Department of Critical Care Medicine, Ghent University Hospital, 9000 Ghent, Belgium.
J Crit Care. 2010 Dec;25(4):641-6. doi: 10.1016/j.jcrc.2009.11.007. Epub 2010 Jan 15.
De-escalation of antimicrobial therapy is often advocated to reduce the use of broad-spectrum antibiotics in critically ill patients. However, little data are available on the application of this strategy in daily clinical practice.
This is a retrospective analysis of all meropenem prescriptions in a surgical intensive care unit (ICU) during 1 year. Age, Acute Physiology and Chronic Health Evaluation II score on admission to the ICU, site of infection, causative organism, duration of meropenem administration, other antibiotic prescription for the same infectious episode for which meropenem was administered, and ICU mortality were recorded. De-escalation was defined as the administration of an antibiotic with a narrower spectrum within 3 days of the start of meropenem.
Data from 113 meropenem prescriptions were available for analysis. Pulmonary (46%) and complicated intraabdominal (31%) infections were the most frequent infections. In 37 patients, meropenem was used after identification of a multiresistant gram-negative organism (MRGN), whereas in 76 patients, empirical treatment with meropenem was started. Empirical prescription of meropenem was de-escalated in 42% of the patients. In the majority of the patients in whom de-escalation was not done, no conclusive cultures were available to guide treatment; also, colonization with MRGN at other sites was frequently associated with non-de-escalation. Patients in whom antibiotics were de-escalated had a trend toward a lower mortality rate (7% vs 21%, P = .12).
De-escalation after empirical treatment with meropenem was performed in less than half of the patients. Reasons for not de-escalating included the absence of conclusive microbiology and colonization with MRGN.
在危重病患者中,常提倡降低抗菌治疗的强度以减少广谱抗生素的使用。然而,关于该策略在日常临床实践中的应用,数据十分有限。
这是对重症监护病房(ICU)中 1 年内所有美罗培南处方的回顾性分析。记录患者的年龄、入 ICU 时的急性生理学和慢性健康评估 II 评分、感染部位、病原体、美罗培南使用时间、为治疗相同感染而开的其他抗生素处方、以及 ICU 死亡率。降阶梯治疗定义为在开始使用美罗培南后 3 天内使用抗菌谱更窄的抗生素。
共 113 例美罗培南处方的数据可用于分析。肺部(46%)和复杂的腹腔内(31%)感染是最常见的感染。在 37 例患者中,在鉴定出多重耐药革兰氏阴性菌(MRGN)后使用了美罗培南,而在 76 例患者中,经验性开始使用美罗培南治疗。在 42%的患者中,美罗培南的经验性处方被降级。在大多数未降级的患者中,没有明确的培养结果可供指导治疗;此外,MRGN 在其他部位定植也常与未降级治疗相关。抗生素降级的患者死亡率有降低的趋势(7%比 21%,P =.12)。
在经验性使用美罗培南治疗后,只有不到一半的患者进行了降阶梯治疗。未降级的原因包括缺乏明确的微生物学证据和 MRGN 定植。