Management Flashcards

1
Q

Management of asymptomatic PAD

A

My management would include non-pharmaceutical and pharmaceutical management targeting modifiable risk factor reduction.
Risk factor reduction- smoking, DM, start Clopidogrel, start a statin
investigation of other vascular beds= AAA once off

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2
Q

Management of intermittent claudication

A

My management for this patient would be both non-pharmacological and pharmacological with emphasis on modifiable risk factor reduction and intervention tailored to lifestyle limitations.
all patients: Reduction of risk factors: smoking, DM, start an antiplatelet, statin,
check the vascular beds: AAA
Patients IC greater than 100: rehabilitation program- supervised exercise
and education about foot care
Patients life style impact: imaging of duplex US and angiography
consider surgical intervention: taking into account patient preference, risk benefit (angioplasty and bypasses limited lifespan about a year). only 10% develop CLI.

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3
Q

Management of critical limb ischemia

A

My management of this patient would involve non-pharmacological and pharmacological treatment with emphasis on risk factor reduction and revascularisation.
RF: smoking, diabetic control, start a statin, checking the other vascular beds: AAA
imaging: arterial tree using CT angiogram and duplex scan if revascularisation is appropriate. (for use in elderly with severe comorbities- primary amputation no imaging needed)

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4
Q

Discuss your revascularisation options in this patient with chronic limb ischemia?

A

The three main options are angioplasty, endarterectomy, and arterial bypass.
Angioplasty- is the procedure where a wire is inserted peripherally from the femoral artery to the site of the lesion (illiac and superficial femoral artery lesions) Then the balloon (using the wire guidance) is inflated at the site of the lesion. Stenting can be considered in illiac but not SFA.
Tight blockages of the common femoral- endarectomy while long occlusions and multi-level stenosis can be treated by bypass.

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5
Q

So as you mentioned the pulse is irregularly irregular. What is the management of atrial fibrillation?

A

My management of atrial fibrillation can be divided into general treatment which includes investigation of underlying precipitants and management of those, specific treatment which can be subdivided into rate and rhythm control and ongoing management.
My first consideration would be red flags: HF, hypotension, a decreasing GCS, and chest pain. This would indicate that the patient is heamodynamically unstable.- senior help. RESUS ATLS guidelines. shock.
conservative: treatment of the underlying cause. Investigations: ECG,
FBC (WBC), UE, TFT, alcohol, Mg, Ca, plus or minus D dimer (PE), troponin *chest pain and suggestive ECG. CXR, ECHO and CTCA (if CAD)
Rate and rhythm control

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6
Q

So the patient with A fib is heamodynamically unstable as you before mentioned… out line your steps of management.

A
  1. ATLS guidelines- Airway high flow non-rebreather mask.
    Breathing (lowering GCS less than 8 calling for anaesthetic review)
    Circulation: wide bore 13G needle IV access.
    First shock, then DC cardioversion, then IV amiodarone
    Important to keep in mind that chronic A fib is unlikely to cause shock, so be vigilant in looking for an alternative cause of shock like sepsis.
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7
Q

So the patient is heamodynamically stable you mentioned the options of rate or rhythm control which do you want and why?

A

if the rate is less than 110 bpm
Beta blockers or non-dihydropyridine calcium channel blockers
heart failure use digoxin as well

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8
Q

So the patient is young and has new onset A Fibrilliation what is your management?

A

rhythm control (not a great choice in elderly, established AF, LA dilatation, and mitral valve disease.
This can be chemical or electrical cardioversion
chemical (flecainide if no structural heart disease or amiodarone- if structure heart disease)
second line is AV ablation

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9
Q

Should this patient be put on anticoagulation?

A

almost all patient’s with A fib need lifelong anticoagulation including 4 weeks prior to DC cardioversion (unless negative TOE)
and 4 weeks afterwards (atrial stunning). To determine the risk /benefit of starting anticoagulation the HASBLED score (risk) and CHA2DS2VASc score. Warfarin, NOACS (apixaban, dabigatran, edoxaban, and rivero alban) or dalteparin

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10
Q

Outline your management for supraventricular tachycardia?

