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Original Article Implementing a Sepsis Resuscitation Bundle Improved Clinical Outcome: A Before-and-After Study
Jeongmin Kim, M.D., Sungwon Na, M.D., Ph.D., Young Chul Yoo, M.D., Ph.D., Shin Ok Koh, M.D., Ph.D.
The Korean Journal of Critical Care Medicine 2014;29(4):250-256.
DOI: https://doi.org/10.4266/kjccm.2014.29.4.250
Published online: November 30, 2014

Department of Anesthesiology and Pain Medicine, Yonsei University College of Medicine, Seoul, Korea

Correspondence to: Sungwon Na, Department of Anesthesiology and Pain Medicine, Yonsei University College of Medicine, 50-1 Yonsei-ro, Seodaemun-gu, Seoul 120-752, Korea, Tel: +82-2-2228-2420, Fax: +82-2-2227-7897, E-mail: nswksj@yuhs.ac
• Received: February 27, 2014   • Revised: June 24, 2014   • Accepted: August 28, 2014

Copyright © 2014 The Korean Society of Critical Care Medicine

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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  • Background
    Unlike other diseases, the management of sepsis has not been fully integrated in our daily practice. The aim of this study was to determine whether repeated training could improve compliance with a 6-h resuscitation bundle in patients with severe sepsis and septic shock.
  • Methods
    Repeated education regarding a sepsis bundle was provided to the intensive care unit and emergency department residents, nurses, and faculties in a single university hospital. The educational program was led by a multidisciplinary team. A total of 175 adult patients with severe sepsis or septic shock were identified (88 before and 87 after the educational program). Hemodynamic resuscitation bundle and timely antibiotics administration were measured for all cases and mortality at 28 days after sepsis diagnosis was evaluated.
  • Results
    The compliance rate for the sepsis resuscitation bundle before the educational program was poor (0%), and repeated training improved it to 80% (p < 0.001). The 28-day mortality was significantly lower in the intervention group (16% vs. 32%, p = 0.040). Within the intervention group, patients for whom the resuscitation bundle was successfully completed had a significantly lower 28-day mortality than other patients (11% vs. 41%, p = 0.004).
  • Conclusions
    Repeated education led by a multidisciplinary team and interdisciplinary communication improved the compliance rate of the 6-h resuscitation bundle in severe sepsis and septic shock patients. Compliance with the sepsis resuscitation bundle was associated with improved 28-day mortality in the study population.
Severe sepsis and septic shock are the leading causes of death in non-cardiac intensive care units (ICU).[1,2] Management of sepsis based on the Surviving Sepsis Campaign (SSC) guidelines[3] has been associated with survival benefits.[49] For the management of severe sepsis, the SSC recommended the implementation of an early goal-directed sepsis resuscitation bundle. Although the guidelines provide a road map for the care of severe sepsis patients, their success depends on the compliance of clinicians. In previous studies a national training program based on the SSC guidelines improved compliance with recommended processes of care for severe sepsis in ICUs. However, a long-term follow-up study showed that the compliance with the 6-hour early goal-directed resuscitation bundle returned to the baseline value, while the compliance with the 24-hour sepsis management bundle remained stable.[10] Considering the impact of the 6-hour early goal-directed resuscitation bundle and the 24-hour sepsis management bundles on clinical outcomes, use of the resuscitation bundle seems to be more strongly associated with clinical outcomes.[4] We designed this before-and-after study to test the hypothesis that a biweekly repetitive educational program for the emergency department (ED) and ICU residents, nurses, and faculties led by a multidisciplinary team could improve the compliance rate for the sepsis resuscitation bundle and further reduce the mortality of severe sepsis and septic shock patients.
This before-and-after study was approved by the Institutional Review Board (IRB) of Severance Hospital (IRB No 4-2009-0295), and the need for informed consent was waived by the IRB. Adult patients aged 18 years or more who were admitted to the ED and diagnosed with severe sepsis/septic shock during a 20-month period after initiation of educational sessions were included as the intervention group (between November 2007 and July 2009). For the control group, patients who were admitted to the ED and diagnosed with severe sepsis/septic shock under the same criteria between January 2006 and September 2007 were included. The clinical data were retrospectively collected by reviewing the electronic medical records (EMR) of the patients. Severe sepsis was defined as sepsis associated with acute organ dysfunction. The term organ dysfunction was defined by the SOFA scoring system.[11] Each subgroup scoring higher than 3 was defined as specific organ failure. Septic shock was defined as acute circulatory failure (systolic blood pressure less than 90 mmHg despite volume resuscitation).[12] We excluded 22 patients who were younger than 18 years, pregnant, with trauma, readmitted within 1 week due to previous diagnosis of sepsis, transferred from another institution, or had a do-not-resuscitate order or a previous history of heart failure. We compared clinicians’ adherence to the SSC guidelines for the implementation of the early goal-directed resuscitation bundle and clinical outcomes of the patients, including 28-day mortality, between the two groups.
