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临床试验/NCT02207114
NCT02207114已完成不适用

Southeastern Pennsylvania Adult and Pediatric Prevention Epicenter Network - Randomized Control Trial

University of Pennsylvania1 个研究点 分布在 1 个国家目标入组 145 人开始时间: 2012年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
145
试验地点
1
主要终点
Duration of antibiotic therapy started upon enrollment for presumed sepsis

研究概览

简要总结

The proposed work will provide critical insights into the potential impact of a biomarker-based algorithm on reducing unnecessary antibiotic use in different adult and pediatric/neonatal ICU's. This proposal will also assess the costs (or savings) of a biomarker-based intervention. Overall, the results of this work will be critical in informing future strategies to eliminate unnecessary antibiotic use and curb the continued rise in antimicrobial resistance.

详细描述

The goal of this project is reduce unnecessary use of antibiotics in the ICU. The purpose of Phase I of the study is to identify the biomarker, or combination of biomarkers, that provides optimal test characteristics in identifying adults and children/neonates with presumed sepsis who have a very low likelihood of bacterial infection. Results of Phase I will result in development of a biomarker-based algorithm to inform need for antibiotic use in ICU patients. In Phase II, the impact of this biomarker-based algorithm on reducing antibiotic use in the ICU will be determined. Costs or savings associated with the algorithm will also be assessed.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
None

入排标准

性别
All
接受健康志愿者
否

入选标准

  • •SIRS Criteria
  • •SIRS is considered to be present when patients have more than one of the following clinical findings:
  • •body temperature >38°C or <36°C
  • •heart rate >90 min-1
  • •respiratory rate of >20 min-1 or a Paco2 of <32 mm Hg
  • •and a white blood cell count of >12,000 cells µL-1 or <4,000 µL-1
  • •new empiric antibiotic therapy is initiated, indicating the suspicion of infection. Accepted criteria for SIRS will be used for the Medical Intensive Care Unit and Surgical Intensive Care Unit populations, with appropriate age-specific vital signs definitions to help make the definitions relevant for the Pediatric Intensive Care Unit population.

排除标准

  • •a code status of "do not resuscitate"
  • •absence of initiation or expansion of antibiotic therapy despite meeting criteria for sepsis
  • •presence of an immunocompromising condition.
  • •An immunocompromising condition will be defined as one of the following:
  • •human immunodeficiency virus (HIV) infection with a t-helper cell (CD4) count <200 cell/mm3; 2) immunosuppressive therapy after organ transplantation
  • •neutropenia (<500 neutrophils/mm3)
  • •active chemotherapy within the 3 months preceding eligibility or
  • •diagnosis of cystic fibrosis.
  • •These criteria all represent conditions in which antibiotic use is much less likely to be decreased regardless of the results of a biomarker and are consistent with exclusion criteria used in past studies of the impact of biomarkers.

研究组 & 干预措施

Observational

No Intervention

9 blood biomarkers (including C reactive protein and Procalcitonin) will be assessed across 3 days. Results will not be shared with the subject's medical team. At 3 days, the definitive diagnosis of infection will be determined using Center for Disease Control (CDC) criteria; this will serve as the gold standard for determining biomarker test characteristics. Additional data to collect: demographics, comorbidities, medication use (like antibiotics), lab cultures, x-rays, sepsis resolution, length of hospital stay, and ultimate outcome (i.e., discharge, death). Phase I will identify the biomarker(s) providing the greatest negative predictive value in identifying patients at very low likelihood bacterial infection.

Biomarker Algorithm Intervention

Experimental

The Algorithm arm is equivalent to the intervention. Biomarker algorithm along with the patient's biomarker assay results will be given to clinical team to assist in deciding to continue antibiotics.

The intervention will consist of using the biomarker identified as useful in Phase I to compile an algorithm along containing the patient's biomarker assay results and providing this as additional information for a clinical team consider using to assist in deciding to continue antibiotics. Biomarker algorithms may be different for adult versus pediatric patients, and across different types of ICUs.

干预措施: Biomarker Algorithm Intervention (Other)

结局指标

主要结局

Duration of antibiotic therapy started upon enrollment for presumed sepsis

时间窗: Two years

The primary outcome is the duration of antibiotic treatment after enrollment, expressed in days. This variable will focus specifically on the antibiotic agents given for the episode of presumed sepsis for which the patient was included in the study.

次要结局

  • Subject's Final Disposition(Participants will be followed for the duration of hospital stay, an expected average of 6 days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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