A sickle cell crisis is a painful episode that may begin suddenly in a person with sickle cell disease.
A sickle cell crisis occurs when sickle-shaped red blood cells clump together and block small blood vessels that carry blood to certain organs, muscles, and bones. This causes mild to severe pain. The pain can last from hours to days. "Painful event" and "painful crisis" are other terms used to describe these episodes. Some people who have sickle cell disease have many painful events, while others have few or none.
The pain can happen in any part of the body. But the most common areas include the:
Treatment depends on the level of pain and how long it lasts. Sometimes, nonprescription, or over-the-counter, pain relievers such as ibuprofen can help. Other times, a person needs stronger pain relief medicine that is prescribed or given by a doctor. Some painful episodes may need IV therapy for fluids and powerful pain medicines, such as morphine, to ease the pain.
You can prepare for a crisis in advance by creating a pain management plan with your doctor. This plan should include not only the types of medicines you can take at home but also other actions you can take at home to relieve pain. Also, your plan helps you know when to call your doctor or go to a hospital.
For more information, see Sickle Cell Disease: Pain Management.
It isn't always possible to know what sets off a crisis, but triggers include dehydration, cold temperatures, infection, stress, and low oxygen intake.
You can help prevent a crisis by:
For more information, see Sickle Cell Disease: Staying Healthy.
|Primary Medical Reviewer||E. Gregory Thompson, MD - Internal Medicine|
|Specialist Medical Reviewer||Martin Steinberg, MD - Hematology|
|Last Revised||January 13, 2012|
To learn more visit Healthwise.org
© 1995-2012 Healthwise, Incorporated. Healthwise, Healthwise for every health decision, and the Healthwise logo are trademarks of Healthwise, Incorporated.