Evidence map›Paper›PMID 38982025›Full record

ArticleJournal of clinical psychology in medical settings2025

Comorbid ADHD and Pediatric Sickle Cell Disease: Prevalence and Risk Factors.

Sarah E Bills, Jeffrey Schatz, Sreya Varanasi, Julia D Johnston, Elizabeth Gillooly

Abstract read
In one paragraph

Article in Journal of clinical psychology in medical settings, 2025. 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
–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

1 citing paper in PubMed.

  1. Review
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

5 authors.

Sarah E BillsBehavioral Medicine and Clinical Psychology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 45229, USA. sarah.bills@cchmc.org.ORCID http://orcid.org/0000-0002-9233-8716
Jeffrey SchatzDepartment of Psychology, University of South Carolina, Columbia, SC, 29208, USA.
Sreya VaranasiDepartment of Psychology, University of South Carolina, Columbia, SC, 29208, USA.
Julia D JohnstonDepartment of Psychology, University of South Carolina, Columbia, SC, 29208, USA.
Elizabeth GilloolyDepartment of Psychology, University of South Carolina, Columbia, SC, 29208, USA.

Funding

Biomedical-Behavioral Interface: Prevention and Developmental Sciences TrainingT32GM081740 · NIGMS · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI PRINZ, RONALD J · 2008 to 2022
$4.5M
Behavioral-Biomedical Interface: Translational and Prevention Sciences TrainingT32GM145226 · NIGMS · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI MICHAEL W BEETS, RONALD J PRINZ · 2023 to 2026
$1.2M
NIGMS NIH HHS T32 GM081740NIGMS NIH HHS T32- GM081740NIGMS NIH HHS T32 GM145226
6 · The paper itself

Abstract

Sickle cell disease (SCD) is a genetic blood condition that places youth at increased risk for deficits in complex attention suggestive of increased risk for Attention-Deficit/Hyperactivity Disorder (ADHD). We used systematic screening to assess the prevalence of ADHD in a clinic-based sample of youth with SCD and explored factors related to ADHD. Caregivers of 107 children with SCD (ages 7-11 years) completed routine psychosocial screening which included inattentive symptoms of ADHD. Follow-up diagnostic procedures were completed for patients with elevated inattentive symptoms to assess for ADHD diagnoses. Biomedical and social-environmental variables were examined from the screening and medical records. Twenty-six percent of patients showed elevated inattentive symptoms with 13% meeting diagnostic criteria for ADHD diagnoses. Most children (75%) who met criteria for ADHD had not been previously diagnosed. Disease severity did not predict inattentive symptoms or ADHD diagnoses, though a measure of chronic inflammation was associated with ADHD. Family functioning was related to elevated inattentive symptoms but not ADHD diagnoses. Children with SCD show relatively high rates of ADHD with many cases not detected through routine care. Screening for ADHD as part of hematology care may be a feasible strategy to improve identification and access to intervention.

Indexed as

Anemia, Sickle CellAttention Deficit Disorder with HyperactivityChildComorbidityFemaleHumansMalePrevalenceRisk FactorsSeverity of Illness IndexADHDNeurodevelopmental outcomesSickle cell diseaseSocial–environmental factorsSystemic inflammation

Identifiers

PMID38982025
PMCPMC11711376

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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.