抗yta引起的急性溶血性输血反应。

Q4 Medicine
M Raos, N Thornton, M Lukic, B Golubic Cepulic
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引用次数: 5

摘要

许多抗yta患者接受多次输注Yt(a+)红细胞(rbc)而无不良反应。然而,抗yta与溶血性输血反应有关。抗体鉴定通常确定抗体的特异性及其临床意义,当涉及临床显著抗体时,证明抗原阴性血的血液需求是合理的。有时,抗体的特异性具有不同的意义。临床意义的变异性是抗yta的一个特点,可能会影响这类患者的临床管理。本病例报告了一例83岁女性抗yta、d -C、-Leab和-HI患者因严重尿路出血和发热入院的不相容输血的结果。患者在紧急医疗事件中输注了1个交叉配型不相容的A、Yt(A +)、D-、C-、E-、S-红细胞单位。在此期间,患者表现出寒战、颤抖和心动过速。血红蛋白和红细胞压积下降。溶血的实验室参数,如总胆红素、直接胆红素和乳酸脱氢酶,都增加了。经临床及实验室评价,认为患者为抗yta所致急性溶血性输血反应。患者成功地接受了退烧药、抗组胺药和皮质类固醇治疗。尿路出血停止。此外,经肠外补铁可改善贫血,无需进一步输血。免疫血液学2021;37:13-17。许多抗yta患者接受多次输注Yt(a+)红细胞(rbc)而无不良反应。然而,抗yta与溶血性输血反应有关。抗体鉴定通常确定抗体的特异性及其临床意义,当涉及临床显著抗体时,证明抗原阴性血的血液需求是合理的。有时,抗体的特异性具有不同的意义。临床意义的变异性是抗yta的一个特点,可能会影响这类患者的临床管理。本病例报告了一例83岁女性抗yta、d -C、-Leab和-HI患者因严重尿路出血和发热入院的不相容输血的结果。患者在紧急医疗事件中输注了1个交叉配型不相容的A、Yt(A +)、D -、C -、E -、S -红细胞单位。在此期间,患者表现出寒战、颤抖和心动过速。血红蛋白和红细胞压积下降。溶血的实验室参数,如总胆红素、直接胆红素和乳酸脱氢酶,都增加了。经临床及实验室评价,认为患者为抗yta所致急性溶血性输血反应。患者成功地接受了退烧药、抗组胺药和皮质类固醇治疗。尿路出血停止。此外,经肠外补铁可改善贫血,无需进一步输血。免疫血液学2021;37:13-17。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Acute hemolytic transfusion reaction caused by anti-Yta.

Many patients with anti-Yta receive multiple transfusions of Yt(a+) red blood cells (RBCs) with no ill effects. However, anti-Yta has been implicated in hemolytic transfusion reactions. Antibody identification typically determines specificity of antibodies and their clinical significance to justify blood requirements for antigen-negative blood when clinically significant antibodies are involved. Occasionally, specificity of antibody is of variable significance. Variability in clinical significance is a characteristic of anti-Yta that may affect the clinical management of such patients. This case reports the outcome of an incompatible transfusion in an 83-year-old female patient with anti-Yta, -D, -C, -Leab, and -HI who was admitted to the hospital for a severe urinary tract hemorrhage and fever. The patient was transfused with 1 crossmatch-incompatible group A, Yt(a+), D-, C-, E-, S- RBC unit in an emergency medical event. During that time, the patient exhibited chills, shivering, and tachycardia. Decreases in hemoglobin and hematocrit were noted. Laboratory parameters for hemolysis, such as total bilirubin, direct bilirubin, and lactate dehydrogenase, were increased. Based on clinical and laboratory evaluation, it was concluded that the patient had an acute hemolytic transfusion reaction caused by anti-Yta. The patient was successfully treated with antipyretics, antihistamines, and corticosteroids. Urinary tract hemorrhaging was stopped. Anemia was additionally improved with parenteral iron supplementation, and further transfusion was not required. Immunohematology 2021;37:13-17.

Many patients with anti-Yta receive multiple transfusions of Yt(a+) red blood cells (RBCs) with no ill effects. However, anti-Yta has been implicated in hemolytic transfusion reactions. Antibody identification typically determines specificity of antibodies and their clinical significance to justify blood requirements for antigen-negative blood when clinically significant antibodies are involved. Occasionally, specificity of antibody is of variable significance. Variability in clinical significance is a characteristic of anti-Yta that may affect the clinical management of such patients. This case reports the outcome of an incompatible transfusion in an 83-year-old female patient with anti-Yta, -D, -C, -Leab, and -HI who was admitted to the hospital for a severe urinary tract hemorrhage and fever. The patient was transfused with 1 crossmatch-incompatible group A, Yt(a+), D–, C–, E–, S– RBC unit in an emergency medical event. During that time, the patient exhibited chills, shivering, and tachycardia. Decreases in hemoglobin and hematocrit were noted. Laboratory parameters for hemolysis, such as total bilirubin, direct bilirubin, and lactate dehydrogenase, were increased. Based on clinical and laboratory evaluation, it was concluded that the patient had an acute hemolytic transfusion reaction caused by anti-Yta. The patient was successfully treated with antipyretics, antihistamines, and corticosteroids. Urinary tract hemorrhaging was stopped. Anemia was additionally improved with parenteral iron supplementation, and further transfusion was not required. Immunohematology 2021;37:13–17.

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来源期刊
Immunohematology
Immunohematology Medicine-Medicine (all)
CiteScore
1.30
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