Evidence map›Paper›PMID 33729042›Full record

ArticleJournal of primary care & community health

Integrating Genomic Screening into Primary Care: Provider Experiences Caring for Latino Patients at a Community-Based Health Center.

Tarika Srinivasan, Erica J Sutton, Annika T Beck, Idali Cuellar, Valentina Hernandez, Joel E Pacyna, Gabriel Q Shaibi, Iftikhar J Kullo, Noralane M Lindor, Davinder Singh and 1 more

Abstract read
In one paragraph

Article in Journal of primary care & community health. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Sustainability in translational genomics research with undiagnosed patients: What is it, why do we need it, and how do we do it?Genetics in medicine : official journal of the American College of Medical Genetics · 2025
    Article
  5. Article
  6. Covering medical care costs for participants in the eMERGE Network: Challenges for equity and implementation.Genetics in medicine : official journal of the American College of Medical Genetics · 2025
    Article
  7. Article
  8. Review
  9. Article
  10. Journal of personalized medicine · 2023
    Article
  11. Article
  12. 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

11 authors.

Tarika SrinivasanHarvard Medical School, Boston, MA, USA.ORCID 0000-0001-5206-1401
Erica J SuttonMayo Clinic, Rochester, MN, USA.
Annika T BeckMayo Clinic, Rochester, MN, USA.
Idali CuellarMayo Clinic, Rochester, MN, USA.
Valentina HernandezMountain Park Health Center, Phoenix, AZ, USA.
Joel E PacynaMayo Clinic, Rochester, MN, USA.ORCID 0000-0002-3103-7805
Gabriel Q ShaibiArizona State University, Phoenix, AZ, USA.
Iftikhar J KulloMayo Clinic, Rochester, MN, USA.
Noralane M LindorMayo Clinic, Rochester, MN, USA.
Davinder SinghMountain Park Health Center, Phoenix, AZ, USA.
Richard R SharpMayo Clinic, Rochester, MN, USA.ORCID 0000-0001-5441-2084

Funding

Genomic Basis of Susceptibility to COVID-19 Infection and its ComplicationsU01HG006379 · NHGRI · MAYO CLINIC ROCHESTER · PI Richard R. Sharp · 2011 to 2026
$16.5M
EMR Phenotypes and Community Engaged Genomic AssociationsU01HG004599 · NHGRI · MAYO CLINIC ROCHESTER · PI CHUTE, CHRISTOPHER G · 2007 to 2010
$3.7M
NHGRI NIH HHS U01 HG004599NHGRI NIH HHS U01 HG006379
6 · The paper itself

Abstract

introductionMinority communities have had limited access to advances in genomic medicine. Mayo Clinic and Mountain Park Health Center, a Federally Qualified Health Center in Phoenix, Arizona, partnered to assess the feasibility of offering genomic screening to Latino patients receiving care at a community-based health center. We examined primary care provider (PCP) experiences reporting genomic screening results and integrating those results into patient care.

methodsWe conducted open-ended, semi-structured interviews with PCPs and other members of the health care team charged with supporting patients who received positive genomic screening results. Interviews were recorded, transcribed, and analyzed thematically.

resultsOf the 500 patients who pursued genomic screening, 10 received results indicating a genetic variant that warranted clinical management. PCPs felt genomic screening was valuable to patients and their families, and that genomic research should strive to include underrepresented minorities. Providers identified multiple challenges integrating genomic sequencing into patient care, including difficulties maintaining patient contact over time; arranging follow-up medical care; and managing results in an environment with limited genetics expertise. Providers also reflected on the ethics of offering genomic sequencing to patients who may not be able to pursue diagnostic testing or follow-up care due to financial constraints.

conclusionsOur results highlight the potential benefits and challenges of bringing advances in precision medicine to community-based health centers serving under-resourced populations. By proactively considering patient support needs, and identifying financial assistance programs and patient-referral mechanisms to support patients who may need specialized medical care, PCPs and other health care providers can help to ensure that precision medicine lives up to its full potential as a tool for improving patient care.

Indexed as

Community Health CentersPrimary Health CareGenomicsHispanic or LatinoHumansPatient Care Teamfederally qualified health centergenomic screeninghealth disparitiesindividualized medicineprimary care

Identifiers

PMID33729042
PMCPMC7975483

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.