A

My management would include acute and chronic treatement using both non-pharmacological and pharmacological approaches. Noting any red flag signs of heart failure, hypotension, decreased GCS, and chest pain, which would need immediate emergency management.

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11
Q

What is your acute treatment for SVT

A

Presence of red flags: ATLS protocol- ABCs calling for senior help

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12
Q

Management of rheumatoid arthritis

A

Management of this patient can be divided into pharmacological and non-pharmacological with the latter involving a multidisciplinary team.
Pharmacological: induce remission and symptom control
non-pharmacological: physiotherapy, OT, podiatry, psychological interventions, rheumatology, and integration with primary care.
Surgery= refractory to medical treatment, stress fracture, worsening function, imminent actual tendon rupture.

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13
Q

You mentioned pharmacological treatment for RA can you elaborate?

A

induce remission:
Disease modifying anti-rheumatic drugs
Methotrexate, Leflunomide, and sulfasalazine
bridging therapy with glucocorticoids (DMARDS takes three months)
failure of two DMARDS (MTX)- biological therapy- TNF inhibitors Etanercept or inflixamab (do chest X-ray before and also interferon test)
symptom control= NSAIDS with PPI

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14
Q

Management of Psoriasis

A

Management of this patient can be divided into pharmacological and non-pharmacological approaches.
non-pharmacological: removal/ avoidance of trigger infection (strep), trauma, drugs (lithium, Beta blockers, anti-microbial, NSAIDS, stress
pharmacological:
topical
systemic
phototherapy

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15
Q

What are the topical treatments for psoriasis?

A
emollients- relieve dryness, fissures, irritation E45 
vitamin D analogues= calcipotriol 
topical steriods- not for face
tar-steriod- descale 
calcineurin inhibitors- tacrolimus
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16
Q

When would you give systemic therapy in psoriasis?

A
large surface area 
pustular psoriasis 
erythrodermic psoriasis 
psoriatic arthropathy
failure of topical agents  
first line is methotrexate 
if rapid response required ciclosporin
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17
Q

What is the management of Giant cell arthritis

A

Management of this patient would involve urgent systemic steroid treatment to preserve vision and induction of remission of the condition.
urgent management:
prednisolone PO bone protection and PPI
gradual dose reduction once sx resolved
treat relapses similarly
long term management *if relapsing disease
methotrexate and toculizumab anti- IL6

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18
Q

Management of gout

A

Management of this patient can be divided into pharmacological and non-pharmacological, with the avoidance of triggers being of particular importance.
Pharmacological can be subdivided into acute and chronic:
acute: symptom relief- NSAIDS indomethacin plus PPI
colchicine (poor compliance due to GI side-effects)
corticosteroids (last resort)
chronic: (2nd time) bridging therapy with NSAID or colchicine (3 months) and do a 24 hour urine uric acid test
little uric acid—{ uricosuric agents- probenecid) greater than 800mg secreted (allopurinol xanthine oxidase inhibitor)
avoid drugs: thiazides, loop diuretics
certain foods: seafood, red meat

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19
Q

Management of scleroderma

A

The management of scleroderma is dependent on it’s severity. It involves the management of the symptoms, which differ depending on organ involvement. This can be divided into pharmacological and non-pharmacological.
no cure—- sx
Raynaud’s= vasodilators CCB, endothelin receptor antagonist
digital ulcers- phosphodiesterase inhibitors- sildenafil
ILD- cyclophosphamide, azathioprine, steriods
pulmonary HTN- endothelin receptor antagonists, sildenafil
GORD- antacids
malnutrition SBO- tetracycline
kidney involvement- ACE inh, ARBs
non pharm- PT, OT, rheumatologist, depression screening, support, integration into primary care

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20
Q

Management of Lupus

A

Management of this patient would involve pharamacological and non-pharmacological treatment. Treatment depends on disease severity and organ involvement.
Pharm-
flares- * mild/moderate/severe
for maintenance

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21
Q

mild flare SLE

A

hydrochloroquine, low dose steriods, skin flare topical steriods

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22
Q

moderate flare of SLE

A

organ involvement steriods, DMARDS, mycophenolate may be needed.

