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About 3,570 results

ALLMedicine™ Sickle Cell Anemia Center

Research & Reviews  1,084 results

Changes in Hydroxyurea Use Among Youths Enrolled in Medicaid With Sickle Cell Anemia Af...
https://doi.org/10.1001/jamanetworkopen.2023.4584
JAMA Network Open; Reeves SL, Peng HK et. al.

Mar 25th, 2023 - Youths with sickle cell anemia (SCA) are at risk of pain crises, stroke, and early death. Complications can be reduced by the oral disease-modifying medication hydroxyurea, and in 2014, the National Heart, Lung, and Blood Institute published revis...

Hydroxyurea underused in youth with sickle cell anemia
https://www.mdedge.com/pediatrics/article/262046/hematology/hydroxyurea-underused-youth-sickle-cell-anemia
Marcia Frellick

Mar 24th, 2023 - Even after endorsement in updated guidelines, hydroxyurea is substantially underused in youth with sickle cell anemia (SCA), new research indicates. SCA can lead to pain crises, stroke, and early death.

TCD screening and spending among children with sickle cell anemia.
https://doi.org/10.37765/ajmc.2023.89333
The American Journal of Managed Care; Reeves SL, Ng S et. al.

Mar 23rd, 2023 - National guidelines recommend that children with sickle cell anemia receive annual transcranial Doppler (TCD) screening to assess stroke risk. Our objectives were to estimate the rate of TCD screening among privately insured children with sickle c...

Hydroxyurea treatment for sickle cell anemia during pregnancy and lactation: Current ev...
https://doi.org/10.1002/phar.2793
Pharmacotherapy Dong M, Ware RE et. al.

Mar 18th, 2023 - Sickle cell anemia (SCA) is a life-threatening genetic condition contributing to high-risk pregnancies affecting both the mother and fetus. With improved management of children with SCA, this life-threatening hematological disorder has evolved int...

Brain BOLD and NIRS response to hyperoxic challenge in sickle cell disease and chronic ...
https://doi.org/10.1016/j.mri.2023.03.002
Magnetic Resonance Imaging; Vu C, Bush A et. al.

Mar 17th, 2023 - Congenital anemias, including sickle cell anemia and thalassemia, are associated with cerebral tissue hypoxia and heightened stroke risks. Recent works in sickle cell disease mouse models have suggested that hyperoxia respiratory challenges can id...

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Guidelines  1 results

Cardiovascular function and treatment in β-thalassemia major: a consensus statement fro...
https://doi.org/10.1161/CIR.0b013e31829b2be6
Circulation Pennell DJ, Udelson JE et. al.

Jun 19th, 2013 - This aim of this statement is to report an expert consensus on the diagnosis and treatment of cardiac dysfunction in β-thalassemia major (TM). This consensus statement does not cover other hemoglobinopathies, including thalassemia intermedia and s...

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Drugs  6 results see all →

Clinicaltrials.gov  164 results

Risk Clinical Stratification of Sickle Cell Disease in Nigeria, Assessment of Efficacy/Safety of Hydroxyurea Treatment
https://clinicaltrials.gov/ct2/show/NCT02149537

Mar 9th, 2023 - The vast majority of births with sickle cell disease (SCD) occur in Africa and 90% are thought to die before the age of five. Hydroxyurea (HU) is the only drug approved by the FDA for the treatment of sickle cell anemia. Although HU is used to tre...

A Study of IMR-687 in Adult Participants With Sickle Cell Anemia (Homozygous HbSS or Sickle-β0 Thalassemia)
https://clinicaltrials.gov/ct2/show/NCT03401112

Mar 8th, 2023 - This is a proof-of-concept study in adult SCA participants, ages 18 to 55 years old, to examine the safety, tolerability, and pharmacokinetic (PK), as well as the potential pharmacodynamic (PD) effects and clinical efficacy, of IMR-687 across a ra...

Kidney Function in Sickle Cell Anemia
https://clinicaltrials.gov/ct2/show/NCT03277547

Mar 6th, 2023 - Sickle cell disease is a severe monogenic disorder which affects approximately 80,000 patients in the US. It is characterized by a vasculopathy with involvement of multiple organs and resulting in complications such as ischemic stroke, pulmonary h...

Sickle Cell Anemia WE CARE
https://clinicaltrials.gov/ct2/show/NCT03716726

Feb 27th, 2023 - Social determinants of health (SDoH)-the conditions in which people are born, grow, work, live, and age-are key drivers of health and health disparities. Children with medical complexity are particularly at-risk given their high healthcare need an...

Dissemination and Implementation of Stroke Prevention Looking at the Care Environment
https://clinicaltrials.gov/ct2/show/NCT04173026

Feb 21st, 2023 - The Dissemination and Implementation of Stroke Prevention Looking at the Care Environment (DISPLACE) study is a multi-center, national, National Heart, Lung and Blood Institute (NHLBI)-funded grant to look at the real-world implementation of strok...

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News  153 results

Hydroxyurea underused in youth with sickle cell anemia
https://www.mdedge.com/pediatrics/article/262046/hematology/hydroxyurea-underused-youth-sickle-cell-anemia
Marcia Frellick

Mar 24th, 2023 - Even after endorsement in updated guidelines, hydroxyurea is substantially underused in youth with sickle cell anemia (SCA), new research indicates. SCA can lead to pain crises, stroke, and early death.

Sickle Cell Disease Patients Miss Out on Decades of Life
https://www.medpagetoday.com/hematologyoncology/hematology/103597

Mar 17th, 2023 - A cohort study of Medicare and Medicaid beneficiaries with sickle cell disease (SCD) showed a life expectancy of just 52.6 years, well below that of the general population. And among SCD patients, survival varied by sex and insurance status. Men, ...

SCD meds: Why such ‘slow uptake’?
https://www.mdedge.com/hematology-oncology/article/261838/anemia/scd-meds-why-such-slow-uptake
Myles Starr

Mar 16th, 2023 - Hydroxyurea (HU) is a safe, effective drug for treating sickle cell disease (SCD), first approved for this condition by the U. S.

High Price for Gene Therapy ― But Cost-Effective in Sickle Cell
https://www.medscape.com/viewarticle/985411

Dec 12th, 2022 - NEW ORLEANS — A gene therapy recently made headlines for becoming the most expensive pharmaceutical ever launched — the price tag was $3.5 million for a one-off treatment with etranacogene dezaparvovec (Hemgenix) for hemophilia B. A gene therapy f...

Children with sickle cell anemia not getting treatments, screening
https://www.mdedge.com/pediatrics/article/258116/hematology/children-sickle-cell-anemia-not-getting-treatments-screening
Marcia Frellick

Sep 21st, 2022 - Fewer than half of children aged 2-16 years with sickle cell anemia are receiving recommended annual screening for stroke, a common complication of the disease, according to a new Vital Signs report from the Centers for Disease Control and Prevent.

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Patient Education  20 results see all →