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1. |
GUEST EDITORIALCombining Drugs and Electroconvulsive TherapySafe and/or Effective? |
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Journal of Clinical Psychopharmacology,
Volume 13,
Issue 2,
1993,
Page 85-86
MAX FINK,
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ISSN:0271-0749
出版商:OVID
年代:1993
数据来源: OVID
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2. |
Acute Interactions of Buprenorphine with Intravenous Cocaine and MorphineAn Investigational New Drug Phase I Safety Evaluation |
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Journal of Clinical Psychopharmacology,
Volume 13,
Issue 2,
1993,
Page 87-99
SIEW TEOH,
JACK MENDELSON,
NANCY MELLO,
JOHN KUEHNLE,
PRADIT SINTAVANARONG,
ERIN RHOADES,
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摘要:
Recent preclinical and clinical studies suggest that buprenorphine, an opioid mixed agonist-antagonist, may be useful for the treatment of dual dependence on cocaine and opiates. This report describes an inpatient clinical evaluation of the safety of buprenorphine alone and in combination with single doses of cocaine and morphine. Twenty subjects with a DSM-III-R diagnosis of concurrent cocaine and opioid dependence were randomly assigned to maintenance treatment with single daily doses of 4 or 8 mg of sublingual buprenorphine for 21 days. Side effects and vital signs were evaluated every day once every 8 hours and for 2 hours after daily buprenorphine administration. The physiologic effects of a single-blind challenge dose of cocaine (30 mg intravenously), morphine (10 mg intravenously), and intravenous saline placebo were measured before and during buprenorphine maintenance. Before buprenorphine maintenance, subjects underwent methadone detoxification followed by a 9-day drugfree period. Three baseline single-blind challenge dose studies were conducted on study days 7, 8, and 9 during the drug-free period. Cardiovascular responses to cocaine and to morphine were equivalent under drugfree and buprenorphine maintenance conditions. Respiration and temperature changes in response to cocaine were also equivalent before and during buprenorphine maintenance. Respiratory rates were slightly lower after morphine administration during maintenance on 8 mg of buprenorphine, but this was not statistically significant. Mild opioid agonist-like side effects were reported during buprenorphine induction and maintenance. These included headache, sedation, nasal discharge, abdominal discomfort, and anxiety. Most opioid agonist side effects decreased within 12 to 14 days. An electrocardiogram and blood chemistry measures were normal before and during buprenorphine maintenance. These data suggest that daily maintenance on buprenorphine is not associated with adverse side effects or toxic interactions with a single acute dose of intravenous cocaine or morphine.
ISSN:0271-0749
出版商:OVID
年代:1993
数据来源: OVID
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3. |
Comparison of the Effects of Zolpidem and Triazolam on Memory Functions, Psychomotor Performances, and Postural Sway in Healthy Subjects |
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Journal of Clinical Psychopharmacology,
Volume 13,
Issue 2,
1993,
Page 100-106
IVAN BERLIN,
DOMINIQUE WAROT,
THIERRY HERGUETA,
PATRICIA MOLINIER,
CHRISTOPHE BAGOT,
ALAIN PUECH,
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摘要:
Zolpidem is a rapid-onset, short-duration imidazopyridine hypnotic drug and is specific agonist of the omega-1 (BZD1) receptors. Its hypnotic characteristics resemble those of triazolam. The aims of this study were to assess the effects of Zolpidem on memory (the main objective), psychomotor performances, and postural sway (secondary objectives) in 18 healthy subjects and to compare them with those of triazolam and placebo. Short-and long-term memory (paired words associate and pictures test), psychomotor performances (critical flicker fusion frequency, choice reaction time, digit symbol substitution test), and postural sway were evaluated before and 1.5, 4, 6, and 8 h after the administration of a single dose of Zolpidem (10 mg), triazolam (0.25 mg), and placebo. For each assessment, the maximal effect for both hypnotic drugs occurred 1.5 hour after intake. Both drugs decreased psychomotor performance, impaired memory, and increased postural sway. The effects of both hypnotic agents were short lasting, and no alterations were found 6 and 8 hours, respectively, after drug intake. No clinically relevant differences were found between Zolpidem and triazolam for memory, psychomotor performance, postural sway, or adverse effects. It may be concluded that Zolpidem, like triazolam, impairs short- and long-term memory, psychomotor performances, and postural sway and that these effects are of short duration.
