0
1
Letter to the Editor   |    
Clonidine Treatment for Hallucinogen Persisting Perception Disorder
ARTURO G. LERNER, M.D.; BORIS FINKEL, M.D.; IGOR OYFFE, M.D., PH.D.; INNA MERENZON, M.D.; MIRCEA SIGAL, M.D.
Am J Psychiatry 1998;155:1460-1460.
View Article Information
Letters to the Editor
To the Editor: We have successfully treated with clonidine three patients who met DSM-IV criteria for hallucinogen persisting perception disorder. We report the most representative case.
Mr. A was a 25-year-old man with a previous history of benzodiazepine, "ecstasy," LSD, and cannabis abuse. There was no other significant medical or psychiatric history. Mr. A reported being bothered by flashbacks of flashes of colors, trails of images of moving objects, body image distortion, and spontaneous imagery. These episodes usually lasted between a fraction of a second and a few minutes. They were severe enough to cause clinically significant distress, anxiety, and impairment in social and occupational functioning. After obtaining written consent, we started Mr. A on a regimen of 0.025 mg of clonidine three times a day. After 1 month of treatment, he reported considerable improvement in both the number of flashbacks and the accompanying anxiety. Over next 2 months, symptoms disappeared completely; we then discontinued the clonidine. Mr. A remained symptom free over a 6-month follow-up period.
Benzodiazepines appear to be useful for some patients who suffer from hallucinogen persisting perception disorder (1), but its abuse potential might be troublesome for those with substance-related disorders.
It was hypothesized that the hyperarousal, traumatic nightmares, and flashbacks that characterize posttraumatic stress syndrome (PTSD) are related to long-term potentiation of locus ceruleus pathways to the hippocampus and amygdala (2). Pharmacological agents that can dampen the hyperarousal associated with PTSD should have a palliative if not a curative role (3). Clonidine suppresses locus ceruleus activity and reduces adrenergic activity (4); thus, it appears to be helpful in the treatment of PTSD (5). We think that LSD-related flashbacks, like PTSD-related flashbacks, may be associated with excessive sympathetic nervous activity; therefore, clonidine may alleviate this condition.
In our experience, clonidine at low doses is well tolerated, has minimal side effects, and has no potential for abuse.
We suggest that clonidine should be considered as an option for certain patients who suffer from LSD-related flashbacks.
Abraham HD: Visual phenomenology of the LSD flashbacks. Arch Gen Psychiatry  1983; 40:884–889[PubMed]
 
van der Kolk B, Greenberg M, Boyd H, Krystal J: Inescapable shock, neurotransmitters, and addiction to trauma: toward a psychobiology of posttraumatic stress. Biol Psychiatry  1985; 20:314–325[PubMed][CrossRef]
 
Friedman MJ: Toward rational pharmacotherapy for posttraumatic stress disorder: an interim report. Am J Psychiatry  1988; 145:281–285 [PubMed]
 
Davidson J: Drug therapy for post-traumatic stress disorder. Br J Psychiatry  1992; 160:309–314[PubMed][CrossRef]
 
Kolb L, Burris BC, Griffiths S: Propranolol and clonidine in the treatment of post traumatic disorders of war, in Post Traumatic Stress Disorder: Psychological and Biological Sequelae. Edited by van der Kolk BA. Washington, DC, American Psychiatric Press, 1984, pp 97–107
 
+
Abraham HD: Visual phenomenology of the LSD flashbacks. Arch Gen Psychiatry  1983; 40:884–889[PubMed]
 
van der Kolk B, Greenberg M, Boyd H, Krystal J: Inescapable shock, neurotransmitters, and addiction to trauma: toward a psychobiology of posttraumatic stress. Biol Psychiatry  1985; 20:314–325[PubMed][CrossRef]
 
Friedman MJ: Toward rational pharmacotherapy for posttraumatic stress disorder: an interim report. Am J Psychiatry  1988; 145:281–285 [PubMed]
 
Davidson J: Drug therapy for post-traumatic stress disorder. Br J Psychiatry  1992; 160:309–314[PubMed][CrossRef]
 
Kolb L, Burris BC, Griffiths S: Propranolol and clonidine in the treatment of post traumatic disorders of war, in Post Traumatic Stress Disorder: Psychological and Biological Sequelae. Edited by van der Kolk BA. Washington, DC, American Psychiatric Press, 1984, pp 97–107
 
+
+

CME Activity

There is currently no quiz available for this resource. Please click here to go to the CME page to find another.
Submit a Comments
Please read the other comments before you post yours. Contributors must reveal any conflict of interest.
Comments are moderated and will appear on the site at the discertion of JBJS editorial staff.

* = Required Field
(if multiple authors, separate names by comma)
Example: John Doe



Related Content
Books
Helping Parents, Youth, and Teachers Understand Medications for Behavioral and Emotional Problems: A Resource Book of Medication Information Handouts, 3rd Edition > Chapter 14.  >
What Your Patients Need to Know About Psychiatric Medications, 2nd Edition > Chapter 84.  >
The American Psychiatric Publishing Textbook of Substance Abuse Treatment, 4th Edition > Chapter 19.  >
The American Psychiatric Publishing Textbook of Psychopharmacology, 4th Edition > Chapter 63.  >
Gabbard's Treatments of Psychiatric Disorders, 4th Edition > Chapter 15.  >
Topic Collections
Psychiatric News