Paeds Flashcards

1
Q

How does infantum roseola present?

A

High fever, mild pharyngitis and lymphadenopathy. Temp returns to normal after 3-4 days, accompanied by appearance of rose-pink macular non-pruritic rash

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2
Q

How does congenital hypothyroidism present?

A

‘Good baby’ - sleep most of time, rarely cry!
Lethargic, poor feeding, constipation, symmetrically poor weight gain.
Coarse facial features with macroglossoa
Hypotonia, large fontanelles
Umbilical hernia

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3
Q

6 year old short for his height, increased subcutaneous fat around trunk, immature facial features, prominent forehead. Dx?

A

Growth hormone deficiency

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4
Q

4 y/o with recent upper respiratory infection now presents with abdo pain, pain in knees and ankles, and non blanching purpuric rash over backs of legs and buttocks
-Dx and what is it?
-most appropriate first line ivx?

A

Henoch-Schönlein Purpura (HSP) - IgA vasculitis. Present with purpuric rash, abdominal pain, arthritis/arthralgia and glomerulonephritis
-Urine dipstick to look for blood and protein

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5
Q

2nd step in asthma Mx for children still having symptoms after salbutamol
-for children under 5?
-children over 5?

A

Under 5 - LRTA ie montelukast
Over 5 - very low dose ICS

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6
Q

Usual age of smiling?
When to refer?

A

6 weeks
Refer at 10 weeks

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7
Q

When can sit without support?
when to refer?

A

7-8 months
Refer at 12 months

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8
Q

When should be able to walk unsupported and know 2-6 words?
When to refer for both?

A

13-15 months
Refer at 18 months

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9
Q

Most common cause of failure to thrive?

A

Non-organic causes ie social problems!

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10
Q

Classic electrolyte and acid-base balance of pyloric stenosis?

A

Hypochloraemic, hypokalaemic metabolic alkalosis

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11
Q

Ivx for pyloric stenosis?
Treatment?

A

-ultrasound
-correct fluid/electrolyte then Ramstedt’s or laparoscopic pyloromyotomy

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12
Q

Testing for Coeliac disease?

A

-patient must have eaten gluten-containing foods for at least 2 meals a day over last 6 weeks
-serological tests: IgA tissue transglutaminase antibody (tTGA) and IgA endomysial antibody (EMA)
-if positive, will need intestinal biopsy (and stay on gluten diet until after this)

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13
Q

Difference between Gillick competence and Fraser guidelines?

A

Gillick competence - determining a child’s capacity to consent

Fraser guidelines as specific to decide if a child can consent to contraceptive or sexual health advice and treatment (‘Fraser is sexy!’)

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14
Q

First line treatment for UTI in kids?

A

Trimethoprim

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15
Q

Day old neonate - bilious vomiting, scaphoid abdomen. USS shows double bubble sign. Dx?

A

Duodenal Atresia

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16
Q

How is Cystic fibrosis inherited and which chromosome does it affect?

A

-Autosomal recessive
-chromosome 7

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17
Q

Other names for erythema infectiosum? What is it caused by?

A

Fifth disease
Slapped cheek disease! (High 5 to face!)
Human parvovirus B19

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18
Q

When does respiratory distress syndrome normally start?

A

Within 4 hours of birth!

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19
Q

Treatment for Scarlett fever?

A

Penicillin

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20
Q

When does intussusception occur?
Which gender more common in?

A

5-10 months
More common in males

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21
Q

Symptoms of Insussusception?
Physical examination?
Ultrasound shows?

A

Vomiting (may be bile stained)
Pulling up legs to chest
Red currant jelly stool

Sausage-shaped mass felt in abdomen

Ultrasound: doughnut/target sign

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22
Q

Treatment for insussusception?

A

BARIUM ENEMA!
Both a method of imaging and treatment!

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23
Q

Risk factors for neonatal jaundice ?

A

Low birthweight (prem/small for dates)
Diabetic mother
Male infants
East Asian ethnicity
High altitude populations

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24
Q

Is physiological jaundice unconjugated or conjugated?

