International Multicentre Prevalence Study on Sepsis (IMPRESS)

European Society of Intensive Care Medicine

Status: Completed

Conditions: Severe Sepsis; Septic Shock

Study type: Observational

Funder types: Other

Identifiers

NCT01943747

IMPRESS

Details and patient eligibility

About

To mark 10 years of the Surviving Sepsis Campaign (SSC), and timed to coincide with World Sepsis Day, on September 13, 2013, the SSC, ESICM and SCCM will be conducting an international point prevalence study of severe sepsis and septic shock. The goal of this project is to determine the world wide burden of severe sepsis and define current practices of sepsis care internationally. The study is a simple data collection exercise for patients presenting with either severe sepsis or septic shock on World Sepsis Day.

Full description

De---identified patient---level data will be collected on patients presenting to a participating intensive care unit or emergency department with severe sepsis or septic shock over a 24 hour period from 00:00 to 24:00 November 07, 2013. De---identified data that is already collected as part of routine clinical care will be collected for this study. Data to be collected includes hospital and ICU characteristics, patient characteristics, severity of illness, and adherence to SSC bundle elements and mortality. It will take between 30---60 minutes to collect and enter data for each patient admitted with severe sepsis or septic shock over the 24 hours study period.

Enrollment: 1,000 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

To be eligible patients must have all of the following:

• Must be admitted or transferred to either the ED or an Intensive Care Unit.
• Have a high clinical suspicion of an infection
• Have sepsis as defined by an infection together with two or more SIRS criteria
• Evidence of acute organ dysfunction and/or Shock.

Exclusion criteria

• Patients less than 18 years of age
• Patients in whom the sepsis has been present from before the beginning of the study period
• Any patients previously included in the study during the same study period