Paeds COPY Flashcards

1
Q

Koplik’s spots

A

Measles

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2
Q

Slapped cheeks

A

Fifth disease aka erythema infectiosum (Parvovirus B19)

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3
Q

Strawberry tongue

A

Scarlet fever + Kawasacki disease

Scarlet fever has an incubation period of 2-4 days and typically presents with:
fever
malaise
tonsillitis
‘strawberry’ tongue
rash - fine punctate erythema (‘pinhead’) which generally appears first on the torso and spares the face although children often have a flushed appearance with perioral pallor. The rash often has a rough ‘sandpaper’ texture. Desquamination occurs later in the course of the illness, particularly around the fingers and toes

Diagnostic features for Kawasaki disease requires a fever >5d with 4 of the following criteria: A) Conjunctival injection B) Mucous membrane changes (dry cracked lips, strawberry tongue) C) Cervical lymphadenopathy D) Polymorphous rash E) Red and oedematous palms/soles, peeling of fingers and toes.

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4
Q

Hypokalaemia, hypotension + alkalosis in a newborn

A

Bartter syndrome

Defect in the ascending limb of the loop of Henle

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5
Q

Most common cause of gastroenteritis in children

A

Rotavirus

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6
Q

1st line treatment for uncomplicated constipation

A

Movicol Paediatric Plain (Polyethylene glycol 3350 + electrolytes)

  • If movicol is not tolerated switch to osmotic laxative
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7
Q

Most common cause of nephrotic syndrome in children

A

Minimal change disease

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8
Q

1st sign of puberty in

  1. Boys
  2. Girls
A
  1. Testicular growth (around 12)

2. Breast development (then height spurt, then menarche)

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9
Q

Grey coating on tonsils + cervical lymphadenopathy in unvaccinated child

A

Diphtheria

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10
Q

Most common cause of croup

A

Parainfluenza

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11
Q

When is the Men B vaccine given? (All 3 dates)

A

2, 4, and 12-13 months

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12
Q

The only childhood congenital syndrome that presents with polydactyly (also with microcephaly, small eyes, clept lip)

A

Patau syndrome (3* 13)

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13
Q

Rocker bottom feet (+ low set ears and micrognathia)

A

Edwards (3* 18)

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14
Q

The only childhood congenital syndrome that presents with macrocephaly (+ macro-orchidism, learning difficulties, long face and large ears)

A

Fragile X

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15
Q

The only childhood congenital syndrome that presents with pectus excavatum (+ webbed neck, short stature + pulmonary stenosis)

A

Noonan Syndrome (aka the male Turners, however affects males and females equally)

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16
Q

The only childhood congenital syndrome that presents with posterior displacement of the tongue (+ micrognathia, cleft palate)

A

Pierre-Robin syndrome

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17
Q

The only childhood congenital syndrome that presents with friendly, extrovert personality (+ short stature, learning difficulties, transient neonatal hypercalcaemia, supravalvular aortic stenosis)

A

William’s syndrome

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18
Q

IM benzylpenicillin doses for suspected meningococcal septicaemia in the community at age…

A
  1. 300mg
  2. 600mg
  3. 1200mg

(always doubles)

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19
Q
  1. 1st line investigation for complications of Kawasaki’s

2. Management

A
  1. Echocardiogram (due to possible coronary artery aneurysms)
  2. High-dose aspirin (one of the very few indications for the use of aspirin in kids). + IV immunoglobulin
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20
Q

Definition of precocious puberty = ‘development of secondary sexual characteristics before the age of ‘____’

  1. Females
  2. Males
A
  1. 8 years

2. 9 years

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21
Q

What are the live attenuated vaccines? (3) + 2 less important ones

A

BCG
MMR
Oral polio

Yellow fever
Oral typhoid

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22
Q

Most common presentation of Wilms’ nephroblastoma

A

Abdominal mass

Also painless haematuria, flank pain, anorexia + fever.

Management - Nephrectomy + chemotherapy

Prognosis - Good, 80% cure rate

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23
Q

Most common complication of Roseola infantum?

A

Febrile Convulsions

Roseola infantum (also known as exanthem subitum, occasionally sixth disease) is a common disease of infancy caused by the human herpes virus 6 (HHV6). It has an incubation period of 5-15 days and typically affects children aged 6 months to 2 years.

Features
high fever: lasting a few days, followed by a
maculopapular rash
febrile convulsions occur in around 10-15%
diarrhoea and cough are also commonly seen

Other possible consequences of HHV6 infection
aseptic meningitis
hepatitis

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24
Q

A baby is born at 32 weeks gestation (i.e. 1 month early), what should happen regarding the normal first set of vaccines beginning at 2 months?

