Pharmacology


Drug class

Findings

Studies

Antidepressantsa

Affect instability

Binks et al. [69]

Herpertz et al. [79]

Nosè et al. [82]

Anger

Binks et al. [69]

Anxiety

Herpertz et al. [79]

Antipsychotics

(Primarily but not exclusively atypicals)

Affect instability

Lieb et al. [71]

Mercer et al. [81]

Anger

Herpertz et al. [79]

Ingenhoven et al. [80]

Lieb et al. [71]

Nosè et al. [82]

Aggression

Herpertz et al. [79]

Ingenhoven et al. [80]

Lieb et al. [71]

Nosè et al. [82]

Global functioning (weak evidence)

Binks et al. [69]

Nosè et al. [82]

Cognitive perceptual symptoms

Binks et al. [69]

Duggan et al. [78]

Herpertz et al. [79]

Ingenhoven et al. [80]

Lieb et al. [71]

Mood stabilizers

Affect instability

Ingenhoven et al. [80]

Lieb et al. [71]

Mercer et al. [81]

Nosè et al. [82]

Anxiety

Ingenhoven et al. [80]

Impulsivity/aggression

Duggan et al. [78]

Anger

Herpertz et al. [79]

Ingenhoven et al. [80]

Lieb et al. [71]

Mercer et al. [81]

Global functioning

Ingenhoven et al. [80]


aMost studies agree that antidepressants are only effective for depression when there is a current comorbid major depressive episode



Nonetheless, a few guidelines should be mentioned and these are elaborated in more detail elsewhere [89]:

1.

There should be a frank discussion of what the patient means when she uses the word depression, and if appropriate, there should be further discussion about how the depression that the patient is suffering differs from that in a major depressive episode. This discussion can address the fact that antidepressant medication effectiveness has been shown in the specific depressive entity of major depressive disorder, but there is little evidence for medication effectiveness in other “depressions.” This does not mean that medications or some medication will not be tried and might even turn out to be helpful, but the benefits one might receive will usually be quite modest at best.

 

2.

Elaborating on the point made above, the patient needs to be told that since the research for effectiveness for these drugs reveals modest effect at best, the greatest amount of progress and improvement will come from the psychotherapeutic work. This does not mean that patients will get no benefit from pharmacologic treatment, but they should work towards not idealizing the pharmacology or any particular pharmacologic agent.

 

3.

There is no data that supports the use of polypharmacy, and it is best to treat with one medication, to appreciate the targeted outcome with or for that medication, and, if after the medication has been tried for a sufficient amount of time, to stop that medication before starting another one. There is no evidence for augmentation of medications in BPD.

 

4.

It is important that all these discussions take place an appreciation by the patient that one of the diagnoses being considered is BPD. In fact such discussions should take place at the initiation of psychopharmacologic treatment [41].

The prescriber should not assume that the patient already has this knowledge, as the patient’s prior experience may have been with a psychiatrist who believed that the patient had treatment-resistant affective illness and approached treatment from the position that finding the right combination of medications is all that the patient needed in order to improve.

 



References



1.

Deutsch H. Some forms of emotional disturbance and their relationship to schizophrenia. Psychoanal Q. 1942;11:301–21.


2.

Hoch P, Polatin P. Pseudoneurotic forms of schizophrenia. Psychiatr Q. 1949;23:248–76.PubMed


3.

Klein M. Notes on some schizoid mechanisms. Int J Psychoanal. 1946;27:99–110 (Reprinted in J Psychother Prac Res. 1996;5:164–79.).PubMed


4.

Knight RP. Borderline states. Bull Menninger Clin. 1953;17:139–50.PubMed


5.

Zilboorg G. Ambulatory schizophrenia. Psychiatry. 1941;4:149–55.


6.

Chopra HD, Beatson JA. Psychotic symptoms in borderline personality disorder. Am J Psychiatry. 1986;143:1605–7.PubMed


7.

Links PS, Steiner M, Mitton J. Characteristics of psychosis in borderline personality disorder. Psychopathology. 1989;22:188–1983.PubMed


8.

Silk KR, Lohr NE, Westen D, Goodrich S. Psychosis in borderline patients with depression. J Personal Disord. 1989;3:92–100.


9.

Frosch J. The psychotic character. Clinical psychiatric considerations. Psychiatr Q. 1964;38:81–96.PubMed


10.

Barnow S, Arens EA, Sieswerda S, Dinu-Biringer R, Spitzer C, Lang S. Borderline personality disorder and psychosis: a review. Curr Psychiatry Rep. 2010;12:186–95.PubMed


11.

Goldberg SC, Schulz SC, Schulz PM, Resnick RJ, Hamer RM, Friedel RO. Borderline and schizotypal personality disorders treated with low-dose thiothixene vs placebo. Arch Gen Psychiatry. 1986;43:680–6.PubMed


12.

Leone NF. Response of borderline patients to loxapine and chlorpromazine. J Clin Psychiatry. 1982;43:148–50.PubMed


13.

Soloff PH, George A, Nathan RS, Schulz PM, Ulrich RF, Perel JM. Progress in pharmacotherapy of borderline disorders. A double-blind study of amitriptyline, haloperidol, and placebo. Arch Gen Psychiatry. 1986;43:691–7.PubMed


14.

American Psychiatric Association. Diagnostic and statistical manual of mental disorders. 5th ed. Arlington: American Psychiatric Publishing; 2013.


15.

Schmideberg M. The treatment of psychopaths and borderline patients. Am J Psychother. 1947;1:45–70.PubMed


16.

Kernberg OF. Borderline personality organization. J Am Psychoanal Assoc. 1967;15:641–85.PubMed


17.

Grinker RR, Werble G, Drye RC. The borderline syndrome. A behavioral study of ego functions. New York: Basic Books; 1968.

Jun 3, 2017 | Posted by in NEUROLOGY | Comments Off on Pharmacology

Full access? Get Clinical Tree

Get Clinical Tree app for offline access