Paeds Flashcards

1
Q

signs of diabetes in children

A

Tired
Thirsty
Toilet more
Thinner

Babies
- heavy nappy
- oral candidiasis
- constipation
- skin infections

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2
Q

investigations for GH deficiency

A

Serum IGF-1 (low)

GH stimulation tests
- Insulin tolerance test
- Argine/glucagon

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3
Q

signs of DKA in children

A

Nausa and vomiting
abdominal pain
ketotic breath
drowsiness
rapid - deep sighing - Kussmaul breathing

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4
Q

start of puberty in boys v girls

A

girls 8-13
- breast budding (s2)

boys 9-14
- testicular enlargement (s2)

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5
Q

causes of jaundice in the first 24 hours of life

A

sepsis

haemolysis (autoimmune, inherited , acquired.. trauma)

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5
Q

jaundice is normal in the first 24 hours of life

a. true
b. false

A

b. false

always pathological - no normal cause of jaundice in the first day of life!!!

  • haemolysis
  • sepsis
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6
Q

ut

causes of jaundice day 2 - 2 weeks

A

physiological

breast milk

sepsis

haemolysis

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7
Q

time period of normal physiological jaundice to occur

A

day 2 - two weeks

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8
Q

why does physiological jaundice occur

A

born with a high number of RBCs and HbF has a shorter lifespan (80-90) days

the liver is immature and doesnt conjugate biliruben quickly enough to keep up

unconjuated

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9
Q

there is prolonged jaundice in breast fed babies

a. true
b. false

A

a. true

unconjugated biliruben remains high and can persist for 12 weeks (if after 3 months become worried and always rule out other causes)

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10
Q

potential treatment for unconjugated jaundice that is prolonged

A

blue light phototherapy

  • 450nm light converts biliruben to water soluable form
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11
Q

when would you start to worry about jaundice

A

prolonged > 2 week in term

> 3 weeks in pre-term

more likely to be pathological

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12
Q

potential causes of jaundice lasting > 2 weeks

A

breast milk (unconjugated)

Hypothyroidism - unconjugated (prevents conjugation)

Extrahepatic - biliary obstruction (CONJUGATED)

Neonatal hepititis - conjugated

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13
Q

signs of biliary atresia

A

prolonged jaundice - conjugated

dark urine

pale stools

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13
Q

tests for biliary atresia

A

split biliruben - conjugated

USS

HIDA/MRCP/Liver biopsy

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14
Q

treatment for biliary atresia

A

kasai portoenterostomy (Connect direct to intestines)

liver transplant often needed

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15
Q

symptoms of pyloric stenosis

A

forceful
projectile vomiting (non- billious)

visible peristlasis

firm round mass ‘olive tumor’ in the upper abdomen (hypertrophic pylorus)

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16
Q

tests for pyloric stenosis

A

ABG
- hypochloraemia
- hypokalaemia
- metabolic alkalosis

USS scan of abdomen!!!

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17
Q

treatment for pyloric stenosis

A

laparoscopic

ramstedts - pyloroyotomy

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18
Q

why do babies get GORD

A
  • Immature LOS
  • Shorter oesophagus
  • Slower gastric emptying time (Stomach stays fuller for longer)
  • Liquid diet
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19
Q

treatment for GORD

A
  • Gaviscon (mixed with feeds – 1st line if breast fed)
  • Thick and easy for formulas (1st line if formula feed)
  • PPIs (2nd line)
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20
Q

type of vomiting in GORD

A

effortless

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21
Q

symptoms of hirshsprungs

A

 acute intestinal obstruction after birth
 Failure to pass meconium with 48 hours
- Chronic constipation
- Abdominal pain and distension
- vomiting
- tight rectum with explosive stool (rectal squirt)

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22
Q

gold standard diagnosis of hirschsprings

A

Rectal biopsy

  • absence of ganglion cells
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23
Q

cause of hirschsprungs

A

congential

Enteric plexus
- myenteric (peristalsis)
- submucosal plexus (fluid secretion, blood flow and absorption)

both are absent!!!!

SECTION DOESN’T RELAX -> becomes constricted -> bowel obstruction -> bowel higher up than effected section becomes dilated and overloaded.

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24
Q

what age group will intusseception become symptomatic

A

3 months - 2 years
under 2 years

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25
Q

what is intussuception

A

Section of the bowel slides or folds into itself (often the ileum enters the cecum): effected section is thickened leading to a palpable mass in the abdomen/narrowed lumen which obstructs the passage of faeces

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26
Q

symptoms of inutssusception

A
  • Acute onset of colicky, severe abdomen pain
  • Bilous of green vomit
    -** Red currant jelly stool (blood mucous and stool)
  • Sausage shaped mass in right upper quadrant **
  • Previous URTI preceding
  • Features of abdominal obstruction (distension, vomiting, absolute constipation).
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27
Q

