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药物诱导性粒细胞缺乏症的临床表现与治疗。

Clinical presentation and management of drug-induced agranulocytosis.

机构信息

Department of Internal Medicine B, University Hospital of Strasbourg, 1 Porte de l'Hôpital, Strasbourg Cedex, France.

出版信息

Expert Rev Hematol. 2011 Apr;4(2):143-51. doi: 10.1586/ehm.11.12.

Abstract

OBJECTIVE

In this article, we report and discuss the clinical presentation and management of idiosyncratic drug-induced agranulocytosis (neutrophil count <0.5 × 10(9)/l).

RESULTS/CONCLUSIONS: Idiosyncratic drug-induced agranulocytosis remains a potentially serious adverse event owing 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. However, several prognostic factors have recently been identified that may be helpful in practice to identify 'susceptible' patients. Old age (>65 years), septicemia or shock, metabolic disorders such as renal failure and a neutrophil count below 0.1 × 10(9)/l are currently consensually accepted as poor prognostic factors. In this potentially life-threatening disorder, modern management with broad-spectrum antibiotics and hematopoietic growth factors (particularly granulocyte colony-stimulating factor) is likely to improve prognosis. Thus, with appropriate management, the mortality rate from idiosyncratic drug-induced agranulocytosis is currently approximately 5%.

摘要

目的

本文报告并讨论了特发性药物诱导性粒细胞缺乏症(中性粒细胞计数<0.5×10(9)/升)的临床表现和治疗。

结果/结论:由于约三分之二住院患者会出现严重败血症伴严重深部组织感染(如肺炎)、败血症和感染性休克,特发性药物诱导性粒细胞缺乏症仍然是一种潜在的严重不良事件。然而,最近已经确定了一些预后因素,这些因素在实践中可能有助于识别“易感”患者。高龄(>65 岁)、败血症或休克、代谢紊乱(如肾衰竭)和中性粒细胞计数<0.1×10(9)/升目前被公认为预后不良的因素。在这种潜在的危及生命的疾病中,广泛使用抗生素和造血生长因子(特别是粒细胞集落刺激因子)的现代治疗方法可能会改善预后。因此,通过适当的治疗,特发性药物诱导性粒细胞缺乏症的死亡率目前约为 5%。

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