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非化疗药物所致中性粒细胞减少症——最新进展

Non-chemotherapy drug-induced neutropenia - an update.

作者信息

Andrès Emmanuel, Mourot-Cottet Rachel

机构信息

a Departments of Internal Medicine, Medical Clinic B , University Hospital of Strasbourg , Strasbourg , France.

b Referral Center of immune cytopenias , University Hospital of Strasbourg , Strasbourg , France.

出版信息

Expert Opin Drug Saf. 2017 Nov;16(11):1235-1242. doi: 10.1080/14740338.2017.1376645. Epub 2017 Sep 17.

Abstract

To date, non-chemotherapy drug-induced severe neutropenia (neutrophil count of ≤0.5 x 10/L) also called idiosyncratic drug-induced agranulocytosis is little discussed in the literature. In the present paper, we report and discuss the clinical data and management of this rare disorder. Areas covered: To do this, we carried out a review of the literature using PubMed database of the US National Library of Medicine. We also used data from the American Society of Hematology educational books, textbooks of Hematology and Internal medicine, and information gleaned from international meetings. Expert opinion: Idiosyncratic agranulocytosis remains a potentially serious adverse event due to the frequency of severe sepsis with severe deep tissue infections (e.g., pneumonia), septicemia, and septic shock in approximately two-thirds of all hospitalized patients. In this context, several prognostic factors have been identified that may be helpful when identifying 'susceptible' patients. Old age (>65 years), septicemia or shock, renal failure, and a neutrophil count ≤0.1 × 10/L have been consensually accepted as poor prognostic factors. In our experience, modern management with pre-established procedures, intravenous broad-spectrum antibiotics and hematopoietic growth factors (particularly G-CSF) is likely to improve the prognosis. Thus with appropriate management, the mortality rate is currently between 5 to 10%.

摘要

迄今为止,非化疗药物引起的严重中性粒细胞减少症(中性粒细胞计数≤0.5×10⁹/L),也称为特发性药物性粒细胞缺乏症,在文献中很少被讨论。在本文中,我们报告并讨论了这种罕见疾病的临床资料及管理。涵盖领域:为此,我们使用美国国立医学图书馆的PubMed数据库进行了文献综述。我们还使用了美国血液学会教育书籍、血液学和内科学教科书的数据,以及从国际会议收集的信息。专家意见:由于约三分之二的住院患者会出现严重的深部组织感染(如肺炎)、败血症和感染性休克等严重脓毒症,特发性粒细胞缺乏症仍然是一种潜在的严重不良事件。在这种情况下,已经确定了几个预后因素,在识别“易感”患者时可能会有所帮助。高龄(>65岁)、败血症或休克、肾衰竭以及中性粒细胞计数≤0.1×10⁹/L已被一致认为是不良预后因素。根据我们的经验,采用既定程序、静脉注射广谱抗生素和造血生长因子(特别是G-CSF)的现代管理方法可能会改善预后。因此,通过适当的管理,目前死亡率在5%至10%之间。

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