A

UNCONJUGATED

(Conjugated bilirubinaemia is ALWAYS pathological - biliary obstruction needs to be ruled out immediately!)

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25
Q

Causes for early jaundice (within first 24 hours):

A

Note: jaundice within 24 hours is PATHOLOGICAL AND NEEDS TO BE CONSIDERED HAEMOLYTIC IN NATURE UNTIL PROVEN OTHERWISE!
-Haemolytic disease (rhesus, ABO incapability, spherocytosis)
-Infection (congenital ie rubella, syphillis or postnatal infection)
-Increased haemolysis secondary to haematoma
-Maternal autoimmune haemolytic anaemia ie SLE
-Enzyme deficiency ie Gilbert’s syndrome

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26
Q

What is roseola infantum caused by?

A

Human herpesvirus (HHV-6)

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27
Q

How does Roseola infantum classically present?

A
  • 3-5 days of high fever
  • Fever resolves, but then gets pink/red macules and papules - start on neck/trunk and spread to extremities

Note- commonly associated with febrile seizures (up to 15%!)

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28
Q

How does Measles classically present?
What is the incubation period?

A

-Fever, maculopapular rash (starts on head/neck then spreads), cough, Coryza, conjunctivitis
-whiteish spots on erythematous buccal mucosa - KOPLIK’S SPOTS

Incubation period is 10 days

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29
Q

How does chickenpox present?
What is the incubation period?

A

-fever, malaise, generalised pruritic, vesicular rash

-incubation period is 14 days

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30
Q

Is Measles notifiable?
What is the exclusion from school?

A

YES
5 days from onset of rash

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31
Q

What causes Scarlet fever?

A

Caused by the exotoxins produced by Strep Pyogenes (Group A Strep!)

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32
Q

How does Scarlet fever present?

A

-Few days of fever and sore throat
-Then, rash (coarse, like sandpaper) that starts on chest/torso then spreads to limbs. Skin sometime peels (desquamation)
-tongue: strawberry tongue

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33
Q

Management and school exclusion for Scarlet fever?

A

Penicillin for 10 days (Azithromycin if pen-allergic)

Child can return to school 24 HOURS after abx started

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34
Q

How does Rubella present?

A

-Prodrome of fever and coryzal symptoms
-Then PINK rash, starts on face and behind ears, spreads to trunk then extremeties

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35
Q

What type of virus causes Rubella?
Is it notifiable?
school exclusion?

A

Togavirus
Yes, NOTIFIABLE
6 days from onset of rash

36
Q

How does erythema infectiosum present?
School exclusion?

A

Prodrome: fever & malaise
Characteristic ‘slapped cheek’ facial rash that spares perioral and periorbital regions (rash disappears after 2w but may come and go for up to a month when hot/exercising!)
No school exclusion! (Once child well)

37
Q

Most common causes of hand foot and mouth disease?
School exclusion?

A

Coxsackie & enterovirus

No recommended school exclusion (once child is well)

38
Q

What type of virus causes Mumps?
School exclusion?

A

Paramyxovirus
5 days from onset of swollen glands

39
Q

When do Milia usually resolve?

A

By 1 month

40
Q

Name for common rash (yellowish pustules and papules with red wheal) that present normally in first week of life?

A

Erythema toxicum neonatorum

41
Q

Treatment for erythema toxicum neonatorum?

A

None, reassure (self-limiting)

42
Q

Risk factors for respiratory distress syndrome?

A

Premature delivery
Male
C sections
Hypothermia
Maternal diabetes
Multiple pregnancy
Family history
Perinatal asphyxia

43
Q

How is respiratory distress syndrome treated?

A

Surfactant replacement therapy is given via endotracheal tube

44
Q

Main extra intestinal manifestations of Coeliac disease?

A

-Dermatitis herpetiformis (blistering skin rash on elbows/knees/buttocks)
-Iron deficiency anaemia
-Short stature & delayed puberty
-Arthritis and arthralgia
-Osteopenia & osteoporosis

45
Q

When can a child normally sit?
When to refer

A

7-8 months
REFER AT 12 MONTHS

46
Q

How does epiglottitis present?
Cause?

