Mood Stabilisers Flashcards

1
Q

Name 5 Mood Stabilisers (including brand names)

A
  • Lithium
  • Sodium Valproate (Epilim)
  • Semi-Sodium Valproate (Depakote)
  • Carbamazepine
  • Lamotrigine
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2
Q

What are the different Mood Stabilisers indicated for?

A
  • Lithium; Bipolar disorder, cyclic mood disorder
  • Sodium Valproates, Carbamazepine and Lamotrigine;
    • anticonvulsants-treatment and management of Epilepsy
    • prophylaxis or adjunct therapy of Bipolar
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3
Q

What is believed to be the mechanism of action for Lithium?

A
  • Lithium is a naturally occuring salt/mineral
  • Works on CNS to improve nerve cell communication-not exactly sure how?
    • May alter NA transport in nerve and muscle cells, thus affecting excitability
    • Changes in gene expression?
    • May decrease levels of 2nd messengers (such as cAMP) inside neuron-this could allow it to selectively modulate responsitiveness of hyperactive neurons that might contribute to manic state)
  • Recent theory that this occurs by activating the CRMP2 protein which is responsible for nerve cell communication.
  • Despite not knowing how, it does work in 1/3 of patients!
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4
Q

What is the general mechanism of action of the anti-convulsant mood stabilisers?

A
  • Reduce abnormal electrical activity in brain via
  • inhibition of voltage-sensitive Na+ channels leading to
  • reduced influx of Na+ ions, preventing
  • neurons from depolarisation and therefore generation of Action Potential
  • These can be ‘use-dependent’-more effective at blocking channels in areas of the brain where action potentials are firing repetitively
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5
Q

How else does Carbamazepine work?

A
  • (other than stabilisation of neuronal membranes via inhibition of voltage-sensitive ion channels)
  • has the ability to inhibit polysynaptic responses?
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6
Q

How else does Lamotrigine work?

A
  • It also inhibits the Ca+ dependent presynaptic release of excitatory NTs such as glutamate
  • Newer!
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7
Q

How else do the Sodium Valproates work?

A

Indirectly by increasing GABA activity. GABA is an inhibitory NT (think Benzos)-Cl ions, hyperpolarisation, inhibit neuronal transmission, reduced chance of AP, exerts stabilising influence, thereby decreasing excessive activity

They do this by;

  • enhancing availability of GABA in synaptic cleft
    • through inhibition of 2 enzymes responsible for GABA inactivation
  • enhancing postsynaptic action of GABA
    • through enhancing opening of receptors
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8
Q

What are the contraindications common to all mood stabilisers?

A
  • Pregnancy
  • Renal Impairments
  • Suicidal thoughts
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9
Q

What are the contrainidications for Lithium?

A
  • Cardiovascular disease
  • Hyperthyroidism
  • Addison’s/Brigada Disease
  • ECT
  • Diuretics or people with sweating/diarrhoea
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10
Q

What are the contraindications for the Sodium Valproates?

A
  • MAOIs or APs
  • Hepatic dysfunction
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11
Q

What are the contraindications for Carbamazepine?

A
  • Chemically related to TCAs, so not if allergic
  • Many drug interactions (TCAs, MAOIs, APs, other anti-seizure drugs)
  • St John’s Wort
  • decrase oral contraceptive efficacy
  • Heart Conditions
  • no alcohol
  • no grapefruit
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12
Q

What are the contraindications for Lamotorgine?

A
  • Parkinsons
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13
Q

What are the side effects of lithium?

A

adverse effects linked to serum levels

  • Tremors
  • Weight gain
  • GI upset-constipation/diarrhoea
  • Polyuria/polydipsia
  • metallic taste
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14
Q

What are the side effects common to anticonvulsants generally?

A
  • Indicators of disorders of
    • Blood (anaemia, bone marrow suppression)
    • Liver (hepatitis)
    • Skin (Stevens-Johnson syndrome)
  • GI disturbances
  • Fatigue
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15
Q

What are the additional side effect of the Sodium Valproates?

A
  • Weight Gain
  • Hair Loss
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16
Q

What are the additional side effects of Carbamazepine/Lamotrigine?

A
  • Water retention and hyponatraemia
17
Q

Why might we talk of polypharmacy with regards to Bipolar disorder?

A

Use of mood stabilisers often accompanied by;

  • antidepressant (depressive episodes)-too much can trigger elation/mania
  • anxiolytics to calm (manic episodes)
  • hypnotics for insomnia (severe episodes)
  • antipsychotic (psychosis during manic episodes)
18
Q

Tell me about the special monitoring requirements for Lithium (please)

A
  • Weekly blood tests until falls within safe range of 0.4-1.0mmol/L then 3 monthly tests-note, must be 12 hours after dose
  • Renal, cardio and thyroid function baseline then 6 monthly
  • Purple Lithium treatment pack (including blood test result booklet, lithium therapy info booklet and lithium alert card)
19
Q

Lithium Patient Education Pertinent Points?

A
  • Lots of things affect Lithium levels (metabolic rate, weight, salt intake, exercise levels and fluid consumption)-it is your responsibility to maintain these to keep you levels stable within safe range.
  • If adjusted and levels fo above 1.5 mmol/L, risk of Lithium Toxicity!
  • can occur at any time + fatal, symptoms include;
    • blurred vision
    • difficulty walking
    • slurred speech
    • irregular heartbeat
    • rash, legs/feet + hands/arms (muscle twiches, swollen, trembling)
20
Q

What are the options regarding pregnancy and mood stabilisers?

A
  • Lithium
    • high risk of heart defects + still-births
    • no breastfeeding
    • levels erratic during pregnancy and childbirth-much increased monitoring
  • Anticonvulsants
    • ‘fetal anticonvulsant syndrome’
    • develomental delay
    • first three months = worst
    • breastfeeding okay
  • Valproate
    • as of April 2018-contraindicated in women of child bearing age because of teratogenic risks. (only prescribed for epilsepy if no suitable alternate treatment and enrolled on Pregnancy Prevention Programme)
21
Q

How is Lithium absorbed, excreted and distributed?

A
  • Absorbed in GI tract
    • Peak at 2-4 hours
  • excreted from kidney, + 80% reabsorbed (during dehydration/sodium dehyradation, more reabsorbed into serum-toxic!)
  • Same distribution in body as water
22
Q

How are the anticonvulsant mood stabilisers absorbed, metabolised and excreted?

A
  • All readily absorbed from GI tract, metabolised in liver and excreted in urine
  • All different durations of action