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本文引用的文献

1
Effects of nutritional intake on disease severity in children with sickle cell disease.营养摄入对镰状细胞病患儿疾病严重程度的影响。
Nutr J. 2016 Apr 30;15(1):46. doi: 10.1186/s12937-016-0159-8.
2
Sickle Cell Disease in Sub-Saharan Africa.撒哈拉以南非洲地区的镰状细胞病
Hematol Oncol Clin North Am. 2016 Apr;30(2):343-58. doi: 10.1016/j.hoc.2015.11.005. Epub 2016 Jan 28.
3
Minireview: Genetic basis of heterogeneity and severity in sickle cell disease.小型综述:镰状细胞病异质性和严重程度的遗传基础
Exp Biol Med (Maywood). 2016 Apr;241(7):689-96. doi: 10.1177/1535370216636726. Epub 2016 Mar 1.
4
Novel insights in the management of sickle cell disease in childhood.儿童镰状细胞病管理的新见解。
World J Clin Pediatr. 2016 Feb 8;5(1):25-34. doi: 10.5409/wjcp.v5.i1.25.
5
Sickle cell disease in adults: developing an appropriate care plan.成人镰状细胞病:制定合适的护理计划。
Clin J Oncol Nurs. 2015 Oct;19(5):562-7. doi: 10.1188/15.CJON.562-567.
6
Evolution of sickle cell disease from a life-threatening disease of children to a chronic disease of adults: The last 40 years.镰状细胞病的演变:从危及儿童生命的疾病到成人慢性病:过去的 40 年。
Am J Hematol. 2016 Jan;91(1):5-14. doi: 10.1002/ajh.24235.
7
Environmental determinants of severity in sickle cell disease.镰状细胞病严重程度的环境决定因素。
Haematologica. 2015 Sep;100(9):1108-16. doi: 10.3324/haematol.2014.120030.
8
Alpha thalassemia among sickle cell anaemia patients in Kampala, Uganda.乌干达坎帕拉镰状细胞贫血患者中的α地中海贫血
Afr Health Sci. 2015 Jun;15(2):682-9. doi: 10.4314/ahs.v15i2.48.
9
[Breastfeeding and the anthropometric profile of children with sickle cell anemia receiving follow-up in a newborn screening reference service].[在新生儿筛查参考服务中接受随访的镰状细胞贫血患儿的母乳喂养与人体测量特征]
Rev Paul Pediatr. 2015 Apr-Jun;33(2):154-9. doi: 10.1016/j.rpped.2014.11.006. Epub 2015 Feb 3.
10
Evaluation of arm span and sitting height as proxy for height in children with sickle cell anemia in Lagos, Nigeria.尼日利亚拉各斯镰状细胞贫血患儿中臂展和坐高作为身高替代指标的评估。
J Am Coll Nutr. 2014;33(6):437-41. doi: 10.1080/07315724.2013.875356. Epub 2014 Jun 25.

患有镰状细胞贫血的儿童生长发育迟缓的相关因素:来自中非的首次报告。

Factors Associated with Growth Retardation in Children Suffering from Sickle Cell Anemia: First Report from Central Africa.

作者信息

Lukusa Kazadi Aimé, Ngiyulu René Makuala, Gini-Ehungu Jean Lambert, Mbuyi-Muamba Jean Marie, Aloni Michel Ntetani

机构信息

Division of Paediatric Haemato-Oncology and Nephrology, Department of Paediatrics, University Hospital of Kinshasa, Faculty of Medicine, University of Kinshasa, Kinshasa, Democratic Republic of the Congo.

Department of Internal Medicine, Faculty of Medicine, University of Kinshasa, Kinshasa, Democratic Republic of the Congo.

出版信息

Anemia. 2017;2017:7916348. doi: 10.1155/2017/7916348. Epub 2017 Jan 30.

DOI:10.1155/2017/7916348
PMID:28250985
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5303847/
Abstract

. The aim of this study was to investigate and determine the risk factors associated with poor growth among SCA children. A cross-sectional study was conducted in Kinshasa, the capital's country. The nutritional status was assessed using the Z scores of the anthropometric indices. We gathered data on the 256 patients, 138 females (53.9%), who entered the study. The mean age at presentation was 8.4 ± 4.9 years of age. Underweight, stunting, and wasting were found, respectively, in 47.7%, 10.5%, and 50.3% of SCA children. A history of hand-foot syndrome, more than 3 blood transfusions, being less than 12 months of age when receiving the first transfusion, more than two severe sickle crises per year, a medical history of severe infections, and the presence of hepatomegaly were associated with poor growth. When comparing sickle cell patients under 12 years of age ( = 159) to a group of 296 age-matched children with normal Hb-AA, a significantly higher proportion of subjects with stunting and underweight were found among SCA. Nutritional status encountered in Congolese sickle cell children has been described for the first time in this study. A high prevalence of poor growth in SCA children was found in our study.

摘要

本研究的目的是调查并确定与镰状细胞贫血(SCA)患儿生长发育不良相关的风险因素。在首都城市金沙萨进行了一项横断面研究。使用人体测量指标的Z评分评估营养状况。我们收集了参与研究的256例患者的数据,其中138例为女性(53.9%)。就诊时的平均年龄为8.4±4.9岁。在SCA患儿中,分别有47.7%、10.5%和50.3%的患儿存在体重不足、发育迟缓及消瘦情况。手足综合征病史、输血超过3次、首次输血时年龄小于12个月、每年发生超过两次严重镰状细胞危象、有严重感染病史以及存在肝肿大与生长发育不良相关。将12岁以下的镰状细胞病患者(n = 159)与一组296名年龄匹配的血红蛋白为正常AA型的儿童进行比较时,发现SCA患儿中发育迟缓和体重不足的比例明显更高。本研究首次描述了刚果镰状细胞病患儿的营养状况。我们的研究发现SCA患儿中生长发育不良的患病率很高。