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23
Q

severe life threatening SLE

A

high dose steriods
mycophenolate
rituximab

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24
Q

For SLE maintenance

A

NSAIDS
steriod sparing agents- azathioprine, MTX
belimumab- add on therapy in antibody and disease where disease activity is high

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25
Q

What are the non- pharmacological management of SLE?

A
general: 
sun block high SPF
cover skin when in sun 
MDT 
physiotherapy 
rheumatology 
specialities- dermatology, cardiology, respiratory
screen for depression, support 
integration into primary care
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26
Q

Management of osteoarthritis

A

management fo OA can be divided into pharmacological and non-pharmacological and also surgical in selected cases.
non-pharm avoid aggrevating factors but remain active
weight loss
foot wear physio
OT
pharm- topical- NSAIDS capsaicin,
oral- paracetamol, NSAIDS
injection- intraarticular or periarticular corticosteroids

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27
Q

What is the surgical management of OA

A
indications- uncontrolled pain, progressive immobility, functional impairment 
surgical procedures- 
washout and debridement 
joint replacement 
arthrodesis- fuse joint 
osteotomy- realign joint
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28
Q

Management of Ank spond

A
Management of ankylosing spondylitis involves both pharmacological and non-pharmacological approaches. 
non-pharm 
patient education 
assess disease severity- BATH index 
avoidance of aggrevating activities 
PT, OT 
Pharmacological
pain relief (nsaids, opioids if severe) 
sulfasalazine - peripheral involvement 
anti- TNF alpha 
infliximab and etanercept
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29
Q

What is the Bath index

A

6 questions
fatigue, morning stiffness duration, severity
spinal pain, arthralgia, enthesitis (inflammation at the site where the tendon meets the bone- achilles)

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30
Q

Management of interstitial fibrosis

A

Management of this patient once confirmed to be interstitial pulmonary fibrosis can be divided into non-pharmacological and pharmacological management and potentially surgical.
non-pharm- using GAP model (gender, age, physiology- FVC and DLCO)
RF = smoking, vaccination
pulmonary rehab and education, assistive breathing techniques,
incorporation into a MDT PT, OT, respiratory nurse specialist, SW and resp physician
Pharm- anti-reflux microaspiration of gastric and oesophageal contents (omeprazole)
avoid- sildenafil, warfarin, azathioprine, co-trimoxazole
nintedanib- receptor blocker for multiple tyrosine kinases that mediate elaboration of fibrogenic growth
perfinidone- anti-fibrotic agent (monitor LFTs for both)
LTOT
palliative care

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31
Q

When would you consider surgery for pulmonary fibrosis

A

consider:
DLCO less than 40%
FVC less than 80%
decrease in pulse ox less than 89%
transplant list:
decrease in FVC greater than 10% 6 month follow up
decrease in DLCO greater than 15% during 6 month follow up
6 minute walk test- oxygen less than 80%
pulmonary HTN

32
Q

What are the contraindication for lung transplantation?

A

end stage HF
chronic substance abuse
mets
psychosis

33
Q

What is the pharmacedical therapy after lung transplant?

A

steriods
calcineurin inhibitor (tacrolimus)
nucleoside blocking agent
azathioprine

34
Q

Management of sarcoidosis

A

Management fo this patient is depenendent of organ involvement, but can be divided into pharmacological and non-pharmacological treatment.
non-pharm- * most patients do not require tx if asymptomatic, non-progressive, or have spontaneous remission.

serveillance- serial imaging, serial PFTs, depending on the center.

