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Antipsychotic-induced rabbit syndrome: Epidemiology, management and pathophysiology
Rabbit syndrome is an antipsychotic-induced rhythmic motion of the mouth/lips, resembling the chewing movements of a rabbit. The movement consists of a vertical-only motion, at about 5Hz, with no involvement of the tongue. Usually, the involuntary movements associated with rabbit syndrome appear aft...
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Published in: | CNS drugs 2004-01, Vol.18 (4), p.213-220 |
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description | Rabbit syndrome is an antipsychotic-induced rhythmic motion of the mouth/lips, resembling the chewing movements of a rabbit. The movement consists of a vertical-only motion, at about 5Hz, with no involvement of the tongue. Usually, the involuntary movements associated with rabbit syndrome appear after a long period (in most cases months or years) of antipsychotic treatment; however, a few patients with the syndrome have had treatment histories with no antipsychotic involvement. The reported prevalence of rabbit syndrome ranges from 2.3 to 4.4% of patients treated with typical antipsychotics. There have been isolated reports of rabbit syndrome in patients treated with the atypical agents risperidone and clozapine. Patients with rabbit syndrome are most often misdiagnosed as having oral tardive dyskinesia. In such cases the key for correct diagnosis is the involvement of tardive tongue movements, which does not occur in rabbit syndrome. The treatment of rabbit syndrome is empirical, reflecting poor understanding of its neuropathology. The first step is to reduce the amount of antipsychotic treatment as much as possible. However, since, in most cases, full withdrawal of antipsychotic treatment is impossible, the syndrome cannot be completely abolished without additional measures. The next stage of treatment involves specific drugs that aim to control the syndrome. Anticholinergic drugs are the best known treatment. Rabbit syndrome does not respond to treatment with levodopa or dopamine agonists. The most striking aspect of this syndrome is its specificity. Rabbit syndrome affects only the buccal region, and within this area it involves a highly stereotyped involuntary movement. This immediately focuses attention on the basal ganglia, in particular the substantia nigra pars reticulata, which is also implicated in oral dyskinesia. Continuing neurophysiological and pharmacological research of the basal ganglia holds the key to better understanding and treatment of this syndrome in the coming years. |
doi_str_mv | 10.2165/00023210-200418040-00002 |
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The movement consists of a vertical-only motion, at about 5Hz, with no involvement of the tongue. Usually, the involuntary movements associated with rabbit syndrome appear after a long period (in most cases months or years) of antipsychotic treatment; however, a few patients with the syndrome have had treatment histories with no antipsychotic involvement. The reported prevalence of rabbit syndrome ranges from 2.3 to 4.4% of patients treated with typical antipsychotics. There have been isolated reports of rabbit syndrome in patients treated with the atypical agents risperidone and clozapine. Patients with rabbit syndrome are most often misdiagnosed as having oral tardive dyskinesia. In such cases the key for correct diagnosis is the involvement of tardive tongue movements, which does not occur in rabbit syndrome. The treatment of rabbit syndrome is empirical, reflecting poor understanding of its neuropathology. The first step is to reduce the amount of antipsychotic treatment as much as possible. However, since, in most cases, full withdrawal of antipsychotic treatment is impossible, the syndrome cannot be completely abolished without additional measures. The next stage of treatment involves specific drugs that aim to control the syndrome. Anticholinergic drugs are the best known treatment. Rabbit syndrome does not respond to treatment with levodopa or dopamine agonists. The most striking aspect of this syndrome is its specificity. Rabbit syndrome affects only the buccal region, and within this area it involves a highly stereotyped involuntary movement. This immediately focuses attention on the basal ganglia, in particular the substantia nigra pars reticulata, which is also implicated in oral dyskinesia. Continuing neurophysiological and pharmacological research of the basal ganglia holds the key to better understanding and treatment of this syndrome in the coming years.