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Continuous Manual Exchange Transfusion for Patients with Sickle Cell Disease: An Efficient Method to Avoid Iron Overload
Published on: March 14, 2017
Adult Sickle Cell Disease: A Five-year Experience of Intensive Care Management in a University Hospital in Oman
Qutaiba Amir Tawfic1, Rajini Kausalya, Dhuha Al-Sajee
1Departments of Anaesthesia & Intensive Care and.
Insights
Acute chest syndrome is the primary reason for intensive care unit (ICU) admission in sickle cell disease (SCD) patients. Inotropic support or mechanical ventilation indicates a higher mortality risk for these patients.
Area of Science:
- Hematology
- Critical Care Medicine
- Genetics
Background:
- Sickle cell disease (SCD) is a prevalent inherited hemoglobinopathy in the Gulf region, including Oman.
- SCD complications frequently necessitate intensive care unit (ICU) admission.
- Understanding ICU admission drivers is crucial for managing SCD patients.
Purpose of the Study:
- To investigate the primary causes for ICU admission among adult SCD patients.
- To identify predictors of mortality in SCD patients admitted to the ICU.
Main Methods:
- Retrospective analysis of adult SCD patients (≥12 years) admitted to Sultan Qaboos University Hospital ICU.
- Data collected from January 1, 2005, to December 31, 2009.
- Analysis included reasons for admission, mortality rates, and impact of supportive measures.
Main Results:
- 56 ICU admissions occurred among 49 SCD patients.
- Acute chest syndrome (69.6%) was the leading cause of ICU admission, followed by painful crises (16.1%).
- Mortality rate was 16.1%; inotropic support and mechanical ventilation significantly predicted mortality.
Conclusions:
- Acute chest syndrome is the predominant reason for ICU admission in SCD patients.
- Inotropic support and mechanical ventilation are indicators of increased mortality risk in this population.
- Non-invasive ventilation, hemofiltration, and transfusions were not significant mortality predictors.
Objectives:
Sickle cell disease (SCD) is an inherited disease caused by an abnormal type of haemoglobin. It is one of the most common genetic blood disorders in the Gulf area, including Oman. It may be associated with complications requiring intensive care unit (ICU) admission. This study investigated the causes of ICU admission for SCD patients.
Methods:
This was a retrospective analysis of all adult patients ≥12 years old with SCD admitted to Sultan Qaboos University Hospital (SQUH) ICU between 1st January 2005 and 31st December 2009.
Results:
A total number of 49 sickle cell patients were admitted 56 times to ICU. The reasons for admission were acute chest syndrome (69.6%), painful crises (16.1%), multi-organ failure (7.1%) and others (7.2%). The mortality for SCD patients in our ICU was 16.1%. The haemoglobin (Hb) and Hb S levels at time of ICU admission were studied as predictors of mortality and neither showed statistical significance by Student's t-test. The odds ratio, with 95% confidence intervals, was used to study other six organ supportive measures as predictors of mortality. The need for inotropic support and mechanical ventilation was a good predictor of mortality. While the need for non-invasive ventilation, haemofiltration, blood transfusions and exchange transfusions were not significant predictors of mortality.
Conclusion:
Acute chest syndrome is the main cause of ICU admission in SCD patient. Unlike other supportive measures, the use of inotropic support and/or mechanical ventilation is an indicator of high mortality rate SCD patient.
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