Evidence map›Paper›PMID 39039947›Full record

ArticleCPT: pharmacometrics & systems pharmacology2024

Population pharmacokinetic modeling of sufentanil in adult Korean patients undergoing cardiopulmonary bypass surgery.

Vipada Khaowroongrueng, Kuk Hui Son, Sang-Min Lee, JiYeon Lee, Chun-Gon Park, Seok In Lee, Dongseong Shin, Kwang-Hee Shin

Abstract read
In one paragraph

Article in CPT: pharmacometrics & systems pharmacology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Observational
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  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Vipada KhaowroongruengResearch and Development Institute, The Government Pharmaceutical Organization, Bangkok, Thailand.ORCID 0009-0003-8710-1284
Kuk Hui SonDepartment of Thoracic and Cardiovascular Surgery, Gil Medical Center, College of Medicine, Gachon University, Incheon, Korea.ORCID 0000-0002-0595-5645
Sang-Min LeeCollege of Pharmacy, Research Institute of Pharmaceutical Sciences, Kyungpook National University, Daegu, Korea.ORCID 0000-0002-9386-1170
JiYeon LeeDepartment of Anesthesiology and Pain Medicine, Gil Medical Center, College of Medicine, Gachon University, Incheon, Korea.ORCID 0000-0003-0327-371X
Chun-Gon ParkDepartment of Anesthesiology and Pain Medicine, Gil Medical Center, College of Medicine, Gachon University, Incheon, Korea.ORCID 0000-0002-8269-5058
Seok In LeeDepartment of Thoracic and Cardiovascular Surgery, Gil Medical Center, College of Medicine, Gachon University, Incheon, Korea.ORCID 0000-0002-8538-4511
Dongseong ShinDepartment of Clinical Pharmacology and Therapeutics, Gil Medical Center, College of Medicine, Gachon University, Incheon, Korea.ORCID 0000-0002-4227-374X
Kwang-Hee ShinCollege of Pharmacy, Research Institute of Pharmaceutical Sciences, Kyungpook National University, Daegu, Korea.ORCID 0000-0002-0915-2700

Funding

National Research Foundation of Korea 2020R1F1A1072586National Research Foundation of Korea 2022K2A9A1A09092375National Research Foundation of Korea RS-2023-00251397
6 · The paper itself

Abstract

Sufentanil is frequently used as an anesthetic agent in cardiac surgery owing to its cardiovascular safety and favorable pharmacokinetics. However, the pharmacokinetics profiles of sufentanil in patients undergoing cardiopulmonary bypass (CPB) surgery remain less understood, which is crucial for achieving the desired level of anesthesia and mitigating surgical complications. Therefore, this study aimed to develop a population pharmacokinetic model of sufentanil in patients undergoing CPB surgery and elucidate the clinical factors affecting its pharmacokinetic profile. Adult patients who underwent cardiac surgery with CPB and were administered sufentanil for anesthesia were enrolled. Arterial blood samples were collected to quantify plasma concentrations of sufentanil and clinical laboratory parameters, including inflammatory cytokines. A population pharmacokinetic model was established using nonlinear mixed-effects modeling. Simulations were performed using the pharmacokinetic parameters of the final model. Overall, 20 patients were included in the final analysis. Sufentanil pharmacokinetics were modeled using a two-compartment model, accounting for CPB effects. Sufentanil clearance increased 2.80-fold during CPB and warming phases, while the central compartment volume increased 2.74-fold during CPB. CPB was a significant covariate affecting drug clearance and distribution volume. No other significant covariates were identified despite increased levels of the inflammatory cytokines, including IL-6, IL-8, and TNF-α during CPB. The simulation indicated a 30 μg loading dose and 40 μg/h maintenance infusion for target-controlled infusion. Additionally, a bolus dose of 60 μg was added at CPB initiation to adjust for exposure changes during this phase. Considering the target sufentanil concentrations, a uniform dosing regimen was acceptable for effective analgesia.

Indexed as

Cardiopulmonary BypassModels, BiologicalSufentanilAdultAgedAnesthetics, IntravenousCytokinesFemaleHumansMaleMiddle AgedRepublic of KoreaAnesthetics, IntravenousCytokinesSufentanil

Identifiers

PMID39039947
PMCPMC11494824

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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.