Rational polypharmacy in the
bipolar affective disorders
by
Post RM, Ketter TA, Pazzaglia PJ, Denicoff K,
George MS, Callahan A,
Leverich G, Frye M.
Biological Psychiatry Branch,
NIMH, Bethesda, MD 20892-1272, USA.
Epilepsy Res Suppl 1996; 11:153-80
ABSTRACT
Bipolar affective illness represents a syndrome not readily treated by single
agents. Approximately 50% of patients are inadequately responsive to lithium and
the majority of patients require supplemental antidepressants, antimanic,
antipsychotic or hypnotic medications. These traditional adjunctive medications
are associated with potential problems. Antidepressants may precipitate mania
(at a rate about double that of placebo) or cause cycle acceleration.
Neuroleptics may be associated with either more profound or longer depressive
phases, and clearly increase the risk of tardive dyskinesia, to which bipolar
patients appear particularly predisposed. Moreover, there are subgroups of
patients who are known to be poorly responsive to lithium. These include
patients with rapid cycling, dysphoric mania, co-morbid drug or alcohol abuse, a
pattern of depression-mania-well interval (D-M-I as opposed to the M-D-I
pattern), and patients without a family history of bipolar illness in
first-degree relatives. There is increasing recognition that the anticonvulsants
carbamazepine and valproate are effective alternatives or adjuncts to lithium in
the acute and long-term treatment of bipolar illness. Ideally, one would want to
assess whether patients who were unresponsive to lithium were responsive to an
anticonvulsant alone prior to utilizing lithium in addition to anticonvulsant
combination therapy. However, from the clinical perspective, it is often more
expedient to use an anticonvulsant adjunctively to lithium to assess the
efficacy of this combination and establish mood stabilization. When lithium is
not discontinued, the increased morbidity during lithium withdrawal also would
not occur and would not confound the evaluation of the new agent. We suggest the
initial use of acute adjuncts to lithium with the anticonvulsants carbamazepine
or valproate (instead of neuroleptics) so that their efficacy can be assessed in
the individual's acute episode, with the likelihood of a positive response in
longer-term prophylaxis. Hypnotic benzodiazepines with anticonvulsant
properties, such as clonazepam or lorazepam, are often used to help to induce
sleep in escalating bipolar patients, and may be useful adjuncts as well.
Patients who were inadequately responsive to either carbamazepine or valproate
alone may be responsive to the anticonvulsant combination. In a similar fashion,
one can also utilize several mood-stabilizing drugs (lithium and an
anticonvulsant such as carbamazepine or valproate) in the treatment of
depressive breakthroughs, and then augment this combination (if necessary) with
a catecholamine-active antidepressant such as bupropion or a serotonin-selective
reuptake inhibitor (SSRI) such as fluoxetine, paroxetine, sertraline or if
necessary a monoamine oxidase inhibitor (MAOI). Once the patient has responded
to a combination of drugs, it becomes problematic to decide whether the last
agent added was the crucial ingredient in helping the patient achieve remission
or that remission might have occurred with this agent alone. A conservative
approach would have merit in patients who are finally stabilized on complex
polypharmacy regimens only after many years of sequential trials; in this
instance, the potential risk of re-exacerbating the illness with a taper of one
of the drugs in the regimen. Rational polypharmacy should thus be implemented
with careful delineation of the prior course of illness (typically using life
chart methodology) and targeted treatment outcomes titrated against side
effects, using sequential clinical trials in individual patients who have not
adequately responded to monotherapy. In this fashion, it is hoped that
pharmacodynamic differences among agents can be maximized and pharmacokinetic
and side effects minimized.
SSRIs
Mania
Lithium
Bipolar II
Cannabis
Valproate
Bupropion
Cyclothymia
Carbamazapine
Bipolar disorders
Prozac for bipolars
Bipolar depression
Bipolar polypharmacy
Bipolar versus unipolar
Social phobia and bipolarity
Ankyrin 3/bipolar disorder
Rapid-cycling bipolar disorder
Drugs which may cause mania
Melancholic bipolar depression
Mood stabilizers for bipolar disorder
Omega 3 fatty acids in bipolar disorder
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