Evidence map›Paper›PMID 41676016›Full record

ArticleJournal of clinical and translational science2026

A method to enable clinical and translational research teams with custom real-world data from electronic health record systems.

Thomas R Campion, Evan T Sholle, Xiaobo Fuld, Cindy Chen, Marcos A Davila, Vinay I Varughese, Curtis L Cole

Abstract read
In one paragraph

Article in Journal of clinical and translational science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

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

7 authors.

Thomas R CampionDepartment of Population Health Sciences, Weill Cornell Medicine, New York, NY, USA.ORCID https://orcid.org/0000-0001-7624-769X
Evan T SholleDepartment of Population Health Sciences, Weill Cornell Medicine, New York, NY, USA.
Xiaobo FuldInformation Technologies & Services Department, Weill Cornell Medicine, New York, NY, USA.
Cindy ChenInformation Technologies & Services Department, Weill Cornell Medicine, New York, NY, USA.
Marcos A DavilaInformation Technologies & Services Department, Weill Cornell Medicine, New York, NY, USA.
Vinay I VarugheseInformation Technologies & Services Department, Weill Cornell Medicine, New York, NY, USA.
Curtis L ColeDepartment of Population Health Sciences, Weill Cornell Medicine, New York, NY, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Custom transformations of real-world data (RWD) from electronic health record (EHR) systems are necessary to define study variables describing health and disease statuses differently among physicians in multiple specialties and basic scientists from a variety of disciplines . To increase RWD use, we hypothesized that a solution supporting three workflows - discovery, collection, and analysis - using existing rather than novel tools and requiring financial commitment from investigators would scale to meet the needs of clinical and translational research teams and ensure regulatory compliance at an academic medical center. Materials and methods: Weill Cornell Medicine (WCM) implemented custom research data repositories (RDRs) consisting of i2b2 for discovery, REDCap for collection, and Microsoft SQL Server for analysis. WCM subsidized the central information technology (IT) department to manage RDRs and required investigators to commit $50,000 for RDR startup and $7500 for annual maintenance. Results: From 2013 through 2025, WCM launched more than 17 custom RDRs for pediatrics, myeloproliferative neoplasms, obstetrics and gynecology, pulmonary and critical care, chronic kidney disease, and ophthalmology among other areas. Custom RDRs enabled academic output (e.g., publications, grants) as well as local quality improvement activities. Discussion: Custom RDRs facilitated delivery of fit-for-purpose data sets derived from EHR systems and other RWD sources. Over time, RDRs have evolved from an infrastructure product delivered by central IT to a data partnership between investigators and IT. Conclusion: Custom RDRs and data partnerships may help increase the use of RWD from EHR and other sources by clinical and translational research teams.

Indexed as

CTSAelectronic health recordenterprise data warehouse for researchreal-world datasecondary use

Identifiers

PMID41676016
PMCPMC12886558

What OpenQuestion holds

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LicenceCC BY
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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.