1) Intervention to improve adherence to the SSC guidelines
The intervention consisted of two components; a multi-disciplinary team and repeated education sessions. The multi-disciplinary team was organized under the participation of the faculties and nurses working in the ICU and ED. Physicians’ subspecialties included emergency medicine, pulmonology, infectious disease, and anesthesiology. The multidisciplinary team provided 2-hour educational sessions during the study period, twice a month, starting in November 2007. The biweekly education sessions encompassed the definition of sepsis, components of the resuscitation bundle, and clinical evidence provided by the recent literature. They also included monthly feedback from the data of the previous month on the basis of the plan-do-study-act process.
2) Management protocol
In the intervention group we managed the patients by following the protocol based on the 6-hour early goal-directed resuscitation bundle.[13] The hemodynamic goal (mean arterial pressure [MAP] > 65 mmHg and central venous pressure [CVP] > 8 mmHg) was achieved with fluid resuscitation and vasopressor infusion. Dobutamine administration or transfusion of packed red blood cells were used to maintain central venous oxygen saturation (ScvO2) over 70%. We also intravenously administered initial empirical antimicrobial therapy within the first 3 hours of diagnosis after appropriate cultures were obtained. Initial empirical anti-infective therapy should include one or more drugs following the 2004 SSC guidelines. Antibiotics selection should be largely determined by institutional guidelines considering the source or focus of infection, the patient’s immunologic status, and whether the infection is nosocomial or community-acquired. The 2004 SSC guidelines also recommend taking into consideration the institution’s specific bacterial resistance patterns. If the patient needed ventilator care due to acute lung injury or acute respiratory distress syndrome, we applied mechanical ventilation using a lung protective strategy including low tidal volume of 6 ml/kg of predicted body weight, plateau airway pressure less than 30 cm H2O, and application of positive end expiratory pressure table of acute respiratory distress syndrome network.
3) Data collection and outcome measures
Demographic data including age, gender, APACHE II score, origin of infection, and organ dysfunction were collected. To evaluate the compliance rate of the early goal-directed resuscitation bundle, we investigated the following items: blood culture before antibiotics, intravenous broad-spectrum antibiotics, and hemodynamic goals including MAP ≥ 65 mmHg, CVP ≥ 8 mmHg, and ScvO2 ≥ 70%.
The primary end point was the comparison of compliance rates for the early goal-directed resuscitation bundle for severe sepsis/septic shock patients during the first 6 hours after the diagnosis, between the two groups. We also compared 28-day mortality and length of stay (LOS) in the ICU and hospital. To evaluate the improvement in the achievement rate of the early goal-directed resuscitation bundle after the intervention process, we compared the rate of measurement of the serum lactate level, insertion of the central venous catheter, insertion of the arterial line, measurement of CVP and ScvO2, and appropriate use of antibiotics. We also compared the time interval from the diagnosis to the start of the monitoring and achievement of the goals. The goals consisted of administering antibiotics within 3 hours of the onset, and achievement of CVP, MAP, and ScvO2 goals within 6 hours.
4) Statistical analysis
To compare continuous data, Student’s t-test or Mann-Whitney test was used. Categorical data were analyzed using the chi-squared test. Mortality was analyzed with the log-rank test and Breslow test, represented by Kaplan-Meier curves. Kaplan-Meier analysis was used to compare LOS in the ICU or hospital and mortality within 28 days.
The intervention group had 87 patients and the control group had 88 patients. Age, sex, and APACHE II score were comparable between the two groups (Table 1). At time-point zero, there were no significant differences in the origin of the infection between the groups. In the study population, the most common origin of sepsis was pneumonia and abdominal infection. The prevalence of organ dysfunction was comparable between the groups. The most common major organ dysfunctions were cardiovascular and respiratory dysfunction.
