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Early sickle cell disease intervention may lower stroke risk

Medical Xpress - Cardiology

Bone marrow transplantation (BMT) can potentially cure sickle cell disease, an inherited and painful blood disorder, but because of its potential drawbacks and costs, patients and caregivers often face the difficult decision of whether to undergo the procedure.

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Researchers identify safety of a potential new treatment to manage complications from sickle cell disease

Medical Xpress - Cardiology

A drug approved to treat pulmonary arterial hypertension may be effective at managing hypertension and end-organ damage in patients with sickle cell disease, according to a new study published in Lancet Haematology.

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Study Reveals Research Gaps on Acute Pancreatitis in Sickle Cell Disease

HCPLive

A systematic review found a higher prevalence of acute pancreatitis in individuals with the HbSS genotype, though a meta-analysis could not be performed.

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Hematology Month in Review: March 2024

HCPLive

Our March 2024 month-in-review in hematology features updates to the anemia pipeline, the latest research in sickle cell disease, and the role of SGLT2 inhibition on hematologic outcomes.

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Abstract TP147: Assessment of Inter-Rater Reliability of Fazekas Scoring on Magnetic Resonance Imaging in Patients With Sickle Cell Disease

Stroke Journal

Background:White matter disease is a common phenomenon in patients with sickle cell disease, that has been linked to cognitive impairment. However, there is no standardized approach for quantification of the cerebral disease burden. However, its utility in sickle cell disease has not yet been established.

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COVID-19 Vaccination Shows Favorable Risk-Benefit in Sickle Cell

HCPLive

A study from the ASH Research Network reports positive antibody response and tolerability after mRNA vaccination in people with sickle cell disease.

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Keli Coleman, MD: Predictors of Hospitalization, Return Visits in Children with SCD

HCPLive

Keli Coleman, MD, discusses findings from her research about the role of pain scores and opioids in predicting hospitalization and return visits in children with sickle cell disease and uncomplicated pain crises.