• Hemoglobinopathies Neurocognitive Risk in Sickle Cell Disease: Utilizing Neuropsychology Services to Manage Cognitive Symptoms and Functional Limitations

    This review in the British Journal of Haematology focuses on neurologic factors that may impact disease severity and overall function in children and adults with sickle cell disease (SCD). The authors describe associations between neurocognition, demographic factors, and social determinants of health in people with SCD. "Integrating neuropsychology into multidisciplinary care for individuals with SCD," they assert, "can assist with identification and management of neurocognitive concerns, intervention development, individualized care plan development, and continued multidisciplinary research."

  • Hemoglobinopathies GRNDaD: Big Data and Sickle Cell Disease

    As the authors of this Blood Advances article note, the Globin Regional Data and Discovery (GRNDaD) registry, developed by sickle cell disease (SCD) healthcare providers from several US sites, will serve as a robust data collection tool for the Health Resources and Services Administration Sickle Cell Treatment Demonstration Program and the newly established National Alliance for Sickle Cell Centers. An important goal of GRNDaD, they explain, "is to identify genetic markers that will help predict outcomes and lead to a better understanding of the natural history of SCD in the modern era of novel therapies," to advance precision medicine in this setting.

  • Hemoglobinopathies The Impact of VO and VOCs

    Rethink Sickle Cell Disease, a patient-information website supported by Novartis, Inc, offers a whiteboard video and several slideshows (referencing current research) explaining how vaso-occlusion (VO) and vaso-occlusive crises (VOC) impact patients with sickle cell disease.

  • Hemoglobinopathies An Overview of Sickle Cell Disease (SCD) and the Impact of Hemoglobin S (Hbs) Polymerization, Anemia, and Hemolysis

    In 3 short videos offered on the SCD Silent Damage website, Andrew Campbell, MD, Director of the Children's National Comprehensive Sickle Cell Disease Program, reviews the prevalence, symptoms, and life impacts of sickle cell disease (SCD); the molecular and cellular processes that underlie sickling; and the role of anemia and hemolysis in SCD. A fourth video uses computer animation to illustrate how hemoglobin S polymerization initiates the pathologic changes and anemia that characterize SCD.

  • Hemoglobinopathies About Sickle Cell Disease

    The US Department of Health and Human Services' Office of Minority Health website offers patient-friendly information about sickle cell disease (SCD), along with current guidelines, research articles, webinars, and recent initiatives related to the management of SCD.

  • Hemoglobinopathies ‘Interesting’ Real-World Data on Sickle Cell Treatment From ASH

    In this short video posted by Healio and created by Marley V. Ghizzone of HemOnctoday, Matthew M. Heeney, MD, highlights interesting findings and trends in sickle cell disease research presented at the 63rd Americal Society of Hematology Annual Meeting and Exposition. Dr. Heeney is Associate Chief of Hematology and Director of the Sickle Cell Program at Boston Children's Hospital; and Associate Professor, Harvard Medical School.

  • Hemoglobinopathies Bone Marrow Transplant and Sickle Cell Disease

    In this 1-hour slide-based webinar, offered by the National Heart, Lung and Blood Institute (NHLBI) through the US Department of Health and Human Services Office of Minority Health, researchers review key findings from selected NHLBI- and National Cancer Institute–funded bone-marrow transplant trials, including those conducted by the Blood and Marrow Transplant Clinical Trials Network. The last presentation is followed by a brief Q&A session.

  • Hemoglobinopathies Research in Sickle Cell Disease: From Bedside to Bench to Bedside

    In their engaging review, researchers from the hematology/oncology division at the Children's National Medical Center, Washington, DC, and the Sickle Cell Branch of the National Heart, Lung and Blood Institute comment that sickle cell disease (SCD) "epitomizes the bidirectional translational research common to many other diseases … starting with a remarkable astute observation of the abnormally shaped red blood cells that motivated decades of bench research that have now translated into new drugs and genetic therapies." Similarly, they write, development of hydroxyurea was initiated by a pediatrician's clinical observation, and research into its molecular mechanism of action has led to development of new fetal hemoglobin (HbF) reactivating agents. Research into mechanisms underlying the transition from HbF to adult Hb is bearing fruit also, with the development of promising genetic therapies. The authors highlight key discoveries that exemplify ways that bidirectional bench-to-bedside research in SCD has contributed to new therapeutic options.

  • Hemoglobinopathies Genetic Therapies in Sickle Cell Disease

    This 1-hour slide-based webinar, offered by the National Heart, Lung and Blood Institute (NHLBI) through the US Department of Health and Human Services Office of Minority Health, provides an overview of genetic therapies for sickle cell disease (SCD). Activities of the Cure Sickle Cell Initiative, an NHLBI-led collaborative research effort to accelerate development of potentially curative genetic therapies for SCD, are highlighted.

  • Hemoglobinopathies Management of Sickle Cell Disease Complications Beyond Acute Chest Syndrome

    This review describes approaches to management of adults with SCD as well as the transition to adult care, highlighting older, newer, and pipeline agents. Management of a variety of complications in SCD—including CNS, musculoskeletal, cardiovascular, splenic, gastrointestinal, and genitourinary effects; aplastic crisis; and COVID-19 infection—is discussed.

  • Hemoglobinopathies Know and Tell

    The Kidney Cancer Association (KCA), an international nonprofit founded in 1990 by a group of patients and doctors in Chicago, provides grants, conducts annual research symposia, and engages in educational and patient advocacy programs. In partnership with the Sickle Cell Disease Association of America, the KCA has launched “Know and Tell,” a program that the KCA says aims “to raise awareness about sickle cell trait and its link to renal medullary carcinoma to promote early identification, proper care, and increasing positive outcomes for patients and families.”

