Use of High Flows in Pediatric Cardiac Surgical Patients

NCT ID: NCT01633801

Last Updated: 2012-08-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

80 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-08-31

Study Completion Date

2012-12-31

Brief Summary

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Humidified high flow nasal prong oxygen therapy is a method for providing oxygen and CPAP. The delivery of high flows decreases dilution of the inhaled oxygen and, by matching patient's peak flow, allows accurate delivery of the set FiO2 throughout the whole inspiratory phase. In addition, a flow-dependent effect of continuous positive airway pressure, possibly due to an air entrainment mechanism, has been documented in healthy volunteers and in patients with COPD.

The investigators working hypothesis is that the use of post-extubation CPAP delivered via nasal cannulae in infants less than 18 months, post-bypass surgery will have better PaCO2 values than infants extubated on to oxygen therapy.

Detailed Description

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After CICU admission, infants with no bleeding, normothermic and hemodynamically stable will be switched from PRVC to SIMV+PSV (10-15cmH20) which should be maintained for 4 hours. An arterial gas analysis will be performed after 20 minutes. Infants with normal gas-exchange are gradually weaned from mechanical ventilation At each weaning step an arterial hemogasanalysis is performed after 20 minutes, to assess if the decreased ventilatory support is tolerated. Increased work of breathing and respiratory acidosis (ph\< 7.3 or pCO2 \> 60 mmHg) are considered criteria to withhold the weaning process. After a 4 hour period on SIMV+PSV the child should be switched to PSV for 30 minutes and then extubated. The following extubation criteria should be reached:

* Satisfactory blood gases with PCO2 under 45mmHg, pH greater than 7.30.
* Fractional inspired oxygen concentration of 65% and or less than the baseline value
* Adequate respiratory frequency according to age without dyspnea

At this point criteria for extubation are reached. Once extubation has taken place the child will be placed either on traditional oxygen therapy or high flow nasal cannulae according to randomization.

Conditions

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Congenital Heart Disease

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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High flows

Group Type OTHER

Use of high flows versus oxygen therapy

Intervention Type DEVICE

Once extubation has taken place the child will be placed either on traditional oxygen therapy or high flow nasal cannulae according to randomization.

oxygen therapy

Intervention Type DEVICE

Once extubation has taken place the child will be placed either on traditional oxygen therapy or high flow nasal cannulae according to randomization.

oxygen therapy

Group Type OTHER

oxygen therapy

Intervention Type DEVICE

Once extubation has taken place the child will be placed either on traditional oxygen therapy or high flow nasal cannulae according to randomization.

Interventions

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Use of high flows versus oxygen therapy

Once extubation has taken place the child will be placed either on traditional oxygen therapy or high flow nasal cannulae according to randomization.

Intervention Type DEVICE

oxygen therapy

Once extubation has taken place the child will be placed either on traditional oxygen therapy or high flow nasal cannulae according to randomization.

Intervention Type DEVICE

Other Intervention Names

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high flow nasal cannulae (via Neonatal Nasal Cannula- Fisher & Paykel) traditional nasal cannulae

Eligibility Criteria

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Inclusion Criteria

* Age: 0-18 months
* Mechanical Ventilation via an endotracheal tube
* Elective surgery
* Post-bypass procedure
* Rachs 2 and above

Exclusion Criteria

* Presence of major congenital malformations
* Presence of neuromuscular disease
* Presence of non drained pneumothorax
* Absent respiratory drive or recurrent apneas
* Hemodynamic instability
* Glasgow coma score (GCS) less than 8
* ECG with evidence of ischaemia or arrhythmias
* Active bleeding
Minimum Eligible Age

1 Day

Maximum Eligible Age

18 Months

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Bambino Gesù Hospital and Research Institute

OTHER

Sponsor Role lead

Responsible Party

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Francesca Giovanna Iodice

Doctor in Medicine

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Francesca Iodice, MD

Role: PRINCIPAL_INVESTIGATOR

Ospedale Bambino Gesu'

Locations

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Francesca Iodice

Rome, Italy, Italy

Site Status RECRUITING

Ospedale Bambino Gesu

Rome, , Italy

Site Status RECRUITING

Countries

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Italy

Facility Contacts

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Francesca Iodice, MD

Role: primary

Francesca Iodice

Role: backup

Francesca G Iodice, M.D.

Role: primary

References

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Testa G, Iodice F, Ricci Z, Vitale V, De Razza F, Haiberger R, Iacoella C, Conti G, Cogo P. Comparative evaluation of high-flow nasal cannula and conventional oxygen therapy in paediatric cardiac surgical patients: a randomized controlled trial. Interact Cardiovasc Thorac Surg. 2014 Sep;19(3):456-61. doi: 10.1093/icvts/ivu171. Epub 2014 Jun 8.

Reference Type DERIVED
PMID: 24912486 (View on PubMed)

Other Identifiers

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BambinoGHRI

Identifier Type: -

Identifier Source: org_study_id