Ventilatory Parameters and Inflammatory Responses of Neonates Ventilated by Different Modes of Ventilation

Sponsor
Gazi University (Other)
Overall Status
Completed
CT.gov ID
NCT01514331
Collaborator
(none)
40
1
2
22
1.8

Study Details

Study Description

Brief Summary

The main purpose of this study is to investigate effects of SIMV+VG (synchronized intermittent mandatory ventilation+volume guarantee) or PSV+VG (pressure support ventilation+volume guarantee) ventilation on vital signs, patient - mechanical ventilation synchrony, ventilation parameters and inflammatory mediators in neonates.

Condition or Disease Intervention/Treatment Phase
  • Other: SIMV+VG mode of ventilation (synchronized intermittent mandatory ventilation+volume guarantee)
  • Other: PSV+VG (pressure support ventilation+volume guarantee)
N/A

Detailed Description

Term or preterm neonates may need mechanical ventilation due to different etiologies. In all patients aim of mechanical ventilation is to promote pulmonary gas exchange, reduce the respiratory work of patient. Ideal mechanical ventilation must minimize pulmonary trauma with low inspiratory pressures that obtains adequate and constant tidal volumes. Ventilation associated pulmonary injury is an important subject that must be considered during mechanical ventilation. Atelectotrauma, volutrauma, barotrauma and biotrauma must be monitored. Volutrauma, barotrauma and oxygen toxicity cause cytokine increase that results in biotrauma. This parenchymal inflammation is a risk factor for chronic lung disease which is an important morbidity of ventilated neonates.

From past to present neonates were ventilated with different ventilation modes including IMV (Intermittent Mandatory Ventilation), SIMV, A/C (Assist Control Ventilation), PSV,HFV (High Frequency Ventilation). Both PSV and SIMV are patient trigger ventilation modes but SIMV is a time cycled and PSV is a flow cycled mode. In recent years hybrid techniques were developed to combine beneficial features of volume and pressure limited ventilation. In commercial ventilation devices these techniques have different names as volume guaranteed pressure limited ventilation (Drager Babylog 8000), pressure regulated volume controlled ventilation (Siemens servo 3000), volume guaranteed pressure support ventilation (VIP Bird Gold).

Since there is not a standard protocol for mechanical ventilation of neonates different countries and even different NICU's use different ventilation protocols.

Literature supports volume targetted ventilation to reduce barotrauma with low maximum inspiratory pressures and to reduce volutrauma with constant tidal volumes. When A/C+VG and SIMV+VG were compared in a crossover trial, more constant tidal volumes were obtained in A/C mode. Inflammatory cytokines have also been measured in different groups of patients with variable ventilatory management techniques. So far there has not been a randomized study published comparing VG+SIMV with VG+PSV in newborns with regards to tidal volume , peak inspiratory pressure variability,or inflammatory cytokines. Therefore in this study the investigators aimed to compare these two ventilation modes with regards to short term outcome.

Study Design

Study Type:
Interventional
Actual Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Official Title:
Determination of Ventilatory Parameters and Inflammatory Responses of Neonates Who Are Ventilated by Volume Guarantee Combined With Synchronized Intermittent Mandatory Ventilation or Pressure Support Ventilation
Study Start Date :
Jan 1, 2012
Actual Primary Completion Date :
Nov 1, 2013
Actual Study Completion Date :
Nov 1, 2013

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: PSV+VG

Neonates who require mechanical ventilation and randomised to pressure support + volume guarantee (PSV+VG) mode

Other: PSV+VG (pressure support ventilation+volume guarantee)
Neonates who need mechanical ventilation will be ventilated with PSV+VG
Other Names:
  • PSV+ VG mode of ventilation
  • Active Comparator: SIMV+VG

    Neonates who require mechanical ventilation and randomised to synchronised intermittant mandatory ventilation + volume guarantee (SIMV+VG) mode

    Other: SIMV+VG mode of ventilation (synchronized intermittent mandatory ventilation+volume guarantee)
    Neonates who need mechanical ventilation will be ventilated with SIMV+VG mode
    Other Names:
  • SIMV + VG mode of ventilation
  • Outcome Measures

