nervous system Flashcards

1
Q

name the different type of dementia

A
  • Alzheimer’s disease (most common)
  • vascular dementia (due to cerebrovascular disease)
  • dementia with Lewy bodies
  • mixed dementia
  • frontotemporal dementia
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2
Q

what are the key symptoms related to dementia?

A

problems reasoning + communication, change in personality, reduced ability to carry out daily activities such as washing + dressing

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3
Q

which HCP must initate drug treatment in newly diagnosed patient vs those currently already on drug therapy?

A

Newly diagnosed patients: initiate drug treatment under the advice of a specialist clinician

Gp may prescribe step-up treatment

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4
Q

Mild to moderate Alzheimers dementia name three 1st line acetylecholinesterase inhibitors

A
  1. donepezil
  2. galantamine
  3. rivastigmine
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5
Q

what is the alternative treatment in mod alzheimers if acetylcholinesterase inhibitors are not tolerated or contra-indicated?

A

memantine (moderate disease)

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6
Q

moderate-severe + severe alzhimers dementia already receiving acetylcholinesterase inhibitor step up?

A
add memantine (may initate primary care)
discontinuing acetylcholinesterase may worsen cognitive function (AVOID)
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7
Q

management of mild-to-mod dementia with lewy bodies (non-alzeimers)

A
  1. Donepezil [unlicensed indication]
  2. rivastigmine [unlicensed indication]

Alternative: If treatment with both donepezil or rivastigmine not tolerated:
- galantamine [unlicensed indication]
Alternative: in whom acetylcholinesterase inhibitors are contra-indicated/not tolerated:
- Memantine hydrochloride [unlicensed indication]

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8
Q

severe dementia with lewy bodies (monotherapy)

A
  1. Donepezil hydrochloride [unlicensed indication]

2. rivastigmine [unlicensed indication]

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9
Q

vascular dementia treatment if suspected co-morbid alzeimers, parkinsons disease dementia, or dementia with lewy bodies treament

A

-Acetylcholinesterase inhibitors [unlicensed indication]
OR
- memantine hydrochloride [unlicensed indication]

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10
Q

Which of the following are not recommended in Frontotemporal dementia or cognitive impairment caused by multiple sclerosis:

A

X Acetylcholinesterase inhibitors

X memantine hydrochloride

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11
Q

Management of cognitive symptoms of dementia - which drugs to AVOID?

A

Drugs cause antimuscarinic effects:  cognitive impairment (AVOID)

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12
Q

what does cognitve symtpoms mean?

A

Cognitive impairment is when a person has trouble remembering, learning new things, concentrating, or making decisions that affect their everyday life. Cognitive impairment ranges from mild to severe.

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13
Q

treatment of cognitive symptoms in dementia?

A

depression- antidepressants e.g. amitriptyline, paroxetine
antipsychotics e.g. olanzapine, quetiapine
antihistamine= chlorphenamine, promethazine
urinary antispasmodics e.g. solifenatic, tolterodine

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14
Q

management non-cogntive symptoms of dementia

A

agitiation, aggression, distress + psychoses, depression, anxiety, sleep disturbancne
- offer counselling, CBT intial step
sleep- increase exersize and activity

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15
Q

antipsyhotics and antidepressants prescribing in dementia

A

antipsychotics- only prescribe if patient risk harming themselves, or causing severe distress,
CHM: increased risk or stroke and death with antipsychoitc + elderly patient with dementia
use lowest does + review every 6 weeks
depression- reserved those pre-existing mental health problems

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16
Q

what is sevre antipsychotic sensitivty reaction in those with dementia with lewy bodies or parkinson disease dementia

A

worsen motor feature of condition some case cause severe antipsychotic sensitivity reaction

17
Q

what is the mechanism of action of acetylcholinesterases?

A

reversible inhibitor of acetylcholinesterase.

examples: donepezil, galantamine, rivastigmine

18
Q

dopaminerigic drugs , NMDA receptor antagonist example and Mechanism of action

A

Memantine

DRUG ACTION =glutamate receptor antagonist

19
Q

which anti-epileptics have a long half life once daily dosing?

A

 Lamotrigine
 perampanel
 phenobarbital
 phenytoin

20
Q

Action to take if monotherapy 1st line anti-epileptic has failed?

A
  • Try monotherapy with a second drug

* Note: Diagnosis should be checked before starting an alternative drug if the first drug showed lack of efficacy.

