Evidence map›Paper›PMID 41307296›Full record

ArticleClinical and translational science2025

Multi-Gene Pharmacogenomic Testing in a Community-Based Setting Is Feasible and Reduces Total Healthcare Costs.

Nihal El Rouby, Josiah D Allen, Tyler Koep, Pat McIntyre, James Kelly, Adarsh Ramesh, Anita Desai-Naik, Jonathan Chiang, Sheena Patel, Carley Brueckner and 6 more

Abstract read
In one paragraph

Article in Clinical and translational science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–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.

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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

16 authors.

Nihal El RoubySt Elizabeth Healthcare, Edgewood, Kentucky, USA.ORCID 0000-0003-1652-3773
Josiah D AllenSt Elizabeth Healthcare, Edgewood, Kentucky, USA.ORCID 0000-0002-2708-2566
Tyler KoepOneOme, Minneapolis, Minnesota, USA.
Pat McIntyreOneOme, Minneapolis, Minnesota, USA.
James KellyOneOme, Minneapolis, Minnesota, USA.
Adarsh RameshOneOme, Minneapolis, Minnesota, USA.
Anita Desai-NaikHumana, Louisville, Kentucky, USA.
Jonathan ChiangHumana, Louisville, Kentucky, USA.
Sheena PatelDivision of Pharmacy Practice and Administrative Sciences, James L. Winkle College of Pharmacy, University of Cincinnati, Cincinnati, Ohio, USA.
Carley BruecknerSt Elizabeth Healthcare, Edgewood, Kentucky, USA.ORCID 0009-0005-0820-8804
Anna CriderSt Elizabeth Healthcare, Edgewood, Kentucky, USA.
Grace MillerSt Elizabeth Healthcare, Edgewood, Kentucky, USA.
Andrea SchumannSt Elizabeth Healthcare, Edgewood, Kentucky, USA.
Jody WallaceSt Elizabeth Healthcare, Edgewood, Kentucky, USA.
Barry WendtSt Elizabeth Healthcare, Edgewood, Kentucky, USA.
Jaime GrundSt Elizabeth Healthcare, Edgewood, Kentucky, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pharmacogenomic (PGx) testing using multi-gene panels (mgPGx) is documented to improve clinical outcomes; however, real-world data on its economic impact remain limited. This study aimed to evaluate the utility and economic value of mgPGx testing among Medicare patients within a community-based health system. We identified Medicare Advantage patients within the primary care setting of a community-based health system hospital who were taking ≥ 1 PGx-guided medication using a stratification algorithm. In total, 1042 patients participated in mgPGx testing. We evaluated the prevalence of PGx medications, polypharmacy involving PGx medications, and actionable results (i.e., a phenotype with PGx guidance and a relevant PGx medication). A Total Cost of Care (TCOC) analysis was performed for a subset of patients (n = 548) who underwent PGx testing and were matched to a control group that did not undergo PGx testing using propensity score matching. Total medical expenses over 12 months, both before and after testing, were compared. Forty-four percent (n = 454/1042) of patients were ≥ 3 PGx-guided medications. Over one-third of patients who were on ≥ 3 PGx medications had ≥ 2 actionable results (35.5%, n = 161/454). The TCOC analysis demonstrated a trend toward a net cost savings of $1827 per member per year (PMPY), with $1582 in medical savings and $245 in pharmacy savings. Polypharmacy with PGx medications is prevalent, and mgPGx led to cost savings. Further research with a larger sample size is needed to replicate the results and assess the long-term impact on healthcare utilization and costs.

Indexed as

Community Health ServicesHealth Care CostsPharmacogenomic TestingAgedAged, 80 and overCost-Benefit AnalysisCost SavingsFeasibility StudiesFemaleHumansMaleMedicare Part CPolypharmacyPrimary Health CareRetrospective StudiesUnited States

Identifiers

PMID41307296
PMCPMC12658616

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.