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Comparison of Two Flow Rates of HHHFNC to Prevent Extubation Failure in Preterm Infants

Primary Purpose

Prematurity, Mechanical Ventilation

Status
Completed
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
HHHFNC 6 liter minute
HHHFNC 3 liters/min
Sponsored by
Mansoura University Children Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prematurity, Mechanical Ventilation

Eligibility Criteria

1 Hour - 30 Days (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Infants born at less than 37 weeks' gestation, required endotracheal intubation and positive pressure ventilation, and are considered ready for extubation by the clinical team. Infants will be enrolled after written informed parental consent is obtained.

Exclusion Criteria:

  • Suspected upper airway obstruction, congenital airway malformations, or major cardiopulmonary malformations

Sites / Locations

  • Neonatal Intensive Care Unit, Mansoura University Children Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

6 liter/min group

3 liter/min group

Arm Description

Infants will be extubated to a HHHFNC (Fisher and Paykel Healthcare , Auckland, New Zealand) at flow rate of 6 L/min. Eligible infants will be enrolled while receiving mechanical ventilation. The timing of extubation will be determined by the clinical team and all infants will start caffeine prior to extubation.

Infants will be extubated to HHHFNC (Fisher and Paykel Healthcare , Auckland, New Zealand) a flow rate of 3 L/min. Eligible infants will be enrolled while receiving mechanical ventilation. The timing of extubation will be determined by the clinical team and all infants will start caffeine prior to extubation.

Outcomes

Primary Outcome Measures

Extubation failure
Extubation failure criteria will be defined as follows: Apnea (respiratory pause >20 seconds), more than 6 episodes requiring physical stimulation in 6 hours or 1 requiring intermittent positive pressure ventilation. Respiratory acidosis with pH <7.25 and Peripheral arterial oxygen saturation (PaCO2) >65 mmHg. ( >15% sustained increase in FiO2 from extubation. 4. Cardiovascular collapse (heart rate <60 beats per minute or shock. 5. Persistent marked/severe retractions. Extubation failure will be deemed to occur if any single criterion was met in any one of the 7 days after extubation. The decision to reintubate an infant and mechanical ventilation variables and subsequent extubation attempts after reintubation will be managed at the discretion of the clinical team.

Secondary Outcome Measures

Mortality
Death within the 96 hour post-extubation period or at any time after randomization.
Total duration of mechanical ventilation
Total duration of mechanical ventilation during NICU admission
Total duration of oxygen supplementation
Total duration of oxygen supplementation during NICU admission
Bronchopulmonary dysplasia (BPD)
BPD defined by oxygen requirement at 36 weeks' post-menstrual age.
Severe BPD
Severe BPD defined as oxygen requirement with fraction of inspired oxygen (FiO2) >0.30 or need for positive pressure support at 36 weeks' post-menstrual age.
The combined outcome variables of death before 36 weeks PMA or BPD
The combined outcome variables of death before 36 weeks PMA or BPD will be used to adjust for occurrence of death after extubation but before the time of assessment of BPD.
The combined outcome variables of death before 36 weeks PMA or severe BPD
The combined outcome variables of death before 36 weeks' post-menstrual age (PMA) or severe BPD will be used to adjust for occurrence of death after extubation but before the time of assessment of BPD.
Other neonatal morbidities (intracranial hemorrhage, pneumothorax, patent ductus arteriosus, necrotizing enterocolitis, and retinopathy of prematurity)
The occurrence of neonatal morbidities occurring before, during the 96 hours post-extubation, and at any time thereafter will be documented (intracranial hemorrhage, pneumothorax, patent ductus arteriosus, necrotizing enterocolitis, and retinopathy of prematurity).

