Bipolar Affective Disorder Flashcards
1
Q
AETIOLOGY:
A
- Genetic
- FHx of bipolar affective disorder/schizophrenia/schizoaffective disorder
- first-degree relatives of patients with bipolar have 7x increased risk of bipolar disorder(10%), 2-3 increased risk of unipolar depression(20-30%), higher risk of schizophrenia/schizoaffective disorder - Environmental
- Childbirth( in previous 6/12)
- 50% untreated bipolar patients experience mania postnatally.
- Recent negative life events
2
Q
MANAGEMENT:
- Tx. setting
- Tx. acute mania/hypomania
- Tx. acute depression in context of bipolar disorder
- Maintenance tx.
A
- may need detention under MHA
- admit if reckless behaviour endangering self/others; impaired judgement; thoughts of self-harm/hurting others/suicide; significant psychotic symptoms; excessive psychomotor agitation with risk of self-injury/dehydration/exhaustion
- may need detention under MHA
- a) If on antidepressant, discontinue gradually.
b) Start antipsychotic(quetiapine/haloperidol/risperidone/olanzapine)
- if not tolerated/ineffective, offer alternative antipsychotic.
- if still not adequate response, consider adding lithium/valproate
- avoid lithium if poorly concordant.
c) if already on mood stabilizers, optimise treatment
- consider adding antipsychotic - a) Pharmacological tx if moderate-severe depression
b) Offer fluoxetine+olanzapine/quetiapine
- if no response/preferred by patient, consider lamotrigine by itself
c) If already on lithium/valproate, consider optimising dose before adding fluoxetine+olanzapine/add quetiapine
- if preferred, can consider adding olanzapine(without fluoxetine) OR lamotrigine.
- if unresponsive, stop additional treatment and add lamotrigine - a) in those with serious adverse risks/repeated hypomanic or depressive eipsode with significant functional impairment.
b) Lithium as first-line. Olanzapine/valproate as alternatives.
- all teratogenic
- lamotrigine considered if majority of episodes depressive
- when started on valproate, liver and haematological function assessed at 6/12
- Lithium levels measured every 3/12. Net benefit after ≥2y
c) Psychological interventions
- consider family intervention
- tailored group or individual psychological intervention
d) ECT
- can precipitate manic episode in bipolar disorder
- useful antimanic agent when severe mania and mixed states.
3
Q
COURSE AND PROGNOSIS:
A
- > 90% with single manic episode have future episodes
- about average 4 mood episodes in 10y - 5-15% have ≥4 mood episodes within 1y
- rapid cycling
- poor prognosis
- respond poorly to lithium - 10-15% completed suicide
4
Q
DYSTHYMIA AND CYCLOTHYMIA:
- Epidemiology and course
- Management
A
- Insidious onset with chronic course, often from childhood/adolescence
- significant number go on to develop more severe mood disorders - Same drugs as in depression and bipolar.
- antidepressants in mild depression can precipitate hypomania
- consider psychological therapies
5
Q
LITHIUM THERAPY:
- Indications
- Adverse effects
- Monitoring
- Lithium toxicity
A
- Prophylaxis in bipolar affective disorder, adjunct in refractory depression
- very narrow therapeutic range(0.4-1.0 mmol/L)
- nausea, vomiting, diarrhoea
weight gain
- nephrotoxicity
- thyroid enlargement, hypothyroidism
- T wave flattening/inversion n on ECG
- idiopathic intracranial hypertension
- fine tremor - Monitor every 3 months. Take reading 12h post-dose
- Monitor renal and thyroid function every 6/12.
- issue patients alert card, information booklet and record book.
- Monitor every 3 months. Take reading 12h post-dose
- > 1.5 mmol/L
- Precipitated by dehydration, diuretics(especially thiazide ones), metronidazole, ACE-inhibitors, NSAIDS, renal failure
- features: coarse tremor, hyperreflexia, acute confusion, seizure, coma
- Mx: Volume resus for mild-moderate toxicity; haemodialysis if severe toxicity; sodium bicarbonate although limited evidence for this.