Powers Jacquelyn M, Buchanan George R, Adix Leah, Zhang Song, Gao Ang, McCavit Timothy L
Division of Hematology and Oncology, Baylor College of Medicine, Houston, Texas2Department of Pediatrics, Baylor College of Medicine, Houston, Texas3Texas Children's Hospital, Houston.
Division of Hematology and Oncology, University of Texas Southwestern Medical Center, Dallas5Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas6Children's Health, Dallas, Texas.
JAMA. 2017 Jun 13;317(22):2297-2304. doi: 10.1001/jama.2017.6846.
Iron-deficiency anemia (IDA) affects millions of persons worldwide, and is associated with impaired neurodevelopment in infants and children. Ferrous sulfate is the most commonly prescribed oral iron despite iron polysaccharide complex possibly being better tolerated.
To compare the effect of ferrous sulfate with iron polysaccharide complex on hemoglobin concentration in infants and children with nutritional IDA.
DESIGN, SETTING, AND PARTICIPANTS: Double-blind, superiority randomized clinical trial of infants and children aged 9 to 48 months with nutritional IDA (assessed by history and laboratory criteria) that was conducted in an outpatient hematology clinic at a US tertiary care hospital from September 2013 through November 2015; 12-week follow-up ended in January 2016.
Three mg/kg of elemental iron once daily as either ferrous sulfate drops or iron polysaccharide complex drops for 12 weeks.
Primary outcome was change in hemoglobin over 12 weeks. Secondary outcomes included complete resolution of IDA (defined as hemoglobin concentration >11 g/dL, mean corpuscular volume >70 fL, reticulocyte hemoglobin equivalent >25 pg, serum ferritin level >15 ng/mL, and total iron-binding capacity <425 μg/dL at the 12-week visit), changes in serum ferritin level and total iron-binding capacity, adverse effects.
Of 80 randomized infants and children (median age, 22 months; 55% male; 61% Hispanic white; 40 per group), 59 completed the trial (28 [70%] in ferrous sulfate group; 31 [78%] in iron polysaccharide complex group). From baseline to 12 weeks, mean hemoglobin increased from 7.9 to 11.9 g/dL (ferrous sulfate group) vs 7.7 to 11.1 g/dL (iron complex group), a greater difference of 1.0 g/dL (95% CI, 0.4 to 1.6 g/dL; P < .001) with ferrous sulfate (based on a linear mixed model). Proportion with a complete resolution of IDA was higher in the ferrous sulfate group (29% vs 6%; P = .04). Median serum ferritin level increased from 3.0 to 15.6 ng/mL (ferrous sulfate) vs 2.0 to 7.5 ng/mL (iron complex) over 12 weeks, a greater difference of 10.2 ng/mL (95% CI, 6.2 to 14.1 ng/mL; P < .001) with ferrous sulfate. Mean total iron-binding capacity decreased from 501 to 389 μg/dL (ferrous sulfate) vs 506 to 417 μg/dL (iron complex) (a greater difference of -50 μg/dL [95% CI, -86 to -14 μg/dL] with ferrous sulfate; P < .001). There were more reports of diarrhea in the iron complex group than in the ferrous sulfate group (58% vs 35%, respectively; P = .04).
Among infants and children aged 9 to 48 months with nutritional iron-deficiency anemia, ferrous sulfate compared with iron polysaccharide complex resulted in a greater increase in hemoglobin concentration at 12 weeks. Once daily, low-dose ferrous sulfate should be considered for children with nutritional iron-deficiency anemia.
clinicaltrials.gov Identifier: NCT01904864.
缺铁性贫血(IDA)影响着全球数百万人,并且与婴幼儿的神经发育受损有关。硫酸亚铁是最常用的口服铁剂,尽管多糖铁复合物可能耐受性更好。
比较硫酸亚铁与多糖铁复合物对营养性缺铁性贫血婴幼儿血红蛋白浓度的影响。
设计、地点和参与者:2013年9月至2015年11月在美国一家三级护理医院的门诊血液科对9至48个月患有营养性缺铁性贫血(通过病史和实验室标准评估)的婴幼儿进行的双盲、优效性随机临床试验;12周的随访于2016年1月结束。
每日一次给予3mg/kg元素铁,以硫酸亚铁滴剂或多糖铁复合物滴剂的形式,持续12周。
主要结局是12周内血红蛋白的变化。次要结局包括缺铁性贫血的完全缓解(定义为在12周访视时血红蛋白浓度>11g/dL、平均红细胞体积>70fL、网织红细胞血红蛋白当量>25pg、血清铁蛋白水平>15ng/mL以及总铁结合力<425μg/dL)、血清铁蛋白水平和总铁结合力的变化、不良反应。
80名随机分组的婴幼儿(中位年龄22个月;55%为男性;61%为西班牙裔白人;每组40名)中,59名完成了试验(硫酸亚铁组28名[70%];多糖铁复合物组31名[78%])。从基线到12周,硫酸亚铁组平均血红蛋白从7.9g/dL升至11.9g/dL,而铁复合物组从7.7g/dL升至11.1g/dL,硫酸亚铁组差异更大,为1.0g/dL(95%CI,0.4至1.6g/dL;P<.001)(基于线性混合模型)。硫酸亚铁组缺铁性贫血完全缓解的比例更高(29%对6%;P=0.04)。12周内,硫酸亚铁组血清铁蛋白水平中位数从3.0ng/mL升至15.6ng/mL,而铁复合物组从2.0ng/mL升至7.5ng/mL,硫酸亚铁组差异更大,为10.2ng/mL(95%CI,6.2至14.1ng/mL;P<.001)。硫酸亚铁组平均总铁结合力从501μg/dL降至389μg/dL,而铁复合物组从506μg/dL降至417μg/dL(硫酸亚铁组差异更大,为-50μg/dL[95%CI,-86至-14μg/dL];P<.001)。铁复合物组腹泻报告比硫酸亚铁组更多(分别为58%对35%;P=0.04)。
在9至48个月患有营养性缺铁性贫血的婴幼儿中,与多糖铁复合物相比,硫酸亚铁在12周时血红蛋白浓度升高幅度更大。对于营养性缺铁性贫血儿童,应考虑每日一次给予低剂量硫酸亚铁。
clinicaltrials.gov标识符:NCT01904864。