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氯氮平使用者发热的临床决定因素及其对治疗管理的意义:叙述性综述。

Clinical determinants of fever in clozapine users and implications for treatment management: A narrative review.

机构信息

Univ. Bordeaux, Inserm, Bordeaux Population Health Research Center, Team Pharmacoepidemiology, UMR 1219, F-33000 Bordeaux, France; Centre Hospitalier Charles Perrens, F-33000 Bordeaux, France.

Centre Hospitalier Charles Perrens, F-33000 Bordeaux, France.

出版信息

Schizophr Res. 2019 Sep;211:1-9. doi: 10.1016/j.schres.2019.07.040. Epub 2019 Aug 1.

Abstract

OBJECTIVES

To identify the clinical determinants of fever in clozapine users and their impact on management of clozapine treatment.

METHODS

Articles published in English or French identified with a MEDLINE, Web of Sciences, Cochrane Library and PsycINFO search, from inception through February 2019, using the term "clozapine" in combination with "fever" OR "hyperthermia" OR "body temperature" OR "pyrexia" OR "febrile" OR "heat" OR "thermoregulation". Information extracted for each medical condition were frequency, time to onset after initiation of clozapine treatment, characteristics of fever, associated symptoms, laboratory tests used for diagnosis, course, lethality, discontinuation of clozapine. Data were synthesized narratively.

RESULTS

Our search yielded 394 unique hits published from 1993 to 2018. We included 73 articles in the review: two meta-analyses, 14 reviews, six epidemiological studies, 11 clinical studies and 40 case reports. During clozapine initiation, fever is most frequently benign and transient but should be closely monitored as it may be the first stage of potentially life-threatening adverse drug reactions (ADR) (agranulocytosis, neuroleptic malignant syndrome myocarditis, hepatitis, pancreatitis, nephritis, colitis, etc.). Other ADR associated with fever are independent of duration of exposure to clozapine (heat stroke, pneumonia, pulmonary embolism, necrotizing colitis). If fever is due to intercurrent infection, therapeutic drug monitoring is recommended to adjust clozapine daily dosage.

CONCLUSION

Benign causes of fever are much more frequent than life-threatening ADR during clozapine treatment. Discontinuation should not be considered as automatic in the event of fever, especially during the early phase of clozapine initiation.

摘要

目的

确定氯氮平使用者发热的临床决定因素及其对氯氮平治疗管理的影响。

方法

通过 MEDLINE、Web of Sciences、Cochrane Library 和 PsycINFO 搜索,以“clozapine”与“fever”或“hyperthermia”或“body temperature”或“pyrexia”或“febrile”或“heat”或“thermoregulation”组合的方式,检索 1993 年至 2019 年 2 月发表的英文或法文文章,提取每个医疗条件的频率、氯氮平治疗开始后发热的发病时间、发热特征、伴随症状、用于诊断的实验室检查、病程、死亡率、氯氮平停药等信息。数据以叙述性方式进行综合。

结果

我们的搜索共产生 394 个独特的结果,发表于 1993 年至 2018 年。我们共纳入 73 篇综述文章:两项荟萃分析、14 项综述、6 项流行病学研究、11 项临床研究和 40 篇病例报告。在氯氮平开始使用时,发热最常是良性和短暂的,但应密切监测,因为它可能是潜在威胁生命的药物不良反应(ADR)(粒细胞缺乏症、恶性神经阻滞剂综合征、心肌炎、肝炎、胰腺炎、肾炎、结肠炎等)的第一阶段。与发热相关的其他 ADR 与氯氮平暴露时间无关(中暑、肺炎、肺栓塞、坏死性结肠炎)。如果发热是由于并发感染引起的,建议进行治疗药物监测以调整氯氮平的日剂量。

结论

在氯氮平治疗期间,良性发热原因比危及生命的 ADR 更为常见。发热时不应自动考虑停药,特别是在氯氮平开始使用的早期阶段。

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