• Br. J. Haematol. · Sep 2010

    Outcome of adults with sickle cell disease admitted to critical care - experience of a single institution in the UK.

    • Kate Gardner, Cathy Bell, Jack L Bartram, Marlene Allman, Moji Awogbade, David C Rees, Max Ervine, and Swee L Thein.
    • Department of Haematological Medicine, King's College Hospital NHS Foundation Trust, Denmark Hill, London, UK.
    • Br. J. Haematol. 2010 Sep 1;150(5):610-3.

    AbstractSickle cell disease (SCD) patients are perceived to have a high mortality when admitted to the Critical Care Unit (CCU). We performed a retrospective analysis of all adult sickle admissions to CCU at a single centre over an 8-year period (1 January 2000 to 31 December 2007). Thirty-eight patients (14 male) were admitted 46 times to CCU; the commonest reasons for admission were acute chest syndrome (14, 30%), multi-organ failure (8, 17%) and planned post-elective surgery (7, 15%). CCU mortality for SCD patients was 19.6%, comparable to a CCU-wide mortality of 17.6% during the study period in the same institution. Re-admission to CCU was high (16% over the 8-year period) but did not increase mortality risk.

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