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An open trial of valproate in borderline
personality disorder.
Stein DJ, Simeon D, Frenkel
M, Islam MN, Hollander E.
Department of Psychiatry,
University of Stellenbosch, Tygerberg, South Africa.
BACKGROUND:
Target symptoms in pharmacotherapy of borderline personality disorder
include mood instability, anxiety, and impulsivity. Valproate appears
useful for the treatment of these target symptoms in several disorders,
and carbamazepine has been found effective for such symptoms in
borderline personality disorder. We therefore conducted a preliminary
open-label trial of valproate in borderline personality disorder.
METHOD: Eleven patients who met DSM-III-R criteria for borderline
personality disorder were entered into an 8-week study of valproate.
Exclusion criteria included current major depression or major medical
disorder. All patients were in psychotherapy at least once a week for a
minimum of 8 weeks prior to starting medication. Valproate was increased
as tolerated to reach blood levels of 50 to 100 micrograms/mL.
Clinician- and self-rated scales were completed each week. RESULTS:
Three patients did not complete the study. Of completers, 4 of 8
patients were responders ("much less" or "less") on clinician-rated
change scores for overall pathology and for mood. Three of 8 patients
were responders on change scores for anxiety, anger, impulsivity, and
rejection sensitivity. There was a significant (p = .03) decrease in
total Symptom Checklist-90 scores between the start and end of the
trial. On the Overt Aggression Scale (Modified), total other-directed
assault did not significantly decrease, but there was a significant (p =
.02) decrease in global subjective irritability. CONCLUSION: Valproate
led to overall improvement in 50% of a small sample of borderline
personality disorder patients who completed an 8-week open trial. The
medication was modestly helpful for mood and irritability as well as for
anxiety, anger, rejection sensitivity, and impulsivity, but specific
therapeutic effects varied from patient to patient. More extensive
controlled trials of anticonvulsants for impulsive personality disorders
are warranted.
Publication Types:
PMID: 7592502 [PubMed - indexed for
MEDLINE]
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