Compliance With the Surviving Sepsis Campaign Bundle: A Multicenter Study From Turkey

Objectives Sepsis bundle compliance is not clear. We evaluated rates of compliance with sepsis bundle protocols among health care providers in Turkey. Methods Our study was carried out retrospectively. Forty-five intensive care units (ICU) participated in this study between March 2, 2018 and October 1, 2018. Results One hundred thirty-eight ICUs were contacted and 45 ICUs agreed to participate. The time taken for the diagnosis of sepsis was less than six hours in 384 (59.8%) patients, while it was more than six hours in 258 (40.2%) patients. The median [interquartile range (IQR)] times for initial antibiotic administration, culturing, vasopressor initiation, and second lactate measurement were 120.0 (60-300) minutes, 24 (12-240) minutes, 40 (20-60) minutes, and 24 (18-24) hours, respectively. The rate of compliance with tissue and organ perfusion follow-up in the first six hours was 0%. The rates of three- and six-hour sepsis bundle protocol compliance were both 0%. The ICU mortality rates for sepsis and septic shock were 22% and 78%, respectively. The ICU mortality rates for sepsis and septic shock were 22% and 78%, respectively. Conclusions The rate of compliance with sepsis bundle protocols was evaluated in Turkey for the first time and determined to be 0%.


Introduction
Sepsis is one of the most common disorders that causes mortality in intensive care units (ICUs) [1]. For the global management of sepsis, international guidelines from the Surviving Sepsis Campaign (SSC) have been published [2]. In 2018, the three-and six-hour bundles were reduced to one hour each by the SSC [3]. Prior observational studies have suggested that the mortality rate and costs of care can be reduced with greater bundle protocol compliance [4,5]. To improve bundle protocol compliance, specific training and infrastructure are necessary [6]; however, according to data from the World Health Organization, the ICUs in 83 countries do not meet minimum standards [7]. The most important reason among those known for ICUs failing to meet standards in this manner is the unavailability of adequate financial support. As compared with developed countries, developing ones typically spend less money and the number of nurses working in these countries is lower [8]; indeed, the number of nurses working in ICUs and the availability of equipment for bronchoscopy, ultrasonography, and hemodynamic monitoring in developing countries are often insufficient to meet patient needs [9]. Moreover, the number of patients per health care professional is high, and the number of beds is limited. Sanitation, electrical resources, ventilation, and patient safety are also often insufficient in hospitals in developing countries [10]. For example, in emergency services, levels of plasma lactate and other biomarkers cannot be measured [11]. Overall, the mortality rate is higher in developing countries [12]. Considering sepsis treatment specifically, according to World Bank data, Turkey is an upper-middle-income country [13]. In developed countries, compatibility with sepsis bundle is high and mortality is low [14]. Sepsis bundle compliance is mandatory in New York [15]. In a previous study conducted in our country, mortality of septic shock was found to be very high [16]. In our country, there is no multicenter study on bundle compliance, which is a mortality-reducing treatment. Our intention was therefore to determine the degree of sepsis bundle protocol compliance in Turkey.

Design and setting
Our study was carried out retrospectively. Every eligible medical center was contacted by phone about participating in this study, and the study protocol was sent to them by email. The study protocol is available at https://forms.gle/GRuqdXyAErt2Vmwz5. In total, 138 intensive care units were contacted. Sixty-eight intensive care units were not appropriate. The reason for this is, in 36 intensive care units, the person-incharge was not defined. Thirty-two intensive care units were specific intensive care units. Seventy intensive care units were eligible for the study. Of these, 35 intensive care units were excluded. The reasons for exclusion were 29 intensive care units did not agree to participate. Six intensive care units provided insufficient data. We worked with 45 intensive care units. In intensive care units, two patients had one nurse and one doctor worked for 24 hours. The study was conducted between March 1, 2018 and October 1, 2018.

Participants
Adult patients older than 18 years were included in this study. All patients with further life expectancy in the ICU were deemed eligible to participate. The inclusion criterion for this study was a diagnosis of sepsis and/or septic shock.

Study data
The prediction or confirmation of infection was performed through 24-hour bedside screening of the study participants. The mortality status of patients discharged from the ICU was determined by reaching the patients or their relatives by phone. The definition of infection was made according to the international sepsis guideline [17]. The presence of sepsis or septic shock was confirmed according to the standards set by the international sepsis datasheet; the definitions of these conditions were produced according to data published in the international sepsis datasheet [2]. The date of admission to the ICU, the infection source, the primary diagnosis, and the comorbidities present were recorded together with the patient's Acute Physiology and Chronic Health Evaluation (APACHE II) score. The Sequential Organ Failure Assessment (SOFA) score was recorded daily. Data on other comorbidities such as solid organ malignancy, diabetes mellitus, cerebrovascular disorders, chronic obstructive pulmonary disease (COPD), asthma, heart failure (New York Heart Association functional classes I-IV), coronary artery disease, liver failure, chronic renal failure (undergoing dialysis or serum creatinine ≥ 2 mg/dL), immunosuppression (neutropenia < 500 mm 3 ), hematologic malignancy, splenectomy, human immunodeficiency virus infection (CD4 < 200 mm 3 ), receipt of chemotherapy or radiotherapy in the last six months prior to hospitalization in the ICU, receipt of corticosteroid treatment, and posttransplant status were also recorded.

