child health Flashcards

1
Q

define innocent murmur

A

soft systolic murmur
due to physiological conditions outside the heart
inconsequential and disappears as child grows older

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2
Q

common causes of cardiac failure in paediatrics

A

neonates: PDA, cortication of aorta, cardiomyopathy
infants: VSD, ASD, cardiomyopathy
children: cardiomyopathy

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3
Q

most common causative organism for infective endocarditis

A

strep. Viridans

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4
Q

dDx of acute cough in a child

A

URTI
croup
asthma
inhaled foreign body

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5
Q

dDx of acute stridor in a child

A

croup
epiglotitis
bacterial tracheitis
inhaled foreign body

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6
Q

common causes of pneumonia in children

A

Viral: RSV, influenza, parainfluenza
bacterial: Strep pneumoniae, mycoplasma (5-14y.o), Grp B strep (neonates)

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7
Q

causes of bronchiolitis

A

RSV, parainfluenza, influenza A, adenovirus

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8
Q

presentation of bronchiolitis

A

cough, dyspnoea, wheeze
hyperinflation, crepitations
seasonal - october-april

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9
Q

management of bronchiolitis

A

self limiting
oxygen
NG feeds and IV fluids if poor feeding

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10
Q

screening for CF

A

Screening – new-born measurement of immunoreactive trypsin levels on neonatal blood spot (heel prick)
If raised blood sent for genetic testing for CF mutations
Sweat test and genetic testing indicated in those missed by screening but presenting with meconium ileus, failure to thrive, recurrent chest infections or malabsorption

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11
Q

presentation of CF

A

recurrent chest infections/airway obstruction
pancreatic insufficiency
DIOS, meconium ileus
infertility (absence of Vas, abnormal cervical mucus)
anaemia
diabetes

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12
Q

management of CF

A

daily physiotherapy
prophylactic Abx (flucloxacillin)
high calorie diet

DIOS/meconium ileus – hydration + lactulose (surgery is 2nd line unless there is complete obstruction or perforation)
Acute RTI - oral amoxicillin (IV tobramycin and ceftazidime if severe) + salbutamol + chest physio + mucolytic
Pancreatic insufficiency – pancreatic enzyme supplements with each meal + fat soluble vitamin supplements

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13
Q

presentation of neonatal sepsis

A
collapse
apnoea or resp. distress
seizure
poor feeding
jaundice
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14
Q

management of hypoxic ischaemic encephalopathy

A

therapeutic cooling to 33.5C, initiated by 6hrs, lasts 72hrs

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15
Q

how is neonatal cataracts screened

A

check red reflex after birth

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16
Q

causes of neonatal jaundice

A

unconjugated
breast milk jaundice, haemolytic anaemias, infections/sepsis, congenital hypothyroidism

conjugated
biliary atresia
a1 antitrypsin deficiency
neonatal hemochromatosis
idiopathic neonatal hepatitis
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17
Q

management of neonatal jaundice

A

phototherapy using UV light fibre optic blankets

exchange transfusion

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18
Q

presentation of downs syndrome

A

generalised hypotonia
short neck with excess skin at nape
brachycephaly
single palmer crease, short hand/fingers and a sandal tow gap in feet
facial features (prominent epicanthic folds, upward slanting palpebral fissures, protruding tongue, flat nose, low set ears)

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19
Q

presentation of edwards syndrome (trisomy 18)

A

microcephaly, small chin, low set ears
overlapping fingers
rocker bottom feet - flexed big toe, prominent heels
VSD, ASD, PDA

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20
Q

presentation of patau’s syndrome

A

holoprosencephaly
structural eye defects
cutis aplasia
cardiac and renal defects

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21
Q

presentation of turner’s syndrome

A

downward turned mouth, downslanting palprbral fissures
webbed neck, wide spaced nipples, lymphodema
streak gonads, lack of secondary sexual development
short stature

