ASCAT Conferences - Abstracts


Abstracts and Poster Presentations

Abstract submission is now closed, please see below a list of the chosen Abstracts.


Basic and Translational

6057305 Early Detection And Clinical Care For Sickle Cell Disorders: The African Research And Innovative Initiative For Sickle Cell Education (Arise)-Consortium On Newborn Screening In Africa (Consa) Newborn Screening Initiative In Kaduna State, Nigeria
6058894 Malaria Infection In Patients With Sickle Cell Disease In Nigeria: Association With Markers Of Hyposplenism
6083244 Pyruvate Kinase Thermostability Is Associated With Red Blood Cell Adhesion, Deformability And Oxygen Affinity In Patients With Sickle Cell Disease
6083283 Cryopreservation Of Sickle Red Blood Cells For Comparison Of Oxygenscan Parameters Between Laboratories To Enable Data Harmonization
6085930 Dynamic Sickling Assay (Dsa): Assessment Of Hemoglobin-Modifying Therapy Dose Response As A Function Of Oxygen Tension
6086151 Mechanism Of Neutrophil Activation  In Scd
6056792 Roxyscan: A Novel Method To Assess Red Blood Cell Resilience To Oxidative Stress In Sickle Cell Disease.
6060861 Discovering Novel Genetic Modifiers Of Haemoglobinopathies: A Large-Scale, Multi-Ethnic, Genome-Wide Association Study Within The Inherent Initiative
6060942 Co-Visualising The Impact Of Sickle Cell: How Can We Use Design Thinking To Investigate And Visualise The Impact Of Sickle Cell?
6070252 <B>Treatment Options For Sickle Cell Disease Patients In France: Transfusion Recommendations And Clinical Practices<|B>
6081428 Establishing Future Research Priorities For Sickle Cell Genomics Through A Priority Setting Partnership
6085030 Blood Transfusion In Pregnant Women With Sickle Cell Disease: A One-Year Retrospective Study
6085343 The Integrated Circulating Lncrna-Mirna-Mrna Network In Beta Thalassemia Patients
6055441 Co-Production Of A Theory-Based Toolbox Of Self-Management Interventions To Support Young Adults With Sickle Cell Disease (Scd) In Saudi Arabia
6056802 Establishing The First National Genomics Research Initiative For Sickle Cell Disorder In England
6073111 A Population-Oriented Genetic Scoring System To Predict Phenotype: A Pathway To Personalized Medicine In Iraqis With Beta-Thalassemia.
6085904 Hemoglobin Co-Arab Mimicking Hbss And Hbsc: A Case Report
5996184 Gene-Environmental Influence Of Space And Microgravity On Red Blood Cells With Sickle Cell Disease : The Time Is Now


Novel Therapies, Gene Therapies and Bone Marrow Transplant

6085456 Transfusion Independence After Exagamglogene Autotemcel In Patients With Transfusion-Dependent Β-Thalassemia
6062402 Safety And Efficacy Of L-Glutamine In Reducing The Frequency Of Vaso-Occlusive Crisis Among Patients With Sickle Cell Disease
6085472 Elimination Of Vaso-Occlusive Crises After Exagamglogene Autotemcel In Patients With Severe Sickle Cell Disease
6048493 Development Of Best-In-Class Gene Editing Therapy For Β-Hemoglobinopathies Using Innovative Transformer Base Editor (Tbe)
6061109 Ascent1 (Trial In Progress): A Phase 2 Trial To Evaluate The Efficacy And Safety Of Oral Decitabine—Tetrahydrouridine (Ndec) In Patients With Sickle Cell Disease
6083335 Evaluation Of The Real-World Use Of Crizanlizumab For People With Sickle Cell Disease:  A National Alliance Of Sickle Cell Centers Study
6084767 Safety And Efficacy Of Rm-001 (Autologous Hbg1|2 Promoter-Modified Cd34+ Hematopoietic Stem And Progenitor Cells) In Patients With Transfusion-Dependent Β-Thalassemia
6086122 The Effect Of Allogeneic Haematopoietic Stem Cell Transplantation On Sickle Cell Disease-Related Organ Damage: A Systematic Review And Meta-Analysis
6047774 Renal Functions Evolution Of 6 Sickle Cell Disease Patients Treated By L-Glutamine
Pharmaceutical Grade For 30 Months: A Real-World Study.
6083201 Hsct In Hemoglobinopathies: A Lebanese Experience Told By The European Arise Project
6051513 Understanding Genome-Wide Mutational Burden In Patients With Sickle Cell Disease: Experience In United Kingdom
6082070 Interim Report Of The Administration Of Hypoxic Red Blood Cells

