Paediatrics Flashcards

1
Q

What are the typical blood gas findings for a baby with pyloric stenosis?

A

Hypochloraemic, hypokalaemic metabolic alkalosis with base excess

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What does a “double bubble” appearance on abdominal x ray indicate?

A

Duodenal atresia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Target like papules on the skin are indicative of what?

A

Erythema multiforme
Arise due to a hypersensitivity reaction due to infection or medications
Large asymptomatic and self-limiting

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What are some duct dependent lesions?

A

Coarctation of the aorta
Hypoplastic left heart syndrome
Critical aortic stenosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What are some features of heart failure in a neonate/ infant?

A
Faltering growth
Breathlessness, especially on feeding
Hepatomegaly
Recurrent chest infections
Tachyonoea
Tachycardia
Poor feeding
Enlarged heart
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

How would an infant with heart failure due to a large VSD be treated?

A

Diuretics
ACEi
Additional calorie input
Surgery at 3-6 months

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What are the features of ADHD?

A

Inattention (e.g. forgetful, easily distracted, won’t listen to instructions, loses things)
Hyperactivity and impulsivity (talks excessively, always “on the go”, runs and climbs when not appropriate, won’t eat their turn etc)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is important to monitor for a patient on methylphenidate?

A

Growth (as it is an appetite suppressant, hence can impair growth)
Also baseline ECG before starting due to potential cardiotoxicity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

How would you manage a baby with gastro-oesophageal reflux?

A

Decrease feed volume and increase feed frequency
If breast fed: alginate e.g. infant gaviscon after each feed
If formula fed: 1-2 week trial of feed thickener, and if that fails stop and add alginate to formulae
If no improvement after 2 weeks, add antacid eg ranitidine, omeprazole

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What is the inheritance pattern of haemophilia?

A

X-linked recessive

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What is the most common congenital cause of stridor in infants?

A

Laryngomalacia

Usually self resolves by 2 years old

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

A 6 month old has a history of episodes of flexion of its head/ arms and trunk and arm extension up to 50 times before stopping. What is the most likely diagnosis?

A
West syndrome (infantile spasms)
Tx with vigabitrin and ACTH
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What drug is first line in West syndrome?

A

Vigabitrin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What are some risk factors for congenital hip dysplasia?

A

Female, oligohydramnios, birth weight >5kg, breech, family history

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What tests are done to examine a baby for congenital hip dysplasia?

A

Barlow test: to dislocate an articulated femoral head

Ortolani test: to relocate a dislocated femoral head

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What imaging is used for Perthes disease?

A

X Ray

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

What is the management of Perthes disease?

A

Stabilise with cast/ brace
Observe if under 6
Oder children will probably need surgery

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

What is the inheritance pattern of Duchenne muscular dystrophy?

A

X linked recessive

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

How may a boy with Duchenne muscular dystrophy present?

A

Delayed walking
Waddling gait
Gower’s sign
Calf pseudohypertrophy (calves enlarged due to fibrous tissue)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

How would you confirm a diagnosis of suspected Duchenne muscular dystrophy?

A

Raised creatine kinase
Genetic testing for dystrophin gene mutation
Muscle biopsy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

What is kernicterus?

A

Irreversible bilirubin induced bran dysfunction

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

What investigation is used to diagnose vesico-reflux?

A

Micturating cystourethrogram

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

What is a micturating cystourethrogram and what is it used to diagnose?

A

Vesico-ureteric reflux
Injecting contrast into the child’s bladder via a catheter and then taking a series of x-rays to etermine whether it is refluxing into the ureters

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

What is the most common cause of nephrotic syndrome in children?

A

Minimal change disease

Adults FSGS, systemic illness eg diabetes, HSP

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Q

What are the features of nephrotic syndrome?

A

Hypoalbuminaemia
Proteinuria
Oedema
Hypercholesterolaemia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
26
Q

How is nephrotic syndrome managed?

A

Course of steroids (initially high, then wean down) 8-12 weeks
Encourage healthy diet with no added salt and no high protein
Prophylactic penicillin V due to infection predisposition

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
27
Q

What are some features of Down syndrome?

A
Brachycephaly
Hypotonia
Epicanthic folds
Flat nasal bridge
Short stature
High arched palate and protruding tongue
Inwards and short little finger
Single palmar crease
Brushfield spots
Small low set ears
Learning difficulty
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
28
Q

What are some medical conditions that people with trisomy 21 are more at risk of?

A
Congenital heart defect (AVSD)
Duodenal atresia, hirschprungs 
Congenital hypothyroidism
ALL
Hearing and visual problems 
Early onset Alzheimer’s
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
29
Q

What are Brushfield spots?

A

Small white spots on the iris that are characteristic of Down syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
30
Q

What are some features of Turners syndrome?

A
Short stature
Webbed neck
Shield shaped chest
Wide space nipple
Puffiness of hands and feet
Low hair line
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
31
Q

How is Turners syndrome managed?

