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摘要:
Drug-induced immune hemolytic anemia (DIIHA) is commonly attributed to cephalosporins. Ceftriaxone is the most frequently administered cephalosporin in patients with sickle cell disease. We present a pediatric patient with severe DIIHA (hemoglobin < 2 g/dl) who survived. Since DIIHA often goes undiagnosed until late in the course, vigilance of DIIHA minimizes unnecessary diagnostic tests and therapies. DIIHA likely remains under-recognized in all patient subpopulations due to its rarity and overlapping presentations with other conditions. Distinction between exacerbation of chronic hemolysis and new onset of acute hemolysis poses a unique challenge in patients with sickle cell disease. A thorough analysis is warranted to better identify factors within the pediatric sickle cell population that may increase the predisposition for DIIHA, particularly due to ceftriaxone.
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篇名 Drug-Induced Hemolytic Anemia: A Fatal Complication Further Under-Recognized in Sickle Cell Disease
来源期刊 血液病期刊(英文) 学科 医学
关键词 SICKLE Cell HEMOLYTIC ANEMIA Blood Bank Pathology
年,卷(期) 2017,(3) 所属期刊栏目
研究方向 页码范围 79-85
页数 7页 分类号 R5
字数 语种
DOI
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研究主题发展历程
节点文献
SICKLE
Cell
HEMOLYTIC
ANEMIA
Blood
Bank
Pathology
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研究来源
研究分支
研究去脉
引文网络交叉学科
相关学者/机构
期刊影响力
血液病期刊(英文)
季刊
2164-3180
武汉市江夏区汤逊湖北路38号光谷总部空间
出版文献量(篇)
110
总下载数(次)
0
总被引数(次)
0
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