USS for intussusception

A

target or dougnut sign

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28
Q

treatment for interussuception

A

therapeutic enemas (contrast, water or air to force folded section of bowel out and into normal position)

surgical reduction

bowel resection if gangrene, or bowel perforation,

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29
Q
  • Red currant jelly stool (blood mucous and stool) and
  • Sausage shaped mass in right upper quadrant

are associated with

A

intussuception

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30
Q

sections of bowel most involved in intussusception

A

the ileum entering the cecum

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31
Q

age range most often affected by intersussception

A

3 months to 2 years

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32
Q

appearance of stool in intersussception

A

red current jelly stool

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33
Q

palpation of abdomen in interussception will find

A

sausage shaped mass in the RUQ

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34
Q

diagnostic of intersussception

A

USS

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35
Q

first line treatment for interussception

A

therapeutic enemas (contrast, water or air to force folded section of bowel out and into normal position)

surgical reduction

bowel resection if gangrene, or bowel perforation,

36
Q

signs of intestinal atresia in pregnancy

A

Polyhydramnios (excess fluid in pregnancy due to inability to swallow)

37
Q

what is intestinal atresia

A
  • Portion of the intestine is completely blocked or absent – preventing the normal passage of foods and fluids.
  • Due to disruption of blood flow to developing intestine during foetal development
  • Most commonly – duodenum
38
Q

downs syndrome is associated with increased risk of intestinal atresia

a. true
b. false

39
Q

symptoms of intestinal atresia

A

bilious vomiting in newborn (24-48 hours)

abdominal distension/failure to pass myconium

polydraminous in pregnancy (unable to swallow fluid)

40
Q

signs of intestinal atresia on Abominal XR

A

double buble sign - dilation of stomach and proximal duodenum

dilated loops of bowel and air flud levels

41
Q

peak incidence of appendicitis

A

Peak incidence 10 to 20 years old
- Less common in young children

42
Q

symptoms of appendicitis

A

Abdominal pain – starts centrally (umbilicus and moves to Right iliac fossa)
- Eventually becomes localised in the Right iliac fossa

Tenderness at McBurney’s point (1/3 distance from ASIS to umbilicus)

Anorexia/loss of appetite

Vomiting and nausea

Fever – low grade

Palpation of Left iliac fossa causes pain in the RIF (rovsings sign)

Guarding and rebound tenderness (increased pain when suddenly releasing pressure of deep palpation

Percussion tenderness – pain and tenderness on percussion

43
Q

Features suggestive of innocent murmur?

A
  • soft < 2/6
  • systolic
  • symptomless
  • situation dependent (gets quieter when standing or only appears when unwell or feverish)
    *no thrills

may not need further investigation

44
Q

Features of murmurs which would prompt further investigation

A

 louder than 2/6
 diastolic
 louder on standing
 failure to thrive, feeding, cyanosis, SOB

45
Q

Name two ejection systolic mumurs

A
  1. aortic stenosis ( 2nd ICS right sternal boarder)
  2. pulmonary stenosis (2nd ICS left sternal boarder)

crescendo descrendo (peak in middle)

46
Q

symptomatic aortic stenosis would cause what symptoms

A

reduced exercise tolerance

exertional chest pain

syncope

47
Q

murmur for aortic stenosis

A

ejection systolic

crescendo decresendo

radiates to carotids

palpable thrill through systole

slow rising pulse + narrow pulse pressure

48
Q

aortic stenosis is assoicated with which conditions

A

Turners
- bicuspid aortic valve

Williams syndrome
- supraclavicular stenosis

49
Q

describe features of murmur in pulmonary stenosis

A

ejection systolic

crescendo-decresendo

2nd ICS - left sternal edge

RADIATES to the BACK

exertional SOB, fatigue and dizziness

50
Q

signs of pulomonary stenosis

A

radiates to the back (ejection systolic murmur)

palpable thrill + RV hypertrophy

raised JVP (giant A wave)

widely split second heart sound!!! (takes longer for RV to empty through narrow valve)

51
Q

o

pulmonary stenosis is associated with what conditions

A

Noonans

Teratology of Fallot

Williams

Congenital rubella syndrome

52
Q

pan-systolic murmurs in children

A
  1. mitral regurgitation - 5th ICS midclavicular
  2. tricuspid regurgiation - 5th left sternal boarder
  3. VSD - louder on left sternal boarder
53
Q

describe murmur in VSD

A

left sternal boarder

pansystolic

54
Q

what kind of murmur in hypertrophic obstructive cardiomyopathy

A

4th ICS left sternal boarder

ejection systolic

55
Q

what two vessels does the ductus arteriolus connect

A

pulmonary artery with the aorta (allowing blood to bypass the lungs in foetus)

usually stops functioning and closes shortly after born

56
Q

what keeps the ductus arteriolus open in utero

A

prostaglandin E2 which is produced by the placenta (falls during birth resulting in closure)

