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Clomipramine treatment of hyperventilation syndrome. 氯丙咪嗪治疗过度通气综合征。
Pub Date : 1980-01-01 DOI: 10.1055/s-2007-1019606
M J Hoes, P Colla, H Folgering

Six patients suffered from a hyperventilation syndrome for 3.4 +/- 1.2 years. They had a lowered PAco2 at rest and an abnormal CO2 response curve. During the entire period they had received unsuccessful treatment with anxiolytics, and had also undergone behaviour therapy for the last 1 -- 2 years without success. Both treatments were discontinued and the patients were placed on clomipramine, 25 mg t.i.d. for 9 months. Their anxiety and hyperventilation attacks diminished after one month of clomipramine, and their fear of attacks an their phobias subsided after two months. Eighteen months after clomipramine therapy had been initiated, they were feeling well without medication. The possible mode of action of clomipramine on the hyperventilation syndrome via central serotonergic mechanism is discussed.

6例患者出现换气过度综合征,持续时间为3.4±1.2年。静息时PAco2降低,CO2响应曲线异常。在整个期间,他们接受了不成功的抗焦虑药物治疗,并且在过去的1 - 2年里也接受了行为治疗,但没有成功。停用两种治疗方法,给予氯丙咪嗪25 mg,每日1次,疗程9个月。服用氯丙咪嗪一个月后,他们的焦虑和过度通气发作减少了,两个月后,他们对发作的恐惧和恐惧症消退了。在氯丙咪嗪治疗开始18个月后,他们在没有药物治疗的情况下感觉良好。探讨氯丙咪嗪通过中枢血清素能机制对过度通气综合征的可能作用模式。
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引用次数: 26
Neuoleptic-related sudden death (proven or a mere hypothesis?). 与新脑相关的猝死(已证实还是仅仅是假设?)
Pub Date : 1980-01-01 DOI: 10.1055/s-2007-1019607
G Ungvári
There are sound theoretical, practical and ethical reasons why, in keeping with the progress of psychopharmacotherapy, the possibility of sudden death during neuroleptic therapy should be periodically reexamined. 11935 patients were treated with neuroleptics at our c1inic over aperiod of eleven years (I. January 1968-3 I. December 1978); eight of them died suddenly and unexpectedly. The sudden death mortality rate of medicated patients was not higher than that of the general population of the same age distribution.
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引用次数: 19
[On the practice of clinical therapy with psychotropic drugs -- retrospective investigation of physicians prescribing practices in a psychiatric hospital (author's transl)]. [关于精神药物临床治疗的实践——对精神病院医生开处方实践的回顾性调查[作者译]。
Pub Date : 1980-01-01 DOI: 10.1055/s-2007-1019604
R Grohmann, A Strauss, C Gehr, E Rüther, H Hippius

1. At the psychiatric hospital of the University of Munich physicians' practices in prescribing psychotropic drugs have been analyzed retrospectively for 1974. Case report of 2,100 patients from a total of 2,118 newly admitted inpatients in 1974 have been evaluated and various methods of analyzing data are compared. 2. 414 (19.7%) patients out of a total of 2100 have not been medicated by any drugs. On the average 2.7 psychotropic drugs/patient have been precribed in the remaining 1,186 patients (80.3%). 3. 37.4% of 4627 applications made have been allotted to neuroleptics. Clozapine has been found to be the drug most extensively used (37.4%). It was prescribed to 595 patients, followed by chloralhydrate (425 patients) and amitriptyline (374 patients). 4. Out of a total of 5373 prescriptions, 2,004 were allotted to a single substance and 3,369 to a combination of different drugs. With regard to combined medications, in 1,856 prescriptions two drugs were combined, in 1,015 three, in 404 four, in 70 five, in 18 six and finally in 6 prescriptions seven medications were applied to one patient. 5. Antidepressants and neuroleptics have been combined on the same patient in 768 prescriptions. As to neuroleptics most frequently clozapine and haloperidol have been prescribed together. 6. The mean time during which a defined combination of drugs was given continuously, never exceeded a quarter of the total time the individual had been admitted to the hospital. 7. It is evident that in clinical practice the combinations of psychotropic drugs are widely used. This pattern of psychopharmacological drug treatment is in conflict with the present accepted rules of psychotropic pharmacotherapy. Furthermore it is a remarkable result of the present studies that in therapeutical practice the single components of drug combinations are changed very often. Compounds with sedative effects are preferred within all classes of psychotropic drugs.

