Meltzer H Y
Dept. of Psychiatry, Case Western Reserve University, Cleveland, OH 44106.
Schizophr Bull. 1992;18(3):515-42. doi: 10.1093/schbul/18.3.515.
The treatment and management of neuroleptic-resistant schizophrenic patients, who comprise 5 to 25 percent of all patients with that diagnosis, are major problems for psychiatry. In addition, another large group of schizophrenic patients, perhaps 5 to 20 percent, are intolerant of therapeutic dosages of neuroleptic drugs because of extrapyramidal symptoms, including akathisia, parkinsonism, and tardive dyskinesia. Because about 60 percent of neuroleptic-resistant schizophrenic patients respond to clozapine and a large percentage of neuroleptic-intolerant patients are able to tolerate clozapine, it should be considered the treatment of choice for such patients until other therapies are proven to be superior. A trial of clozapine alone should usually be continued for up to 6 months before it is terminated or supplemental agents are tried. Plasma levels of clozapine may be useful to guide dosage. The major side effects of clozapine are granulocytopenia or agranulocytosis (1%-2%) and a dose-related increase in the incidence of generalized seizures. Psychosocial treatments such as education of the patient and the family about the nature of the illness, rehabilitation programs, social skills training, and assistance in housing are generally needed to obtain optimal benefit from clozapine, as with other somatic therapies. If clozapine is unavailable, unacceptable, or not tolerated, a variety of approaches may be employed to supplement typical antipsychotic drugs for patients who do not respond adequately to these agents alone. These include lithium; electroconvulsive therapy; carbamazepine or valproic acid; benzodiazepines; antidepressant drugs; reserpine; L-dopa and amphetamine; opioid drugs; calcium channel blockers; and miscellaneous other pharmacologic approaches. The evidence for the efficacy of these ancillary somatic therapies in treatment-resistant patients is relatively weak. Polypharmacy should be tried only for discrete periods and with clear goals. If these are not achieved, supplemental medications should be discontinued. Psychosurgery is not a recommended alternative at this time.
抗精神病药难治性精神分裂症患者占所有确诊患者的5%至25%,其治疗和管理是精神病学面临的主要问题。此外,另一大组精神分裂症患者,可能占5%至20%,由于锥体外系症状,包括静坐不能、帕金森症和迟发性运动障碍,无法耐受治疗剂量的抗精神病药物。由于约60%的抗精神病药难治性精神分裂症患者对氯氮平有反应,且很大比例的抗精神病药不耐受患者能够耐受氯氮平,在其他疗法被证明更优之前,应将其视为这类患者的首选治疗方法。单独使用氯氮平的试验通常应持续长达6个月,然后再终止或尝试添加其他药物。氯氮平的血药浓度可能有助于指导用药剂量。氯氮平的主要副作用是粒细胞减少或粒细胞缺乏症(1% - 2%)以及癫痫发作发生率与剂量相关的增加。与其他躯体治疗一样,通常需要进行心理社会治疗,如向患者及其家属介绍疾病性质、康复计划、社交技能培训以及住房援助等,以便从氯氮平治疗中获得最佳疗效。如果无法获得氯氮平、氯氮平不可接受或患者不耐受,可以采用多种方法来补充典型抗精神病药物,用于单独使用这些药物反应不佳的患者。这些方法包括锂盐;电休克治疗;卡马西平或丙戊酸;苯二氮䓬类药物;抗抑郁药;利血平;左旋多巴和苯丙胺;阿片类药物;钙通道阻滞剂;以及其他各种药理学方法。这些辅助躯体疗法在难治性患者中的疗效证据相对较弱。联合用药应仅在特定时间段内尝试,并设定明确目标。如果未达到目标,应停用补充药物。目前不推荐采用精神外科手术作为替代治疗方法。