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Long-Term Outcomes after Protocolized Sedation versus Usual Care in Ventilated Pediatric Patients
R Scott Watson1,2, Lisa A Asaro3, James H Hertzog4
11 Department of Pediatrics, University of Washington, Seattle, Washington.
Insights
A goal-directed sedation protocol for intubated children did not harm long-term functional status or quality of life. This sedation strategy did not increase post-traumatic stress disorder risk in children recovering from acute respiratory failure.
Area of Science:
- Pediatric critical care medicine
- Pediatric intensive care
- Sedation and analgesia
Background:
- Assessing the long-term effects of nurse-implemented, goal-directed sedation protocols in intubated children is crucial.
- Understanding the impact on postdischarge functional status, quality of life, and PTSD risk is unknown.
Purpose of the Study:
- To compare postdischarge outcomes in children with acute respiratory failure randomized to a sedation protocol versus usual care.
- To evaluate the effects of a sedation strategy on functional status, health-related quality of life, and PTSD risk.
Main Methods:
- A cluster-randomized trial involving 1,360 pediatric patients from 31 centers.
- Follow-up assessments conducted 6 months post-ICU discharge via mail, electronic, and telephone surveys.
- Utilized validated instruments including the Pediatric Overall Performance Category, Pediatric Cerebral Performance Category, quality of life questionnaires, and PTSD symptom scales.
Main Results:
- Functional status worsened from baseline in 20% of patients, with no difference between treatment arms.
- Decline in functional status was more prevalent in children with pre-existing impairments.
- No significant differences were observed in health-related quality of life or risk of post-traumatic stress disorder between the sedation protocol and usual care groups.
Conclusions:
- A sedation strategy promoting wakefulness and minimizing sedative/analgesic exposure does not result in long-term harm.
- Postdischarge morbidity following acute respiratory failure is a common concern in pediatric patients.
- The findings support the safety of goal-directed sedation protocols in this population.
Rationale:
Whether a nurse-implemented goal-directed sedation protocol resulting in more awake yet calm intubated children affects postdischarge functional status, health-related quality of life, or risk for post-traumatic stress disorder is unknown.
Objectives:
To compare postdischarge outcomes in children with acute respiratory failure cluster-randomized to a sedation protocol or usual care.
Methods:
A stratified random sample of 1,360 patients from 31 centers in the RESTORE (Randomized Evaluation of Sedation Titration for Respiratory Failure) trial was assessed by mail, electronically, and/or telephone 6 months after ICU discharge. In treatment group comparisons, we controlled for age, baseline functional status, and severity of illness.
Measurements And Main Results:
We used the Pediatric Overall Performance Category and the Pediatric Cerebral Performance Category to characterize functional status, the Infant and Toddler Quality of Life Questionnaire (97-item full-length version) (<2 yr old) or Pediatric Quality of Life Inventory (≥2 yr old), and the Child Post-traumatic Stress Disorder Symptom Scale (≥8 yr old and developmentally able). Functional status worsened from baseline to follow-up in 20%. Decline in functional status did not differ by treatment arm and was more common among those with baseline impairment than those with baseline normal function (27 vs. 18%; P < 0.001). There were no significant differences in health-related quality of life total scores by treatment arm. Scores indicating risk of post-traumatic stress disorder occurred in 30%, with no difference between treatment arms.
Conclusions:
A sedation strategy that allows patients to be more awake and exposes them to fewer sedative and analgesic medications produces no long-term harm. However, postdischarge morbidity after acute respiratory failure is common. Clinical trial registered with www.clinicaltrials.gov (NCT00814099).
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