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Consensus Standards and Recommendations for Developmental and Cognitive Surveillance, Screening, and Evaluation in Sickle Cell Disease: Executive Summary From the National Alliance of Sickle Cell Centers Neurocognitive Workgroup

Pediatric Blood & Cancer·July 21
HematologyOncologyPediatricsPractice changingNeurocognitive ImpairmentNeurodevelopmental DisordersSickle Cell DiseaseExpert Consensus / Clinical Practice GuidelineMixed

Summary

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What was studied

Expert consensus standards and recommendations for neurodevelopmental and neurocognitive surveillance, screening, and evaluation across the lifespan in individuals with sickle cell disease (SCD), developed by the National Alliance of Sickle Cell Centers Neurocognitive Workgroup.

Key findings

The workgroup produced consensus-based standards, an accompanying clinical algorithm, and supplemental implementation guidance for identifying and supporting neurodevelopmental and neurocognitive difficulties in SCD across the lifespan; no quantitative outcome data are reported.

Study limitations

Recommendations are based on expert consensus rather than primary clinical trial evidence, which limits the strength of the evidence base. No sample size or comparative outcomes are reported in this executive summary format.

Clinical implications

Clinicians caring for patients with SCD should implement structured neurodevelopmental and neurocognitive surveillance and screening at regular intervals across the lifespan, following the published algorithm. Early identification and referral for support are emphasized as key goals.

Related Questions

Explore related topics

What neurocognitive screening tools are recommended for children with sickle cell disease?How often should cognitive surveillance be performed in adults with sickle cell disease?What interventions are available for neurodevelopmental difficulties in sickle cell disease?

Publication Details

Year
2026
Journal
Pediatric Blood & Cancer
Source
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