ReviewLife (Basel, Switzerland)2026
Target-Controlled Infusion for Caesarean Delivery Under General Anesthesia: From Conventional Pharmacokinetic Models to Physiologically Based Pharmacokinetic Modeling.
Review in Life (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Target-controlled infusion (TCI) enables the precise delivery of intravenous anesthetics based on pharmacokinetic-pharmacodynamic (PK-PD) models and represents a key component of total intravenous anesthesia (TIVA). However, its use in obstetric anesthesia remains limited, as current TCI algorithms are derived from non-pregnant populations and do not account for pregnancy-related physiological changes or maternal-fetal drug distribution. This narrative review examines the clinical application of TIVA-TCI in caesarean delivery under general anesthesia, summarizing evidence from recent observational studies and national audits, which suggest feasibility but limited adoption in routine obstetric practice. Pregnancy induces significant alterations in drug distribution, protein binding, metabolism, and clearance, which may affect anesthetic pharmacokinetics and fetal exposure. Physiologically based pharmacokinetic (PBPK) modeling is explored as a complementary approach that may improve understanding of maternal-fetal drug disposition by integrating physiological and drug-specific parameters. Although promising, these model-based strategies require further validation before clinical implementation. Overall, current evidence supports the cautious use of TIVA-TCI in selected obstetric settings while highlighting the need for pregnancy-specific pharmacokinetic models and prospective clinical studies.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.