Transfusion management of sickle cell disease.

No abstract is available for this paper.

• Publication year

  1993

• Venue

  Blood

• Publication date

  Unknown publication date

• Fields of study

  Medicine

• Identifiers
  DOI 10.1182/blood.v81.5.1109.bloodjournal8151109PMID 8443373
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Alloantibody responses in multiply transfused sickle cell patients.

  2008cited by this paper
• Increasing Whole Blood Oxygen Affinity During Rapid Exchange Transfusion: a Potential Hazard

  2003cited by this paper
• Perioperative management for cholecystectomy in sickle cell disease.

  1993cited by this paper
• The declining risk of post-transfusion hepatitis C virus infection.

  1992cited by this paper
• The risk of transfusion-transmitted infection.

  1992cited by this paper
• Neurologic events after partial exchange transfusion for priapism in sickle cell disease.

  1992cited by this paper
• A modified transfusion program for prevention of stroke in sickle cell disease.

  1992cited by this paper
• The use of transcranial ultrasonography to predict stroke in sickle cell disease.

  1992cited by this paper
• Hepatitis C virus infection in post-transfusion hepatitis. An analysis with first- and second-generation assays.

  1992cited by this paper
• Hydroxyurea: effects on hemoglobin F production in patients with sickle cell anemia.

  1992cited by this paper
• Less intensive long-term transfusion therapy for sickle cell anemia and cerebrovascular accident.

  1992cited by this paper
• Stroke in sickle cell disease: demographic, clinical, and therapeutic considerations.

  1991cited by this paper
• Bone marrow transplantation for sickle cell anemia.

  1991cited by this paper
• Sickle cell vaso-occlusion.

  1991cited by this paper
• HEPATITIS C VIRUS INFECTION IN POST-TRANSFUSION HEPATITIS - AN ANALYSIS WITH FIRST - AND SECOND - GENERATION ASSAYS

  1991cited by this paper
• Hepatitis B virus: a comprehensive strategy for eliminating transmission in the United States through universal childhood vaccination. Recommendations of the Immunization Practices Advisory Committee (ACIP).

  1991cited by this paper
• Transfusion-related chronic liver disease in sickle cell anemia.

  1991cited by this paper
• Vascular occlusion in sickle cell disease: current concepts and unanswered questions.

  1991cited by this paper
• Beyond hemoglobin polymerization: the red blood cell membrane and sickle disease pathophysiology.

  1991cited by this paper
• A randomized controlled trial of recombinant interferon-alpha in chronic hepatitis C in hemophiliacs.

  1991cited by this paper
• Increased blood requirements during long-term transfusion therapy for sickle cell disease.

  1991cited by this paper
• Evaluation of screened blood donations for human immunodeficiency virus type 1 infection by culture and DNA amplification of pooled cells.

  1991cited by this paper
• The effect of radiological contrast media in animal models of experimental thrombosis.

  1991cited by this paper
• Management of pregnancy in sickle cell syndromes.

  1991cited by this paper
• Platelets, coagulation, and fibrinolysis in sickle cell disease: their possible role in vascular occlusion.

  1991cited by this paper
• High risk of recurrent stroke after discontinuance of five to twelve years of transfusion therapy in patients with sickle cell disease.

  1991cited by this paper
• Use of continuous flow erythrocytapheresis in pregnant patients with sickle cell disease

  1991cited by this paper
• Contrast media-related thromboembolic risks: effects of blood mixed with contrast media in contact with angiographic catheters.

  1991cited by this paper
• Pain in sickle cell disease. Rates and risk factors.

  1991cited by this paper
• Problems of chronic transfusion in sickle cell disease

  1991cited by this paper
• Problems in transfusion therapy.

  1990cited by this paper
• Acute transfusion reactions.

  1990cited by this paper
• Alloimmunization in sickle cell anemia and transfusion of racially unmatched blood.