To Patients With Transfusion-Dependent Hematologic Malignancies And Burns
6054171 Recurrence Of Alpha Thalassemia With High Hemoglobin H Levels Post-Transplant: A Case Study
6058058 Closing The Knowledge Gaps -Post Hct-Dubai Thalassemia Center Experience
6060966 The Hibiscus-Kids Study: A Single-Arm, Open-Label, Phase 1|2 Study To Evaluate The Pharmacokinetics And Safety Of Etavopivat In Pediatric Patients With Sickle Cell Disease


Artificial intelligence, deep learning and other technological advancements in hemoglobinopathies

6085810 Utilising Digital, Longitudinal Tracking Of Wearable Metrics And Patient-Reported Outcomes To Predict Vaso-Occlusive Crises In Sickle Cell Disease
6035523 The Diagnostic Accuracy Of A Deep-Learning-Trained Software System For Evaluating Liver Iron Concentration From Magnetic Resonance Images Of Patients With Inherited Transfusion Dependent Anemias In South Africa.
6074951 Use Of Machine Learning To Predict 30-Day Reutilization Of Care For Patients With Sickle Cell Disease Treated For Vaso-Occlusive Crisis
6077929 Outcome Of Retrospective Pediatric Feasibility Study With Artificial Intelligence (Ai) Based, Machine Learning (Ml) Tool Predicting The Individual Absolute Risk Of Acute Graft-Versus-Host Disease
6085225 The Sickle Cell And Thalassaemia Blood Group Genotyping Programme And The Development Of A Novel Blood Group Genotyping Array
6036647 Sickle Cell Trait E-Learning Counseling Program For Rural Health Department Nurses
6080928 Association Between Fetal Hemoglobin Parameters And Disease Severity In Sickle Cell Disease Patients In Tanzania.
6060664 Validation Of A Fully Automated Method Of Analysing Mr Images For Evaluation Of Liver Iron Concentration In A Population Of Thalassemia Major Patients Following Curative Stem Cell Transplantation In Lebanon
6082550 Applying Machine Learning To Detect Co-Inheritance Of Alpha-Thalassemia With Other Beta-Globin Gene Hemoglobinopathies
6085136 Utilizing Social Media Educational Videos To Disseminate Vital Information About Sickle Cell Disease To Parents: A Medical Education Project
6077976 Establishing Standard Of Care In Predicting Serious Complications For Patients Planned To Receive An Allogeneic Hematopoietic Stem Cell Transplantation


