Neurology - Level 1 Flashcards

1
Q

Definition of stroke?

A

o Syndrome of rapid onset of cerebral deficit lasting >24 hours with no apparent cause except vascular
o Complete – deficit becomes maximal <6 hours
o Stroke in evolution – progression during first 24 hours

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2
Q

Definition of ischaemic stroke?

A

 Due to ischaemia and death of tissue following vascular occlusion or stenosis

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3
Q

Definition of haemorrhagic stroke?

A

 Due to collection of blood from rupture of blood vessel within the brain (intercerebral) or between brain and arachnoid tissues (subarachnoid)

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4
Q

Definition of TIA?

A

o Sudden focal deficit lasting <24 hours with complete recovery and no evidence of acute infarction

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5
Q

Epidemiology of stroke?

A
2nd commonest cause of death worldwide
7% of deaths in UK
Rates higher in Asians and Africans
Incidence 1 in 1000
Men > Women
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6
Q

Risk factors of stroke?

A
  • Hypertension, AF, Valve disease
  • DM, PCV, Syphilis
  • Smoking, Obesity, Alcohol, High cholesterol, clotting factors, OCP
  • Hx of TIA
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7
Q

Aetiology of stroke?

A
  • Ischaemic (85%) – embolism/thrombosis/artherosclerosis
  • Haemorrhagic (15%) – intracranial, SAH
  • Rare – Venous thrombosis, sudden BP drop, lesion, carotid artery dissection
  • TIA – microembolism from atherosclerotic plaques or mural thrombi
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8
Q

Symptoms of TIA - carotid artery symptoms?

A
  • Sudden onset of focal deficit usually lasting 5-15 minutes

o Hemiparesis – unilateral weakness to one side of body
o Hemiplagia – flaccid and then spastic
o Aphasia – speech problems
o Ataxia, vertigo, syncope
o Amaurosis Fugax – sudden transient loss of vision in one eye
o Hemianopia

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9
Q

Symptoms of TIA - vertebrobasilar symptoms?

A
o	Diplopia
o	Vertigo
o	Vomiting
o	Choking and dysarthria
o	Ataxia
o	Hemisensory loss
o	Visual loss
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10
Q

Symptoms of stroke - cerebral infarction?

A
  • Sudden onset focal deficit ongoing or persisted for >24 hours and cannot be explained by another condition

o Symptoms of TIA, Sensory loss, hemiplegia (flaccid and then spastic), dysphagia, hemianopia

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11
Q

Symptoms of stroke - brainstem infarction?

A

o Lateral medullary syndrome – vertigo, Horner’s, facial numbness, ataxia, nystagmus
o Locked in syndrome

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12
Q

Symptoms of stroke - lacunar haemorrhage?

A

o Pure motor, sensory, ataxic hemiparesis, cognition intact

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13
Q

Symptoms of stroke - cerebral haemorrhage?

A

Sudden LOC, severe headache and meningism

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14
Q

Oxford Bamford Stroke Classification - Total Anterior Circulation Stroke (TACS)?

A

o Large stroke – both the middle and anterior cerebral arteries

o All 3 of following:

 Unilateral weakness (and/or sensory deficit) of face, arm and leg
 Homonymous hemianopia
 Higher cerebral dysfunction (dysphasia, visuospatial disorder)

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15
Q

Oxford Bamford Stroke Classification - Partial Anterior Circulation Stroke (PACS)?`

A

o Less severe than TACS, part of anterior circulation compromised

o 2 of the following:

 Unilateral weakness (and/or sensory deficit) of face, arm and leg
 Homonymous hemianopia
 Higher cerebral dysfunction (dysphasia, visuospatial disorder)

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16
Q

Oxford Bamford Stroke Classification - Posterior Circulation Stroke (POCS)?

A

o Damage to area supplied by posterior circulation (cerebellum and brainstem)

o 1 of the following:

 Cranial nerve palsy and contralateral motor/sensory deficit
 Bilateral motor/sensory deficit
 Conjugate eye movement disorder (horizontal gaze palsy)
 Cerebellar dysfunction (vertigo, nystagmus, ataxia)
 Isolated homonymous hemianopia

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17
Q

Oxford Bamford Stroke Classification - Lacunar Syndrome (LACS)?

