Aerosolized Dornase Alfa (DNase I) for the Treatment of Severe Respiratory Failure in COVID-19: A Randomized Controlled Trial - Scorecard - MDSpire

Aerosolized Dornase Alfa (DNase I) for the Treatment of Severe Respiratory Failure in COVID-19: A Randomized Controlled Trial

  • By

  • Per Åkesson

  • Lisa Mellhammar

  • Magnus Rasmussen

  • Malin Inghammar

  • Sara Jesperson

  • Fredrik Månsson

  • Elin Economou Lundeberg

  • John Walles

  • Martin Wallberg

  • Attila Frigyesi

  • Adam Linder

  • April 24, 2025

  • 0 min

Share

Clinical Scorecard: Inhaled Dornase Alfa (DNase I) for Managing Severe Respiratory Failure in COVID-19: Results from a Randomized Controlled Study

At a Glance

CategoryDetail
ConditionSevere respiratory failure with hypoxia in acute COVID-19
Key MechanismsNeutrophil extracellular traps (NETs) contribute to lung inflammation, increased sputum viscosity, and impaired gas exchange; DNase I degrades NETs
Target PopulationHospitalized adults (≥18 years) with COVID-19 and oxygen saturation ≤90% without supplemental oxygen
Care SettingHospital wards and intensive care units

Key Highlights

  • Randomized placebo-controlled trial of inhaled dornase alfa (2.5 mg twice daily for 5 days) versus placebo in 76 hospitalized COVID-19 patients with hypoxia
  • No significant difference in primary outcome (time to oxygen cessation or hospital discharge) or secondary outcomes including mortality and length of stay
  • Subanalysis by age (<65 vs ≥65 years) showed no benefit of dornase alfa; study stopped early due to emergence of Omicron variant

Guideline-Based Recommendations

Diagnosis

  • Confirm COVID-19 diagnosis by PCR testing
  • Assess oxygen saturation ≤90% without supplemental oxygen to identify severe respiratory failure

Management

  • Standard of care oxygen support for hypoxic COVID-19 patients
  • Inhaled dornase alfa is not recommended for improving hypoxia based on current evidence

Monitoring & Follow-up

  • Monitor oxygen saturation regularly (at least twice daily) after cessation of supplemental oxygen
  • Observe for adverse events during inhaled therapy

Risks

  • Potential allergy to dornase alfa contraindicates use
  • No significant adverse events observed in trial; however, no clinical benefit demonstrated

Patient & Prescribing Data

Hospitalized adult COVID-19 patients with hypoxia (oxygen saturation ≤90%)

Inhaled dornase alfa administered twice daily for 5 days did not improve oxygenation or clinical outcomes compared to placebo

Clinical Best Practices

  • Use standard oxygen therapy protocols for hypoxic COVID-19 patients
  • Avoid off-label use of inhaled dornase alfa for COVID-19 respiratory failure outside clinical trials
  • Consider heterogeneity of viral variants and vaccination status when interpreting treatment effects
  • Further research needed to evaluate DNase I effects in other respiratory infections

References

Original Source(s)

Related Content