Week 1 - D - Pharmacology- Neuropathic pain, Depression (SSRI, SNRI, TCA, MAOI, Atypicals)&Bipolar disorder (acute&mood stabilisation) Flashcards

1
Q

Antidepressant drugs have lots of different clinical use Moderate/severe depresion Dysthymia - how long does dysthymia last? Generalised anxiety Panic disorder, OCD, PTDS Premenstrual dysphoria Bulima nervosaa Neruropathic pain

1st line for neuropathic pain & trigeminal neuralgia?

A

Dysthymia is persistent mild depression lasting longer than 2 years - in some patients this progresses to major depression - (major encompasses moderate to severe usually)

1st line treatment for trigeminal neuralgia - carbamazepine

If this fails - lamotrigine, gabapentin or phenytoin (basically stick with the anti-epileptics for trigeminal neuralgia)

1st line treatment for neuropathic pain - 1st line is amitryptlyine or gabapentin or pregablin or duloxetine

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2
Q

How does carbamezapine (1st line for trigeminal neuralgia), lamotrogine, gabapentin and phenytoin (all three are 2nd line options) work? How does amitryptiline work, and gabapentin and pregablin and duloxetine? (all 1st line options for neuropathic pain that isnt trigeminal neuralgia)

A

* Carbamezapine - Na+ channel blocker - stabalises inactivated Na+ channels - anti-convulsant

* Lamotrigine - Na+ channel blocker- anti-convulsant

* Phenyotin - believed to be a Na+ channel blocker

Amitryptiline - tricyclic antidepressant, selectively blocks reuptake of monoamines into the presynaptic terminal (mainly serotonin (5HT) and noradrenaline)

Gabapentin/pregablin - GABA analogue - blocks voltage gated Ca 2+ channels decreasing release of glutamate & substance P

Duloxetine-SNRI -blocks reuptake of serotonin&noradrenaline

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3
Q

What are the three main classes of antidepressants?

A

Monoamine reuptake inhibitors (SSRIs, tricylics, SNRIs, other non-selective reuptake inhibtiors) Monoamine oxidase inhibitors Atypical drugs - they exhibit post-synaptic effects

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4
Q

Name 3 types of monamine? Monoamine neurotransmitters are neurotransmitters and neuromodulators that contain one amino group that is connected to an aromatic ring by a two-carbon chain (such as -CH2-CH2-).

A

Monoamine refer to specific neurotransmitters eg Noradrenaline Serotonin Dopamine

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5
Q

What do monoamine reuptake inhibitors do?

A

These stop the reuptake of the monoamines (noradrenaline, serotonin and dopamine) resulting in an increase in concentrations of neurotransmitters in the synapse

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6
Q

What is the monoamine hypothesis?

A

This hypothesis stipulates that depression results from a functional deficit of monoamine transmitters particularly serotonin and noradrenaline Drugs that deplete the stores of monoamines can therefore induce low mood And therefore drugs that treat depression will work by increasing the concentrations of monoamines

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7
Q

What are the different types of anti-depressants mainly?

A

Monoamine reuptake inhibitors (SSRIs, Tricyclics, SNRIs, Other-non selective uptake inhibtors) Monoamine oxidase inhibitors Atypicals - exhibit post-synaptic effects

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8
Q

How do monoamine oxidase inhibitors work? (MAOI)

A

Monoamine oxidase inhibitors can either be reversible or irreversible of monoamine oxidase A or B Monoamine oxidase inhibitors prevent the action of monoamine oxidase which catalyses the activation and inactivation of monoamine neurotransmitters

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9
Q

MAOI - Inhibit monoamine oxidase -> decreased breakdown of the monoamine neurotransmitters (norepinephrine, serotonin, dopamine) leading to increased levels in the synapse Why are they not used first line?

A

They are highly effective in patients with treatment resistant depression but patients need to be able to follow the dietary restrictions which is difficult

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10
Q

What are examples of irreversible and reversible MAOIs?

