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Completed

NCT Number: NCT03111303

Mechanical Ventilation Parameters in HAP Patients

Hospital-acquired pneumonia (HAP) in patients in intensive care often requires the mechanical ventilation (MV). Management and weaning from MV are given by specificity of this type of pulmonary inflammation. Enrolled in the retrospective, observational study were all patients older than 18 years staying at the ICU of University Hospital in Olomouc, between 1 January 2011 and 31 December 2016. The determination of the parameters of the MV, ICU length of stay, hospital length of stay and mortality in HAP group were compared with the control group of patients without HAP.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

About this study

Hospital-acquired pneumonia (HAP) development influences the parameters of mechanical ventilation, intensive care unit (ICU) length of stay, hospital length of stay, need of tracheostomy, bronchoscopy, reconnection to MV and mortality. We respect HAP definition: acute inflammation of the respiratory bronchioles, alveolar structures and pulmonary interstitium. Clinically it is defined as the presence of newly developed or progressive infiltrates on chest radiographs plus at least two other signs of respiratory tract infection: temperature >38 °C, chest pain, purulent sputum, leukocytosis or leukopenia, signs of inflammation on auscultation, cough and/or respiratory insufficiency. HAP is defined as pneumonia that occurs 48 hours or more after admission, which was not incubating at the time of admission. A retrospective, observational study processing data on all consecutive intensive care patients older than 18 years of age between 1 January 2011 and 31 December 2015. The aim was to determine the incidence of potential risk factors and their impact on the development of HAP. The primary outcome was investigation of the relationship between mechanical ventilation parameters and the presence of early- and late-onset HAP. Enrolled in the study were patients staying at the ICU of the Department of Anesthesiology and Intensive Care Medicine, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, between 1 January 2011 and 31 December 2016. The participants were all patients older than 18 years of age consecutively admitted to the ICU.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18+
  • Need of Mechanical ventilation (Pressure controlled mechanical ventilation or Pressure support ventilation)

Exclusion criteria

  • Organ donor
  • Need Volume controlled mechanical ventilation
  • no mechanical ventilation

Treatment and study plan

Mechanical ventilation

Device

Connection to mechanical ventilator

Primary outcomes

  1. length of mechanical ventilation

    Time frame: during MV

    days of MV

Secondary outcomes

  1. ICU length of stay

    Time frame: 1 month

    length of stay in ICU

  2. Hospital length of stay (LOS)

    Time frame: 1 month

    length of hospital stay

  3. Mortality

    Time frame: 1 month

    mortality during Hospital LOS

Other outcomes

  1. Inspiratory pressure

    Time frame: during MV

    most high inspiratory pressure during MV

  2. Positive end expiratory pressure (PEEP)

    Time frame: during MV

    most high PEEP during MV

Sponsors and collaborators

Lead sponsor

University Hospital Olomouc

Other

Registry information

Official study title

Nosocomial Pneumonia as a Factor Influencing Parameters of Mechanical Ventilation: Results of a Retrospective, Observational Study

Important dates

Study start
2011
Primary completion
2016
Study completion
2017
First posted
Apr 12, 2017
Registry last updated
Oct 26, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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