缺铁性贫血和地中海贫血共存的特点:铁治疗对红细胞参数和血红蛋白亚型的影响

ISRN Hematology Pub Date : 2014-03-12 eCollection Date: 2014-01-01 DOI:10.1155/2014/293216
Sarika Verma, Ruchika Gupta, Madhur Kudesia, Alka Mathur, Gopal Krishan, Sompal Singh
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引用次数: 39

摘要

背景。缺铁性贫血(IDA)与β地中海贫血(BTT)共存一直是研究的热点。然而,我国尚无研究评价铁治疗对合并IDA和BTT患者的效果。方法。在两年的时间里,纳入了30例合并IDA和BTT的患者。所有患者均进行全血细胞计数、血清铁研究,并使用BIORADTM血红蛋白检测系统进行地中海贫血筛查。患者接受适当剂量的口服铁治疗,为期20周,之后重复所有调查。采用适当的统计学方法对治疗前后资料进行比较。结果。除两名患者外,所有患者均为成年人,女性明显占优势。口服铁治疗组血红蛋白、红细胞指标改善有统计学意义(P < 0.05),血清铁、铁蛋白、HbA2水平变化有统计学意义(P < 0.001)。总铁结合能力水平显著降低。结论。本研究显示,缺铁性贫血在β地中海贫血特征患者中经常发生,这可能会混淆后者的诊断。因此,在怀疑有地中海贫血特征的患者中,应发现并纠正缺铁。
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Coexisting iron deficiency anemia and Beta thalassemia trait: effect of iron therapy on red cell parameters and hemoglobin subtypes.

Background. Coexistence of iron deficiency anemia (IDA) and beta thalassemia trait (BTT) has been the topic of few studies. However, no study from our country was found evaluating the effect of iron therapy in patients with concomitant IDA and BTT. Methods. Over a period of two years, 30 patients with concomitant IDA and BTT were included. All the patients had a complete blood count, serum iron studies, and thalassemia screening using BIORADTM hemoglobin testing system. The patients received oral iron therapy in appropriate dosages for a period of twenty weeks, after which all the investigations were repeated. Appropriate statistical methods were applied for comparison of pre- and posttherapy data. Results. All except two patients were adults with a marked female preponderance. Oral iron therapy led to statistically significant improvement in hemoglobin, red cell indices (P < 0.05), and marked change in serum iron, ferritin, and HbA2 levels (P < 0.001). There was a significant reduction in the total iron binding capacity levels. Conclusion. The present study shows the frequent occurrence of iron deficiency anemia in patients with beta thalassemia trait, which can potentially confound the diagnosis of the latter. Hence, iron deficiency should be identified and rectified in patients with suspicion of beta thalassemia trait.

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