paeds Flashcards

1
Q

causes of dehydration main categories

A

reduced intake

increased loss

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2
Q

causes of dehyrdration

A

REDUCED INTAKE

  • dysphagia /neurodisability (cleft palate, developmental delay, cerebral palsy)
  • vomitting (gastroenteritis, GORD, URTI, chemo)
  • behavioural/ psych (food refusal, anorexia)
  • child neglect

INCREASED LOSS

  • gut (gastroenteritis, IBD, stoma)
  • kidneys (renal tubular disease, nephrogenic diabetes insipidus, renal dysplasia)
  • lungs (cystic fibrosis, cardio/resp diseases)
  • skin (burns, cystic fibrosis, sepsis/fever)
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3
Q

signs of dehydration - mild (5% water loss), moderate, severe (10%)

A

thirst
dry lips
restless, irritable

sunken eyes
reduced skin turgor
decreased urine output

anuria
cold, mottled peripheries, hypotension
reduced conciousness

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4
Q

dehydration complications

A

constipation
developmental delays
UTI
failure to thrive, malnutrition

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5
Q

managment principles of rehydration for different levels of dehydration

A
Not dehydrated (eg elective surgery) = maintenance
Dehydrated = maintenance + correct deficit
Shocked = maintenance + correct deficit + bolus (C as part of ABCDE - part of their resuscitation)
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6
Q

maintaince of hydration formula

A

first 10kg = 100ml/kg (10x100)
second 10kg = 50ml/kg
all other kg = 20ml/kg

this = daily total. so divide by 24 for hourly amount

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7
Q

how to calculate estimated weight

A

Estimated weight (kg) = (age +4 ) x2

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8
Q

defecit correction for hydration formula

A

Deficit % x 10 x weight (kg)

Over 24h or 48h

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9
Q

fluid bolus for dehydration amount

A

20mls/kg of 0.9%

Sometimes 10ml/kg more
Sometimes less than 20 – give 10ml/kg of 0.9%
- Trauma
- DKA

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10
Q

what is monitored in dehydration

A
BP
HR
O2 sat
RR
Capillary refill
Temperature 
Appearance and behaviour
- Lips dry
- Sunken eyes
- Skin turgor
- Restless 
- Reduced consciousness 
U/Es
Urine output
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11
Q

ondasteron =

A

prevents vomitting. try in dehydrated, esp gastroentiris

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12
Q

when are fluids given orally/ IV for dehydration

A

flexible but generally 5% (mild) - oral; 10% severe - IV

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13
Q

toddlers diarrhea

A

Foul smelling, watery. May contain mucus or undigested material
No other thriving problems in baby
Exclusion diagnosis (infection, malabsorption)

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14
Q

extra things to ask in paeds history

A

Feeding /hydration

  • How often
  • How much
  • How long on breast
  • Fed overnight
  • Wet nappy - how many, how much wetness (heaviness of nappy)
  • Bowels opening - diarrhea

Fever

  • If checking temperature, how – Under arm best, What reading, Since when
  • Any action eg paracetamol

Rashes
- inc Non-blanching -septicaemia

Behaviour

  • Are they their usual selves
  • How happy - have you seen them smile today

Contacts

  • Who lives at home? Are they well?
  • Anyone ill at school
  • Been abroad?

Ask about birth history

  • How many weeks
  • Mode of birth (vaginal, elective, emergency, instrumental)
  • Any time in neonatal unit after birth
  • Feeding

Development

  • “Have you got any concerns about development?”
  • Ask about milestones - independent walking etc
  • Growth

vaccination history

  • Are they up to date
  • Flu
  • Any extra?
  • Preterm have additional winter vaccines
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15
Q

extra things to ask in paeds history

A

Feeding /hydration

  • How often
  • How much
  • How long on breast
  • Fed overnight
  • Wet nappy - how many, how much wetness (heaviness of nappy)
  • Bowels opening - diarrhea

Fever

  • If checking temperature, how – Under arm best, What reading, Since when
  • Any action eg paracetamol

Rashes
- Non-blanching -septicaemia

Behaviour

  • Are they their usual selves
  • How happy - have you seen them smile today

Contacts

  • Who lives at home? Are they well?
  • Anyone ill at school
  • Been abroad?

