|
|
| You are here: DOH Home » EHSPHL Home » PHL Home » NBS Home »Publications | Search | Employees |
| Splenic Sequestration Crisis | |
Splenic Sequestration Crisis
WHAT IS THE SPLEEN AND WHAT DOES IT DO?
In sickle cell anemia the spleen usually does not work after 4-6 months of age. It has been damaged by the sickled red blood cells (RBC's) and is not able to remove bacteria from the blood. This means that bacteria can grow in the blood and cause septicemia or blood poisoning (infection of the blood). Some children with sickle cell anemia normally have enlarged (big) spleen. This is usually seen up to age 5 years. Spleen enlargement is rare after age 5 - by this age, the spleen is usually shriveled up and therefore you are not able to feel it. Children with Hemoglobin Sickle C disease (SC disease - a milder form of sickle cell disease) may have a big spleen, but this does not happen until that are about 4 years of age or older. Also, the spleen functions more normally in Sickle C disease.
WHAT IS SPLENIC SEQUESTRATION? (SPLEEN CRISIS)When sickled cells block the blood vessels leading out of the spleen, blood stays in the spleen instead of flowing through it. This causes the spleen to get bigger. When this happens the blood count (hemoglobin and hematocrit) falls and the spleen gets very large and easy to feel. This is called splenic sequestration crisis (or "spleen crisis"). Splenic sequestration can sometimes be painful.
WHAT ARE THE SYMPTOMS OF SPLENIC SEQUESTRATION?Your child may experience any of the following symptoms:
•••• A child can have a seriously low blood count without many symptoms. Sometimes the only symptoms is that he/she is not as active as usual.
WHO CAN GET SPLENIC SEQUESTRATION?Infants and young children with sickle cell anemia who are between the ages of 2 months and 4 years are at greatest risk of splenic sequestration and blood poisoning. Sequestration crisis can occur in older children with SC disease and Sickle Beta-Plus Thalassemia. In these cases, the spleen remains enlarged or has the capability to enlarge.
IS SPLENIC SEQUESTRATION SERIOUS?Any enlargement of the spleen must be monitored. Parents should be taught how to feel for their child's spleen at their regular check-up visit. They need to know how their child's spleen usually feels so that when he/she seems sick, they can feel the spleen to see if it is bigger. Acute splenic sequestration crisis can be serious and a potentially life-threatening problem if the spleen suddenly enlarges with a large drop in the blood count. The child needs to see a doctor immediately. When the spleen gradually gets bigger over several weeks, the blood count does not change much and therefore it may not be as serious.
WHAT IS THE TREATMENT FOR SEQUESTRATION SERIOUS?A blood transfusion is given if the blood count is dangerously low. Minor episodes of splenic sequestration are common. You will notice moderate increases in spleen size associated with a decrease in hemoglobin levels. These minor episodes usually resolve spontaneously, but require monitoring of spleen size and blood counts. If a child experiences several episodes of splenic sequestration, surgery to remove the spleen may be considered.
CAN SPLENIC SEQUESTRATION HAPPEN MORE THAN ONCE?Yes. An infant or child that has had one episode of splenic sequestration is likely to have other episodes. Copyright & Disclaimer
DISCLAIMER TDH does not endorse any of the products, vendors, consultants, or documentation referenced in this website. Any mention of vendors, products, or services is for informational purposes only. TDH does not collect or track personal information from its website visitors. Generic information from server logs may be used to track the number of hits to the site, and to find out what types of browser software are used by visitors. This information will be used only in aggregate form, and used solely for improving website design. |
DOH Home | Access Washington | Privacy Notice | Disclaimer/Copyright Information
|
Washington
State Department of Health Last
Update :
11/20/2006 09:39 AM
|