A

Give vaccines as per normal timetable (i.e. don’t account for premature)

25
Most common cause of death in the first year of life?
SIDS
26
Most common cause of Bronchiolitis
RSV (also mycoplasma, adenovirus)
27
What are the 4 components of Tetralogy of Fallot? | *TOF generally presents at 1-2 months
ventricular septal defect (VSD) right ventricular hypertrophy right ventricular outflow tract obstruction, pulmonary stenosis overriding aorta
28
Most common cause of hypertension in children
Renal parenchymal disease (+ renal vascular disease, coarctation of the aorta, phaeochromocytoma, congenital adrenal hyperplasia)
29
1st line management of minimal change glomerulonephritis?
Prednisolone Good prognosis - full recovery however 80% will have recurrences
30
Acyanotic congenital heart disease causes (5)
VSD - most common! ASD PDA Coartation of aorta aortic valve stenosis
31
Cyanotic congenital heart disease causes (4)
Tetralogy of Fallot (most common) Transposition of great arteries (TGA) Tricuspid atresia Pulmonary Valve Stenosis
32
What is the most appropriate way to confirm a diagnosis of pertussis?
Nasal swab Management - oral course of erythromycin to reduce spread. However does not alter course of illness
33
What 5 criteria make up the APGAR score?
Pulse Respiratory effort Colour Muscle tone Reflex irritability
34
Treatment for threadworms
Hygiene measures + single dose mebendazole for all the family
35
1st line management for uncomplicated enuresis (bed wetting) 1. Below the age of 5 2. Below the age of 7 3. Above the age of 7
1. Reassure, bed wetting is common until age 5 2. Enuresis alarm 3. Desmopressin
36
What is the causative agent of roseola infantum
HHV6
37
When is the oral rotavirus vaccine given?
2 + 3 months
38
1st line management of absence seizures
Sodium valproate + ethosuximide (Good prognosis, 95% become seizure free in adolescence) SE of Sodium valproate: Weight gain + hair loss
39
Causative organism of hand, foot and mouth
Coxsackie A16 virus (occasionally enterovirus 71)
40
Investigation to confirm DDH if clinically suspected
Ultrasound
41
How long should a child with chickenpox be excluded from school?
Until 5 days after skin lesions have APPEARED
42
Treatment for HSP
Analgesia for arthralgia Treatment of nephropathy is generally supportive. There is inconsistent evidence for the use of steroids and immunosuppressants
43
What is the investigation of choice to diagnose vesicoureteric reflux?
Micturating cystourethrogram
44
Most appropriate initial investigation for suspected coeliac disease
IgA TTG antibodies Coeliac HLA-DQ2 association Diagnosis: jejunal biopsy showing subtotal villous atrophy anti-endomysial and anti-gliadin antibodies are useful screening tests
45
What birth weight = fetal macrosomia?
>4kg
46
Most common palsy due to shoulder dystocia?
Erb's palsy
47
Pink maculopapular rash, initially on face before spreading to the whole body + suboccipital and postauricular lymph nodes
Rubella
48
Causative organism for Scarlet fever
Group A haemolytic streptococci
49
What length of school exclusion is recommended for kids with head lice
None.
50
At what age should a child be referred if they are not walking?
18 months
51
'Jittery' newborn with absent philtrum + dysmorphic feathures
Fetal alcohol syndrome
52
saddle-shaped nose
Fetal alcohol syndrome
53
'Onion skin-like' appearance on X-ray
Ewing's sarcoma
54
Positive technetium-99m pertechnetate scan
Meckel's diverticulum
55
Anosmia + low LH / FSH / Testosterone in male adolescent
Kallman's Syndrome Kallman's syndrome is a recognised cause of delayed puberty secondary to hypogonadotrophic hypogonadism. It is usually inherited as an X-linked recessive trait. Kallman's syndrome is thought to be caused by failure of GnRH-secreting neurons to migrate to the hypothalamus. The clue given in many questions is lack of smell (anosmia) in a boy with delayed puberty Features 'delayed puberty' hypogonadism, cryptorchidism anosmia sex hormone levels are low LH, FSH levels are inappropriately low/normal patients are typically of normal or above average height Cleft lip/palate and visual/hearing defects are also seen in some patients
56
1st test to perform on a child who presents with jaundice after 14 days
Split Bilirubin. Need to rule out biliary atresia
57
Management of UTI in... 1. 3 months
1. Admit and treat with IV antibiotics | 2. 3 day course of oral antibiotics (usually trimethoprim)
58
Cyanotic heart defect with no murmur
Transposition of the great vessels