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2008 Psychoeducation Workshops |
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Toronto, ON
Wednesday, Junuary 16, 2008 |
2007 Psychoeducation Workshops |
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Montreal, QC Friday, April 27, 2007
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Vancouver, BC Saturday, April 14, 2007 |
CANMAT
Bipolar Updates at
CPA CPD Institute: Collaborative Forums in Mental Health |
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Ottawa, ON
Friday, March 30, 2007 |
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Halifax, NS
Friday, April 27, 2007 |
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Vancouver, BC Friday, May 4
2007 |
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Montreal, QC Friday, June 1, 2007 |
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Toronto, ON Friday, June 8, 2007 |
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MAINTENANCE PHASE/PROPHYLACTIC
TREATMENT (see
algorithm)
If the patient has remained stable through the continuation phase of treatment,
the clinican, patient and family need to consider the value of prophylactic
mood stabilizer treatment, which can reduce morbidity and mortality risks
and improve the quality of life. The decision is relatively easier in
patients who have had recurrent episodes, where the illness is very severe,
or where there is a strong family history of bipolar disorder. Unfortunately
the vast majority of patients have recurrent episodes. It is difficult,
if not impossible, to accurately predict the very small minority of patients
diagnosed with bipolar disorder who will never have a further episode
of mood disorder during their lifetime. Hence, the recommendation for
prophylactic treatment should be the rule. There should be very good reason
not to recommend robust prophylactic treatment in a patient with a well
diagnosed bipolar disorder. Apart from the rare patient who cannot tolerate
any treatment, the other situation where the decision to recommend indefiniate
prophylaxis may be deferred is in patients with a single episode of hypomania
with no history of depression and no family history of bipolar disoder.
However, even with these patients every effort should be made to ensure
mood stabilizer treatment for about a year. When medication is being discontinued
this should be done on a gradual basis over about 3 months, but not less
than 1 month. Patients who discontinue treatment should have access to
regular monitoring, rapid reassessment and treatment if required.
Lithium is the medication with proven prophylactic efficacy in bipolar
disorder. It has been used in large numbers of patients, tested in double-blind
conditions, and used over many years. It has proven efficacy in classical,
non-rapid cycling, non-mixed states, primary bipolar disorder at serum
levels of 0.8-1.1 mmols/l. There is an increased risk of relapse at serum
levels below 0.8 mmols/l, particularly below 0.6 mmols/l. There is growing
evidence from several open studies that Divalproex has significant prophylactic
efficacy similar to Lithium. At two recent conferences, the results of
a double blind multicentre study comparing Lithium, Divalproex and placebo
in the prophylaxis of bipolar disorder showed that Divalproex and Lithium
had equal efficacy and were superior to placebo in patients with moderate
to severe illness. This study is as yet unpublished. Divalproex may also
be useful in early onset bipolar disorder and in secondary bipolar disorder.
There is some good evidence that Carbamazepine has prophylactic efficacy,
but, more recently, its efficacy has come into question in long term use
and in rapid cycling conditions. It too, like Divalproex, is useful in
secondary bipolar disorder.
Few patients manage a lifetime of bipolar disorder with monotherapy. Most
patients require short or long term polytherapy with mood stabilizers
and or ECT. A very small sub-group of patients may be totally refractory
to mood stabilizers and may require an atypical neuroleptic, like Clozapine,
or maintenance ECT.
Serum levels of medication and other monitoring/investigations of bodily
systems should be conducted as clinically indicated, but no less than
once every 6 months.
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| Over one million Canadians suffer from some form of depressive illness. |
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