Abstract
Background
Bloodstream infection (BSI) is a common urgent condition at the emergency department (ED). However, current guidelines for diagnosis do not specify the juncture at which blood cultures should be taken. The decision whether or not to obtain hemoculture is based solely upon clinical judgment and potential outcomes of inappropriately ordered cultures. This study aimed to find clinical factors present on ED arrival that are predictive of bloodstream infection.
Methods
This study was conducted retrospectively at the ED of a single tertiary care hospital in Thailand. We included adult patients with suspected infection based on blood culture who were treated with intravenous antibiotics during their ED visit. Independent positive predictors for positive blood culture were calculated by logistic regression analysis.
Results
A total of 169,578 patients visited the ED during the study period, 12,556 (7.40%) of whom were suspected of infection. Of those, 8177 met the study criteria and were categorized according to blood culture results (741 positive; 9.06%). Six clinical factors, including age over 55 years, moderate to severe CKD, solid organ tumor, liver disease, history of chills, and body temperature of over 38.3 °C, were associated with positive blood culture.
Conclusions
Clinical factors at ED arrival can be used as predictors of bloodstream infection.
Keywords: Bloodstream infection, Bacteremia, Blood cultures, Rapid diagnosis, Emergency department
Background
Bloodstream infection (BSI) is a common urgent condition at the emergency department (ED) [1, 2]. In 2010, the annual incidence of bloodstream infection increased to 38.1 persons per 100,000, and the mortality rate was as high as 50% [3]. Early diagnosis and appropriate antimicrobial therapy are a key to improving patient outcomes [4], particularly among individuals displaying either septic shock or sepsis [5, 6].
Current guidelines recommend obtaining hemoculture in patients suspected of sepsis in order to diagnose BSI [5, 7], as positive blood culture is an important factor in determining the appropriate antibiotic treatment [5, 8]. However, the guidelines do not specify when blood cultures ought to be procured. Furthermore, the decision as to whether to take hemoculture is based solely upon clinical judgment, which could result in unnecessary cultures [8–10]. There are several predictors of bloodstream infection at the ED such as blood pressure less than 60 mmHg, procalcitonin levels over 2 μg/L, and C-reactive protein> 10 mg/dL [11]. Shapiro et al. developed a clinical score for bloodstream infection at the ED with a decent validation of 83% [12]. However, obtaining this score may require laboratory results, which could result in delayed sepsis management [6]. Hence, this study examined only clinical factors present on ED arrival to determine which, if any, were predictive of bloodstream infection.
Methods
Study design and ethical approval
This study was conducted retrospectively as part of an ED infection project at Khon Kaen University’s Srinagarind Hospital, a tertiary care hospital with approximately 60,000 annual ED visits. Inclusion criteria were age > 18 years, suspicion of infection based on blood culture collection, and initiation of intravenous antibiotics during the ED visit. Cases with cardiac arrest or trauma, those referred from other hospitals, those who had previously received antibiotics, and those missing clinical data were excluded. The study period took place between January 1st, 2016 and December 31st, 2018. The study protocol was approved by the Khon Kaen University Ethics Committee in Human Research (HE631115).
Source of data and microbiological methods
Blood cultures at the ED each consist of two aerobic bottles. Those with a pathogen similar to at least one sample with clinical relevance were considered positive for bloodstream infection. Pathogens (e.g., coagulase-negative Staphylococci, Corynebacterium spp., Propionibacterium spp., Viridans group streptococci, Micrococcus spp., and Bacillus spp.) were considered as such if they were isolated from a patient twice or more consecutively with clinical relevance [7, 13, 14]. Clinical data of eligible patients were retrieved from the computerized hospital database and chart records. Data were subsequently categorized as comorbid conditions, ED arrival parameters, and parameters beyond the initial hour following presentation at the ED. Comorbid conditions were defined according to the Charlson Comorbidity Index (CCI) [15]. ED arrival parameters included history of fever or chills, vital signs, and sepsis scores including Systemic Inflammatory Response Syndrome (SIRS) score, quick Sepsis-related Organ Failure Assessment (qSOFA), and National Early Warning Score (NEWS). Parameters beyond the initial hour post ED arrival included white blood cell count and lactate levels.
