Biomarkers from distinct biological pathways improve early risk stratification in medical emergency patients: the multinational, prospective, observational TRIAGE study

被引:77
|
作者
Schuetz, Philipp [1 ,6 ]
Hausfater, Pierre [2 ]
Amin, Devendra [3 ]
Amin, Adina [3 ]
Haubitz, Sebastian [1 ]
Faessler, Lukas [1 ]
Kutz, Alexander [1 ]
Conca, Antoinette [4 ]
Reutlinger, Barbara [4 ]
Canavaggio, Pauline [2 ]
Sauvin, Gabrielle [2 ]
Bernard, Maguy [7 ,8 ]
Huber, Andreas [5 ]
Mueller, Beat [1 ,6 ]
机构
[1] Kantonsspital Aarau, Univ Dept Med, Div Gen & Emergency Med, CH-5001 Aarau, Switzerland
[2] Grp Hosp Pitie Salpetriere, AP HP, Emergency Dept, F-75634 Paris, France
[3] Morton Plant Hosp, Dept Crit Care, Clearwater, FL 33756 USA
[4] Kantonsspital Aarau, Dept Clin Nursing Sci, CH-5001 Aarau, Switzerland
[5] Kantonsspital Aarau, Dept Lab Med, CH-5001 Aarau, Switzerland
[6] Univ Basel, Med Fac, Basel, Switzerland
[7] Hop La Pitie Salpetriere, Biochem Dept, Paris, France
[8] Univ Paris 05, Paris, France
来源
CRITICAL CARE | 2015年 / 19卷
基金
瑞士国家科学基金会;
关键词
COMMUNITY-ACQUIRED PNEUMONIA; OUTCOME PREDICTION; SEVERITY INDEX; ISCHEMIC-STROKE; STABLE PEPTIDE; PROADRENOMEDULLIN; COPEPTIN; PROCALCITONIN; HOSPITALIZATION; INFECTIONS;
D O I
10.1186/s13054-015-1098-z
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Introduction: Early risk stratification in the emergency department (ED) is vital to reduce time to effective treatment in high-risk patients and to improve patient flow. Yet, there is a lack of investigations evaluating the incremental usefulness of multiple biomarkers measured upon admission from distinct biological pathways for predicting fatal outcome and high initial treatment urgency in unselected ED patients in a multicenter and multinational setting. Method: We included consecutive, adult, medical patients seeking ED care into this observational, cohort study in Switzerland, France and the USA. We recorded initial clinical parameters and batch-measured prognostic biomarkers of inflammation (pro-adrenomedullin [ProADM]), stress (copeptin) and infection (procalcitonin). Results: During a 30-day follow-up, 331 of 7132 (4.6 %) participants reached the primary endpoint of death within 30 days. In logistic regression models adjusted for conventional risk factors available at ED admission, all three biomarkers strongly predicted the risk of death (AUC 0.83, 0.78 and 0.75), ICU admission (AUC 0.67, 0.69 and 0.62) and high initial triage priority (0.67, 0.66 and 0.58). For the prediction of death, ProADM significantly improved regression models including (a) clinical information available at ED admission (AUC increase from 0.79 to 0.84), (b) full clinical information at ED discharge (AUC increase from 0.85 to 0.88), and (c) triage information (AUC increase from 0.67 to 0.83) (p < 0.01 for each comparison). Similarly, ProADM also improved clinical models for prediction of ICU admission and high initial treatment urgency. Results were robust in regard to predefined patient subgroups by center, main diagnosis, presenting symptoms, age and gender. Conclusions: Combination of clinical information with results of blood biomarkers measured upon ED admission allows early and more adequate risk stratification in individual unselected medical ED patients. A randomized trial is needed to answer the question whether biomarker-guided initial patient triage reduces time to initial treatment of high-risk patients in the ED and thereby improves patient flow and clinical outcomes.
引用
收藏
页数:11
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