Emergency management of sepsis: The simple stuff saves lives

Issue: BCMJ, vol. 54 , No. 4 , May 2012 , Pages 176-182 Clinical Articles

ABSTRACT: Many emergency depart­ments have implemented sepsis protocols since the 2001 publication of results from the early goal-directed therapy trial, which showed early targeted resuscitation lowers mortality. As part of an attempt to im­prove clinical and operational outcomes for emergency departments across British Columbia, we review­ed sepsis management literature and considered sepsis protocol im­plementation in the province’s emergency departments. During the literature review we found that many observational studies confirmed an association between implementation of emergency sepsis protocols and decreased mortality. The literature also confirmed that septic pa­tients who have elevated serum lactate and do not clear serum lactate rapidly have increased mortality, and that delay in administration of antibiotics after onset of septic shock was associated with increas­ed mortality. Two BC-based initiatives, the Evidence to Excellence Sepsis Collaborative and Clinical Care Management, support improvements in management of sepsis in BC emergency departments, which should include early identification of septic pa­tients, rapid and appropriate fluid resuscitation, lab tests (serum lactate and blood cultures), antibiotic administration, and source control of infection. Close clinical monitoring and biomarker (lactate) monitoring are also necessary during resuscitation to optimize safety and efficacy.

Research supports using protocols that include delivering antibio­tics within minutes of identifying septic patients in the emergency department.

In 2001 the New England Journal of Medicine published results of a randomized control trial by Rivers and colleagues of early goal-directed therapy (EGDT) that represented a significant advancement in the emergency department (ED) management of sepsis.[1

EGDT relies on invasive monitoring with arterial and central venous catheters that allows clinicians to normalize central venous pressure (CVP) with intravenous fluids and mean arterial pressure (MAP) with vasopressors. Blood transfusions and cardiac inotropes are also used in EGDT to ensure adequate oxygen delivery to peripheral tissues, as confirmed by normal central venous oxygen saturation (ScvO2). 

This RCT showed that patients receiving EGDT after presenting to the emergency department with severe sepsis or septic shock had an absolute mortality reduction of 16% compared with a control group. Although this single-centre study has been criticized, the findings were so dramatic that most members of the medical community endorsed the protocols recommended by Rivers soon after publication.[2]

Over the ensuing years, EDs around the world have implemented sepsis protocols, many with variations on the original EGDT, and two common themes have emerged in the subsequent evaluations. First, it is difficult to perform the full EGDT protocol in a busy emergency department[3-5] be­cause of the time needed to place the various invasive catheters and perform the complex resuscitation, and because many departments are not set up to measure ScvO2. 

Second, clinicians have found significant improvements in mortality of severely septic patients by implementing only key steps in the EGDT protocol rather than all steps.[6-9] These key steps are des­cribed below.[6,8-11
Screening of septic patients 
Timely recognition and management of trauma and myocardial infarction[12,13] have long been recognized as critical to optimal outcomes for these conditions; however, the evidence to support timeliness in sepsis management has only emerged over the last 10 years.[1,11] Once septic patients devel­op macrovascular shock (refractory hy­po­tension) or microvascular shock (elevated lactate), they are on the steep part of the mortality curve and immediate identification and intervention is critical to avert rapid deterioration and death.[14-16

In order to screen a large volume of emergency department pa­tients for sepsis in a timely manner, personnel require a high index of suspicion and an effective screening mech­anism. Triage education and tools, such as sepsis posters and tri­age checklists, are needed to identify patients with severe sepsis or septic shock. 

In screening for sepsis, two or more of a possible four criteria for systemic inflammatory response syndrome (SIRS) signify the presence of a potentially severe infection.2 The four SIRS criteria are: 

•    Heart rate > 90 beats/min. 
•    Respiratory rate > 20 breaths/min. 
•    A high (≥ 38°C) or low (< 36°C) temperature. 
•    Abnormal white blood cell count ([> 12000/cubic mm or < 4000/cubic mm]); several BC protocols substitute WBC with an altered level of consciousness as a marker of severity of illness at triage as a WBC is not initially available.

