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Diagnostic Modalities for VAP Detection

A

Assiut University

Status

Completed

Conditions

Ventilator Associated Pneumonia

Treatments

Diagnostic Test: bronchoalveolar lavage

Study type

Interventional

Funder types

Other

Identifiers

NCT04911244
VAP diagnosis

Details and patient eligibility

About

asses diagnostic performance of different methods for detection of ventilator associated pneumonia.

Full description

Ventilator associated pneumonia (VAP) is a common cause of nosocomial infection, that can complicate mechanical ventilation and is related to significant utilization of health-care resources.

The diagnosis of VAP is subjected to considerable interobserver variability. The Centers for Disease Control and Prevention (CDC) definition of VAP uses a combination of clinical, radiographic, and micro-biological criteria for diagnosis, but in the absence of a definite diagnostic test, the accurate diagnosis and treatment of VAP is limited.

The clinical pulmonary infection score (CPIS) was developed to objectively diagnose VAP and assign points on the basis of clinical and radiographic data, but its role in diagnosing pneumonia remains controversial .

Lung ultrasound (LUS) is a simple, non irradiating, noninvasive, cost-effective, bedside technique. It has been successfully applied for monitoring aeration and monitoring antibiotic efficacy in ventilator-associated pneumonia (VAP). However, no scientific evidence is yet available on whether LUS reliably improves the diagnosis of VAP.

Quantitative bacterial cultures of the specimen obtained from the lower airways using bronchoscope were proposed for VAP diagnosis with a cut off value of 104 colony-forming unit/ml. However, microbiological cultures cannot guide the early clinical management of patients with a suspected VAP, as they need at least 24 hours for preliminary results. So, starting antibiotics remains a challenge. Moreover, bronchoscopy is not always easy to perform in hypoxemic patients and not promptly available in all ICUs. Therefore, it can be replaced by tracheal aspirate microbiological samples.

Enrollment

100 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All adult patients mechanically ventilated for at least 48 hours in Respiratory ICU were included in the study.

who had:

  • Clinically suspected VAP according to simplified Clinical Pulmonary Infectious Score exceeding 6.

  • Or new or extension of a radiological image with at least two of the following clinical criteria:

    • Body temperature ≥ 38.5 ° C or <36 ° C.
    • Leukocytes> 10 * 103 / ml or <4 * 103/ ml or > 10% immature cells (in the absence of other known causes).
    • Purulent tracheal secretions.
    • Hypoxemia with PaO2 <60 mmHg or a PaO2 / FiO2 <300.

Exclusion criteria

  • Patients with diagnosis of community acquired pneumonia or hospital acquired pneumonia before starting of mechanical ventilation.
  • Patients who are contraindicated for bronchoscopy

Trial design

100 participants in 2 patient groups

VAP group
Experimental group
Description:
patients confirmed diagnosis of VAP with bronchoalveolar lavage
Treatment:
Diagnostic Test: bronchoalveolar lavage
Non VAP group
Experimental group
Description:
patients confirmed not VAP with bronchoalveolar lavage
Treatment:
Diagnostic Test: bronchoalveolar lavage

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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