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SSRIs and
Discontinuation Events
by Bob Knies RN, MSN, CEN
Depression has been described as, "a
disease state characterized by complex alterations in several CNS
neurotransmitters and receptor systems" (Leonard, 1992). Part of the
treatment involves antidepressant drugs that are known to cause adaptive
changes in several CNS receptor systems, how they effect the changes and the
intricacies of their action remain unknown. Thus, the action of
Selective Serotonin Reuptake Inhibitors
(SSRIs) cannot be simply explained as the inhibition of serotonin (5-HT)
reuptake.
Natural serotonin dysfunction has been
suggested as a cause for
depression, migraines and selected anxiety disorders (Gardner & Lynd,
1998).
Serotonin is a monoamine neurotransmitter produced by
several central cell bodies within the brain. It is a vasoconstrictor, and
inhibitory neurotransmitter especially for dopamine (Caley, 1997).
The effect of serotonin on platelet activity
has been indicated in studies of depression (Doogan & Caillard, 1988;
Muck-Seler et al. 1991; Price, 1990). These studies have shown that serotonin
affect platelet density and reduces serotonin re-uptake. The antidepressant
activity of SSRIs is not only due to their inhibition of serotonin reuptake,
term administration of these drugs to patients with depression have shown that
platelet serotonin uptake increases (Leonard, 1992).
Recently, a growing
number of discontinuation reactions have been described relating
to SSRIs. Discontinuation reactions have been reported for all the SSRIs in
clinical use today (Haddad, 1997).They are: Fluoxetine (Prozac); Fluvoxamine
(Luvox); Paroxetine (Paxil); and Sertraline (Zoloft). Although no double-blind
studies comparing discontinuation from different SSRIs have been published,
data on relative incidence of discontinuation symptoms have been gleaned from
several venues (Haddad, 1997).
The symptoms have been misdiagnosed or
diagnosed as a side effect of another disease, syndrome or medication. There
are several terms used to categorize these symptoms such as,
SSRI Discontinuation
Syndrome (Haddad, 1997), or Serotonergic Withdrawal Syndrome (Dominguez
& Goodnick, 1995). Remember, that a syndrome is a group of symptoms. The
four most common symptoms in one study included dizziness, nausea, lethargy,
and headache (Haddad, 1997). Other symptoms include anxiety, parasthesia,
confusion, tremor, sweating, insomnia, irritability, memory problems, and
anorexia.
Dilsaver and colleagues (1987), divided
symptoms of tricyclic antidepressant discontinuation into five main
groups:
- GI and general somatic distress symptoms
(lethargy, nausea, headache) often associated with anxiety or agitation.
- Sleep disturbance (insomnia, excessive
dreaming).
- Movement disorders (akathisia,
parkinsonism).
- Behavioral activation on a continuum to
mania.
- Miscellaneous symptoms (cardiac
arrhythmias).
Except for cardiac arrhythmias these symptoms
have been seen with SSRI discontinuation (Haddad, 1997).
Several novel symptoms or symptom clusters,
which fall outside the Dilsaver et al. (1987) group are discussed in the
literature, which suggests that the symptoms of SSRI discontinuation may be
more varied than those seen with tricyclic antidepressants. These include:
- Problems with balance (dizziness, ataxia,
vertigo).
- Sensory abnormalities including shock-like
sensations (paresthesia, numbness).
- Aggressive and impulsive behavior.
In summary, the data on SSRI discontinuation
reactions are derived from databases, published reports and adverse drug event
forms that have reported to national monitoring bureaus. The incidence varies
significantly from one SSRI to another, the consensus is that the majority of
discontinuation symptoms occur with paroxetine (Paxil) and lowest with
fluoxetine (Prozac), and varied with the others. Many symptoms overlap making
the diagnosis difficult. In particular, psychiatric discontinuation symptoms
(depressed mood, agitation, or irritability) may be mistaken for a relapse of
depressive symptoms (Haddad, 1997). There is a need for more methodologically
based studies to more clearly define the syndrome, determine causality and
interventions.
References:
Caley, C.F. (1997). Extrapyramidal reactions
and the selective serotonin-reuptake inhibitors. The Annals of Pharmacotherapy,
31, 1481-1489.
Dilsaver, S.C., Greden, J.F. & Snider, R.M. (1987). Antidepressant
withdrawal syndromes: Phenomenology and pathophysiology. International Clinical
Psychopharmacology, 2, 1-19.
Dominguez, R.A. & Goodnick, P.J. (1995). Adverse events after the abrupt
discontinuation of paroxetine. Pharmacotherapy, 15, (6), 778-780.
Doogan, D.P., & Caillard, V. (1988). Sertraline: A new antidepressant.
Journal of Clinical Psychiatry, 49 (supplement), 46-51.
Garder, D.M., & Lynd, L.D. (1998). Sumatriptan contraindications and the
serotonin syndrome. The Annals of Pharmacology, 32, 32-38.
Haddad, P. (1997). Newer antidepressants and the discontinuation syndrome.
Journal of Clinical Psychiatry, 57, (7), 17-21.
Leonard, B.E. (1992). Pharmacological differences of serotonin reuptake
inhibitors and possible clinical relevance. Drugs, 43, Supplement 2, 3-10.
Muck-Seler, D., Jakovlevic, M., & Deanovic, Z. (1991). Effect of
antidepressant treatment on platelet 5-HT content and relation to therapeutic
outcome in unipolar depressive patients. Journal of Affective Disorders, 23,
157-164.
Price, L.H. (1990). Serotonin reuptake inhibitors in depression and
anxiety, an overview. Annals of Clinical Psychiatry, 2, 165-172.
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