“Everyone screens to some extent”: Barriers and facilitators of developmental screening among children with sickle cell disease: A mixed methods study

Author:

Hoyt Catherine R.123ORCID,Luo Lingzi4,Rice Hannah E.5,Shivakumar Nirmala6,Housten Ashley J.15,Picinich Abigail2,Qashou Nai2,Harris Kelly M.15ORCID,Varughese Taniya2,King Allison A.12567ORCID

Affiliation:

1. Program in Occupational Therapy Washington University School of Medicine St. Louis Missouri USA

2. Department of Pediatrics Washington University School of Medicine St. Louis Missouri USA

3. Department of Neurology Washington University School of Medicine St. Louis Missouri USA

4. School of Global Public Health New York University New York New York USA

5. Department of Surgery Division of Public Health Sciences Washington University School of Medicine St. Louis Missouri USA

6. Department of Medicine Washington University School of Medicine St. Louis Missouri USA

7. Department of Education Washington University School of Medicine St. Louis Missouri USA

Abstract

AbstractBackgroundDevelopmental delays are common among children with sickle cell disease (SCD). Existing guidelines support consistent screening to increase the identification of deficits and support referral to rehabilitative interventions, yet adherence remains variable. This study sought to assess current practices and identify barriers and facilitators to improve developmental screening for children 0–3 years with SCD.ProcedureA mixed methods approach, guided by the Exploration and Preparation stages of the Exploration, Preparation, Implementation, and Sustainment (EPIS) framework, assessed developmental screening practices among primary care providers and hematologists. Phase 1 included the SCD Developmental Surveillance and Screening Guideline and Practice Survey. Phase 2 included the SCD Developmental Screening Organizational Survey alongside semi‐structured interviews. Descriptive and qualitative methods summarized the findings.ResultsThirty‐three providers from general pediatrics and hematology completed phase 1. Use of standardized developmental screening measures was variable, with the most frequently used being the Modified Checklist for Autism in Toddlers (77%) and the Ages and Stages Questionnaire (55%). Fifteen providers participated in phase 2, and reported they were most likely to engage in changes to improve their practice (mean = 4.4/5) and least likely to support spiritual health and well‐being (mean = 3.5/5). Three themes emerged:(i) developmental screening is not standardized or specific to SCD, (ii) children with SCD benefit from a multidisciplinary team, and (iii) healthcare system limitations are a barrier.ConclusionsDevelopmental screening is inconsistent and insufficient for young children with SCD. Providers are interested in supporting children with SCD, but report a lack of standardized measures and consistent guidance as barriers.

Publisher

Wiley

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