Evidence map›Paper›PMID 38025152›Full record

ArticleThe journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG2023

Multidisciplinary Approach to Deciphering Etoposide Infusion Reactions and Potential Role of Polyethersulfone Filter Membranes.

Nicholas Miles, Andi Masters, Zeruesenay Desta, Jennifer L Goldman, Sarah L Suppes, Emma M Tillman

Open access · bronzeAbstract read
In one paragraph

Article in The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

6 authors at 3 institutions in 1 country.

Nicholas MilesDivision of Clinical Pharmacology (NM, ZD, ET), Indiana University School of Medicine, Indianapolis, IN.
Andi MastersIndiana University Comprehensive Cancer Center (AM), Indiana University School of Medicine, Indianapolis, IN.
Zeruesenay DestaDivision of Clinical Pharmacology (NM, ZD, ET), Indiana University School of Medicine, Indianapolis, IN.
Jennifer L GoldmanDepartment of Pediatrics (JLG), Children's Mercy Hospital and the University of Missouri-Kansas City, Kansas City, MO.
Sarah L SuppesDivision of Clinical Pharmacology (SLS), Toxicology, and Therapeutic Innovation, Children's Mercy Hospital, Kansas City, MO.
Emma M TillmanDivision of Clinical Pharmacology (NM, ZD, ET), Indiana University School of Medicine, Indianapolis, IN.
Indiana University – Purdue University Indianapolis · USChildren's Mercy Hospital · USIndiana University School of Medicine

Funding

Indiana University Comprehensive Training in Clinical PharmacologyT32GM008425 · NIGMS · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI Zeruesenay Desta, Michael Thomas Eadon · 1992 to 2026
$7.7M
Genomic and drug-drug interaction mechanisms of interindividual variability in drug dispositionR35GM145383 · NIGMS · INDIANA UNIVERSITY INDIANAPOLIS · PI Zeruesenay Desta · 2022 to 2026
$2.0M
NIGMS NIH HHS R35 GM145383NIGMS NIH HHS T32 GM008425
6 · The paper itself

Abstract

purposeEtoposide, a topoisomerase II inhibitor used clinically to treat cancer, has been associated with severe anaphylactic infusion related adverse drug reactions (ADRs). In a previous study we identified a hydrophilic polyethersulfone filter as a possible cause of increased rates of pediatric etoposide infusion reactions. In this multidisciplinary follow-up analytical study, we aimed to assess the chemical structure of etoposide after passing through the same hydrophilic polyethersulfone filter.

methodsAn etoposide 0.4 mg/mL infusion was prepared under aseptic conditions and then passed through a standard IV infusion set with an in-line filter in place. Samples were taken in triplicate using a needle-less access system to include sampling sites directly from the IV bag port and from the IV tubing both before and after the in-line filter. Samples were diluted into mobile phase, then an aliquot was injected into a high-performance liquid chromatography mass spectrometry HPLC-MS (Thermo TSQ Quantum Ultra) system coupled to a Diode Array Detector (DAD) (Thermo Dionex Ultimate 3000). Etoposide was monitored using a selected reaction monitoring scan (SRM) of 606.2/228.8 and wavelengths of 210, 220, 254, and 280 nm for 30 minutes.

resultsNo detectable differences were observed upon comparing the three samples. Based on these results, a chemical change in etoposide resulting from an in-line filter is unlikely to be the primary cause of increased rates of infusion reactions.

conclusionPharmacists working in healthcare systems, observe many ADRs, but rarely have the resources necessary to investigate the potential etiology or causality. This report highlights importance of multi-disciplinary collaboration to investigate serious ADRs.

Indexed as

drug-related side effects and adverse reactionsEtoposidepolyethersulfone filter

Identifiers

PMID38025152
PMCPMC10681083
OpenAlexW4389100786

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.