Assessing the Effect of the Surviving Sepsis Campaign Treatment Guidelines on Clinical Outcomes in a Community Hospital

Author:

Patel Gita Wasan1,Roderman Nicki2,Gehring Hollie3,Saad John4,Bartek William5

Affiliation:

1. Clinical Pharmacy Coordinator, Pharmacy Department, The Medical Center of Plano, Plano, TX

2. Clinical Nurse Specialist, Critical Care Unit, The Medical Center of Plano

3. Emergency Department, The Medical Center of Plano

4. Emergency Medicine, Emergency Department, The Medical Center of Plano

5. Intensive Care Unit, The Medical Center of Plano

Abstract

Background: Bundles yield a reduction in mortality in patients with sepsis, but the majority of the data is from large academic centers. The ability of a community hospital to implement a sepsis bundle successfully, however, has not been investigated. Objective: To examine the effect of a collaborative 2-part sepsis bundle on clinical outcomes and mortality at a community hospital. Methods: The study included all patients with severe sepsis/septic shock over the age of 18 years admitted to the intensive care unit (ICU) from 2006 to 2007 who were not treated with a bundle (n = 53) and those who were treated with a bundle (n = 59). Data collected included demographics; initiation of vasopressors; days on vasopressors; blood glucose; use of drotrecogin alfa (activated), steroids, and ventilator; ICU/hospital lengths of stay; ventilator days; time to culture; time to first dose of antibiotics; time to transfer from emergency department to ICU; fluid resuscitation in the first 24 hours; percentage of patients started on dialysis; and mortality. Results: Demographics; blood glucose; use of drolrecogin alfa (activated), steroids and ventilator; ICU/hospital lengths of stay; and ventilator days were statistically similar between groups. Median time to cultures, first dose of antibiotics, and transfer to ICU were all reduced with the bundle. Percentage of non-bundle patients on vasopressors was 87% versus 66.7% of bundle patients (p = 0.011) and number of median days on vasopressors was reduced. Fewer bundle patients were initiated on dialysis (0%) versus non-bundle patients (14.8%) (p = 0.02). Median fluid administered in the first 24 hours was 2200 mL (10-13,996 mL) for non-bundle patients and 7143 mL (1000-19,104 mL) for bundle patients (p < 0.001). Mortality was 61.1% in the non-bundle group versus 20% with the bundle (p < 0.001). Conclusions: Implementation of a 2-part sepsis bundle based on the Surviving Sepsis Campaign Guidelines can yield a positive impact on clinical outcome and mortality in a nonacademic, community hospital setting.

Publisher

SAGE Publications

Subject

Pharmacology (medical)

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