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Encephalopathy with combined lithium-risperidone administration.联用锂盐和利培酮导致的脑病。
Acta Psychiatr Scand. 2008 May;117(5):394-5; discussion 396. doi: 10.1111/j.1600-0447.2008.01165.x. Epub 2008 Mar 10.
2
Lithium in mood disorders: increasing evidence base, declining use?锂盐在心境障碍中的应用:证据基础增加,使用量却在下降?
Br J Psychiatry. 2007 Dec;191:474-6. doi: 10.1192/bjp.bp.107.043133.
3
Atypical antipsychotics: newer options for mania and maintenance therapy.非典型抗精神病药物:用于躁狂症和维持治疗的新选择。
Bipolar Disord. 2005;7 Suppl 4:21-33. doi: 10.1111/j.1399-5618.2005.00212.x.
4
Atypical antipsychotics for bipolar disorder.用于双相情感障碍的非典型抗精神病药物。
Psychiatr Clin North Am. 2005 Jun;28(2):325-47. doi: 10.1016/j.psc.2005.01.001.
5
A pooled analysis of 2 placebo-controlled 18-month trials of lamotrigine and lithium maintenance in bipolar I disorder.一项对两项为期18个月的安慰剂对照试验进行的汇总分析,这两项试验涉及拉莫三嗪和锂盐用于双相I型障碍的维持治疗。
J Clin Psychiatry. 2004 Mar;65(3):432-41. doi: 10.4088/jcp.v65n0321.
6
Valproate for acute mood episodes in bipolar disorder.丙戊酸盐用于双相情感障碍的急性情绪发作
Cochrane Database Syst Rev. 2003(1):CD004052. doi: 10.1002/14651858.CD004052.
7
Rationale for long-term treatment of bipolar disorder and evidence for long-term lithium treatment.双相情感障碍长期治疗的理论依据及锂盐长期治疗的证据
J Clin Psychiatry. 2002;63 Suppl 10:5-12.
8
Topiramate versus bupropion SR when added to mood stabilizer therapy for the depressive phase of bipolar disorder: a preliminary single-blind study.在双相情感障碍抑郁发作期,联用心境稳定剂治疗时,托吡酯与缓释安非他酮的比较:一项初步单盲研究。
Bipolar Disord. 2002 Jun;4(3):207-13. doi: 10.1034/j.1399-5618.2002.01189.x.
9
Lithium therapy at the millennium: a revolutionary drug used for 50 years faces competing options and possible demise.千年之际的锂盐治疗:一种使用了50年的革命性药物面临着竞争选择和可能的淘汰。
Bipolar Disord. 1999 Dec;1(2):67-70. doi: 10.1034/j.1399-5618.1999.010201.x.
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Lithium neurotoxicity at therapeutic level--a case report.治疗剂量下的锂神经毒性——一例报告
J Indian Med Assoc. 1999 Nov;97(11):473-4.

可逆性锂神经毒性:文献综述

Reversible lithium neurotoxicity: review of the literatur.

作者信息

Netto Ivan, Phutane Vivek H

机构信息

Parmar Plaza Clinic, Fatimanagar, Pune, Maharashtra, India.

出版信息

Prim Care Companion CNS Disord. 2012;14(1). doi: 10.4088/PCC.11r01197.

DOI:10.4088/PCC.11r01197
PMID:22690368
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3357580/
Abstract

OBJECTIVE

Lithium neurotoxicity may be reversible or irreversible. Reversible lithium neurotoxicity has been defined as cases of lithium neurotoxicity in which patients recovered without any permanent neurologic sequelae, even after 2 months of an episode of lithium toxicity. Cases of reversible lithium neurotoxicity differ in clinical presentation from those of irreversible lithium neurotoxicity and have important implications in clinical practice. This review aims to study the clinical presentation of cases of reversible lithium neurotoxicity.

DATA SOURCES

A comprehensive electronic search was conducted in the following databases: MEDLINE (PubMed), 1950 to November 2010; PsycINFO, 1967 to November 2010; and SCOPUS (EMBASE), 1950 to November 2010. MEDLINE and PsycINFO were searched by using the OvidSP interface.

STUDY SELECTION

A combination of the following search terms was used: lithium AND adverse effects AND central nervous system OR neurologic manifestation. Publications cited include articles concerned with reversible lithium neurotoxicity.

DATA EXTRACTION

The age, sex, clinical features, diagnostic categories, lithium doses, serum lithium levels, precipitating factors, and preventive measures of 52 cases of reversible lithium neurotoxicity were extracted.

DATA SYNTHESIS

Among the 52 cases of reversible lithium neurotoxicity, patients ranged in age from 10 to 80 years and a greater number were female (P = .008). Most patients had affective disorders, schizoaffective disorders, and/or depression (P < .001) and presented mainly with acute organic brain syndrome. In most cases, the therapeutic serum lithium levels were less than or equal to 1.5 mEq/L (P < .001), and dosage regimens were less than 2,000 mg/day. Specific drug combinations with lithium, underlying brain pathology, abnormal tissue levels, specific diagnostic categories, and elderly populations were some of the precipitating factors reported for reversible lithium neurotoxicity. The preventive measures were also described.

CONCLUSIONS

Reversible lithium neurotoxicity presents with a certain clinical profile and precipitating factors for which there are appropriate preventive measures. This recognition will help in early diagnosis and prompt treatment of lithium neurotoxicity.

摘要

目的

锂神经毒性可能是可逆的或不可逆的。可逆性锂神经毒性被定义为锂神经毒性病例,即患者即使在锂中毒发作2个月后仍能康复且无任何永久性神经后遗症。可逆性锂神经毒性病例的临床表现与不可逆性锂神经毒性病例不同,在临床实践中具有重要意义。本综述旨在研究可逆性锂神经毒性病例的临床表现。

数据来源

在以下数据库中进行了全面的电子检索:MEDLINE(PubMed),1950年至2010年11月;PsycINFO,1967年至2010年11月;以及SCOPUS(EMBASE),1950年至2010年11月。通过OvidSP界面检索MEDLINE和PsycINFO。

研究选择

使用以下检索词组合:锂与不良反应与中枢神经系统或神经表现。引用的出版物包括与可逆性锂神经毒性相关的文章。

数据提取

提取了52例可逆性锂神经毒性病例的年龄、性别、临床特征、诊断类别、锂剂量、血清锂水平、诱发因素和预防措施。

数据综合

在52例可逆性锂神经毒性病例中,患者年龄在10至80岁之间,女性患者较多(P = 0.008)。大多数患者患有情感障碍、分裂情感障碍和/或抑郁症(P < 0.001),主要表现为急性器质性脑综合征。在大多数情况下,治疗性血清锂水平小于或等于1.5 mEq/L(P < 0.001),给药方案小于2000 mg/天。与锂的特定药物组合、潜在的脑部病变、异常的组织水平、特定的诊断类别和老年人群是报道的可逆性锂神经毒性的一些诱发因素。还描述了预防措施。

结论

可逆性锂神经毒性具有一定的临床特征和诱发因素,对此有适当的预防措施。这种认识将有助于锂神经毒性的早期诊断和及时治疗。