Bipolar Flashcards

1
Q

Bipolar Depression (old name: Manic depression)

A
  • Occurs in about 1% of the adult population
  • Symptoms typically develop in late adolescence/early adulthood
  • Women show an increased incidence over men (around 20%)
  • Shows strong genetic component
  • Characterised by dramatic mood swings, from overtly “high” to the “low” of very sad or hopeless
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2
Q

Diagnosis

A
  • Defined in the Diagnosis and statistical manual for mental disorders DSM-IV
  • It can be difficult since patients often enjoy the manic or hypomanic episodes so may only visit GP when depressed, also symptoms can be confused with anxiety or schizophrenia
  • A questionnaire may be used by the doctor if mania suspected. These may include questions like-
    • Have you ever found yourself to be abnormally talkative and speaking-very quickly?
    • Have you been so manic that people thought you were not yourself
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3
Q

Symptoms of a ‘high’ (mania)

A
  • Overly good, euphoric mood
  • Increased energy, activity and restlessness
  • Racing thoughts, talking fast, jumping from one idea to the next
  • Provocative, intrusive or aggressive behaviour
  • Needs little sleep
  • Unrealistic beliefs in one’s abilities and powers
  • Increased sexual drive
  • Abuse of drugs, particularly cocaine, alcohol and sleeping medications
  • A denial that anything is wrong
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4
Q

A bipolar range of mood from depression to mania

A
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5
Q

Cycling

A
  • Mania (peak)
  • Depression (bottom)
  • Normality (middle)
  • 4 episodes over 12 months are known as rapid cycling
  • Some patients have multiple episodes with a single week or even day
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6
Q

Cycling of mania and depression

A
  • Bipolar I disorder- recurrent episodes of mania and possibly depression
  • Bipolar II disorder- Recurrent episodes of hypomania and depression
  • Can NOT giving antidepressants
    • The graph will mood upwards with a greater period of time being spent in mania
  • We try to dampen the graph so the oscillations will stay around the normal mood line
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7
Q

Dont give antidepressents

A
  • If left untreated Bipolar will deteriorate into a worse and worse condition
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8
Q

Clinical Intervention in mania

A
  • There are two principle aims in the treatment of bipolar disorder
    • Short term control of acute maina
    • Long term (prophylactic) treatment to maximise the time interval between episodes
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9
Q

Treatment of acute mania

A
  • Over mania is controlled with neuroleptic Olanzepine (nb atypical anti-psychotics not only block D2 receptors but also 5-HT2A receptors)
  • Valporate but remember restrictions in women of childbearing age. Carbamezapine can be used but note the greater risk of cardiotoxicity and increased propensity for drug interactions
    • Blocking excitability
  • nb the therapeutic benefit of mood stabilisers is delayed
  • If sedation is a priority a BZ such as lorazepam can be administered
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10
Q

Mood stablising drugs

A
  • Lithium carbonate most commonly used as prophylactic to control mania as well as depression
  • Recent use as prophylactic or in acute phase has increased as they have better side-effect and safety profile
  • Has to build up for 6 months or more
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11
Q

Li- MOA

We don’t actually no

A
  • Mood
    • Decrease in: Mania; Depression; Mood stabilisation; Suicidality
  • Cognition
    • Altered cognitive function
  • Structure
    • Neuroprotective: Increase global grey matter vol; Amygdala, hippocampus, PFC
  • Neurotransmission- Increased GABA: Decreased excitatory transmission
  • Cellular and intracellular changes: 2nd messenger (PKC, Ionositol, AC; increased anti-oxidant; Neuroprotective
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12
Q

Patient care

A
  • An important aspect is the teaching of patients to recognise the early symptoms of manic relapse
  • Compliance with the lithium treatment is particularly important
  • Monitoring of lithium blood concentrations after 1 week and then every 3 months
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13
Q

Lithium PK

A
  • Lithium is rapidly absorbed from the GI tract
  • Li has an elimination half lifeof 24 hr
  • Steady state levels are thus not obtained until about day 5
  • Li dose must be titrated carefully to obtain blood levels between 0.5-1.2 mmol/L
  • Severe toxicity occurs above 2 mmol/L
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14
Q

Side effects of Li

A
  • Approximately 30% of patients can not tolerate the ADR
  • Therapeutic plasma levels of Li are associated with
    • GI discomfort and nausea
    • Neurological symptoms (which may dissipate) such as fatigue, malaise, muscle weakness
    • Decreased water reabsorption by the kidney
    • Weight gain. This is a frequent cause of non-compliance
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15
Q

Li- Long half-life but narrow therapeutic window

Moderate

A
  • Moderate (1.5-2.0 mmol/L
    • GI
      • Vomiting
      • Abdominal pain
      • Dry mouth
    • Neurological
      • Ataxia
      • Dizziness
      • Slurred speech
      • Lethargy or excitement
      • Muscle weakness
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16
Q

Severe (2-2.5 mmol/L)

A
  • GI
    • Anorexia nervosa
    • Persistent vomiting
  • Neurological
    • Blurred vision
    • Muscle fasciculation
    • Clonic limb movements
    • Convulsions
    • Delirium
    • Syncope
    • Coma
    • Circulatory failure
17
Q

w

A