Statistical analysis
Eligible patients were categorized into two groups based on whether their blood culture results were positive or negative. Descriptive statistics were used to compare differences in studied variables between the two groups. Factors associated with positive blood culture were calculated via logistic regression analysis. Univariate and multivariate logistic regression were applied to calculate the unadjusted/adjusted odds ratios (95% confidence interval) of each factor. All statistical analyses were performed using STATA version 10.1 (College Station, Texas, USA).
Results
Patient characteristic and microbiology data
A total of 169578 patients visited the ED during the study period, of which 12556 (7.40%) were suspected of infection according to the hospital database. After exclusion, 8177 individuals met the study criteria and were categorized according to blood culture results as either positive for bloodstream infection (741 patients; 9.06%) or negative/non-pathogen bacteremia (7436 patients; 90.94%), as shown in Fig. 1. Almost all variables studied differed significantly between groups (Table 1), with the exception of AIDS prevalence (2.16% in the positive group and 1.44% in the negative group; p 0.125). The most common Gram-negative and positive pathogens were Escherichia coli (274 patients; 36.98%) and Streptococcus (76 patients; 10.26%), respectively.
Fig. 1.

Study flow of patients with suspected infection presenting at the emergency department and blood culture results
Table 1.
Baseline characteristics of patients with suspected infection presenting at the emergency department categorized by blood culture results
| ALL patients (n = 8177) n (%) | Positive blood culture (n = 741) n (%) | Negative blood culture (n = 7436) n (%) | p-value | |
|---|---|---|---|---|
| Demographics | ||||
| Age, yrs. –median (range) | 62 (18–100) | 62 (18–100) | 64 (18–100) | < 0.001 |
| Male | 4275 (52.28) | 415 (56.01) | 3860 (51.90) | 0.003 |
| CCI –median (range) | 3 (0–13) | 4 (0–13) | 3 (0–13) | < 0.001 |
| Comorbidity | ||||
| Age > 55 years | 5231 (63.97) | 537 (72.47) | 4694 (63.13) | < 0.001 |
| Hypertension | 2149 (26.28) | 235 (31.71) | 1914 (25.74) | < 0.001 |
| Solid organ malignancy | 1878 (22.97) | 231 (31.17) | 1647 (22.15) | < 0.001 |
| Diabetes mellitus | 1729 (21.14) | 194 (26.18) | 1535 (20.64) | < 0.001 |
| Liver disease | 1190 (14.55) | 191 (25.78) | 999 (13.43) | < 0.001 |
| Moderate to severe CKD | 639 (7.81) | 86 (11.61) | 553 (7.44) | < 0.001 |
| AIDS | 123 (1.50) | 16 (2.16) | 107 (1.44) | 0.125 |
| History of chills | 515 (6.30) | 101 (13.63) | 414 (5.57) | < 0.001 |
| Clinical presentation at triage zone | ||||
| Respiratory rate > 22/min | 5369 (65.66) | 573 (77.33) | 4796 (64.50) | < 0.001 |
| Temperature > 38.3 °C | 2658 (32.51) | 349 (47.10) | 2309 (31.05) | < 0.001 |
| Heart rate > 120/min | 921 (11.26) | 105 (14.17) | 816 (10.97) | < 0.001 |
| Hypotension (SBP < 90 or MAP < 65 mmHg) | 611 (7.47) | 96 (12.96) | 515 (6.93) | < 0.001 |
| Met Sepsis criteria | ||||
| SIRS ≥2 | 6149 (75.20) | 651 (87.85) | 5498 (93.94) | < 0.001 |
| qSOFA ≥2 | 1230 (15.04) | 140 (18.89) | 1060 (14.25) | < 0.001 |
| NEWS ≥7 | 2917 (35.67) | 259 (34.95) | 1759 (23.66) | < 0.001 |
| Lactate values | (n = 4694) | (n = 575) | (n = 4119) | |
| First lactate, mmol/L-median | 1.88 (0.01–28.33) | 2.50 (0.01–18.71) | 1.80 (0.01–28.33) | < 0.001 |
| First lactate > 2 mmol/L | 2193 (46.72) | 383 (51.69) | 1810 (23.34) | < 0.001 |
CKD chronic kidney disease, SBP systolic blood pressure, MAP mean arterial pressure, SIRS Systemic Inflammatory Response Syndrome, qSOFA quick Sepsis-related Organ Failure Assessment, NEWS National Early Warning Score
Clinical factors predictive of bloodstream infection
There were four significant comorbid conditions, two factors at ED arrival, and three factors beyond the first hour (Table 2). The six significant predictors for positive blood culture on ED arrival were age over 55 years, moderate to severe CKD, solid organ tumor, liver disease, history of chills, and body temperature over 38.3 °C. Liver disease had the highest adjusted odds ratio at 2.04 (95% CI of 1.59, 2.61). The adjusted odds ratio of independent factors ranged from 1.33 to 2.04 (Table 2). Beyond the first hour after ED arrival, lactate level and white blood cell count were both significant factors, with adjusted odds ratios ranging from 1.10 to 2.48.
