Pulmonary Infections and Barotrauma Associated With MV IN PICU

March 29, 2023 updated by: Abdelrahman Mahmoud Ezzat, Assiut University

Frequencies, Risk Factors and Outcome of Ventilation-Associated Lung Complications At Paediatric Intensive Care Unit (PICU)

This study aims to determine the incidence, risk factors and outcome of ventilation associated common complication in the PICUs at Assiut University Children Hospital in Egypt.

Study Overview

Status

Active, not recruiting

Intervention / Treatment

Detailed Description

A constellation of adverse effects and complications may be associated with mechanical ventilation,The following are the Commonest Complications of Mechanical Ventilation

  1. Ventilator-associated pneumonia.
  2. Ventilator-induced lung injury.
  3. Ventilation induce Hemodynamic compromise leads to ARDS. Ventilator-Associated Pneumonia (VAP) It refers to nosocomial pneumonia occurring 48 hours or more after initiation of mechanical ventilation (MV)

It is the second most common HAI after blood stream infection in the paediatric age group, accounting for about 20% of all HAIs in the paediatric intensive care units (PICUs) and has a rate of 2.9- 21.6 per 1000 ventilator days.The risk factors responsible for VAP occurrence can be classified into:

A-Host related factors: include associated co-morbidities B-Device-related factors: include the endotracheal tube, the ventilation circuit, and the presence of a nasogastric or an orogastric tube.

C-Personnel related factors: include improper hand hygiene and inadequate use of personal protective equipment.

VAP is associated with increased hospital morbidity; mortality; duration of hospitalization by an average of 7-9 days per patient; and health care costs . The incidence rates of VAP are higher in developing countries with limited resources.

Ventilator-associated lung injury (VALI) It is the lung damage by application positive or negative pressure to the lung by mechanical ventilation.

The prevalence of VALI in children admitted to the paediatric intensive care unit (PICU) may approximate 10%.

Types of VALI:

  • Voltrauma (This is damage caused by over-distension)
  • Barotrauma (destructive entry of pressurised airway gases into the parenchyma, or into blood vessels.)
  • Biotrauma (is known to upregulate pulmonary cytokine production)
  • Oxygen toxicity (This is the damage caused by a high concentration of inspired oxygen)
  • Recruitment /de-recruitment injury (atelectotrauma)
  • Shearing injury Risk factors for VALI: blood product transfusion, acidaemia, and history of restrictive lung disease. larger tidal volume.

investigators observed lower mortality among children ventilated with Vt ~8 mL/kg actual bodyweight compared with ~10 mL/kg in a before-after retrospective study .

Ventilation induce Hemodynamic compromise leads to ARDS:

Definition: Decrease in mean arterial pressure of 60 mm Hg or an absolute decrease to a systolic blood pressure < 80 mm Hg in the first 2 hours after intubation, required treatment for LTH with vasopressors.

primary factor influencing mortality in acute respiratory distress syndrome (ARDS) Incidence: 28.6% of patients intubated in the emergency department developed post-intubation hypotension, tatistically significant association between LTH and hyper carbic (PCO2 > 50 mm) chronic obstructive pulmonary disease

Study Type

Observational

Enrollment (Anticipated)

50

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Assuit
      • Assiut, Assuit, Egypt, 2063045
        • PICU

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

1 month to 16 years (Child)

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

children aged one month to up to 16 years Intubated and connected to MV for at least 48hrs.

Description

Inclusion Criteria:

  • children aged one month to up to 16 years Intubated and connected to MV for at least 48hrs.

Exclusion Criteria:

  • Neonates and cases connected to M.V less than 48 hours.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
assess right sided heart failure post ventilator acquired pneumonia
Time Frame: one year from april 2022 to april 2023
use modified ross score for evaluation of heart failure post mechanical ventilation
one year from april 2022 to april 2023

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Asess the risk factors associated with barotrauma on mechanical ventilation
Time Frame: one year from april 2022 to april 2023
previous chronic lung disease .previous NICU or PICU admission
one year from april 2022 to april 2023

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 1, 2022

Primary Completion (Anticipated)

April 30, 2023

Study Completion (Anticipated)

June 30, 2023

Study Registration Dates

First Submitted

January 9, 2023

First Submitted That Met QC Criteria

March 29, 2023

First Posted (Actual)

March 31, 2023

Study Record Updates

Last Update Posted (Actual)

March 31, 2023

Last Update Submitted That Met QC Criteria

March 29, 2023

Last Verified

March 1, 2023

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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