Paeds Flashcards

1
Q

When is meningococcal vaccine given?

A

2 months, 4 months and 12-13 months

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2
Q

What is the difference between cephalhaematoma, caput succadeneum and craniosynostosis

A

Cephalhaematoma:
* Doesnt cross suture lines.
* Appears a couple of days after instrumental delivery.
* Is due to bleeding between the periosteum and the skull.

Succadeneum
* Sewlling appears immediately after birth
* Generalised superficial scalp oedema, which crosses suture lines.
* Associated with prolonged labour.

Craniosynostosis:
* Premature closure of cranial sutures, causing deformity of the skull.

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3
Q

How to manage reflux in babies?

A

1) Nurse 30 degrees head up. Advise they should sleep on back, ensure not being overfed, trial smaller more frequent feeds.
2) If bottle fed add thickener
3) If not trial alginate (gaviscon)
4) IF unexplained feeding difficulty/distressed/faltering growth then trial PPI (used to be ranitidine but now withdrawn)

5) Metoclopramide but under specialist advice. If really bad they’ll consider Nissens fundoplication

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4
Q

Features of Williams syndrome

A
  • Small upturned nose
  • Long philtrum (upper lip length)
  • Wide mouth
    *Full lips
    *Small chin
    *Puffiness around the eyes.

**Associated with Aortic stenosis.

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5
Q

How to manage food allergy in children?

A

First establish whether IgE or non IgE mediated.

IgE mediated = Bad(E) - more likely to have more severe GI sx AND chest involvement so things like wheeze.

To manage IgE mediated they need skin prick testing.

Non IgE mediated - Eliminate the allergen for 2-6 weeks then slowly reintroduce with a ladder. E.g. if eggs then start with cooked eggs before scrambled.

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6
Q

Is transposition of the great arteries cyanotic or acyanotic?
How is this managed?

A

cyanotic.
Need to keep the ductus arteriosus open with prostaglandins.
Surgery = definitive

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7
Q

3 cyanotic congenital cardiac problems?

A

CT
Transposition of great vessels
Tetralogy of Fallot
Tricuspid atresia.

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8
Q

Tetralogy of fallot features?
What would you see on XR?

A

VSD
Pulmonary stenosis
RVH
Overriding aorta (should be over LV but actually its in the middle so gets blood from right heart too).

CXR will show a boot shaped heart

Usually presents age 1-2 months however can be as late as 6 months. Children get ‘tet spells’ - upset get cyanosed, inc RR and can LOC

Management is surgery usually in first year of life.

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9
Q

How to manage CMPA
1) If formula fed
2) If breastfeeding

Prognosis?

A

1) eHF extensive hydrolysed formula. If not working then amino acid based formula.

2)Eliminate cow’s milk protein from maternal diet. Consider prescribing calcium supplements to mum.
Use eHF milk when breastfeeding stops, until 12 months of age and at least for 6 months

IgE mediated - 55% will be milk tolerant by 5.
Non-IgE mediated - most children will be milk tolerant by 3.
Challenge is often performed in the hospital setting as anaphylaxis can occur.

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10
Q

When would you refer a child to have vaccines at hospital and why?

A

Babies born under 28 weeks - risk of apnoea.

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11
Q

What is Edwards syndrome?

A

Trisomy 18
Get micrognathia, low-set ears, rocker bottom feet and overlapping of fingers - Edward’s syndrome

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12
Q

Management of Kawasakis

A

High-dose aspirin - usually can’t give this in children due to risk of
Reye’s syndrome but do for this.

IVIG

echo- ? coronary artery aneurysms

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13
Q

Kawasaki features

A

High-grade fever which lasts for > 5 days.

Conjunctivitis
Red palms of the hands and the soles of the feet which later peel
Eyes -conjunctival injection
Lymphadenopathy(cervical)
Mouth sore, strawberry tongue

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14
Q

How can you tell adrenal cause of precocious puberty from other causes?

A

Small testes if adrenal hyperplasia.

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15
Q

Pink Mac pap rash that starts on the face then spreads to body. Suboccipital and post auricular lymphadenopathy.

A

Rubella

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16
Q

Child presents with fever, malaise and tonsillitis associated with a ‘strawberry’ tongue and a fine punctate erythematous rash sparing the area around the mouth

A

Scarlet fever

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17
Q

What is Hirschsprung’s disease ?