A

Irreversible - phenelzine Reversible - moclobemide

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11
Q

MAOIs are Highly effective in some patients with treatment resistant depression but patients need to be able to follow the diet and medication restrictions What are side effects of MAOI?

A

Postural hypotension Reduces metabolism of other drugs potentiating their effects Insomnia Peripheral oedema Cheese crisis aka hypertensive crisis

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12
Q

What needs to be avoided in diet when taking MAOIs due to the risk of hypertensive crisis? What causes the hypertensive crisis?

A

Foods containing the ingredient tyramine need to be avoided Tyramine is a very potent release of noradrenaline and is usually broken down by MAO-A. If taking a MAOI and a high tyramine meal is taken, then this noradrenaline accumualtion can cause a hypertensive crisis Foods high in tyamine - CHEESE (hence the cheese crisis), alcohol and many others Symptoms of crisis - headache, SOB, nosebleed

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13
Q

How do tricylic anti-depressants work? What are examples of tricyclic agents?

A

Tricyclics work by blocking the reuptake of monoamine neurotransmitters in the presynaptic terminals - increasing their time in the synaptic cleft (mainly noradrenaline and serotonin) * Amitriptyline * Imipramine * Clomipramine * Lofeparmine

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14
Q

What are common side effects of tricylic anti-depressants? What happens in amitryptiline toxicity?

A

Anti-cholinergic so dry mouth , blurred vision, constipation, urinary retention - they block your parasympathetics Sedation Weight gain Also cardiovascular - eg postural hypotension, tachycardia, arrhythmia Amitryptiline is cardiotoxic in overdose

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15
Q

How do selective serotonin reuptake inhibitors (SSRIs) work? Name 3 examples

A

Selective serotonin reuptake inhibitors - SSRIs These work by selectively inhibiting the serotonin reuptake in the presynaptic terminals increasing serotonin (5HT) in the synaptic cleft 4 examples * Fluoxetine * Citalopram * Paroxetine * Sertraline

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16
Q

Common side effects of SSRIs? What can SSRIS cause transiently in patients of what age group?

A

GI side effects Anxiety Sexual dysfunction Headache Hyponatraemia Can cause a transient increase in self-harm / suicidal ideation in patients aged under 25 years of age

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17
Q

Why can SSRIs cause cause hyponatraemia? What other anti-depressant class can cause this?

A

Many drugs including tricyclic antidepressants, and all SSRIs can cause SIADH. This increased water retention causes increased sodium loss leading to a hyponatraemia. Antidepressant-induced SIADH has been reported mostly in patients above 65 years of age, mostly due to the use of fluoxetine.

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18
Q

What is the other main monoamine reuptake inhibitor? What is its mode of action? (dual reuptake inhibitor) Name 2 examples?

A

This would be serotonin and noradrenaline reuptake inhibitors (SNRIs) - they block the reuptake of serotonin and noradrenaline in the presynaptic terminals Duloextine and venlafaxine

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19
Q

What are the side effects of SNRIs?

A

They are similar to SSRIs but lack the major blocking side effects so have fewer side effects than tricyclics Side effects GI effects Anxiety Sexual dysfunction

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20
Q

Give two examples of atyical drugs? Atyical drugs worked via mixed receptor effects

A

Mirtazapine and bupropion

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21
Q

What type of atypical is mirtazpine? (how does it work) What are its side effects and what can it block if given with SSRIs?

A

Mirtazapine as a noradrenergic and specific serotonergic antidepressant (NaSSA) Blocks alpha2, 5-HT2 and 5-HT3 receptors Side effects include weight gain and sedation Can block the serotenergic side effects f given with SSRIs

22
Q

What is the combination of mirtazapine and venflafaxine known as?

A

Basically if monotherapy with SSRIs and/or mirtazapine hasnt worked then give SNRIs SNRIs- not usually first line due to higher risk of side effects than SSRIs. Commonly used when SSRI and/or mirtazapine haven’t worked. Venlafaxine is excellent in combination with mirtazapine when monotherapy hasn’t worked (“California Rocket Fuel”)

23
Q

How does the atypical bupropion work?