MDT- PT, resp nurse, SW, intergration into primary care
Pharm- steriods… second line methotrexate, azathioprine

35
Q

Management of COPD

A

Management of this patient can be divided into non-pharmacological and pharmacological the latter being dependent on the GOLD classification of the patient.
non- pharm-
education, vaccination, oxygen therapy, pulmonary rehab, nutrition, co-morbid depression and anxiety, integration into primary care, and MDT
GOLD classification
divided into ABCD the severity is dependent on the mMrC score and the exacerbation history. mMrc greater than 2 higher level. and a exacerbation history of greater than 2 in the past 12 months is considered significant.
A SAMA/ SABA
B LAMA/ LABA
C ICS plus LABA or LAMA
D triple therapy- ICS/ LABA/ LAMA consider antibiotic prophylaxis azithromyocin

36
Q

Pharmacological management of COPD= inhaler types

A

beta agonists SABA- salbutamol inh (100-200 mcg) or nebs 2.5 mg 4 hourly
LABA salmeterol
amtimuscarinics- SAMA ipratropium (40 mcg QDS)
LAMA tiotropium
inhaled steriods
beclomethasone 100 mcg 2 buds BD
mucolytics- carbocystine
phosphodiesterase 4 inhibitors Roflumilast 500 mcg OD * anti-inflammatory

37
Q

What is your management for an acute exacerbation of COPD

A

scoring to local hospital guidelines
Amoxicillin 1 g TDS
if penicillin allergic
Clarithromycin 500 mg BD

38
Q

what is the management for Bronchiectasis?

A

Managment of this patient would focus on treating the underlying cause, any exacerbations, exacerbation prevention, pharmacological therapy and surgery if localised disease
exacerbation - broad spectrum antibiotics, P. Aeruginosa colonisation (difficulty in eradicating)
chest prevention: chest physiotherapy, smoking cessation, nutrition, saline, mucolytics, vaccinations.

39
Q

Management of CF

A

management of this patient requires long term follow-up and management of acute exacerbations. This can be subdivided into pharmacological and non-pharmacological therapy.
Non- pharm:
MDT
dietitation- high caloric intake
PT, respiratory consultant annual check up
survallience- DM, psych, malabsorption

40
Q

What are the routine bloods for CF?

A

FBC, Coag, B12, creatinine, Calcium, IG G/m/e Vitamen A and E
coag, CRP. LFTs, phosphate, aspergillosis serology, U and E, eGFR, TFTs, Mg, iron

41
Q

What is the pharmacological treatment for CF

A

Pharmacological
respirtory- mucolytics, bronchodilators,
endocrine- insulin
digestive- enzyme replacement creon, fat soluble vitamin supplement, diabetic drugs if ddx, ursodeoxycholic acid, CFTR modulators

42
Q

What are come examples of CFTR modulators?

A
Ivacaftor 
G551D 
Lumicaftor 
F508 del mutation 
reduced exacerbation and better FEV1
43
Q

What is the acute management for Cf?

A

oxygen
IV antibiotics
mucolytics
chest physiotherapy

44
Q

Management fo RA lung disease?

A

same as RA
symptoms RA- ILD with steriods, and steriod sparing agents
mycophenolate, azathioprine, cyclophosphamide

45
Q

Management of a pleural effusion

A

Management is based upon diagnostic aspiration and chest drain.
fluid removal is best if slow less than 2 litres in 24 hours
if recurrent:
pleurodesis
with talc
surgery: rarely needed plerectomy

46
Q

Management of kyphoscoliosis

A

Management of kyphoscoliosis depends on the degree of deformity and how it is affecting the patient, but can involve conservative, pharmacological therapies and definitive surgical correction.
conservative:
PT, shoe lift (leg length des), braces, weight loss, mobility aids
referral: if pain, neurogenic claudication, cauda equina
medical:
analgesia and epidural analgesia plus or minus glucosteriods if radicular pain
surgical- relieve of sx and restoration of normal anatomy.

47
Q

Management of pulmonary HTN

A

Management of this patient would involve a pharmacological and non pharmacological approach based upon treating the underlying causes and reducing pulmonary vascular resistance.
HF pharm- ACE inh, B blocker, duiretics, anticoagulation non-pharm same as weigh HF
reduction of pulmonary vascular resistance
pharm- LTOT, CCB nifedipine, selective vasodilator tx
NO pathway- sildenafil
prostaglandin analogues- lioprost
bosentan- endothelin receptor antagonists
Heart and lung transplant
Pharm

48
Q

Management of asthma

A

Management of this patient is based on the relief and control of symptoms (using the gina assessment of asthma control) and also the management fo any acute exacerbations.
Acute management is subdivided into mild, moderate, and severe this is based on the Peak flow of the patient, the ox sats, speech, respiratory rate and pulse.