    Primary Outcome Measures

    1. IL-1beta levels in tracheal aspirate material [Baseline and 72 hours of mechanical ventilation]

      Tracheal aspirate will be analyzed for the mediator level and change from baseline will be reported

    2. IL-6 level in tracheal aspirate [Baseline and 72 hours of mechanical ventilation]

      Tracheal aspirate will be analyzed for IL6 level and the change from baseline will be reported

    3. IL-8 in tracheal aspirate material [Baseline and 72 hours of mechanical ventilation]

      Tracheal aspirate will be analyzed for the mediator level and change from baseline will be reported

    4. IL-10 level in tracheal aspirate material [Baseline and 72 hours of mechanical ventilation]

      Tracheal aspirate will be analyzed for the mediator level and change from baseline will be reported

    5. TNF alfa in tracheal aspirate material [Baseline and 72 hours of mechanical ventilation]

      Tracheal aspirate will be analyzed for the mediator level and change from baseline will be reported

    6. tidal volume variability [72 hours of mechanical ventilation or entire ventilation time if extubated earlier]

      variability in tidal volume measured with babyview program

    7. peak inspiratory pressure variability [72 hours of mechanical ventilation or entire ventilation time if extubated earlier]

      variability in peak inspiratory pressure measured with babyview program

    8. respiratory rate variability [72 hours of mechanical ventilation or entire ventilation time if extubated earlier]

      changes in respiratory rate, tacypnea rate

    9. oxygen saturation variability [72 hours of mechanical ventilation or entire ventilation time if extubated earlier]

      changes in oxygen saturation, desaturation rate, hyperoxy rate

    10. lowest carbondioxide level (mmHg) [72 hours of mechanical ventilation or entire ventilation time if extubated earlier]

      ratio of hypocarbic blood gases and least pCo2 level

    11. highest carbondioxide level (mmHg) [72 hours of mechanical ventilation or entire ventilation time if extubated earlier]

      ratio of hypercarbic blood gases and highest pCo2 level

    12. lowest oxygen level (mmHg) [72 hours of mechanical ventilation or entire ventilation time if extubated earlier]

      ratio of hypoxic blood gases and least pO2 level

    13. highest oxygen level (mmHg) [72 hours of mechanical ventilation or entire ventilation time if extubated earlier]

      ratio of hyperoxic blood gases and highest pO2 level

    Secondary Outcome Measures

    1. bronchopulmonary dysplasia [36 weeks corrected age]

      Oxygen requirement at 36 weeks corrected age

    2. patent ductus arteriosus [in the first week of post natal life of the patient]

      Presence of hemodynamically significant patent ductus arteriosus in the first 7 days of life

    3. necrotizing enterocolitis [36 weeks corrected age]

      Necrotising entercolitis defined by clinical and radiological findings

    4. intraventricular hemorrhage [during first week]

      Intraventricular hemorrhage diagnosed by head ultrasound

    5. pneumothorax [during first 3 days]

      Air leak diagnosed by chest x-ray

    6. pulmonary interstitial emphysema [during first week]

      Air leak diagnosed by x-ray

    7. pulmonary hemorrhage [during first week]

    8. retinopathy of prematurity [until 36 weeks corrected age]

      Retinal disease diagnosed by indirect opthtalmoscopic exam

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A to 24 Hours
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • neonates with respiratory distress who need mechanical ventilation

    • gestational age less than or equal to 37 weeks

    • neonates who need mechanical ventilation within first 24 hours

    Exclusion Criteria:
    • neonates who need mechanical ventilation other than conventional ventilation

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Gazi University Hospital, Department of Pediatrics, Division of Newborn Medicine Besevler Ankara Turkey 06500

    Sponsors and Collaborators

    • Gazi University

    Investigators

    • Principal Investigator: Ebru N Ergenekon, MD, Gazi University, Division of newborn Medicine

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Ebru Ergenekon, Prof.Dr, Gazi University
    ClinicalTrials.gov Identifier:
    NCT01514331
    Other Study ID Numbers:
    • 01/2011-68
    First Posted:
    Jan 23, 2012
    Last Update Posted:
    Nov 20, 2013
    Last Verified:
    Nov 1, 2013
    Keywords provided by Ebru Ergenekon, Prof.Dr, Gazi University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 20, 2013