Clinical, public health and epidemiological studies

6061186 Treatment Of Sickle Cell Disease With Voxelotor Through The Uk Early Access To Medicines Scheme
6074996 Rise Up Campaign: Raising The Bar On Patient Involvement In Clinical Development
6032410 Efficacy, Safety And Pharmacokinetics Of A New, Ready To Use, Liquid Hydroxyurea In Children With Sickle Cell Anemia.
6052021 National Long-Term Follow-Up Of Children With Sickle Cell Disease Diagnosed By Newborn Screening In The Netherlands: Overview Of The Morbidity And Mortality
6083296 Cardiac Mechanics And Ventricular Dimensions In Children And Adolescents With Sickle Cell Disease
6054676 Global, Regional, And National Burden Of Thalassemia Disease: A Systematic Analysis Of The Global Burden Of Disease Study 2019
6072862 Key Factors In Prevention Of Stroke With Transcranial Doppler Velocities In Children With Sickle Cell Disease: Results From A Single Italian Center Experience
6085095 Clinical Sensory Testing For Neuropathic Pain And Health Related Quality Of Life In Young Patients With Sickle Cell Disease
6052063 Analysis Of Volatile Organic Compounds In Exhaled Air In Patients With Sickle Cell Disease During Vaso-Occlusive Episodes
6054155 Newborn Screening For Sickle Cell Disease, Implementation At The Hospital Materno Infantil Dr Manuel Pedro Azancot De Menezes, Angola
6058361 <B>Use Of Race And Ethnicity In Sickle Cell Disease Research <B>
6081386 Prevalence And Predictors Of Hydroxyurea Use Among Sickle Cell Disease Patients Attending Clinics In Tanzania
6085193 Clinical Profile And Evaluation Of Iron Overload In Transfusion-Dependent Thalassemia Patients From Cipto Mangunkusumo Hospital, Indonesia
6059844 A Community Outreach And Awareness Event For Sickle Cell Disease - How Well Is Sickle Cell Disease Understood?
6060720 Descriptive Epidemiological Study Of Adults With Sickle Cell Disease In Uk: Experience From 5 Years Of A Single-Centre In West London, United Kingdom
6061237 Understanding The Health Landscape Of Tribal Population In Central India: Assessing The Prevalence Of Thalassemia And Sickle Cell Anemia.
6062449 Genetic Variability In Pregnant Patients With Sickle Cell Disease In Luanda, Angola.
6078033 A "Centaur" (Β Chain Coding Gene With A Δ Promoter) "De Novo" Hb Variant Inducing High Hbf Production, Protects Against Dependent Blood Transfusion In A Predictable Case Of Severe Beta Thalassemia
6085227 Delineation Of The Molecular Basis Of Borderline Haemoglobin A2 In Malaysian Population
6060839 Rare Anaemia Disorders European Epidemiological Platform: From Public Health To Research Projects<B>
6048122 New Update Of The Spanish Registry Of Hemoglobinopathies And Rare Anemias. Sickle Cell Patients
6082702 The Pilot Study Of The Clingen Hemoglobinopathy Variant Curation Expert Panel
6083194 Recurrent Pulmonary Embolism During Acute Chest Syndrome In A Child With Sickle Cell Disease. What'S The Role Of Anticoagulation Therapy?
6085501 Outcome Of Administration Of Hydroxyurea On The Occurrence Of Pulmonary Hypertension Among Children With Sickle Cell Anaemia At Jos University Teaching Hospital, Jos, Nigeria
6085990 Characterising The Real-World Use Of Transfusion Therapy Among Patients With Sickle Cell Disease And As A Second Line To Hydroxyurea Treatment
6075184 The Natural History And Clinical Outcomes In Sickle Cell Disease: A Multi-Centre Uk Study
6085578 Newborn Screening For Sickle Cell Disease In Kaduna State, Nigeria: Building A Sustainable Primary Health Care (Phc) Model
6022788 Frequency And Predictors Of Hospitalisation Of Children With Sickle Cell Disease At Komfo Anokye Teaching Hospital
6060019 Sickle Cell Trait Prevalence In São Tomé E Príncipe: Starting Small To Unleash Sickle Cell Epidemiology In Lusophone Africa
6076256 Fat Embolism Syndrome In Sickle Cell Disease: Clinical, Laboratory And Radiological Features And Outcome.
6082358 The Readability And Quality Of Online Information On Sickle Cell Retinopathy For Patients
6083247 An Epidemiological Study Of Rh Phenotypes In Patients With Sickle Cell Disorder In Relation To The Blood Donor Population In The West Of Scotland.
6083294 Risk Factors, Types And Outcome Of Stroke Among Sickle Cell Disease Children Attended Public Hospitals, Khartoum, Sudan 2022.
6085413 Establishing Advanced Therapy Program For Sickle Cell Disease At Muhimbili University Of Health And Allied Sciences In Tanzania
6086121 Clinical Profiles Of Children With Sickle Cell Anaemia On Hydroxyurea And The Pattern Of Its Uptake: Experience From Jos University Teaching Hospital, North Central Nigeria
6086467 "Those That Can Heal, Can Harm"- Ceftriaxone Induced Hemolysis In Children With Sickle Cell Disease
6048965 Evaluating The Use Of Hydroxycarbamide In Children With Sickle Cell Disease: A Single-Centre Audit
6074643 The Systemic Blood Pressure Level In Sudanese Children With Sickle Cell Anemia In Fathelrahman El-Bashir Health Center
6076838 Awareness Of Sickle Cell Disease Among University Undergraduates In Nigeria: An Ecological Model Study In A Low-And Middle-Income Country Setting  <B><|B>
6082332 Investigating Publication Trends In Sickle Cell Retinopathy Over The Last 60 Years.
6082337 Automated Red Blood Cell Exchange Versus Manual Transfusion In Adult Patients With Sickle Cell Disease: A Brazilian Single Centre Experience
6082783 A Pilot Study Of The International Hemoglobinopathy Research Network (Inherent)
6085922 Assessment Of Sickle Cell Disease Among Undergraduates Of Tertiary Institutions In Kaduna State, Nigeria
6086164 Screening With Imaging And Non-Imaging Transcranial Doppler Screening In Children With Sickle Cell Anaemia In India
6058144 Trials In Progress: The Randomized, Double-Blind, Placebo-Controlled Phase 1 B Crosswalk-A And Phase 2A Crosswalk-C Trials - Crovalimab For The Treatment And Prevention Of Vasa-Occlusive Episodes In Sickle Cell Disease
6082446 Association Between Fetal Hemoglobin Parameters And Disease     Severity In Sickle Cell Disease Patients In Tanzania.
6082540 Prevalence And Determinants Of Progressive Kidney Disease Among  Patients  With Sickle Cell  Attending Muhimbili National Hospital
6086158 Platelet To Lymphocyte Ratio And Sickle Cell Nephropathy
6022815 Artherogenic Index Of Plasma (Aip) Of Pregnant Women Attending Barau Dikko Teaching Hospital And How Aip Affects Pregnant Sickle Cell Disease (Scd) Patients.
6085708 Relationship Between Platelet Counts, Mean Platelet Volume, Plateletcrit In Iron Deficiency Anemia And B-Thalassemia Major; A Comparative Study
6032547 Healthcare Professionals Involved In Sickle Cell Disease Management In Nigeria Needs: A Grounded Theory Approach
5943365 Spontaneous Epidural Hematoma: A Case Report Of Rare Crisis Of Sickle Cell Disease


