Predictors and Outcomes of Ventilated Hospital-acquired Pneumonia

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-100
SponsorAssiut University

About this trial

Hospital-acquired pneumonia (HAP) is defined as an infection of the pulmonary parenchyma that develops in patients admitted to hospital for more than 48 hours and that was not incubating at the time of admission. It represents one of the most common and serious nosocomial infections, associated with significant morbidity, prolonged hospitalisation, and increased mortality in critically ill patients.

The aetiology of HAP is primarily driven by micro-aspiration of bacteria colonising the oropharynx and upper gastrointestinal tract. Pathogen distribution is shaped by the duration of hospitalisation, prior antibiotic exposure, local epidemiology, and patient characteristics. Multidrug-resistant (MDR) organisms are particularly prevalent in patients with prolonged inpatient stay and intensive care unit (ICU) admission, as critically ill patients become rapidly colonised with nosocomial pathogens.

Ventilator-associated pneumonia (VAP), a subgroup of nosocomial pneumonia, occurs in patients requiring tracheal intubation and mechanical ventilation for at least 48 hours. A clinically important and increasingly recognised entity is ventilated HAP (v-HAP), defined as HAP that subsequently requires tracheal intubation and mechanical ventilation. Emerging evidence indicates that v-HAP carries the highest mortality among nosocomial pneumonia subtypes in ICU patients - exceeding VAP - while non-ventilated ICU-acquired HAP carries the lowest mortality.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

Post operative patients

Tracheostomized patients

Comatosed patient since admission

Suspected aspiration

Trial population

* Adult patients (age ≥18 years) admitted to the Chest Department or Respiratory ICU, Assiut University Hospitals * Diagnosis of HAP confirmed according to standard clinical, radiological, and microbiological criteria * Hospital admission for more than 48 hours prior to pneumonia onset * Ability to provide informed consent

Trial design

Design model

Other

Time perspective

Cross-sectional

Treatments tested in this trial

  • mechanical ventilation (MV)

    Behavioral

    need for mechanical ventilation

Treatment groups

151 Participants
are divided into 1 treatment group
Group A: HAP1 intervention

Trial outcomes

Primary outcomes

1

Prevalence of mechanical ventilation among HAP patients (v-HAP rate).

Time frame
1 year

Secondary outcomes

Other outcomes

Sponsors and contacts

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