Furthermore, studies have consistently shown that even in the face of hemodynamic stability, elevated lactate levels are associated with an increased mortality, necessitating the need for early measurement of lactate levels.[14,15,17

Patients with a serum lactate level > 4.0 mmol/L have a sharp decline in survival, which is why EGDT and the majority of other sepsis protocols chose this value for entry into aggressive management algorithms.[1,15] These algorithms require centres to perform rapid lactate testing and deliver the results to the clinician.[1,18] The lactate readings can be obtained through either point-of-care testing devices or arterial/venous blood gas analysis.[19,20

Once identified in the emergency department, patients with severe sepsis or septic shock will require aggressive source control, fluid resuscitation, and antibiotic therapy.[21
Identifying and controlling the source of sepsis
Source control dates back to the origins of medicine.[22] The need to drain abscesses and remove foreign bodies has been recognized since the fourth century BC, and the modern management of sepsis still relies on such surgical therapy. Identifying an infectious source and removing it, if possible, remains a core principle. 

The Surviving Sepsis Campaign guidelines recommend that a specific anatomic source diagnosis of infection be sought within 6 hours of presentation.[2] This requires blood cultures and often re­quires ultrasound or CT imaging; other cultures (e.g., urine, CSF, synovial fluid) may also be required.

Once identified, the focus of infection should be drained or removed with the least physiologic insult, such as through a percutaneously placed drain. Concurrent with surgical therapy, aggressive resuscitation, and early administration of antibiotics, samples should be taken from all potentially infected sites for cultures.

Fluid resuscitation
With the introduction of the Swan-Ganz pulmonary artery catheter in the 1970s, it became common to use fluid resuscitation to optimize a patient’s hemodynamic status based on oxygen transport, even attempting supranormal oxygen delivery.[23] Although ac­cepted by many clinicians at the time, studies since have produced conflicting results.[24-26

In 1995 Gattinoni and colleagues published the results of a well-designed, multicentre randomized control trial that concluded there was no benefit from supranormal oxygen delivery (although it is important to note that the patients entered in the trial were often enrolled relatively late into their disease process, even up to 72 hours after sepsis recognition).[26] A subsequent meta-analysis suggested that only early fluid resuscitation and normalization of hemodynamic para­meters are associated with improved survival.[27]

These studies and an understanding of the cardiovascular pathophysiology of sepsis led Rivers to conduct his EGDT trial, which showed that beginning interventions as soon as severe sepsis is recognized is required to achieve favorable outcomes.[1] One key finding of this trial was that pa­tients in the treatment arm received more intravenous fluids early in the course of their resuscitation. Numerous observational studies looking at the initiation of sepsis protocols in emergency departments[6-8,28-32] convincingly demonstrate that early ag­gressive resuscitation of the septic patient is associated with decreased mortality.[33]

Patients with sepsis and evidence of global hypoperfusion may require 6 to 10 L of crystalloid in their initial resuscitation.[34,35] Several recently pub­lished studies suggest that there is a danger of overresuscitation in this patient population, as there is with patients undergoing burn resuscitation.[36-38]

Although some patients may require several litres of crystalloid early in their disease, it remains un­clear at which point fluid administration may cause increased morbidity. Furthermore, optimal (meaning both safe and effective) fluid resuscitation may not require all of the invasive monitoring used in the original EGDT protocol. Accordingly, researchers and clinicians seek better targets for resuscitation that are less invasive than ScvO2, such as circulating biomarkers to titrate resuscitation.

Monitoring serum lactate clearance
Currently, serum lactate clearance shows the most promise as a reasonable biomarker alternative to invasive resuscitation monitoring. Studies have found that septic patients who do not clear serum lactate by 10% in the first 2 to 6 hours have an increased mortality.[39,40

Two recently published studies examined the association of targeting lactate clearance as a resuscitation goal with mortality. In 2010 Arnold and colleagues published results of a multicentre trial in which patients were randomized to con­ventional in­vasive monitoring (EGDT) or a ther­apy target guided by serial lactate clearance of 20% every 2 hours in addition to conventional invasive monitoring.[39

They found a significantly reduced ICU length of stay and both ICU and hospital mortality in the lactate clearance group when adjusting for predefined baseline mortality risk factors. Also in 2010, Jones and colleagues published results of a multicentre noninferiority trial comparing two groups of patients: one assigned to normalization of CVP, MAP, and ScvO2 according to EGDT protocols, and one to normalization of CVP, MAP, and a lactate clearance of 10% in the first 6 hours.[41

Although the authors found no significant difference in in-hospital mortality rates between the groups (i.e., noninferiority), suggesting that lactate clearance may be used instead of central venous oxygen saturation as a resuscitation target in severe sepsis, the study had two limitations. First, caregivers could not be blinded to the treatment groups of patients. 