Ask about birth history

  • How many weeks
  • Mode of birth (vaginal, elective, emergency, instrumental)
  • Any time in neonatal unit after birth
  • Feeding

Development

  • “Have you got any concerns about development?”
  • Ask about milestones - independent walking etc
  • Growth

vaccination history

  • Are they up to date
  • Flu
  • Any extra?
  • Preterm have additional winter vaccines
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16
Q

kawasaki presentation / diagnosis

A

Fever (Essential)

4 out of 5 of:

  • Skin rash - diffuse
  • Conjunctivitis - red eyes
  • Periphery change - Peeling of fingers / swelling / red / pain
  • Cracked lips, Swollen red tongue
  • Swollen neck lymph gland - painful, solitary, large
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17
Q

non blanching rash- what are you thinking of

A

meningitis septicaemia

also could be ITP and HSP

if just face/neck/conjunctival petichiae - may be due to retching/ vomitting –> pressure

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18
Q

ASD triad

A

Rituals

  • Certain order in bedroom, fixed on daytimes
  • rigid, resist change

Unusual /delayed language
- May have seen speech and language therapist, language may appear stilted

Social difficulty

  • Lack of theory of mind, can’t read others
  • Lack of understanding unspoken social rules, idioms, body language
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19
Q

PTSD triad

A

Intrusive sensations, memories/ flashbacks

Avoidance
- Of places, of talking/ thinking about it

Anxiety

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20
Q

kocher’s criteria

A
Kocher's criteria
Fever >38.5
CRP>20 
ESR >40 in first hr
Cannot bear weight
WBC >12

for septic arthritis (limping child)

also - pain often at rest
any age

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21
Q

most common UTI cause. treat with what

A

e coli
cefcefotaxime
If unresponsive to this, meropenem (a carbapenem) (broader)

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22
Q

flucoxycylin good for what

A

staph aureus

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23
Q

perthes disease

A
3-10y
Self limiting
Ischaemia → necrosis of femoral head
Unilateral  
Seen on X ray 
Pain, effusion, limited range of motion
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24
Q

Transient synovitis

A

3-10y
Usually following resp infection (but the effusion is sterile!)
Usually no pain at rest/passive movements

