Evidence map›Paper›PMID 42190900›Full record

ArticleThe Journal of pediatrics2026

Talking About Future Disability: Qualitative Analysis of Family Meetings in Neonatal and Pediatric Intensive Care Units.

Ryan F Sutyla, Katelyn A Young, Saisha Dhar, Nikhita Nanduri, Sarah Jean Barton, Monica Lemmon

Abstract read
In one paragraph

Article in The Journal of pediatrics, 2026. 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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1 · What the graph read from it

What it found

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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

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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

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5 · Who and what money

Authors and funding

6 authors.

Ryan F SutylaDepartment of Pediatrics, Duke University Medical Center, Durham, NC. Electronic address: ryan.sutyla@duke.edu.
Katelyn A YoungDuke University School of Medicine, Durham, NC.
Saisha DharVanderbilt University School of Medicine, Nashville, TN.
Nikhita NanduriDuke University School of Medicine, Durham, NC.
Sarah Jean BartonDepartment of Orthopaedic Surgery, Duke University School of Medicine, Durham, NC; Duke University Divinity School, Durham, NC.
Monica LemmonDepartment of Pediatrics, Duke University Medical Center, Durham, NC.

Funding

Decision Making for Infants with Neurologic ConditionsK23NS116453 · NINDS · DUKE UNIVERSITY · PI LEMMON, MONICA · 2020 to 2024
$942k
NINDS NIH HHS K23 NS116453
6 · The paper itself

Abstract

objectiveTo evaluate the language used to discuss a child's disability and understand themes related to its use. STUDY

designThis descriptive qualitative study was embedded in a qualitative study examining family meeting dynamics and decision-making in pediatric and neonatal intensive care units. Family meetings involved an infant 1 year old or younger and were held to discuss neurologic prognosis or goals of care. We performed a secondary, post hoc analysis of family meeting content to characterize language used to discuss current and/or future disability.

resultsA total of 68 family meetings were screened; 45 (66%) included disability language. Disability was referenced by explicitly naming disability, sharing information about disability characteristics, and using problematic language. We identified 5 themes that further characterized disability language: (1) euphemisms for disability, (2) invoking the healthy other, (3) the intersection between quality of life and disability, (4) using the medical model to contextualize disability, and (5) disability's impact on the child's family.

conclusionsThe language used by family members and clinicians to discuss and contextualize disability provides important insight into how disability is addressed in pediatric and neonatal intensive care units. These findings emphasize the importance of including topics related to disability in medical education and can inform further work to develop training tools to aid pediatric clinicians in discussing disability effectively.

Indexed as

Children with DisabilitiesCommunicationIntensive Care Units, NeonatalIntensive Care Units, PediatricProfessional-Family RelationsDecision MakingFemaleHumansInfantInfant, NewbornMaleQualitative ResearchQuality of Lifedisabilityfamily experiencefamily meetingslanguageneonatal ICUpediatric ICU

Identifiers

PMID42190900
PMCPMC13238138

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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.