Evidence map›Paper›PMID 26712558›Full record

Trial reportJournal of clinical pharmacology2016

Theophylline Population Pharmacokinetics and Dosing in Children Following Congenital Heart Surgery With Cardiopulmonary Bypass.

Adam Frymoyer, Felice Su, Paul C Grimm, Scott M Sutherland, David M Axelrod

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of clinical pharmacology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. No Requirement for Targeted Theophylline Levels for Diuretic Effect of Aminophylline in Critically Ill Children.Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies · 2018
    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

5 authors at 1 institution in 1 country.

Adam FrymoyerDepartment of Pediatrics, Stanford University, Stanford, CA, USA.
Felice SuDepartment of Pediatrics, Stanford University, Stanford, CA, USA.
Paul C GrimmDepartment of Pediatrics, Stanford University, Stanford, CA, USA.
Scott M SutherlandDepartment of Pediatrics, Stanford University, Stanford, CA, USA.
David M AxelrodDepartment of Pediatrics, Stanford University, Stanford, CA, USA.
Stanford University · US

Funding

Spectrum Stanford Center for clinical and Translational Research and EducationUL1TR001085 · NCATS · STANFORD UNIVERSITY · PI CULLEN, MARK RICHARD, GREENBERG, HARRY BERNARD · 2013 to 2017
$37.1M
Pharmacology of Aminophylline for Acute Kidney Injury in Neonates and ChildrenK23HD079557 · NICHD · STANFORD UNIVERSITY · PI FRYMOYER, ADAM · 2014 to 2018
$732k
NCATS NIH HHS UL1 TR001085NICHD NIH HHS K23 HD079557
6 · The paper itself

Abstract

Children undergoing cardiac surgery requiring cardiopulmonary bypass (CPB) frequently develop acute kidney injury due to renal ischemia. Theophylline, which improves renal perfusion via adenosine receptor inhibition, is a potential targeted therapy. However, children undergoing cardiac surgery and CPB commonly have alterations in drug pharmacokinetics. To help understand optimal aminophylline (salt formulation of theophylline) dosing strategies in this population, a population-based pharmacokinetic model was developed using nonlinear mixed-effects modeling (NONMEM) from 71 children (median age 5 months; 90% range 1 week to 10 years) who underwent cardiac surgery requiring CPB and received aminophylline as part of a previous randomized controlled trial. A 1-compartment model with linear elimination adequately described the pharmacokinetics of theophylline. Weight scaled via allometry was a significant predictor of clearance and volume. In addition, allometric scaled clearance increased with age implemented as a power maturation function. Compared to prior reports in noncardiac children, theophylline clearance was markedly reduced across age. In the final population pharmacokinetic model, optimized empiric dosing regimens were developed via Monte Carlo simulations. Doses 50% to 75% lower than those recommended in noncardiac children were needed to achieve target serum concentrations of 5 to 10 mg/L.

Indexed as

Models, BiologicalAdolescentAminophyllineCardiopulmonary BypassCardiotonic AgentsChildChild, PreschoolDose-Response Relationship, DrugDouble-Blind MethodFemaleHeart Defects, CongenitalHumansInfantMaleMonte Carlo MethodTheophyllineAminophyllineCardiotonic AgentsTheophyllineacute kidney injuryaminophyllinecongenital heart defectpediatricpharmacokinetics

Identifiers

PMID26712558
PMCPMC4927421
OpenAlexW2216762931

What OpenQuestion holds

Textmetadata
LicenceTDM
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.