Paediatrics Flashcards

1
Q

Gross Motor Milestones

A
3 Months - head control
6 Months - rolls front to back, back straight when held sitting
7-8 Months - sits without support
9 Months - pulls to standing, crawls
12 Months - cruises, walks with one hand held
12-15 Months - walks unaided
18 Months - squats to pick things up
2 years - runs
3 years - rides a tricycle
4 years - hops on one leg
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2
Q

Gross motor milestones - when to be concerned (2 things)

A

Not sitting without support by 12 months

Not walking without support by 18 months.

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3
Q

Age at which continence usually achieved

A

3 to 4 years

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4
Q

Management of Nocturnal Eneuresis (4 things)

A

1) rule out other causes e.g. constipation, diabetes, UTI
2) advise on fluid intake, diet, toileting behaviour
3) give rewards for agreed behaviour i.e. toileting before bed
4) failing these measures, generally enuresis alarm for children under 7 or desmopressin for children over 7 years. (depending on family needs and preferences.)

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5
Q

Causes of Microcephaly

A
Normal Varient
Familial
Congenital Infection
Perinatal brain injury
FAS
syndromes e.g. Patau
craniocyntosis
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6
Q

Presentation of Heart failure in Infants (4)

A

Breathlessness worse on exertion e.g. feeding
sweating
poor feeding
recurrent chest infections

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7
Q

Causes of Heart Failure in Infants

A

< 2 weeks - duct dependant systemic circulations e.g. coarctation of the aorta
> 2 weeks - VSD as the pulmonary vasculature resistance falls

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8
Q

Risk assessment in febrile children -colour

A

Green - normal
Amber - pallor reported by care giver
Red - pale or mottled

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9
Q

Risk assessment in febrile children - Activity

A

Green - responds normally, content, easily rousable or awake, not crying or strong cry
Amber - not responding normally to social cues, no smile, takes time to wake, decreased activity
red - no response to social cues, appears ill, does not wake or does not stay awake when roused, weak, high pitched or continuous cry.

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10
Q

Risk assessment in febrile children - Respiratory

A

Amber - nasal flaring, tachyponea (>50b/m in 6-12 months or >40b/p in ae >12 months), 02 sats = 95% in air, Crackles in the chest.
red - grunting, tachyponea >60 bpm, moderate or severe chest indrawing

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11
Q

Risk assessment in febrile children - circulation and hydration

A

green - normal skin and eyes, moist mucous membranes
amber - tachycardia >160 b/m in <12 mnths, >150 b/m in 12-24 mnths, >140 b/m in 2-5yrs, cap refil >/= 3 secondsm dry mucous membranes, poor feeding, reduced urine output
red - reduced skin turgor

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12
Q

Risk assessment in febrile children - other

A

green - no amber or red signs
amber - age 3-6 mnths temp >39 degrees, fever for 5 days or more, rigors, swelling of a joint or limb, non-weight bearing or not using an extremety.
red - age <3 months temp >38, non blanching rash, bulging fontanelle, neck stiffness, status epilepticus, focal neurology, focal seizures.

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13
Q

management of febrile illness in infants

A

GREEN - supportive care at home, advice when to seek help
AMBER - safety net or paeds specialist review
RED - urgent referal to paeds specialist

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14
Q

What would these parameters be in early (compensated) shock in a child? BP, HR, Resp rate, appearance, urine output

A
BP - Normal
HR - tachy
RR - tachy
appearance - pale or mottled
UP - reduced
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15
Q

What would these parameters be in late (decompensated) shock in a child? BP, HR, Resp appearance, urine output

A
BP - hypo
HR - Brady
Resp - acidotic
appearance - blue
UO - absent
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16
Q

Fluid Bolus in children

A

20ml/kg (15ml/kg in neonates) in 10 mins of saline

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17
Q

initial management of duct dependent congenital heart disease

A

prostaglandins e.g. alprostadil as they maintain patency of the ductus arteriosus

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18
Q

Red flags for constipation (5) (and two amber)

A

reported from first few weeks of life
Meconium passed later than 48 hrs post birth
‘ribbon’ stools
previously undiagnosed leg weakness or locomotor delay
abdominal distension
Amber - safeguarding concern, faltering growth

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19
Q

Causes of Constipation in Children

A
Majority are Idiopathic
dehydration
low-fibre diet
opiate medication
anal fissure
over enthusiastic potty training
hypothyroidism
hirschsprung's disease
hypercalcaemia
learning disability
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20
Q

what is Hirschsprung’s Disease?

A

the absence of ganglions in a segment of the bowel causing loss of peristalsis and ability to move stool through the intestine

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21
Q

What is perthes’ disease and who gets it?

A

degenerative condition of the hips, typically affecting boys (5:1) aged 4 - 8 years. It is due to AVN of the femoral epiphysis.

