Long-Term Inhalative Sedation in Children With Pulmonary Diseases
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Updated: Dec 8, 2025

Halogenated Agent Delivery in Porcine Model of Acute Respiratory Distress Syndrome via an Intensive Care Unit Type Device
Published on: September 24, 2020
Jochen Meyburg1, David Frommhold2,3, Johann Motsch4
1Department of General Pediatrics, University Children's Hospital, Heidelberg, Germany.
Insights
Long-term inhalative sedation (LTIS) is safe and feasible in children, even those with severe lung disease. This approach may allow faster reduction of other sedatives, but close monitoring for side effects is essential.
Area of Science:
- Pediatric Intensive Care
- Respiratory Medicine
- Anesthesiology
Background:
- Recent studies suggest beneficial effects of long-term inhalative sedation (LTIS) in adult patients with acute respiratory distress syndrome (ARDS).
- LTIS offers a potential alternative for sedation in critically ill patients.
Purpose of the Study:
- To evaluate the safety and feasibility of LTIS in children with severe respiratory diseases.
- To compare LTIS outcomes in children with lung disease versus those with normal lung function.
- To explore the potential of LTIS for pediatric patients with ARDS.
Main Methods:
- Single-center retrospective study.
- Analysis of 37 LTIS courses in 29 pediatric intensive care unit (PICU) patients (July 2011-July 2019).
- Utilized the AnaConDa® device for LTIS administration.
Main Results:
- LTIS was feasible in all pediatric patients, including those with severe lung impairment.
- Concomitant intravenous sedatives were reduced more rapidly in children with lung diseases.
- Cardiocirculatory depression occurred in all patients, but severe side effects were rare.
Conclusions:
- LTIS is a feasible sedation method for children, even with significant respiratory compromise.
- A prospective trial investigating LTIS for pediatric ARDS is warranted.
- Close monitoring of cardiocirculatory function during LTIS is crucial.
Objectives:
To describe safety and feasibility of long-term inhalative sedation (LTIS) in children with severe respiratory diseases compared to patients with normal lung function with respect to recent studies that showed beneficial effects in adult patients with acute respiratory distress syndrome (ARDS).
Design:
Single-center retrospective study.
Setting:
12-bed pediatric intensive care unit (PICU) in a tertiary-care academic medical center in Germany.
Patients:
All patients treated in our PICU with LTIS using the AnaConDa® device between July 2011 and July 2019.
Measurements And Main Results:
Thirty-seven courses of LTIS in 29 patients were analyzed. LTIS was feasible in both groups, but concomitant intravenous sedatives could be reduced more rapidly in children with lung diseases. Cardiocirculatory depression requiring vasopressors was observed in all patients. However, severe side effects only rarely occured.
Conclusions:
In this largest cohort of children treated with LTIS reported so far, LTIS was feasible even in children with severely impaired lung function. From our data, a prospective trial on the use of LTIS in children with ARDS seems justified. However, a thorough monitoring of cardiocirculatory side effects is mandatory.
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