A

rare but think of it if it takes a long time for child to pass meconium, or later in life if child is constipated.

Parasympathetic Auerbach and Meissner plexuses affected.

Ix: AXR, rectal biopsy is gold standard,

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18
Q

Slapped cheek proper name

A

erythema infectiosum

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19
Q

Virus that causes Hand foot and mouth?

A

Coxsackie A16

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20
Q

What does parainfluenza cause?

A

Croup

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21
Q

What does haemophilus influenzae cause?

A

acute epiglottitis
exacerbation of bronchiectasis
IECOPD

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22
Q

Child with fever, conjunctivitis, white spots on buccal mucosa, rash starting behind ears

A

Measles

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23
Q

Child with fever, fine punctate erythematous rash with ‘sandpaper’ texture, strawberry tongue

A

Scarlett fever

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24
Q

Puberty in females

Age??
First signs?

A

First sign is breast development at around 11.5 years of age (range = 9-13 years)

Height spurt reaches its maximum early in puberty (at 12) , before menarche

menarche at 13 (11-15)
there is an increase of only about 4% of height following menarche

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25
Q

Puberty in males

Age?
First signs?

A

First sign is testicular growth at around 12 years of age (range = 10-15 years)

testicular volume > 4 ml indicates onset of puberty

maximum height spurt at 14

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26
Q

How to diagnose vesicoureteric reflux in children

A

Micturating cystourethrogram

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27
Q

When would NICE say to image the urinary tract?

A

infants < 6 months who present with a first UTI which responds to treatment should have an ultrasound within 6 weeks.

children > 6 months who present with a first UTI which responds to treatment do not require imaging unless there are features suggestive of an atypical infection or recurrent infection

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28
Q

When should a DMSA scan be done?
Why?

A

4-6 months after an initial infection
To look for renal scarring

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29
Q

When would you do MCUG and why?

A

Identifies vesicoureteric reflux. Only recommended for infants younger than 6 months who present with atypical or recurrent infections

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30
Q

How to manage acute mild-mod asthma in children?

A

Bronchodilator therapy
give a beta-2 agonist via a spacer (for a child < 3 years use a close-fitting mask)
give 1 puff every 30-60 seconds up to a maximum of 10 puffs
if symptoms are not controlled repeat beta-2 agonist and refer to hospital

Steroids should be given to all children with an exacerbation and
treatment should be given for 3-5 days

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31
Q

Scarlet fever causative organism

A

Group a haemolytic strep

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32
Q

Most common cause of meningitis in kids over 3m?

A

Neisseria meningitidis
Haemophilus influenzae
Streptococcus pneumoniae

33
Q

Most common cause of meningitis in kids over 3m?

A

Neisseria meningitidis
Haemophilus influenzae
Streptococcus pneumoniae

34
Q

Most common cause of meningitis in neonates?

A

GBStrep
Listeria
E coli

35
Q

Which abx for meningitis in children?

A

< 3 months: IV amoxicillin (or ampicillin) + IV cefotaxime
> 3 months: IV cefotaxime (or ceftriaxone)

36
Q

Who should have screening for DDH?
How and when is this done?

A

-First-degree family history of hip problems in early life

  • breech presentation at or after 36 weeks

-multiple pregnancy

Positive Barlow/ortolanis

USS At 6 wks

37
Q

Scarlet fever management

A

Pen V

38
Q

Most common osteomyelitis pathogen

A

staph aureus

39
Q

Most common osteomyelitis pathogen in sickle cell

A

Salmonella

40
Q

Imaging of choice in ? osteomyelitis

A

MRI

41
Q

What Is the most common form of JIA?

A

pauciarticular (oligoarthritis)

42
Q

What is pauciarticular (oligoarticular) JIA?
Which joints?

A

When 4 or fewer joints affected.

Typically affects knees, ankles, and wrists.

43
Q

Demographics of pauciarticular JIA?

A

Commonly affects F>M and ages 2-4

44
Q

Extra joint manifestations of pauciarticular JIA?

A

Uveitis
Growth problems (ie one leg longer than other)
Joint damage

45
Q

Is JIA autoimmune?

A

Yes

46
Q

What are the main JIA subtypes?

