抗菌药物在发热性中性粒细胞减少症患者中的应用。

B E De Pauw, J M Raemaekers, T Schattenberg, J P Donnelly
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引用次数: 0

摘要

未标记:本分析的目的是评估一种更个性化的经验抗生素治疗发热性中性粒细胞减少症的可行性,并探讨修改初始方案的原因。设计、环境和研究对象:主要来源是来自全球35个中心进行的一项非盲法大型试验的发热性中性粒细胞减少癌患者数据库。这是由来自奈梅亨大学医院血液科连续系列随机试验的患者数据补充的。干预措施:标准化了诊断程序,定义了可能的感染类型,并记录了修改经验方案的原因。主要结局指标:发热性中性粒细胞减少发作的生存率,微生物学和临床定义的与致病微生物有关的感染的发展,以及治疗结果。结果:单药治疗与联合治疗同样有效,总死亡率<或= 7%,其中21%的中性粒细胞减少发作伴有临床定义的感染证明是致命的,而没有焦点的发作只有4%。在治疗结束时,在多中心试验中,60%的病例添加了经验性方案,而在我们自己的机构中,这一比例为39%,在许多病例中,仅仅是因为持续发烧。结论:针对发热性嗜中性粒细胞减少的癌症患者,通过补充经验方案,制定个性化定制抗生素治疗指南是实现最佳抗感染策略的可行选择。
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Empirical and subsequent use of antibacterial agents in the febrile neutropenic patient.

Unlabelled: The objective of this analysis were an assessment of the feasibility of a more individually tailored approach of empirical antibiotic therapy in febrile neutropenia and an exploration of the reasons to modify the initial regimen.

Design, setting and subjects: The main source was a database on febrile neutropenic cancer patients from an unblinded large trial conducted in 35 centres world-wide. This was supplemented by data from patients enrolled in a consecutive series of randomized trials at the Department of Haematology, University Hospital Nijmegen.

Interventions: Diagnostic procedures were standardized, types of possible infections defined and the reasons for modifying an empirical regimen were recorded.

Main outcome measures: Survival of the febrile neutropenic episode, development of microbiologically and clinically defined infection in relation to causative organisms, and results of modification.

Results: Monotherapy was as effective as combination therapy with an overall mortality of < or = 7%, with 21% of neutropenic episodes accompanied by a clinically defined infection proving fatal compared with only 4% of episodes without a focus. At the end of treatment the empirical regimen had been added to in 60% of cases in the multicentre trial, in contrast to 39% in our own institution, in many cases simply because of continuing fever.

Conclusion: The development of local guidelines for individually tailoring antibiotic therapy by complementing the empirical regimen is a feasible option for achieving an optimal anti-infective strategy for febrile neutropenic cancer patients.

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