Evidence map›Paper›PMID 26566962›Full record

ArticleBMC anesthesiology2015

Paracetamol pharmacokinetics and metabolism in young women.

Karel Allegaert, Mariska Y Peeters, Bjorn Beleyn, Anne Smits, Aida Kulo, Kristel van Calsteren, Jan Deprest, Jan de Hoon, Catherijne A J Knibbe

Open access · goldAbstract read
In one paragraph

Article in BMC anesthesiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 14% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. Pooled it
  2. Biological sex differences in pharmacokinetics and adverse drug reactions.Naunyn-Schmiedeberg's archives of pharmacology · 2026
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  8. Mechanistic Coupling of a NovelFrontiers in pediatrics · 2021
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  9. Anatomical and physiological alterations of pregnancy.Journal of pharmacokinetics and pharmacodynamics · 2020
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  14. Induction of Biofilm Formation inAntibiotics (Basel, Switzerland) · 2018
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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

9 authors at 3 institutions in 2 countries.

Karel AllegaertNICU, University Hospitals Leuven, Herestraat 49, 3000, Leuven, Belgium. karel.allegaert@uzleuven.be.
Mariska Y PeetersDepartment of Clinical Pharmacy, St Antonius hospital, Nieuwegein, The Netherlands. r.peeters@antoniusziekenhuis.nl.
Bjorn BeleynDepartment of Development and Regeneration, Cluster Organ Systems, KU Leuven, Leuven, Belgium. bjorn_beleyn@hotmail.com.
Anne SmitsNICU, University Hospitals Leuven, Herestraat 49, 3000, Leuven, Belgium. anne.smits@uzleuven.be.
Aida KuloCenter for Clinical Pharmacology, University Hospitals Leuven, Leuven, Belgium. aida.kulo@gmail.com.
Kristel van CalsterenDepartment of Development and Regeneration, Cluster Organ Systems, KU Leuven, Leuven, Belgium. kristel.vancalsteren@uzleuven.be.
Jan DeprestDepartment of Development and Regeneration, Cluster Organ Systems, KU Leuven, Leuven, Belgium. jan.deprest@uzleuven.be.
Jan de HoonDepartment of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium. jan.dehoon@uzleuven.be.
Catherijne A J KnibbeDepartment of Clinical Pharmacy, St Antonius hospital, Nieuwegein, The Netherlands. c.knibbe@antoniusziekenhuis.nl.
KU Leuven · BEOrgan Recovery Systems (Belgium) · BESt. Antonius Ziekenhuis · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThere is relevant between individual variability in paracetamol clearance in young women. In this pooled study, we focused on the population pharmacokinetic profile of intravenous paracetamol metabolism and its covariates in young women.

methodsPopulation PK parameters using non-linear mixed effect modelling were estimated in a pooled dataset of plasma and urine PK studies in 69 young women [47 at delivery, 8/47 again 10-15 weeks after delivery (early postpartum), and 7/8 again 1 year after delivery (late postpartum), 22 healthy female volunteers with or without oral contraceptives].

resultsPopulation PK parameters were estimated based on 815 plasma samples and 101 urine collections. Compared to healthy female volunteers (reference group) not on oral contraceptives, being at delivery was the most significant covariate for clearance to paracetamol glucuronide (Factor = 2.03), while women in early postpartum had decreased paracetamol glucuronidation clearance (Factor = 0.55). Women on contraceptives showed increased paracetamol glucuronidation clearance (Factor = 1.46). The oestradiol level did not further affect this model. Being at delivery did not prove significant for clearance to paracetamol sulphate, but was higher in pregnant women who delivered preterm (<37 weeks, Factor = 1.34) compared to term delivery and non-pregnant women. Finally, clearance of unchanged paracetamol was dependent on urine flow rate.

conclusionsCompared to healthy female volunteers not on oral contraceptives, urine paracetamol glucuronidation elimination in young women is affected by pregnancy (higher), early postpartum (lower) or exposure to oral contraceptives (higher), resulting in at least a two fold variability in paracetamol clearance in young women.

Indexed as

AcetaminophenAdolescentAdultAnalgesics, Non-NarcoticFemaleFollow-Up StudiesHumansPostpartum PeriodPregnancyYoung AdultAcetaminophenAnalgesics, Non-Narcotic

Identifiers

PMID26566962
PMCPMC4644344
OpenAlexW2172374524

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.