Second, after normalization of CVP and MAP, very few pa­tients required further therapy to normalize their ScvO2 or to clear their lactate—that is, the planned intervention was not much different between treatment groups, which could explain why outcomes did not differ between groups. While there is growing evidence for resuscitation with a target of lactate clearance, and the use of this biomarker is simple and appealing, further research needs to be conducted before lactate clearance can be recommended as a resuscitation biomarker in severe sepsis. 

Three large government-funded RCTs are now underway and each is designed to determine the ideal method of sepsis resuscitation: ProCESS (Protocolized Care for Early Septic Shock, NCT00510835 at www.clinicaltrials.gov), a US trial; ARISE (Austral­asian Resuscitation in Sepsis Evaluation, NCT00975793 at www.clinicaltrials.gov); and ProMISe (Protocolised Management in Sepsis), a UK trial. These trials will be performed in different countries, but the groups have planned for a prospective combined meta-analysis that they hope will provide a final answer to this hotly debated question. 

Antibiotic administration
The importance of rapid initiation of antibiotic therapy for life-threatening infections has become increasingly apparent in the last few decades, 
as demonstrated by improved outcomes in patients with meningitis and community-acquired pneumonia who receive antimicrobials early rather than later in the course of their disease.[42,43] In the last 6 years several retrospective studies have shown a strong positive relationship between prompt antimicrobial administration and improved outcome in severe sepsis or septic shock.[44-46]

The most commonly quoted study shows that in the first 6 hours after development of septic shock every hour of delay in initiating antibiotic therapy was associated with a 7.6% increase in mortality.[44] This led the international Surviving Sepsis Campaign to recommend that patients with severe sepsis and septic shock receive rapid initiation (beginning in less than 1 hour) of antimicrobials.[2]

One prospective study evaluated the individual components of the Surviving Sepsis Campaign “bundle” or group of therapies and their association with survival in 316 patients with severe sepsis or septic shock. Early ad­ministration of antimicrobials (i.e., after less than 120 min from identification) and early collection of blood for cultures were the only interventions associated with lower mortality.[47

Another prospective observational study examined the relationship be­tween components of the Surviv­ing Sep­­sis Campaign bundle and outcome.[48] In a study of 2796 severe sepsis or septic shock patients they found that early administration of antimicrobials was one of only two interventions associated with significantly reduced mortality. 

A more recent study of septic shock found there was no association between each hour delay in initiating antibiotic therapy and mortality. However, patients who had antimicrobials administered after onset of hypotension had higher mortality than did patients who had antimicrobials given before hypotension.[49]

Thus, there has been some controversy about these guidelines because of the retrospective nature of the re­search from which they are derived. Fortunately, interventional studies supporting early administration of antimicrobials have recently been publish­ed.[50] To our knowledge, there is only one preliminary report of a randomized control trial of early versus later initiation of antibiotic therapy in severe sepsis.[51

This Australian study examined the benefit of prehospital administration of antimicrobials in 198 septic shock patients, all of whom required long transport times from rural areas. They showed that administering antimicrobials 3.4 hours ear­lier, on average, resulted in an absolute risk reduction of 28-day mortality of 14.3% (P = .049). It should be noted that this study has not been peer re­viewed. 

Although there are several key components to the early management of septic patients, none may be as simple or as important as early initiation of antibiotics. The development of systems that allow clinicians to deliver antimicrobials within minutes of identifying septic patients is likely the single greatest lifesaving improvement that many emergency departments can implement.

