Sufentanil Disposition and Pharmacokinetic Model-Based Dosage Regimen for Sufentanil in Ventilated Full-Term Neonates
Language English Country Switzerland Media print-electronic
Document type Journal Article, Observational Study
PubMed
34077940
DOI
10.1159/000515787
PII: 000515787
Knihovny.cz E-resources
- Keywords
- Critical care, Dosage regimen, Neonate, Pharmacokinetics, Sufentanil,
- MeSH
- Models, Biological * MeSH
- Gestational Age MeSH
- Humans MeSH
- Drug Monitoring methods MeSH
- Infant, Newborn MeSH
- Analgesics, Opioid administration & dosage pharmacokinetics MeSH
- Retrospective Studies MeSH
- Sufentanil administration & dosage pharmacokinetics MeSH
- Body Weight MeSH
- Tissue Distribution MeSH
- Respiration, Artificial * MeSH
- Dose-Response Relationship, Drug MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Infant, Newborn MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Observational Study MeSH
- Names of Substances
- Analgesics, Opioid MeSH
- Sufentanil MeSH
INTRODUCTION: Sufentanil is a potent synthetic opioid used for analgesia in neonates; however, data concerning drug disposition of sufentanil and dosage regimen are sparse in this population. Therefore, the aim of the study was to explore sufentanil disposition and to propose optimal loading and maintenance doses of sufentanil in ventilated full-term neonates. METHODS: Individual sufentanil pharmacokinetic parameters were calculated based on therapeutic drug monitoring data using a 2-compartmental model. Linear regression models were used to explore the covariates. RESULTS: The median (IQR) central volume of distribution (Vdc) and clearance (CL) for sufentanil were 4.7 (4.1-5.4) L/kg and 0.651 (0.433-0.751) L/h/kg, respectively. Linear regression models showed relationship between Vdc (L) and GA (r2 = 0.3436; p = 0.0452) as well as BW (r2 = 0.4019; p = 0.0268). Median optimal sufentanil LD and MD were 2.13 (95% CI: 1.78-2.48) μg/kg and 0.29 (95% CI: 0.22-0.37) μg/kg/h, respectively. Median daily COMFORT-B (IQR) scores ranged from 6 to 23 while no significant relationship between pharmacokinetic parameters and COMFORT-B scores was found. DISCUSSION/CONCLUSION: Body weight and gestational age were found as weak covariates for sufentanil distribution, and the dosage regimen was developed for a prospective trial.
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