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25
Slipped upper femoral epiphysis
Onset of puberty Tall and thin or short and obese Pain, leg length shortening seen on X ray
26
what could cause limping
``` Toxic synovitis = most common - Benign, self limiting Infection - osteomyelitis, septic arthritis - systemically unwell, prev infection Fracture Tumour - Pain, tender, mass possibly Arthritis Slipped upper femoral epiphysis - Onset of puberty - Tall and thin or short and obese - Pain, leg length shortening Perthes disease - Self limiting - Ischaemia → necrosis of femoral head - Unilateral - Pain, effusion, limited range of motion ``` could be foot, leg, thigh, hip, knee, spine, testiclar or abdomen
27
presentation of malignancy (general)
Localised mass - Lymphadenopathy - Organomegaly - Soft tissue or bony mass - Airway obstruction as a result Disseminated disease → infiltrates bone marrow → anaemia → infections, bruising Headaches, increase ICP signs (brain tumour) Fever, weight loss, fatigue
28
leukaemia - commonness - symptoms - investigations
Leukaemia is common esp ALL ``` Fatigue Fever Frequent infections Lymphadenopathy hepato/splenomegaly Anaemia - pale, bruising Bone/ joint pain ``` ``` Blood film - see blastocyte Serum chemistry CXR Bone marrow aspirate Lumbar puncture ``` Chemo Haemopoetic stem cell transplant
29
CNS tumours presentation and treament
``` Presentation Headache, often worse lying Vomiting, esp early morn Papilloedema Nystagmus Ataxia Behavioural changes Squint ``` ``` Treatment Surgical resection Radiotherapy Chemo palliative care ```
30
negative long term effects of cancer treatment
``` Endocrine (brain surgery) Intellectual cardiac/renal toxicity - chemo Fertility Psychological ```
31
wilms =?
nephroblastoma
32
ADHD criteria
3 key symptoms = inattention, hyperactivity, impulsivity 6 symptoms of inattention - Lack of attention to detail, careless mistakes - Difficulty sustaining attention - Does not seem to listen when spoken to directly - Fails to finish tasks - Difficulty organizing - Avoids or dislikes tasks that require sustained mental effort - Often loses things needed for tasks - Easily distracted by extraneous stimuli - Forgetful in daily activities OR 6 symptoms of hyperactivity or impulsivity - fidgets/taps hands/legs / squirms in seat - Leaves seats when expected to stay in seat (school, eating, activity) - runs/ climbs in inappropriate situations - Unable to play/ leisure quietly - “On the go” - Talks excessively - Blurts out answer before question finished - Difficulty waiting their turn - Interrupts or intrudes Present before 12y Present in 2 or more settings Must affect functioning No better diagnosis
33
ADHD treatment
Nonpharmalogical - Parent management and training = 1st line - ---Plan for day, routine - ---Positive reinforcement - ---Brief, specific instructions - ---Incentives eg star chart - ---Keep social interactions with others short and sweet - ---Regular exercise - ---Regular and healthy diet - ---Support from school - CBT Pharmacological - Not advised for pre-school children - Stimulant - ---Increase dopamine in brain - ---Ritalin (short acting) - ---Delmosart (long acting) - ---Lisdexamfetamine - Non stimulant - ---Reduce norepinephrine breakdown - ---SNRI - atomoxetine - ---Guanfacine - Combined therapy - Side effects - ---Anxiety - ---Reduced appetite - ---Hypertension - ---Psychosis (rare)
34
MODY - what might make you suspcious that t1dm is acc mody - diagnosis
Lots of family with DM C peptide robust No antibodies for insulin Genetic testing
35
JIA - commonnes - when - diagnosis - features
Most common inflammatory condition Juvenile = Onset before 16th birthday Idiopathic = no other identified cause- diagnosis of exclusion Rule out: - Reactive arthritis (following other infection) - Malignancies inc blood born ones like leukaemia - Non accidental injury - Septic arthritis ``` Arthritis = joint swelling (or painful restriction of movement) - lasting 6w Features - Persistent joint swelling - Joint stiffness - esp morning - Loss of range of movement - Pain - Warmth - Colour change - Joint deformity - Accelerated bone growth - if one leg longer ```
36
oligoarticular JIA
4 or fewer joints involved Typically lower limb associated with chronic anterior uveitis
37
polyarticular JIA
More than four joint involved More rapid bony destruction Often small joints eg hand/feet
38
Psoriatic JIA
May be before / after / same time as joint problems Family link common Dactylitis , nail pitting - can diagnose it even if child has not yet developed psoriasis often associated with chronic anterior uveitis
39
Enthesitis -related JIA
Akin to ankylosing spondylitis in adults Plantar fasciitis - sore underside of feet Lower back joints sacroileus often involved
40
systemic arthitis JIA
``` Auto-inflammatory Spiking fever Rash Lymphadenopathy Hepatosplenomegaly Fluid effusions - eg ascites ```
41
chronic anterior uveitis
