|
1. |
Clozapine and Fluvoxamine, a Curious Complexity |
|
Journal of Clinical Psychopharmacology,
Volume 18,
Issue 2,
1998,
Page 101-102
Richard I. Shader,
David J. Greenblatt,
Preview
|
|
ISSN:0271-0749
出版商:OVID
年代:1998
数据来源: OVID
|
2. |
Therapeutic Equivalence of Risperidone Given Once Daily and Twice Daily in Patients With Schizophrenia |
|
Journal of Clinical Psychopharmacology,
Volume 18,
Issue 2,
1998,
Page 103-110
N.P.V. Nair,
Preview
|
|
摘要:
A study was conducted to determine whether once-daily administration of risperidone was as effective and safe as twice-daily administration. In a double-blind 6-week trial, 211 patients with acute exacerbation according to DSM-III-R criteria were randomly assigned to receive risperidone at 8 mg once daily or 4 mg twice daily. The primary efficacy measure was the treatment response rate, defined as a 20% or greater reduction in total Positive and Negative Syndrome Scale (PANSS) scores. Severity of extrapyramidal symptoms was assessed by the Extrapyramidal Symptom Rating Scale. The percentage of patients who showed a treatment response at endpoint was not significantly different between groups (76%, once-daily; 72%, twice-daily), nor was the median time to first treatment response (14 days, both groups). Significant reductions in PANSS total and subscale scores and PANSS-derived Brief Psychiatric Rating Scale were observed in both groups, with no significant between-group differences. Extrapyramidal Symptom Rating Scale scores did not differ significantly between groups. There were no clinically relevant changes in vital signs, electrocardiograms, or clinical laboratory test results in either group. Gradual dosage titration over the first 3 days of treatment was well-tolerated in both groups. The median trough plasma concentrations of risperidone, 9-hydroxyrisperidone, and risperidone plus 9-hydroxyrisperidone were significantly lower with once-daily than with twice-daily administration; median plasma concentrations measured within the first 8 hours after administration tended to be higher with once-daily administration. These differences did not affect the safety and efficacy of risperidone. Risperidone given once daily at 8 mg is as effective as twice-daily administration of 4 mg in the treatment of acute exacerbations of schizophrenia. Both regimens were equally well-tolerated. (J Clin Psychopharmacol 1998;18:103-110)
ISSN:0271-0749
出版商:OVID
年代:1998
数据来源: OVID
|
3. |
Risperidone Versus Haloperidol and Amitriptyline in the Treatment of Patients With a Combined Psychotic and Depressive Syndrome |
|
Journal of Clinical Psychopharmacology,
Volume 18,
Issue 2,
1998,
Page 111-120
Florian Muller-Siecheneder,
Matthias J. Muller,
Andreas Hillert,
Armin Szegedi,
Hermann Wetzel,
Otto Benkert,
Preview
|
|
摘要:
In a multicenter, double-blind, parallel group trial, the efficacy of risperidone (RIS) was compared with a combination of haloperidol and amitriptyline (HAL/AMI) over 6 weeks in patients with coexisting psychotic and depressive symptoms with either a schizoaffective disorder, depressive type, a major depression with psychotic features, or a nonresidual schizophrenia with major depressive symptoms according to DSM-III-R criteria. A total of 123 patients (62 RIS; 61 HAL/AMI) were included; the mean daily dosage at endpoint was 6.9 mg RIS versus 9 mg HAL combined with 180 mg AMI. Efficacy results for those 98 patients (47 RIS; 51 HAL/AMI) who completed at least 3 weeks of double-blind treatment revealed in both treatment groups large reductions in the Positive and Negative Syndrome Scale-derived Brief Psychiatric Rating Scale (RIS 37%; HAL/AMI 51%) and the Bech-Rafaelsen Melancholia Scale total scores (RIS 51%; HAL/AMI 70%). The reductions in the Brief Psychiatric Rating Scale and the Bech-Rafaelsen Melancholia Scale scores in the total group were significantly larger in the HAL/AMI group than in the