  1990cited by this paper
• Long-term management of splenic sequestration in children with sickle cell disease.

  1990cited by this paper
• Red Cell Alloantibodies in Patients with Thalassemia

  1990cited by this paper
• Transfusion reactions in thalassemia. A survey from the Cooleycare programme. The Cooleycare Cooperative Group.

  1990cited by this paper
• Clinical significance of white cell antibodies in febrile nonhemolytic transfusion reactions

  1990cited by this paper
• Transmission of HIV by transfusion of screened blood.

  1990cited by this paper
• The treatment of Cooley's anemia.

  1990cited by this paper
• Transfusion of racially unmatched blood.

  1990cited by this paper
• Incidence of red cell antibodies after multiple blood transfusion

  1990cited by this paper
• Modified method of exchange transfusion in sickle cell disease

  1990cited by this paper
• Transfusion and alloimmunization in sickle cell disease. The Cooperative Study of Sickle Cell Disease.

  1990cited by this paper
• The sickle erythrocyte in double jeopardy: autoxidation and iron decompartmentalization.

  1990cited by this paper
• The variable expression of sickle cell disease is genetically determined.

  1990cited by this paper
• An assay for circulating antibodies to a major etiologic virus of human non-A, non-B hepatitis.

  1990cited by this paper
• Treatment of Cooley's anemia.

  1990cited by this paper
• Detection of antibody to hepatitis C virus in prospectively followed transfusion recipients with acute and chronic non-A, non-B hepatitis.

  1989cited by this paper
• Mortality in children and adolescents with sickle cell disease. Cooperative Study of Sickle Cell Disease.

  1989cited by this paper
• Hepatitis C: and miles to go before we sleep.

  1989cited by this paper
• Isolation of a cDNA clone derived from a blood-borne non-A, non-B viral hepatitis genome.

  1989cited by this paper
• Transfusion Management of Patients with Sickle Cell Disease a

  1989cited by this paper
• Complications of plasma exchange

  1989cited by this paper
• Increased incidence of hepatitis B markers in children with sickle-cell anemia

  1989cited by this paper
• Newborn Screening for Sickle Cell Disease and Other Hemoglobinopathies

  1989cited by this paper
• Exposure of patients to human immunodeficiency virus through the transfusion of blood components that test antibody-negative.

  1989cited by this paper
• Frequencies of hepatitis B, delta and human immune deficiency virus markers in multitransfused Saudi patients with thalassaemia and sickle-cell disease.

  1989cited by this paper
• Treatment of chronic hepatitis C with recombinant interferon alfa. A multicenter randomized, controlled trial.

  1989cited by this paper
• Prophylactic red‐cell transfusions in pregnant patients with sickle cell disease. A randomized cooperative study

  1989cited by this paper
• Recombinant interferon alfa therapy for chronic hepatitis C. A randomized, double-blind, placebo-controlled trial.

  1989cited by this paper
• Splenic phagocytic function in children with sickle cell anemia receiving long-term hypertransfusion therapy.

  1989cited by this paper
• Leg ulcers in patients with sickle cell disease.

  1989cited by this paper
• Newborn screening for sickle cell disease and other hemoglobinopathies.

  1989cited by this paper
• Prophylactic red-cell transfusions in pregnant patients with sickle cell disease. A randomized cooperative study.

  1988cited by this paper
• Immunogenicity of hepatitis B vaccine in children with sickle cell anemia.

  1988cited by this paper
• Beneficial effect of blood transfusion in children with sickle cell chest syndrome.

  1988cited by this paper
• Elective Cholecystectomy in Children with Sickle Hemoglobinopathies: Successful Outcome Using a Preoperative Transfusion Regimen

  1988cited by this paper
• Citrate toxicity during massive blood transfusion.

  1988cited by this paper
• Is there treatment for sickle cell anemia?

  1988cited by this paper
• Sickle cell states and the anaesthetist

  1988cited by this paper
• Risk of alloimmunization and delayed hemolytic transfusion reactions in patients with sickle cell disease.

