Evidence map›Paper›PMID 36264219›Full record

ArticlePaediatric anaesthesia2023

Acetaminophen pharmacokinetics in infants and children with congenital heart disease.

Jay Holladay, Peter Winch, James Morse, Brian J Anderson, Christopher T McKee, Julie Rice-Weimer, Joseph D Tobias

Open access · bronzeAbstract read
In one paragraph

Article in Paediatric anaesthesia, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 29% of its field
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

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.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 4 citations in OpenAlex.

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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

7 authors at 2 institutions in 2 countries.

Jay HolladayDepartment of Anesthesiology & Pain Medicine, Nationwide Children's Hospital, Columbus, Ohio, USA.ORCID 0000-0003-0112-311X
Peter WinchDepartment of Anesthesiology & Pain Medicine, Nationwide Children's Hospital, Columbus, Ohio, USA.ORCID 0000-0001-8183-8507
James MorseDepartment of Anesthesiology, University of Auckland, Auckland, New Zealand.ORCID 0000-0001-7500-0062
Brian J AndersonDepartment of Anesthesiology, University of Auckland, Auckland, New Zealand.ORCID 0000-0002-2826-3019
Christopher T McKeeDepartment of Anesthesiology & Pain Medicine, Nationwide Children's Hospital, Columbus, Ohio, USA.
Julie Rice-WeimerDepartment of Anesthesiology & Pain Medicine, Nationwide Children's Hospital, Columbus, Ohio, USA.
Joseph D TobiasDepartment of Anesthesiology & Pain Medicine, Nationwide Children's Hospital, Columbus, Ohio, USA.
Nationwide Children's Hospital · USUniversity of Auckland · NZ

Funding

Heart Center Intramural Funding Program of Nationwide Children's Hospital
6 · The paper itself

Abstract

backgroundAcetaminophen is routinely used for perioperative analgesia in children undergoing major surgical procedures. There are few estimates of acetaminophen pharmacokinetic parameters in children with congenital heart disease, especially those with cyanotic heart disease.

aimsThe current study prospectively investigated differences in acetaminophen pharmacokinetics following surgery using cardiopulmonary bypass in children with cyanotic and acyanotic congenital heart disease.

methodsChildren (2-6 years, 9-23 kg) presenting for median sternotomy for Fontan palliation (cyanotic patients) or two ventricle surgical repair (acyanotic patients) were eligible for inclusion. A single intravenous dose of acetaminophen (15 mg/kg) was administered at the start of sternal closure after separation from cardiopulmonary bypass. The time-course of acetaminophen concentrations were described using non-linear mixed effects models. One and two-compartment disposition models with first-order elimination were tested. Pharmacokinetic parameter estimates were scaled using allometry and standardized to a 70 kg person.

resultsThere were 208 acetaminophen concentrations assayed from 30 children, 15 with cyanotic, and 15 with acyanotic heart disease. A 2-compartment model best described acetaminophen PK. Parameter estimates (population parameter variability, PPV%; 95% confidence interval, CI) were clearance CL 15.3 L.h-1.70 kg-1 (22.2%; 13.8-16.7), intercompartment clearance Q 45.4 L.h-1.70 kg-1 (22.4%; 25.2-61.9), central volume of distribution V1 33.5 L.70 kg-1 (23.2%; 25.9-38.8), peripheral volume of distribution V2 32.1 L.70 kg

conclusionsAcetaminophen pharmacokinetics were characterized using a 2-compartment model with first-order elimination following cardiac bypass surgery in children. Population pharmacokinetic parameter estimates were similar to other studies in children. No differences were detected between patients with cyanotic and acyanotic heart disease.

Indexed as

AcetaminophenHeart Defects, CongenitalChildHumansAcetaminophenacetaminophencardiopulmonary bypasscongenital heart diseaseparacetamolpharmacokinetics

Identifiers

PMID36264219
PMCPMC10100048
OpenAlexW4306910616

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.