1. 回顾分析了慕尼黑大学精神病院1974年医师开精神药物处方的情况。本文对1974年2118例新住院患者中2100例患者的病例报告进行了评估,并对各种分析数据的方法进行了比较。2. 2100例患者中有414例(19.7%)未接受任何药物治疗。其余1186名病人(80.3%)平均每名病人服用2.7种精神药物。3.在4627份申请中,有37.4%被分配给抗精神病药物。氯氮平是使用最广泛的药物(37.4%)。595名患者服用了该药,其次是氯醛(425名患者)和阿米替林(374名患者)。4. 在总共5373张处方中,2004张分配给单一药物,3369张分配给不同药物的组合。在联合用药方面,1856张处方中有两种药物联合用药,1015张处方中有三种药物联合用药,404张处方中有四种药物联合用药,70张处方中有五种药物联合用药,18张处方中有六种药物联合用药。5. 抗抑郁药和抗精神病药在同一个病人身上联合使用的处方有768张。至于抗精神病药,最常见的是氯氮平和氟哌啶醇一起开。6. 连续给予特定药物组合的平均时间,从未超过个人住院总时间的四分之一。7. 显然,在临床实践中,精神药物的联合使用是广泛的。这种精神药理学药物治疗模式与目前公认的精神药物治疗规则相冲突。此外,目前研究的一个显著结果是,在治疗实践中,药物组合的单一成分经常发生变化。在所有类别的精神药物中,具有镇静作用的化合物是首选的。
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引用次数: 11
Hydergine: a review of 26 clinical studies. 盐酸:26项临床研究综述。
Pub Date : 1979-11-01 DOI: 10.1055/s-0028-1094637
R J McDonald

This report reviews 26 clinical drug trials which investigated the effectiveness of Hydergine, a dihydrogenated ergot alkaloid, used frequently in geriatric psychopharmacology. The methodological characteristics and significant results for each study are presented in outline form. In total, 32 symptoms were assessed in six or more studies. Therapeutic benefits following Hydergine treatment occurred in the areas of cognitive dysfunctions, mood depression, and the composite scores as measured by subjective clinical behavioral rating scales. It is suggested that the improvement reported in cognitive functions and mood depression is a reflection of the global change observed by clinicians in patients' overall behavior duirng the interview. This conclusion that Hydergine does produce some global improvement indicates that further research with Hydergine is warranted, provided more objective instruments are employed such as those described in the report.

本报告回顾了26项临床药物试验,这些试验调查了Hydergine的有效性,Hydergine是一种二氢化麦角生物碱,经常用于老年精神药理学。每项研究的方法学特征和重要结果以大纲形式呈现。在6项或更多的研究中,总共评估了32种症状。hyderine治疗后的治疗效果出现在认知功能障碍、情绪抑郁和主观临床行为评定量表测量的综合得分方面。这表明,报告的认知功能和情绪抑郁的改善反映了临床医生在访谈期间观察到的患者整体行为的整体变化。Hydergine确实产生了一些全球性的改善,这一结论表明,如果采用报告中描述的更客观的工具,Hydergine的进一步研究是有必要的。
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引用次数: 22
Antidepressive treatment and mood swing patterns in endogenous depression. 内源性抑郁症的抗抑郁治疗和情绪波动模式。
Pub Date : 1979-11-01 DOI: 10.1055/s-0028-1094640
F Strian, W Albert, C Klicpera

In 105 patients with endogenous depression treated with antidepressants or ECT the course of the depressive state was evaluated by means of a self-rating mood scale (Befindlichkeits-Skala by von Zerssen). The scale was filled out every second day. The course of the depressive mood was computed by various algorithms for each patient. Two different courses of depressive mood could be identified: some patients showed a relatively continuous decline in the depressive mood, whereas others showed strong fluctuations. Although there were some correlations between type of treatment and extent of mood swings, other factors also seemed to be relevant. Thus, there appears to be an interaction between treatment effects and spontaneous rhythms.

