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不同并发症风险的中性粒细胞减少患者发热的管理。

Management of fever in neutropenic patients with different risks of complications.

作者信息

Klastersky Jean

机构信息

Department of Medicine, Institut Bordet, Service de Medicine, Brussels, Belgium.

出版信息

Clin Infect Dis. 2004 Jul 15;39 Suppl 1:S32-7. doi: 10.1086/383050.

Abstract

Risk stratification of febrile neutropenic patients can have important implications in terms of management. The first prospectively validated risk scoring system was developed in 1992. A subsequent scoring system was developed in 2000, in which a score of < or =21 predicts a <5% risk for severe complications. Oral combination therapy in an ambulatory or home care setting is acceptable for low-risk patients. Hospital admission is mandatory for high-risk patients. Intravenous monotherapy can be given if neutropenia is anticipated to be of short duration; it is also acceptable if neutropenia is expected to be more prolonged but the patients is stable and do not have an infectious focus. All other patients should receive combination therapy with an aminoglycoside, if infection with a gram-negative pathogen is suspected, or a glycopeptide, if a gram-positive organism is suspected. However, antimicrobial therapy with coverage against gram-negative organisms should always be provided because of the significant mortality associated with these infections.

摘要

发热性中性粒细胞减少患者的风险分层对治疗具有重要意义。首个经过前瞻性验证的风险评分系统于1992年开发。随后在2000年又开发了一个评分系统,其中评分≤21分预示严重并发症风险<5%。低风险患者可在门诊或家庭护理环境中接受口服联合治疗。高风险患者必须住院。如果预计中性粒细胞减少持续时间较短,可给予静脉单药治疗;如果预计中性粒细胞减少持续时间较长,但患者病情稳定且无感染灶,也可接受静脉单药治疗。所有其他患者,如果怀疑感染革兰氏阴性病原体,应接受含氨基糖苷类的联合治疗;如果怀疑感染革兰氏阳性菌,则应接受含糖肽类的联合治疗。然而,由于革兰氏阴性菌感染相关的显著死亡率,始终应提供覆盖革兰氏阴性菌的抗菌治疗。

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