Awareness, access, and communication: provider perspectives on early intervention services for children with sickle cell disease

PurposeThis study aimed to identify determinants influencing the utilization of early intervention services among young children with sickle cell disease (SCD) based on perspectives from medical and early intervention providers.Design and methodsEarly intervention and medical providers from the catc...

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Main Authors: Andrew M. Heitzer (Author), Erin MacArthur (Author), Mollie Tamboli (Author), Ashley Wilson (Author), Jane S. Hankins (Author), Catherine R. Hoyt (Author)
Format: Book
Published: Frontiers Media S.A., 2024-03-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Andrew M. Heitzer  |e author 
700 1 0 |a Erin MacArthur  |e author 
700 1 0 |a Mollie Tamboli  |e author 
700 1 0 |a Ashley Wilson  |e author 
700 1 0 |a Jane S. Hankins  |e author 
700 1 0 |a Jane S. Hankins  |e author 
700 1 0 |a Catherine R. Hoyt  |e author 
245 0 0 |a Awareness, access, and communication: provider perspectives on early intervention services for children with sickle cell disease 
260 |b Frontiers Media S.A.,   |c 2024-03-01T00:00:00Z. 
500 |a 2296-2360 
500 |a 10.3389/fped.2024.1366522 
520 |a PurposeThis study aimed to identify determinants influencing the utilization of early intervention services among young children with sickle cell disease (SCD) based on perspectives from medical and early intervention providers.Design and methodsEarly intervention and medical providers from the catchment area surrounding St. Jude Children's Research Hospital and Washington University were recruited (20 total providers). Interviews were completed over the phone and audio recorded. All interviews were transcribed verbatim, coded, and analyzed using inductive thematic analysis.ResultsThree overarching themes were identified from both groups: Awareness (e.g., lack of awareness about the EI system and SCD), Access (e.g., difficulties accessing services), and Communication (e.g., limited communication between medical and early intervention providers, and between providers and families). Although these three themes were shared by medical and early intervention providers, the differing perspectives of each produced subthemes unique to the two professional fields.ConclusionsEarly intervention services can limit the neurodevelopmental deficits experienced by young children with SCD; however, most children with SCD do not receive these services. The perspectives of early intervention and medical providers highlight several potential solutions to increase early intervention utilization among young children with SCD. 
546 |a EN 
690 |a sickle cell 
690 |a early intervention 
690 |a developmental 
690 |a cognitive 
690 |a occupational therapy 
690 |a physical therapy 
690 |a Pediatrics 
690 |a RJ1-570 
655 7 |a article  |2 local 
786 0 |n Frontiers in Pediatrics, Vol 12 (2024) 
787 0 |n https://www.frontiersin.org/articles/10.3389/fped.2024.1366522/full 
787 0 |n https://doaj.org/toc/2296-2360 
856 4 1 |u https://doaj.org/article/fc598380a1ce4b868c972bcf8b977ce7  |z Connect to this object online.