Silent - no signs/ symptoms Can cause blindness Often present in JIA, so all children with JIA/suspected JIA are screened several times a year Especially connected to oligoarticular and psoriatic JIA
42
what should you screen for when you see dysmorphic features
cardiac conditions Trisomy 21 - VSD - AVSD - Tetralogy of fallot Turners syndrome - Coarctation of aorta - Bicuspid aortic valves - Aortic stenosis - Aortic dissection (later in life) Noonans 22q11p.2 deletion syndrome
43
complex congenital cardiac conditions
= combination of congenital cardiac conditions
44
pulmonary vascular resistance pre and post birth
High pulmonary vascular resistance (alveoli closed) so blood bypasses lungs After birth, baby takes breaths, alveoli open, so pulmonary vascular resistance falls, so blood goes to lungs rather than to L side of body
45
physiological fetal circulation shunt closing and why
After birth, baby takes breaths, alveoli open, so pulmonary vascular resistance falls, so blood goes to lungs rather than to L side of body Oxygen presence also reduces prostaglandins so ductus arteriosus tissue contracts and closes (first shunt to close) Then L side pressure increases so less foramen ovale activity so closes The umbilicus is cut - so no blood from placenta to umbilical vein and ductus venosus - so this shunts closes too
46
types of ASD
Ostium secundum - in middle of septum Ostium primum - at bottom of atrial septum, closer to AV valves, associated with AVSD Sinus venosus defect - at top of septum - rare and hard to pick up with echo
47
ASD presentation
``` Asymptomatic when younger Only if large will immediate lung effects transpire Fixed and widely split S2 sound Systolic murmur in pulmonary region Palpitations ```
48
VSD presentation
Pulmonary oedema (Pulmonary artery blood is mixed. High pressure → increased pulmonary blood flow) Infection of IE around defect Asymptomatic often until pulmonary vascular resistance falls Poor feeding Failure to thrive Tachypnoea Gallop rhythm, 3rd heart stand, thrill Pan systolic murmur, best heart in lower left sternal edge, radiating to axilla and upper sternal edge Hepatomegaly Oedema
49
AVSD =? Presentation
Atrial and septal septum defect, involving the crux of the heart and leaflets (so worse than ASD +VSD) Common in trisomy 21 So important to look for dysmorphism in cardiac examination ``` Poor feeding Failure to thrive Tachypnoea Gallop rhythm, 3rd heart stand, thrill Can lead to to pulmonary vascular disease rapidly Murmur arises from valvular regurgitation Hepatomegaly Oedema ```
50
patent ductus arteriosus presentation
``` Preterm Pulmonary oedema (High pressure blood into lungs from aorta to pulm artery) Poor feeding Failure to thrive Tachypnoea Easily palpable femoral pulses Gallop rhythm (3rd heart sound), thrill Continuous machinery murmur Hepatomegaly Oedema ```
51
types of L-->R shunts management
ASD VSD AVSD patent ductus arteriosis ``` Increase calorie intake NG feeds Diuretics ACE i Surgical or catheter device occlusion ```
52
coarctation of aorta signs
Weak femoral pulses-- Compare to brachial Pre and post ductal difference in o2 saturations - IF duct is open (Open aids survival - bypasses coarctation ) 4 limb BP - upper/lower limb discrepancy If ductus arteriosus closing/ closed - collapsed and acidotic Murmur over back if older child
53
aortic stenosis signs
(aortic valve narrowing) LV must work harder → hypertrophy → failure Weak pulses upper and lower limb (less volume ejected from LV) Thrill in suprasternal region and carotid area Ejection systolic murmur in aortic area If critical → collapsed and acidotic
54
pulmonary stenosis signs
RV must work harder → hypertrophy → failure Ejection systolic murmur in L upper sternal edge Murmur radiates to back Heave - RV - L sternal border
55
tetraolgy of fallot features
1. VSD 2. infundibular/ muscular thickening at base of pulmonary artery - blocks outflow When severe, low o2 saturation, blood goes through VSD rather than lungs = hypercyanotic spell 3. Overriding aorta Sits on top of VSD, septum deviated towards L 4. RV hypertrophy (due to 2nd point- stenosis)
56
tetralogy of fallot presentation investigations management
Cyanosis Acidosis Collapse /death Investigations Check for 22q deletion (genetic) ``` Management Managing hypercyanotic spells - Propranolol - BT shunt (Blood taken from head and neck arteries to lungs) Surgical repair - 6-9m ```
57
Transposition of great arteries =? presentation management
Aorta not connected to L as planned, but the R. and visa versa with pulmonary artery Deoxygenated blood from body goes to body → central cyanosis Oxygenated blood form pulmonary veins into L heart then back to lungs Foramen ovale helps - allows some mixing of blood. If and when this closes … : Cyanosis Acidosis Collapse /death Management Atrial septostomy - mixing of circulations via hole in foramen ovale being widened
58
what is in septic screen
bloods urine sample (ideally clean catch) LP
59
meningococcal antibiotics - pre hospital - <3 m - >3m
