Sepse: Critical Analysis of New Sepse Studies and Definitions and Retrospective Evaluation of Sepse Protocol Implementation at Hospital Unimed Volta Redonda
Trial Snapshot
- Phase
- Not Applicable
- Sponsor
- Enrollment
- 506
- Locations
- 1
- Primary Endpoint
- Adherence to the sepsis protocol
Study Overview
Brief Summary
Research in the databases Lilacs, BIREME, SciELO by the terms: systemic inflammatory response syndrome (SIRS), sepsis, severe sepsis and septic shock and their equivalents in the English language. Selection of the main articles of the last five years to study and contextualize the reality presented since the implantation of the HUVR sepsis protocol. Statistical analysis of data since the implementation of the sepsis protocol in the HUVR, in July 2014 until June 2016.
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Retrospective
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •All individuals who had a confirmed or suspected sepsis diagnosis and had a sepsis protocol completed during the study period.
Exclusion Criteria
- •Individuals with confirmed or suspected sepsis in the study period who did not complete the protocol.
- •Individuals under the age of 18
Outcomes
Primary Outcomes
Adherence to the sepsis protocol
Time Frame: From 2014 to 2016
Implementation of the measures recommended in the sepsis protocol
Secondary Outcomes
- Sepsis mortality rate(From 2014 to 2016)
Investigators
Vicente Lopes da Silva Junior
Principal Investigator
Unimed Volta Redonda