A

o Subcortical stroke secondary to small vessel disease (no loss of higher cerebral function)

o	1 of the following:
	Pure sensory stroke
	Pure motor stroke
	Sensori-motor stroke
	Ataxic hemiparesis
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18
Q

Initial Assessment in A&E of stroke?

A
FAST tool/Rossier Tool --- Stroke unlikely if score 0 or less
	Facial Weakness (asymmetrical) (1)
	Arm Weakness (asymmetrical) (1)
	Leg weakness (asymmetrical) (1)
	Speech disturbance (1)
	Visual field defect (1)
	Loss of consciousness or syncope (-1)
	Seizure (-1)
ABCDE assessment – protect airway
Vital signs – BP, pulse, O2 sats, HR, temp
Blood glucose
ECG
Neurological assessment (fundoscopy)
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19
Q

Management of TIA - initial assessment?

A
-	ABCD2 (not used anymore)
o	Age >60
o	BP >140/90
o	Clinical weakness (2)/speech problem (1)
o	Duration >1hr (2)/<1hr (1)
o	Diabetes (1)
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20
Q

Management of TIA - initial management?

A

o Aspirin 300mg immediately (with PPI)

o Refer for urgent (within 24 hours of symptoms) assessment with specialist

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21
Q

Management of TIA - brain imaging?

A

CT
 Do not offer CT scan unless suspicion of alternative diagnosis that CT could detect

MRI
 After specialist assessment in TIA clinic, consider to determine territory of ischaemia or haemorrhage – perform on same day

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22
Q

Management of TIA - further management?

A

Carotid imaging and carotid endarterectomy
 Extent measured using NASCET or ECST
 Surgery when symptomatic & NASCET >50% or ECST >70% stenosed
 Stenting alternative if patient unable to have endarterectomy

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23
Q

Management of TIA - secondary prevention?

A

 Clopidogrel 75mg daily
 Dipyridamole MR + aspirin
• Dipyridamole MR alone if aspirin contraindicated/not tolerated

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24
Q

Management of stroke - initial assessment?