Clinical, infection and nutritional deficiencies

6046197 Sickle Cell Disease And Gut Health - Prevalence Of Intestinal Parasites And Gut Microbiome Analysis In <C>Angolan Children
6040027 Antibiotic Prophylaxis Before Dental Procedures For Individuals With Sickle Cell Disease With Total Hip Replacement -- A Scoping Review
6047119 Identification Of Optimal Thalassemia Carrier Screening Strategies In The Setting Of Limited Public Resources
6065460 Long-Term Efficacy, Survival And Complications After Splenectomy In Transfusion-Dependent Beta-Thalassemia Patients
6045628 Burden Of Alloimmunization In Sickle Cell Disease Patients In Africa: A Systematic Review With Meta-Analysis
6085429 Analyzing Treatment Patterns And Clinical Outcomes Within The First 24 Hours Of Hospitalization In Patients With Sickle Cell Disease And Infection: Evidence From A Retrospective Cohort Study
6085513 Invasive Bacterial Infection In Children With Sickle Cell Anaemia In A Tertiary Hospital In South Eastern Nigeria.<B>
6085954 Phenotypic Variability Of Sickle Cell Disease In The Arabian Gulf: Influence Of Fetal Hemoglobin Among Kuwaiti And Omani Patients
6086186 Diagnosing Osteoporosis In Children With Transfusion-Dependent Thalassemia: Focus On Vertebral Compression Fractures And The Associated Factors
6078044 Co-Existence Of Sickle Cell Disease And Autoimmune Digestive Diseases. Report Of Three Pediatric Cases From Two Hospitals In Barcelona Area
6077245 The Need To Develop A Nutrition Protocol And Mobile Application For Scd In Nigeria
6085202 Sudden Bilateral Loss Of Vision In A 5-Year-Old Child Known To Have Sickle Cell Disease.


