| Literature DB >> 25308571 |
Lori E Crosby1,2, Lisa M Shook2,3, Russell E Ware2,3,4, William B Brinkman2,5,6.
Abstract
Clinical trials have demonstrated hydroxyurea's efficacy in improving health outcomes for children with sickle cell anemia (SCA) who have medical complications. New NHLBI clinical guidelines will recommend offering hydroxyurea to young patients regardless of clinical severity. Shared decision making may be an effective approach for implementing this practice change. Decision aids that help patients/parents feel empowered to make this decision and help providers feel comfortable in discussing hydroxyurea as a preventive treatment may facilitate shared discussions between families and providers. We recommend six strategies providers can use to facilitate these discussions while decision aids and tools are being developed. Pediatr Blood Cancer 2015;62:184-185.Entities:
Keywords: decision‐making; guidelines; pediatrics; sickle cell anemia; therapeutics
Mesh:
Substances:
Year: 2014 PMID: 25308571 PMCID: PMC5278638 DOI: 10.1002/pbc.25124
Source DB: PubMed Journal: Pediatr Blood Cancer ISSN: 1545-5009 Impact factor: 3.167