Considering each of the resuscitation bundle items, antibiotics were more frequently given within 3 hours in the intervention group (85% vs. 41%, p < 0.001). The rate of achieving hemodynamic goals was also higher in the intervention group (CVP 83% vs. 27%, p < 0.001; MAP 98% vs. 89%, p = 0.013; CVP and MAP, 94% vs. 25%, p < 0.001). ScVO2 level was incommensurable because it was not measured in the control group. The rate of patients who achieved all hemodynamic goals within 6 hours after diagnosis (80% vs. 0%, p < 0.001) was definitely higher in the intervention group (Table 2).
The time from the diagnosis to the achievement of variables of the early goal-directed resuscitation bundle were compared between the two groups. After completing the training program, the times to administering antibiotics, insertion of central venous catheter, and achievement of CVP and MAP goals were significantly reduced (118 vs. 245 min, p < 0.001; 40 vs. 122 min, p = 0.0007; 135 vs. 197 min, p = 0.0163; 91 vs. 179 min, p < 0.001, respectively).
The patients in the intervention group showed a significantly lower mortality rate at 28 days after the diagnosis (16% vs. 32%, p = 0.04) than those in the control group. Kaplan-Meier plots of the probability of remaining alive are shown in Fig. 1. The Breslow test showed statistical significance in the difference in 28-day mortality between the groups (Fig. 1, p = 0.040). LOS in the ICU analyzed by Kaplan-Meier test was significantly longer in the control group (Fig. 2, p = 0.001), while LOS in the hospital was not significantly different between the two groups (Fig. 3, p = 0.078). Discontinuation of the training for 4 months reduced the goal achievement rate and increased the 28-day mortality rate, although they were restored after resuming the program (Fig. 4).
In the intervention group, 17 patients did not have their resuscitation goals completed, while the remaining 70 patients did. There was a statistically significant difference in the 28-day mortality rate in the patients who did or did not complete the bundle (11% vs. 41%, p = 0.004), while LOS in the ICU and LOS in the hospital were not significantly different according to the bundle completion rate. (p = 0.062)
Norepinephrine (53% vs. 34%, p = 0.019) was more frequently administered in the intervention group, compared with the control group. Fewer patients received dopamine (50% vs. 91%, p < 0.001) and dobutamine (4% vs. 19%, p = 0.006) in the intervention group, respectively. Steroids were more frequently administered in the intervention group, compared with the control group (34% vs. 19%, p = 0.036), and there was no significant difference in the use of vasopressin (14% vs. 7%, p = 0.138).
The present study showed that quality improvement action including repeated education provided by a multidisciplinary team could improve the adherence to SCC guidelines, thereby improving clinical outcomes in severe sepsis and septic shock patients. The adherence rate to the SCC guidelines before education or quality improvement actions was poor, a finding consistent with previous studies.[10,14] In our study, a specially organized multi-disciplinary team with good collaboration and a training program improved the management process of severe sepsis and septic shock patients. Trzeciak et al.[9] showed that effective emergency medicine and collaborative critical care improved the early achievement rate of goal-directed therapy. Our collaborative sepsis management team showed improved compliance and outcomes.
A nation-wide study demonstrated that a training program based on the SCC guidelines improved compliance with the recommended processes of care for severe sepsis in the ICU.[10,15] However, Ferre also showed a discrepancy in adherence to the protocol for the early goal-directed resuscitation bundle and the 24-hour management bundle. In this study, compliance with the protocol for the sepsis management bundle was maintained even after the 1-year follow-up was finished, while the compliance for the early goal-directed resuscitation bundle returned to the baseline level.
In the intervention group, we found a significant relationship between the achievement rate of the early goal-directed resuscitation bundle as recommended by the SCC guidelines and the mortality rate. Recent studies showed that non-compliance with the 6-hour sepsis resuscitation bundle increased mortality while non-compliance with the 24-hour sepsis management bundle did not.[4]
Studies have been conducted on the effect of education in clinical fields and reports have revealed the effect of education on the behavior of the medical staff.[16] Ordinary didactic approaches such as printed materials or practice guidelines for health care providers, including physicians, failed to change their behavior.[17] Only evidence-based educational approaches are known to have an impact on health care providers’ behavior. Such approaches include interactive educational activities, sequenced and multifaceted interventions, educational outreach or academic detailing, and audit and feedback to physicians.[18,19] Constant re-educational programs were essential for the successful implementation of the sepsis bundle.