RIS group (p <0.01), mostly because of significant differences in the subgroup of patients suffering from depression with psychotic features, whereas treatment differences in the other diagnostic subgroups were not significant. The incidence of extrapyramidal side effects as assessed by the Extrapyramidal Symptom Rating Scale was slightly higher under RIS (37%) than under HAL/AMI (31%). Adverse events were reported by 66% of RIS and 75% of HAL/AMI patients. The results of this trial suggest that the therapeutic effect of HAL/AMI is superior to RIS in the total group of patients with combined psychotic and depressive symptoms. However, subgroup differences have to be considered. (J Clin Psychopharmacol 1998;18:111-120)
ISSN:0271-0749
出版商:OVID
年代:1998
数据来源: OVID
|
4. |
A Controlled Trial of Ondansetron, a 5-HT3Antagonist, in Benzodiazepine Discontinuation |
|
Journal of Clinical Psychopharmacology,
Volume 18,
Issue 2,
1998,
Page 121-131
Myroslava K. Romach,
Howard L. Kaplan,
Usoa E. Busto,
Gail Somer,
Edward M. Sellers,
Preview
|
|
摘要:
Serotonin is implicated in the etiology of anxiety disorders and in the anxiolytic actions of benzodiazepines.Preclinical studies with 5-HT (33 months entered, and 97 completed a randomized double-blind discontinuation treatment program during which they received either ondansetron 2 mg twice daily or placebo and flexibly tapered their benzodiazepine over a 6-week period. There were no significant differences between the patients who had entered and completed treatment. Three weeks postmedication, 63% of the patients discontinued use of benzodiazepine. The percentage of reduction of benzodiazepine daily dosage at all time points in the treatment trial was similar for the ondansetron and placebo groups. Ondansetron had no significant effects on severity of withdrawal symptoms or levels of anxiety. High placebo response may have prevented detection of an ondansetron effect. At 1 year follow-up, 68% of patients reported that they stopped using benzodiazepine. Patient characteristics were more important than ondansetron in tapered benzodiazepine discontinuation. (J Clin Psychopharmacol 1998;18:121-131)
ISSN:0271-0749
出版商:OVID
年代:1998
数据来源: OVID
|
5. |
Imipramine in the Treatment of Social Phobia |
|
Journal of Clinical Psychopharmacology,
Volume 18,
Issue 2,
1998,
Page 132-135
H. Blair Simpson,
Franklin R. Schneier,
Raphael B. Campeas,
Randall D. Marshall,
Brian A. Fallon,
Sharon Davies,
Donald F. Klein,
Michael R. Liebowitz,
Preview
|
|
摘要:
We report the results of an 8-week open trial of imipramine in 15 patients with social phobia. Nine patients completed the trial; six dropped out early because of adverse effects. The mean reduction in the Liebowitz Social Anxiety Scale was 15% and 18% for the intent-to-treat and completer groups, respectively; the overall response rate (based on the Clinical Global Impression Scale of 1 or 2, very much or much improved) was 20% (3/15) and 22% (2/9), respectively. The results from this open trial do not support the efficacy of imipramine as a treatment for social phobia. (J Clin Psychopharmacol 1998;18:132-135)
ISSN:0271-0749
出版商:OVID
年代:1998
数据来源: OVID
|
6. |
A Meta-Analysis of the Effects of Venlafaxine on Anxiety Associated With Depression |
|
Journal of Clinical Psychopharmacology,
Volume 18,
Issue 2,
1998,
Page 136-144
Richard L. Rudolph,
Richard Entsuah,
Rohini Chitra,
Preview
|
|
摘要:
