Evidence map›Paper›PMID 42276543›Full record

ArticleCancer control : journal of the Moffitt Cancer Center

An Informatics Approach to Enhance Care for Childhood, Adolescent and Young Adult Cancer Survivors Through Population Health Management.

David H Noyd, Lindsey Coons, Jonathan D Bank, Emily Larimer, Gayle Garson, Vicky Aliferakis, Taylor Giovannetti, Carlos Villavicencio, Yu-Hsiang Lin, Michael G Leu and 2 more

Abstract read
In one paragraph

Article in Cancer control : journal of the Moffitt Cancer Center. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

12 authors.

David H NoydBen Towne Center for Childhood Cancer and Blood Disorders Research and the Department of Pediatrics, Seattle Children's Hospital, University of Washington, Seattle, WA, USA.
Lindsey CoonsSeattle Children's Hospital, Seattle, WA, USA.
Jonathan D BankSeattle Children's Hospital, Seattle, WA, USA.
Emily LarimerBen Towne Center for Childhood Cancer and Blood Disorders Research and the Department of Pediatrics, Seattle Children's Hospital, University of Washington, Seattle, WA, USA.
Gayle GarsonSeattle Children's Hospital, Seattle, WA, USA.
Vicky AliferakisSeattle Children's Hospital, Seattle, WA, USA.
Taylor GiovannettiSeattle Children's Hospital, Seattle, WA, USA.
Carlos VillavicencioSeattle Children's Hospital, Seattle, WA, USA.
Yu-Hsiang LinSeattle Children's Hospital, Seattle, WA, USA.
Michael G LeuSeattle Children's Hospital, Seattle, WA, USA.
Eric J ChowBen Towne Center for Childhood Cancer and Blood Disorders Research and the Department of Pediatrics, Seattle Children's Hospital, University of Washington, Seattle, WA, USA.
Carrie L HeikeSeattle Children's Hospital, Seattle, WA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

IntroductionAdolescent and young adult (AYA) cancer survivors are at significant risk for late treatment-related effects yet face challenges when transitioning to survivorship-focused care and longitudinal follow-up. Population-level tools in the electronic health record (EHR) offer a pragmatic approach to track patients and optimize care.MethodsThe Seattle Children's Hospital Cancer Survivor Program created a population health management system, using tools embedded within the EHR, based on a validated registry of AYA survivors. We developed a dynamic dashboard to make care gaps visible survivorship care, provide exposure-based pulmonary and cardiac toxicity surveillance, and support transition to adult care. We also built reports to facilitate real-world data analysis of the transition to survivorship care and longitudinal follow-up in a retrospective cohort of AYA survivors. We analyzed data from the cohort to explore subgroup differences in survivorship care.ResultsAmong survivors who finished treatment between January 1, 2021, and April 30, 2022 (n=220), 47% completed a long-term follow-up visit. There were no differences in the likelihood of follow-up based on age categories (p=0.36). For survivors with established long-term follow-up (n=743), 76% received longitudinal care. Compared with children, adolescent survivors (OR 0.51, 95% CI 0.29-0.9), emerging young adults (OR 0.39, 95% CI 0.24-0.63), and young adults (OR 0.10, 95% CI 0.05-0.18) were less likely to have a survivorship visit in the preceding 30 months. This difference was attenuated when analysis was restricted to survivors <22 years old and adjustment for years off therapy, with OR of 0.67 (95%CI 0.37-1.21) and 0.82 (0.45-1.50) among AYAs compared to children as the referent group.ConclusionAn EHR embedded population health platform represents a feasible approach to measure longitudinal follow-up care and transitions among AYA survivors. Clinical informatics tools have the potential to drive innovation and enhance evidence-based, guideline-concordant care to mitigate late effects in this population.

Indexed as

Cancer SurvivorsNeoplasmsPopulation Health ManagementAdolescentAdultChildElectronic Health RecordsFemaleHumansMaleRetrospective StudiesTransition to Adult CareYoung Adultadolescent, and young adult cancerchildhoodclinical cancer informaticslate effectspopulation healthsurvivorship

Identifiers

PMID42276543
PMCPMC13260967

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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.