Standardization and protocolization are important for improving clinical practice.[20] Many researchers tried to demonstrate that implementation of an evidence-based management protocol improved clinical outcomes of sepsis patients, but their results were not consistent.[57,9,14,21] Most of the trials used more rigorous fluid management earlier in the treatment protocol, more appropriate antibiotics therapy, and shorter LOS in the ICU or hospital, and the effects of the tested interventions on mortality varied. A few studies demonstrated mortality benefits,[6,22] while others did not.[21] These inconsistent results were thought to be related to clinicians’ adherence to the protocol. Nguyen et al. demonstrated that the completion of early goal-directed therapy was significantly associated with lower mortality[7] (odds ratio, 0.36; 95% confidence interval, 0.17–0.79; p = 0.01). Compared to previous studies, the completion rate after intervention in our study was relatively high. This high rate might result from the fact that we organized the clinical pathway with a periodic survey of the treatment process and continuous provision of training sessions.
The time to administration of broad-spectrum antibiotics was improved after intervention in this study, while the administration rate itself did not show significant changes. Similar improvement in earlier administration of antimicrobial agents was noticed in several recent studies.[21].
Among vasopressors, dopamine and norepinephrine are most frequently used, and are recommended by the SCC guidelines. In our study, there was a noticeable change in the use of vasopressors. More vasopressin and less dopamine were used in the intervention group. This change was thought to result from the physicians’ concerns about the arrhythmogenicity of dopamine and relative deficiency of vasopressin.[23,24] In addition, during the study periods, more physicians would tend to use steroids in patients with septic shock who, despite adequate fluid replacement, required vasopressor therapy to maintain adequate blood pressure. Therefore, steroid use showed a significant difference between the two groups in the course of time (34% vs. 19%, p = 0.036).
As demonstrated by Rivers,[22] time-dependant characteristics of sepsis management required involved clinicians to make standardized protocols, but its multi-disciplinary nature made implementation of protocols challenging. The present study confirmed that the sepsis resuscitation bundle, as well as the treatment bundle, could be implemented and maintained by continuously conducting surveys and education, and benefit sepsis patients with standardized care and early admission to the ICU.
Limitations of this study are as follows. Since creating a multi-disciplinary team, provision of repeated training, and formulating a resuscitation bundle implement pathway were simultaneously carried out, we could not differentiate the impacts of each factor. Moreover, since the control group data were retrospectively collected, randomization could not be performed. However, since all patients who were admitted to the ED and diagnosed as having severe sepsis/septic shock between January 2006 and September 2007 were allocated to the control group, selection bias would be minimal. Random allocation of patients to the intervention group would not be ethical, so the comparison between the intervention and control groups could be performed only observationally. In our institution, moreover, since patients’ data were recorded in the EMR system according to the institutional guidelines, we gathered all parameters relevant to the resuscitation bundle and patients’ outcome. Another important limitation was that we did not know how long the effect of training could be maintained and we could not confirm the ideal interval between training sessions. However, discontinuation of the training program for 4 months reduced the goal achievement rate and increased the 28-day mortality rate, although the goal achievement rate and mortality rate were restored after resuming the training (Fig. 4). We would like to suggest that repeated training with an interval between training sessions of at least 2 or 3 months is necessary to maintain improved compliance and clinical outcomes. The other limitation was that our hypothesis was based upon a premise that we could exclude the effect of the 24-hour sepsis management bundle on the clinical outcome. However, compliance with the 6-hour early goal-directed resuscitation bundle was in connection with the 24-hour sepsis management bundle.
In conclusion, we demonstrated that implementation of an evidence-based management protocol for severe sepsis or septic shock patients improved clinical outcomes. Repeated exposure to an educational program and interdisciplinary communication was helpful to maintain a high completion rate for the management bundles, which in turn decreased ICU mortality in sepsis patients.