Full Information

First Posted
February 10, 2016
Last Updated
February 22, 2020
Sponsor
Mansoura University Children Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02681315
Brief Title
Comparison of Two Flow Rates of HHHFNC to Prevent Extubation Failure in Preterm Infants
Official Title
HHHFNC to Prevent Extubation Failure in Preterm Infants: A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2017
Overall Recruitment Status
Completed
Study Start Date
March 2016 (Actual)
Primary Completion Date
January 2018 (Actual)
Study Completion Date
January 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Mansoura University Children Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a randomized controlled trial (RCT) to evaluate the influence of two flow rates (6 liter/min versus 3 liter/min) of Heated-Humidified High-Flow-Nasal-Cannula (HHHFNC) on rates of extubation failure in mechanically ventilated preterm infants.
Detailed Description
HHHFNC has been proposed as an alternative to nasal continuous positive airway pressure (nCPAP) in neonatal intensive care units (NICUs) for preventing extubation failure. In a recent international survey on periextubation practices in extremely preterm infants, nCPAP was the most common type of respiratory support used (84%) followed by nasal intermittent positive pressure ventilation (55%) and HHHFNC (33%). Moreover, HHHFNC appears to have efficacy and safety similar to those of nCPAP when applied immediately post-extubation to prevent extubation failure in preterm infants. and resulted in significantly less nasal trauma in the first 7 days post-extubation than nCPAP. However, the best flow rates of HHHFNC to prevent extubation failure remains to be known. This RCT aims to compare the efficacy and safety of postextubation respiratory support via HHHFNC at two different flow rates (6 L/min. versus 3 L/min) regarding successful extubation after a period of endotracheal positive pressure ventilation. We hypothesized that postextubation respiratory support via HHHFNC at a flow rate of 6 L/min. will result in a greater proportion of preterm infants being successfully extubated after a period of endotracheal positive pressure ventilation compared with HHHFNC at a flow rate of 3 L/min.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prematurity, Mechanical Ventilation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
6 liter/min group
Arm Type
Experimental
Arm Description
Infants will be extubated to a HHHFNC (Fisher and Paykel Healthcare , Auckland, New Zealand) at flow rate of 6 L/min. Eligible infants will be enrolled while receiving mechanical ventilation. The timing of extubation will be determined by the clinical team and all infants will start caffeine prior to extubation.
Arm Title
3 liter/min group
Arm Type
Active Comparator
Arm Description
Infants will be extubated to HHHFNC (Fisher and Paykel Healthcare , Auckland, New Zealand) a flow rate of 3 L/min. Eligible infants will be enrolled while receiving mechanical ventilation. The timing of extubation will be determined by the clinical team and all infants will start caffeine prior to extubation.
Intervention Type
Device
Intervention Name(s)
HHHFNC 6 liter minute
Intervention Description
Infants allocated to HHHFNC at 6 L/min. will be extubated to a HHHFNC flow of 6 L/min. Eligible infants will be enrolled while receiving mechanical ventilation. The timing of extubation will be determined by the clinical team and all infants will start caffeine prior to extubation.
Intervention Type
Device
Intervention Name(s)
HHHFNC 3 liters/min
Intervention Description
Infants allocated to HHHFNC at 3 L/min. will be extubated to a HHHFNC flow of 3 L/min. Eligible infants will be enrolled while receiving mechanical ventilation. The timing of extubation will be determined by the clinical team and all infants will start caffeine prior to extubation.
Primary Outcome Measure Information:
Title
Extubation failure
Description
Extubation failure criteria will be defined as follows: Apnea (respiratory pause >20 seconds), more than 6 episodes requiring physical stimulation in 6 hours or 1 requiring intermittent positive pressure ventilation. Respiratory acidosis with pH <7.25 and Peripheral arterial oxygen saturation (PaCO2) >65 mmHg. ( >15% sustained increase in FiO2 from extubation. 4. Cardiovascular collapse (heart rate <60 beats per minute or shock. 5. Persistent marked/severe retractions. Extubation failure will be deemed to occur if any single criterion was met in any one of the 7 days after extubation. The decision to reintubate an infant and mechanical ventilation variables and subsequent extubation attempts after reintubation will be managed at the discretion of the clinical team.
Time Frame
the 7 days after extubation
Secondary Outcome Measure Information:
Title
Mortality
Description
Death within the 96 hour post-extubation period or at any time after randomization.
Time Frame
within the 96 hour post-extubation period or at any time after with expected average of 5 weeks
Title
Total duration of mechanical ventilation
Description
Total duration of mechanical ventilation during NICU admission
Time Frame
During NICU admission with expected average of 5 weeks
Title
Total duration of oxygen supplementation
Description
Total duration of oxygen supplementation during NICU admission
Time Frame
During NICU admission with expected average of 5 weeks
Title
Bronchopulmonary dysplasia (BPD)
Description
BPD defined by oxygen requirement at 36 weeks' post-menstrual age.
Time Frame
at 36 weeks' post-menstrual age.
Title
Severe BPD
Description
Severe BPD defined as oxygen requirement with fraction of inspired oxygen (FiO2) >0.30 or need for positive pressure support at 36 weeks' post-menstrual age.
Time Frame
at 36 weeks' post-menstrual age.
Title
The combined outcome variables of death before 36 weeks PMA or BPD
Description
The combined outcome variables of death before 36 weeks PMA or BPD will be used to adjust for occurrence of death after extubation but before the time of assessment of BPD.
Time Frame
at 36 weeks' post-menstrual age.
Title
The combined outcome variables of death before 36 weeks PMA or severe BPD
Description
The combined outcome variables of death before 36 weeks' post-menstrual age (PMA) or severe BPD will be used to adjust for occurrence of death after extubation but before the time of assessment of BPD.
Time Frame
at 36 weeks' post-menstrual age
Title
Other neonatal morbidities (intracranial hemorrhage, pneumothorax, patent ductus arteriosus, necrotizing enterocolitis, and retinopathy of prematurity)
Description
The occurrence of neonatal morbidities occurring before, during the 96 hours post-extubation, and at any time thereafter will be documented (intracranial hemorrhage, pneumothorax, patent ductus arteriosus, necrotizing enterocolitis, and retinopathy of prematurity).
Time Frame
baseline, during the 96 hours post-extubation, and at any time thereafter during NICU stay with an expected average of 5 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Hour
Maximum Age & Unit of Time
30 Days
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Infants born at less than 37 weeks' gestation, required endotracheal intubation and positive pressure ventilation, and are considered ready for extubation by the clinical team. Infants will be enrolled after written informed parental consent is obtained. Exclusion Criteria: Suspected upper airway obstruction, congenital airway malformations, or major cardiopulmonary malformations
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hesham Abdel-Hady
Organizational Affiliation
Mansoura University Children"s Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Neonatal Intensive Care Unit, Mansoura University Children Hospital
City
Mansourah
State/Province
Dakahlia
ZIP/Postal Code
35516
Country
Egypt