A

Bupropion is a dopamine uptake inhibitor

24
Q

What is important to note about all anti-depressants?

A

They all take several weeks to have onset

25
Q

Which drugs are most commonly given as the first line treatment for depression? Name examples? When should they be taken and why?

A

This would be the SSRIs - selective serotonin reuptake inhibitors * Citaloram * Fluoxetine * Paraoxetine * Sertaline Should take in the morning to avoid insomnia - a known side effect

26
Q

What are the options for the second line treatment of depression?

A

* SNRI - serotonin and noradrenaline reuptake inhibitors * * Tricylcics - blocks reuptake of monoamines in the synaptic cleft (mainly serotnonin and noradrenaline) * * Atypicals - mirtazapine (noradrenergic and specific serotonergic antidepressant NaSSA) or bupropion (dopamine uptake antagonist)

27
Q

Which drug is commonly out of the three options mentioned used as second line in the treatment of depression? When may this drug be used 1st line?

A

Mirtazapine - may be used first line in patients with insomnia and/or poor appetite Often used though when SSRIs dont work

28
Q

SNRIs are not usually first line due to higher risk of side effects than SSRIs When are they usually used? When are tricyclics used?

A

SNRIs are usualy used if treatment has not responded to SSRIs or mirtazapine Tricylcics are used after SNRI, avoid in those with cardiac problems

29
Q

If the patients hasnt responded to the different Monoamine reuptake inhibitors or the atypical drugs What is the treatment that can be given? Give two examples

A

Monoamine oxidase inhibitors - prevent the oxidation and inactivation of monamines by the enzyme monoamine oxidase Can be irreversible - phenelzine Can be reversible - Moclobemide

30
Q

What are the side effects associated with MAOIs?

A

Postural hypotension Peripheral oedema Insomnia Hypertensive crisis - due to foods containing cheese which require MAO to break it down - tyramine increases noradenaline production which leads to increased BP Also potentiates effects of other drugs by blocking their metabolism

31
Q

What is non-response to an antidepressant defined as? How long should the treatment be continued after resolution of depressive symptoms at first appearance?

A

Non-responsive treatment to an antidepressant can be defined as no or inadequate response after six weeks at maximum or best tolerated dose - swap the antidepressant Continue treatment fora after at least 6 months after a full resolution of symptoms after a first episode

32
Q

How long should treatment be continued after a recurrence of depression? How long should anti-depressant treatment be continued after a third episode?

A

After a recurrence, continue treatment for at least 12, up to 24 months after full resolution of symptoms After third episode, continue indefinitely if willing

33
Q

Electroconvulsive therapy is a very effective treatment for depression What are the indications for the use of ECT in the treatment of depression?

A

It is recommended that electroconvulsive therapy (ECT) is used only to achieve rapid and short-term improvement of severe depressive symptoms after an adequate trial of other treatment options has proven ineffective and/or when the condition is considered to be potentially life-threatening, in individuals with: * catatonia * a prolonged or severe manic episode.

34
Q

What is catatonia? What condition is it typically seen in?

A

Cataonia is the abnormality of movement and behaviour arising from a disturbed mental state (typically schizophrenia)

35
Q

What are the common catatonic behaviours?

A

Patients can present as Rigid or in a stupor Staying in uncomfortable positions without moving Performing erratic movements Echolalia - repetition of words or behaviours

36
Q

How long are the typical course lengths of ECT? What should happen to the medication when ECT is about to be started?

A

Typical course lentghs are 6-12 sessions (usually 2 per week) Current medication should be reduced and continued when starting ECT

37
Q

What are the side effects of ECT?

A

Short-term side-effects headache nausea memory loss of events prior to ECT short term retrograde amnesia Long-term side-effects some patients report impaired memory

38
Q

What are the principles of treating bipolar disorder?

A

The acute treatment is to raise the mood in depressive and to decrease the mood in manic bouts However for long term - give a mood stabilizer

39
Q

Which drug is usually used 1st line to treat the depressive episodes in bipolar disorder if this is what they present with?