Pre-hospital - benzylpenicillin >3months - ceftriaxone <3months - cefotaxime + amoxicillin/ ampicillin (Group B strep cover)
60
meningococcal purpura cause
neisseria meningitidis. Wbc engulf endotoxins → endothelial damage in blood vessels → capillary leakage
61
meningococcal prophylaxis for close contacts
Prophylactic antibiotics (within 24h) -- ciprofloxacin for prolonged close contact - siblings, roomates, parents, partner (not classmates, friends, visiting family) within 7 days of illness
62
systemic JIA tx
NSAIDS/ aspirin High dose corticosteroids DMARDs if corticosteroids not successful
63
kawasaki tx
``` Aspirin - Painkiller - Anti-inflammatory - Anti-platelet - High dose until fever goes, then low dose for 6-8w IV immunoglobulin - gamma globulin - Reduces heart risk and fever - If ineffective → corticosteroids Fluids Monitor heart (aneurysm (rupture, MI, HF), myocarditis, tachy, pleural effusions) ```
64
what is reyes syndrome
liver / brain damage | possible effect of aspirin (in children)
65
broncholitis xray and clinical presentation
thickened airways - air struggles to leave so wheeze and hyperinflated chest diaphragm level at more than 6 ribs visible cant breath out, exhausted form breathing effort - maybe on ventilator
66
NEC pathophysiology
Bugs produce air in the wall of the bowel. Then air is absorbed in veins !
67
TTN causes and pathophysiology
TTN - lungs wet from C Section/grand multip -- less squeezing during birth so not prepared for lung clearance. Difficulty breathing, but resolves
68
where does diaphragm normally lie (xray)
Diaphragm at 3/4th rib with expiration And this gives a more consolidated picture so important to rule out poor inflation Diaphragm at 5/6th rib with inspiration If overinflated, could be bronchiolitis
69
first/ second line for antidepressants
Fluoxetine first line | Citalopram / sertraline second line
70
why is iron deficiency common in children investigation results treatment
Children have poor intake and increased demand Especially with breastfeeding (over cow's milk), picky toddlers, growth and infection increases requirement Adults get most of their iron from recycled red blood cells whereas children need to get more from their diet Low ferritin, low serum iron, increased total iron binding capacity (TIBC) as compensation, high ZPP minimum 3 months oral iron (compliance is challenging) and also address cause (change diet)
71
G6PD presentation and cause
``` Lack of glucose 6 phosphate dehydrogenase ⇒ haemolysis X linked (boys) ``` Presentation Acute severe haemolysis -- broad beans, prescribed drugs, infection Neonatal jaundice Chronic haemolysis
72
which is more common ALL or AML
ALL (most common childhood cancer). good prognosis though, slightly better than the slightly less common AML
73
what should you prevent in sickle cell patients
pain / crises (hydration, warmth, transfusion) infection -- aplastic crisis often precipitated by parvovirus (slapped cheek virus) - rbc production switched off temporarily but this has large effects as their rbc lifespan is shorter (anaemia with low reticulocyte count)
74
sickle cell patient develops Pain, hypoxia, fever, sometimes CXR signs ... - diagnosis - tx
Acute chest syndrome Transfusion, oxygen, antibiotics, incentive spirometry
75
normal and abnormal gross motor development - newborn - 3months - 6 months - 6-8months - 9 months - 1 yr - 2 yr - 3 yr - 4yr - 5yr
Newborn Flexed arms and legs Equal movements in all limbs Head lag, floppy 3 months Start pushing up on arms, lift head when on tummy Turn head side to side Minimal head lag ``` 6 months Hands on ground, with head up whilst on tummy Rolls - Front to back - 4-6m - Back to front - 6m Crawling 6-9m ``` 6-8m Tripod sitting, supported sitting, Rounded back, arms in front of their legs ``` 9 months Pull up on furniture → standing Sit unsupported (SOME SAYS 6M, SO TRIPOD BEFORE?) - Not sitting by 1 year = worried Cruising ``` 1 year Walking - No walking by 18 months - consider muscular dystrophy for boys (check Creatinine Kinase) 2 years Steps Throw ball overarm 3 years Jumps Ride tricyle 4 years Hops Use bat 5 years Ride a bike
76
when worried about no walking
No walking by 18 months - consider muscular dystrophy for boys check Creatinine Kinase should be 1 year
77
when worried about no sitting unsupported
Not sitting by 1 year = worried | should be 6months
78
speech and language and hearing and abnormal landmarks ``` 3m 9m 1y 2y 3y 4y 5y ```
3 months Laughs and squeals Turn to sound 9 months ‘mama’/’dada’ 1 year One word - No clear words by 18 months - could be hearing problem, learning disability, autism or an isolated speech/ language problem 2 years 2 words joined together Name body parts x10 3 years Short sentences, mainly understandable Can follow 2 - step commands 4 years Colours Count to 5 objects Fluent in 4 word sentences 5 years Knows meanings of words (e.g. what is a lake?)
79
when worried by no words
No clear words by 18 months - could be hearing problem, learning disability, autism or an isolated speech/ language problem should be 12m
