Below are the best information and knowledge on the subject sickle cell crisis treatment compiled and compiled by our own team alltopus:
1. Sickle cell anemia – Diagnosis and treatment – Mayo Clinic
Date Submitted: 12/19/2020 06:05 PM
Average star voting: 4 ⭐ ( 46446 reviews)
Match with the search results: Management of sickle cell anemia is usually aimed at avoiding pain episodes, relieving symptoms and preventing complications. Treatments might include …. read more
2. Complications and Treatments of Sickle Cell Disease | CDC
Date Submitted: 06/17/2020 04:32 AM
Average star voting: 5 ⭐ ( 79200 reviews)
Summary: People with sickle cell disease (SCD) start to have signs of the disease during the first year of life, usually around 5 months of age. Symptoms and complications of SCD are different for each person and can range from mild to severe. Learn more.
Match with the search results: Another treatment, which can actually cure SCD, is a stem cell transplant (also called a bone marrow transplant); this procedure infuses healthy ……. read more
3. Sickle Cell Disease Treatment & Management: Approach Considerations, Hydroxyurea Therapy, Transfusion
Date Submitted: 11/15/2020 12:40 PM
Average star voting: 4 ⭐ ( 33550 reviews)
Summary: Sickle cell disease (SCD) and its variants are genetic disorders resulting from the presence of a mutated form of hemoglobin, hemoglobin S (HbS) (see the image below). The most common form of SCD found in North America is homozygous HbS disease (HbSS), an autosomal recessive disorder first described by Herrick in 1910.
Match with the search results: Vaso-occlusive crisis is treated with vigorous intravenous hydration and analgesics. Intravenous fluids should be of sufficient quantity to ……. read more
4. Sickle Cell Crisis: Symptoms, Causes, Treatment, Prevention
Date Submitted: 10/08/2019 08:00 PM
Average star voting: 5 ⭐ ( 91301 reviews)
Summary: Sickle cell crisis can be very painful and you never know when it might come on. Learn the symptoms, what to do when you have a crisis, and how you can help prevent it.
Match with the search results: You can also try a heating pad, hot bath, or a massage. Physical therapy may provide some relief, too. And don’t forget to tend to your mind….. read more
5. Sickle Cell Crisis
Date Submitted: 03/19/2021 04:28 PM
Average star voting: 4 ⭐ ( 79268 reviews)
Summary: Sickle cell disease (SCD) is a group of inherited red blood cell disorders affecting about 1 in 500 African American children and 1 in 36,000 Hispanic American children. SCD results in anemia and “sickle cell crisis” (SCC). The main clinical feature of sickle cell disease is the ”acute painful crisis,’’ which often requires hospitalization. The term “sickle cell crisis” is used to describe several acute conditions such as the vaso-occlusive crisis (acute painful crisis), aplastic crisis, splenic sequestration crisis, hyperhemolytic crisis, hepatic crisis, dactylitis, and acute chest syndrome. Other acute complications include pneumonia, meningitis, sepsis and osteomyelitis, stroke, avascular necrosis, priapism, and venous thromboembolism.
Match with the search results: Vaso-occlusive Crisis Management. Rapid pain assessment and initiation of analgesia should be undertaken promptly….. read more
6. Approach to Vaso-occlussive Crisis in Adults with Sickle Cell Disease
Date Submitted: 01/12/2021 06:18 AM
Average star voting: 3 ⭐ ( 65457 reviews)
Summary: The vaso-occlusive crisis, or sickle cell crisis, is a common painful complication of sickle cell disease in adolescents and adults. Acute episodes of severe pain (crises) are the primary reason that these patients seek medical care in hospital emergency departments. Frequently, however, the pain is incompletely treated. Despite advances in pain management, physicians are often reluctant to give patients adequate dosages of narcotic analgesics because of concerns about addiction, tolerance and side effects. It is important to recognize a pain crisis early, correct the inciting causes, control pain, maintain euvolemia and, when necessary, administer adequate hemoglobin to decrease the hemoglobin S level. The family physician and the hematologist must work together to treat acute pain episodes promptly and effectively, manage the long-term sequelae of chronic pain and prevent future vaso-occlusive crises.
Match with the search results: …. read more
7. Sickle cell disease – Treatment
Date Submitted: 11/07/2020 08:11 AM
Average star voting: 3 ⭐ ( 74675 reviews)
Summary: Read about the main treatments for sickle cell disease, including medications to prevent pain, blood transfusions and stem cell transplants.
Match with the search results: Nonnarcotic Analgesics for Mild Pain in Sickle Cell Disease ; Naproxen (Naprosyn). 500 mg initially, then 250 mg every 6 to 8 hours ; Fenoprofen ( ……. read more
8. Sickle Cell Disease | Sickle Cell Anemia | MedlinePlus
Date Submitted: 01/01/2021 04:40 AM
Average star voting: 3 ⭐ ( 93539 reviews)
Summary: Sickle cell disease (or sickle cell anemia) causes your body to produce abnormally shaped red blood cells. Learn about symptoms and treatment.
Match with the search results: Stem cell or bone marrow transplants are the only cure for sickle cell disease, but they’re not done very often because of the significant risks involved. Stem ……. read more
9. Sickle Cell Disease in Children
Date Submitted: 04/03/2020 06:12 PM
Average star voting: 3 ⭐ ( 78402 reviews)
Summary: Sickle cell disease is an inherited blood disorder that is present at birth. Children with SCD make an abnormal type of hemoglobin. This is the protein in red blood cells that carries oxygen to all parts of the body.
Match with the search results: The only cure for SCD is bone marrow or stem cell transplantation. Because these transplants are risky and can have serious side effects, they ……. read more
10. Sickle Cell Disease (for Teens) – Nemours KidsHealth
Date Submitted: 04/23/2020 01:58 AM
Average star voting: 5 ⭐ ( 83818 reviews)
Summary: Sickle cell disease is a blood disorder that makes red blood cells change shape and cause health problems. Find out more in this article for teens.
Match with the search results: Therapies to prevent pain episodes in SCD including hydroxyurea, L-glutamine, and others are discussed separately. (See “Hydroxyurea use in sickle cell disease” ……. read more