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22
Q

presentation of Perthes’

A

Hip pain, progressive over weeks
limp
stiffness and reduced ROM

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23
Q

radiographical changes in perthes’

A

widening of joint space, decreased femoral head size, femoral head flattening

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24
Q

management of perthes’

A

Cast and braces to keep femoral head in acetabulum

if older than 6 consider surgical management

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25
Q

What is Juvenile idiopathic arthritis

A

arthritis occurring in someone less than 16 years old lasting more than 6 weeks.

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26
Q

Types of JIA and their features (5)

A

Pauciarticular - most common, 4 or less joints effected, medium sized joints e.g. knees, shoulders elbows
Systemic-onset JIA -anaemia, thrombocytosis, lecucytosis and rasied ESR present
RF positive JIA - RF is positive, nodules on extensor surface of tendons
Polyarticular JIA - 4 or more joints effected
Ethesitis related JIA - inflammationof the entheses present (site of tendon and ligament insertion into bone.)

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27
Q

What is plagiocephaly?

A

parallelogram shaped head - normal in infants due to sleeping on back. usually resolves between 3-5 years. Reassure and recommend moving cot/ focus of attention, encouraging supervised supported sitting out during the day and supervised tummy time.

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28
Q

What is biliary atresia and when does it occur?

A

oliteration or discontinuity of the extrahepatic biliary system, resulting in obstructive jaundice. Usually presents in first few weeks of life.

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29
Q

Fine motor developmental milestones - general

A

3 months - reaches for objects, holds rattle briefly
6 months - holds in palmar grasp, passess objects from one hand to the other
9 months - points with finger, early pincer
12 months - good pincer, bangs toys together

30
Q

visual developmental milestiones

A

3 months - fixes and follows to 180 degrees

6 months - visually insatiable - looking around in every direction

31
Q

Towers of Bricks milestones

A

15 months - tower of 2
18 months - tower of 3
2 years - tower of 6
3 years - tower of 9

32
Q

drawing milestones

A
18 months - circular scribble
2 years - copies vertical line
3 years - copies circle
4 years - copies cross
5 years - copies square and triangle
33
Q

book milestones

A

15 months - looks at pages and pats pages
18 months - turns several pages at a time
2 years - turns pages one at a time

34
Q

What is Croup

A

URTI most common in 6mnths to 3 yrs causing laryngeal oedema and secretions caused by parainfluenza viruses.

35
Q

features of croup

A

stridor
barking cough
fever
coryzal symptoms

36
Q

severity of croup

A

mild - occasional barking cough, no stridor, no recessions, well child
moderate - frequent barking cough, audible stridor at rest, some suprasternal and sternal wall retraction at rest. No or little distress, child can be placated and is interested in surroundings
severe - frequent barking cough, prominent stridor, marked sternal retractions, significant distress, lethargy or restlessness, tachycardia, hypoxia

37
Q

management of Croup

A

oral dexamethasone 0.15mg/kg
admit if moderate or severe, child under 6mnths old, known upper airway abnormalities, uncertain diagnosis. In emergencies give high flow oxygen and nebulised adrenaline.

38
Q

What are infantile spasms?

A

type of childhood epilepsy which typically first present in 4-8mnths. they carry a poor prognosis.

39
Q

Presentation of infantile spasms

A

‘salaam’ attacks - flexion of head, trunk and arms, followed by extension of the arms, lasting a few seconds but may be repeated many times.
progressive learning disability.

40
Q

investigation of infantile spasms

A

CT - brain disease in 70%

EEG - hypsarrhythmmia in 66%

41
Q

management of infantile spasms

A

vigabatrin first line (prevents breakdown of GABA)

ACTH

42
Q

complications of respiratory distress syndrome at birth

A

renal failure and retinopathy of prematurity

43
Q

What is transient synovitis and how should it be managed.

A

Acute hip pain following a viral infection in 2 to 10 years. There may be a low grade fever. Rest and analgesia.

44
Q

What is Ebstein’s anomaly?

A

CHD where the tricuspid valve is positioned low, in the right ventricle resulting in a large atrium and small ventricle. It is associated with tricuspid regurg and Wolff-Parkinson White and may be caused by intrauterine lithium exposure.

45
Q

Features of Turner’s Syndrome (12)

A
short stature
shield chest
widely spaced nipples
webbed neck
bicuspid aortic valve (15%), coarctation of the aorta (5-10%)
primary amenorrhoea
cystic hygroma (often diagnosed prenatally)
high-arched palate
short fourth metacarpal
multiple pigmented naevi
lymphoedema in neonates (especially feet)
gonadotrophin levels will be elevated
46
Q

5 Red flags and 2 amber flags for constipation in children

A

Present since the first few weeks of life
>48hrs to meconium passage
‘ribbon’ stools
new leg weakness or locomotor delay
Abdominal distention
Amber: Faltering growth and safeguarding concerns

