Clinical evaluation of the BioFire Respiratory Pathogen Panel for the guidance of empirical antimicrobial therapy in critically ill patients with hospital-acquired pneumonia: A multicenter, quality improvement project

IF 3.7 3区 医学 Q1 ANESTHESIOLOGY
Cécile Poulain , Yoann Launey , Marwan Bouras , Karim Lakhal , Laura Dargelos , Lise Crémet , Sophie-Anne Gibaud , Stéphane Corvec , Philippe Seguin , Bertrand Rozec , Karim Asehnoune , Fanny Feuillet , Antoine Roquilly
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Abstract

Background

We aimed to determine whether implementing antimicrobial stewardship based on multiplex bacterial PCR examination of respiratory fluid can enhance outcomes of critically ill patients with hospital-acquired pneumonia (HAP).

Methods

We conducted a quality improvement study in two hospitals in France. Adult patients requiring invasive mechanical ventilation with a diagnosis of HAP were included. In the pre-intervention period (August 2019 to April 2020), antimicrobial therapy followed European guidelines. In the «intervention» phase (June 2020 to October 2021), treatment followed a multiplex PCR-guided protocol. The primary endpoint was a composite endpoint made of mortality on day 28, clinical cure between days 7 and 10, and duration of invasive mechanical ventilation on day 28. The primary outcome was analyzed with a DOOR strategy.

Results

A total of 443 patients were included in 3 ICUs from 2 hospitals (220 pre-intervention; 223 intervention). No difference in the ranking of the primary composite outcome was found (DOOR: 50.3%; 95%CI, 49.9%–50.8%). The number of invasive mechanical ventilation-free days at day 28 was 10.0 [0.0; 19.0] in the baseline period and 9.0 [0.0; 20.0] days during the intervention period (p = 0.95). The time-to-efficient antimicrobial treatment was 0.43 ± 1.29 days before versus 0.55 ± 1.13 days after the intervention (p = 0.56).

Conclusion

Implementation of Rapid Multiplex PCR to guide empirical antimicrobial therapy for critically ill patients with HAP was not associated with better outcomes. However, adherence to stewardship was low, and the study may have had limited power to detect a clinically important difference.

用于指导医院获得性肺炎重症患者经验性抗菌治疗的 BioFire 呼吸道病原体样本临床评估:多中心质量改进项目。
背景:我们的目的是确定基于呼吸液多重细菌 PCR 检查的抗菌药物管理能否提高医院获得性肺炎(HAP)重症患者的治疗效果:我们在法国两家医院开展了一项质量改进研究。方法:我们在法国的两家医院开展了一项质量改进研究,研究对象包括需要进行有创机械通气并确诊为 HAP 的成人患者。在干预前阶段(2019 年 8 月至 2020 年 4 月),抗菌治疗遵循欧洲指南。在 "干预 "阶段(2020 年 6 月至 2021 年 10 月),治疗遵循多重 PCR 指导方案。主要终点是由第 28 天的死亡率、第 7 至 10 天的临床治愈率和第 28 天有创机械通气持续时间组成的复合终点。主要结果采用 DOOR 策略进行分析:两家医院的 3 个重症监护室共纳入 443 名患者(干预前 220 人;干预后 223 人)。主要综合结果的排名没有差异(DOOR:50.3%;95%CI:49.9% 至 50.8%)。基线期第 28 天无创机械通气天数为 10.0 [0.0; 19.0]天,干预期为 9.0 [0.0; 20.0]天(P = 0.95)。干预前的有效抗菌治疗时间为 0.43+/-1.29 天,干预后为 0.55+/-1.13 天(p = 0.56):结论:采用快速多重 PCR 技术指导 HAP 重症患者的经验性抗菌治疗与更好的治疗效果无关。然而,患者对抗菌药物管理的依从性较低,因此该研究可能无法检测出具有重要临床意义的差异。
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来源期刊
CiteScore
6.70
自引率
5.50%
发文量
150
审稿时长
18 days
期刊介绍: Anaesthesia, Critical Care & Pain Medicine (formerly Annales Françaises d''Anesthésie et de Réanimation) publishes in English the highest quality original material, both scientific and clinical, on all aspects of anaesthesia, critical care & pain medicine.
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