80
normal and abnormal fine motor/ vision landmarks ``` 8w 2-3m 4m 6m 8m 1y 1.5y 2y 3y 4 5 6 7 10 ```
8w Follow movement in horizontal plane ``` 2-3 months Hands not closed anymore Blink at bright lights Hold gaze of caregivers Follow movement in all planes ``` 4 months Palmar grasp of object, both hands Hand regard- Stare at hands, in midline, understand they are theirs 6 months Transfer object one hand to other Foot regard Object permanence 8 months Take object in each hand - Hand preference before 18 months - consider neurological condition such as cerebral palsy 1 year Scribbles with crayon Basic pincer grip Casting 1.5 years 2 cube tower 2years Horizontal scribble ``` 3 years 8 cube tower Draw circle Bridge/train out of blocks Colour matching Red green colour blindness recognisable at this point ``` 4 years Cross drawing Steps out of cube blocks 5 Square drawing 6 Triangle drawing 7 Diamond drawing 10 Cube drawing
81
hand preference is worrying at what age
Hand preference before 18 months - consider neurological condition such as cerebral palsy
82
normal/ abnormal social interaction and self care landmarks ``` 6w 2m 6m 9m 1y 2y 3y 4y ```
6 weeks Spontaneous smile No smiling by 3 months may be a sign of visual impairment, as well as autism and learning disability 2m Coo 6 months Finger feeds object permanece 9 months Wave goodbye Stranger anxiety, upset when caregivers leave 1 year Finger feeds 2 years Help dress self Feed a doll 3 years Play with others, name a friend Worried if not interested in playing with friends by 3 Dress self 4 years dress/ undress without help Simple board game Cultery use
83
at what age should children be playing with peers
3y
84
at what point do we worry about lack of smile
No smiling by 3 months may be a sign of visual impairment, as well as autism and learning disability should be 6w
85
global impairment defined as what
delay in 2 or more domains Gross motor Fine motor and vision Speech, language and vision Social interaction and self care skills
86
sore legs may suggest
meningococcal septicaemia
87
what age is consistent with febrile convulsions
1-3y mainly but 3m -5y
88
unequal pupils associated with?
intracranial bleed
89
boggy head swelling indicates
underlying skull fracture
90
``` classification of infants toddlers children adolescents ```
infants 0-27d toddlers 28d - 23m children 2y-11y adolescents 12-16-18y
91
which age category can have less fat soluble drugs
neonates - less bile acid so less fat absorption
92
chloramphenicol and babies
unable to metabolise (no enzyme) grey baby syndrome --> vomitting, poor feeding, cyanosis, hypotension, CV and resp issues --> death so avoid or use CLOSE monitoring
93
rashes + the following - abdo pain - recent burn - bleeding gums - cough / sore eyes - red eyes - joint pains
- abdo pain - HSP - recent burn - toxic shock syndrome - bleeding gums/ nose bleeds - leukaemia - cough / sore eyes - measles - red eyes - kawasaki - joint pains - meningioccal sepsis, HSP, JIA, leukaemia
94
which centiles are considered the outer ranges of normal for - height - height velocity
Height : 3-97th centile | Height velocity : 25-75th centile
95
early/ delayed puberty ages for boys and girls. and what is the marker for puberty
Girls - breast 13 = delayed 8= early Boys - testes 14 = delayed 9= early Late is more common and okay for boys. Early is more common and okay for girls
96
how do you distinguish hormonal vs malnutrtion issue in regards to growth
Height and weight problem = malabsorption issue (weight not affected by hormone issue)
97
test to distinguish true and pseudo precicious puberty
GnRH test Test between true and pseudo precocious puberty LH, FSH measured and remeasured after GnRH injection ``` True = levels rise Pseudo = levels stay low ``` ``` True = central (cause = hypothalamus/pit - early HPG axis maturation) - more internal charactherisitcs ? eg testes size and periods? maybe not though Pseudo = peripheral (induced by sex steroids, gonadatrophin /HPG axis independant) - more secondary characteristics? eg pubic hair. maybe not though ```
98
discuss 2 chromosomal hypogonadic conditions - name - chromosomal tagline - features
``` Klinefelter syndrome 47XXY Primary hypogonadism Gynacomastia Azzospermia Reduced secondarys sexual characteristics Small testicular volume <5mls Lower IQ Tall ``` ``` Turners 45XO Hypergonadotropic hypogonadism Short stature, neck webbing, low posterior hairline, prominent ears CV and renal malformations Recurrent ear infections ```
99
what is a fluid challenge
= rehydration attempt 5ml diarolyte given every 5 mins diarrhea/ vomitting noted reveiwed regularly
100
acute scrotum pain differential diagnosis investigations
``` testicular torsion (main one) Torsion of hydatid aka appendix testis Trauma Epididymo-orchitis Acute hydrocele Idiopathic scrotal oedema UTI ``` Examination ! Urine dip ! Surgery exploration NOT US - doesn't rule out testicular torsion
