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

Br J Haematol. 2010 Sep;150(5):610-3. doi: 10.1111/j.1365-2141.2010.08271.x. Epub 2010 Jun 15.

Abstract

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 19.6%, 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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Chest Syndrome / etiology
  • Adult
  • Anemia, Sickle Cell / complications
  • Anemia, Sickle Cell / therapy*
  • Critical Care*
  • Female
  • Humans
  • Intensive Care Units
  • Length of Stay / statistics & numerical data
  • Male
  • Middle Aged
  • Multiple Organ Failure / etiology
  • Retrospective Studies
  • Treatment Outcome
  • Young Adult