A

Conservative: psychological support, educational supportive eg sitting at front of class if poor hearing

Medical: growth hormone, Oestrogen therapy for puberty

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
32
Q

What is the chromosome abnormality in Klinefelter syndrome?

A

47, XXY

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
33
Q

DiGeorge syndrome leads to what symptoms?

A

CATCH-22 (deletion on chromosome 22 causing…
Cardiac abnormalities (often TOF)
Abnormal faces
Thymus aplasia (lack of T cells so immunocompromised)
Cleft palate
Hypocalcaemia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
34
Q

At what age should a child be able to smile?

A

6 weeks

Refer at 10 weeks if not

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
35
Q

What is the limit age for sitting unsupported?

A

9 months

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
36
Q

What is the limit age for a child feeding the self with a spoon?

A

18 months

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
37
Q

What is the triad of signs in ADHD?

A

Impulsivity
Hyperactivity
Inattention

38
Q

Which if nephrotic or nephritic syndrome will show hypercholesterolaemia?

A

Nephrotic syndrome

Due to response of liver to hypoalbuminaemia, so cholesterol production also increases

39
Q

What rate is an insulin infusion given at for a patient presenting with DKA?

A

0.1 units/kg/hour

40
Q

Hand foot and mouth disease is caused by which organism?

A

Cocksackie virus

41
Q

A sausage shaped abdominal mass and red current jelly stools are characteristic signs of which condition?

A

Intussuscpetion

42
Q

Transposition of the great arteries and tetralogy of fallot are both cyanosis heart lesions, but how does the timing of their presentation differ?

A

TGA presents soon after birth

Tetralogy presents at 1-2 months of age (shunt becomes R to L, “tet spells”)

43
Q

Which condition is the most common cause of pulmonary hypoplasia?

A

Diaphragmatic hernia

Can also be caused by oligohydramnios

44
Q

Barlow and Ortolani tests are used to aid the diagnosis of what?

A

Congenital hip dysplasia
Confirmed with USS
Barlows dislocats, ortolanis relocates

45
Q

What is the most common cause of gastroenteritis in children?

46
Q

What are the 4 primitive reflexes?

A

Grasp
Moro
Walking
Rooting

47
Q

At approximately what age does a child start crawling?

48
Q

What is the triad seen in haemolytic uraemic syndrome?

A

Acute renal failure
Thrombocytopenia
Haemolytic anaemia

49
Q

What is haemolytic uraemic syndrome most classically caused by?

A

E Coli gastroenteritis producing Shiga toxins

50
Q

What are the different types of cerebral palsy?

A

Spastic (most common, due to UMN of motor cortex damage)
Dystonic (due to basal ganglia damage)
Ataxic (due to cerebellar damage)

51
Q

How does spastic cerebral palsy present?

A

Can be either hemiplegic (but worse for arms than legs), diplegic, or paraplegic
Diplegic has characteristic scissor gait
All present with spasticity, hyper-reflexia, increased tone, Babinski reflex positive

52
Q

What is a febrile convulsion?

A

Seizures in children aged 6months to 6years caused by fever

That have had no history of an afebrile seizures

53
Q

What is the difference between a simple and complex febrile convulsion?

A

Simple: lasts less than 15 minutes, generalised tonic clonic seizure, no more than one in the same episode of illness

Complex: lasts >15 minutes, focal seizures, recurs in the same episode of illness

54
Q

What advice would you give to parents of a child presenting with febrile convulsions?

A
That they are very common
Likely to recur in future
No risk of brain damage
No significant increased epilepsy risk
Antipyretics are not shown to help
55
Q

What is the investigation of choice to diagnose infantile spasms?

A

EEG which will show hysarrythmia

56
Q

3Hz per second spike and wave activity on EEG is characteristic of what?

A

Absence seizures

57
Q

How will a child with absense seizures present?

A

Usually begin aged 4 to 6
“Daydreaming” with simple automatisms e.g. lip smacking, fumbling fingers
No post ictal phase
Normal neurological exam

58
Q

What is the first line medication for absence seizures?

A

Valproate

Be aware of carbamazepine as this can worsen absence seizures!

59
Q

Which drug is first line for focal seizures?

A

Carbamazepine

2nd line is lamotrigine

60
Q

Which drugs are used for different types of epilepsy management?

A

Tonic clonic: 1st line valproate 2nd lamotrigine 3rd carbamazepine
Absence: valproate
Myoclonic: valproate
Focal: 1st line is carbamazepine 2nd is lamotrigine

Avoid carbamazepine in absence/ myclonic as they can worsen it

61
Q

What non medical treatments can be recommended for epilepsy management?

A

Ketogenic diet
Epilepsy support group
Inform DVLA if they can drive
Vagal nerve stimulation

62
Q

Which type of seizure is ethosuximide used for?

A

Absence seizures

63
Q

What drugs are used in status epilepticus?

A

Community: buccal midazolam or rectal diazepam
Hospital: IV lorazepam then IV phenytoin infusion if seizure state persists

64
Q

Liver damage and hair loss are side effects of which anti epileptic drug?