101
testicular torsion - when does it happen - symptoms inc late signs - how long until death of testicle - tx/diagnosis
``` Neonatal / puberty - main times Pain often so severe → vomit Tender all over 6h from onset until ischaemia/death Redness and swelling are LATE signs Surgery needed- This is the diagnosis too! ```
102
Torsion of hydatid aka appendix testis - what is that - symptoms (compared to dif diagnosis) - tx
Remnant of mullerian duct Pain less severe, more localised to upper testicle (compared to testicular torsion) Can sometimes see blue dot - as infarct through skin Surgery not necessary
103
Idiopathic scrotal oedema presentation
Red, swollen on one side
104
non retractile foreskin | - worrying?
Up until puberty, this is normal - Reassurance - may have .... Mysterious swelling - Smegma = skin secretions trapped due to non-rectralie foreskin -- also Reassurance , will get better when foreskin retracts ``` Unless BXO (balanitis xerotica obliterans) (Then worrying!): White scarred appearance of foreskin inc when retracted (unlike pink/red = healthy) Circumcision needed ```
105
hypospadias - what is this - what should you check and why - tx
Urethra opening is below where it should be (along shaft/ at base) Don't circumcised - skin used to reconstruct urethra later on Check testicles are palpable Undescended may indicate sex disorder - congenital adrenal hyperplasia - unusual hormone synthesis XX but exposed to hormones during pregnancy. Clitoromegaly rather than glans. Virilized genitalia
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when should you def not circumcise someone
hypospadias (urethra opening below where it should be) | skin used to reconstruct urethra later on
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groin swelling differential diagnosis investigations to distinguish
Inguinal hernias - Boys more- testicular descent opens up canal more - Priority to younger - more complications eg strangulation of hernia Hydroceles - Often left alone, unless large or hasn't subsided for ages - Hydroceles transilluminate (less so for pediatric -- skin and bowel thinner so bowel hernias also transilluminate) - Hernias may have cough impulse - Swelling just in scrotum = hydrocele, but swelling between testicle and superficial inguinal ring = hernias
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when capillary haemoangiomas cant be left | normal course of action
near airway / eyes (blindness) - removal if left alone (unproblematic place), they grow, then reduce on their own (not present at birth)
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when do you worry about lymphadenopathy
Mostly fine Worry if >2cm in diameter Rapidly enlarging Inflamed for more than 2 weeks then May be leukaemia
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what neck swelling moves when tongue stuck out
thyroglossal cyst
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undescended testis - how long til worry - investigations
Do nothing for first 6 months, as most sort themselves out Often palpable along line of descent - important to palpate (may indicate congenital adrenal hyperplasia- sex disorder- XX but exposed to hormones during pregnancy. Clitoromegaly rather than glans. Virilized genitalia ) Investigations Examination under anaesthetic if unable to palpate - laparoscopy
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umbilical hernias | - worry?
hardly ever strangulate | so leave alone if less than 4 -5 years old (As cause more problems for adults), and less than 2 cm
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umbilicus granuloma - looks like what - tx
fleshy growth on belly button | Treat with salt and water
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omphalitis =? | tx
Omphalitis = infected umbilicus Infection can spread centrally rapidly IV antibiotics
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anorexia screening
SCOFF S- do you make yourself Sick because you're uncomfortably full? C- do you worry that you’ve lost Control over how much you eat? O- have you recently lost more than 6 kilograms (about One stone) in three months? F- do you believe you’re Fat when others say you’re thin? F- would you say that Food dominates your life?
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anorexia clinical signs
``` Dry skin Lanugo hair Orange skin and palms Cold hands and feet Bradycardia Drop in BP on standing Oedema Week proximal muscles - squat test ```
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faltering growth definition
description (not diagnosis) of inadequate weight gain/ growth 1 + centile drop if birth weight below 9th centile 2+ centile drop if birth weight 9-91st centile 3+ centile drop if birth weight above 91st centile weight below 2nd centile (regardless of birthweight)
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newborn weight loss - what is normal - what is concerning - investigations