49
Q

Acute management of asthma

A

management is according to Advanced Trauma Life support guidelines. ABCs and ABG constantly reassess ox
oxygen maintain sats 94-98%
Beta 2 agonist- nebulised salbutamol 5 mg 4 hourly
Predisolone 40-50 mg or IV hydrocortisone 100 mg 6 hourly
Ipratropium bromide 0.5 mg via nebuliser
consider ICU and Mg sulphate 1.2 -2 mg over 20 minutes
r/p PEF 15-30 minutes after initiation of tx

50
Q

Chronic management fo Asthma (right before discharge)

A

on discharge meds for 12-24 hours and education about inh tech
PEF grater than 75% best or predicted
tx with oral and inh steriods plus bronchodilator tx
write an asthma action plan
GP follow up in 2 working days
follow up appointment in 4 weeks.

51
Q

Chronic management of asthma

A
short acting b agonist 
regular preventor steriods
add on therapy LABA to low dose ICS 
This is according to the 2016 guidlines of the BTS 
1SABA plus low dose ICS
2 SABA plus low dose ICS and LABA
3 SABA plus medium dose ICS and LABA 
4 SABA plus medium dose ICS and LABA and additional agents (leukotrine R antagonist (monteluklast) or theophylline  
5 SABA plus above plus orla steroids
52
Q

Management of pneumonia

A

Management of this patient would involve calculating his CURB 65 score and pharmaceutical and non pharmaceutical interventions.
Non- pharm: fluids, chest PT, address any other co-morbilidad, and follow up chest x ray at 6 weeks.
Pharm- according to the GAP app
CAP (score 1) amoxicillin (2) amox plus clarithromyocin. (3) co-amox plus clarithromyocin
aspiration: co amox
COPD exacerbation: amoxicillin 7 days
HAP - 8 days (2) pip taz
(3) pip taz plus clarithromyocin plus gent (if unstable) plus vanc

53
Q

Management of polycystic kidney disease

A

non-pharmacological increase water intake to 3-4 litres *supress ADH and urine osmolalaity reduce cyst size
low sodium diet
cyst decompression
MDT approach with primary care

54
Q

Management of PKD pharm

A

treat the HTN target 130/80 first line ACEI or ARB then thiazide diuretic
statin- increased risk of CVD
tolvaptan- vasopressin receptor analogue
octeotide (somatostatin) does not alter disease progression.
RRT

55
Q

Management of testicular torsion

A

emergency surgery
fixation of the testes
NPO analgesia and fluids etc

56
Q

Management of Bell’s palsy

A

Bell’s palsy can be managed conservatively
with physiotherapy, massage, electrical stimulation, lubricating eye drops
early treatment with corticosteroids
acyclovir

57
Q

What is the treatment for Parkinson’s

A
Parkinson is amovement disorder due to dopamine depletion of the substantia niagra 
treatment can be divided into pharmacological and non-pharmacological 
if life limiting symptoms: dopamine L dopa and carbidopa (sinemet) 
if non life limiting can start on dopamine agonist (non-ergot derived Pramipraxole 
MAO-B inhibitor selegine (inhibiting breakdown of dopamine) 
COMT inh (entacapone)
58
Q

What is the treatment for Huntington’s disease?

A
There is no cure
but there is symptomatic relief 
psychiatric symptoms- atypical antipsychotics decreased risk of extrapyramidal SE 
chorea: reserpine 
depression SSRIs 
dystonia: botulinum toxin
59
Q

What is the treatment for Motor Neuron Disease

A

The treatment can be divided into conservative and non conservative and disease modifying medications
patient educationa dn counselling of family
MDT neurologist, GP palliative nurse, physio, OT, Dietician
symtomatic relief:
drooling: amitriptyline (anticholingeric)
dysphagia: blend food, NGTm PEG feeds
dysarthria SLP
respiratory failure: NIV
muscle weakness physio, walking aids
spasticity: botulinum toxin, baclofen
pain- analgesia ladder
disease modifying Riluzole (3 months longer)

60
Q

What is the treatment Amyotrophic Lateral Sclerosis

A

supportative there is no cure for ALS

drooling anticholinergic like amitriptyline

61
Q

What is the treatment for foot drop?

