Evidence map›Paper›PMID 38497946›Full record

ArticleJournal of the American Medical Informatics Association : JAMIA2024

Genomics in nephrology: identifying informatics opportunities to improve diagnosis of genetic kidney disorders using a human-centered design approach.

Katrina M Romagnoli, Zachary M Salvati, Darren K Johnson, Heather M Ramey, Alexander R Chang, Marc S Williams

Abstract read
In one paragraph

Article in Journal of the American Medical Informatics Association : JAMIA, 2024. 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

6 authors.

Katrina M RomagnoliDepartment of Population Health Sciences, Geisinger Clinic, Danville, PA 17822, United States.
Zachary M SalvatiDepartment of Genomic Health, Geisinger, Danville, PA 17822, United States.
Darren K JohnsonDepartment of Genomic Health, Geisinger, Danville, PA 17822, United States.
Heather M RameyDepartment of Genomic Health, Geisinger, Danville, PA 17822, United States.
Alexander R ChangDepartment of Population Health Sciences, Geisinger Clinic, Danville, PA 17822, United States.
Marc S WilliamsDepartment of Genomic Health, Geisinger, Danville, PA 17822, United States.

Funding

Real-time genetic diagnosis at the point of careR01HG011799 · NHGRI · GEISINGER CLINIC · PI WILLIAMS, MARC S. · 2021 to 2025
$4.6M
NHGRI NIH HHS R01 HG011799NIH HHS R01HG011799
6 · The paper itself

Abstract

backgroundGenomic kidney conditions often have a long lag between onset of symptoms and diagnosis. To design a real time genetic diagnosis process that meets the needs of nephrologists, we need to understand the current state, barriers, and facilitators nephrologists and other clinicians who treat kidney conditions experience, and identify areas of opportunity for improvement and innovation.

methodsQualitative in-depth interviews were conducted with nephrologists and internists from 7 health systems. Rapid analysis identified themes in the interviews. These were used to develop service blueprints and process maps depicting the current state of genetic diagnosis of kidney disease.

resultsThemes from the interviews included the importance of trustworthy resources, guidance on how to order tests, and clarity on what to do with results. Barriers included lack of knowledge, lack of access, and complexity surrounding the case and disease. Facilitators included good user experience, straightforward diagnoses, and support from colleagues. DISCUSSION: The current state of diagnosis of kidney diseases with genetic etiology is suboptimal, with information gaps, complexity of genetic testing processes, and heterogeneity of disease impeding efficiency and leading to poor outcomes. This study highlights opportunities for improvement and innovation to address these barriers and empower nephrologists and other clinicians who treat kidney conditions to access and use real time genetic information.

Indexed as

GenomicsKidney DiseasesNephrologyGenetic TestingHumansInterviews as TopicNephrologistsgenomic medicinehuman-centered designnephrology

Identifiers

PMID38497946
PMCPMC11105128

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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.