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Published on: January 17, 2011
Update on total intravenous anesthesia in children
Vinícius Caldeira Quintão1,2,3, Ricardo Vieira Carlos2,3, Britta S von Ungern-Sternberg4,5,6,7
1Department of Pediatrics, Faculdade de Medicina, Universidade de São Paulo.
Insights
Pediatric total intravenous anesthesia (TIVA) is advancing with improved precision and safety. Recent evidence shows benefits in reduced side effects and environmental impact, with a call for better training and tools for wider adoption.
Area of Science:
- Anesthesiology
- Pediatric Pharmacology
- Pharmacokinetics and Pharmacodynamics
Background:
- Pediatric total intravenous anesthesia (TIVA) practice requires updated frameworks.
- Advances in pharmacokinetics-pharmacodynamics (PK-PD) are crucial for pediatric anesthesia.
Purpose of the Study:
- To summarize recent evidence in pediatric TIVA.
- To highlight advances in PK-PD, target-controlled infusion (TCI), electroencephalography (EEG)-guided titration, emerging agents, safety, and sustainability.
- To provide an updated, practical framework for pediatric TIVA.
Main Methods:
- Review of recent evidence in pediatric TIVA.
- Analysis of pharmacokinetic-pharmacodynamic patterns.
- Evaluation of target-controlled infusion models and EEG-guided strategies.
Main Results:
- Clearer developmental PK-PD patterns and refined propofol-remifentanil dosing.
- Growing use of dexmedetomidine; remimazolam shows promise but lacks pediatric data.
- EEG-guided and combined PK-EEG strategies enhance infant safety; TIVA reduces adverse events and environmental impact.
Conclusions:
- Pediatric TIVA is advancing towards precision, safety, and sustainability.
- Moderate effect-site targets and opioid titration are key, especially in neonates.
- Wider adoption requires improved training, TCI tools, and addressing regulatory barriers.
Purpose Of Review:
To summarize recent evidence in pediatric total intravenous anesthesia (TIVA), highlighting advances in pharmacokinetics-pharmacodynamics, target-controlled infusion (TCI), electroencephalography (EEG)-guided titration, emerging agents, safety, and sustainability, and to provide clinicians with an updated, practical framework for pediatric TIVA practice.
Recent Findings:
Recent evidence highlights major advances in pediatric TIVA, including clearer developmental pharmacokinetic-pharmacodynamic patterns, refined propofol-remifentanil dosing, and growing use of dexmedetomidine. Remimazolam shows promise but currently has limited pediatric evidence. Universal TCI models improve dosing accuracy across ages, while EEG-guided and combined pharmacokinetics-EEG strategies enhance safety in infants. TIVA reduces emergence delirium, postoperative nausea and vomiting, and perioperative respiratory adverse events; supports neurophysiologic monitoring; and yields substantially lower environmental greenhouse gas emissions than inhalation anesthesia.
Summary:
Pediatric TIVA is moving toward greater precision, safety, and sustainability. Moderate effect-site targets, opioid titration, and early down-titration remain central, particularly in neonates. Propofol infusion syndrome is exceedingly rare, and organ-protective effects of TIVA are reported in major surgery. Despite clinical and environmental advantages, adoption varies globally due to limited training, variable pump availability, and regulatory barriers. Expanding structured education and pediatric-specific TCI tools is essential for broader implementation.
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