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Patients with sickle cell disease are nearly half as likely to report satisfaction in the care they received at an emergency department as they are from their primary care provider, according to a new study.
The findings, based on a one-time survey of adults and adolescents with the inherited blood disease who reported to EDs with acute pain issues, shows the effect a lack of emphasis on quality, individualized care for sickle cell patients may have on their response to symptoms.
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