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
26063193
Citation
Al-Mandari H, Shalish W, Dempsey E, Keszler M, Davis PG, Sant'Anna G. International survey on periextubation practices in extremely preterm infants. Arch Dis Child Fetal Neonatal Ed. 2015 Sep;100(5):F428-31. doi: 10.1136/archdischild-2015-308549. Epub 2015 Jun 10.
Results Reference
background
PubMed Identifier
24915914
Citation
Collaborative Group for the Multicenter Study on Heated Humidified High-flow Nasal Cannula Ventilation. [Efficacy and safety of heated humidified high-flow nasal cannula for prevention of extubation failure in neonates]. Zhonghua Er Ke Za Zhi. 2014 Apr;52(4):271-6. Chinese.
Results Reference
background
PubMed Identifier
23260098
Citation
Collins CL, Holberton JR, Barfield C, Davis PG. A randomized controlled trial to compare heated humidified high-flow nasal cannulae with nasal continuous positive airway pressure postextubation in premature infants. J Pediatr. 2013 May;162(5):949-54.e1. doi: 10.1016/j.jpeds.2012.11.016. Epub 2012 Dec 20.
Results Reference
background
PubMed Identifier
23955516
Citation
Collins CL, Barfield C, Horne RS, Davis PG. A comparison of nasal trauma in preterm infants extubated to either heated humidified high-flow nasal cannulae or nasal continuous positive airway pressure. Eur J Pediatr. 2014 Feb;173(2):181-6. doi: 10.1007/s00431-013-2139-8. Epub 2013 Aug 18.
Results Reference
background

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Comparison of Two Flow Rates of HHHFNC to Prevent Extubation Failure in Preterm Infants

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