnosis of cerebral palsy?
None as clinical diagnosis | But MRI can show where the injury is depending on the cause + if spasticity then look at corticospinal tracts for damage
139
Which specialists are involved in the care of a child with cerebral palsy?
``` Doctor (paediatrician) Specialist nurse Speech and language therapist Physiotherapist Occupational therapist Dietician Psychologist ```
140
When would botox be prescribed in a child with cerebral palsy?
Excessive spasticity
141
CASE A kid with a squint - left eye pointing outwards but moves inwards when the other eye is covered Diagnosis?
Exotropia | Non-paralytic as moves back when the other eye is covered
142
What are the causes of a exotropic wang eye?
Congenital Difference in visual acuity Space occupying lesion (if paralytic)
143
How would you treat a child with an exotropic wang eye?
Patch on good eye Frosted glass in glasses on good eye side Surgery to correct (to prevent amblyopia)
144
What is the complication associated with long term untreated exotropic wang eye?
Amblyopia (blindness in affected eye)
145
How would you investigate a paralytic squint?
Imaging of the head and orbit (MRI) | To look for tumours
146
How would you treat status epilepticus?
``` Benzodiazepine 2nd dose benzodiazepine Paraldehyde IV phenytoin Rapid sequence induction - intubation + general anaesthesia - usually makes it stop ```
147
How do you define status epilepticus?
Seizure lasting 30 mins or longer
148
CASE Infant born at 27 weeks gestation, following SROM 48 hours before. He is dependent on oxygen to maintain his saturations in the normal ranges, and is working hard to breathe. Differentials?
``` Respiratory distress syndrome Infection - sepsis, pneumonia Heart disorders - PDA, VSD, ToF Blood disorders eg sickle cell Meconium aspiration Diaphragmatic hernia Persistent pulmonary hypertension of the newborn ```
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Outline the pathophysiology of respiratory distress syndrome
Surfactant deficiency Leads to: - Alveolar collapse - Increased work of breathing - Hypoxia
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How would you manage a child with respiratory distress syndrome?
Oxygen with CPAP Surfactant - intubate and inject into the lungs - improves in one minute + antenatal steroids usually
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What are the clinical features of respiratory distress syndrome?
Tachypnoea over 60bpm Sternal or subcostal recession Grunting Cyanosis if severe Within FOUR HOURS OF BIRTH
152
What antibiotics would you use if you suspected GBS infection in a newborn? (+ route)
IV benpen + gentamicin
153
What are the possible reasons why a premature neonate could develop hypoglycaemia in the hours after birth?
Prematurity - increased risk of hypoglycaemia (due to decreased glycogen storage) Not been fed Glucose usually dips in the first few hours after birth anyway
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How would you manage a premature baby who has developed hypoglycaemia after birth?
Feed Keep warm 2ml/kg 10% dextrose bolus 20ml/kg 0.9% saline bolus
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How would you feed a premature baby?
``` If <34 weeks - don't have suck and swallow so feed via NG tube Otherwise enterally (normally) ``` Start slowly and build
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Why would you not build up feeds to quickly?
Risk of NEC
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How do you monitor the adequacy of nutrition given to babies?
Plot height and weight on centile chart and correct for gestational age
158
What are the differentials for sudden deterioration / looking pale in a premature baby?
Shock: - Sepsis - Hypoxia - Hypovolaemia - IVH
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How would you identify interventricular haemorrhage in a premature baby?
Cranial ultrasound - through anterior fontanelle
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What are the long term problems associated with prematurity?
Retinopathy of prematurity Hearing loss Respiratory distress syndrome and chronic lung disease Intracranial haemorrhage
161
How do you assess jaundice clinically?
Looking where it starts and progresses - usually starts at head and progresses down to the feet
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What investigations would you perform in a baby who is jaundiced?
Blood bilirubin level - assess conjugated vs unconjugated Blood typing G6PD Blood film Direct Coombs test - haemolytic disease of the newborn basically
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How do you know when to treat a baby who is jaundiced?
Look at the level | Under 24 hours - usually need to treat as not physiological
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How would you treat a baby with jaundice?
Phototherapy | Antibiotics if suspected infection
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What is the harmful complication of jaundice?
Kernicterus - encephalopathy due to deposition of unconjugated bilirubin in the basal ganglia When unconjugated bilirubin exceeds albumin binding capacity
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What are the causes of jaundice that occur within the first 2 days of life?
Haemolysis - Rhesus incompatibility - ABO incompatibility - G6PD deficiency - Spherocytosis - Pyruvate kinase deficiency - Congenital infection
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What are the causes of jaundice that occur within 2-14 days of life?
Physiological Breast milk jaundice Could be infection
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What are the causes of jaundice lasting longer than 2 weeks?
``` BILIARY ATRESIA Infection Polycythaemia Crigler-Najjar syndrome Hypothyroidism Pyloric stenosis Bile duct obstruction Neonatal hepatitis ```
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How would you investigate a neonate with prolonged jaundice (>2 weeks)?
HIDA scan - isotope scan showing the structure of the biliary tree - for biliary atresia
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What disease is important to identify in a baby with prolonged jaundice?
Biliary atresia - as can lead to cirrhosis, portal hypertension, liver failure
171
What are the differentials in an inconsolable neonate who is not moving a limb?
NAI | Osteogenesis imperfecta
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What features would you look out for on an examination of a child with an inconsolable neonate who is not moving a limb?
Bruising / marks (NAI) | Blue sclera - for OI
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How would you investigate a child with a suspected fracture / immobile limb?
``` Skeletal survey - rib fractures in OI Clotting screen if bruising CT head to look for haemorrhage - NAI Skin biopsy for OI Ophthalmology - retinal haemorrhages (shaken baby) ```
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What is the mode of inheritance of osteogenesis imperfecta?
Autosomal dominant
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What other agencies would need to be involved if NAI was suspected?
Police | Social services
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What would be appropriate analgesia for a fracture in a neonate?
Calpol - paracetamol Sucrose Feeding
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How would you treat osteogenesis imperfecta?
Bisphosphonates