Unmet legal and social advocacy needs of children with sickle cell disease: Implications for health care payer costs

Rajan A. Sonik, Sarah Teasdale, Susan L. Parish, Maria Champigny and Philippa G. Sprinz

Children and Youth Services Review, 2018, vol. 84, issue C, 76-81

Abstract: Previous studies of advocacy needs faced by children and families have not differentiated needs that require attorney involvement (“legal advocacy needs”) from needs best addressed by social workers or lay advocates (“social advocacy needs”). Studies have also not examined the relationship between either type of need and health care costs. We developed a novel, replicable process to differentiate between legal advocacy needs and social advocacy needs. We then collected cross-sectional data from a sample of 52 children with sickle cell disease who were at least 1year of age, a population with high advocacy needs and high health care costs. Mean annual health care costs to payers for children whose families had a least one legal advocacy need were $16,314, compared to $5552 for children in families with no legal advocacy needs (P=0.007). After adjusting for covariates, the presence of a legal advocacy need was associated with $12,040 more in health care costs to payers (P=0.02). Whether interventions to prevent and resolve legal advocacy needs can reduce health care costs by addressing the social determinants of health warrants future study.

Keywords: Anemia, sickle cell; Legal services; Social determinants of health; Health care costs (search for similar items in EconPapers)
Date: 2018
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Persistent link: https://EconPapers.repec.org/RePEc:eee:cysrev:v:84:y:2018:i:c:p:76-81

DOI: 10.1016/j.childyouth.2017.11.023

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