A
o	FAST tool/Rossier Tool
	Stroke unlikely if score 0 or less
•	Facial Weakness (asymmetrical) (1)
•	Arm Weakness (asymmetrical) (1)
•	Leg weakness (asymmetrical) (1)
•	Speech disturbance (1)
•	Visual field defect (1)
•	Loss of consciousness or syncope (-1)
•	Seizure (-1)
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25
Management of stroke - initial management?
o ABCDE assessment – protect airway o Vital signs – BP, pulse, O2 sats, HR, temp o Oxygen (only if O2 <95%)
26
Management of stroke - initial investigations?
o Blood glucose ---- Maintain at 4-11mmol/l with IV glucose and insulin in T1DM o ECG o Neurological assessment (fundoscopy) o NBM if choking risk – NG tube within 24 hours, gastrostomy if needed o Blood tests ---- ESR, FBC, glucose, U&Es
27
Management of stroke - imaging?
CT scan
28
Management of stroke - when to perform CT within 1 hour?
If indications for thrombolysis (<4.5 hours) On anticoagulant or Bleeding tendency GCS<13 Progressing or fluctuating symptoms Papilledema, Neck stiffness, Severe headache
29
Management of stroke - when to perform CT within 24 hours?
 If no indications for immediate brain scanning
30
Management of stroke - further imaging?
o If thrombectomy indicated – CT contrast angiography & add on CT perfusion imaging (or MR equivalent) if indicated beyond 6 hours of symptom onset
31
Management of stroke - management of confirmed ischaemic stroke?
o Aspirin 300mg (orally or rectal/enteral if dysphagia) once haemorrhagic excluded  Add PPI if previous dyspepsia  Continue aspirin 300mg daily until 2 weeks after stroke  Then start definitive long-term antithrombotic treatment
32
Management of ischaemic stroke - thrombolysis - when is it indicated and how? Post-thrombolysis management?
 <4.5 hours onset and haemorrhage been excluded on CT  IV recombinant tissue plasminogen activator (alteplase 0.9mg/kg over 1h)  CT 24-hour post lysis to identify bleeds
33
Management of ischaemic stroke - thrombectomy - when is it done and why?
ASAP and within 6 hours of symptoms, with IV thrombolysis if: • Acute ischaemia stroke and confirmed occlusion of proximal anterior circulation on CTA or MRA ASAP in people who were well 6-24 hours previously • Acute ischaemia stroke and confirmed occlusion of proximal anterior circulation on CTA or MRA • AND salvagable on CT/MRI with limited core infarct Pre Stroke mRS <3 and NIHSS >5
34
Management of ischaemic stroke - cerebral sinus thrombosis?
• Full-dose LMWH and then warfarin (INR2-3)
35
Management of ischaemic stroke - ischaemic stroke with AF?
Aspirin 300mg for first 2 weeks before anticoagulation treatment
36
Management of ischaemic stroke - haemorrhagic stroke with DVT/PE?
• Treat with anticoagulation or caval filter to prevent further pulmonary emboli
37
Management of haemorrhagic stroke - initial management?
Refer to neurosurgery Managing hydrocephalus  Previously fit people – consider surgical intervention
38
Management of haemorrhagic stroke - medical treatment initially - when?
 Small deep haemorrhages  Lobar haemorrhage without either hydrocephalus or rapid neurological deterioration  Large haemorrhage and significant comorbidities  GCS <8, unless due to hydrocephalus  Posterior fossa haemorrrhage
39
Management of haemorrhagic stroke - reversing anticoagulation?
 If receiving warfarin (and have elevated INR) – use IV vitamin K and prothrombin complex concentrate
40
Management of haemorrhagic stroke - blood pressure control?
 Offer to all, without exclusions, if present within 6 hours of symptoms and systolic blood pressure between 150-220: • Aim for 130-140 within 1 hour of starting treatment and maintain for at least 7 days • Use IV labetalol 5mg bolus for rapid control, GTN infusion used for long-term hospital control until titrated onto oral medications
41
Management of haemorrhagic stroke - When not to offer BP control?
* Structural cause (tumour, arteriovenous malformation, aneurysm) * GCS<6 * Having early neurosurgery to evacuate haematoma * Massive haematoma with poor prognosis
42
Management of stroke in specialist stroke unit?
Admit everyone with stroke directly to specialist acute stroke unit after initial assessment Swallow Function (specialist assessment within 24 hours and not >72 hours)  NG tube and fed within 24 hours unless had thrombolysis  Nasal bridle tube or gastrostomy if unable to tolerate NG tube  Refer to dietician  Amend oral medications Early Mobilisation  Help patients sit out of bed, walk as soon as able Statin Treatment  Do not start in acute stroke but continue if already on statin