105例内源性抑郁症患者接受抗抑郁药或电休克治疗,采用自评情绪量表(Befindlichkeits-Skala by von Zerssen)评估抑郁状态的过程。天平每隔一天填一次。通过不同的算法计算每个患者的抑郁情绪病程。可以确定两种不同的抑郁情绪过程:一些患者的抑郁情绪表现出相对持续的下降,而另一些患者则表现出强烈的波动。虽然治疗类型和情绪波动程度之间存在一些相关性,但其他因素似乎也相关。因此,治疗效果和自发节律之间似乎存在相互作用。
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引用次数: 7
Endocrinological changes in patients with sexual dysfunction under long-term neuroleptic treatment. 长期抗精神病药物治疗对性功能障碍患者内分泌系统的影响。
Pub Date : 1979-11-01 DOI: 10.1055/s-0028-1094639
M Arató, A Erdös, M Polgár

Endocrine changes induced by dopaminergic inhibition may play a part in the development of sexual dysfunction (reduced libido/potency) in schizophrenic patients on long-term neuroleptic treatment. Prolactin, testosterone, LH and FSH serum level determinations by radioimmunoassays were performed in 24 schizophrenic males on long-acting fluphenazine decanoate treatment. Of these patients, sexual dysfunction was present in 17 cases, in 10 patients sexual activity remained unchanged. As compared to the 15 healthy controls (7.33 +/- 0.91 ng/ml), a significant increase of prolactin concentrations was found, i.e. 28.2 +/- 5.15 in the impotent groups, and 16.7 +/- 2.12 in the non-impotent group. The difference between the latter two mean values was, however, not significant. In the patients with normal sexual activity the increase of LH concentration was highly significant. It might be assumed that normal sexual behaviour despite neuroleptic treatment and hyperprolactinaemia is related to the high concentration of LH, though the mechanism of increased LH secretion has not been cleared as yet. The testosterone and FSH concentrations showed no differences in various groups.

多巴胺能抑制引起的内分泌变化可能在长期接受抗精神病药物治疗的精神分裂症患者性功能障碍(性欲/效力降低)的发展中起作用。用放射免疫法测定24例经长效癸酸氟那嗪治疗的男性精神分裂症患者血清催乳素、睾酮、黄体生成素和卵泡刺激素水平。在这些患者中,17例存在性功能障碍,10例性活动保持不变。与15名健康对照(7.33 +/- 0.91 ng/ml)相比,催乳素浓度显著增加,阳痿组为28.2 +/- 5.15,非阳痿组为16.7 +/- 2.12。然而,后两个平均值之间的差异并不显著。在性活动正常的患者中,LH浓度升高非常显著。虽然目前还不清楚促黄体生成素分泌增加的机制,但我们可以认为,抗精神病药物治疗和高催乳素血症后正常的性行为与高浓度的LH有关。各组间睾酮和卵泡刺激素浓度无明显差异。
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引用次数: 27
Endorphins in schizophrenia: hemodialysis/hemoperfusion are ineffective in clearing beta-Leu5-endorphin and beta-endorphin from human plasma. 精神分裂症中的内啡肽:血液透析/血液灌流对清除人血浆中的- leu5 -内啡肽和-内啡肽无效。
Pub Date : 1979-11-01 DOI: 10.1055/s-0028-1094636
V Höllt, G Hillebrand, B Schmidt, H J Gurland

Beta-Leu5-endorphin, a relative of "normal" beta-endorphin in which leucine is substituted for methionine at position 5 of the latter, has previously been found in high concentrations in the dialysate of schizophrenics. Its removal from plasma by means of hemodialysis has been claimed to relive the symptoms of schizophrenia. Using a highly sensitive radioimmunoassay of equal sensitivity to beta-endorphin and beta-leu5-endorphin, we have compared the plasma immunoreactivity of three schizophrenic patients befofe and after performance of their first session of membrane hemoperfusion. As compared to normal subjects, plasma beta-endorphin-like immunoreactivity was not greatly elevated in the schizophrenic patients before hemoperfusion.However, instead of the expected decrease, a consistent increase in the plasma levels of immunoreactive beta-endorphin was detected after hemoperfusion. In vitro experiments in which two different membranes and hemodialysis as well as hemoperfusion were used, revealed that synthetic beta-leu5-endorphin (and beta-endorphin) from human plasma was not cleared with any of these methods. This finding is inconsistent with the hypothesis that the claimed therapeutic effects of hemodialysis in schizophrenics are due to the removal of a beta-endorphin-like material from the plasma. Consequently, it seems to be unprobable that high concentrations of beta-leu5-endorphin occur in the dialysate or ultrafiltrate of schizophrenics.

