Prediction of levobupivacaine concentrations in neonates and infants following neuraxial rescue blocks
dc.contributor.author | Frawley, Geoff | |
dc.contributor.author | Ignacio Cortinez, Luis | |
dc.contributor.author | Anderson, Brian J. | |
dc.date.accessioned | 2025-01-20T23:51:26Z | |
dc.date.available | 2025-01-20T23:51:26Z | |
dc.date.issued | 2021 | |
dc.description.abstract | Aim Pharmacokinetic simulation was used to characterize levobupivacaine disposition after regional anesthetic rescue for failed spinal anesthesia in neonates and infants. | |
dc.description.abstract | Methods Population pharmacokinetics of levobupivacaine were estimated after spinal blockade in a cohort of neonates and infants (n = 25, postnatal age 5-18 weeks, gestation 21-41 weeks, weight 2.4-6 kg). Total levobupivacaine concentrations were assayed 3-4 times in the first hour after spinal levobupivacaine 1 mg kg(-1) administration. Parameters were estimated using nonlinear mixed-effects models and supported by priors. Covariates included postnatal age and total body weight. Parameter estimates were used to simulate total levobupivacaine concentrations after a primary spinal levobupivacaine 1 mg kg(-1) with rescue caudal levobupivacaine 1.5-2.5 mg kg(-1). | |
dc.description.abstract | Results A one-compartment model with a mature clearance 21.5 L h(-1) 70 kg(-1) (CV 47.3%) and central volume 189 L 70 kg(-1) (CV 37%) adequately described time-concentration profiles. Clearance maturation was described using a maturation half-time of 11.5 weeks postnatal age. The absorption half-time for spinal levobupivacaine was 2.6 min (CV 56.8%). The upper (97.5% prediction) for peak concentrations after rescue caudal levobupivacaine were 1.5 mg kg(-1), 2 mg kg(-1), and 2.5 mg kg(-1) was 2.05 mg L-1, 2.5 mg L-1, and 2.9 mg L-1 respectively. | |
dc.description.abstract | Conclusion Total bupivacaine concentrations greater than 2.5 mg L-1 are associated with neurotoxicity in adults. Predicted concentrations after either a repeat spinal or a caudal rescue dose of levobupivacaine 1.5 mg kg(-1) 1 h after spinal levobupivacaine administration are below the neurotoxic concentration threshold. | |
dc.fuente.origen | WOS | |
dc.identifier.doi | 10.1111/pan.14170 | |
dc.identifier.eissn | 1460-9592 | |
dc.identifier.issn | 1155-5645 | |
dc.identifier.uri | https://doi.org/10.1111/pan.14170 | |
dc.identifier.uri | https://repositorio.uc.cl/handle/11534/94813 | |
dc.identifier.wosid | WOS:000640878400001 | |
dc.issue.numero | 6 | |
dc.language.iso | en | |
dc.pagina.final | 664 | |
dc.pagina.inicio | 655 | |
dc.revista | Pediatric anesthesia | |
dc.rights | acceso restringido | |
dc.subject | levobupivacaine | |
dc.subject | neonates pharmacokinetics | |
dc.subject | toxicity | |
dc.subject | variability | |
dc.title | Prediction of levobupivacaine concentrations in neonates and infants following neuraxial rescue blocks | |
dc.type | artículo | |
dc.volumen | 31 | |
sipa.index | WOS | |
sipa.trazabilidad | WOS;2025-01-12 |