Opioid responsiveness in patients with neuroleptic-induced akathisia.
Identifieur interne : 005130 ( PubMed/Corpus ); précédent : 005129; suivant : 005131Opioid responsiveness in patients with neuroleptic-induced akathisia.
Auteurs : A. Walters ; W. Hening ; S. Chokroverty ; S. FahnSource :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 1986.
English descriptors
- KwdEn :
- Acetaminophen (therapeutic use), Adult, Aged, Akathisia, Drug-Induced, Antipsychotic Agents (adverse effects), Codeine (therapeutic use), Dextropropoxyphene (therapeutic use), Female, Humans, Male, Middle Aged, Naloxone (adverse effects), Psychomotor Agitation (drug therapy), Receptors, Opioid (physiology).
- MESH :
- chemical , adverse effects : Antipsychotic Agents, Naloxone.
- chemical , physiology : Receptors, Opioid.
- chemical , therapeutic use : Acetaminophen, Codeine, Dextropropoxyphene.
- drug therapy : Psychomotor Agitation.
- Adult, Aged, Akathisia, Drug-Induced, Female, Humans, Male, Middle Aged.
Abstract
Five patients with either acute or tardive neuroleptic-induced akathisia (5 weeks to 1 1/2 years duration) were videotaped before, during, and after a 2-week trial of propoxyphene (Darvon), 100 mg q.i.d., or acetaminophen (Tylenol) with 30 mg codeine, two tabs, q.i.d. Three "blinded" observers, experienced in movement disorders, rated the involuntary movements shown on the videotapes and agreed that, on opioids, all patients showed substantial to complete improvement of their stereotyped restless akathitic movements. Matching placebo was not beneficial. One patient who had improved on opioids was challenged with naloxone while on the opioids. There was a brief but severe reactivation of the akathisia. Our results suggest that opioids offer a selective therapy for patients with neuroleptic-induced akathisia and further suggest that the endogenous opiate system may be involved in patients with neuroleptic-induced akathisia.
DOI: 10.1002/mds.870010206
PubMed: 2904116
Links to Exploration step
pubmed:2904116Le document en format XML
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<author><name sortKey="Walters, A" sort="Walters, A" uniqKey="Walters A" first="A" last="Walters">A. Walters</name>
<affiliation><nlm:affiliation>Department of Neurology, UMDNJ-Rutgers Medical School, New Brunswick 08903.</nlm:affiliation>
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<author><name sortKey="Hening, W" sort="Hening, W" uniqKey="Hening W" first="W" last="Hening">W. Hening</name>
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<author><name sortKey="Chokroverty, S" sort="Chokroverty, S" uniqKey="Chokroverty S" first="S" last="Chokroverty">S. Chokroverty</name>
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<author><name sortKey="Fahn, S" sort="Fahn, S" uniqKey="Fahn S" first="S" last="Fahn">S. Fahn</name>
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<author><name sortKey="Walters, A" sort="Walters, A" uniqKey="Walters A" first="A" last="Walters">A. Walters</name>
<affiliation><nlm:affiliation>Department of Neurology, UMDNJ-Rutgers Medical School, New Brunswick 08903.</nlm:affiliation>
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<author><name sortKey="Hening, W" sort="Hening, W" uniqKey="Hening W" first="W" last="Hening">W. Hening</name>
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<author><name sortKey="Chokroverty, S" sort="Chokroverty, S" uniqKey="Chokroverty S" first="S" last="Chokroverty">S. Chokroverty</name>
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<term>Antipsychotic Agents (adverse effects)</term>
<term>Codeine (therapeutic use)</term>
<term>Dextropropoxyphene (therapeutic use)</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Naloxone (adverse effects)</term>
<term>Psychomotor Agitation (drug therapy)</term>
<term>Receptors, Opioid (physiology)</term>
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<keywords scheme="MESH" type="chemical" qualifier="adverse effects" xml:lang="en"><term>Antipsychotic Agents</term>
<term>Naloxone</term>
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<keywords scheme="MESH" type="chemical" qualifier="physiology" xml:lang="en"><term>Receptors, Opioid</term>
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<term>Aged</term>
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<front><div type="abstract" xml:lang="en">Five patients with either acute or tardive neuroleptic-induced akathisia (5 weeks to 1 1/2 years duration) were videotaped before, during, and after a 2-week trial of propoxyphene (Darvon), 100 mg q.i.d., or acetaminophen (Tylenol) with 30 mg codeine, two tabs, q.i.d. Three "blinded" observers, experienced in movement disorders, rated the involuntary movements shown on the videotapes and agreed that, on opioids, all patients showed substantial to complete improvement of their stereotyped restless akathitic movements. Matching placebo was not beneficial. One patient who had improved on opioids was challenged with naloxone while on the opioids. There was a brief but severe reactivation of the akathisia. Our results suggest that opioids offer a selective therapy for patients with neuroleptic-induced akathisia and further suggest that the endogenous opiate system may be involved in patients with neuroleptic-induced akathisia.</div>
</front>
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<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
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<ArticleTitle>Opioid responsiveness in patients with neuroleptic-induced akathisia.</ArticleTitle>
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<Abstract><AbstractText>Five patients with either acute or tardive neuroleptic-induced akathisia (5 weeks to 1 1/2 years duration) were videotaped before, during, and after a 2-week trial of propoxyphene (Darvon), 100 mg q.i.d., or acetaminophen (Tylenol) with 30 mg codeine, two tabs, q.i.d. Three "blinded" observers, experienced in movement disorders, rated the involuntary movements shown on the videotapes and agreed that, on opioids, all patients showed substantial to complete improvement of their stereotyped restless akathitic movements. Matching placebo was not beneficial. One patient who had improved on opioids was challenged with naloxone while on the opioids. There was a brief but severe reactivation of the akathisia. Our results suggest that opioids offer a selective therapy for patients with neuroleptic-induced akathisia and further suggest that the endogenous opiate system may be involved in patients with neuroleptic-induced akathisia.</AbstractText>
</Abstract>
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