Table 2.
Factors associated with positive blood culture in patients suspected of infection presenting at the emergency department
| Factors | Unadjusted Odds Ratio (95% CI) | aAdjusted Odds Ratio (95% CI) | p-value |
|---|---|---|---|
| Comorbid conditions | |||
| Age > 55 | 1.54 (1.30–1.81) | 1.33 (1.04–1.72) | 0.02 |
| Sex | 0.84 (0.73–0.99) | 0.94 (78.1–1.13) | 0.52 |
| Emergency severity index level | 0.62 (0.55–0.70) | 0.87 (0.71–1.13) | 0.18 |
| CCI | 1.13 (1.09–1.06) | 0.98 (0.92–1.04) | 0.46 |
| Liver disease | 2.24 (1.87–2.67) | 2.04 (1.59–2.61) | < 0.01 |
| Diabetes mellitus | 1.36 (1.15–1.62) | 1.08 (0.89–1.30) | 0.45 |
| Moderate to severe CKD | 1.63 (1.28–2.08) | 1.68 (1.22–2.32) | 0.01 |
| Solid organ tumor | 1.59 (1.35–1.87) | 1.40 (1.09–1.80) | 0.01 |
| Hypertension | 1.34 (1.13–1.57) | 1.14 (0.92–1.41) | 0.24 |
| On arrival parameter | |||
| History of Chills | 2.67 (2.12–3.38) | 1.94 (1.43–2.62) | < 0.01 |
| Temperature > 38.3 °C | 1.40 (1.32–1.50) | 1.77 (1.39–2.25) | < 0.01 |
| Heart rate > 120 /min | 1.01 (1.00–1.01) | 0.96 (0.73–1.26) | 0.76 |
| SBP < 90 or MAP < 65 | 2.01 (1.59–2.54) | 1.22 (0.86–1.71) | 0.26 |
| Respiratory rate > 22/min | 1.03 (1.02–1.04) | 0.89 (0.71–1.26) | 0.32 |
| SIRS criteria ≥2 | 2.5 (2.03–3.20) | 1.21 (0.94–1.53) | 0.26 |
| qSOFA criteria ≥2 | 1.79 (1.49–2.15) | 1.20 (0.94–1.53) | 0.15 |
| NEWS ≥7 | 1.73 (1.47–2.04) | 0.93 (0.73–1.18) | 0.53 |
| Beyond first hour parameter | |||
| bLactate level | 1.13 (1.10–1.16) | 1.10 (1.07–1.14) | < 0.01 |
| WBC > 11,000 /microliter | 1.31 (1.12–1.52) | 1.28 (1.03–1.59) | 0.03 |
| WBC < 3000 /microliter | 2.30 (1.70–3.13) | 2.48 (1.68–3.66) | < 0.01 |
CCI Charlson Comorbidity Index, CKD chronic kidney disease, SBP systolic blood pressure, MAP mean arterial pressure, SIRS Systemic Inflammatory Response Syndrome; qSOFA quick Sepsis-related Organ Failure Assessment, NEWS National Early Warning Score, WBC white blood cell
a adjusted by the studied factors shown in this table
b initial lactate level in mmol/L.
