首页> 外文期刊>The journal of maternal-fetal & neonatal medicine >Total dose iron dextran infusion versus oral iron for treating iron deficiency anemia in pregnant women: a randomized controlled trial
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Total dose iron dextran infusion versus oral iron for treating iron deficiency anemia in pregnant women: a randomized controlled trial

机译:总剂量铁葡聚糖输注对孕妇治疗缺铁性贫血的口服熨斗:随机对照试验

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Study objective: To test safety, efficacy, and cost-effectiveness of total dose infusion (TDI) of low molecular weight (LMW) iron dextran for treatment of iron deficiency anemia (IDA) during pregnancy in comparison to oral ferrous fumarate. Design: Prospective interventional randomized controlled trial (RCT). Design classification. Canadian Task Force II3. Setting: Antenatal clinic and causality unit of a tertiary care referral facility and University Hospital. Patients: A total 66 anemic pregnant women (hemoglobin level between 7-10 g/dl). Intervention: Administration of a LMW iron dextran as a TDI (group A) or Oral iron ferrous fumarate 60 mg elemental iron three times daily (group B) followed by remeasurement of hemoglobin after 4 weeks. Measures and main results: The main outcome measure was clinical and laboratory improvement of anemia after 4 weeks of starting the therapy. Both groups showed a significant clinical improvement of anemia 4 weeks post-therapy. However, the first improvement of symptoms was significantly faster in group A. Complete blood count (CBC) as well as all iron indices were improved in both groups after 4 weeks of therapy, but were significantly better in group A than B. Side effects in group B were mainly gastrointestinal (GIT) while one case of mild hypersensitivity to TDI and another one case of local reaction at the site of injection were reported in group A. Conclusions: It is concluded that despite being equally effective in improving both clinical and laboratory evidence of IDA, TDI allows iron restoration with a single dose faster than oral iron therapy with a reasonable safety profile. It is a good example of office one-stop therapy. Nevertheless, noninvasive selfusage at home is a clear advantage of the cheaper oral iron therapy which makes it the first choice for treating IDA in the second and third trimesters of pregnancy in tolerable cases.
机译:研究目的:测试低分子量(LMW)铁葡聚糖总剂量输注(TDI)的安全性,疗效和成本效益,与口服富马酸盐相比,妊娠期间孕缺血性贫血(IDA)。设计:前瞻性介入随机对照试验(RCT)。设计分类。加拿大特遣部队II3。设置:第三级护理转诊设施和大学医院的产前诊所和因果关系。患者:总共66例贫血妇女(7-10克/ DL之间的血红蛋白水平)。干预:将LMW铁葡聚糖作为TDI(A组)或口服铁铁料型60mg元素铁,每日三次(B组),然后在4周后重新测量血红蛋白。措施和主要结果:主要结果措施是在开始治疗的4周后贫血后临床和实验室改善。两组两组均显示治疗后4周的贫血症临床改善。然而,A组症状的第一次改善在A组中明显更快。在治疗4周后,两组的全部血统(CBC)以及所有铁指数都得到改善,但在B组中显着更好。副作用B组主要是胃肠道(Git),而对TDI的一种情况下对TDI的一个案例和另一个在注射部位的局部反应的情况下报告了A组。结论:尽管在改善临床和实验室方面同样有效IDA的证据,TDI允许使用单剂量比口服铁疗法更快的铁恢复,合理的安全性。这是办公室一站式治疗的一个很好的例子。然而,在家中的非侵入性自我是一种清晰的口服铁疗法的清晰优势,使其成为在耐受案件中治疗妊娠的第二和第三个三个月的IDA的首选。

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