药物警戒在行动:利用 VigiBase 数据提高氯氮平的安全性。

IF 2 3区 医学 Q2 MEDICINE, GENERAL & INTERNAL
Patient preference and adherence Pub Date : 2024-11-12 eCollection Date: 2024-01-01 DOI:10.2147/PPA.S495254
Carlos De Las Cuevas, Emilio J Sanz, Jose de Leon
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引用次数: 0

摘要

目的:氯氮平是一种抗精神病药物,1989 年获准在美国用于治疗耐药性精神分裂症。在获批之前,几乎没有进行过随机试验,通过药物警戒发现了可能致命的氯氮平药物不良反应(ADR),如粒细胞减少症和心肌炎。世卫组织全球数据库 VigiBase 是国际药物警戒工作的基石,用于在上市后监测期间识别 ADR。本系统性文献综述探讨了 VigiBase 近期研究对氯氮平药物不良反应知识的进一步贡献:2024 年 9 月 5 日,我们使用 "氯氮平和 VigiBase "在 PubMed 上进行了文章检索。在 29 篇文章中,排除了 11 篇,结果部分描述了 18 篇:所有氯氮平不良反应均在两项 VigiBase 研究中有所描述。其中一项关于妊娠的研究表明,与其他抗精神病药物相比,使用氯氮平的风险并没有增加;另一项研究报告了截至 2023 年 1 月 15 日的 191,557 例氯氮平 ADR,其中包括 22,956 例死亡病例,并关注了前四大报告国(美国、英国、加拿大和澳大利亚)的报告风格。在三项 VigiBase 研究中描述了感染情况,其中氯氮平治疗与感染、呼吸道吸入和肺炎有关。快速滴定可导致氯氮平诱发的局部炎症,包括心肌炎、心包炎或胰腺炎,或全身炎症,如药物反应伴嗜酸性粒细胞增多和全身症状(DRESS)综合征。VigiBase 的四项研究描述了氯氮平诱发的炎症,其中两项针对所有年龄段(心肌炎和 DRESS),两项针对年轻人(心肌炎,另一项针对心包炎和胰腺炎)。九项 VigiBase 研究还描述了其他特定的不良反应(血液恶性肿瘤、横纹肌溶解症、淤血、癫痫发作、糖尿病、药物性帕金森病、戒断症状和自杀行为):结论:呼吸道吸入-吸入性肺炎-肺炎和其他感染是导致氯氮平治疗患者死亡的重要原因。在 VigiBase 的所有自杀行为标签中,氯氮平与其他抗精神病药物相比具有抗自杀作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pharmacovigilance in Action: Utilizing VigiBase Data to Improve Clozapine Safety.

Purpose: Clozapine is an antipsychotic which was approved in 1989 for treatment-resistant schizophrenia in the United States (US). There were few randomized trials before its approval and potentially lethal clozapine adverse drug reactions (ADRs), such as agranulocytosis and myocarditis were identified by pharmacovigilance. VigiBase, the WHO global database, is a cornerstone of international pharmacovigilance efforts for ADR identification during post-marketing surveillance. This systematic review of the literature explores additional contributions to the knowledge of clozapine ADRs from recent VigiBase studies.

Methods: Using the terms "clozapine AND VigiBase" we conducted an article search in PubMed on September 5, 2024. Of the 29 articles, 11 were excluded and 18 described in the Results section.

Results: All clozapine ADRs were described in two VigiBase studies. One on pregnancy indicated no increased risk with clozapine compared with other antipsychotics; the other reported 191,557 clozapine ADRs, including 22,956 fatal outcomes through January 15, 2023, and paid attention to the reporting style of the top 4 reporting countries (the US, the United Kingdom, Canada and Australia). Infections were described in three VigiBase studies where clozapine treatment was associated with infections, respiratory aspiration, and pneumonia. Rapid titration can lead to localized clozapine-induced inflammations including myocarditis, pericarditis or pancreatitis, or generalized inflammations such as drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome. Clozapine-induced inflammation was described in four VigiBase studies, two focused on all ages (myocarditis and DRESS) and two on youth (myocarditis and another on pericarditis and pancreatitis). Other specific ADRs were described in nine VigiBase studies (hematological malignancies, rhabdomyolysis, sialorrhea, seizures, diabetes mellitus, drug-induced parkinsonism, withdrawal symptoms, and suicidal behaviors).

Conclusion: The spectrum of respiratory aspiration - aspiration pneumonia - pneumonia and other infections are significant causes of fatal outcomes in clozapine-treated patients. Clozapine had anti-suicidal effects versus other antipsychotics across all VigiBase labels of suicidal behavior.

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来源期刊
Patient preference and adherence
Patient preference and adherence MEDICINE, GENERAL & INTERNAL-
CiteScore
3.60
自引率
4.50%
发文量
354
审稿时长
6-12 weeks
期刊介绍: Patient Preference and Adherence is an international, peer reviewed, open access journal that focuses on the growing importance of patient preference and adherence throughout the therapeutic continuum. The journal is characterized by the rapid reporting of reviews, original research, modeling and clinical studies across all therapeutic areas. Patient satisfaction, acceptability, quality of life, compliance, persistence and their role in developing new therapeutic modalities and compounds to optimize clinical outcomes for existing disease states are major areas of interest for the journal. As of 1st April 2019, Patient Preference and Adherence will no longer consider meta-analyses for publication.
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