Paediatric arthritis Flashcards

(46 cards)

1
Q

important factor on spetic arthritis

A

surgical emergency

-irreparable changes in the articular cartilage occur within HOURS of inoculation

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2
Q

top 3 organisms for septic arthitis

A

staphylococcus aureus

strep pneumonia

Haemophilus influenzae (incidence falling with immunisation)

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3
Q

presentation of septic arthiris excluding the joint 3

A

systemically unwell
-fever
-headache

-may have another focus of infection (septicasemia, pharyngitis, meningitis, cellulitis)

joints issues

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4
Q

presentation of septic arthitis regarding the joint 5

A

exquisitely painful

hot

swollen

red

held immobile (pseudoparalysis)

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5
Q

how can joint presentation differ in septic arthitis

A

joints covered by lots of muscel or subcut itssue (particulary hip) will not be red hot or swollen

those signs are more common in superfical joints

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6
Q

how can presentation in septic arthitis differ

A

presentation may be more subtle- particulary in neonates
-only physical signs may be irritability and (more importatnly) pseudoparalysis

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7
Q

fact about pesuoparalysis in a neonate 1

A

is the result of bone/joint sepsis until proven otherwise

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8
Q

differentials for septic arthritis 2

A

transient synovitis

reactive arthritis

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9
Q

how to differentiate transient synovitis and reactive arthritis from septic arthritis 4

A

pyrexia >38.5 within last week

inability to weight bear through that limb

raised ESR >40mm/h

WBC >12x10(9)/l

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10
Q

management of septic arthritis 4

A

ABC- resusitaction if unwell

urgent aspiration (usually under GA) with immediate microscopy and gram stain, subsequenent culure and sensitivity

blood cultures- minimum of 2 (not always postiive)

High dose IV ABx

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11
Q

classical presentation of osteomyelitits 3

A

acutely unwell child

pyrexia

local erythema and tenderness

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12
Q

what often procedes a subacute presentation of osteomyelitis 1

A

recent varicella zoster infection
-common
-scratching typically introduced haematogenous spread of S. aureus)

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13
Q

subacute presentation of osteomyelitis 4

A

point tenderness (often near metaphyses)

night pain

Limp

Remember- Fever may be absent

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14
Q

management of osteomyelitis

A

blood culture

bone aspiration - if absecee is present

High dose IV ABx

Splintage of the limb

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15
Q

Abx for septic arthritis 3

A

fluclos

vanc

gent if MRSA

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16
Q

ABx for osteomyelitis 3

A

fluclox

metro

gent

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17
Q

more insidious cause of septic arthritis and osteomyelitis 1

how to diagnose- 1

A

tuberculosis

quickly by PCR (cultures take over 6 weeks)

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18
Q

most common cause of joint swelling in children

A

reactive arthitis

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19
Q

overview of causes of reactive arhtitis

A

usually by an unidentified viral infection

short lived and self limiting illness
-if persists -> consider other causes

20
Q

what causes rheumatic fevere

A

streptococcal pyogenes infection

21
Q

symtpoms of rhuematic fever (overview) 4

A

carditis
arthritis
neuro features
rash

22
Q

neuroogical features in rhuematic fever

A

sydenham chorea
-rapid ivoluntary movements of the limbs, trunnk and facial muscles

23
Q

rash in rhuematic fever 1

A

erythema marginatum

24
Q

raised biochem in rheuamtic fevere 3

A

raised ESR

ASO titre
DNase B

25
managemtn of reheumatic fever 4
antibiotics: oral penicillin V anti-inflammatories: NSAIDs are first-line treatment of any complications that develop e.g. heart failure -need life long penicillin prophylaxis
26
how is rhuematic fever assocaited with joints
can cause reactive arhtitis
27
symtpoms of HLA B27 assoacited reactive syndrome
reactive arthitis urethrisi conjunctivits ± plantar fascitis
28
what else is HLA B27 associated reactive syndrome called
REiters syndrome
29
what type of infections lead to HLA B27 associated reactive syndrome
post enteric or genitourinary infection -Yersinia -SHigella -Salmonella -E coli -STDs
30
managemtn of reactive arthitis in HLA B27 associated reactive syndrome
self-limiting conditino once infection treated
31
what else is transient synovitis of the hip called
irritable hip
32
who gets transient synovitis of the hip
idiopathic disorder in children ,3-10yo -often preceded by infection
33
presentation of transient synovitis of the hip 3
sudden or gradual onset of hip pain+ limp hip is held flexed and externally roated -pain can refer to knee
34
biochem in transient synovitis of the hip
ESR and WCC are normal or mildly raised
35
managment of transient synovitis of the hip 2
conservative -analgesi and allow child to rest until happy to weight bear -condition should resolve after one week -> if symptoms prolonged or recurrent-> may need to revist diagnosis
36
overview of discitis
unclear if infective aetiiologu of the spine -usually self limiting and not associated w culture or organisms peak onset 1-3 years -child refuse to walk ± low grade fever diangosis can be confusion -should have well localised tendernes of spine -radiographs normal until alte indisase -MRI helpful -if in doubt-> ABx
37
overview of juvenile idiopathic arthritis
childhood onset of chornic inflammatory arhtitis of unknown aeitology -no single diagnostic test and investigation aims to exclude other diagnoses
38
esentatino of juvenile idiopathic arthritis
PERSISTENT joint swelling in one or more joints inflammatory featurtes of early morning stiffness and warmth clinical diagnosis w no diagnostic tests
39
what occurs in 1/3 of juvenile idopathic arthirits
chornic anterior uveitis -leading cause of child blindness
40
managemnt of chronic anterior uveitis 2
early referral for regular eye screening by slit lapm -screening by ophthalmologist -key to early diagnosis and preservation of vision
41
types of connective tissue disease in children 4
systemic lupus erythematous (SLE) dermatomyositis scleroderma (particulary localised) Vasculitis
42
two vascultic conditions more common in children than adults
Henoch Schonlein Purpura Kawasaki disae
43
why is henoch schonlein purura important in children 1
because of the assocated renal disease
44
why is kawasaki disease important
associagted mortality assocaited w coronary artery aneurysms -preventable with early diagnosis and treatment with IVIG
45
key early features of kawasaki disease 10
high and persistent evere (>39.5) for 5 days rash red palms, soles and perineum Miserable ( v important sign reflecting aspectic menigeal irritatoin) mucositis non-purluent conjunctivits arthtis high platelet count lymphadenopthy high acute phase response
46
late features of kawasaki disease 5
aneurysms peeling skin cardiac ischaemia myocardial infarctoin claudication- where other aneuryms have occured