Prognostic Biomarkers in Predicting Mortality in Respiratory Patients With Ventilator-Associated Pneumonia

Sponsor
Assiut University (Other)
Overall Status
Completed
CT.gov ID
NCT04739748
Collaborator
(none)
136
1
20
6.8

Study Details

Study Description

Brief Summary

The aim of this study is to evaluate prognostic efficiency RDW and NLR for mortality prediction in respiratory patients with VAP.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: complete blood picture

Detailed Description

Ventilator-associated pneumonia (VAP) is the most common nosocomial infection. VAP continues to be a leading cause of morbidity and mortality in the nosocomial setting. Red cell distribution width (RDW) and neutrophil-lymphocyte ratio (NLR) are prognostic factors to mortality in different diseases.

Study Design

Study Type:
Observational
Actual Enrollment :
136 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Prognostic Biomarkers in Predicting Mortality in Respiratory Patients With Ventilator-Associated Pneumonia
Actual Study Start Date :
Apr 6, 2018
Actual Primary Completion Date :
Dec 7, 2019
Actual Study Completion Date :
Dec 7, 2019

Arms and Interventions

Arm Intervention/Treatment
Respiratory ICU patient

patient in RICU that developed ventilator-associated pneumonia

Diagnostic Test: complete blood picture
Measure the red blood cell distribution width (RDW), the neutrophil-lymphocyte ratio (NLR).

Outcome Measures

Primary Outcome Measures

  1. Hospital Mortality [45 days]

    The number of patients who not Survive after developing ventilator-associated pneumonia in their stay in the Respiratory Intensive Care Unit.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Respiratory failure needs mechanical ventilator support > 48 hrs. VAP was defined as an acute lower respiratory tract infection in mechanically ventilated patient > 48 hrs with a new or progressing infiltrate on chest radiograph and who met at least two of the following clinical criteria: body temperature >38°C or <36°C with no other recognized cause, white blood cell count >10,000 /mm3 or <5000 /mm3, or a macroscopically purulent tracheal aspirate

  • Only the first VAP episode was included

Exclusion Criteria:
  • Neutropenia (< 500 cells/ml) before the development of VAP.

  • Conditions are known to influence total and differential WBC counts such as chronic inflammatory conditions, hematologic disorders, history of chemotherapy, or radiotherapy within 4 weeks before enrollment.

  • Conditions are known to affect RDW as anemia due to nutritional deficiency (ie, iron, vitamin B12, and folic acid).

  • Patients with HIV/AIDS

Contacts and Locations

Locations

Site City State Country Postal Code
1 Chest Department-faculty of medicine-Assuit university Assuit Egypt

Sponsors and Collaborators

  • Assiut University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Nermeen Aly Mahmoud Abdel Aleem, lecture in Faculty of medicine,Assiut University, Assiut University
ClinicalTrials.gov Identifier:
NCT04739748
Other Study ID Numbers:
  • IRB17300520
First Posted:
Feb 5, 2021
Last Update Posted:
Feb 8, 2021
Last Verified:
Feb 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Nermeen Aly Mahmoud Abdel Aleem, lecture in Faculty of medicine,Assiut University, Assiut University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 8, 2021