Evidence map›Paper›PMID 24297680›Full record

ArticleClinical pharmacokinetics2014

Influence of gestational age and body weight on the pharmacokinetics of labetalol in pregnancy.

James H Fischer, Gloria E Sarto, Jennifer Hardman, Loraine Endres, Thomas M Jenkins, Sarah J Kilpatrick, Hyunyoung Jeong, Stacie Geller, Kelly Deyo, Patricia A Fischer and 1 more

Open access · greenAbstract read
In one paragraph

Article in Clinical pharmacokinetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 2 pooled it
2.7field-weighted citation impact, top 11% 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

25 citing papers in PubMed, 2 syntheses or guidelines pooled it, 51 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Mechanisms of altered hepatic drug disposition during pregnancy: small molecules.Expert opinion on drug metabolism & toxicology · 2025
    Review
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  15. Anatomical and physiological alterations of pregnancy.Journal of pharmacokinetics and pharmacodynamics · 2020
    Review
  16. Review
  17. Article
  18. Pharmacokinetic studies in pregnancy.Seminars in perinatology · 2020
    Review
  19. Review
  20. Review
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

11 authors at 3 institutions in 1 country.

James H FischerDepartment of Pharmacy Practice, College of Pharmacy, University of Illinois at Chicago, 833 S Wood Street, Room 164, Chicago, IL, 60612, USA, jfischer@uic.edu.
Gloria E Sarto
Jennifer Hardman
Loraine Endres
Thomas M Jenkins
Sarah J Kilpatrick
Hyunyoung Jeong
Stacie Geller
Kelly Deyo
Patricia A Fischer
Keith A Rodvold
University of Illinois Chicago · USUniversity of Wisconsin–Madison · USFroedtert Hospital · US

Funding

UIC Program for Interdisciplinary Careers in Women's Health ResearchK12HD055892 · NICHD · UNIVERSITY OF ILLINOIS AT CHICAGO · PI GELLER, STACIE E. · 2007 to 2016
$4.9M
Altered drug metabolism in pregnancyR01HD065532 · NICHD · UNIVERSITY OF ILLINOIS AT CHICAGO · PI JEONG, HYUNYOUNG · 2011 to 2015
$1.7M
NICHD NIH HHS K12 HD055892NICHD NIH HHS R01 HD065532
6 · The paper itself

Abstract

BACKGROUND AND

objectivesLabetalol is frequently prescribed for the treatment of hypertension during pregnancy; however, the influence of pregnancy on labetalol pharmacokinetics is uncertain, with inconsistent findings reported by previous studies. This study examined the population pharmacokinetics of oral labetalol during and after pregnancy in women receiving labetalol for hypertension.

methodsData were collected from 57 women receiving the drug for hypertension from the 12th week of pregnancy through 12 weeks postpartum using a prospective, longitudinal design. A sparse sampling strategy guided collection of plasma samples. Samples were assayed for labetalol by high-performance liquid chromatography. Estimation of population pharmacokinetic parameters and covariate effects was performed by nonlinear mixed effects modeling using NONMEM. The final population model was validated by bootstrap analysis and visual predictive check. Simulations were performed with the final model to evaluate the appropriate body weight to guide labetalol dosing.

resultsLean body weight (LBW) and gestational age, i.e. weeks of pregnancy, were identified as significantly influencing oral clearance (CL/F) of labetalol, with CL/F ranging from 1.4-fold greater than postpartum values at 12 weeks' gestational age to 1.6-fold greater at 40 weeks. Doses adjusted for LBW provide more consistent drug exposure than doses adjusted for total body weight. The apparent volumes of distribution for the central compartment and at steady-state were 1.9-fold higher during pregnancy.

conclusionsGestational age and LBW impact the pharmacokinetics of labetalol during pregnancy and have clinical implications for adjusting labetalol doses in these women.

Indexed as

Gestational AgeAdolescentAdultAntihypertensive AgentsBody WeightDose-Response Relationship, DrugFemaleHumansHypertension, Pregnancy-InducedLabetalolLongitudinal StudiesPregnancyProspective StudiesYoung AdultAntihypertensive AgentsLabetalol

Identifiers

PMID24297680
PMCPMC4310214
OpenAlexW2061556591

What OpenQuestion holds

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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.