TOTB: Sickle Cell Pain Crises

Sickle cell pain crises are a hallmark of sickle cell disease, presenting significant challenges and requiring swift, compassionate management from internal medicine residents. These painful episodes, driven by vaso-occlusive processes, can lead to severe discomfort and distress in patients, necessitating a comprehensive understanding of their pathophysiology and individualized treatment strategies. In this blog post, we will delve into the mechanisms behind sickle cell crises, key assessment techniques, and evidence-based approaches to pain management and crisis prevention, empowering you to provide empathetic and effective care for patients experiencing these debilitating events.