TREATMENT OF THE NEUROLEPTIC-NONRESPONSIVE SCHIZOPHRENIC PATIENT

被引:249
作者
MELTZER, HY [1 ]
机构
[1] VET ADM MED CTR,PSYCHIAT RES,CLEVELAND,OH 44106
关键词
D O I
10.1093/schbul/18.3.515
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
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 add; 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 dear goals. If these are not achieved, supplemental medications should be discontinued. Psychosurgery is not a recommended alternative at this time.
引用
收藏
页码:515 / 542
页数:28
相关论文
共 221 条
[1]   CLOZAPINE - PHARMACOKINETIC INVESTIGATIONS AND BIOCHEMICAL EFFECTS IN MAN [J].
ACKENHEIL, M .
PSYCHOPHARMACOLOGY, 1989, 99 :S32-S37
[2]  
ACKENHEIL VM, 1977, ARZNEIM FORSCH DRUG, V26, P1156
[3]   AGRANULOCYTOSIS INDUCED BY CLOZAPINE WITH THE EARLY ADDITION OF TRIFLUOPERAZINE - A CASE-REPORT [J].
ADAMS, CE ;
RICCIO, M ;
MCCARTHY, D ;
BARNES, TRE ;
HIRSCH, SR .
INTERNATIONAL CLINICAL PSYCHOPHARMACOLOGY, 1990, 5 (04) :287-290
[4]   CLONAZEPAM HALOPERIDOL COMBINATION THERAPY IN SCHIZOPHRENIA - A DOUBLE-BLIND STUDY [J].
ALTAMURA, AC ;
MAURI, MC ;
MANTERO, M ;
BRUNETTI, M .
ACTA PSYCHIATRICA SCANDINAVICA, 1987, 76 (06) :702-706
[5]  
American Psychiatric Association, 1980, DIAGN STAT MAN MENT, V3rd
[6]  
American Psychiatric Association, 1987, DSM 3 R DIAGN STAT M, V3rd
[7]   AGRANULOCYTOSIS IN PATIENTS TREATED WITH CLOZAPINE - STUDY OF FINNISH EPIDEMIC [J].
AMSLER, HA ;
TEERENHOVI, L ;
BARTH, E ;
HARJULA, K ;
VUOPIO, P .
ACTA PSYCHIATRICA SCANDINAVICA, 1977, 56 (04) :241-248
[8]  
ANDERSON ES, 1991, J CLIN PSYCHIAT, V52, P102
[9]   BEHAVIORAL EFFECTS OF L-DOPA IN SCHIZOPHRENIC PATIENTS [J].
ANGRIST, B ;
SATHANANTHAN, G ;
GERSHON, S .
PSYCHOPHARMACOLOGIA, 1973, 31 (01) :1-12
[10]  
Angst J., 1971, PHARRNACKOPSYCHIATRI, V4, P192