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 Rees, Max Ervine, Swee L. Thein

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    28 Citations (Scopus)

    Abstract

    P>Sickle 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 center dot 6%, comparable to a CCU-wide mortality of 17 center dot 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.
    Original languageEnglish
    Pages (from-to)610-613
    Number of pages4
    JournalBritish Journal of Haematology
    Volume150
    Issue number5
    DOIs
    Publication statusPublished - Sept 2010

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