Neuro and musc Flashcards

(27 cards)

1
Q

What are the indications of a CT in children?

A

CT in an hour if one of the follow:

  • more than 3 episodes of vomiting
  • LOC for more than 5 mins
  • high impact trauma/injury
  • abnormal drowsiness
  • amnesia >5 mins
CT in an hour if one or more of the follow:
NAI
GCS less than 14 
GCS less than 15 2 hours after 
basal skull fracture 
focal neurological deficit
bruising in child under 1 and 5 cm laceration 
suspected open/depressed skull fracture
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what is the treatment for west syndrome?

A

vigabatrin and steroids

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What are the side effects of anti epileptic drugs?

A

Valporate - weight gain, hair loss, liver failure
Lamotrigine - severe skin rash (steven johns syndrome) EXACERBATES MYOCLONIC SEIZURES
Carbamazepine - rash, neutropenia, SIADH (hyponatraemia) EXACERBATES ABSENT SEIZURES
Levetericitam - sedation (rare)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Name some causes of myoclonic seizures in children

A

3-12 yr - Benign rolandic epilepsy - happen during sleep, face and upper limb seizures, hyper-salivation

12-18 yr - juvenile myoclonic epilepsy - happens after waking up

progressive myoclonic epilepsy - gets worse

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

When do you admit a febrile seizure?

A
first seizure
last longer than 15 mins 
happened more than once in 24 hours
unknown cause 
under 18 months
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

How do you differentiate between transient synovitis and septic arthritis?

A
septic 
Temp >38
ESR>40
WCC>12 
unable to weight-bare
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What are the 3 types of JIA?

A

systemic - hepatosplenomegaly, fever, malaise, salmon pink rash

polyarticular - painful swollen joints, small and large joints, can be ANA +

pauciarticular - painful swollen joints <5 joints, large joints, can be ANA +

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

How do you treat osteomyelitis and septic arthritis?

A

Fluclox IV
Pen allergic - clindamycin
MRSA - vancomycin
grame -ve - cefotaxime

surgical debridement/joint wash out

Sepctic - IV 2 weeks, oral 4 weeks
OM - IV until CPR stable for 2 days then oral

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What is osteochondritis dissecans?

A

pain after exercise, catching locking, giving way - caused by reduced blood flow = avascular necrosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What is chondromalacia patella?

A

posterior degenration of patella cartilage - pain on running, getting up, painless at first but gets painful on REPEATED USE

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What is Osgood-Schlatter?

A

inflammation of patella tendon - frequent small fracture - overuse injury = REST, NSAIDS, ICE PACKS

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

How do you manage perthes?

A

<6 monitor and manage with splints

>6 surgery

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

How do you manage JIA?

A

NSAIDS
steroids
DMARDS - methotrexate, sulfasalazine
TNF alpha inhibitors

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What is the difference between transient synovitis and reactive arthritis?

A

TS - hip joint, under 3 MUST BE RAPID ASSESSED, after URTI

RA - preceded by GI infection

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

describe the difference in presentation between extradural, subdural and such arachnoid haemorrages?

A

extradural - LUCID phase, then deteriorate quickly, usually from direct trauma affecting middle meningieal artery
subdural - gradual deterioration, caused by NAI (shaken baby syndrome)
subarachnoid - RAPID ONSET HEADACHE, rare in children, caused by aneurysm or AVM - DO NOT DUE LP

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What are the causes of intraventricular haemorrhage?

A

ECMO - in prems or congenital CMV infection

17
Q

How to babies with intraventricular haemorrhage present?

A

drowsy, apnoea, absent moro reflex, low tone, tense fontanelle

18
Q

How do you manage intraventricular haemorrhage?

A

fluid replacement
anticonvulsants
acetazolamide
Ventriculo-peritineal shunt if hydrocephalus

19
Q

What are the 2 types of hydrocephalus and their causes?

A

Communicating - obstruction after CSF exits ventricles
meningitis, SAH

Non communicating - obstruction in ventricles
- can be acquired or congenital

CONGENITAL - aqueduct stenosis, dandy walker malformation (4th ventricle enlarged), Chiari malformation
ACQUIRED - aqueduct stenosis

20
Q

What are the signs and symptoms of hydrocephalus?

A

ACUTE - vomiting, impaired consiousness

CHRONIC - failure to thrive, developmental delay, increased skull circumference, tense fontanelle

21
Q

What is the management for Tics?

A

Conservative - sleep hygiene and stress management

Exposure response prevention - deal with the feeling before tic so they can get used to it

Medication

  • anti psychotics - risperidone
  • clonidine - ticks and adhd
  • clonazepam
  • tetrabenazine - treat tics caused by huntingtons
  • botulinum
22
Q

what is the pathogenesis of duchennes?

A

x linked
deletion of dystrophin
lack of connection between cytoskeleton and ECM
influx of ca2+ breaks down calmodulin which releases free radicals = myofibre necrosis

present 1-3yrs and diagnosed at 5 yrs, life expectancy 35

23
Q

What are some signs and symptoms of duchennes?

A

waddling gait, tip toeing, decreased tone, mount stairs one at a time, runs slowly and tires easily

24
Q

How do you manage duchennes?

A

physio
CPAP due to weak intercostale muscles
steroids
heart protecting meds - carvediol

surgery if needed to strengthen achilles heal or scoliosis

25
how is myotonic dystrophy different to duchennes?
progressive loss, starting from small muscle to large whereas duchennes affects large muscles adult onset - 20-30years
26
What is the diagnostic criteria for neurofibromatosis type 1?
>6 cafe au lait spots >1 neurofibroma optic glioma/ visual impariment
27
What is tuberous sclerosis?
cutaneous signs - ash leaf patch, angiofibromata (butterfly facial distribution) neurological - infantile spasms and seizures can cause development of nodules in the brain - subependymal giant cell astrocytoma