ISSN:0271-0749
出版商:OVID
年代:1993
数据来源: OVID
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4. |
Open Prospective Trial of Fluoxetine for Posttraumatic Stress Disorder |
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Journal of Clinical Psychopharmacology,
Volume 13,
Issue 2,
1993,
Page 107-113
LINDA NAGY,
C. MORGAN,
STEVEN SOUTHWICK,
DENNIS CHARNEY,
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摘要:
Twenty-seven patients with combat-related posttraumatic stress disorder (PTSD) entered an open, prospective, 10-week trial of fluoxetine, beginning with 20 mg/day and increasing to 80 mg/ day until response was optimal or side effects prohibited dose increase. Nineteen patients completed 3 or more weeks and were included in the data analysis. Total Clinician-Administered PTSD Scale scores decreased from a mean of 64.5 at baseline to 42.7 at endpoint (F=7.17p< 0.001), and improvement was significant in each of the three PTSD subscales (reexperiencing, avoidance/ numbing, and hyperarousal). Depression and anxiety ratings showed similar improvements, and suicidally ratings did not increase. Global improvement scores decreased from 4.0 at baseline to 2.67 at endpoint (F= 12.08,p< 0.001); however, improvement in social and occupational functioning was minimal. Appreciable improvement tended to occur after 6 weeks, suggesting that higher fluoxetine doses and/or duration than that used for depression may be indicated in this population. Panic attack frequency decreased by at least 50% in six of eight patients who kept panic diaries. The high dropout rate reflects problems with side effects, anxiety symptoms, external events, and substance abuse. Our data suggest that fluoxetine is effective in reducing reexperiencing, avoidance, and hyperarousal symptoms of PTSD, and this improvement is independent of comorbid panic disorder. In addition, fluoxetine appears to be effective in reducing panic attacks in PTSD patients. The efficacy of fluoxetine for some PTSD patients is interesting in light of emerging neuropharmaco-logic data suggesting serotonergic dysregulation in some PTSD patients. Noradrenergic hypotheses are also discussed. The findings should be confirmed by double-blind, placebo-controlled studies.
ISSN:0271-0749
出版商:OVID
年代:1993
数据来源: OVID
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5. |
Imipramine Is Effective After Unsuccessful Cognitive TherapySequential Use of Cognitive Therapy and Imipramine in Depressed Outpatients |
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Journal of Clinical Psychopharmacology,
Volume 13,
Issue 2,
1993,
Page 114-119
JONATHAN STEWART,
MARY MERCIER,
VITO AGOSTI,
MARY GUARDINO,
FREDERIC QUITKIN,
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摘要:
As a partial test of whether the same or different patients benefit from cognitive therapy and tricyclic antidepressant agents, depressed outpatients first received cognitive therapy, then nonresponders were treated with either imipramine or placebo. If the two treatments were effective for the same subgroup of patients, imipramine should not be more effective than placebo because potential responders should already have been removed by treatment with cognitive therapy. Alternatively, if cognitive therapy and imipramine are effective for different subtypes of depressive disorder, then imipramine ought to be more effective than placebo for patients failing to benefit from cognitive therapy because some potential imipramine failures would already have been removed. Thirty-six depressed outpatients were treated with weekly cognitive therapy for 16 weeks with 17 (47%) responding. Nonresponders were then randomly assigned to imipramine or placebo for 6 weeks to a maximum dose of 300 mg of imipramine per day. Of 12 patients completing the double-blind medication trial, all 5 assigned to imipramine had a clear-cut response, whereas none of the other seven benefited from placebo (χ2= 12.00;p= 0.001). Although the numbers are small, these results suggest rejection of the hypothesis that imipramine is effective for the same subpopulation of depressed patients as is cognitive therapy.
ISSN:0271-0749
出版商:OVID
年代:1993
数据来源: OVID
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6. |
The Assessment and Clinical Implications of Haloperidol Acute‐Dose, Steady‐State, and Withdrawal Pharmacokinetics |
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Journal of Clinical Psychopharmacology,
Volume 13,
Issue 2,
1993,
Page 120-127
VIKRAM KHOT,
C. DeVANE,
ESA KORPI,
DIANE VENABLE,
LLEWELLYN BIGELOW,
RICHARD WYATT,
DARRELL KIRCH,
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摘要:
In order to evaluate comprehensively haloperidol pharmacokinetics under fixed-dose treatment conditions, psychiatric patients were studied after treatment with an acute dose, during maintenance therapy, and after withdrawal from haloperidol following steady-state conditions. After single doses, haloperidol appeared rapidly in serum, achieving peak concentration at a mean of 4.5 hours. The range of observed elimination half-life was broad, between 8.5 and 66.6 hours, with a mean of 19.5 hours. Under conditions of chronic dosing, serial measurements of steady-state serum concentration revealed intrapatient coefficients of variation between 2 and 72%. The mean for all patients was 26.4%. Body clearance decreased nonsignificantly, and elimination half-life increased significantly after chronic dosing compared with kinetic parameters determined after a single dose. The concentration of haloperidol in serum obtained at 8 hours after a single dose correlated most strongly (r= 0.73;p< 0.0001) with steady-state concentration resulting from chronic dosing. A value of 4 ng/ml or lower determined 8 hours after a single oral dose of 0.2 mg/kg identified patients who did not accumulate haloperidol during chronic dosing of 0.4 mg/kg per day above a presumed therapeutic range for haloperidol of 5 to 15 ng/ml. The implications of these data for the clinical use of haloperidol are discussed.
