镰状细胞病儿童的营养评估

R Williams, E O George, W Wang
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摘要

与同龄人相比,患有镰状细胞病的儿童身高和体重都有所下降。虽然发育不良的确切原因尚未确定,但增加的卡路里和蛋白质需求以及锌、叶酸和维生素A、C和E的缺乏可能是因素。为了确定营养摄入不足是否导致这种生长不良,我们对镰状细胞病家庭的营养知识和实践进行了调查。61例患者中位年龄为8岁(范围13个月至17岁)参加了这项研究。合并纯合子S血红蛋白(镰状细胞)病(Hb SS, n = 34)和镰状β零型地中海贫血(Hb S β零型地中海贫血,n = 2)患者;19%的人身高低于第五个百分位数。其他镰状血红蛋白C病(Hb SC, n = 21)和镰状β +地中海贫血(Hb β(+)-地中海贫血,n = 4)患者分组,4%的患者身高低于第5百分位(P = 0.043)。90%的研究患者或他们的父母都熟悉美国农业部食物指南金字塔上列出的食物类别,但大多数患者未能从这些类别中摄入适量的食物。虽然三分之二的患者每天食用推荐数量的肉类,但只有20%到31%的其他食物被食用。这可能与低社会经济地位有关。与Hb SC组相比,Hb SS组患者食用面包(P < 0.037)和牛奶(P < 0.022)的数量明显减少。59%的家庭收入低于贫困水平,79%的家庭参加了食品援助计划。我们得出结论,镰状细胞病患者的营养摄入往往不足。对镰状细胞病患者的教育应侧重于(1)特定的营养需求,合理分配膳食摄入量,(2)如何在有限的收入下提供营养膳食,(3)增加热量和蛋白质摄入量的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nutrition assessment in children with sickle cell disease.

Children with sickle cell disease have decreased height and weight when compared with their peers. Although exact reasons for poor growth have not been established, increased calorie and protein needs and deficiencies in zinc, folic acid, and vitamins A, C, and E may be factors. To determine whether inadequate nutrient intake contributes to this poor growth, we conducted a survey of the nutrition knowledge and practices of families affected by sickle cell disease. Sixty-one patients with a median age of 8 years (range, 13 months to 17 years) participated in the study. Patients with homozygous S hemoglobin (sickle cell) disease (Hb SS, n = 34) and sickle beta zero thalassemia (Hb S beta zero-thalassemia, n = 2) were combined; 19% were below the fifth percentile for height. The other patients, with sickle hemoglobin C disease (Hb SC, n = 21) and sickle beta plus thalassemia (Hb beta(+)-thalassemia, n = 4), were grouped, and 4% were below the fifth percentile for height (P = .043). Ninety percent of the study patients or their parents were familiar with the food groups indicated on the US Department of Agriculture's Food Guide Pyramid, but most patients failed to consume appropriate amounts from those groups. Although two thirds of the patients ate the recommended number of servings daily from the meat group, only 20% to 31% of the recommended servings from each of the other food groups was consumed. This was possibly related to low socioeconomic status. The patients in the Hb SS group ate significantly less from the bread (P < .037) and milk (P < .022) categories than the patients in the Hb SC group. Fifty-nine percent of families had incomes below the poverty level, and 79% participated in a food assistance program. We conclude that the nutrient intake of patients with sickle cell disease is often inadequate. Education for patients with sickle cell disease should focus on (1) specific nutrient needs, with proper distribution of dietary intake among the food groups, (2) ways to provide nutritious meals on a limited income, and (3) methods for increasing calorie and protein intake.

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