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Home > Patient & Family Resources > Health Library > Sickle Cell Crisis
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A sickle cell crisis is a painful episode that may begin suddenly in a person who has 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.
It isn't always possible to know what sets off a crisis. But triggers include dehydration, cold temperatures, infection, stress, and low oxygen intake.
Here are some tips for preventing a crisis.
Current as of:
April 29, 2021
Author: Healthwise StaffMedical Review: E. Gregory Thompson MD - Internal MedicineAdam Husney MD - Family MedicineMartin J. Gabica MD - Family MedicineMartin Steinberg MD - Hematology
Current as of: April 29, 2021
Author: Healthwise Staff
Medical Review:E. Gregory Thompson MD - Internal Medicine & Adam Husney MD - Family Medicine & Martin J. Gabica MD - Family Medicine & Martin Steinberg MD - Hematology
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