Discussion
The positive blood culture rate in this study (9.06%) was comparable with those in previous studies (up to 12.4%) [11, 16]. Subjecting low-risk patients to unnecessary blood culture may yield false positives and increase healthcare costs [12]. As previously reported [12, 17–19], fever and older age are independently associated with positive blood culture at the ED. Although body temperature over 38.3 degrees celsius is one criterion included in the SIRS score [5], only 47.10% of patients in this group had positive cultures (Table 1). The proportion of patients in the positive group with respiratory rate over 22 times/min was higher than that of those with high body temperature (77.33% vs 47.10%). However, this difference was not significant after adjustment for other factors (Table 2). This implies that body temperature alone may not be an adequate indicator of positive blood culture and that it should, instead, be considered in combination with the other five independent factors.
History of chills, which is an indicator of pyrogenic cytokines, is another predictor of positive blood culture. Previous studies by Tokuda et al. and Holmqvist et al. showed history of chills to be associated with positive blood culture, regardless of severity (mild to shaking) [20, 21]. However, these studies had smaller populations and adjusted for fewer other variables than did our study. The former adjusted for only age and body temperature (n = 526), while the latter adjusted for age, sex, vomiting, and antibiotic use (n = 479).
This study’s findings regarding co-morbid diseases and laboratory tests differed from those of some previous studies [17, 18]. One study, for example, found that the prevalence of liver cirrhosis, chronic kidney disease, and malignancy did not differ significantly between those with and those without positive blood culture [17], whereas our study found a correlation between these co-morbid diseases and blood culture positivity. These differences may have been due to our larger study population or the fact that we used clinical factors (with no laboratory results) to predict positive blood cultures in order to allow for more rapid assessment of risk. However, there have been other studies that have reported findings similar to ours [19, 22–24]. For example, one previous study found that cirrhotic patients had a higher incidence of bloodstream infection than non-cirrhotic patients [24].
Strengths and limitations
In this study, we enrolled a large population to determine predictors for positive blood culture in ED patients with suspicion of infection. However, there were some limitations to this study. Although we employed a large sample size, clinical data were missing in some cases due to the retrospective study design. Such cases were excluded (261 patients). Second, blood cultures were performed based on the judgement of the attending physicians at a single ED. Further studies are thus required to validate and confirm the results of this study. Finally, the results may not be universal for other setting such as community hospitals [25, 26].
Conclusions
Six clinical factors, including age over 55 years, moderate to severe CKD, solid organ tumor, liver disease, history of chills, and body temperature of over 38.3 °C were associated with blood culture positivity. Consideration of these clinical factors may allow for more rapid assessment of positive blood culture risk in ED patients suspected of infection.
Acknowledgments
We would like to acknowledge Dr. Dylan Southard for editing the MS via the KKU Publication Clinic (Thailand).
Abbreviations
- AUROC
Associated area under the ROC
- BSI
Bloodstream infection (BSI)
- CCI
Charlson Comorbidity Index
- CKD
Chronic kidney disease
- ED
Emergency department
- +LR
Positive likelihood ratio
- -LR
Negative likelihood ratio
- MAP
Mean arterial pressure
- NEWS
National Early Warning Score
- qBSI score
Quick Bloodstream Infection score
- ROC curve
Receiver operating characteristic curves
- SIRS
Systemic Inflammatory Response Syndrome (SIRS)
- SBP
Systolic blood pressure
Authors’ contributions
Conceptualization and Methodology: P.P., N.L. and K.A.; data validation: P.P., N.L. and K.I.; data curation and investigation: P.P., K.A. and S.S.; writing—original draft and formal analysis: P.P., K.S. and V.C.; writing—review and editing: All authors; supervision: P.P. and K.A. All authors have read and agreed to the published version of the manuscript.
Funding
This study was funded by a grant from the Khon Kaen University Faculty of Medicine (Thailand; Grant Number MN63202). The funders played no role in the design of the study, collection, analysis or interpretation of data, or writing of the manuscript.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Declarations
Ethics approval and consent to participate
The study period took place between January 1st, 2016 and December 31st, 2018 using study protocols approved by the Khon Kaen University Ethics Committee in Human Research (HE631115).
