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A Novel Rescue Technique for Difficult Intubation and Difficult Ventilation
Published on: January 17, 2011
Recombinant human deoxyribonuclease shortens ventilation time in young, mechanically ventilated children
Joachim Riethmueller1, Thomas Borth-Bruhns, Matthias Kumpf
1Department of Pediatrics, University Children's Hospital, Tübingen, Germany. joachim.riethmueller@med.uni-tuebingen.de
Insights
Dornase alfa, a recombinant human deoxyribonuclease I, may reduce ventilation duration and PICU stay in ventilated infants. This study found dornase alfa beneficial and safe for fluid-restricted children requiring mechanical ventilation.
Area of Science:
- Biochemistry
- Pediatric Critical Care
- Pharmacology
Background:
- Recombinant human deoxyribonuclease I (dornase alfa) is an established inhaled mucoactive agent for cystic fibrosis.
- The potential use of dornase alfa in ventilated, fluid-restricted pediatric patients remains under investigation.
Purpose of the Study:
- To evaluate the efficacy and safety of dornase alfa in reducing reintubation rates, ventilation duration, pediatric intensive care unit (PICU) stay, and ventilation complications in ventilated, fluid-restricted infants.
- To explore the potential benefits of dornase alfa in fluid-restricted children, particularly those expected to require prolonged mechanical ventilation after cardiac surgery.
Main Methods:
- A randomized, placebo-controlled, double-blind clinical study involving 100 infants.
- Administration of dornase alfa versus placebo in ventilated, fluid-restricted children.
- Assessment of reintubation rates, ventilation duration, PICU stay, ventilation complications, and costs.
Main Results:
- Reintubation rates were similar between the dornase alfa and placebo groups (7% vs. 9%).
- The dornase alfa group showed a lower incidence of atelectasis (6 vs. 17), shorter median ventilation time (2.2 vs. 3.4 days), and shorter median PICU stay (7 vs. 8 days).
- Mean costs were reduced in the dornase alfa group (4,830 vs. 6,320), and no adverse effects were observed.
Conclusions:
- Dornase alfa demonstrated beneficial effects and a favorable safety profile in ventilated, fluid-restricted infants.
- The findings suggest dornase alfa may be valuable from the first day of mechanical ventilation, especially for children anticipated to require >3 days of ventilation post-cardiac surgery.
Abstract:
Recombinant human deoxyribonuclease I (dornase alfa) is currently used as an inhaled mucoactive agent in the treatment of cystic fibrosis. In a randomized, placebo-controlled, double-blind clinical study in 100 infants, we investigated whether the therapeutic use of dornase alfa can be extended to ventilated, fluid-restricted children to reduce reintubation rate, ventilation duration, pediatric intensive care unit (PICU) stay, and ventilation complications. While reintubation rates were similar for dornase alfa 7% vs. placebo 9% (odds ratio, 0.77; confidence interval, 0.11-4.9), the incidence of atelectasis (6 vs. 17, respectively; P-value 0.051), median ventilation time (2.2 vs. 3.4 days, respectively; P-value 0.043), median length of PICU stay (7 vs. 8 days, respectively; P-value 0.051), and mean costs (4,830 vs. 6,320, respectively) were lower in the dornase alfa group. No adverse effects were observed, even in critically ill patients. We found that dornase alfa was beneficial and safe. Our findings also indicate that dornase alfa is possibly of value from the first day of mechanical ventilation onward, particularly when longer ventilation (>3 days) is expected in fluid-restricted children after cardiac surgery.
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