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Syndrome and Aspiration Pneumonia in Intensive Care

Syndrome and Aspiration Pneumonia in Intensive Care

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01881672
Acronym
SPIRE
Enrollment
250
Registered
2013-06-20
Start date
2012-11-30
Completion date
2015-04-30
Last updated
2016-08-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

ICU Patients, In State of Coma (Define by Glasgow ≤ 8), No Antibiotic Treatment, Under Mechanical Ventilation

Keywords

Aspiration pneumonia, Coma, Mechanical ventilation

Brief summary

Inhalation is a common condition in patients with impaired their awareness requiring protection of the upper airway by endotracheal intubation. This inhalation may lead to chemical pneumonitis and/or bacterial pneumonia. Only the latter requires the administration of antibiotics. Patients developing such a bacterial pneumonia, has a mortality, duration of mechanical ventilation and length of ICU stay increased. However, the proportion of patients with such bacterial pneumonia, bacterial ecology and morbidity that are little known. The aim of this study is to determine the frequency of bacterial pneumonia in patients admitted to the ICU for coma and treated with mechanical ventilation

Interventions

None listed

Sponsors

Centre Hospitalier Departemental Vendee
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Altered consciousness defined by a Glasgow Coma Scale score less than or equal to 8 before protection of the upper airway by endotracheal intubation * Patient under mechanical ventilation

Exclusion criteria

* Patient with pre-existing impairment of laryngeal function in Parkinson's disease, Alzheimer's disease, amyotrophic lateral sclerosis, laryngeal cancer, radiotherapy laryngeal * Patient under guardianship * Inpatient without consent * Pregnant woman * Patient previously treated with antibiotics for more than 24 hours at the time of ICU admission * Patient with infection at ICU admission which justified probabilist antibiotic treatment * Lack of social security * Refusal of the patient or their next of kind

Design outcomes

Primary

MeasureTime frameDescription
Determine the frequency of bacterial pneumonia in patients admitted to the ICU for coma and treated with mechanical ventilationICU DischargeParticipants will be followed for the duration of ICU stay, an expected average of 4 days

Secondary

MeasureTime frameDescription
Quantify the use of antibiotics during the ICU stay for patients admitted to the ICU for coma and treated with mechanical ventilationICU DischargeParticipants will be followed for the duration of ICU stay, an expected average of 4 days
Description of the bacterial flora identified in respiratory specimens.ICU DischargeParticipants will be followed for the duration of ICU stay, an expected average of 4 days
Identification of predictive factors for development of bacterial pneumoniaICU DischargeParticipants will be followed for the duration of ICU stay, an expected average of 4 days

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026