Venlafaxine is the first member of a novel class of antidepressants that inhibits the reuptake of both serotonin and norepinephrine.Clinical trials of venlafaxine have demonstrated its efficacy and safety in the treatment of patients diagnosed with major depression. Because patients who have depression also often have anxiety, recent investigations have focused on determining whether venlafaxine can relieve symptoms of anxiety in depressed patients. We performed a pooled analysis of six short-term trials of venlafaxine, retrospectively measuring anxiety in anxious depressed patients using the Hamilton Rating Scale for Depression (HAM-D), Anxiety/Somatization factor and Anxiety Psychic item scores. Three studies were placebo-controlled, and three were placebo- and active-drug-controlled; active controls were imipramine in two trials and trazodone in the third trial. Patients were categorized as having anxiety accompanying depression if baseline HAM-D Anxiety Psychic item scores were 2 or greater. Anxious depressed patients treated with venlafaxine showed greater improvement than those treated with placebo beginning at week 3, according to the HAM-D Anxiety/Somatization factor score, and beginning at week 1, according to the Anxiety Psychic item score. Both effects were maintained at week 6 of treatment (and at week 12 in the one study of longer duration). Finally, treatment with venlafaxine resulted in a highly significant (p <or= to 0.001) improvement in depression scores in patients who were anxious at baseline, compared with placebo-treated patients. The results of this analysis demonstrate that venlafaxine is more effective than placebo in reducing symptoms of anxiety in depressed patients and suggest that venlafaxine may afford a monotherapy option for treating patients who have a comorbid diagnosis of depression with anxiety. (J Clin Psychopharmacol 1998;18:136-144)
ISSN:0271-0749
出版商:OVID
年代:1998
数据来源: OVID
|
7. |
Nefazodone in Major DepressionAdjunctive Benzodiazepine Therapy and Tolerability |
|
Journal of Clinical Psychopharmacology,
Volume 18,
Issue 2,
1998,
Page 145-153
Karl Rickels,
Edward Schweizer,
W. George Case,
Nicholas DeMartinis,
David J. Greenblatt,
Laura A. Mandos,
Felipe Garcia Espana,
Preview
|
|
摘要:
One hundred sixty-six patients suffering from major depressive disorders were treated for 8 weeks with nefazodone in an open study in dosage ranges from 200 to 600 mg. This report focuses primarily on the first week of therapy and on the concomitant use of several benzodiazepines, one of which is not metabolized by the cytochrome system (temazepam). Triazolam response was further evaluated as a function of two nefazodone dosage regimens provided during the first week of therapy, one group receiving nefazodone 200 mg/day for 7 days, and another group receiving nefazodone 200 mg/day for 3 days, followed by 4 days with 400 mg/day. Finally, a comparison of three different nefazodone dosages, the third being 400 mg from day 1 on, was also carried out. Outcome measures included Hamilton Rating Scale for Depression total and the total of the three Hamilton Rating Scale for Depression insomnia items, as well as global improvement, a daily completed sleep questionnaire, and adverse event assessment.A combination of nefazodone with a benzodiazepine (BZ) caused more sedation than nefazodone alone; triazolam, the BZ with the shortest half-life and the highest dependence on the cytochrome 450 system for its metabolism, caused the least amount of sedation, and alprazolam and diazepam, the two daytime benzodiazepines, caused the most sedation. Triazolam caused significant and identical reduction of insomnia in both nefazodone groups. Compared with nefazodone 200 mg given as monotherapy, insomnia was significantly improved-not only by triazolam, but also alprazolam and diazepam, but not temazepam. The addition of nefazodone raised triazolam plasma levels to almost 500%, the plasma level of desmethyl-diazepam 87%, and that of alprazolam 34%. Temazepam plasma levels remained unchanged.When prescribing nefazodone with a benzodiazepine, one should expect an improved sleep pattern initially, but at the cost of clinically relevant daytime sedation.The prediction that temazepam, the only BZ not dependent on the cytochrome mechanism for metabolism, should be the least sedating, and triazolam, because of its cytochromic metabolism interference with nefazodone should be the most sedating, could not be confirmed. In fact, triazolam 0.25 mg capsules seem to be the safest treatment of choice when one has to combine a benzodiazepine with nefazodone in initial stages of therapy, at least of the four benzodiazepines tested in this study. (J Clin Psychopharmacol 1998;18:145-153)