β - leu5 -endorphin是“正常”β -endorphin的一种近亲,其中亮氨酸取代了蛋氨酸的第5位,以前在精神分裂症患者的透析液中发现了高浓度。据称,通过血液透析将其从血浆中去除可以缓解精神分裂症的症状。使用对-内啡肽和-白细胞- 5-内啡肽同等敏感性的高灵敏度放射免疫测定,我们比较了三名精神分裂症患者在第一次膜血液灌流前后的血浆免疫反应性。与正常人相比,血液灌流前精神分裂症患者血浆β -内啡肽样免疫反应性没有明显升高。然而,血液灌流后检测到血浆免疫反应性β -内啡肽水平的持续升高,而不是预期的下降。使用两种不同的膜和血液透析以及血液灌流的体外实验显示,从人血浆中合成的β -leu5-内啡肽(和β -内啡肽)没有被任何这些方法清除。这一发现与先前的假设不一致,即血液透析对精神分裂症患者的治疗效果是由于从血浆中去除-内啡肽样物质。因此,高浓度的-leu5-内啡肽似乎不太可能出现在精神分裂症患者的透析液或超滤液中。
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引用次数: 1
Effect of lithium carbonate on circadian periodicity in humans. 碳酸锂对人类生理周期的影响。
Pub Date : 1979-11-01 DOI: 10.1055/s-0028-1094638
A Johnsson, B Pflug, W Engelmann, W Klemke

Five groups of two volunteers lived during four weeks under arctic summer conditions (Spitsbergen) isolated in huts, without time information. They received lithium carbonate or placebo. All showed free-run of their circadian temperature and activity/rest rhythms with periods longer than 24 hours. Under lithium carbonate, a period-lengthening effect can be shown. This could help to understand theprophylactic effect of lithium salts in manic-depressive episodes.

五组两名志愿者在北极夏季条件下(斯匹次卑尔根岛)与世隔绝的小木屋里生活了四周,没有时间信息。他们分别服用碳酸锂或安慰剂。所有动物的昼夜温度和活动/休息节律均自由运行,周期超过24小时。碳酸锂作用下,可以表现出周期延长效应。这有助于理解锂盐对躁狂抑郁发作的预防作用。
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引用次数: 53
Monitoring plasma concentrations of psychotropic drugs as an aid to treatment. 监测精神药物的血浆浓度以辅助治疗。
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引用次数: 0
Studies on the distribution of 14C-sulpiride and its metabolites in the rat and guinea pig. 14c -舒必利及其代谢物在大鼠和豚鼠体内分布的研究。
Pub Date : 1979-11-01 DOI: 10.1055/s-0028-1094641
K Dross, A Hopf

After ip. injection of 14C-labelled sulpiride in rats, about one third is metabolized while the other two thirds are excreted unchanged in feces and urine. The highest level of its metabolites was found in the liver (about 65% of total radioactivity). In the brain, 90% of the radioactivity consisted of unchanged sulpiride, which seems to be responsible for the central effects of the drug. The highest concentrations within the brain were found in the median eminence, circumventricular organs, plexus, and pineal body.

在ip。大鼠注射14c标记的舒必利后,约三分之一被代谢,其余三分之二不变地随粪便和尿液排出体外。其代谢产物在肝脏中含量最高(约占总放射性的65%)。在大脑中,90%的放射性物质是由未改变的磺胺嘧啶组成的,这似乎是该药产生中枢效应的原因。脑内浓度最高的部位为正中隆起、脑室周围器官、神经丛和松果体。
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引用次数: 4
期刊
Pharmakopsychiatrie, Neuro-Psychopharmakologie
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