Evidence map›Paper›PMID 36777987›Full record

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

Physical Compatibility of Y-site Pediatric Drug Administration: A Call for Question of US Pharmacopeia Standards.

Emma L Ross, Kirsten Petty, Allison Salinas, Jarrett Bremmer, Cheng Her, John F Carpenter

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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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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Emma L RossDepartment of Pharmacy (ELR, KP, AS), Children's Hospital Colorado, Aurora, CO.
Kirsten PettyDepartment of Pharmacy (ELR, KP, AS), Children's Hospital Colorado, Aurora, CO.
Allison SalinasDepartment of Pharmacy (ELR, KP, AS), Children's Hospital Colorado, Aurora, CO.
Jarrett BremmerDepartment of Pharmacy (JB), University of Colorado Skaggs School of Pharmacy and Pharmaceutical Science, Aurora, CO.
Cheng HerDepartment of Basic Science (CH, JFC), University of Colorado Skaggs School of Pharmacy and Pharmaceutical Science, Aurora, CO.
John F CarpenterDepartment of Basic Science (CH, JFC), University of Colorado Skaggs School of Pharmacy and Pharmaceutical Science, Aurora, CO.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo evaluate the physical intravenous Y-site compatibility of 29 combinations of medications at commonly used pediatric concentrations using both existing and novel techniques.

methodsMedication combinations included were selected by a varied group of pediatric inpatient pharmacists, and then assessed by 3 independent reviewers for existing literature. For each combination, 2 different medications were mixed together in a 1:1 ratio and incubated at room temperature for 4 hours to simulate Y-site administration. Each sample was then analyzed using the US Pharmacopeia (USP) <788> recommended analytical technique of light obscuration (LO) in addition to novel flow imaging (FI) microscopy and backgrounded membrane imaging (BMI). Physical compatibility was determined using USP chapter <788> large volume particle count limits for all techniques.

resultsA total of 29 different medication combinations were studied. Five combinations met criteria for compatibility by all 3 techniques. The remaining 24 combinations reached the threshold to be considered incompatible by at least 1 of the 3 techniques. Light obscuration, BMI, and FI identified 14%, 59%, and 76% of combinations as incompatible, respectively. All samples deemed incompatible by LO were also incompatible by at least 1 of the other 2 techniques. Flow imaging and BMI results agreed in 69% of samples tested.

conclusionsMost combinations tested were found to be incompatible by at least 1 of the 3 instruments used. Light obscuration appears to have reduced accuracy for identifying particulate resulting in physical medication incompatibility when compared with the novel techniques of FI and BMI.

Indexed as

drug stabilityintravenous administrationintravenous infusionparticulate matterpediatrics

Identifiers

PMID36777987
PMCPMC9901315

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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.