ISSN:0271-0749
出版商:OVID
年代:1998
数据来源: OVID
|
8. |
Benzodiazepine-Receptor Ligands in HumansAcute Performance-Impairing, Subject-Rated and Observer-Rated Effects |
|
Journal of Clinical Psychopharmacology,
Volume 18,
Issue 2,
1998,
Page 154-166
Craig R. Rush,
Deanna L. Armstrong,
Jeffrey A. Ali,
Peggy J. Pazzaglia,
Preview
|
|
摘要:
The study presented here compared the acute performance-impairing, subject-rated, and observer-rated effects of quazepam (15, 30, and 45 mg), triazolam (0.1875, 0.375, and 0.5625 mg), zolpidem (7.5, 15, and 22.5 mg), and placebo in nine healthy, non-drug-abusing humans. Quazepam, a trifluoroethylbenzodiazepine, was chosen for study because, when compared with triazolam, a triazolobenzodiazepine, it is a relatively weak benzodiazepine-receptor ligand, and it may bind selectively to the BZ1benzodiazepine-receptor subtype. Zolpidem, an imidazopyridine, is the most commonly prescribed hypnotic and was chosen for study because it is biochemically distinct from benzodiazepine hypnotics and also purportedly binds selectively to the BZ1benzodiazepine-receptor subtype. Triazolam was chosen as the reference compound because it binds nonselectively to BZ1and BZ2benzodiazepine-receptor subtypes. Triazolam, zolpidem, quazepam, and placebo were administered orally in a double-blind, crossover design. Triazolam and zolpidem produced orderly dose- and time-related impairment of learning, performance, and recall, and produced sedative-like subject- and observer-rated drug effects. The behavioral pharmacologic profile of zolpidem and triazolam was indistinguishable in that at peak effect, the absolute magnitude of drug effect was comparable across the various measures. Quazepam, by contrast, did not impair performance on any task to a statistically significant degree, nor did it produce significant sedation as measured by subject- and observer-rated drug-effect questionnaires. Whether these effects are a result of the unique benzodiazepine-receptor binding profile of quazepam or the testing of insufficient dosages is unknown. Future research could extend the findings presented here by testing higher dosages of quazepam. (J Clin Psychopharmacol 1998;18:154-166)
ISSN:0271-0749
出版商:OVID
年代:1998
数据来源: OVID
|
9. |
Serum Levels of Valproate and Carbamazepine in Breastfeeding Mother-Infant Pairs |
|
Journal of Clinical Psychopharmacology,
Volume 18,
Issue 2,
1998,
Page 167-169
Katherine L. Wisner,
James M. Perel,
Preview
|
|
摘要:
Few data are available about the use of anti-convulsants during breastfeeding. In this article, three women with bipolar disorder who insisted upon breastfeeding their infants were studied.One mother was treated with carbamazepine (CBZ) and two were treated with valproate (VLP) monotherapy.Mother and infant serum levels were assessed when maternal steady-state was reached.The infant whose mother took CBZ developed a serum level that was 15% of the total maternal CBZ.Free CBZ was 20% of maternal values. The two infants whose mothers took VLP developed low serum levels (1.5 and 6.0% of maternal values).In the series, the serum levels of both CBZ and VLP were lower than previously reported values.However, information is limited and careful monitoring is recommended. (J Clin Psychopharmacol 1998;18:167-169)
ISSN:0271-0749
出版商:OVID
年代:1998
数据来源: OVID
|
10. |
Clozapine Induced Atrial Fibrillation |
|
Journal of Clinical Psychopharmacology,
Volume 18,
Issue 2,
1998,
Page 170-170
Robert A. Jr Low,
Matthew A. Fuller,
Anand Popli,
Preview
|
|
ISSN:0271-0749
出版商:OVID
年代:1998
数据来源: OVID
|
|