Sepsis best practices in BC
In 2008, the BC Ministry of Health funded Evidence 2 Excellence, an academic emergency health care initiative to establish interprofessional collaboration that supports improvements in emergency department management of sepsis. Evidence 2 Excellence employs an electronic community of practice, popularized by Wenger and colleagues,[52] to engage stakeholders across the pro­vince in networking to deepen their knowledge and skills.[53

Inspired by the Institute for Healthcare Improvement’s Breakthrough Series collaborative model,[54,55] Evidence 2 Excellence partnered with the UBC eHealth Strategy Office and the BC Patient Safety and Quality Council to conduct two Sepsis Collaboratives for clinical and operational improvement, the first in 2008–2009 involving 20 emergen­cy departments, and the second in 2009–2010 involving another 18 teams throughout BC. 

Research funding from the Canadian Institutes of Health Research is being used for a 3-year study to examine how to introduce best practices in sepsis provincially into different emergency departments with a variety of locations, patient mixes, case volumes, staffing and trainee arrangements, resources, and other aspects of practice. Thus, a critical strength of this study is that it is “real world” and therefore highly generalizable. 

While this study will not finish until later this year, early results suggest that even though the evidence for sepsis care is straightforward to understand, using the evidence in different, highly varied clinical contexts is difficult. 

Following the initial success of Evidence 2 Excellence, the BC Ministry of Health made sepsis one of nine topics in its Clinical Care Management initiative. The purpose of Clinical Care Management is to improve the quality of patient care in BC through a well-supported system-wide approach that promotes implementation of evidence-based clinical best practices and reports on the results. 

The BC Patient Safety and Quality Council is mandated to support implementation across the province, and is partnering with Evidence 2 Excellence to continue the improvement work in sepsis care. 

One of the first steps in the process was the development of new provincial guidelines for sepsis care (see Figure on next page). These guidelines were developed and approved by Evidence 2 Excellence faculty and the Sepsis Care Clinical Expert Group, which has the knowledge and peer credibility to make these recommendations. 

In addition to following the sepsis guidelines, emergency departments are re­quired to collect data and report on key pro­cess and outcome measures to ensure that BC residents are receiving optimal sepsis care. BC Patient Safety and Quality Council has appointed a clinical lead, Dr David Sweet, to provide the clinical expertise and to support health authorities with their improvement work. 

Support is tailored to the needs of individual sites and entails ongoing assessment and feedback. The BC Patient Safety and Quality Council has designed implementation tools for clinicians interested in ini­tiating sepsis protocols in their de­partments. These tools include im­provement guides, examples of sepsis pro­to­cols, posters, and data collection tools, all available at www.clinicalcaremanagement.ca. It is expected that within 1 year all emergency de­partments in BC seeing over 10000 patients annually will be engaged in sepsis improvement and will be act­ively reporting process and outcome measurements for septic patients to the Ministry of Health, including the following: 

•    Percentage of patients who received antibiotics by time goal.
•    Percentage of patients who had blood drawn for cultures before IV antibiotic therapy was initiated.
•    Percentage of patients who received initiation of a second litre of crystalloid by time goal.
•    Percentage of patients who had appropriate lactate measurements by time goals.
•    Mortality.

The identification and management of patients with sepsis has evolved since the landmark study by Rivers and colleagues1 10 years ago and will continue to evolve. A literature review indicates that key steps to optimize outcome when managing sepsis in the emergency department include:

•    Early triage and identification of patients.
•    Rapid and appropriate fluid resuscitation.
•    Lab testing (blood cultures), antibiotic administration, and source control of infection.
•    Close clinical and biomarker (lactate) monitoring. 

The evidence for making dramatic improvements in outcomes for septic patients is compelling; however, we continue to have a gap in care for these patients in our province because of the difficulty of safely and effectively applying evidence to clinical practice. The reasons for this difficulty are multifactorial and involve the core challenges of knowledge translation: clinician engagement, availa­bility of resources, and capacity for measurement and data collection. 

Great strides have been made in sepsis care across BC as a result of the commitment and dedication of health care providers working in EDs across the province and through the support provided by Evidence 2 Excellence and the Clinical Care Management initiative. Sepsis care will continue to improve and be sustained across the province and beyond as we meet the challenges of knowledge translation. To learn more and get involved in improving BC sepsis care we invite you to join the BC Sepsis Network.

