Evidence map›Paper›PMID 18226244›Full record

ArticleBMC medical informatics and decision making2008

Integration of modeling and simulation into hospital-based decision support systems guiding pediatric pharmacotherapy.

Jeffrey S Barrett, John T Mondick, Mahesh Narayan, Kalpana Vijayakumar, Sundararajan Vijayakumar

Registry-linked trialAbstract read
In one paragraph

Article in BMC medical informatics and decision making, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02624037 (Precision IFX), which is not on this map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
–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

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.

NCT02624037 nacompletednot on this mapstarted 2015, after this paper: background citation

Precision IFX: Using a Pharmacokinetic Dashboard to Optimize and Individualize Infliximab Dosage for Pediatric Inflammatory Bowel Disease Patients

TypeinterventionalSponsorIcahn School of Medicine at Mount SinaiRan2015 to 2020Enrolled189ConditionsInflammatory Bowel DiseaseArmsIndividualized Dosage Precision IFX Dashboard
3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Methotrexate for high-grade osteosarcoma in children and young adults.The Cochrane database of systematic reviews · 2011
    Pooled it
  2. Article
  3. Review
  4. The Coming of Age of Model-Informed Precision Therapeutics for Children.The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG · 2025
    Article
  5. Article
  6. Treatment of evolving cancers will require dynamic decision support.Annals of oncology : official journal of the European Society for Medical Oncology · 2023
    Review
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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

5 authors.

Jeffrey S BarrettDepartment of Pediatrics, Division of Clinical Pharmacology and Therapeutics, The Children's Hospital of Philadelphia, USA. barrettj@email.chop.edu
John T Mondick
Mahesh Narayan
Kalpana Vijayakumar
Sundararajan Vijayakumar

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDecision analysis in hospital-based settings is becoming more common place. The application of modeling and simulation approaches has likewise become more prevalent in order to support decision analytics. With respect to clinical decision making at the level of the patient, modeling and simulation approaches have been used to study and forecast treatment options, examine and rate caregiver performance and assign resources (staffing, beds, patient throughput). There us a great need to facilitate pharmacotherapeutic decision making in pediatrics given the often limited data available to guide dosing and manage patient response. We have employed nonlinear mixed effect models and Bayesian forecasting algorithms coupled with data summary and visualization tools to create drug-specific decision support systems that utilize individualized patient data from our electronic medical records systems.

methodsPharmacokinetic and pharmacodynamic nonlinear mixed-effect models of specific drugs are generated based on historical data in relevant pediatric populations or from adults when no pediatric data is available. These models are re-executed with individual patient data allowing for patient-specific guidance via a Bayesian forecasting approach. The models are called and executed in an interactive manner through our web-based dashboard environment which interfaces to the hospital's electronic medical records system.

resultsThe methotrexate dashboard utilizes a two-compartment, population-based, PK mixed-effect model to project patient response to specific dosing events. Projected plasma concentrations are viewable against protocol-specific nomograms to provide dosing guidance for potential rescue therapy with leucovorin. These data are also viewable against common biomarkers used to assess patient safety (e.g., vital signs and plasma creatinine levels). As additional data become available via therapeutic drug monitoring, the model is re-executed and projections are revised.

conclusionThe management of pediatric pharmacotherapy can be greatly enhanced via the immediate feedback provided by decision analytics which incorporate the current, best-available knowledge pertaining to dose-exposure and exposure-response relationships, especially for narrow therapeutic agents that are difficult to manage.

Indexed as

Clinical Pharmacy Information SystemsComputer SimulationDecision Support Systems, ClinicalHospitals, PediatricSystems IntegrationAlgorithmsAntimetabolites, AntineoplasticBayes TheoremChildHumansMedical Records Systems, ComputerizedMethotrexateNeoplasmsPharmacy Service, HospitalPhiladelphiaAntimetabolites, AntineoplasticMethotrexate

Identifiers

PMID18226244
PMCPMC2254609

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Registered trials

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.