  1988cited by this paper
• Hepatitis B vaccine in sickle-cell anemia.

  1988cited by this paper
• A new approach to neocyte transfusion: Preliminary report

  1988cited by this paper
• Iron-chelating therapy.

  1988cited by this paper
• Sickle Cell Chronic Lung Disease: Prior Morbidity and the Risk of Pulmonary Failure

  1988cited by this paper
• Membrane-associated sickle hemoglobin: a major determinant of sickle erythrocyte rigidity.

  1987cited by this paper
• Transfusion and exchange transfusion in sickle cell anaemias, with particular reference to iron metabolism.

  1987cited by this paper
• Viscosity of mixtures of sickle and normal red cells at varying hematocrit levels

  1987cited by this paper
• Experience with donors matched for minor blood group antigens in patients with sickle cell anemia who are receiving chronic transfusion therapy

  1987cited by this paper
• Painful sickle cell crises precipitated by stopping prophylactic exchange transfusions.

  1987cited by this paper
• Life threatening sickle chest syndrome treated with extracorporeal membrane oxygenation.

  1987cited by this paper
• Urological complications of sickle cell disease in a pediatric population.

  1987cited by this paper
• Leukocyte depletion of red cell units at the bedside by transfusion through a new filter

  1987cited by this paper
• Estimates of need for transfusions during hypertransfusion therapy in sickle cell disease.

  1986cited by this paper
• Bacteremia in sickle hemoglobinopathies.

  1986cited by this paper
• The incidence of development of irregular red cell antibodies in patients with sickle cell anemia

  1986cited by this paper
• Red cell alloimmunization in sickle cell disease

  1986cited by this paper
• Frozen storage of 11 units of sickle cell red cells for autologous transfusion of a single patient

  1986cited by this paper
• Acute chest syndrome in children with sickle cell disease. A retrospective analysis of 100 hospitalized cases.

  1986cited by this paper
• Broadening the base of a rare donor program by targeting minority populations

  1986cited by this paper
• Prophylaxis with oral penicillin in children with sickle cell anemia. A randomized trial.

  1986cited by this paper
• A Potential Hazard

  1986cited by this paper
• Cerebrovascular accident during a delayed hemolytic transfusion reaction in a patient with sickle cell anemia.

  1986cited by this paper
• Exchange

  1985cited by this paper
• Acute splenic sequestration in homozygous sickle cell disease: natural history and management.

  1985cited by this paper
• Long‐term cryopreservation of red cells from patients with sickle cell disease

  1985cited by this paper
• Liver Involvement in Sickle Cell Disease

  1985cited by this paper
• Intracranial hemorrhage in children with sickle cell disease.

  1985cited by this paper
• Vascular occlusion and infarction in sickle cell crisis and the sickle chest syndrome.

  1985cited by this paper
• Sickle erythrocyte adherence to vascular endothelium. Morphologic correlates and the requirement for divalent cations and collagen-binding plasma proteins.

  1985cited by this paper

• Functional biomarkers for sickle cell disease

  2024cites this paper
• 5607225 ADDITION OF THERAPEUTIC PLASMA EXCHANGE TO RED CELL EXCHANGE IMPROVES OUTCOMES OF FAT EMBOLISM SYNDROME IN SICKLE CELL DISEASE

  2023cites this paper
• 5597311 THE EFFECT OF MUSIC AND DANCE AS FORMS OF PHYSICAL ACTIVITY ON THE HEALTH STATUS OF PEOPLE WITH SICKLE CELL DISEASE: A SYSTEMATIC REVIEW OF THE LITERATURE

  2023cites this paper
• Managing the Cerebrovascular Complications of Sickle Cell Disease: Current Perspectives

  2023cites this paper
• 5567917 COST COMPARISON OF TRANSFUSION CHOICES IN OMAN FOR PATIENTS SUFFERING FROM SICKLE CELL DISEASE

  2023cites this paper
• A retrospective study for association between post‐transfusion hemoglobin S level and pre‐transfusion hemoglobin S level at the next scheduled transfusion

  2023cites this paper
• Global burden of transfusion in sickle cell disease.