57
Q

what direction is the shunt in PDA

A

from left to right (high pressure aorta -> into the pulmonary arteries)

the additional blood creates pressure within the pulmonary circulation

58
Q

signs that there is a PDA

A
  • increased HR
    dyanamic apex beat
    bounding pulses
    SOB, difficulty sleeping
    poor weight gain
    LTRI
59
Q

risk factors for PDA

A

preterm

downs

diabetes/rubella in mother

60
Q

murmur heard in PDA

A

Continuous crescendo-decrescendo machinery murmur
**- Loudest below the clavicle **

Normal S1 but S2 can be difficult to hear over the murmur

61
Q

what is given to close the PDA

A

IV ibuprofen or indomethacin

prostaglandin inhibitors

(surgical if doesnt work and symptomatic)

good chance of closure in term babies

62
Q

signs of aortic co-artaction in newborn

A

weak or absent femoral pulse!!! - checked on first day baby check

63
Q

co-artaction is common in turner syndrome

a. true
b. false

64
Q

radial-femoral delay is a late sign in

A

coarctation of the aorta

65
Q

what might you see in the blood pressure in aortic coarctation

A

increased pressure in limbs supplied by vessels proximal to it (e.g. ARMS)

and decreased pressure distal to the narrowing (limbs)

66
Q

murmur heard in coarctation of the aorta

A

Harsh systolic murmur – left sternal edge

/loudest on the back /left scapula

67
Q

what might compensate /delay deterioration in coaratation of the aorta

A

if the PDA is open - can compensate (and then becomes suddenly unwell when it closes)

reopen PDA with prostaglandin E1 and E2 to stabalise

68
Q

what are the 4 abnormalities in fallots teratology

A
  1. Pulmonary valve stenosis - due to narrowing of the RV outflow tract
  2. Large VSD
  3. Overiding aorta (sticks into RV)
  4. RV hypertrophy - due to (R-L shunt)
69
Q

risk factors for fallots teratology

A

increased maternal age

alcohol

maternal diabetes

diGeorge/Downs

congenital rubella

70
Q

where is the blood shunted in teratory of fallot

A

right to left shunt

The overriding aorta and pulmonary stenosis encourage blood to be shunted from right to left

71
Q

treatment of teratoly of fallot

A

Correction operation at 6 months
- Once 5kg bodyweight

72
Q

treatment for Tet spells

A
  • Give high flow 02
  • IV Fluid
  • IV beta blockers
  • Phenylephrine infusion
  • Sodium bicarb (will be acidotic)
  • Beta-blocker – reduce spasm/outflow tract
  • IV morphine

tet spells are emergencys

73
Q

what is transposition of the great arteries

A

(pulmonary trunk comes out of LV and back to lungs) and aorta out of RV

If no shunt – between vessels (ASD or PDA) survival is low

74
Q

Causes of a pan-systolic murmur:

A

VSDs, mitral regurgitation and tricuspid regurgitation.

74
Q

shunting of blood is in what direction in transposition of the great arteries

A

right to left – Deoxygenated blood bypasses the lungs and enters systemic circulation causing cyanosis

CENTRAL cyanosis (blue tongue and lips) due to
 RIGHT to left shunt

Blue baby – Is IMMEDIATE in neonatal period – newborn will be cyanotic

75
Q

heart defects associated with turners

A
  • Bicuspid aortic valve -> stenosis/regurgitation
  • Coarctation of aorta – usually descending (increased afterload on heart)
76
Q

thickening (hypertrophy) of the left ventricle muscle, particularly affecting the ventricular septum

A

Hypertrophic obstructive cardiomyopathy (HOCM)

thickening reduces the space inside the ventricle and blocks blood flow up to the aorta (left ventricle outflow tract obstruction.

77
Q

Arrhythmia and sudden death often occur during exertion, when there is extra demand on the heart in what condition

A

Hyoertrophic obstructive cardiomyopathy

78
Q

what is cause of HOCM

A

autosomal dominant genetic condition resulting from a defect in the genes for sarcomere proteins.

can occur via de nova mutation (new mutation) without familey history

78
Q

diagnosis of HOCM

A

echocardiogram or cardiac MRI

79
Q

treatment for whooping cough

A

azithromycin or clarithromycin if onset of cough is within the last 21 days

80
Q

when does cows milk allergy typically present?

A

first 3 months of life in formula feed infants

rarely - seen in breast fed infants

81
Q

what type of immune reactions take place in Cows milk protein allergy

A

both immediate IgE

and non immediate (non IgE)

82
Q

features of CMPA

A

regurgitation and vomiting

diarrhoea

urticaria, atopic eczema

wheeze, chronic cough

rare - angioodema/anphylaxis

83
Q

diagnosis of CMPA

A

clinical (improvement once stoped)

Skin prick/patch

total IgE and specigic IgE RAST for cows milk

84
Q

treatment for CMPA

A

extensive hydrolysed formula = eHF

85
Q

what kind of mass would you see in intusseption

A

sausage shaped - upper left quandrant

86
Q

medication for febrile seizures

A

buccal or rectal midazolam