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22
Q

presentation of fragile X syndrome

A
long face, prominent ears, large chin
macroorchidism
learning difficulties
connective tissue problems, hyperflexibable joints, flat feet
behavioural problems: ADD, Autism
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23
Q

causes of intellectual developmental disability

A

Genetics - down’s, fragile X
acquired - fetal alcohol/drug exposure, rubella
perinatal - intraventricular haemorrhage, hypoxic ischaemic encephalopathy
post natal - brain injury

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24
Q

benefits of breast milk

A

baby
all the macronutrients needed for growth and metabolism
protects child against infections
promotes development of the gut
reduces cardiovascular disease and autoimmune conditions in the child

mother
reduces risk of breast and ovarian cancer
reduces risk of diabetes
reduces risk of post natal depression

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25
Q

define cerebral palsy

A

An umbrella term referring to a non-progressive disease of the brain originating during the antenatal, neonatal, or early postnatal period when brain neuronal connections are still developing.

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26
Q

risk factors for cerebral palsy

A
prematurity
maternal illness (thyroid, TORCH, factor V leiden)
birth asphyxia
neonatal sepsis
head injury prior to 3 years
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27
Q

what are the TORCH infections

A
toxoplasmosis
other (syphilis, VZV, parvovirus)
rubella
cytomegalovirus
HSV
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28
Q

presentation of cerebral palsy

A

motor abnormalities (delayed development, paralysis, weakness, ataxia, chorea)
spasticity
feeding difficulties
speech impairment/delay in speech development
delay in cognitive/intellectual development

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29
Q

complications of cerebral palsy

A

epilepsy
behavioural problems
poor growth
osteoporosis

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30
Q

management of cerebral palsy

A

physiotherapy
speech and language therapy
botulinum toxin
surgery

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31
Q

presentation of neural tube defects

A
paralysis or sensory loss in legs
LL weakness and loss of reflexes
neurogenic bladder and bowel
hydrocephalus
chiari II malformation - learning difficulties
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32
Q

management of NT defects

A

neurosurgical repair of the cele - antenatally or by 3 months
ventriculoperitoneal shunt for hydrocephalus
IV Abx to prevent neonatal meningitis

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33
Q

presentation of musclular dystrophy

A

DMD - onset at 3, wheelchair by 12
BMD - onset at 11, wheelchair not needed/in later life

loss of limb strenghth
loss of muscle tone and reflexes
calf hypertrophy
scoliosis and lumbar lordosis
positive gowers sign
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34
Q

diagnosis of muscular dystrophy

A

genetic testing
elevated creatinine kinase
monitor resp and cardio function

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35
Q

management of muscular dystrophy

A
genetic counselling
physiotherapy
oral pred 
resp support (positive pressure ventilation)
scoliosis surgery
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36
Q

define febrile seizure

A

A febrile seizure as a seizure occurring in the presence of fever in a child between the ages of 6 and 60 months who do not have an intracranial infection, metabolic disturbance, or history of afebrile seizures

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37
Q

presentation of febrile seizure

A
simple = tonic clonic with no focal features for < 10mins
complex = focal features or >10mins or recurrent seizures within 24 hrs

majority are simple, last 5 mins and has a rapid recovery
follows a recent fever/infection

38
Q

investigations for a febrile seizure

A

clinical diagnosis - routine investigations (imaging and bloods) not required for first simple seizure
rule out menigitis if there is nuchal rigidity = LP
EEG and MRI if recurrent complex seizure or less the 6 months old

39
Q

management of febrile seizures

A

paracetamol

if ongoing for > 5mins = diazepam

40
Q

presentation of osteomylitis

A
acutly unwell child
pyrexic
local erythema and tenderness (often near metaphysis)
recent history of VZV is common
night pain
limp
41
Q

management of osteomyelitis

A

bone aspiration if abscess
IV Abx
splintage of the limb

42
Q

presentation of juvenile idiopathic arthritis

A

persistent joint swelling in one or more joints
EMS
asymptomatic anterior uveitis

43
Q

salter harris classification

A

classification of growth plate injuries

I to V

44
Q

what is perthes disease

A

necrosis of part of the femoral capital epiphysis and growth disturbance in the physeal and articular cartilage leading to deformity of the femoral head and degenerative joint disease