Consent for publication
Not applicable.
Competing interests
The authors declare that they have no competing interests.
Footnotes
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
References
- 1.Boyles TH, Davis K, Crede T, Malan J, Mendelson M, Lesosky M. Blood cultures taken from patients attending emergency departments in South Africa are an important antibiotic stewardship tool, which directly influences patient management. BMC Infect Dis. 2015;15:410. 10.1186/s12879-015-1127-1. [DOI] [PMC free article] [PubMed]
- 2.Anderson DJ, Moehring RW, Sloane R, Schmader KE, Weber DJ, Fowler VG, et al. Bloodstream infections in community hospitals in the 21st century: a multicenter cohort study. PLoS One. 2014;9(3):e91713. 10.1371/journal.pone.0091713. [DOI] [PMC free article] [PubMed]
- 3.Cheung Y, Ko S, Wong OF, Lam HSB, Ma HM, Lit CHA. Clinical experience in management of bloodstream infection in emergency medical ward: A preliminary report. Hong Kong J Emerg Med. 2019:102490791989049.
- 4.Timsit J-F, Ruppé E, Barbier F, Tabah A, Bassetti M. Bloodstream infections in critically ill patients: an expert statement. Intensive Care Med. 2020;46:266–284. doi: 10.1007/s00134-020-05950-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Rhodes A, Evans LE, Alhazzani W, Levy MM, Antonelli M, Ferrer R, et al. Surviving Sepsis campaign: international guidelines for Management of Sepsis and Septic Shock: 2016. Intensive Care Med. 2017;43:304–377. doi: 10.1007/s00134-017-4683-6. [DOI] [PubMed] [Google Scholar]
- 6.Levy MM, Evans LE, Rhodes A. The surviving Sepsis campaign bundle: 2018 update. Intensive Care Med. 2018;44:925–928. doi: 10.1007/s00134-018-5085-0. [DOI] [PubMed] [Google Scholar]
- 7.Miller JM, Binnicker MJ, Campbell S, Carroll KC, Chapin KC, Gilligan PH, et al. A guide to utilization of the microbiology Laboratory for Diagnosis of infectious diseases: 2018 update by the Infectious Diseases Society of America and the American society for Microbiologya. Clin Infect Dis. 2018;67:813–816. doi: 10.1093/cid/ciy584. [DOI] [PubMed] [Google Scholar]
- 8.Long B, Koyfman A. Best clinical practice: blood culture utility in the emergency department. J Emerg Med. 2016;51:529–539. doi: 10.1016/j.jemermed.2016.07.003. [DOI] [PubMed] [Google Scholar]
- 9.Lamy B, Dargère S, Arendrup MC, Parienti J-J, Tattevin P. How to optimize the use of blood cultures for the diagnosis of bloodstream infections? A State-of-the Art. Front Microbiol. 2016;7:697. 10.3389/fmicb.2016.00697. [DOI] [PMC free article] [PubMed]
- 10.Coburn B, Morris AM, Tomlinson G, Detsky AS. Does this adult patient with suspected bacteremia require blood cultures? JAMA. 2012;308:502–511. doi: 10.1001/jama.2012.8262. [DOI] [PubMed] [Google Scholar]
- 11.Chase M, Klasco RS, Joyce NR, Donnino MW, Wolfe RE, Shapiro NI. Predictors of bacteremia in emergency department patients with suspected infection. Am J Emerg Med. 2012;30:1691–1697. doi: 10.1016/j.ajem.2012.01.018. [DOI] [PubMed] [Google Scholar]
- 12.Shapiro NI, Wolfe RE, Wright SB, Moore R, Bates DW. Who needs a blood culture? A prospectively derived and validated prediction rule. J Emerg Med. 2008;35:255–264. doi: 10.1016/j.jemermed.2008.04.001. [DOI] [PubMed] [Google Scholar]
- 13.Dargère S, Cormier H, Verdon R. Contaminants in blood cultures: importance, implications, interpretation and prevention. Clin Microbiol Infect. 2018;24:964–969. doi: 10.1016/j.cmi.2018.03.030. [DOI] [PubMed] [Google Scholar]