  • Hemoglobinopathies Emergency Department Sickle Cell Care Coalition

    On its website, the American College of Emergency Physicians provides information about EDSC3, its Emergency Department Sickle Cell Care Coalition, created with the help of multiple public, private, and professional partners to optimize the delivery and performance metrics of evidence-based emergency care for patients with SCD in the United States. EDSC3 also disseminates relevant research findings to local, regional, and national stakeholders; provides patient and provider education about appropriate management of SCD-related pain; and supports patient advocacy and community outreach in this area.

  • Hemoglobinopathies THALIA Mobile App

    The Thalassemia International Foundation (TIF) introduced its free THALIA app in February. It can be downloaded to Apple and Android devices and is available in English, French, and German, with more languages to be added in the near future. The app enables users to organize medical and blood transfusion appointments; receive medication alerts; score disease symptoms, as well as pain and mood levels; monitor progress and share graphs; and read news and educational material from TIF.

  • Hemoglobinopathies Secure-SCD Registry

    A team of clinicians from the Medical College of Wisconsin has developed an online registry to monitor outcomes of COVID-19 in pediatric and adult patients with sickle cell disease across the United States. The registry contains only de-identified data, in accordance with HIPAA standards, and the data entered by providers caring for these patients are stored on secure servers. Data will be shared directly on covidsicklecell.org, through social media (@SickleCellWI), and in scholarly publications.

  • Hemoglobinopathies Cooley Anemia

    This up-to-date open-source document from StatPearls (available on the National Center for Biotechnology Information online bookshelf) is an excellent introduction to the etiology/epidemiology, diagnosis, and treatment of beta-thalassemia, also called Cooley anemia. Specific transfusion-related complications are highlighted.

  • Hemoglobinopathies Sickle Cell Disease CDE Highlight Summary

    Earlier in 2021, the Cure Sickle Cell Initiative (CureSCi) of the National Heart, Lung and Blood Institute (NHLBI) finalized the first set of set of core data elements, or CDEs, for investigations of genetic therapies for SCD. Its Sickle Cell Disease Genetic Studies Highlight Summary Document provides useful recommendations to investigators for evaluation of patients with SCD enrolled in clinical trials in this area, as well as for study domains including disease- and treatment-related events, assessments and examinations, treatment and intervention data, and outcomes and endpoints.

  • Hemoglobinopathies Hemoglobinopathies Project

    The APHL website offers access to informational webinars on alpha and beta thalassemia; oral sessions on detecting and reporting alpha thalassemia in newborns; and presentations highlighting current best practices for hemoglobinopathy screening, confirmation, and follow-up. APHL’s Newborn Screening Hemoglobinopathies Workgroup is also available to answer emailed screening-related questions, with a 1-week turnaround.

  • Hemoglobinopathies Cooley’s Anemia Foundation Website

    This is an excellent resource for both patients and healthcare providers. Clinicians can access relevant webinars and grand rounds programs, as well as information about clinical trials and thalassemia-related medical research grants and fellowships. Patients and caregivers can read in-depth information about thalassemia and its management; find treatment centers; explore physician Q&A articles on specific aspects of this illness; and view patient stories. Educational brochures are available as downloadable PDFs.

  • Hemoglobinopathies Hemoglobinopathies: Current Practices for Screening, Confirmation and Follow-Up

    This document provides guidance on hemoglobinopathy laboratory testing and follow-up technique, in support of early detection of hemoglobin disorders. It includes an overview of laboratory structure and discusses algorithms for testing, reporting, and follow-up from several programs in the US.

  • Hemoglobinopathies NIH: Sickle Cell Disease

    This resource contains comprehensive patient-education information and links to NIH-sponsored clinical trials. There is also a section for healthcare professionals, with research updates and tips (on hydroxyurea, pain management, healthy living) to share with patients.

  • Hemoglobinopathies Evidence-Based Management of Sickle Cell Disease: Expert Panel Report, 2014

    These science-based guidelines for best-practice care were developed by a multicenter panel of healthcare professionals selected by NHLBI’s leadership. The guidelines highlight commonly encountered issues in SCD, such as routine health maintenance, detection and treatment of SCD acute and chronic complications and comorbidities, and indications for and monitoring of hydroxyurea and blood transfusion therapy.

  • Hemoglobinopathies Thalassemia

    Multimedia resources for patients, offering fact sheets, educational materials, webinars, and personal stories about thalassemia. For healthcare professionals, current virtual grand rounds and webinars on various aspects of thalassemia management.


  • Hemoglobinopathies The Year’s Best in Sickle Cell Disease

    This brief but intriguing roundup in The Hematologist, a publication of the American Society of Hematology, highlights cutting-edge clinical trials of the past year focused on gene therapy for sickle cell disease.

  • Hemoglobinopathies Sickle Cell Disease

    Updated for 2021, this GeneReviews® e-book provides comprehensive, up-to-date information about sickle cell disease (SKD) diagnosis, supportive care, and treatment options, as well as SKD-related genetic testing and counseling.

  • Hemoglobinopathies American Society of Hematology (ASH) Sickle Cell Disease Initiative: Resources for Clinicians

    Comprehensive multimedia information for clinicians, including current research, management guidelines and toolkits, and patient education resources.

  • Hemoglobinopathies Expert Opinions for Specific Non-malignant Hematologic Diseases

    Learn more about European clinicians’ perspective on management of sickle cell disease and thalassemia during the COVID-19 pandemic, with recommendations from the European Hematology Association.