Acute Pain
Volume 7, Issue 1 , Pages 1-3, May 2005

Sickle cell pain management meets technology: Everybody wins

  • Jason Sawyer

      Affiliations

    • Corresponding Author InformationTel.: +1 416 480 6100x2945; fax: +1 416 480 6039.

Acute Pain Service, Sunnybrook & Women's College Hospital, M3-200 Department of Anesthesia, 2075 Bayview Avenue, Toronto, Ont., Canada M4N 3M5

Received 1 March 2005; accepted 16 March 2005.

Summary 

Sickle cell disease is a chronic disease characterized by frequent exacerbations of its symptomatology. Intense pain is a hallmark of a sickle cell crisis, yet unfortunately, inadequate pain management in this population is well documented. Frequent visits to the Emergency Department (ED) by those in crisis expose them to several barriers that inhibit effective care, particularly pain management. Suspicion of drug seeking behaviour based on ethnicity or race, requests for specific drugs and doses, administration of large doses of opioid without relief, and a general lack of knowledge regarding pain management among healthcare professionals are some of these barriers. Using information technology, an effort was undertaken to simultaneously address many of the barriers to pain management for sickle cell crisis patients in the emergency department, and enhance the quality of pain management they receive.

Keywords: Sickle cell, Information technology, Pain management, Emergency department

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PII: S1366-0071(05)00008-2

doi:10.1016/j.acpain.2005.03.003

Acute Pain
Volume 7, Issue 1 , Pages 1-3, May 2005