43
When to perform decompressive hemicranectomy in stroke?
 If middle cerebral infarction within 48 hours who: • >15 on NIHSS • Decreased level of consciousness, score of 1 or more on item 1a of NIHSS • Signs on CT of infarct in >50% MCA territory
44
When to image carotid arteries in stroke?
 Carotid imaging and carotid endarterectomy • Extent measured using NASCET or ECST • Surgery when symptomatic & NASCET >50% or ECST >70% stenosed • Stenting alternative if patient unable to have endarterectomy
45
Rehabilitation teams involved in stroke?
o Inpatient stroke rehabilitation service o Offer training in care for family members, carers o May need SALT, OT, orthoptics, physiotherapy, fitness training
46
AF stroke prevention following acute stroke?
• Aspirin 300mg for 2 weeks, then restart anticoagulation (warfarin/DOAC) and stop aspirin
47
Secondary prevention of ischaemic stroke or TIA?
Control risk factors – HTN, DM, HF, BP (<130/80) Atorvastatin 80mg daily (started 48h after ischaemic stroke) Clopidogrel 75mg daily (dipyridamole 200mg + aspirin 75mg if clopidogrel contraindicated or not tolerated)
48
Follow up after acute stroke?
o Follow up at specialist clinic in 6 weeks | o 6-month primary care and then annually with specialist
49
General advice given to stoke patients?
``` o No LMWH for 2 months o Inform DVLA – no driving for 1 month o Assessment to return to work and may need support o Encourage physical activity o Stop smoking o Keep low salt intake o Reduce alcohol o Physio/OT assessments ```
50
Complications of stroke?
- Cerebral oedema - Seizures - VTE - Mobility problems – falls, ataxia, hemiparesis - Sensory/Communication problems - Visual/Cognitive impairment - Continence problems - Pain
51
Definition of meningitis?
- Inflammation of the meninges
52
Pathogenesis of meningitis?
o Micro-organisms reach meninges by direct extension from ears, nasopharynx, head injury or blood o Invasion of the blood stream o Attachment to and invasion of the meninges o Induction of inflammation with leak of proteinscerebral oedema (hydrocephalus) o Alteration in cerebral blood flow and metabolism o Cerebral vasculitis
53
Acute bacterial of meningitis pathology?
o Pia-arachnoid gather polymorphs and layers of pus o May form adhesions and cause cranial nerve palsies o Chronic – brain covered in tubercles
54
Pathology of viral meningitis?
o Lymphocytic inflammation without pus | o Little cerebral oedema
55
Epidemiology of viral meningitis?
- Viral Meningitis is most common o Enteroviruses = more common in autumn and winter o 95% have complete recovery with no neurological complications
56
Epidemiology of bacterial meningitis?
o 80% of cases of bacterial meningitis occur in <16yr olds in UK o 5-10% mortality o Meningococcus:  causes majority of bacterial infections in >2m.  This has ↓ since intro of MenB/MenC vaccine
57
Risk Factors of meningitis?
o Impaired Immunity  Young age, complement defects, splenic defects from sickle-cell disease or asplenia (Strep pneumonia and Hib susceptibility) o Factors associated with low socio-economic status
58
Causative organisms of viral meningitis?
 Enteroviruses (80%)  EBV, CMV, VZV, HSV  Adenovirus  Mumps (pre-MMR)
59
Causative organisms of bacterial meningitis?
```  Neisseria meningitidis  S. pneumoniae  S. aureus  Streptococcus Group B  TB ```
60
Causative organisms of fungal meningitis?
 Cryptococcus neoformans |  Candida Albicans
61
Symptoms of meningitis?
o Fever o Headache, neck stiffness, photophobia - meningism o Altered Consciousness, seizures o Nausea & Vomiting, anorexia o Rash – petechial non-blanching rash in meningococcal septicaemia o Focal cranial nerve signs common in tuberculous or cryptococcal meningitis
62
Signs of meningitis?
Neck Stiffness – meningeal irritation prevents neck flexion  Not always present in infants Brudzinski’s Sign  Flexion of the neck with the child supine causes flexion of the knees and hips Kernig’s Sign  In supine position, when knee and hip are flexed, extension of knee leads to pain Rash – Purpuric or petechial:  Usually non-blanching (but may initially be blanching)  Characteristic of meningococcal infection
63
Signs of raised ICP?
