Overview

Samu Save Sepsis: Early Goal Directed Therapy in Pre Hospital Care of Patients With Severe Sepsis and/or Septic Shock

Status:
Completed
Trial end date:
2019-02-09
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to determine whether an aggressive strategy of severe sepsis patients since pre hospital care, including early antibiotics administration, hemodynamic optimization, and opotherapy when indicated, could reduce mortality
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Assistance Publique - Hôpitaux de Paris
Treatments:
Anti-Bacterial Agents
Ceftriaxone
Cortisol succinate
Hydrocortisone
Hydrocortisone 17-butyrate 21-propionate
Hydrocortisone acetate
Norepinephrine
Penicillanic Acid
Piperacillin
Piperacillin, Tazobactam Drug Combination
Tazobactam
Criteria
Inclusion Criteria:

All patients fulfilling the following criteria:

- Age ≥ 18 years

- Patient with suspected severe infection defined by the existence of a suspected
infection AND

- Hypotension before vascular fluid loading AND/OR

- Lactataemia greater than 4 mmol/l AND/OR

- Glasgow scale lower than 13 AND/OR

- Mottling score greater than 2

- Patient with a septic shock

Exclusion Criteria:

- Age <18 years or Unable

- Pregnant

- Severe concomitant pathology requiring urgent care(i.e.epilepsy)

- Status "not to be reanimated" life expectancy less than 6 months with no indication of
reanimation support ( prior decision on care limitation).

- Fulminans purpura

- True allergy to beta-lactam defined by an angioedema or by an anaphylactic shock
during a prior exposure to beta-lactam.

- Patient who have already received hemodynamic optimization or antibiotic treatment
before the MICU's (Mobile Intensive Care Unit) care.