Competing interests
Dr Russell holds stock in Sirius Genomics Incorporated, which has submitted patents related to the genetics of sepsis and its treatment that are owned by the University of British Columbia and licensed to Sirius Genomics. The University of British Columbia has also submitted a patent related to the use of vasopressin in septic shock. Dr Russell is named as an inventor on these patents. Dr Russell has received consulting fees from Ferring Pharmaceuticals (which manufactures vasopressin and is developing a selective V1a agonist), from Astra­Zeneca (which is developing an anti-TNF-alpha product), from BioCritica (which sells activated protein C in the US), and from Sirius Genomics. Dr Russell has received grant support from Sirius Genomics, Ferring Pharmaceuticals, AstraZeneca, and Eli Lilly, and speaking honoraria from Pfizer and Eli Lilly.

This article has been peer reviewed.


1.    Rivers E, Nguyen B, Havstad S, et al. Early goal-directed therapy in the treatment of severe sepsis and septic shock. N Engl J Med 2001;345:1368-1377.
2.    Dellinger RP, Levy MM, Carlet JM, et al. Surviving Sepsis Campaign: International guidelines for management of severe sepsis and septic shock: 2008. Crit Care Med 2008;36:296-327. Erratum in Crit Care Med 2008;36:1394-1396.
3.    Reade MC, Huang DT, Bell D, et al.; British Association for Emergency Medicine; UK Intensive Care Society; UK Society for Acute Medicine; Australasian Resuscitation in Sepsis Evaluation Investigators; Protocolized Care for Early Septic Shock Investigators. Variability in management of early severe sepsis. Emerg Med J 2010;27:110-115.
4.    Jones AE, Kline JA. Use of goal-directed therapy for severe sepsis and septic shock in academic emergency departments. Crit Care Med 2005;33:1888-1889.
5.    Durthaler JM, Ernst FR, Johnston JA. Managing severe sepsis: A national survey of current practices. Am J Health Syst Pharm 2009;66:45-53.
6.    Micek ST, Roubinian N, Heuring T, et al. Before-after study of a standardized hospital order set for the management of septic shock. Crit Care Med 2006;
7.    Ferrer R, Artigas A, Levy MM, et al.; Edusepsis Study Group. Improvement in process of care and outcome after a multicenter severe sepsis educational program in Spain. JAMA 2008;299:2294-2303.
8.    Lin SM, Huang CD, Lin HC, et al. A modified goal-directed protocol improves clinical outcomes in intensive care unit patients with septic shock: A randomized controlled trial. Shock 2006;26:551-557.
9.    Barochia AV, Cui X, Vitberg D, et al. Bundled care for septic shock: An analysis of clinical trials. Crit Care Med 2010;38:668-678.
10.    Perel A. Bench-to-bedside review: The initial hemodynamic resuscitation of the septic patient according to Surviving Sepsis Campaign guidelines—does one size fit all? Crit Care 2008;12:223.
11.    Levy MM, Dellinger RP, Townsend SR, et al.; Surviving Sepsis Campaign. The Surviving Sepsis Campaign: Results of an international guideline-based performance improvement program targeting severe sepsis. Crit Care Med 2010;
12.    Hollenberg S. Top ten list in myocardial infarction. Chest 2000;118:1477-1479.
13.    Mullins RJ, Mann NC. Population-based research assessing the effectiveness of trauma systems. J Trauma 1999;47:S59-S66.
14.    Trzeciak S, Dellinger RP, Chansky ME, et al. Serum lactate as a predictor of mortality in patients with infection. Intensive Care Med 2007;33:970-977.
15.    Shapiro NI, Howell MD, Talmor D, et al. Serum lactate as a predictor of mortality in emergency department patients with infection. Ann Emerg Med 2005;45:524-528.
16.    Mikkelsen ME, Miltiades AN, Gaieski DF, et al. Serum lactate is associated with mortality in severe sepsis independent of organ failure and shock. Crit Care Med 2009;37:1670-1677.
17.    Meregalli A, Oliveria RP, Friedman G. Occult hypoperfusion is associated with increased mortality in hemodynamically stable, high-risk, surgical patients. Crit Care 2004;8:R60-R65.
18.    Moore LJ, Jones SL, Kreiner LA, et al. Validation of a screening tool for the early identification of sepsis. J Trauma 2009;