drop is normal up until 4th day of life, this is normally recovered by 3w Be worried if losing more than 10% of birth weight assess feeding (discussion/ observation) feeding support monitoring
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faltering growth investigations
- monitor height/length and weight regularly (Measure more often if more concerned and if younger) - Measure parents - work out mid-parental centile (2 centiles below may suggest undernutrition of growth disorder - assess feeding - If 2y+, BMI centile - Nutritional blood tests - any supplementation needed?
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faltering growth causes (in categories)
Not enough in - Ineffective suckling/ bottle feeding - Feeding aversion (problems with parental interaction, GORD (avoid pain)) - Physical disorder to disturb feeding eg tongue tied - neglect - anorexia Not absorbed - Anaemia - Billiary atresia - Cystic fibrosis - Inborn errors of metabolism - Coeliac - Infections - Cows milk allergy CMA Too much used up - Prematurity - Chronic infections / illness - -- HIV, TB - -- Asthma - -- Hyperthyroidism - -- IBD - -- Malignancy - -- Renal failure - -- Congenital heart disease Abnormal central control of growth / appetite
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gower's manoevre
for duchenne's (m)/ beckers (f, milder)). or hip girdle weakness Lie on their back. How quickly can they stand up Long time from lying to sitting then crawl themselves up legs to wide based stance due to proximal weakness Creatine kinase test next step!
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types of strabismus
Manifest = obvious deviation of one eye - Esotropia = one eye straight ahead, one eye turned inwards - Exotropia = one eye straight ahead, one eye turned outwards - Hypertropia one eye straight ahead, one eye turned upwards - Hypotropia = one eye straight ahead, one eye turned downwards Latent = when one eye close / occluded under a cover, then the eye deviates - Esophoria = one eye straight ahead, one eye turned inwards - Exophoria = one eye straight ahead, one eye turned outwards - Hyperphoria one eye straight ahead, one eye turned upwards - Hypophoria = one eye straight ahead, one eye turned downwards
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strabismus aetiology
Genetic component Refractive error - need of glasses - Long sighted - hypermetropia - Anisotropia - difference in refractive error of each eye → amblyopia (one eye seeing better than the other even with correction of refractive error) Neurological defects eg cerebral palsy
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what about... 1. sudden onset strabismus 2. strabismus in first few months
1. urgent referral - this is worrying. normally not sudden onset 2. If first few months, this may be physiological - transient newborn misalignment (reducing by 2m, stopped by 4m)
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strabismus examination (inc what refers to what strabismus)
Corneal reflection - With pen torch, looking for white dot reflection In pupil and slightly nasal but central, and symmetrical. if white dot is displaced - strabismus Cover test - Light + Get child to focus on something 33cm away and then 6m away - Eye not covered moves position when cover on other eye put on/removed - One at a time with gap between → manifest - One after the other straight away → latent Measure visual acuity -- each eye separately!! - V young- Whether they look towards stripes or not (levelled) - Picture based - either at top or bottom of card, point/ eye movements - Snellen / picture naming
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strabismus tx
Better prognosis if caught earlier ``` Glasses Prisms Eye exercises Surgery - on extraocular muscles by weakening/strengthening them Botox injected into muscles - but wears off - Would need repeating - Can be diagnostic tool ```
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what is pseudostrabismus and why might this occur
Eyes are straight, and are being used normally but appear unusual: - Broad epicanthus (nose bridge) - wide interpupillary distance - Or narrow! ^ - Facial asymmetry eg Unilateral ptosis - Deep set eyes
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Amblyopia = ?
one eye seeing better than the other even after correction of refractive error
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jump/ hop test and blowing out/sucking in tummy in abdo exam
unable to do this with guarding / peritoneal irritation
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classic age of presentation and colour of vomit: pyloric stenosis malrotation intersussception
pyloric stenosis- 4w, milky malrotation- 24h, green intersussception- 6m, milky then green
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where is intersussception mass ususally felt USS appearance cause treatment
right upper quadrant - sausage shaped mass donut usually idiopathic air enema fluid surgery sometimes