45
Q

presentation of perthes disease

A

mainly occurs in 4-8 year olds
groin/knee pain
limp#
reduced hip abduction and internal rotation

46
Q

presentation of a slipped upper femoral epiphysis (SUFE)

A

early adolescence
hip pain - may have referred knee pain
affect limb often externally rotated - foot points out while walking
associated with hypothyroidism, chronic renal failure, radiotherapy, growth hormone therapy

47
Q

what is DDH

A

neonatal hip instability

acetabular dysplasia with or without subluxation and frank dislocation of the hip joint

48
Q

presentation of DDH

A

screened for at birth and 6 weeks - positive barlows and ortilani test

in older children
limp
asymmetrical groin creases
leg length discrepancy
reduced hip abduction
49
Q

causes of chronic diarrhoea in children

A
toddler's diarrhoea
constipation overflow
post infectious foot intolerance e.g. lactose
IBD
malabsorption (CF, coeliac)
50
Q

causes of acute diarrhoea in children

A

infections (rotavirus, enterovirus, E coli, salmonella)
starvation stools
intussusception

51
Q

investigations for a bleeding/bruised child

A
FBC, coag
BC, WCC, CRP (infection)
XM (major haemorrhage)
BP and urinalysis (HSP)
skeletal survey, CT head, retinoscopy (NAI)
52
Q

presentation of idiopathic thrompocytopenia

A

acute onset bruising/petechiae
absence of systemic symptoms
epistaxis common following a recent viral illness

53
Q

management of ITP

A
limit high impact activities
platelet transfusion if bleeding
IVIG
steroids
splenectomy
54
Q

haemophilia summary

A

type A = factor 8 deficiency
type B = factor 9 deficiency
presents with spontaneous joint/muscle bleed or from minor trauma, raised lumpy bruises
investigations - prolonged APTT, clotting screen
management with recombinant factor administration IV

55
Q

von willie brand disease summary

A

deficiency of factor 8: VWF ratio = decrease platelet adhesion
presents with mucosal bleeding (gums, GI, epistaxis, menorrhagia), prolonged bleeding post trauma
investigations: prolonged APTT, reduced F8:VWF, no platelet aggregation on co factor assay
manage with prophylactic desmopressin or recombinant factor 8 for bleeding episodes

56
Q

presentation of a brain tumour

A
raised ICP (morning headaches, vomiting, papilloedema)
focal seizure
neurological deficit
endocrine disorders
57
Q

investigation for suspected brain tumours

A

brain/spinal MRI
tumour biopsy
endocrine screen
CSF cytology and tumour markers

58
Q

differentials for a child with an abdominal mass

A

neuroblastoma
wilm’s tumour
hepatoblastoma
germ cell tumour

59
Q

biochemical disturbances seen in tumour lysis syndrome

A

hyperuricaemia
hyperkalaemia
hypophosphatemia
hypocalcaemia

if untreated can lead to AKI, seizures, cardiac arrhythmias, death

60
Q

management of tumour lysis syndrome

A

IV fluids
allopurinol
manage hyperkalaemia (insulin/dextrose, calcium gluconate, calcium resonium, salbutamol)
dialysis

61
Q

presentation of measles

A

prodrome (fever, coryza, cough, koplik spots)
maculopapular rash behind ears, migrates to face then trunk
complications: otitis media, interstitial pneumonitis

62
Q

presentation of chicken pox

A
fever
malaise
headache
abdo pain
itch crops of erythematous macules, papules and vesicles
63
Q

infectious period of chicken pox

A

2 days before symptoms to 5 days post rash

64
Q

management of chicken pox

A

supportive
aciclovir for high risk patients
vaccination for high risk patients
post exposure prophylaxis (VZ IVIG) if immunocompromised

65
Q

presentation of parvovirus B19

A

low grade fever
malaise
maculopapular spots on cheeks (gives slapped cheeks appearance)
rash on trunk and limbs (lacy appearance)