A

For the treatment of depression options include: Fluoxetine combined with olanzapine, or Olanzapine alone, or Quetiapine alone, or If these do not work can try lamotrigine. And after successful treatment move to a long term mood stabilizer

40
Q

If a person develops mania or hypomania and is not taking an antipsychotic or mood stabiliser, offer what drugs?

A

Usually offer an atypical or typical antipsychotic to treat the acute mania episode (haloperidol (typical), quetiapine, olanzapine, risperidone (atypicals) - generally the atypicals are used) or Try valproate semisodium

41
Q

What is the most effective treatment for stabilizing bipolar disorder and how is it thought to work?

A

This would be lithium carbonate Thought to work by blocking phsophatidylinositol pathway or inhibiting glycogen synthase kinase 3B

42
Q

What is the hypothesis by which lithium is thought to work?

A

Thought to work via the inositol depletion hypothesis

43
Q

What are the side effects of lithium? Why is the drug dangerous?

A

The side effects - GI upset, sedation, feeling of weakness, fine tremor, polyuria - causes diabetes insipidus, ankle swelling, renal impairment, hypoparathyroidism and hypothyroidism

44
Q

What are the toxic effects of lithium?

A

Vomiting, diarrhoea, ataxia, coarse tremor, drowsiness, convulsions, coma

45
Q

If patient compliance is good, what needs to be seen as normal before commencing a patient on lithium? What must be checked when making sure lithium is in the therapeutic range?

A

* If the patient compliance is good, then check to make sure U&Es, TFTs and ECG is normal and then start the patient on lithium Get patient to therapeutic range by checking U&Es every 7 days and checking lithium levels 12 hours after each dose until within stable range Stable range is when 12 hours after last dose the lithium levels are in therapeutic range in the blood

46
Q

After the patient then continues on lithium when concentrations are stable, how often are lithium level, U&Es and TFTs checked?

A

After starting lithium levels should be performed weekly and 12 hours after each dose change until concentrations are stable * Once established, lithium blood level should ‘normally’ be checked every 3 months * Check TFTs and U&Es every 6 months

47
Q

If hypothryoidism does happen, what do you do to the lithium? What type of diabetes insipdus does the lithium cause? How do you monitor the lithium after you change its dose?

A

If patient becomes hypothyroid, then do not stop the lithium but instead prescribe levothyroxine Lithium causes nephrogenic diabetes insipidus where the kidneys do not respond to ADH After a change in dose, lithium levels should be taken a week later and 12 hours after the last dose

48
Q

What are causes of lithium toxicity? What is the treatment?

A

Causes - increased dose, dehydration (pshyical illness, exercise, alcohol, decreased fluid intake), drug interaction and reduced salt intake Treatment - stop lithium, IV fluids and may need dialysis if severe

49
Q

What other drugs can be used in the long term treatment of bipolar disorder? Usually options when lithium is not giving good control Give drug examples of both options

A

Anticonvulsatns can be used as mood stabiliser - valproic acid, lamotrigine and carbamezapine Antipsychotic drugs can be used - usually atypicals - olanzapine, quetiapine, aripiprazole

50
Q

What is the mode of action anti-psychotics? What are the side effects?

A

Anti-psychotics - dopamine antagonism and 5HT antagonism Side effects - Sedation and weight gain, metabolic syndrome (insulin resistance, fatness) (also get galactorrhea and gynaecomastia due to blocking of dopamine and increased prolactin) Extrapydramidal side effects

51
Q

What are side effects of the different anticonvulsant options?

A

Anti-convulsants Side effects Carbamezapine - can cause SIADH and pancytpenia Valproic acid - teratogenic, weight gain, thrombocytopenia Lamotrigine - Steven-johnson syndrome

52
Q

Which drug mentioned in this card set is dangerous for suicidal people as it can be used to easily overdose?

A

This would be tricyclic antidepressants - side effects is in overdose they are cardiotoxic