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    Sickle cell disease: acute complications and management

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    Author
    Hodges, Ross
    Keyword
    Emergency Medical Services
    Acute Chest Syndrome
    Sickle Cell Disease
    Anaemia
    Clinical Management
    Journal title
    Journal of Paramedic Practice
    
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    URI
    http://hdl.handle.net/20.500.12417/755
    DOI
    10.12968/jpar.2011.3.11.608
    Abstract
    Abstract published with permission. Sickle cell disease is a genetic blood disorder resulting in the sickling of red blood cells (RBC) when exposed to certain conditions. Historically, sickle cell care has been poor and often delayed, but in recent years, several key publications have helped provide guidance and uniformity on how to manage acute crises, ensuring all patients receive a high level of care. The sickling of RBC can lead to acute complications, some of which are potentially life-threatening. The sickling can occur anywhere in the body, producing a wide array of symptoms. For this reason, it is paramount that prehospital clinicians conduct a thorough assessment and, where appropriate, initiate treatment prior to arrival at the hospital. The most common symptom that clinicians will need to manage is severe pain. Many patients will have an individualized treatment plan detailing how they are best managed following an acute crisis and where possible it should be followed.
    ae974a485f413a2113503eed53cd6c53
    10.12968/jpar.2011.3.11.608
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