Evidence map›Paper›PMID 38051389›Full record

ReviewPediatric nephrology (Berlin, Germany)2024

Medication patterns and dosing guidance in pediatric patients supported with intermittent hemodialysis or continuous kidney replacement therapy.

Autumn M McKnite, Danielle J Green, Raoul Nelson, Simon C Brewer, Kevin M Watt

Open access · greenAbstract readReview
In one paragraph

Review in Pediatric nephrology (Berlin, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 31% 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

4 citing papers in PubMed, 2 citations in OpenAlex.

  1. Observational
  2. Article
  3. Article
  4. 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.

Autumn M McKniteDepartment of Pharmacology and Toxicology, University of Utah, Salt Lake City, UT, USA. autumn.mcknite@neuro.utah.edu.ORCID 0000-0001-7985-2991
Danielle J GreenDepartment of Pediatrics, Division of Pediatric Critical Care, University of Utah, Salt Lake City, UT, USA.
Raoul NelsonDepartment of Pediatrics, Division of Pediatric Nephrology, University of Utah, Salt Lake City, UT, USA.
Simon C BrewerDepartment of Geography, University of Utah, Salt Lake City, UT, USA.
Kevin M WattDepartment of Pediatrics, Division of Pediatric Critical Care, University of Utah, Salt Lake City, UT, USA.
University of Utah · US

Funding

Multidisciplinary Pulmonary and Critical Care Training ProgramT32HL105321 · NHLBI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Ramsey Hachem, Robert Paine · 2010 to 2026
$4.5M
Physiologically-Based Pharmacokinetic Approach to Determine Dosing on Extracorporeal Life SupportR01HD097775 · NICHD · UNIVERSITY OF UTAH · PI WATT, KEVIN M · 2019 to 2023
$2.7M
Home vs. Clinic Collection of Human Milk in Evaluating the Pharmacokinetics of Four MedicationsR21HD104412 · NICHD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHAMBERS, CHRISTINA, WATT, KEVIN M · 2021 to 2022
$682k
Investigation of Drug-Drug and Drug-Circuit Interactions in Children on Continuous Renal Replacement TherapyF31DK130542 · NIDDK · UNIVERSITY OF UTAH · PI MCKNITE, AUTUMN · 2022 to 2023
$74k
NHLBI NIH HHS 2T32HL105321NHLBI NIH HHS T32 HL105321NICHD NIH HHS R01 HD097775NICHD NIH HHS R21 HD104412NIDDK NIH HHS F31 DK130542NIDDK NIH HHS F31DK130542
6 · The paper itself

Abstract

backgroundHemodialysis is a life-saving technology used during periods of acute or chronic kidney failure to remove toxins, and maintain fluid, electrolyte and metabolic balance. While this technology plays an important role for pediatric patients with kidney dysfunction, it can alter the pharmacokinetic behavior of medications placing patients at risk for suboptimal dosing and drug toxicity. The ability to directly translate pharmacokinetic alterations into dosing recommendations has thus far been limited and dosing guidance specific to pediatric hemodialysis patients is rare. Despite differences in dialysis prescription and patient populations, intermittent (iHD) and continuous kidney replacement therapy (CKRT) patients are often pooled together. In order to develop evidence-based dosing guidelines, it is important to first prioritize drugs for study in each modality.

methodsHere we aim to identify priority drugs in two hemodialysis modalities, through: 1) Identification of hospitalized, pediatric patients who received CKRT or intermittent hemodialysis (iHD) using a machine learning-based predictive model based on medications; 2) Identification of medication administration patterns in these patient cohorts; and 3) Identification of the most commonly prescribed drugs that lack published dosing guidance.

resultsNotable differences were found in the pattern of medications and drug dosing guidance between iHD and CKRT patients. Antibiotics, diuretics and sedatives were more common in CKRT patients. Out of the 50 most commonly administered medications in the two modalities, only 34% and 28% had dosing guidance present for iHD and CKRT, respectively.

conclusionsOur results add to the understanding of the differences between iHD and CKRT patient populations by identifying commonly used medications that lack dosing guidance for each hemodialysis modality, helping to pinpoint priority medications for further study. Overall, this study provides an overview of the current limitations in medication use in this at-risk population, and provides a framework for future studies by identifying commonly used medications in pediatric CKRT and iHD patients.

Indexed as

Acute Kidney InjuryContinuous Renal Replacement TherapyKidney Failure, ChronicAnti-Bacterial AgentsChildHumansPharmaceutical PreparationsRenal DialysisRenal Replacement TherapyAnti-Bacterial AgentsPharmaceutical PreparationsContinuous kidney replacement therapyIntermittent hemodialysisPediatricsPharmacokineticsPharmacology

Identifiers

PMID38051389
PMCPMC11332978
OpenAlexW4389339566

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.