Evidence map›Paper›PMID 42440320›Full record

ArticleJAMA network open2026

Coping Strategies and Social Support for Transition Readiness Among Youth With Sickle Cell Disease.

Apoorva S Iyengar, Tanisha Belton, Jack Chen, Tisheya Ward, Olivia Teng, Banu Aygun, Abena Appiah-Kubi, Nataly Apollonsky, Donna Boruchov, Biree Andemariam and 7 more

Abstract read
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Article in JAMA network open, 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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0citing papers 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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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

17 authors.

Apoorva S IyengarDepartment of Pediatrics, Northwell Health, New Hyde Park, New York.
Tanisha BeltonPolicyLab, Division of General Pediatrics, Children's Hospital of Philadelphia, Pennsylvania.
Jack ChenDepartment of Pediatrics, Northwell Health, New Hyde Park, New York.
Tisheya WardDepartment of Pediatrics, Northwell Health, New Hyde Park, New York.
Olivia TengDepartment of Pediatrics, Northwell Health, New Hyde Park, New York.
Banu AygunDepartment of Pediatrics, Northwell Health, New Hyde Park, New York.
Abena Appiah-KubiDepartment of Pediatrics, Northwell Health, New Hyde Park, New York.
Nataly ApollonskyDrexel University College of Medicine, Philadelphia, Pennsylvania.
Donna BoruchovConnecticut Children's Medical Center, Hartford.
Biree AndemariamNew England Sickle Cell Institute, University of Connecticut Health, Farmington.
Omar NissDepartment of Pediatrics, Cincinnati Children's Hospital Medical Center, Ohio.
Lori E CrosbyDepartment of Pediatrics, Cincinnati Children's Hospital Medical Center, Ohio.
Lisa SchwartzDivision of Oncology, Children's Hospital of Philadelphia, Pennsylvania.
Lamia BarakatDivision of Oncology, Children's Hospital of Philadelphia, Pennsylvania.
Kim Smith-WhitleyPolicyLab, Division of General Pediatrics, Children's Hospital of Philadelphia, Pennsylvania.
Sophia JanDepartment of Pediatrics, Northwell Health, New Hyde Park, New York.
Caren SteinwayDepartment of Pediatrics, Northwell Health, New Hyde Park, New York.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Suboptimal transitions from pediatric to adult health care can negatively impact disease outcomes, medication regimen adherence, and disease self-management in adulthood. Little is known about whether the presence of coping strategies in young adults (YAs) with sickle cell disease (SCD) is associated with higher transition readiness scores. Objective: To evaluate whether coping strategies and social support are associated with higher transition readiness scores in YAs with SCD. Design, Setting, and Participants: This cross-sectional study was a subanalysis of baseline data from a prospective randomized clinical trial of YAs aged 17 to 25 years with SCD planning to transition to an adult sickle cell clinic within the next 12 months at 5 institutions across Connecticut, New York, Ohio, and Pennsylvania. The recruitment period was from January 15, 2019, to December 31, 2022. Analysis used data from this time period and was conducted from September 30, 2024, to June 30, 2025. Main Outcomes and Measures: Measures included the Transition Readiness Assessment Questionnaire (TRAQ) to assess transition readiness, the Medical Outcomes Study-Social Support Survey (MOS-SSS) emotional/informational subscale to assess social support, and the Brief-COPE (problem-focused, emotion-focused, and avoidant subscales) to assess coping strategies. Bivariate and multivariable linear regression analyses were used to assess differences of transition readiness. Covariates included worry (PedsQL Sickle Cell Disease Module worry I), age, gender, SCD disease severity, and social support. Results: The final cohort included 373 YAs (mean [SD] age, 18.9 [1.9] years; 190 female [51.5%]), with 335 of 367 reporting race as Black (91.3%) and 335 of 365 reporting ethnicity as non-Hispanic/Latino (91.8%). Unadjusted analysis found that overall coping (mean difference, 0.14; 95% CI, 0.01-0.27; P = .03), problem-focused coping (mean difference, 0.18; 95% CI, 0.09-0.27; P < .001), and the emotional/informational subscale of the MOS-SSS (mean difference, 0.13; 95% CI, 0.07-0.19; P < .001) were associated with higher transition readiness scores. Adjusted linear regression analysis showed that problem-focused coping (mean difference, 0.10; 95% CI, 0.003-0.19; P = .04) was associated with transition readiness even after adjusting for age, gender, disease severity, worry, recruitment site, and social support. Conclusions and Relevance: In this cross-sectional study in a national cohort of adolescents and YAs with SCD, problem-focused coping strategies were associated with higher levels of transition readiness. These findings suggest important intervention targets for supporting transitioning adolescents with SCD.

Indexed as

Adaptation, PsychologicalAnemia, Sickle CellCoping SkillsSocial SupportTransition to Adult CareAdolescentAdultCross-Sectional StudiesFemaleHumansMaleProspective StudiesSurveys and QuestionnairesYoung Adult

Identifiers

PMID42440320
PMCPMC13366194

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.