66
Q

presentation of mumps

A

prodrome (fever, anorexia, headache)

painful salivary and submandibular gland swelling

67
Q

presentation of rubella

A

prodrome (coryza, tender cervical lymphadonopathy)
fine maculopapular rash - face spreads to trunk
arthralgia

68
Q

most common causes of meningitis in children

A

bacterial: neisseria meningitidis, strep pneumonia
viral: enterovirus, HSV (meningoencephalitis)

69
Q

presentation of bacterial meningitis in a child

A
fever, lethargy 
high pitched or irritable cry (cannot be soothed by parents)
poor feeding
apnoeic or cyanotic attacks
seizure
bulging fontanelle
70
Q

management of bacterial meningitis

A

suspected
IV ceftriaxone
+ amoxicillin and gentamicin if under 6 weeks

confirmed
N. menigiditis = cefotaxime fir 7 day
strep. pneumonae = cefotaxime for 14 days

71
Q

presentation of meningococcal meningitis/sepsis

A

fever + petechial/purpuric rash
hypovolaemic shock
DIC
metabolic derangements (low, K, Ca, Mg, PO4)

72
Q

complications of prematurity

A
sepsis
PDA
RDS
ROP
osteopenia
NEC
intraventricular haemorrhage
73
Q

what is potters syndrome

A

bilateral renal agenesis

74
Q

indications for dialysis

A
severe volume overload
severe hyperkalaemia
symptomatic uraemia
severe metabolic acidosis
removal of toxins
75
Q

causes of HTN in young people

A

coarctation of aorta
pheochromocytoma or neuroblastoma (catecholamine release)
congenital adrenal hyperplasia
renal tumour, renal parenchymal disease (release of renin)

76
Q

management of minimal change GN

A
prednisolone
furosemide if symptomatic oedema
pneumococcal vaccination
penicillin prophylaxis for risk of encapsulated organism
salt/fluid restriction
77
Q

causes of deafness in children

A

acquired
pre natal - rubella infection
perinatal - hypoxia, kernicterus
postnatal - menigitis, head injury, ototoxic drugs e.g. cisplatin

congenital
usher’s, pendred’s

78
Q

management if deafness in children

A

hearing rehab with bilateral, digital, behind-the-ear hearing aids
cochlear implantation

79
Q

most common cause of nasal obstruction in children

A

hypertrophy of the adenoids

associated with snoring and green rhinorrhoea

80
Q

management of irritant contact napkin dermatitis

A

frequent nappy changes
avoidance of soaps and wipes
emollient and zinc based preparation after each nappy change
topical steroid if inflamed
if candida infection (satellite papules and pustules) - clotrimazole

81
Q

what is juvenile plantar dermatosis

A

erythema, hyperkeratosis and fissuring of the anterior plater surface
associated with sweating and sports footwear

82
Q

management of juvenile plantar dermatoses

A

avoidance of occlusive footwear and synthetic socks
aluminium hydrochloride to reuce sweating
urea based emollients for hyperkeratosis and fissuring
steroids

83
Q

what is impetigo

A

highly contagious skin infection cause by s aureus

annular erythema with honey colour crust, may become bullous

84
Q

management of impetigo

A

flucloxacillin

prevention of spread
dont share towels or bath with other children
antiseptic in bath

85
Q

molluscum contagiosum

A

small pearly umbilicated papules causes by MCV.

self limiting

86
Q

management of tinea capatis

A

ketaconazole shampoo

oral griseofulvin or terbinafine

87
Q

investigations for Down’s

A

screening: maternal b HCG, PAPP-A, nuchal translucency on US, maternal age

those deemed high risk offered chorionic villous sampling and amniocentesis.

88
Q

duodenal atresia presentation

A

bilious vomiting after birth
double bubble finding on abdominal x ray
associated with downs

89
Q

presentation of intussesception

A

classic triad of abdominal pain, red current jelly stools and vomiting

signs: abdominal mass, distention, pallor, absent bowel sounds
X ray: target lesion/doughnut sign

90
Q

management of intussesception

A
contrast enema (air enema) +/- Abx
surgical reduction +/-resection