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情感障碍与迟发性运动障碍。

Affective disorders and tardive dyskinesia.

作者信息

Casey D E

机构信息

Psychiatry Service, V.A. Medical Center, Portland, OR 97207.

出版信息

Encephale. 1988 Sep;14 Spec No:221-6.

PMID:2905650
Abstract

Evidence from multiple lines of study indicate that mood disorders, particularly depression, are a risk factor for developing tardive dyskinesia (TD). Important patient and treatment factors include: 1) frequent retrospective rediagnosis of affective disorders instead of schizophrenia when the long-term course of illness and response is evaluated, and 2) TD onset after relatively brief (few months to few years) exposure to low to moderate neuroleptic doses. Mechanisms underlying this increased sensitivity to TD are unknown. It has been hypothesized that the cyclic mono- and catecholamine activity during mood changes makes the brain more vulnerable to the direct neuroleptic effects or the compensatory processes initiated by these drugs. There may also be an interaction between neuroleptic drugs and antidepressant agents which produce greater vulnerability to TD. Additionally, neuroleptic drug use may be different in affective disorders, such as high doses for short time periods with mania. Treating TD in patients with mood disorders is often difficult. The psychiatric diagnosis should be the first priority in treatment regimens. Then, strategies for addressing TD should be considered. Occasionally lithium and/or antidepressants may be effective in treating both affective disorders and TD in some patients. Specific drug therapies for TD have not been consistently effective. Therefore, the passage of time may be the best treatment approach. Preventing TD should receive the highest priority. In the short term, neuroleptic drugs should be limited to managing acute psychotic symptoms in patients with mood disorders. In the long term, neuroleptics should be reserved for manic or depressive symptoms that do not respond to standard therapy.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

多项研究证据表明,情绪障碍,尤其是抑郁症,是迟发性运动障碍(TD)发生的一个风险因素。重要的患者和治疗因素包括:1)在评估疾病的长期病程和反应时,频繁地对情感障碍而非精神分裂症进行回顾性重新诊断;2)在相对较短的时间(几个月至几年)内接触低至中等剂量的抗精神病药物后出现TD。这种对TD敏感性增加的潜在机制尚不清楚。据推测,情绪变化期间的循环单胺和儿茶酚胺活性使大脑更容易受到抗精神病药物的直接作用或这些药物引发的代偿过程的影响。抗精神病药物和抗抑郁药物之间也可能存在相互作用,从而使患者对TD更易感性增加。此外,在情感障碍中使用抗精神病药物可能有所不同,例如在治疗躁狂症时短时间使用高剂量药物。治疗患有情绪障碍的TD患者通常很困难。在治疗方案中,精神科诊断应是首要任务。然后,应考虑应对TD的策略。偶尔,锂盐和/或抗抑郁药物可能对某些患者的情感障碍和TD都有效。针对TD的特定药物治疗并不总是有效。因此,时间推移可能是最佳的治疗方法。预防TD应得到最高优先级。短期内,抗精神病药物应仅限于控制情绪障碍患者的急性精神病症状。从长远来看,抗精神病药物应仅用于对标准治疗无反应的躁狂或抑郁症状。(摘要截选至250字)

相似文献

1
Affective disorders and tardive dyskinesia.情感障碍与迟发性运动障碍。
Encephale. 1988 Sep;14 Spec No:221-6.
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