Papilledema (rare) ↓ level of consciousness Focal neurology • VI nerve palsy • Cushing reflex (High BP, Low HR, Cheyne-Stokes breathing (irregular and apnoeas))
64
Investigations of meningitis?
- Bloods – FBC, LFTs, U&E, glucose, coagulation screen, CRP - Blood cultures, throat swabs, rectal swabs, serology - Head CT scan if suspicion of raised ICP - Lumbar puncture usually done after CT unless GCS 15 and no raised ICP o Send CSF for M, C&S
65
Management of meningitis - if meningococcal disease?
o Admit to hospital with 999 o If in community/GP then give IM/IV 1.2g Benzylpenicillin (single dose) before admission  Children 1-9 – 600mg  Children <1 – 300mg
66
Management of meningitis - if no non-blanching rash?
o Admit to hospital with 999 | o Do not give antibiotics unless urgent transfer not possible
67
Management of meningitis - initial management and investigations?
 15L/min O2 if needed  IV fluids, pressure area care and monitor conscious level  In child <16 years • Bloods (FBC, CRP, coagulation, glucose, VBG, PCR for N.meningitides) • Blood culture  Adults • FBC, U&E, coagulation • CXR • Urine culture, nasopharyngeal swabs, stool virology
68
Management of meningitis - imaging?
 If reduced consciousness (GCS<9 or drop of 3 or more) or focal neurological signs, perform CT scan
69
Management of meningitis - lumbar puncture?
 Contraindicated if: • Signs of raised ICP (reduced consciousness, bad headache, papilloedema) • Focal neurology • Severse shock • Sepsis  WBC count, examination, Gram stain, total protein and glucose concentations, culture and PCR
70
Management of meningitis - if septic signs predominate?
```  Do not LP  Antibiotics Adults and child 3 months -50 years o IV Cefotaxime (2g, OD) for 10 days o Add vancomycin if prolonged or multiple use of other antibacterials in last 3 months/travelled outside UK with highly resistant pneumococci ``` Adults over 50 o IV cefotaxime + amoxicillin for 10 days o If over 55 or immunocompromised, add ampicillin Neonates and child <3 months o IV Amoxicillin + Cefotaxime for 14 days  Critical care team input  If shocked, ICU for fluids, intubation, inotropes
71
What antibiotics to give in meningitis - if 3 months - 50 years?
o IV Cefotaxime (2g, OD) for 10 days o Add vancomycin if prolonged or multiple use of other antibacterials in last 3 months/travelled outside UK with highly resistant pneumococci
72
What antibiotics to give in meningitis - over 50?
o IV cefotaxime/ceftriaxone + amoxicillin/ampicillin for 10 days
73
What antibiotics to give in meningitis - neonate and <3 months?
o IV Amoxicillin + Cefotaxime for 14 days
74
Management of meningitis - if meningitic signs predominate?
Assess ICP signs • If raised ICP – ICU and no LP • If no raised ICP – do LP Antibiotics • Adults and child 3 months -50 years - IV Cefotaxime (2g, OD) for 10 days - Add vancomycin if prolonged or multiple use of other antibacterials in last 3 months/travelled outside UK with highly resistant pneumococci • Adults over 50 - IV cefotaxime + amoxicillin for 10 days - If over 55 or immunocompromised, add ampicillin • Neonates and child <3 months - IV Amoxicillin + Cefotaxime for 14 days Dexamethasone 0.15mg/kg, up to 10mg QDS if LP reveals: • Purulent CSF, WBC >1000, protein >1g/l, bacteria on Gram stain • Give within 4 hours of antibiotics but not after 12 hours
75
Management of meningitis - subsequent management?
o Discuss antibiotic therapy with microbiology o IV fluids if needed o Isolate for 1st 24 hours
76
Management of meningitis -antibiotics depending on cause?
o Meningococci – Benzylpenicillin or cefotaxime for 7 days o Pneumococci – Cefotaxime +/- dexamethasone for 14 days o H.influenzae – Cefotaxime +/- dexamethasone for 10 days o Listeria – Amoxicillin + gentamicin for 21 days (stop gentamicin after 7 days)
77
Management of meningitis -prophylaxis?
o Rifampicin or ciprofloxacin to all household contacts
78
Management of meningitis - discharge advice?
o Notify relevant Health Authorities o Hospital Follow Up with paediatrician 4-6 weeks after discharge o Audiological Assessment in children within 4 weeks of being fit to test, preferably before discharge
79
Complications of meningitis?
- During Illness: o Convulsions, cerebral oedema, circulatory shock, DIC - Neurological o Hearing loss (10%), visual impairment, cerebral palsy, vasculitis o Hydrocephalus, cerebral abscess
80
