Exchange Transfusion, Whole Blood
"Exchange Transfusion, Whole Blood" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Repetitive withdrawal of small amounts of blood and replacement with donor blood until a large proportion of the blood volume has been exchanged. Used in treatment of fetal erythroblastosis, hepatic coma, sickle cell anemia, disseminated intravascular coagulation, septicemia, burns, thrombotic thrombopenic purpura, and fulminant malaria.
Descriptor ID |
D005078
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MeSH Number(s) |
E02.095.135.469
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Exchange Transfusion, Whole Blood".
Below are MeSH descriptors whose meaning is more specific than "Exchange Transfusion, Whole Blood".
This graph shows the total number of publications written about "Exchange Transfusion, Whole Blood" by people in this website by year, and whether "Exchange Transfusion, Whole Blood" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2006 | 0 | 1 | 1 |
2007 | 0 | 1 | 1 |
2014 | 0 | 1 | 1 |
2020 | 0 | 1 | 1 |
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Below are the most recent publications written about "Exchange Transfusion, Whole Blood" by people in Profiles.
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Sunlight for the prevention and treatment of hyperbilirubinemia in term and late preterm neonates. Cochrane Database Syst Rev. 2021 07 06; 7:CD013277.
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The rise and fall of heterologous transfusion. J Anesth Hist. 2020 09; 6(3):127-132.
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Effectiveness of red blood cell exchange, partial manual exchange, and simple transfusion concurrently with iron chelation therapy in reducing iron overload in chronically transfused sickle cell anemia patients. Transfusion. 2016 07; 56(7):1707-15.
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Back to the future: the renaissance of whole-blood transfusions for massively hemorrhaging patients. Surgery. 2014 May; 155(5):883-6.
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Sickle cell disease caused by Hb S/Qu?bec-CHORI: treatment with hydroxyurea and response. Pediatr Blood Cancer. 2007 Aug; 49(2):207-10.
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Successful mobilization and transplantation of filgrastim mobilized hematopoietic stem cells in sickle cell-hemoglobin C disease. Bone Marrow Transplant. 2006 Jun; 37(11):1065-6.
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Dural venous sinus thrombosis in a patient with sickle cell disease: case report and literature review. Am J Hematol. 2006 Apr; 81(4):290-3.
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Fetal and neonatal hematologic parameters in red cell alloimmunization: predicting the need for late neonatal transfusions. Fetal Diagn Ther. 1993 May-Jun; 8(3):161-4.
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Chronic relapsing thrombotic thrombocytopenic purpura in infants with large von Willebrand factor multimers during remission. J Pediatr. 1992 Jan; 120(1):49-53.
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Exchange transfusion in premature newborns: effect of maturity on thyrotropin and thyroxine responses. Endocrinol Exp. 1987 Dec; 21(4):269-73.