A

Sodium valproate

65
Q

What are some side effects of carbamazepine?

A

Rash
P450 inducer
Agranulocytosis
Aplastic anaemia

66
Q

What are some criteria of neurofibromatosis type 1?

A
Neurofibromatas
6 or more cafe at lait spots
Axillray freckling
Lisch nodules of the iris
1st degree relative with NF-1
67
Q

Depigmented skin patches and roughened patches of skin are both features of with neurocutaneous disorder?

A

Tuberous sclerosis

68
Q

What antibiotic (and what length of tx) would you give for a child with a sore throat that scores a 3 on the centor criteria?

A

Penicillin V 10 days (erythromycin if penicillin allergic)

Avoid amoxicillin as this will cause a widespread rash if it is EBV

69
Q

What are some prevention tips you can tell parents of to minimise the likelihood if UTIs in their child?

A
Good hydration
Fully complete voiding 
Encourage regular voiding every few hours
Avoid constipation 
Avoid scented bubble baths
Wipe front to back
Cotton underwear, not tight/ nylon
70
Q

At what age does the anterior fontanelle close?

71
Q

What signs can be elicited when examining a patient with suspected bacterial meningitis?

A

Brudzinski sign: flexion of neck with child supine causes flexion of knees and hips

Kernigs sign: pain when attempting to extended a knee that is flexed (hip also flexed and child is supine)

72
Q

What are some common bacterial causes of meningitis in children and adults?

A

Neisseria meningitidis, h influenzae, strep pneumoniae

Neonates: GBS, Listeria, E Coli

73
Q

What’re some examples of live attenuated vaccines?

A

MMR
Rotavirus
BCG

74
Q

Which vaccines are only offered to at risk babies?

A
Hepatitis B (those born to hepatitis B infected mums)
BCG (if born in area of high incidence or parent/ grandparent born in high incidence country)
Whooping cough (offered to pregnant women from 20 weeks)
75
Q

What are features to distinguish between viral induced wheeze and bronchiolitis?

A

Viral induced wheeze follows URTI, usually caused by rhinovirus, no crepitations heard on auscultation, usually in 2-5 year olds. Tx supportive but can also offer beta-2 agonists and ipatropium bromide

(Bronchiolitis in under 2’s and has fine crepititations, usually RSV)

76
Q

How would you treat a neonate with persistent pulmonary hypertension of the newborn?

A
Nitric oxide (potent vasodilator)
Mechanical ventilation
ECMO is severe
77
Q

What are some red flag signs and symptoms for a child presenting with headache?

A

Symptoms: if persistent and less than 6y/o, if duration <6months, worse at nighttime or in morning, worse when coughing or lay down, early morning nausea and vomiting, seizures, behavioural changes, development regression

Signs: raised fontanelle, papilloedema, growth abnormalities, skin lesions suggestive neurocutaneous syndromes, neurological signs e.g. weakness, ataxia, squint

78
Q

What is the most common cause of ambiguous genitalia in newborns?

A

Congenital adrenal hyperplasia

79
Q

Define failure to thrive

A

Poor weight gain in a child with a drop down 2 centile spaces
Aka weight faltering

80
Q

What gene s associated with coeliac disease?

81
Q

Which food groups will have to be avoided when following a gluten free diet?

A

Wheat
Rye
Barley
Oats (most commercial oats have contaminated gluten)

82
Q

What are some complications of coeliac disease?

A
Osteoporosis
Non-Hodgkin’s lymphoma
Malignancy in oesophagus and bowel
Anaemia
Thyroid
Hyposplenism 
Infertility
Hyposplenism
83
Q

Which test is most specific for coeliac disease?

A

Endomysial antibody titre

84
Q

What rash is associated with coeliac disease?

A

Dermatitis herpetiformis

Intensely pruritic blistering lesions on extensor surfaces, can be treated with Dapsone

85
Q

Dermatitis herpetiformis is associated with which condition?

A

Coeliac disease

86
Q

What are some risk factors for coeliac disease?

A
T1DM
FHx
IgA deficient
Autoimmune thyroid disease
T21, 45XO
IBD
HLA-DQ2 gene
87
Q

What is the management of SUFE?

A

Always surgical, urgent referral to orthopaedics
(Internal fixation usually with single screw)
Best rest and non weight bearing until surgery

88
Q

Kocher criteria is used in the diagnosis of what?

A

Septic arthritis

89
Q

What are some differentials for a limping child?

A

SUFE, Perthes, congenital hip dysplasia, transient synovitis, septic arthritis, osteosarcoma, trauma (e.g. #)

90
Q

How would you manage a child with suspected septic arthritis?

A

Joint aspiration before abx
IV flucloxacillin 4/52
Analgesia
May require arthroscopic lavage

91
Q

What are the categories of development in children?

A

Gross motor
Fine motor
Speech and language
Emotional, social and behavioural

92
Q

What is colic?

A

Repeated episodes of crying in an otherwise healthy and well-fed child under the age of 3 months