</description><identifier>ISSN: 1172-7047</identifier><identifier>EISSN: 1179-1934</identifier><identifier>DOI: 10.2165/00023210-200418040-00002</identifier><identifier>PMID: 15015902</identifier><language>eng</language><publisher>Hong Kong: Adis International</publisher><subject>Animals ; Antipsychotic Agents - adverse effects ; Biological and medical sciences ; Clozapine - adverse effects ; Diagnosis, Differential ; Drug toxicity and drugs side effects treatment ; Dyskinesia, Drug-Induced - epidemiology ; Dyskinesia, Drug-Induced - etiology ; Dyskinesia, Drug-Induced - physiopathology ; Dyskinesia, Drug-Induced - therapy ; Humans ; Medical sciences ; Pharmacology. Drug treatments ; Rabbits ; Risperidone - adverse effects ; Toxicity: nervous system and muscle</subject><ispartof>CNS drugs, 2004-01, Vol.18 (4), p.213-220</ispartof><rights>2004 INIST-CNRS</rights><rights>COPYRIGHT 2004 Wolters Kluwer Health, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c384t-ef3d4efe458ca6620354106f2f9fb523368fcc296938170a3d78c297c57a20723</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15565312$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15015902$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SCHWARTZ, Miguel</creatorcontrib><creatorcontrib>HOCHERMAN, Shraga</creatorcontrib><title>Antipsychotic-induced rabbit syndrome: Epidemiology, management and pathophysiology</title><title>CNS drugs</title><addtitle>CNS Drugs</addtitle><description>Rabbit syndrome is an antipsychotic-induced rhythmic motion of the mouth/lips, resembling the chewing movements of a rabbit. The movement consists of a vertical-only motion, at about 5Hz, with no involvement of the tongue. Usually, the involuntary movements associated with rabbit syndrome appear after a long period (in most cases months or years) of antipsychotic treatment; however, a few patients with the syndrome have had treatment histories with no antipsychotic involvement. The reported prevalence of rabbit syndrome ranges from 2.3 to 4.4% of patients treated with typical antipsychotics. There have been isolated reports of rabbit syndrome in patients treated with the atypical agents risperidone and clozapine. Patients with rabbit syndrome are most often misdiagnosed as having oral tardive dyskinesia. In such cases the key for correct diagnosis is the involvement of tardive tongue movements, which does not occur in rabbit syndrome. The treatment of rabbit syndrome is empirical, reflecting poor understanding of its neuropathology. The first step is to reduce the amount of antipsychotic treatment as much as possible. However, since, in most cases, full withdrawal of antipsychotic treatment is impossible, the syndrome cannot be completely abolished without additional measures. The next stage of treatment involves specific drugs that aim to control the syndrome. Anticholinergic drugs are the best known treatment. Rabbit syndrome does not respond to treatment with levodopa or dopamine agonists. The most striking aspect of this syndrome is its specificity. Rabbit syndrome affects only the buccal region, and within this area it involves a highly stereotyped involuntary movement. This immediately focuses attention on the basal ganglia, in particular the substantia nigra pars reticulata, which is also implicated in oral dyskinesia. Continuing neurophysiological and pharmacological research of the basal ganglia holds the key to better understanding and treatment of this syndrome in the coming years.</description><subject>Animals</subject><subject>Antipsychotic Agents - adverse effects</subject><subject>Biological and medical sciences</subject><subject>Clozapine - adverse effects</subject><subject>Diagnosis, Differential</subject><subject>Drug toxicity and drugs side effects treatment</subject><subject>Dyskinesia, Drug-Induced - epidemiology</subject><subject>Dyskinesia, Drug-Induced - etiology</subject><subject>Dyskinesia, Drug-Induced - physiopathology</subject><subject>Dyskinesia, Drug-Induced - therapy</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Pharmacology. Drug treatments</subject><subject>Rabbits</subject><subject>Risperidone - adverse effects</subject><subject>Toxicity: nervous system and muscle</subject><issn>1172-7047</issn><issn>1179-1934</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNptkUtv3CAURlHUqHn-hcpS1a7i5PI0dDeK0jZSpCzSrhGDYYbKBhc8C__72Jlp2koRC7iX812BDkIVhmuCBb8BAEIJhpoAMCyBQQ1L7widYtyoGivK3r2cSd0Aa07QWSm_ZoJRId6jE8wBcwXkFD2t4hiGMtltGoOtQ2x31rVVNut1GKsyxTan3n2p7obQuj6kLm2mq6o30Wxc7-JYmdhWgxm3adhOZX9_gY696Yq7POzn6OfXux-33-uHx2_3t6uH2lLJxtp52jLnHePSGiEIUM4wCE-88mtOKBXSW0uUUFTiBgxtGzmXjeWNIdAQeo4-7-cOOf3euTLqPhTrus5El3ZFEyDzVLmAH_fgxnROh-jTmI1dYL3CSinMJGUzdf0GNa_l4zZF58Pc_y8g9wGbUynZeT3k0Js8aQx68aT_eNKvnvSLpzn64fD03bp37d_gQcwMfDoApljT-WyiDeUfjgtOMaHPJEmZDA</recordid><startdate>20040101</startdate><enddate>20040101</enddate><creator>SCHWARTZ, Miguel</creator><creator>HOCHERMAN, Shraga</creator><general>Adis