A
  • Oligoarticular (4 or fewer joints affected)
  • Polyarticular (5 or more joints)
  • Systemic JIA ( presents with fever, rash, and arthritis)
  • Enthesitis - where tendons and ligaments attach to bone are inflamed.
    Psoriatic JIA - associated with psoriasis
47
Q

Polyarticular arthritis subtypes and which joints are affected?

A

RF +ve:
- Symmetric joint involvement,
- Small joints of the hands and feet affected.

RF-ve
-Larger joints such as the knee, hip, and shoulder.

48
Q

DDH risk factors

A

+ve FHx
oligohydramnios
Breech
Incorrect swaddling

49
Q

Imaging choice for DDH

A

4-6m and under - USS

Over 4-6m X ray

50
Q

Which out of Barlow and Ortolani dislocates the hip?

A

Barlows.
Ortolani puts it back in

51
Q

What happens in Perthes disease?

A

Idiopathic osteonecrosis of the femoral head.

52
Q

How old are perthes children

A

4-8
Boys>girls

53
Q

What staging is used in Perthes

A

Catterall

54
Q

Who gets SUFE

A

Boys aged 10-15
Overweight usually

55
Q

SUFE management

A

Surgery

56
Q

Transient synovitis age

A

3-10

57
Q

How high transient synovitis present

A

Recent URTI/ bacterial infection.
Pain, limp
Boys
May have a low grade fever

58
Q

Kocher criteria?

A

Used to help determine if transient synovitis/ septic joint.

Criteria:
1. Non-weight bearing
2. Temperature >38.5°
3. White cell count >12,000 cells/mm3
4. ESR >40mm/hr

higher the number, higher the risk of septic joint

59
Q

Transient synovitis management

A

Conservative
Tell them to come back in 48h to review and ensure improving.
Tell them to come back in a week to ensure fully resolved.

60
Q

What is Osgood schlatter?

What might you see on examination?

A

inflammation of the patellar ligament where it attaches to the tibial tuberosity.

Point tenderness over the tibial tuberosity. Can get swelling and X ray changes but don’t need X ray unless worried about something else

61
Q

What is chondromalacia patellae?

A

Softening of the cartilage of the patella
Common in teenage girls
Characteristically anterior knee pain on walking up and down stairs and rising from prolonged sitting
Usually responds to physiotherapy

62
Q

Osteochondritis dissecans classic presentation

A

knee pain. Knee might lock or clunk.

63
Q

Who must have a USS referral for DDH?

A

All breech babies after 36 weeks
Positive first degree FHx
Multiple pregnancy

All need USS at 6 weeks to look for DDH

64
Q

Is Perthes usually painful?

A

No

65
Q

How to manage inguinal hernia

A

surgery

66
Q

How to manage infantile umbilical hernias

A

Conservative. Majority resolve by age 4-5

67
Q

charcots triad

A

fever, jaundice, RUQ pain.
Sign of ascending cholangitis

68
Q

What to do if someone on insulin but needs planned surgery

A

Reduce OD dose by 20% on day before and day of

69
Q

When would you worry about jaundice in babies

A

If under 24 hours old or above 2 weeks.

If above 2 weeks need a split bili - tells you if its conj or unconj - looking for biliary atresia. Get higher conj

In between = physiological jaundice,

70
Q

Continuos machine murmur

A

PDA

71
Q

What heart issues to downs syndrome babies get

A

Atrioventricular septal defects

72
Q

Reasons to refer febrile convulsion for same day

A

18 U CAN Consume Fosters

under 18 minths
Unclear diagnosis
Complex seizuure
Abx use recently
Neuro deficit
Consciousness decreased prior
First fit

73
Q

HUS triad

A

Thrombocytopenia
Normocytic anaemia
AKI

74
Q

What do contacts of pts with meningococcal meningitis get?

A

Oral ciprofloxacin or rifampicin is used as prophylaxis for contacts of patients with meningococcal meningitis
*if pneumococcal meningitis don’t usually need unless an outbreak in a cluster.

75
Q

Can coeliacs cause IDA?

A

YEs

76
Q

What are antistreptolysin o titres associated with

A

Henoch

77
Q

Double bubble sign on imaging?

A

duodenal atresia

78
Q
A