Propofol for palliative sedation: A systematic review of clinical outcomes, safety, and ethical implications.

Λεπτομέρειες βιβλιογραφικής εγγραφής
Τίτλος: Propofol for palliative sedation: A systematic review of clinical outcomes, safety, and ethical implications.
Συγγραφείς: Almeida-Jardim L; Palliative Medicine Center, Faculty of Medicine, University of Lisbon, Lisboa, Portugal., Reis-Pina P; Palliative Medicine Center, Faculty of Medicine, University of Lisbon, Lisboa, Portugal.; Acute Palliative Care Inpatient Unit, Local Health Unit of Santa Maria, Lisboa, Portugal.
Πηγή: Palliative medicine [Palliat Med] 2026 Oct; Vol. 40 (9), pp. 1302-1321. Date of Electronic Publication: 2026 Jul 31.
Τύπος έκδοσης: Systematic Review; Journal Article
Γλώσσα: English
Στοιχεία περιοδικού: Publisher: SAGE Publications Country of Publication: England NLM ID: 8704926 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1477-030X (Electronic) Linking ISSN: 02692163 NLM ISO Abbreviation: Palliat Med Subsets: MEDLINE
Imprint Name(s): Publication: London : SAGE Publications
Original Publication: London : New York, NY : Cambridge University Press, North American distributors, Edward Arnold ; c1987-
Ιατρικοί όροι (MeSH): Propofol*/therapeutic use , Propofol*/adverse effects , Palliative Care*/methods , Palliative Care*/ethics , Hypnotics and Sedatives*/therapeutic use, Humans ; Female ; Adult ; Male
Περίληψη: Background: Palliative sedation is used to relieve refractory suffering in terminally ill patients. Propofol, an intravenous anesthetic, may offer advantages due to its rapid onset and short half-life.
Aim: To evaluate the role of propofol in palliative sedation, focusing on symptom control, sedation depth, survival time, safety, and ethical implications.
Design: Systematic review registered in PROSPERO (CRD42025643575; February 6, 2025).
Data Sources: Scopus, MEDLINE, and Web of Science were searched for English-language studies (2005-2024) on propofol use in adult terminally ill patients. Studies comparing propofol with other sedatives or non-sedated controls were included; those involving anesthetic or intensive care settings were excluded. Risk of bias and certainty of evidence were assessed. Results were synthesized narratively.
Results: Ten non-randomized studies were included (observational, cross-sectional, cohort, case series, and before-and-after designs), mostly of moderate quality, conducted in Europe (n = 7) involving 4072 patients (28,3% received palliative sedation), mainly with cancer. Symptom control was reported in 73%-100% of cases, target sedation depth was achieved in 52%-100%, although outcome definitions and measurement methods varied. Survival ranged from 19 h to 38 days. Propofol was used alone (n = 4) or with other sedatives (n = 6). Respiratory depression was the main safety concern. Ethical issues included absence of explicit consent and rare reports of life-shortening intent.
Conclusions: Propofol may be considered as a rescue option in selected refractory cases managed by experienced teams; however, given the low to very low certainty of available evidence, findings should be interpreted cautiously and supported by institutional protocols and further prospective research.
Competing Interests: Declaration of conflicting interestsThe authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.
Contributed Indexing: Keywords: deep sedation; ethics; medical; palliative care; patient safety; propofol; survival rate; symptom burden; terminal care
Substance Nomenclature: YI7VU623SF (Propofol)
0 (Hypnotics and Sedatives)
Entry Date(s): Date Created: 20260731 Date Completed: 20260927 Latest Revision: 20261009
Update Code: 20261009
PubMed Central ID: PMC13612869
DOI: 10.1177/02692163261465774
PMID: 42533745
Βάση Δεδομένων: MEDLINE
Περιγραφή
ISSN:1477-030X
DOI:10.1177/02692163261465774