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氯氮平与发热:一例氯氮平持续治疗病例

Clozapine and Fever: A Case of Continued Therapy With Clozapine.

作者信息

Bruno Valentina, Valiente-Gómez Alicia, Alcoverro Oscar

机构信息

*Psychiatry Department, Benito Menni CASM, Hospital General de Granollers; †Psychiatry Department, Benito Menni CASM, Hospital Benito Menni; ‡FIDMAG Germanes Hospitalàries Research Foundation, Barcelona; and §Centro de Investigación Biomédica en Red de Salud Mental, Madrid, Spain.

出版信息

Clin Neuropharmacol. 2015 Jul-Aug;38(4):151-3. doi: 10.1097/WNF.0000000000000088.

Abstract

Clozapine is a major atypical antipsychotic drug used in treatment-resistant schizophrenia (Patel and Allin. Ther Adv Psychopharmacol 2011;1:25-29). It interferes with dopamine binding to D1, D2, D3, and D5 receptors but has high affinity to D4. It also has an anticholinergic effect and antagonizes α-adrenergic, histaminergic, and serotoninergic receptors (Oerther and Ahlenius. J Pharmacol Exp Ther 2000;292:731-736). Clozapine has proved effective in treating positive and negative symptoms in patients with refractory schizophrenia, thus accounting for its frequent use. Despite its effectiveness, this drug is not without its adverse effects. The most well known is agranulocytosis. There are, however, many others, such as myocarditis, aspiration pneumonia, ileus, fever, hyperglycemia, hyperlipidemia, hypertriglycemia, tachycardia, and weight gain, among others (Bruijnzeel et al. Asian J Psychiatr 2014;11:3-7). Fever induced by clozapine is a common phenomenon (Lowe et al. Ann Pharmacother 2007;41:1700-1704), which usually occurs in the first 4 weeks of treatment, and its prevalence oscillates from 0.5% and 55%, depending on the study (Jeong et al. Schizophr Res 2002;56:191-193; Young et al. Schizophr Bull 1998;24:381-390). The fever lasts for 2.5 days on average, and unless the treatment is discontinued, it generally abates between day 8 and 16 of treatment (Kohen et al. Ann Pharmacother 2009;43:143-146). There are several different theories about the physiopathological mechanism; it could be a variation of malignant neuroleptic syndrome, an infection secondary to neutropenia, and allergic reaction or the emergence of the immunomodulating effect of clozapine. Some case reports in the bibliography have shown that patients in treatment with clozapine can develop a mild leukocytosis, but the presence of other concurrent symptoms, which indicate infection, is not common (Tham and Dickson. J Clin Psychiatry 2002;63:880-884). The theory of an allergic reaction is unsupported because of the fact that the fever does not recur after reintroducing clozapine. So we question, "What would be the attitudes to follow when we find clozapine-induced fever (Nielsen et al. J Clin Psychiatry 2013;74:603-613)?" The management of patients with clozapine-induced fever should include a complete blood picture, liver and renal function tests, a creatine kinase test urine culture, and a chest x-ray. A nasopharyngeal aspirate can also be useful to exclude infection (Pui-yin Chung et al. Can J Psychiatry 2008;53:857-862). On the other hand, some drugs have been suggested for treatment of fever induced by clozapine. The use of acetaminophen, in the treatment of the fever induced by clozapine, is supported by many studies (Jeong et al. Schizophr Res 2002;56:191-193). In one of these, clozapine was suspended and restarted successfully after 1 week. However, in some studies, such as the case report of Tremeau et al (Clin Neuropharmacol 1997;20:168-170), clozapine was reduced instead of discontinued. In other studies, the recommendation is continuating clozapine treatment (Martin and Williams. J Psychiatry Neurosci 2013;38:E9-E10).

摘要

氯氮平是一种主要用于治疗难治性精神分裂症的非典型抗精神病药物(帕特尔和阿林。《治疗进展:精神药理学》2011年;1:25 - 29)。它干扰多巴胺与D1、D2、D3和D5受体的结合,但对D4受体具有高亲和力。它还具有抗胆碱能作用,并拮抗α - 肾上腺素能、组胺能和5 - 羟色胺能受体(厄特和阿伦纽斯。《药理学与实验治疗学杂志》2000年;292:731 - 736)。氯氮平已被证明对治疗难治性精神分裂症患者的阳性和阴性症状有效,因此被频繁使用。尽管其有效,但这种药物并非没有不良反应。最广为人知的是粒细胞缺乏症。然而,还有许多其他不良反应,如心肌炎、吸入性肺炎、肠梗阻、发热、高血糖、高脂血症、高甘油三酯血症、心动过速和体重增加等(布鲁因泽尔等人。《亚洲精神病学杂志》2014年;11:3 - 7)。氯氮平引起的发热是一种常见现象(洛维等人。《药物治疗学年鉴》2007年;41:1700 - 1704),通常发生在治疗的前4周,其发生率根据研究不同在0.5%至55%之间波动(郑等人。《精神分裂症研究》2002年;56:191 - 193;杨等人。《精神分裂症通报》1998年;24:381 - 390)。发热平均持续2.5天,除非停药,一般在治疗的第8天至16天之间消退(科恩等人。《药物治疗学年鉴》2009年;43:143 - 146)。关于生理病理机制有几种不同的理论;它可能是恶性神经阻滞剂综合征的一种变体、中性粒细胞减少继发的感染、过敏反应或氯氮平免疫调节作用的出现。参考文献中的一些病例报告表明,接受氯氮平治疗的患者可能会出现轻度白细胞增多,但伴有其他表明感染的并发症状并不常见(谭和迪克森。《临床精神病学杂志》2002年;63:880 - 884)。过敏反应理论不成立,因为重新使用氯氮平后发热不会复发。所以我们质疑,“当我们发现氯氮平引起的发热时应采取什么态度(尼尔森等人。《临床精神病学杂志》2013年;74:603 - 613)?”氯氮平引起发热的患者管理应包括全血细胞计数检查、肝肾功能检查、肌酸激酶检查、尿培养和胸部X光检查。鼻咽抽吸物检查也有助于排除感染(钟佩茵等人。《加拿大精神病学杂志》2008年;53:857 - 862)。另一方面,有人建议使用一些药物来治疗氯氮平引起的发热。许多研究支持使用对乙酰氨基酚治疗氯氮平引起的发热(郑等人。《精神分裂症研究》2002年;56:191 - 193)。其中一项研究中,氯氮平停药1周后成功重新使用。然而,在一些研究中,如特雷莫等人的病例报告(《临床神经药理学》1997年;20:168 - 170),是减少氯氮平用量而不是停药。在其他研究中,建议继续氯氮平治疗(马丁和威廉姆斯。《精神病学与神经科学杂志》2013年;38:E9 - E10)。

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