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Published on: December 5, 2025
High-frequency oscillatory ventilation versus synchronized intermittent mandatory ventilation plus pressure support
Huiqing Sun1, Rui Cheng, Wengqing Kang
1Department of Pediatrics, Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Insights
High-frequency oscillatory ventilation (HFOV) significantly reduced death and bronchopulmonary dysplasia (BPD) in preterm infants with severe respiratory distress syndrome (RDS). HFOV also improved long-term neurodevelopmental outcomes compared to synchronized intermittent mandatory ventilation plus pressure support ventilation (SIMV-PSV).
Area of Science:
- Neonatal Medicine
- Pediatric Critical Care
- Respiratory Physiology
Background:
- Mechanical ventilation and surfactant therapy are standard for preterm respiratory distress syndrome (RDS).
- The impact of ventilation strategies on bronchopulmonary dysplasia (BPD) and neurodevelopment is debated.
- This study compares high-frequency oscillatory ventilation (HFOV) with synchronized intermittent mandatory ventilation plus pressure support ventilation (SIMV-PSV) in severe RDS.
Purpose of the Study:
- To compare the efficacy and safety of HFOV versus SIMV-PSV in preterm infants with severe RDS.
- To evaluate the effects of ventilation strategy on mortality, BPD, and neurodevelopmental outcomes.
- To assess secondary outcomes including hospitalization duration and specific morbidities.
Main Methods:
- Randomized controlled trial involving 366 preterm infants with severe RDS.
- Infants were assigned to HFOV (n=184) or SIMV-PSV (n=182).
- Surfactant was administered if PaO2/FIO2 < 200 mm Hg after 2 hours; primary outcomes were mortality or BPD.
Main Results:
- The incidence of death or BPD was significantly lower with HFOV (P=.001).
- HFOV group showed shorter ventilation/hospitalization duration and reduced surfactant needs (P<.001).
- Fewer infants in the HFOV group experienced moderate/severe neurological disability at 18 months (P=.03).
Conclusions:
- Initial HFOV in preterm infants with severe RDS decreases mortality and BPD incidence.
- HFOV improves long-term neurodevelopmental outcomes compared to SIMV-PSV.
- The combination of HFOV and surfactant effectively reduces adverse outcomes in this population.
Background:
Mechanical ventilation and surfactants are the standard treatment of preterm respiratory distress syndrome (RDS). The effects of the primary ventilation model on bronchopulmonary dysplasia (BPD) and long-term neurodevelopment outcomes are controversial. The purpose of this study was to compare the efficacy and safety of high-frequency oscillatory ventilation (HFOV) and synchronized intermittent mandatory ventilation plus pressure support ventilation (SIMV-PSV) in preterm infants with severe RDS.
Methods:
A total of 366 eligible preterm infants were randomly assigned to treatment with HFOV (n = 184) or SIMV-PSV (n = 182). Surfactant was applied if PaO2/FIO2 was < 200 mm Hg after 2 hours of ventilation. Primary outcomes were mortality or incidence of BPD. Secondary outcomes were duration of ventilation and hospitalization, surfactant requirements, pneumothorax, retinopathy of prematurity ≥ stage 2, and neurodevelopment at 18 months of corrected age.
Results:
Survival and complete outcome data were available for 288 infants at 18 months of corrected age. The incidence of death or BPD was significantly higher in the SIMV-PSV group (P = .001). The duration of mechanical ventilation and hospitalization was shorter and the incidence of surfactant requirement and retinopathy of prematurity was lower in the HFOV group (P < .001, P = .002, P = .04, respectively). Moderate or severe neurological disability was less frequent in the HFOV group than in the SIMV-PSV group at 18 months (P = .03). The combination of HFOV and surfactant dramatically reduced negative outcomes in preterm infants with severe RDS.
Conclusions:
Initial ventilation with HFOV in preterm infants with severe RDS reduces the incidence of death and BPD, and improves long-term neurodevelopment outcomes. (ClinicalTrials.gov NCT01496508).
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