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Addressing Inconsistent Protocols for ED Physicians and Nurses
Hospital emergency departments have varying intake protocols for SCD patients, and some have no protocols at all, which creates confusion and challenges for patients seeking care. The Assistant Secretary for Health has released guidelines for the emergency treatment of Sickle Cell Disease but these are not often followed. As a result, many ED doctors and nurses are not trained in administering the proper medications or correctly diagnosing a patient’s symptoms. These issues can be compounded by racial bias and social stigmas towards patients seeking opioids.
As one idea, HHS could introduce an ongoing, nationwide training curriculum for nurses and doctors to provide a comprehensive review of SCD protocols and patient treatment. These programs could work in tandem with hospital networks and be piloted in major states. This program could include analyzing data to show the impact of training on patient outcomes or other data-driven approaches to improving care.
What data would be needed to help improve protocols for personnel in the Emergency Department?
Good Morning, Here is something I drafted a while back