19.    Jansen TC, van Bommel J, Mulder PG, et al. The prognostic value of blood lactate levels relative to that of vital signs in the pre-hospital setting: A pilot study. Crit Care 2008;12:R160.
20.    Shapiro NI, Fisher C, Donnino M, et al. The feasibility and accuracy of point-of-care lactate measurement in emergency department patients with suspected infection. J Emerg Med 2010;39:89-94. 
21.    Sweet D, Jaswal D, Fu W, et al. Effect of an emergency department sepsis protocol on the care of patients admitted to the intensive care unit. CJEM 2010;
22.    Jimenez MF, Marshall JC. Source control in the management of sepsis. Intensive Care Med 2001;27:49-62.
23.    Swan HJ, Ganz W, Forrester J, et al. Catheterization of the heart in man with use of a flow-directed balloon-tipped cath­eter. N Engl J Med 1970;283:447-451.
24.    Russell JA, Phang PT. The oxygen delivery/consumption controversy. Approaches to management of the critically ill. Am J Respir Crit Care Med 1994;149:533-537.
25.    Shoemaker WC, Appel PL, Kram HB, et al. Temporal hemodynamic and oxygen transport patterns in medical patients. Septic shock. Chest 1993;104:1529-1536.
26.    Gattinoni L, Brazzi L, Pelosi P, et al. A trial of goal-oriented hemodynamic therapy in critically ill patients: SvO2 Collaborative Group. N Engl J Med 1995;333:1025-1032. 
27.    Kern JW, Shoemaker WC. Meta-analysis of hemodynamic optimization in high-risk patients. Crit Care Med 2002;30:1686-1692.
28.    Gao F, Melody T, Daniels DF, et al. 
The impact of compliance with 6-hour 
and 24-hour sepsis bundles on hospital 
mortality in patients with severe sepsis: A prospective observational study. Crit Care 2005;9:R764-R770.
29.    Nguyen HB, Corbett SW, Steele R, et al. Implementation of a bundle of quality indicators for the early management of severe sepsis and septic shock is associated with decreased mortality. Crit Care Med 2007;35:1105-1112.
30.    Jones AE, Focht A, Horton JM, et al. Prospective external validation of the clinical effectiveness of an emergency department-based early goal-directed therapy protocol for severe sepsis and septic shock. Chest 2007;132:425-432.
31.    Zambon M, Ceola M, Almeida-de-Castro R, et al. Implementation of the Surviving Sepsis Campaign guidelines for severe sepsis and septic shock: We could go faster. J Crit Care 2008;23:455-460.
32.    Kortgen A, Niederprum P, Bauer M. Implementation of an evidence-based “standard operating procedure” and outcome in septic shock. Crit Care Med 2006;34:943-949.
33.    Jones AE, Brown MD, Trzeciak S, et al. The effect of a quantitative resuscitation strategy on mortality in patients with sepsis: A meta-analysis. Crit Care Med 2008;
34.    Task Force of the American College of Critical Care Medicine, Society of Critical Care Medicine. Practice parameters for hemodynamic support of sepsis in adult patients in sepsis. Crit Care Med 1999;
35.    Otero RM, Nguyen HB, Huang DT, et al. Early goal-directed therapy in severe sepsis and septic shock revisited: Concepts, controversies, and contemporary findings. Chest 2006;130:5:1579-1595.
36.    Saffle JIL. The phenomenon of “fluid creep” in acute burn resuscitation. J Burn Care Res 2007;28:382-395.
37.    Vincent JL, Sakr Y, Sprung CL, et al. Sepsis in European intensive care units: Results of the SOAP study. Crit Care Med 2006;34:344-353.
38.    Boyd JH, Forbes J, Nakada TA, et al. Fluid resuscitation in septic shock: A positive fluid balance and elevated central venous pressure are associated with increased mortality. Crit Care Med 2011;39:259-265.
39.    Arnold RC, Shapiro NI, Jones AE, et al. Multicenter study of early lactate clearance as a determinant of survival in pa­tients with presumed sepsis. Shock 2009;32:35-39.
40.    Nguyen HB, Rivers EP, Knoblich BP, et al. Early lactate clearance is associated with improved outcome in severe sepsis and septic shock. Crit Care Med 2004;32:
41.    Jones AE, Shapiro NI, Trzeciak S, et al. Lactate clearance vs central venous oxygen saturation as goals of early sepsis therapy: A randomized clinical trial. JAMA 2010;303:739-746.
42.    Tunkel AR, Hartman BJ, Kaplan SL, et al. Practice guidelines for the management of bacterial meningitis. Clin Infect Dis 2004;39:1267-1284.
43.    Meehan TP, Fine MJ, Krumholz HM, et al. Quality of care, process, and outcomes in elderly patients with pneumonia. JAMA 1997;278:2080-2084. 
44.    Kumar A, Roberts D, Wood KE, et al. Duration of hypotension before initiation of effective antimicrobial therapy is the critical determinant of survival in human septic shock. Crit Care Med 2006;34:
45.    Garey KW, Rege M, Pai MP, et al. Time to initiation of fluconazole therapy impacts mortality in patients with candidemia: A multi-institutional study. Clin Infect Dis 2006;43:25-31.
46.    Gaieski DF, Mikkelsen ME, Band RA, et al. Impact of time to antibiotics on survival in patients with severe sepsis or septic shock in whom early goal-directed therapy was initiated in the emergency department. Crit Care Med 2010;38:
47.    de Sousa AG, Fernandes CJ Jr, Santos GPD, et al. The impact of each action in the Surviving Sepsis Campaign measures on hospital mortality of patients with severe sepsis/septic shock. Einstein 2008;
48.    Ferrer R, Artigas A, Suarez D, et al. Effectiveness of treatments for severe sepsis: A prospective, multicenter, observational study. Am J Respir Crit Care Med 2009;
49.    Pukarich MA, Trzeciak S, Shapiro NI, et al. Association between timing of antibiotic administration and mortality from septic shock in patients treated with a quantitative resuscitation protocol. Crit Care Med 2011;39:2066-2071.
50.    Funk DJ, Kumar A. Antimicrobial therapy for life-threatening infections: Speed is life. Crit Care Clin 2011;27:53-76.
51.    Chamberlain D. Prehospital administer­ed intravenous antimicrobial protocol for septic shock: A prospective randomized clinical trial [poster]. Presented at 29th International Symposium on Intensive Care and Emergency Medicine, Brussels, Belgium, 24-27 March 2009.
52.    Wenger E, McDermott R, Snyder W. Cultivating communities of practice. Boston, MA: Harvard Business Review Press; 2002.
53.    Ho K, Jarvis-Selinger S, Norman CD, et al. Electronic communities of practice: Guidelines from a project. J Contin Educ Health Prof 2007;30:139-143.
54.    Kilo C. A framework for collaborative improvement: Lessons from the Institute for Healthcare Improvement’s Breakthrough Series. Qual Manage Health Care 2001;6:1-13.
55.    Wilson T, Plsek P, Berwick D, et al. Learning from around the world: Experiences and thoughts of collaborative improvement from seven countries. Boston, MA: Institute for Healthcare Improvement; 2001.

Dr Sweet is a clinical assistant professor in the Department of Emergency Medicine at the University of British Columbia, and holds attending positions in emergency medicine and critical care medicine at Vancouver General Hospital and Surrey Memorial Hospital. He is also clinical lead for sepsis (clinical care management) with the BC Patient Safety and Quality Council. Dr Marsden is a clinical professor in the Department of Emergency Medicine at UBC and a physician in the emergency department at St. Paul’s Hospital. Dr Ho is an associate professor in the Department of Emergency Medicine at UBC and a physician in the emergency department at Vancouver General Hospital. Ms Krause is executive director of the BC Patient Safety and Quality Council. Dr Russell is a pro­fes­sor in the Division of Critical Care Medicine at UBC,   principal investigator of the James Hogg Centre for Cardiovascular and Pulmonary Research, and a member of the Division of Critical Care Medicine, St. Paul’s Hospital and University of British Columbia.

David Sweet, MD,, Julian Marsden, MD,, Kendall Ho, MD, FRCPC, Christina Krause, MSc,, James A. Russell, MD,. Emergency management of sepsis: The simple stuff saves lives. BCMJ, Vol. 54, No. 4, May, 2012, Page(s) 176-182 - Clinical Articles.

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