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Pediatric palliative sedation therapy with propofol: recommendations based on experience in children with terminal
Doralina L Anghelescu1, Hunter Hamilton, Lane G Faughnan
1Division of Anesthesiology, St. Jude Children's Research Hospital, Memphis, Tennessee 38105, USA. doralina.anghelescu@stjude.org
Insights
Propofol palliative sedation therapy (PST) offers a valuable option for pediatric oncology patients with intractable end-of-life suffering. This study details its use and proposes an algorithm for patient selection.
Area of Science:
- Pediatric oncology
- Palliative care
- Pharmacology
Background:
- Palliative sedation therapy (PST) for children using propofol is not extensively documented.
- Intractable end-of-life suffering in pediatric oncology patients requires effective management strategies.
Observation:
- Three pediatric oncology patients (aged 6-15) received propofol PST within 20 days of death.
- Medication consumption (opioids, supportive) decreased in two patients during PST.
- One patient required sedation as the primary comfort measure due to persistent high pain scores.
Findings:
- Propofol PST was successfully administered to pediatric patients with intractable end-of-life suffering.
- Clinical notes indicated improved comfort and rest for all patients receiving propofol PST.
- Propofol infusions were continued until the time of death in all observed cases.
Implications:
- Propofol PST is a viable palliative option for pediatric patients facing intractable suffering.
- An algorithm for selecting pediatric candidates for propofol PST is proposed.
- This approach may improve end-of-life care in pediatric oncology.
Background:
The use of propofol for palliative sedation of children is not well documented.
Objective:
Here we describe our experience with the use of propofol palliative sedation therapy (PST) to alleviate intractable end-of-life suffering in three pediatric oncology patients, and propose an algorithm for the selection of such candidates for PST.
Patients And Methods:
We identified inpatients who had received propofol PST within 20 days of death at our institution between 2003 and 2010. Their medical records were reviewed for indicators of pain, suffering, and sedation from 48 hours before PST to the time of death. We also tabulated consumption of opioids and other symptom management medications, pain scores, and adverse events of propofol, and reviewed clinical notes for descriptors of suffering and/or palliation.
Results:
Three of 192 (1.6%) inpatients (aged 6-15 years) received propofol PST at the end of life. Consumption of opioids and other supportive medications decreased during PST in two cases. In the third case, pain scores remained high and sedation was the only effective comfort measure. Clinical notes suggested improved comfort and rest in all patients. Propofol infusions were continued until the time of death.
Conclusions:
Our experience demonstrates that propofol PST is a useful palliative option for pediatric patients experiencing intractable suffering at the end of life. We describe an algorithm that can be used to identify such children who are candidates for PST.
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