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ABSTRACT: Background
The management of acute and chronic pain for individuals living with sickle cell disease (SCD) is a clinical challenge. This reflects the paucity of clinical SCD pain research and limited understanding of the complex biological differences between acute and chronic pain. These issues collectively create barriers to effective, targeted interventions. Optimal pain management requires interdisciplinary care.Objective
These evidence-based guidelines developed by the American Society of Hematology (ASH) are intended to support patients, clinicians, and other health care professionals in pain management decisions for children and adults with SCD.Methods
ASH formed a multidisciplinary panel, including 2 patient representatives, that was thoroughly vetted to mini
SUBMITTER: Brandow AM
PROVIDER: S-EPMC7322963 | biostudies-literature | 2020 Jun
REPOSITORIES: biostudies-literature