Definitions of data
Definitions were made according to the Third International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3). Sepsis was considered when an elevation of the Sepsis-related Organ Failure Assessment (qSOFA) score of two or more points occurred outside the ICU or an elevation of the SOFA score of two or more points occurred in the ICU in patients with suspected or proven infection. The qSOFA score is obtained by awarding one point per item when the following are positive: respiratory rate of at least 22 breaths/min, alteration in mental status, Glasgow Coma Scale score of less than 15 points, and systolic blood pressure of 100 mmHg or less. When the SOFA score was two or more points, a preliminary diagnosis of sepsis was made after the exclusion of other probable causes of organ failure and the patient was admitted to the ICU. If the SOFA score manifested an elevation of two or more points, the diagnosis of sepsis was made. Septic shock was defined as a systolic blood pressure of less than 90 mmHg, a mean blood pressure of less than 65 mmHg despite sufficient fluid loading, or a blood lactate level of more than 4 mmol/L (36 mg/dL).

Statistical analysis
Quantitative data were expressed as mean (with 95% confidence interval of mean) and standard deviation from the mean and were compared between groups using Student's t-Test. Categorical or qualitative data were expressed as frequency with corresponding percentages and were compared between survivors and non-survivors using Chi-square or Fisher's Exact Test. Level of significance was set at 5% or 0.05 and p < 0.05 was considered significant. Statistical analysis was completed using the Statistical Package for the Social Sciences version 23.0 software program (IBM Corp., Armonk, NY, USA) and Stata software version 15.1 (Stata Corp LLC, College Station, TX, USA).

Results
A total of 138 ICUs were screened and data were collected from 45 ICUs (Figure 1).

FIGURE 1: Data collection from intensive care units
The demographic characteristics of the included patients considering their mortality in view of bundle compliance were similar ( Table 1).

Variables
All

TABLE 2: Bundle compliance of patients
The 2018 SSC one-hour bundle protocol compliance rate was also 0%. The rate of obtaining an appropriate culture in the first three-hour bundle was 31%, while the rate of using appropriate antibiotics at an appropriate time was 50%. Additionally, the rate of initial administration of an appropriate fluid bolus was 12% and the mean fluid bolus volume was 1,113 ± 676 mL. Further, the initiation of a vasopressor drug if the mean blood pressure was less than 65 mmHg presented a rate of 11.5%, while the rate of second lactate measurement was 0%. The rate of assessing at least two items among the parameters of central venous pressure (CVP) measurement, central venous oxygen saturation (ScvO)2, cardiac ultrasonography, dynamic testing, and passive lower-extremity elevation testing -besides the vital signs, cardiopulmonary findings, capillary refilling, and cutaneous findings -to determine the volume and perfusion status of a patient was 0.3%. The median number of days that a mechanical ventilator was used was 10 (interquartile range: 5-23 days). The mortality rate due to sepsis in the intensive care unit was 22%. The mortality rate due to septic shock in the intensive care unit was 78%.

Discussion
In our study involving 45 ICUs, we determined that the one-hour bundle compliance rate was 0%. Also, we found that the three-and six-hour bundle compliance rates were each 0%. These results are quite low when compared to those recorded from both developing and developed countries [5,18]. In our study, the most significant deviation from compliance was seen with the absence of recurrent lactate measurements within the one-and six-hour bundles. In a similar study conducted in Asian countries with high-and middle-level incomes, those with low middle and middle-level incomes reported a rate of compliance with the six-hour resuscitation bundle of 6.9% and a mortality rate of 50% [19]. In a study conducted in Bangladesh, which is a low-income country, the six-hour resuscitation bundle compliance rate was 0%, with the hospital mortality rate being 49.2% [20]. In a multicenter study performed in Asia, the team reported a level of 7.6% bundle compliance. After the sepsis training was given to physicians, the bundle compliance rate was 37.5% [18].
A study of developed and developing countries reported a total three-hour bundle compliance rate of 19%. In this study, the highest three-hour bundle compliance was found in North America, with 29%. Mortality is reduced with greater bundle protocol compliance and the highest six-hour compliance is in western Europe, found as 36% [5]. On the contrary, the lowest bundle compliance was found to be 26% in Africa and Central Asia. In large retrospective studies in the United States of America, it has been found that mortality decreases with bundle compliance [21][22].
Multicenter sepsis study was carried out in Turkey. In this study, sepsis bundle compliance is very low and mortality is high [5]. Among the ways to increase sepsis bundle compliance are education (meeting, bedside training, etc.) and increasing the standardization of sepsis treatment (predefined order sets, screening tools, sepsis teams) [ [26].
The primary limitation of our study was that it was conducted only in tertiary ICUs and does not represent the conditions of other ICUs or hospital wards. There is therefore a need to conduct clinical trials in developing countries.

Conclusions
In conclusion, we found bundle compliance very low and mortality high in Turkey. Studies are needed to increase the compliance of sepsis bundle (effect of training, impact of the team, screening and feedback).

Additional Information Disclosures
Human subjects: Consent was obtained or waived by all participants in this study. Katip Çelebi University Ethics Committee issued approval 77/2017. Approved by the Ethics Committee of Katip Çelebi University. Animal subjects: All authors have confirmed that this study did not involve animal subjects or tissue.

Conflicts of interest:
In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.