21
Q

changing one antiepileptic to another:

A

BE CAUTIOUS

• slowly withdrawing the first drug only when the new regimen has been established

22
Q

use of 2 or more antiepileptic (may be necessary)

A

• concurrent use of antiepileptic drugs increases the risk of adverse effects and drug interactions.
• If combination therapy does not bring about worthwhile benefits, revert to the regimen (monotherapy or combination therapy) that provided the best balance between tolerability and efficacy.
 A single antiepileptic drug should be prescribed wherever possible.

23
Q

MHRA: antiepileptics advice on switching brands

A
  • potential harm of switching patient stabilised

- report of loss seizure, worsening SEs, explained as chance associations, casual role of switching cannot be ruled out

24
Q

minimise risk of swithcing anti-epileptics brands?

A

3 risk categories
if desirable GP must specifiy product, prescribe brand or generic + manufacturer name
advice relates to only treatment of epilepsy
report yellow card scheme any suspected ADR
pharmacist ensure continuity of supply ,

25
Q

action if a specific brand not available

A

it may be necessary to dispense a product from a different manufacturer to maintain continuity of treatment of that antiepileptic drug. Such cases should be discussed and agreed with both the prescriber and patient (or carer):

26
Q

category 1 antiepileptics must be maintained specific manufacturer product

A
[CPPP]
	Carbamazepine
	phenobarbital
	phenytoin
	primidone
27
Q

category 2- maintain brand based on clinical judgement, based on seizure frequency, treatment history, potential implication of patient having breakthrough seizure, + consider non-clinical factors

A
[CROP CEL TVZ]
	Clobazam 
	rufinamide
	oxcarbazepine
	perampanel

 clonazepam
 Eslicarbazepine acetate
 lamotrigine

 topiramate
 valproate
 zonisamide.

28
Q

category 3 (doesnt matter)- uncessary maintain specific manufacturer brand consider product name, packaging, appearance, etc + consider patient disability

A
[BELL TV  GP]
	Brivaraceta
	ethosuximide
	lacosamide
	levetiracetam

 tiagabine
 vigabatrin

 gabapentin
 pregabalin

29
Q

what is antiepileptic hypersensitivty syndrome

A

rare fatal syndrome associated some antiepileptics

30
Q

risk of antiepileptic hypersensitivty syndrome with the following drugs

A
[ROLL C PPP]
	rufinamide
	oxcarbazepine
	lacosamide
	lamotrigine
	Carbamazepine
	phenobarbital
	phenytoin
	Primidone

theoretical risk:
 Eslicarbazepine
 stiripentol
 Zonisamide

31
Q

symptoms of antiepileptic hypersensitivty syndrome?

A
Symptoms (week 1-8 of exposure):
most common:
	 fever
	 rash
	 lymphadenopathy
Other systemic signs:
	liver dysfunction
	Haematological
	renal, and pulmonary abnormalities
	vasculitis
	multi-organ failure
32
Q

action to take if hypersensitivty occurs anti-epileptics

A

If signs or symptoms occur the drug should be withdrawn immediately!!! the patient must not be re-exposed, and expert advice should be sought

33
Q

MHRA alert for all anti-epileptics

A

MHRA advised all antiepileptic drugs are associated with a small increased risk of suicidal thoughts and behaviour.
Symptoms may occur as early as one week after starting treatment

Advise patients to report:
• mood changes
• distressing thoughts
• feelings about suicide or harming themselves

34
Q

interaction with anti-epileptics

A
  • may increase toxicity without an increase in antiepileptic effect
  • usually caused by hepatic enzyme induction or inhibition
  • Displacement from protein binding sites is not usually a problem.
  • Interactions are highly variable and unpredictable
35
Q

antiepileptic withdrawal

A

withdrawn under specialist supervision

  1. Avoid abrupt withdrawal, particularly of barbiturates and benzodiazepines, because this can precipitate severe rebound seizures.
  2. Reduction in dosage should be gradual+ case of barbiturates, withdrawal of the drug may take months!
  3. The decision to withdraw antiepileptic from a seizure-free patient, and its timing, is often difficult and depends on individual circumstances.
  4. Even in patient’s seizure-free for several years, a significant risk of seizure recurrence on drug withdrawal
  5. In patients receiving several antiepileptic drugs, only one drug should be withdrawn at a time.