International</general><general>Wolters Kluwer Health, Inc</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope></search><sort><creationdate>20040101</creationdate><title>Antipsychotic-induced rabbit syndrome: Epidemiology, management and pathophysiology</title><author>SCHWARTZ, Miguel ; HOCHERMAN, Shraga</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c384t-ef3d4efe458ca6620354106f2f9fb523368fcc296938170a3d78c297c57a20723</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Animals</topic><topic>Antipsychotic Agents - adverse effects</topic><topic>Biological and medical sciences</topic><topic>Clozapine - adverse effects</topic><topic>Diagnosis, Differential</topic><topic>Drug toxicity and drugs side effects treatment</topic><topic>Dyskinesia, Drug-Induced - epidemiology</topic><topic>Dyskinesia, Drug-Induced - etiology</topic><topic>Dyskinesia, Drug-Induced - physiopathology</topic><topic>Dyskinesia, Drug-Induced - therapy</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Pharmacology. Drug treatments</topic><topic>Rabbits</topic><topic>Risperidone - adverse effects</topic><topic>Toxicity: nervous system and muscle</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SCHWARTZ, Miguel</creatorcontrib><creatorcontrib>HOCHERMAN, Shraga</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><jtitle>CNS drugs</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SCHWARTZ, Miguel</au><au>HOCHERMAN, Shraga</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antipsychotic-induced rabbit syndrome: Epidemiology, management and pathophysiology</atitle><jtitle>CNS drugs</jtitle><addtitle>CNS Drugs</addtitle><date>2004-01-01</date><risdate>2004</risdate><volume>18</volume><issue>4</issue><spage>213</spage><epage>220</epage><pages>213-220</pages><issn>1172-7047</issn><eissn>1179-1934</eissn><abstract>Rabbit syndrome is an antipsychotic-induced rhythmic motion of the mouth/lips, resembling the chewing movements of a rabbit. The movement consists of a vertical-only motion, at about 5Hz, with no involvement of the tongue. Usually, the involuntary movements associated with rabbit syndrome appear after a long period (in most cases months or years) of antipsychotic treatment; however, a few patients with the syndrome have had treatment histories with no antipsychotic involvement. The reported prevalence of rabbit syndrome ranges from 2.3 to 4.4% of patients treated with typical antipsychotics. There have been isolated reports of rabbit syndrome in patients treated with the atypical agents risperidone and clozapine. Patients with rabbit syndrome are most often misdiagnosed as having oral tardive dyskinesia. In such cases the key for correct diagnosis is the involvement of tardive tongue movements, which does not occur in rabbit syndrome. The treatment of rabbit syndrome is empirical, reflecting poor understanding of its neuropathology. The first step is to reduce the amount of antipsychotic treatment as much as possible. However, since, in most cases, full withdrawal of antipsychotic treatment is impossible, the syndrome cannot be completely abolished without additional measures. The next stage of treatment involves specific drugs that aim to control the syndrome. Anticholinergic drugs are the best known treatment. Rabbit syndrome does not respond to treatment with levodopa or dopamine agonists. The most striking aspect of this syndrome is its specificity. Rabbit syndrome affects only the buccal region, and within this area it involves a highly stereotyped involuntary movement. This immediately focuses attention on the basal ganglia, in particular the substantia nigra pars reticulata, which is also implicated in oral dyskinesia. Continuing neurophysiological and pharmacological research of the basal ganglia holds the key to better understanding and treatment of this syndrome in the coming years.</abstract><cop>Hong Kong</cop><cop>Auckland</cop><pub>Adis International</pub><pmid>15015902</pmid><doi>10.2165/00023210-200418040-00002</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Antipsychotic Agents - adverse effects Biological and medical sciences Clozapine - adverse effects Diagnosis, Differential Drug toxicity and drugs side effects treatment Dyskinesia, Drug-Induced - epidemiology Dyskinesia, Drug-Induced - etiology Dyskinesia, Drug-Induced - physiopathology Dyskinesia, Drug-Induced - therapy Humans Medical sciences Pharmacology. Drug treatments Rabbits Risperidone - adverse effects Toxicity: nervous system and muscle |
title | Antipsychotic-induced rabbit syndrome: Epidemiology, management and pathophysiology |
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