- 14.Manian FA. IDSA guidelines for the diagnosis and Management of Intravascular Catheter-Related Bloodstream Infection. Clin Infect Dis. 2009;49:1770–1771. doi: 10.1086/648113. [DOI] [PubMed] [Google Scholar]
- 15.Charlson ME, Pompei P, Ales KL, MacKenzie CR. A new method of classifying prognostic comorbidity in longitudinal studies: development and validation. J Chronic Dis. 1987;40:373–383. doi: 10.1016/0021-9681(87)90171-8. [DOI] [PubMed] [Google Scholar]
- 16.Lindvig KP, Nielsen SL, Henriksen DP, Jensen TG, Kolmos HJ, Pedersen C, et al. Mortality and prognostic factors of patients who have blood cultures performed in the emergency department: a cohort study. Eur J Emerg Med. 2016;23:166–172. doi: 10.1097/MEJ.0000000000000250. [DOI] [PubMed] [Google Scholar]
- 17.Jessen MK, Mackenhauer J, Hvass AMSW, Ellermann-Eriksen S, Skibsted S, Kirkegaard H, et al. Prediction of bacteremia in the emergency department: an external validation of a clinical decision rule. Eur J Emerg Med. 2016;23:44–49. doi: 10.1097/MEJ.0000000000000203. [DOI] [PubMed] [Google Scholar]
- 18.Su C-P, Chen TH-H, Chen S-Y, Ghiang W-C, Wu GH-M, Sun H-Y, et al. Predictive model for bacteremia in adult patients with blood cultures performed at the emergency department: a preliminary report. J Microbiol Immunol Infect. 2011;44:449–455. doi: 10.1016/j.jmii.2011.04.006. [DOI] [PubMed] [Google Scholar]
- 19.James MT, Laupland KB, Tonelli M, Manns BJ, Culleton BF, Hemmelgarn BR, et al. Risk of bloodstream infection in patients with chronic kidney disease not treated with dialysis. Arch Intern Med. 2008;168(21):2333–2339. doi: 10.1001/archinte.168.21.2333. [DOI] [PubMed] [Google Scholar]
- 20.Tokuda Y, Miyasato H, Stein GH, Kishaba T. The degree of chills for risk of bacteremia in acute febrile illness. Am J Med. 2005;118(12):1417. doi: 10.1016/j.amjmed.2005.06.043. [DOI] [PubMed] [Google Scholar]
- 21.Holmqvist M, Inghammar M, Påhlman LI, Boyd J, Åkesson P, Linder A, et al. Risk of bacteremia in patients presenting with shaking chills and vomiting - a prospective cohort study. Epidemiol Infect. 2020;148:e86. doi: 10.1017/S0950268820000746. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Wan Q, Ye Q, Zhou J. Mortality predictors of bloodstream infections in solid-organ transplant recipients. Exp Clin Transplant. 2013;11:211–214. doi: 10.6002/ect.2012.0093. [DOI] [PubMed] [Google Scholar]
- 23.Zhao H, Gu X, Zhao R, Shi Y, Sheng J. Evaluation of prognostic scoring systems in liver cirrhosis patients with bloodstream infection. Medicine. 2017;96(50):e8844. 10.1097/MD.0000000000008844. [DOI] [PMC free article] [PubMed]
- 24.Thulstrup AM, Sørensen HT, Schønheyder HC, Møller JK, Tage-Jensen U. Population-based study of the risk and short-term prognosis for bacteremia in patients with liver cirrhosis. Clin Infect Dis. 2000;31:1357–1361. doi: 10.1086/317494. [DOI] [PubMed] [Google Scholar]
- 25.Jingmark S, Kuhirunyaratn P, Theeranut A, Nonjui P. Subjective well-being and related factors among community-dwelling elderly in Udon Thani Province, Thailand. Asia Pac J Sci Technol. 2020;25:APST-25-01-09. [Google Scholar]
- 26.Chaiear N, Nirarach K, Kawamatawong T, Krisorn P, Burge PS. Proportion of workers having work-related asthma symptoms in a cassava factory, Nakhon Ratchasima province, Thailand. Asia Pac J Sci Technol. 2020;25:APST-25-02-08. [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
