Adult sickle cell disease: A five-year experience of intensive care management in a university hospital in Oman

Qutaiba Amir Tawfic, Rajini Kausalya, Dhuha Al-Sajee, Jyoti Burad, Ahmed K. Mohammed, Aravind Narayanan

Research output: Contribution to journalArticle

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Abstract

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 noninvasive 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.

Original languageEnglish
Pages (from-to)177-183
Number of pages7
JournalSultan Qaboos University Medical Journal
Volume12
Issue number2
Publication statusPublished - May 2012

Fingerprint

Oman
Sickle Cell Anemia
Critical Care
Intensive Care Units
Mortality
Acute Chest Syndrome
Artificial Respiration
Abnormal Hemoglobins
Sickle Hemoglobin
Noninvasive Ventilation
Hemofiltration
Inborn Genetic Diseases
Blood Transfusion
Hemoglobins
Odds Ratio
Confidence Intervals
Students

Keywords

  • Acute chest syndrome
  • Anemia
  • Oman
  • Sickle cell

ASJC Scopus subject areas

  • Medicine(all)

Cite this

Adult sickle cell disease : A five-year experience of intensive care management in a university hospital in Oman. / Tawfic, Qutaiba Amir; Kausalya, Rajini; Al-Sajee, Dhuha; Burad, Jyoti; Mohammed, Ahmed K.; Narayanan, Aravind.

In: Sultan Qaboos University Medical Journal, Vol. 12, No. 2, 05.2012, p. 177-183.

Research output: Contribution to journalArticle

Tawfic, Qutaiba Amir ; Kausalya, Rajini ; Al-Sajee, Dhuha ; Burad, Jyoti ; Mohammed, Ahmed K. ; Narayanan, Aravind. / Adult sickle cell disease : A five-year experience of intensive care management in a university hospital in Oman. In: Sultan Qaboos University Medical Journal. 2012 ; Vol. 12, No. 2. pp. 177-183.
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