A

Sore throat, muffled voice, drooling, fever, anterior neck tenderness, oynophagia (pain swallowing), cervical lymphadenopathy

Hib!

47
Q

Is neck xray done in epiglottitis, what may it show?

A

Thumbprint sign (inflammed glottis)

48
Q

If CXR done for Croup, what may it show?

A

Steeple sign (subglottic narrowing)

49
Q

14 y/o asylum seeker, purulent blood-stained nasal discharge, fever, inflamed pharynx with greyish membrane, enlarged lymph nodes - Dx?

A

Diptheria! (Dipped in grey!)
-nasal discharge that becomes purulent and blood stained
-‘bull neck’ - enlarged cervical lymph nodes

50
Q

What is Extracorporeal membrane oxygenation (ECMO) used for?

A

Severe heart/lung dysfunction ie PRIMARY PULMONARY HYPERTENSION or RESPIRATORY DISTRESS SYNDROME

51
Q

What is a port-wine stain?

A

Named after colour! Reddish/purple
Vascular birthmark PRESENT AT BIRTH

52
Q

What is a Stork bite?

A

Telangiectatic naevus
Pink, FLAT, irregularly shaped mark on back of neck/forehead/eyelid/top lip
Skin is not thickened, feels the same as rest of body

53
Q

Definitions of ‘atypical’ UTIs in children?

A

-seriously ill/septicaemia
-poor urine flow
-abdominal/bladder mass
-raised creatinine
-failure to respond to abx in 48 hours
-NON-E COLI ORGANISMS!

54
Q

Treatment for <3 months with suspected UTI?

A

URGENT REFERRAL

55
Q

Management for >3 y/o with:
Upper UTI
Lower UTI?

A

Upper - most need urgent referral!
-7-10 days co-Amox or cefalexin

Lower - 3 days of either
-Trimethoprim, nitrofurantoin, amoxicillin or cefalexin

56
Q

Commonest epilepsy syndrome in childhood?

A

-Benign Rolandic epilepsy (prev called partial seizures)
-Usually 7-10 years
-More common in boys
-Often at night, involve one side of face, causing gurgling/grunting/dribbling
-generally outgrown by puberty!

57
Q

3 month old with severe eczema and D&V. Most likely Dx?

A

Cow’s Milk Protein Allergy

NOTE in most young kids, CMPA rather than lactose intolerance which is IgE-mediated!

58
Q

What to do if suspected CMPA?
Likely CMPA?

A

Suspected - try a ‘comfort’ milk ie Aptamil where some of protein is hydrolysed so it is less allergenic

Likely - prescribe EHF (extensively hydrolysed feeds) and refer

59
Q

Features of INNOCENT heart murmur

A

-soft
-position dependent
-otherwise healthy
-occurs during systole or both (MURMURS DURING DIASTOLE ARE ALWAYS PATHOLOGICAL)
-no palpable thrill
-physiological splitting of S2

60
Q

8 y/o with recurrent nosebleeds and bleeding gums over past week. Multiple bruises, no organomegaly. Low platelets, normal clotting. Dx and what is it?

A

ITP (idiopathic thrombocytopaenic purpura)
-acute, transient disorder, affecting older kids 2-4 y/o, usually occurs after infection or immunisation

61
Q

Management of ITP?

A

Usually just advice and support, and repeat FBC in 10 days

62
Q

5 days baby present with bleeding gums and from umbilical wound, otherwise well. Likely Dx?

A

Hemorrhagic disease of newborn (or vitamin K deficiency bleeding!)

63
Q

Quick way to estimate weight of child?

A

(Age + 4) x2

64
Q

Blood spot tests which 9 things?

A

‘Come Cuddle/Hug My Magnificent PIGS’

Congenital hypothyroidism
Cystic Fibrosis
Homocystinuria
MCADD
Maple syrup urine disease
Phenyl ketonuria
Isovalaeric acidaemia
Glutaric acidaemia type 1
Sickle cell disease

65
Q

When is blood spot test done?

66
Q

Which children get Necrotising enterocolitis and when?

A

Premature/underweight neonates
Usually 2nd to 3rd week of life

67
Q

Risk factors for NEC?