No potential conflict of interest relevant to this article was reported.

Fig. 1.
Comparison of the 28-day survival rate between the intervention and control groups. Kaplan-Meier curves depicting the probability of survival of patients with severe sepsis or septic shock in the intervention group and the control group according to the length of survival (p = 0.04 by Breslow test) + means censored data.
kjccm-2014-29-4-250f1.gif
Fig. 2.
Comparison of LOS in the ICU between the intervention and control groups. Kaplan-Meier curves depict the probability of remaining in the ICU for patients with severe sepsis or septic shock in the intervention group and the control group according to the LOS in the ICU (p = 0.001 by Log Rank test) + means censored data. LOS: length of stay; ICU: intensive care unit.
kjccm-2014-29-4-250f2.gif
Fig. 3.
Comparison of the number of days in hospital between the intervention and the control groups. Kaplan-Meier curves depict the probability of remaining in the hospital for patients with severe sepsis or septic shock in the intervention group and the control group according to the LOS in hospital (p = 0.078 by Breslow test) + means censored data. LOS: length of stay.
kjccm-2014-29-4-250f3.gif
Fig. 4.
Relationship between training and outcome. The x-axis shows the 22-month study period divided into 4-month intervals comparing the goal achievement rates between each period, and the y-axis shows the 28-day mortality rate (A) and the achievement rate of the early goal-directed resuscitation bundle (B). C indicates the time period when training was carried out.
kjccm-2014-29-4-250f4.gif
Table 1.
Demographic data, origin of infection, and organ dysfunction
Intervention (n = 87) Control (n = 88) p value
APACHE II 20.0 ± 6.6 21.4 ± 5.7 0.133
Age, yr 64.3 ± 12.3 64.7 ± 14.7 0.847
Male 46 (53) 44 (50) 0.818
Origin of infection
  Pneumonia 33 (38) 30 (34) 0.828
  Acute abdomen 20 (23) 21 (24) 0.888
  UTI 13 (15) 18 (21) 0.695
  Meningitis 2 (2) 1 (1) 0.313
  Soft tissue infection 7 (8) 4 (5) 0.215
  Others 10 (12) 8 (9) 0.702
  Multiple infection sites 3 (3) 5 (6) 0.384
Organ dysfunction*
  Cardiovascular 66 (76) 66 (75) 0.966
  Respiratory 48 (55) 59 (67) 0.145
  Renal 28 (32) 23 (48) 0.475
  Hepatic 15 (17) 21 (24) 0.369
  Coagulation 9 (10) 16 (18) 0.206
  Neurologic 10 (12) 15 (17) 0.203

Values are presented as mean ± SD or n (%).

* Organ dysfunction was defined by SOFA scoring greater than 3. APACHE II: acute physiology and chronic health evaluation; UTI: urinary tract infection.