  2023cites this paper
• Comprehensive guide to managing a chronic automated red cell exchange program in sickle cell disease

  2022cites this paper
• Management of acute chest syndrome in patients with sickle cell disease: a systematic review of randomized clinical trials

  2022cites this paper
• Incidence of Red Cell Antibody Formation Following Massive Transfusion Protocol: Experience of a Single Institution

  2022cites this paper
• Therapeutic approach to pediatric patients with acute chest syndrome: national multicenter survey of non invasive ventilation (NIV) and transfusion.

  2021cites this paper
• Pre-sedation Assessment

  2021cites this paper
• Ex Vivo Activation of Red Blood Cell Senescence by Plasma from Sickle-Cell Disease Patients: Correlation between Markers and Adhesion Consequences during Acute Disease Events

  2021influential citation
• Automated RBC Exchange has a greater effect on whole blood viscosity than manual whole blood exchange in adult patients with sickle cell disease

  2020cites this paper
• Delayed Hemolytic Transfusion Reaction in a Sickle Cell Disease Patient: A Case Report

  2020cites this paper
• Preclinical Evaluation of a Novel Lentiviral Vector Driving Lineage-Specific BCL11A Knockdown for Sickle Cell Gene Therapy

  2020cites this paper
• Assessment of Vitamin D Level and Osteoporosis in Children with Sickle Cell Anemia

  2020cites this paper
• Blood Transfusion Frequency and Indications in Yemeni Children with Sickle Cell Disease

  2020cites this paper
• Identification of Clinical and Laboratory Parameters Associated with the Development of Acute Chest Syndrome during Vaso-Occlusive Episodes in Children with Sickle Cell Disease: A Preliminary Step before Assessing Specific and Early Treatment Strategies

  2019cites this paper
• Transfusion Therapy in Sickle Cell Disease

  2019cites this paper
• Simple chronic transfusion therapy, a crucial therapeutic option for sickle cell disease, improves but does not normalize blood rheology: What should be our goals for transfusion therapy?

  2018cites this paper
• Effect of Sex Hormones and Prolactin on Sickle Cell Erythrocytes Polymerization in PortHarcourt, Rivers State, Nigeria

  2018cites this paper
• Oxygen‐dependent flow of sickle trait blood as an in vitro therapeutic benchmark for sickle cell disease treatments

  2018cites this paper
• Vascular access for red blood cell exchange

  2018cites this paper
• Whole‐exome sequencing of sickle cell disease patients with hyperhemolysis syndrome suggests a role for rare variation in disease predisposition

  2018cites this paper
• Early Noninvasive Ventilation and Nonroutine Transfusion for Acute Chest Syndrome in Sickle Cell Disease in Children: A Descriptive Study

  2018cites this paper
• Guidelines on red cell transfusion in sickle cell disease. Part I: principles and laboratory aspects

  2017cites this paper
• Guidelines on red cell transfusion in sickle cell disease Part II: indications for transfusion

  2017cites this paper
• Alloimmunisation in Sickle Cell Disease Presenting As Haemolytic Crisis

  2017cites this paper
• Sickle Cell Disease: A Brief Update.

  2017cites this paper
• Alloimmunisation and nephropathy in sickle cell disease patients in Jeddah, Saudi Arabia

  2017cites this paper
• Iron in neurodegenerative disorders: being in the wrong place at the wrong time?

  2017cites this paper
• Anti-Toxoplasma gondii antibodies in patients with beta-hemoglobinopathies: the first report in the Americas

  2017cites this paper
• Transfusion Therapy in Children With Sickle Cell Disease.