Complications of meningitis?
- During Illness: o Convulsions, cerebral oedema, circulatory shock, DIC - Neurological o Hearing loss (10%), visual impairment, cerebral palsy, vasculitis o Hydrocephalus, cerebral abscess
81
Pathology of subarachnoid haemorrhage?
Rupture of blood vessel into subarachnoid space o Berry aneurysm at junction of posterior communicating with internal carotid or anterior communicating with anterior cerebral or bifurcation of middle cerebral o Associated with polycystic kidneys, coarctation, Ehlers-Danlos syndrome
82
Epidemiology of subarachnoid haemorrhage?
- Accounts for 5% of strokes | - Typical age between 30-60
83
Risk factors of subarachnoid haemorrhage?
``` o Smoking o Alcohol o Family history o Post-menopause o Increased BP o Bleeding disorder ```
84
Aetiology of subarachnoid haemorrhage?
o Rupture of Berry aneurysm in circle of Willis (mostly) o Arteriovenous malformations o Tumours o Connective tissue disorders
85
Symptoms of subarachnoid haemorrhage?
o Sudden onset, severe headache – often occipital o “Worst pain ever”, “kicked in back of head” o Nausea and vomiting o Neck pain o Photophobia o Collapse and coma o May be preceded by sentinel headache
86
Signs of subarachnoid haemorrhage?
o Meningism o Retinal, vitreous bleeds o Focal neurology may indicate site
87
Investigations of subarachnoid haemorrhage?
Assess airway and breathing, if unconscious open airway and contact ICU - May need RSI, tracheal intubation and ventilation IV access – check BMG, FBC, clotting, U&Es Emergency CT scan (<12 hours) - 90% detected ``` Lumbar puncture (if CT negative, no CI and >12 hours) o Blood early on and yellow after hours – bilirubin from Hb – xanthochromia ``` CT angiogram – localise source of bleed
88
Severity assessment of subarachnoid haemorrhage?
- Hunt and Hess Scale | o Grade 1-5 to assess severity
89
Management of subarachnoid haemorrhage - initial management?
o O2 if saturations low o IV fluids resuscitation o Analgesia (codeine PO or morphine IV) and antiemetic o If GCS <8, agitated – may need tracheal intubation
90
Management of subarachnoid haemorrhage - further management - general measures?
o Refer to neurosurgery  Bed rest  Control BP (<140mmHg)
91
Management of subarachnoid haemorrhage - further management - neurosurgery?
 Endovascular coiling (after CT angiography) |  Stenting/Clipping
92
Management of subarachnoid haemorrhage - further management - medical management?
 Nimodipine (60mg PO every 4 hours) – reduces vasospasm |  Mannitol IV (if raised ICP)
93
Complications of subarachnoid haemorrhage?
o Rebleeding – 20% in 1st few days o Cerebral ischaemia o Hydrocephalus o Hyponatraemia
94
Describe normal gait cycle?
Stance phase - limb with foot on ground, heel strike-toe off, hip abductors contract to prevent pelvis dropping on contralateral side Swing phase - foot off ground, toe-off, foot plantar flexes to push foot off ground, knee and hip flex and foot dorsiflexes after toe off so to not drag
95
Description of hemiplegic gait?
Asymmetrical gait, one limb normal while other stiff (spastic) Affected limb held in extension, toes may drag on floor Affected leg swings around (circumducts) during swing phase
96
Clinical features of hemiplegic gait?
``` Increased tone with clasp-knife Hyperreflexia Upgoing plantars (positive Babinski) Reduced power Sensory deficit ```
97
DDx of hemiplegic gait?
Unilateral upper motor neuron lesion CONTRALATERAL SIDE TO AFFECTED LIMB - Ischaemic stroke, brain tumour, trauma, MS, space-occupying lesion HEMISECTION OF SPINAL CORD (BROWN-SEQUARD SYNDROME) OF IPSILATERAL SIDE - prolapsed disc, spinal spondylosis, spinal tumour, spinal infarct
98
Description of diplegic (scissoring) gait?
Similar to hemiplegic but bilateral Limbs stiff and held in extension, feet inverted, hips drawn together Circuduction of both legs during swing phase
99
Clinical findings of diplegic (scissoring) gait?
``` Increased tone with clasp-knife Hyperreflexia Upgoing plantars (positive Babinski) Reduced power Sensory deficit ```
100
DDx of diplegic gait?
Spinal cord lesion - prolasped disc, spinal spondylosis/tumour/infarct, transverse myelitis, syringomelia Bilateral brain lesion - cerebral palsy, MS, bilateral brain infarcts, paraspinal meningioma MND
101
Description of Parkinsonian (festinant) gait?
