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Clinical Trials/RBR-6y2q4d5
RBR-6y2q4d5
Terminated
N/A

se of the Guaranteed Volume mode as a ventilatory weaning strategy in Premature Newborns

niversidade Federal do Rio Grande do Norte0 sitesOctober 20, 2022

Overview

Phase
N/A
Intervention
Not specified
Conditions
Respiratory Distress Syndrome, Newborn
Sponsor
niversidade Federal do Rio Grande do Norte
Status
Terminated
Last Updated
2 years ago

Overview

Brief Summary

Introduction: The diaphragm of preterm newborns is flat, weak, and horizontally inserted in the rib cage. Consequently, it hampers the lever mechanism during muscle contraction, reduces the efficiency of pulmonary ventilation and chest expansion, and increases energy expenditure. Objective: To assess chest expansion using inductance plethysmography in preterm newborns during assist-control ventilation and inspiratory pressure control with and without volume guarantee (VG and AC-PC, respectively). Methods: This is a crossover clinical trial. Ventilatory (peak pressure, minute volume, dynamic compliance, and airway resistance) and autonomic outcomes (heart rate, respiratory rate, and peripheral oxygen saturation) were measured at 0, 30, and 60 minutes after initiation of ventilation. Paired t-test compared ventilation modes and times (0, 30, and 60 minutes). Results: We included ten preterm newborns (mean gestational age of 30 ± 1.89 weeks and weight of 964 ± 167.1 grams). VG increased chest expansion and peripheral oxygen saturation and reduced respiratory distress compared with AC-PC. Conclusion: VG may increase chest expansion and peripheral oxygen saturation and reduce respiratory distress and heart rate compared with AC-CP mode. Also, inductance plethysmography may be viable for measuring chest expansion during mechanical ventilation.

Registry
who.int
Start Date
October 20, 2022
End Date
April 10, 2021
Last Updated
2 years ago
Study Type
Observational

Investigators

Sponsor
niversidade Federal do Rio Grande do Norte

Eligibility Criteria

Inclusion Criteria

  • Premature newborns (gestational age equal to or less than 32 weeks), diagnosed with Respiratory Distress Syndrome and birth weight of up to 1,500g, intubated and in a weaning protocol. The protocol maintained an inspired fraction of oxygen lower than 50%, mandatory respiratory rate lower than 30 cycles per minute, peak pressure equal to or lower than 25cmH2O, and end expiratory pressure lower than or equal to 6 centimeters of water.

Exclusion Criteria

  • Using medications with side effects on the respiratory system were not included and those preterm newborns who presented clinical worsening and/or need to increase ventilatory parameters were excluded.

Outcomes

Primary Outcomes

Not specified

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