Abstract

BackgroundBlood biomarkers are increasingly used to diagnose, guide therapy in, and risk-stratify community-acquired pneumonia (CAP) patients in emergency departments (EDs). How pre-analytic factors affect these markers’ initial levels in this population is unknown.MethodsIn this secondary analysis of consecutive ED patients with CAP from a large multicentre antibiotic stewardship trial, we used adjusted multivariate regression models to determine the magnitude and statistical significance of differences in mean baseline concentrations of five biomarkers (procalcitonin [PCT], C-reactive protein [CRP], white blood cells count [WBC], proadrenomedullin [ProADM], copeptin) associated with six pre-analytic factors (antibiotic or corticosteroid pretreatment, age, gender, chronic renal failure or chronic liver insufficiency).ResultsOf 925 CAP patients (median age 73 years, 58.8% male), 25.5% had antibiotic pretreatment, 2.4%, corticosteroid pretreatment, 22.3%, chronic renal failure, 2.4% chronic liver insufficiency. Differences associated with pre-analytic factors averaged 6.1% ±4.6%; the three largest statistically significant changes (95% confidence interval) were: PCT, +14.2% (+2.1% to +26.4%, p = 0.02) with liver insufficiency; ProADM, +13.2% (+10.2% to +16.1%, p < 0.01) with age above median; CRP, -12.8% (-25.4% to -0.2%, p = 0.05) with steroid pretreatment. In post hoc sensitivity analyses, reclassification statistics showed that these factors did not result in significant changes of biomarker levels across clinically used cut-off ranges.ConclusionsDespite statistically significant associations of some pre-analytic factors and biomarker levels, a clinically relevant influence seems unlikely. Our observations reinforce the concept of using biomarkers in algorithms with widely-separated cut-offs and overruling criteria considering the entire clinical picture.Trial registrationIdentifier ISRCTN95122877.Electronic supplementary materialThe online version of this article (doi:10.1186/1471-2253-14-102) contains supplementary material, which is available to authorized users.

Highlights

  • Blood biomarkers are increasingly used to diagnose, guide therapy in, and risk-stratify communityacquired pneumonia (CAP) patients in emergency departments (EDs)

  • For this purpose, circulating levels of biomarkers associated with bacterial infection and inflammation, procalcitonin (PCT), as well as C-reactive protein (CRP) and white blood cells count (WBC), are increasingly considered in the initial assessment of patients with signs or

  • The study sample comprised all 925 confirmed CAP patients included in the ProHOSP trial

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Summary

Introduction

Blood biomarkers are increasingly used to diagnose, guide therapy in, and risk-stratify communityacquired pneumonia (CAP) patients in emergency departments (EDs). To improve outcomes in community-acquired pneumonia (CAP), management guidelines emphasize early diagnosis to enable a timely start of appropriate antimicrobial therapy [1,2] For this purpose, circulating levels of biomarkers associated with bacterial infection and inflammation, procalcitonin (PCT), as well as C-reactive protein (CRP) and white blood cells count (WBC), are increasingly considered in the initial assessment of patients with signs or Before admission, CAP patients presenting to the emergency department (ED) frequently have received pretreatment with antibiotics or corticosteroids. These patients are often elderly and may have varying degrees of kidney or liver dysfunction. Previous literature has addressed such associations only in healthy volunteers or critical care patients, populations differing greatly from ED patients with CAP in pretreatment, age, gender composition, comorbidity, and general state [12,13,14,18]

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