Evidence map›Paper›PMID 38225886›Full record

ArticleJournal of genetic counseling2024

Families' experiences accessing care after genomic sequencing in the pediatric cancer context: "It's just been a big juggle".

Blake Vuocolo, Amanda M Gutierrez, Jill O Robinson, Alva M Recinos, Lauren R Desrosiers, Mary A Majumder, Juan Carlos Bernini, Jonathan Gill, Timothy Griffin, Gail E Tomlinson and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of genetic counseling, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
3.5field-weighted citation impact, top 9% of its field
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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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

15 authors at 4 institutions in 1 country.

Blake VuocoloDepartment of Molecular and Human Genetics, School of Health Professions, Baylor College of Medicine, Houston, Texas, USA.
Amanda M GutierrezCenter for Medical Ethics and Health Policy, Baylor College of Medicine, Houston, Texas, USA.
Jill O RobinsonCenter for Medical Ethics and Health Policy, Baylor College of Medicine, Houston, Texas, USA.
Alva M RecinosDepartment of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.
Lauren R DesrosiersDepartment of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.
Mary A MajumderCenter for Medical Ethics and Health Policy, Baylor College of Medicine, Houston, Texas, USA.
Juan Carlos BerniniDepartment of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.
Jonathan GillUT MD Anderson Cancer Center, Children's Cancer Hospital, Houston, Texas, USA.
Timothy GriffinDepartment of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.
Gail E TomlinsonUT Health Science Center, Greehey Children's Cancer Research Institute and Division of Pediatric Hematology-Oncology, San Antonio, Texas, USA.
Kelly VallanceCook Children's Hematology and Oncology, Cook Children's Hospital, Forth Worth, Texas, USA.
Amy L McGuireCenter for Medical Ethics and Health Policy, Baylor College of Medicine, Houston, Texas, USA.
D Williams ParsonsDepartment of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.
Sharon E PlonDepartment of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.
Sarah ScollonDepartment of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.ORCID 0000-0003-2017-0245
Baylor College of Medicine · USChildren's Cancer Center · USCook Children's Medical Center · USThe University of Texas MD Anderson Cancer Center · US

Funding

Measuring Perceptions of Utility of Clinical Genome Sequencing: Instrument Testing and ValidationU01HG006485 · NHGRI · BAYLOR COLLEGE OF MEDICINE · PI MCGUIRE, AMY L, PARSONS, DONALD W. · 2012 to 2021
$22.1M
National Human Genome Research Institute and the National Cancer Institute U01HG006485National Society of Genetic CounselorsNHGRI NIH HHS U01 HG006485Texas Society of Genetic Counselors
6 · The paper itself

Abstract

Access to genomic sequencing (GS) and resulting recommendations have not been well described in pediatric oncology. GS results may provide a cancer predisposition syndrome (CPS) diagnosis that warrants screening and specialist visits beyond cancer treatment, including testing or surveillance for family members. The Texas KidsCanSeq (KCS) Study evaluated implementation of GS in a diverse pediatric oncology population. We conducted semi-structured interviews (n = 20) to explore experiences of KCS patients' families around learning about a CPS diagnosis and following up on recommended care. We used qualitative content analysis to develop themes and subthemes across families' descriptions of their experiences accessing care and to understand which factors presented barriers and/or facilitators. We found participants had difficulty differentiating which follow-up care recommendations were made for their child's current cancer treatment versus the CPS. In families' access to follow-up care for CPS, organizational factors were crucial: travel time and distance were common hardships, while coordination of care to streamline multiple appointments with different providers helped facilitate CPS care. Financial factors also impacted families' access to CPS-related follow-up care: having financial assistance and insurance were facilitators for families, while costs and lack of insurance posed as barriers for patients who lost coverage during transitions from pediatric to adult care, and for adult family members who had no coverage. Factors related to beliefs and perceptions, specifically perceiving the risk as less salient to them and feeling overwhelmed with the patient's cancer care, presented barriers to follow-up care primarily for family members. Regarding social factors, competing life priorities made it difficult for families to access follow-up care, though having community support alleviated these barriers. We suggest interventions to improve coordination of cancer treatment and CPS-related care and adherence to surveillance protocols for families as children age, such as care navigators and integrating longitudinal genetic counseling into hereditary cancer centers.

Indexed as

NeoplasmsAdolescentAdultChildFamilyFemaleGenetic Predisposition to DiseaseGenomicsHealth Services AccessibilityHumansMaleTexasaccess to caregenomic researchpediatric cancerunderrepresented populations

Identifiers

PMID38225886
PMCPMC11247135
OpenAlexW4390915415

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.