ISSN:0271-0749
出版商:OVID
年代:1993
数据来源: OVID
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7. |
Prolongation of the Corrected QT and Torsades de Pointes Cardiac Arrhythmia Associated with Intravenous Haloperidol in the Medically III |
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Journal of Clinical Psychopharmacology,
Volume 13,
Issue 2,
1993,
Page 128-132
ERAN METZGER,
ROHN FRIEDMAN,
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摘要:
Consultation psychiatrists are frequently called upon by their medical and surgical colleagues to assist in the management of agitated, delirious patients in the intensive care unit. Intravenous haloperidol has a reputation for safe and effective sedation of these patients and has been found to be free of many of the dangerous anticholinergic and cardiac side effects of the lower-potency neuroleptics. The authors report the cases of three patients who developed torsades de pointes arrhythmia or lengthening of the Q-T interval during treatment with intravenous haloperidol. The cases suggest that the use of intravenous haloperidol should be accompanied by cardiac monitoring and that risk factors for torsades de pointes during haloperidol treatment may include dilated cardiomyopathy and a history of alcohol abuse.
ISSN:0271-0749
出版商:OVID
年代:1993
数据来源: OVID
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8. |
A Systematic Approach to the Classification and Pharmacotherapy of Nonpsychotic Major Depression and Dysthymia |
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Journal of Clinical Psychopharmacology,
Volume 13,
Issue 2,
1993,
Page 133-144
DAVID OSSER,
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摘要:
Nonpsychotic depressive and dysthymic states are reclassified and reorganized in order to maximize relevance to clinical psychopharmacology. In the initial phase of assessment, patients are divided into two easily recognized categories: moodnonreactive (autonomous) depression and mood-reactive depression. After family and past history of response and cost of drug are considered, a tricyclic antidepressant is usually selected for autonomous depression patients, and mood-reactive depression patients are initially given a serotonin reuptake inhibitor. Nonresponders from either category are changed to the alternative medication or have it added to their first drug. Nonresponders to both of these initial trials are then assessed for the presence of atypical depression symptoms by the Columbia criteria. If these symptoms are present, the patients may be offered a third medication trial with a monoamine oxidase inhibitor. Bupropion could be the choice if the monoamine oxidase inhibitor cannot be given expeditiously. This completes the initial assessment and treatment phase.Autonomous and mood-reactive patients who do not respond to this sequence of interventions are then reassessed for the presence of characterologic syndromes and comorbidity with some frequently encountered conditions. These may determine the choice of medication and the prognosis for a positive result from the next choices selected. When possible, specific recommendations are given for the various situations.
ISSN:0271-0749
出版商:OVID
年代:1993
数据来源: OVID
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9. |
Gepirone and the Treatment of Panic DisorderAn Open Study |
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Journal of Clinical Psychopharmacology,
Volume 13,
Issue 2,
1993,
Page 145-148
JOHN PECKNOLD,
LORENZ LUTHE,
MARIE-HÉLÈNE SCOTT-FLEURY,
STEPHEN JENKINS,
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摘要:
Gepirone, an azapirone, is a potent 5-hydroxy-tryptamine 1A (5-HTIA) agonist. We report an uncontrolled 6-week study in 21 patients (4 men, 17 women: mean age, 36.71 years) with a concurrent DSM-HI-R diagnosis of generalized anxiety disorder and panic disorder with agoraphobia. After a 2-week medication-free period, patients were started on 2 mg of gepirone per day increasing over 3 weeks to 12 mg/day. Three patients dropped out in the first week, and one patient violated the protocol. They were therefore excluded from analysis. Two patients who dropped out at weeks 4 and 5 because they found the treatment ineffective were included. Twelve of the 17 patients (70.6%) had at least a 50% reduction in their panic attacks by week 6, and 9 of them had at least a 50% reduction by week 3. Ten patients had “0” panic attacks by week 6 (59%). On the Hamilton Anxiety Scale, 65% had a 50% or greater reduction in total score, mostly beginning in week 1. On Global Assessment, by week 6,11 were much improved or better (65%). Adverse effects were rare and consisted of stomach upset, dizziness, or headaches. This preliminary study suggests the possible efficacy of gepirone in panic disorder.
ISSN:0271-0749
出版商:OVID
年代:1993
数据来源: OVID
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10. |
Erratum |
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Journal of Clinical Psychopharmacology,
Volume 13,
Issue 2,
1993,
Page 149-149
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PDF (421KB)
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ISSN:0271-0749
出版商:OVID
年代:1993
数据来源: OVID
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