Table 2.
Compliance to sepsis resuscitation bundle within 6 hours from diagnosis
Intervention (n = 87) Control (n = 88) p value
Antibiotics administered within 3 h 74 (85) 36 (41) < 0.001
Blood culture before antibiotics 84 (97) 79 (90) 0.140
CVP ≥ 8 mmHg 72 (83) 24 (27) < 0.001
MAP ≥ 65 mmHg 86 (99) 78 (89) 0.013
All measured goals 70 (80) 0 (0) < 0.001

Values are presented as mean ± SD or n (%). CVP: central venous pressure; MAP: mean arterial pressure.

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    Implementing a Sepsis Resuscitation Bundle Improved Clinical Outcome: A Before-and-After Study
    Image Image Image Image
    Fig. 1. Comparison of the 28-day survival rate between the intervention and control groups. Kaplan-Meier curves depicting the probability of survival of patients with severe sepsis or septic shock in the intervention group and the control group according to the length of survival (p = 0.04 by Breslow test) + means censored data.
    Fig. 2. Comparison of LOS in the ICU between the intervention and control groups. Kaplan-Meier curves depict the probability of remaining in the ICU for patients with severe sepsis or septic shock in the intervention group and the control group according to the LOS in the ICU (p = 0.001 by Log Rank test) + means censored data. LOS: length of stay; ICU: intensive care unit.
    Fig. 3. Comparison of the number of days in hospital between the intervention and the control groups. Kaplan-Meier curves depict the probability of remaining in the hospital for patients with severe sepsis or septic shock in the intervention group and the control group according to the LOS in hospital (p = 0.078 by Breslow test) + means censored data. LOS: length of stay.
    Fig. 4. Relationship between training and outcome. The x-axis shows the 22-month study period divided into 4-month intervals comparing the goal achievement rates between each period, and the y-axis shows the 28-day mortality rate (A) and the achievement rate of the early goal-directed resuscitation bundle (B). C indicates the time period when training was carried out.
    Implementing a Sepsis Resuscitation Bundle Improved Clinical Outcome: A Before-and-After Study
    Intervention (n = 87) Control (n = 88) p value
    APACHE II 20.0 ± 6.6 21.4 ± 5.7 0.133
    Age, yr 64.3 ± 12.3 64.7 ± 14.7 0.847
    Male 46 (53) 44 (50) 0.818
    Origin of infection
      Pneumonia 33 (38) 30 (34) 0.828
      Acute abdomen 20 (23) 21 (24) 0.888
      UTI 13 (15) 18 (21) 0.695
      Meningitis 2 (2) 1 (1) 0.313
      Soft tissue infection 7 (8) 4 (5) 0.215
      Others 10 (12) 8 (9) 0.702
      Multiple infection sites 3 (3) 5 (6) 0.384
    Organ dysfunction*
      Cardiovascular 66 (76) 66 (75) 0.966
      Respiratory 48 (55) 59 (67) 0.145
      Renal 28 (32) 23 (48) 0.475
      Hepatic 15 (17) 21 (24) 0.369
      Coagulation 9 (10) 16 (18) 0.206
      Neurologic 10 (12) 15 (17) 0.203
    Intervention (n = 87) Control (n = 88) p value
    Antibiotics administered within 3 h 74 (85) 36 (41) < 0.001
    Blood culture before antibiotics 84 (97) 79 (90) 0.140
    CVP ≥ 8 mmHg 72 (83) 24 (27) < 0.001
    MAP ≥ 65 mmHg 86 (99) 78 (89) 0.013
    All measured goals 70 (80) 0 (0) < 0.001
    Table 1. Demographic data, origin of infection, and organ dysfunction

    Values are presented as mean ± SD or n (%).

    Organ dysfunction was defined by SOFA scoring greater than 3. APACHE II: acute physiology and chronic health evaluation; UTI: urinary tract infection.

    Table 2. Compliance to sepsis resuscitation bundle within 6 hours from diagnosis

    Values are presented as mean ± SD or n (%). CVP: central venous pressure; MAP: mean arterial pressure.


    ACC : Acute and Critical Care
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