A

-Maternal illicit drug use/HIV/chorioamnionitis
-Prematurity/low weight
-Congenital abnormalities
-Low flow/perfusion states ie placental abruption leading to neonatal shock
-Feeding type - preterm formula

68
Q

Symptoms of NEC

A

Poor feeding, vomiting (may be bile stained) lethargy, abdo tenderness/distention
Blood/mucous in stools

69
Q

How to confirm NEC and what would it show?

A

Abdo xray
Pathognomic findings:
-PNEUMATOSIS INTESTINALIS (gas in wall of intestine)
-PORTAL VENOUS GAS

Earlier signs:
Dilated, gas filled loops of bowel
Extraluminal (free) air

70
Q

Management of NEC?

A

NBM
Nasogastric tube for decompression
IVF/TPN and IV abx
Surgery if necrosis suspected
Intubation/ventilation for apnoea

71
Q

Features of EDWARDS syndrome

A

Ears - low set, malformed
Development issues with thumbs/hands
Weird palate - cleft
Absent radius
Rocker bottom feet
Don’t mess with me (clenched fist)
Small head and jaw (microcephaly, micrognathia)

72
Q

Which trisomy is;
-Edward’s
-Patau

A

Edwards = 18
Patau = 13

73
Q

Karyotype for Turner’s syndrome?
Girls/boys affected?
Classical features?

A

45XO - 1 X chromosome missing/partially missing! X chromosome ‘turned’ into O

Only GIRLS

Short stature (because missing chromosome!)
Gonadal dysgenesis - primary and secondary amenorrhea
Lymphoedema

74
Q

Klinefelter’s syndrome chromosome abnormality?

Affects boys or girls?

Features?

A

Extra X chromosome (47XXY)

BOYS ONLY

Tall (because extra chromosome!)
Long arms and legs
Gymaecomastia
Central obesity
Small firm testicles

75
Q

Which are the TORCH infections that are passed from mother to child during pregnancy/birth?

A

Toxoplasma gondii
Others (VZV, Parvovirus B19, Zika)
Rubella
CMV
HSV

76
Q

Bloody mucousy stools in children - how to determine NEC vs intussusception?

A

NEC: 2nd to 3rd week of life in generally PREMATURE babies

Intussusception: infants 3-12 months, drawing up legs

77
Q

Infant with instestinal obstruction within hours of birth, ‘soap bubble’ on abdomen xray. Dx?
Tx?

A

Meconium ileus!
Therapeutic enemas
If fails - surgery

78
Q

Hirschprung’s disease
-associated with which condition?
-what is it?
-when does it usually present?
-presentation
-investigations?
-mx?

A

-Down’s syndrome
-partial/complete colonic obstruction associated with absence of ganglion cells
-from newborn up to 1 year of life
-NOT PASSING MECONIUM for 48 hours, abdo distension, vomiting
-RECTAL BIOPSY
-surgery

79
Q

Usual age of presentation for pyloric stenosis?
Examination finding ?

A

Typically 3-6 week
Olive shaped mass in R upper abdomen

80
Q

What is HARTNUP disease?
Symptoms?

A

Abnormality of renal/intestinal transport involving amino acids
-red, scaly, photosensitive rash
-neurological abnormalities- ataxia, unsteady gait, dysarthria, tremors, spasticity

81
Q

How is fragile X inherited?

A

X linked DOMINANT (not so fragile!)

-commonest inherited cause of learning disability!

82
Q

How is fragile X inherited?

A

X linked DOMINANT

-commonest inherited cause of learning disability!

83
Q

First line treatment for absence seizures?

A

Ethosuximide
Or valproate
Or Lamotrigine

84
Q

Where and when does a dermoid cyst present?

A

Young children
Lumps on lateral eyebrow ‘D for devil horns!!’

85
Q

Forceps delivery - Several hours after birth, swelling that doesn’t cross suture lines, can take months to resolve. Dx? Where is the bleed?

A

CEPHALOHAEMATOMA
Between periosteum and skull

86
Q

Forceps - swelling present from birth, crosses suture lines, resolves within days

A

Caput succedaneum