Observational Study on Intubation in Septic Shock (INTUBATIC)

University Hospital, Angers

Status: Completed

Conditions: Septic Shock

Study type: Observational

Funder types: Other

Identifiers

NCT02780466

2015-96

Details and patient eligibility

About

Septic shock is common in intensive care and its mortality remains high. While new treatments have not improved survival, optimization of known and widely used techniques has allowed reduction in mortality. Thus improving care given to patients starts with making better use of existing resuscitation techniques. Among these practices, mechanical ventilation is widespread in the management of patients with septic shock. In large studies published in recent years in Europe and North America, 40 to 85% of patients receive invasive mechanical ventilation. It therefore appears that a significant proportion of patients are never intubated during treatment and management of their septic shock. There is no specific recommendation from critical care societies concerning mechanical ventilation in the treatment of septic shock. Apart from indisputable situations such as impaired consciousness or acute respiratoire distress, the decision whether to ventilate mechanically or not is left to the discretion of the physician.

The aim of this study is to analyze intubation practice in septic shock patients and its impact on 28-day survival.

This multicentric and observational study will be conducted in 30 French ICUs.

Enrollment: 859 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• older than 18 years old
• Admitted in the ICU for septic shock
• Introduction of vasopressors ( norepinephrine or adrenaline ) in the ICU or within 24 hours of ICU admission
• Suspected or proven infection

Exclusion criteria

• Intubation before the introduction of vasopressors
• Decision of withdrawing or withholding care at admission
• Pregnant woman
• Patient not affiliated to the social security insurance
• Refusal of participation in the study

Trial design

859 participants in 1 patient group

Patients with septic shock