Alloimmunization and hyperhemolysis in sickle cell disease
F Pirenne, C Pondarré - Hematology, 2023 - ashpublications.org
Alloimmunization against red blood cell antigens and delayed hemolytic transfusion reaction
(DHTR) are major barriers to transfusion in sickle cell disease (SCD). In SCD, DHTR is a …
(DHTR) are major barriers to transfusion in sickle cell disease (SCD). In SCD, DHTR is a …
Successful treatment with plasma exchange in life‐threatening hyperhemolytic syndrome unrelated to sickle cell disease.
A Shaulov, D Rund, D Filon, B Nachmias… - …, 2023 - search.ebscohost.com
Introduction: Hyperhemolytic syndrome (HHS) is a severe form of delayed transfusion
reaction primarily described in sickle cell anemia patients which is characterized by a …
reaction primarily described in sickle cell anemia patients which is characterized by a …
“Don't add fuel to the fire”-Hyperhemolysis Syndrome in a pregnant woman with compound Sickle cell disease/ß0-thalassemia-Case report and review of the literature
A Rihsling, H Simeunovic, S Sanchez, C Henny… - Acta …, 2023 - karger.com
Hyperhemolysis Syndrome (HHS) is a rare and severe post-transfusion complication
characterized by the destruction of both recipient and donor red blood cells (RBC). The …
characterized by the destruction of both recipient and donor red blood cells (RBC). The …
儿科住院拟输血患者意外抗体阳性结果分布及影响因素横断面研究
李正峰， 王佳， 陈萍， 甘珊， 李好， 段灵， 陈鑫， 杨柳春… - 临床输血与检验, 2023 - lcsxyjy.com
目的分析儿科住院患者意外抗体分布情况以及性别, 年龄, 输血史对患者意外抗体产生的影响.
方法采集4 345 例住院患者血液标本进行意外抗体筛查, 利用谱细胞对抗体初筛阳性标本进行 …
方法采集4 345 例住院患者血液标本进行意外抗体筛查, 利用谱细胞对抗体初筛阳性标本进行 …
[HTML][HTML] Delayed Hemolytic Transfusion Reaction With Hyperhemolysis Syndrome Due to Anti-M Alloantibody in Myelofibrosis: A Case Report
MS Alsoreeky, LK Lutfi, AA Altamimi, TH Haddad… - Cureus, 2023 - ncbi.nlm.nih.gov
Hyperhemolysis syndrome (HHS) and delayed hemolytic transfusion reaction (DHTR)
commonly occur in patients with sickle cell disease (SCD) and thalassemia, due to the need …
commonly occur in patients with sickle cell disease (SCD) and thalassemia, due to the need …
[HTML][HTML] Transfusion in sickle cell disease: Management of complications including iron overload
INTRODUCTION—Individuals with sickle cell disease (SCD) have chronic anemia that can
worsen abruptly for various reasons such as splenic sequestration or transient red cell …
worsen abruptly for various reasons such as splenic sequestration or transient red cell …
The management of fatal hyperhemolysis in a sickle cell anemia patient transfused in a remote Island in North Andaman
PPA Shahid, PS Shaiji, Y Hameed - Journal of Medical Society, 2023 - journals.lww.com
Hyperhemolysis following red cell transfusion is a potentially fatal complication in sickle cell
disease patients. Red cell alloimmunization can lead to a delayed hemolytic reaction further …
disease patients. Red cell alloimmunization can lead to a delayed hemolytic reaction further …
A Cross-sectional Study on the Distribution and Influencing Factors of Unexpected Antibody Positive Results in Pediatric Hospitalized Patients Planning to Receive …
LI Zhengfeng, W Jia, C Ping - JOURNAL OF CLINICAL TRANSFUSION AND … - lcsxyjy.com
Objective To analyze the distribution of unexpected antibodies of pediatric inpatients and the
impact of gender, age, and blood transfusion history on antibody production. Methods Blood …
impact of gender, age, and blood transfusion history on antibody production. Methods Blood …