47
Q

Epiglottitis causative organism

A

Haemophilus infleunzae type B

48
Q
Pyloric stenosis
Who gets it?
Features
Diagnosis
Treatment
A

M>F, 4-6 weeks old
Projectile non bile stained vomiting
Diagnosis is made by test feed or USS
Treatment: Ramstedt pyloromyotomy (open or laparoscopic)

49
Q

Acute appendicitis
Who gets it?
Presentation

A

Uncommon under 3 years

When occurs may present atypically

50
Q
Intussusception
What is it? Where does it usually occur?
Age?
Presentation?
Management?
A

Telescoping bowel
Proximal to or at the level of, ileocaecal valve
6-9 months of age
Colicky pain, diarrhoea and vomiting, sausage-shaped mass, red jelly stool.
Treatment: reduction with air insufflation

51
Q
Malrotation
What is it?
Associated conditions?
Complications?
Diagnosis?
Management?
A

High caecum at the midline
Feature in exomphalos, congenital diaphragmatic hernia, intrinsic duodenal atresia
May be complicated by the development of volvulus, an infant with volvulus may have bile stained vomiting
Diagnosis is made by upper GI contrast study and USS
Treatment is by laparotomy, if volvulus is present (or at high risk of occurring then a Ladd’s procedure is performed

52
Q
Hirschsprung's disease	
What is it?
Presentation
Diagnosis
Management
A

Absence of ganglion cells from myenteric and submucosal plexuses
Delayed passage of meconium and abdominal distension
Full-thickness rectal biopsy for diagnosis
Treatment is with rectal washouts initially, after that an anorectal pull through procedure

53
Q

Oesophageal atresia
Associations
Presentation

A

Associated with tracheo-oesophageal fistula and polyhydramnios
May present with choking and cyanotic spells following aspiration

54
Q

Meconium ileus
Presentation
associated diagnosis
Management

A

Usually delayed passage of meconium and abdominal distension
The majority have cystic fibrosis
PR contrast studies may dislodge meconium plugs and be therapeutic, NG N-acetyl cysteine useful,
Infants who do not respond will require surgery to remove the plugs

55
Q

Biliary atresia
Presentation
Investigation finding
Management

A

Jaundice > 14 days
Increased conjugated bilirubin
Urgent Kasai procedure

56
Q
Necrotising enterocolitis	
Who gets it?
Features
X-ray findings
Risk factor
Management
A

Premature babies
Early features include abdominal distension and passage of bloody stools
X-Rays may show pneumatosis intestinalis and evidence of free air
Increased risk when empirical antibiotics are given to infants beyond 5 days
Treatment is with total gut rest and TPN, babies with perforations will require laparotomy

57
Q

Mesenteric adenitis

Presentation and management

A

Central abdominal pain and URTI

Conservative management

58
Q

VACTERL conditions

A
Vertebral defects
Anal atresia
Cardiac defects
Tracheo-esophageal fistula
Renal anomalies
Limb abnormalities
59
Q

Management of UTI

A

Under 3 months - refer same day to paeds
Over 3 months - upper UTI - refer to hospital
- lower UTI - 3 days Abx and safety netting

60
Q

when to admit a child with bronchiolitis

A

RR over 60 breaths/minute
difficulty with breastfeeding or inadequate oral fluid intake (50–75% of usual volume
clinical dehydration

61
Q
Patau syndrome (trisomy 13)
4x features
A

Microcephalic, small eyes
Cleft lip/palate
Polydactyly
Scalp lesions

62
Q

Edward’s syndrome (trisomy 18)

4x feautres

A

Micrognathia
Low-set ears
Rocker bottom feet
Overlapping of fingers

63
Q

Fragile X

5x features

A
Learning difficulties
Macrocephaly
Long face
Large ears
Macro-orchidism
64
Q

Noonan syndrome

4x features

A

Webbed neck
Pectus excavatum
Short stature
Pulmonary stenosis

65
Q

Pierre-Robin syndrome*

3x features

A

Micrognathia
Posterior displacement of the tongue (may result in upper airway obstruction)
Cleft palate

66
Q

Prader-Willi syndrome

3x features

A

Hypotonia
Hypogonadism
Obesity

67
Q

William’s syndrome

5x features

A
Short stature
Learning difficulties
Friendly, extrovert personality
Transient neonatal hypercalcaemia
Supravalvular aortic stenosis
elfin facies
68
Q

Cri du chat syndrome (chromosome 5p deletion syndrome)

5x features

A

Characteristic cry (hence the name) due to larynx and neurological problems
Feeding difficulties and poor weight gain
Learning difficulties
Microcephaly and micrognathism
Hyperteloris

69
Q

Causes of Hypertension in children (6)

A
Renal parenchymal disease
renal vascular disease
coarctation of the aorta
phaeochromocytoma
congenital adrenal hyperplasia
essential or primary hypertension
70
Q

Imaging developmental dysplasia of the hip

A

newborn - ultrasound

>4.5 months - X-ray