- Poster presentation
- Open Access
Influence of rhDNAse on the duration of mechanical ventilation in intensive care patients: interim analysis of the LUFIT trial
© BioMed Central Ltd 2006
- Published: 21 March 2006
- Placebo Group
- Mechanical Ventilation
- Cystic Fibrosis
- Paediatric Patient
To investigate whether rhDNAse is able to reduce the duration of ventilation in adult mechanically ventilated intensive care patients.
After approval of the local ethics committees we conducted a double-blind, placebo-controlled, randomised, multicentre national trial. Patients were stratified into two subgroups depending on their status as surgical or nonsurgical. The trial was started within 48 hours after the start of mechanical ventilation and lasted until weaning was successful. Patients in the active treatment group received 2.5 ml rhDNAse endotracheally twice a day. Patients in the placebo group received the same amount of normal saline. This interim analysis reviewed 98 nonsurgical patients. Data from 85 patients were included in the analysis.
Forty-four patients in the study group and 41 patients in the placebo group were analysed. Factors such as gender, weight, smoking habit, chronic pre-existing diseases and prevalence of COPD were distributed equally in both groups. Three patients died in the rhDNAse group versus eight in the placebo group. The median duration of ventilation was 140 hours (CI 120–200 hours) in the rhDNAse and 324 hours (CI 178–442 hours) in the placebo group.
This interim analysis suggests that rhDNAse may have the potential to reduce the duration of ventilation in adult nonsurgical intensive care patients. This confirms results obtained in paediatric patients . Data from surgical patients will be presented as soon as the interim analysis in that group is completed.