Ageing and end organ damage

6017055 Age-Related Transfusion Requirements In Hospitalized Patients With Sickle Cell Disease Taking Either Voxelotor Or Hydroxyurea


Health services and outcomes research including psychology

6024855 Impact Of A Peer-To-Peer Round Table Pilot Educational Program For Healthcare Professionals In Rural Ghana To Upscale Their Knowledge In The Management Of Sickle Cell Disease
6058521 A Multicenter, Retrospective Study On Real-World Experience Of Patients With Sickle Cell Disease Treated With Voxelotor
6061147 Follow Up Of Babies Identified Through Newborn Screening For
Sickle Cell Disease: Implementation Of A Nurse-Led Care Pathway
At A Teaching Hospital In Ghana
6057021 Finding Common Ground: A Pan-Disease Advisory Council To Uncover Shared Unmet Needs In Hemolytic Anemias
6061124 Using Community-Based Participatory Research And Human Centered Design To Develop Simulation Scenarios For Young Adults Living With Sickle Cell Disease
6070504 Healthcare Resource Use, Economic Burden And In-Patient Mortality In Patients With Alpha- And Beta-Thalassemia Compared To Matched Controls In The Real-World Setting
6083293 Mortality And Clinical Complications Among Patients With Transfusion-Dependent Β-Thalassemia In England
6083308 Mortality And Clinical Complications Among Patients With Sickle Cell Disease With Recurrent Vocs In England
6085032 Cerebral Blood Flow And Its Association With Cognition In Paediatric Patients With Sickle Cell Anaemia
6085385 Complementary And Integrative Medicine In Pediatric Patients With Sickle Cell Disease
6083327 "Do People Living With Sickle Cell Receive Fair Treatment For Pain In The Emergency Room?" Institutional Racism Changes Perceptions Of Justice.
6055466 How Is Fatigue Managed In Children And Young People With Sickle Cell Disease? A Qualitative Study
6061282 Principles For Implementation Of Sickle Cell Disease Point Of Care Newborn Screening Program In Sub-Saharan Africa
6061509 Leveraging Quality Improvement To Optimize Engagement Approaches That
Strengthen Multi-Stakeholder Partnerships In Sickle Cell Disease Transition
6061565 Sickle Cell Disease Newborn Screening: Parents' Experiences Of Receiving Positive Test Results At Korle Bu Teaching Hospital, Ghana
6075717 A Systematic Literature Review Of Biomarkers And Their Association With Clinical Outcomes In Sickle Cell Disease
6081452 Factors Affecting Adequate Pain Control In Patients With Sickle Cell Disease At Mwananyamala And Muhimbili Hospitals In
Dar Es Salaam
6083225 Developing A Structured Approach To Feedback For Sickle Cell Patients In East Midlands: Transitioning To The Picker Questionnaire
6083251 Patient Report Quality Of Life Measures In Sickle Cell: A Uk Multi -Center Study
6085434 Healthcare Resource Utilization Among Patients With Sickle Cell Disease With Recurrent Vaso-Occlusive Crises In England
6085442 Healthcare Resource Utilization Among Patients With Transfusion-Dependent Beta-Thalassemia In England
6085517 Quality Of Life And Psychiatric Symptoms At Baseline And After 7 Years Follow-Up Of Ghanaian Adults Living With Sickle Cell Disease
6055898 Specialist Sickle Cell Nursing Workforce: Current Level, The Impact On Patients & Clinicians, And What Needs To Happen
6060731 Empowering Healthcare Professionals And Patients Through The Sickle Cell Education Series: A Systematic Review Of An Innovative Online Teaching Platform
6061118 Unraveling Pain And Stress In Younger And Older Adults Living With Sickle Cell Disease
6081524 Evaluating The Quality Of Life Among Transfusion Dependent Thalassemia Patients Using The World Health Organization'S Quality Of Life Instrument (Whoqol-Bref)
6081979 Scr.Net Empowering Vision: The Sickle Cell Retinopathy Network'S Mission To Transform Care And Research
6034912 Development Of A Patient-Centered, Patient-Engaged Research Dissemination And Translation Model
6047995 Economic Burden Of Sickle Cell Anemia On Uninsured Patients: A Case Study From Muhimbili National Hospital, Tanzania
6073110 Study To Assess Patients' And Healthcare Workers' Needs Involved In Sickle Cell Disease Management
6073430 Health Technologies To Manage Scd Complications: Questionnaire-Based Prospective Study For Healthcare Facilities
6077412 Collaborative Approaches To Quality Improvement: A Darzi Fellowship In Sickle Cell Disease
6078030 Building A Better Path- Improving Sickle Cell Healthcare Transition With Engaging Workshops
6082688 Engaging Young People In A Transition Pathway -Creation Of A Digital  Resource
6085971 Empowering Teenagers With Sickle Cell Disease: Transforming Healthcare Transition Through Interactive Workshops.

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