This clinical study aims to improve pain management for individuals with sickle cell disease who are experiencing vaso-occlusive crisis and/or acute chest syndrome while in intensive care. Sickle cell disease is an inherited blood disorder where red blood cells become crescent-shaped and can block blood vessels, causing severe pain episodes. The study focuses on how the kidneys process morphine, which is commonly used to treat severe pain in these patients.
The research evaluates how well the kidneys filter blood (called glomerular filtration) and how this affects morphine processing in the body. By measuring kidney function using iohexol clearance (a reference method) and comparing it to a kidney function estimation tool (CKD-Epi score), researchers hope to determine when standard morphine doses might not provide adequate pain relief for certain patients.
Understanding the relationship between kidney function and morphine effectiveness could help doctors identify which patients need higher initial doses of pain medication. This would allow for more personalized pain management strategies for people with sickle cell disease during painful crises, potentially improving treatment outcomes and patient comfort.



France