A
conservative 
orthotics and splits 
physiotherapy 
non conservative 
surgical decompression
62
Q

What is the treatment for Guillian Barre syndrome?

A
Supportive and disease modifying 
monitor inspiratory force and vital capacity PFTs and need for ICU 
autonomías dysfunction- monitoring 
CVS manage BP and arrhythmias (sinus tachycardia) 
bowel and bladder care catherter 
pain control- analgesia 
rehabilitation 
disease modifying 
IVIG (0.4g/kg daily for 5 days) 
plasma exchange peres is
63
Q

What is the treatment for Myasthenia Gravis?

A

Pharmacological
anticholinesterase agents (pyridostigamine 30mg TDS)
chronic immunosupression (steriods, azathioprine, cyclosporine)
Plasmapharesis plus or minus IVIG for crisis
surgical: thymectomy

64
Q

What is the treatment for Lambert Eaton Mysathenic syndrome?

A

treatment:
underlying condition- small cell lung cancer with resection
need for acetylcholine
so increase release: diaminopyridine. guanidine
decrease the breakdown with pyridostigmine
immunosuppresion

65
Q

What is the treatment for MS

A

Involvement of a Multidisciplinary team
acute: methyprednisone 1000 my IV daily for 3-7 days
symptom treatment
patient education
spasticity- baclofen
bladder dysfunction- oxybutin
pain- TCAs
depression TCAS
disease modifying treatment: 1st ABCs (Avonex, Betaseron, Copolymer) all interferon Betas
Monoclonal antibodies- Natalizumab acts as alpha 4 intergrin antagonist used in severe relapsing remitting MA that is unresponsive to interferon.

66
Q

What is the treatment for spinal cord compression?

A

Emergency:
treat with high dose steriods IV
ultimately need to do surgical decompression
symptomatic relief:
mobilization of patient: avoid bed sores
cathertisation- urinary retention
manual evacuation of faeces
passive physio- avoid formation of contratares
Baclofen, botulinum toxin spasticity
LMWH- thromboprophylaxis

67
Q

What is the treatment for Cauda Equina?

A

surgical decompression in less than 48 hours

consult with radio oncology for symtomatomatic relief in malignancy

68
Q

What is the treatment for subacute degeneration of the spinal cord?

A

B12 injection with variable response

69
Q

How do you treat an acute relapse in MS

A

oral methylprednisolone 0.5 g daily for 5 days

if severe consider IV

70
Q

What is the treatment for transverse myelitis?

A

High dose steriod in acute

plasmapheresis

71
Q

What is the treatment of Myasthenia gravis?

A

cholinesterase inhibitors pyridostigmine
steiods- prednisolone
azathioprine- steriod sparing agents
other immunosuppression MTX
plasma exchange and IV immunoglobulin used in crisis and severe MG with sevre bulbar and respitory compromise
surgical thymectomy

72
Q

Charcot Mary Tooth disease treatment?

A

evaluate all pd for weakness booth distal and proximal, psyical conditioning, ambulatory, balance coordination, and manual dexterity.
daily exercises may improvise function with ADLs
orthotics to stabilise the ankles
ortho surgery

73
Q

What drugs should you avoid in CMT

A
vincristine 
amiodarone 
cisplatin 
metronidazole 
nitrofurantoin
74
Q

What is the treatment for myotonic dystrophy?

A
genetic counselling 
pre natal dx if family history 
muscle pain- NSAIDS, TCAs, Mexiletine 
myotonia
mexiletine- check ECG for QT prolongation
alveolar hypoventilation regular use of incentive spirometers 
nutrition 
screen for depression 
MDT
75
Q

What drugs should not be offered as first line treatment for PD?

A

ergot derived dopamine agonists because of the monitoring
considered in patients who have developed dyskinesia or motor fluctuations
second line if not sx controlled enough