  2017cites this paper
• Alloimmunization in Patients with Sickle Cell Disease and Thalassemia: Experience of a Single Centre in Oman

  2017cites this paper
• Magnetic resonance imaging in pediatric sickle cell anemia

  2016cites this paper
• Unique aspects of red blood cell transfusion in pediatric patients

  2016cites this paper
• Management of sickle cell disease: challenges and risks of transfusion

  2016cites this paper
• Evidence of benefits from using fresh and cryopreserved blood to transfuse patients with acute sickle cell disease

  2016cites this paper
• Examination of Reticulocytosis among Chronically Transfused Children with Sickle Cell Anemia

  2016cites this paper
• Prophylactic red blood cell exchange may be beneficial in the management of sickle cell disease in pregnancy

  2015cites this paper
• Pattern and prevelence of alloimmunization in multiply transfused patients with sickle cell disease in Nigeria

  2015cites this paper
• Surgical management of osteonecrosis of the femoral head in patients with sickle cell disease.

  2015cites this paper
• Hematopoietic Stem Cell Transplantation in Adult Sickle Cell Disease: Problems and Solutions

  2015cites this paper
• How we treat delayed haemolytic transfusion reactions in patients with sickle cell disease

  2015cites this paper
• Manifestaciones cardiovasculares de anemia de células falciformes

  2015cites this paper
• EVALUATION OF IRON STATUS AMONG SUDANESE PATIENTS WITH SICKLE CELL DISEASE RECEIVING CHRONIC RED BLOOD CELL TRANSFUSION

  2015cites this paper
• Sickle Cell Disease in Sub-Saharan Africa: Molecular Mechanisms Underlying Episodic Crises, Current and Emerging Therapeutic Strategies in Treatment

  2015cites this paper
• A rapid paper‐based test for quantifying sickle hemoglobin in blood samples from patients with sickle cell disease

  2015cites this paper
• Sickle Cell Disease – Current Treatment and New Therapeutical Approaches

  2015cites this paper
• Red Blood Cell Alloimmunization in Sickle Cell Disease Patients in Tanzania.

  2014cites this paper
• Hypertransfusion Therapy in Sickle Cell Disease in Nigeria

  2014cites this paper
• Sickle cell patients face death in the ICU*.

  2014cites this paper
• Pulmonary Disease BoarD reView manual management of acute Chest syndrome and other Pulmonary Complications of sickle Cell Disease

  2014cites this paper
• Computerized Physician Order Entry Improves Compliance With a Manual Exchange Transfusion Protocol in the Pediatric Intensive Care Unit

  2014cites this paper
• Genomic analyses of RH alleles to improve transfusion therapy in patients with sickle cell disease.

  2014cites this paper
• The acute chest syndrome of sickle cell disease

  2013cites this paper
• Post-transfusion and maternal red blood cell alloimmunization in Uganda

  2013cites this paper
• Effect of inositol hexaphosphate–loaded red blood cells (RBCs) on the rheology of sickle RBCs

  2013cites this paper
• Drug-loaded sickle cells programmed ex vivo for delayed hemolysis target hypoxic tumor microvessels and augment tumor drug delivery.

  2013cites this paper
• Comparison of automated red cell exchange transfusion and simple transfusion for the treatment of children with sickle cell disease acute chest syndrome

  2013cites this paper
• Red blood cell alloimmunization in sickle cell disease: prevalence in 2010

  2013cites this paper
• Red blood cell alloimmunization and antigen matching in sickle cell disease – the African perspective

  2012cites this paper
• Quantitative MRI analysis of salivary glands in sickle cell disease.