- Short-stepping, shuffling gait - Minimal arm swing - Hesitancy when asked to start, turn around and stop - Stooped posture - Hypomimia (expressionless) - Hypokinetic gait
102
Clinical features of Parkinsonian (festinant) gait?
Tremor (pin-rolling) Rigidity (cog-wheel) Bradykinesia
103
DDx of Parkinsonian (festinant) gait?
Parkinson's Disease Parkinsonian disorders - Vascular Parkinson's disorder - Dementia with Lewy Body - Parkinson's plus syndrome (multisystem atophy with cerebellar signs, progressive supranuclear palsy with vertical gaze palsy) - drug induced (antipsychotics, domperidone)
104
Description of ataxic gait?
``` Broad-based Unsteady Foot stamping Veer towards side of lesion Heel-toe may elicit ataxia ```
105
Clinical features of ataxic gait?
Cerebellar - nystagmus, dysarthria, past-pointing, dysdiadokinesia, intension tremor Sensory - impaired proprioception and vibration, positive Romberg's sign Vestibular - vertigo, nausea and vomiting
106
DDX of ataxic gait?
Unilateral cerebellar disease - Ischaemia (PCA infarct), haemorrhagic stroke, space occupying lesion Bilateral cerebellar disease - MS, alcoholism, B12 deficiency, Drugs (phenytoin, carbamazepine, lithium, barbituates), Frederich's ataxia, Spinocerebellar ataxia, Ataxic telangiectasia, Multisystem atrophy
107
Description of high-stepping gait (neuropathic)?
Caused by motor weakness of nerves supplying ankle dorsiflexor muscles (tibialis anterior) Foot drop - weakness of dorsiflexion, so foot drops and toes drag To prevent toes from dragging, knee and hips flex creating high stepping gait Foot stamps on floor
108
Clinical features of high-stepping gait (neuropathic)?
Ankle-foot orthoses - aid to keep ankle fixed in dorsiflexion Unilateral foot drop with sensory impairment - common peroneal nerve disease Bilateral distal muscle weakness with foot drop - MND, peripheral neuropathies Reflexes - reduced in peripheral neuropathies, brisk with ungoing plantars and fasciculations in MND
109
DDx of high-stepping gait?
Weakness of tibialis anterior supplied by common peroneal nerve (L4-S1) Due to - Isolated palsy due to trauma or compression around fibula head - MND - L5 radiculopathy - Polyneuropathy (diabetic neuropathy, Charcot Marie Tooth, vasculitis, GBS)
110
Description of sensory gait (stomping)?
Caused by peripheral sensory nerve impairment Cannot sense where foot is so slams foot on ground
111
Clinical features of sensory gait (stomping)?
Romberg's positive Stomping exacerbated by dark Impaired sensation of feet
112
DDx of sensory gait (stomping)?
``` B12 deficiency Tabes Dorsalis (syphilis) Diabetes Vasculitis Charcot-Marie Tooth GBS ```
113
Description of myopathic gait? (Waddling or Trendelenburg)
Hip abductors weak so cannot contract and stabilise pelvis during stance phase Pelvis tilts down on contralateral side Conpensation - lateral flexing of torso away from leg
114
Clincial features of myopathic gait? (Waddling or Trendelenburg)
Trendelenberg's sign positive | Signs of proximal myopathy
115
DDx of myopathic gait? (Waddling or Trendelenburg)
``` Hyperthyroidism Hypothyroidism Cushing's syndrome Acromegaly PMR Polymyositis Dermatomyositis Duchenne's muscular dystrophy Becker's muscular dystrophy Myotonic dystrophy ```
116
Description of choreiform (hyperkinetic) gait?
Normal gait with involuntary movements through body (grimacing, lip smacking, writhing, dance-like)
117
DDx of choreiform (hyperkinetic) gait?
Huntington's disease Cerebral palsy Wilson's disease Dopaminergic medications
118
Description of antalgic (painful) gait?
Gait painful, shortened length of time in stance phase on affected leg
119
DDx of antalgic (painful) gait?
Osteoarthritis Inflammatory joint disease Lower limb fracture Nerve entrapment
120
LP findings in bacterial meningitis?
``` Opening Pressure - elevated WBC Count - >1000 WBC - polymorphs (neutrophils) Protein - Increased CSF-to-serum glucose - Decreased ```
121
LP findings in viral meningitis?
``` Opening Pressure - Normal WBC Count - <100 WBC - Lymphocytes Protein - Normal CSF-to-serum glucose - normal ```
122
LP findings in fungal meningitis?
``` Opening Pressure - Normal/Elevated WBC Count - Normal/Elevated WBC - Lymphocytes Protein - Elevated CSF-to-serum glucose - Low ```
123
LP findings in TB meningitis?
``` Opening Pressure - Normal/Elevated WBC Count - Normal/Elevated WBC - Lymphocytes Protein - Elevated CSF-to-serum glucose - Low ```