  2012cites this paper
• Sickle‐cell disease and the heart: review of the current literature

  2012cites this paper
• Efficacy of homologous inositol hexaphosphate‐loaded red blood cells in sickle transgenic mice

  2012influential citation
• The prevention and management of alloimmunization in sickle cell disease: the benefit of extended phenotypic matching of red blood cells

  2012cites this paper
• Guidelines for the Primary Prevention of Stroke: A Statement for Healthcare Professionals From the American Heart Association/American Stroke Association

  2011cites this paper
• Identification of RHCE and KEL alleles in large cohorts of Afro‐Caribbean and Comorian donors by multiplex SNaPshot and fragment assays: a transfusion support for sickle cell disease patients

  2011cites this paper
• Sickle Cell Disease (Exchange Transfusion)

  2011cites this paper
• How I treat acute chest syndrome in children with sickle cell disease.

  2011cites this paper
• CXCL1 and its receptor, CXCR2, mediate murine sickle cell vaso‐occlusion during hemolytic transfusion reactions

  2011cites this paper
• Factors that influence health-related quality of life in adolescents with sickle cell disease

  2011cites this paper
• Guidelines for the Primary Prevention of Stroke: A Guideline for Healthcare Professionals From the American Heart Association/American Stroke Association

  2011cites this paper
• Pharmacoeconomic Considerations in Treating Iron Overload in Patients with β-Thalassaemia, Sickle Cell Disease and Myelodysplastic Syndromes in the US

  2011cites this paper
• DORES OSTEO-ARTICULARES Um Caso da Doença da HbSC/alfa-talassémia

  2011cites this paper
• Hepatitis B virus infection in Nigerian children with sickle cell anaemia.

  2011cites this paper
• [Musculoskeletal pain: a case of disease HbSC/alpha-thalassemia].

  2011cites this paper
• Red blood cell alloimmunization in sickle cell disease patients in Uganda

  2010cites this paper
• A Palliative Care Approach in Treating Patients With Sickle Cell Disease Using Exchange Transfusion

  2010cites this paper
• A 49-year-old woman with acute respiratory failure.

  2010cites this paper
• Acute chest syndrome in sickle cell disease

  2010cites this paper
• Delayed Hemolytic Transfusion Reaction in Sickle Cell Disease

  2010cites this paper
• Best practices for transfusion for patients with sickle cell disease

  2009influential citation
• Introduction to antibodies and complement.

  2009cites this paper
• Sickle cell disease and stroke.

  2009cites this paper
• Molecular biology of the Rh system: clinical considerations for transfusion in sickle cell disease.

  2009cites this paper
• Current strategies for the management of children with sickle cell disease

  2009cites this paper
• Sickle cell disease and stroke Running Head: Left: VERDUZCO and NATHAN Right: SICKLE CELL DISEASE AND STROKE

  2009cites this paper
• Corticosteroids and increased risk of readmission after acute chest syndrome in children with sickle cell disease

  2008cites this paper
• [Stroke prevention in sickle-cell disease: results, hurdles and future perspectives].

  2008cites this paper
• Advances in clinical research in sickle cell disease

  2008cites this paper
• Derivation of a risk assessment tool for emergency department patients with sickle cell disease

  2008cites this paper
• Étude d ’ une cohorte de 206 patients drépanocytaires adultes transfusés : immunisation , risque transfusionnel et ressources en concentrés globulaires Study of 206 transfused sickle cell disease patients : Immunization , transfusion safety and red blood cell supply

  2008cites this paper
• The pharmacotherapy of sickle cell disease

  2008cites this paper
• A Single-Institution Experience With Treatment of Severe Acute Chest Syndrome: Lack of Rebound Pain With Dexamethasone Plus Transfusion Therapy

  2008cites this paper
• Chapter 29 – Managing Pain during Pregnancy and Lactation

  2008cites this paper
• Cholecystectomy in sickle cell disease patients: is there more acute chest syndrome after laparoscopy? A case controlled study.

  2008cites this paper
• Perioperative transfusion of patients with sickle cell disease undergoing surgery at the University Hospital of the West Indies (UHWI).

  2008cites this paper
• Acute myocardial infarction in sickle cell disease: a systematic review.

  2008cites this paper