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接受输血治疗的地中海贫血患者的临床和代谢并发症

Clinical and Metabolic Complications in patients with thalassemia undergoing transfusion therapy.

作者信息

Raghuwanshi Babita, Kumari Suchitra, Sahoo Durgesh Prasad

机构信息

Department of Transfusion Medicine and Blood Bank, AIIMS, Bhopal, Madhya Pradesh, India.

Department of Biochemistry, AIIMS Bhubaneswar, Odisha, India.

出版信息

J Family Med Prim Care. 2020 Feb 28;9(2):973-977. doi: 10.4103/jfmpc.jfmpc_845_19. eCollection 2020 Feb.

DOI:10.4103/jfmpc.jfmpc_845_19
PMID:32318453
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7113988/
Abstract

BACKGROUND

The transfusions in patients with thalassemia are a double-edged sword as the patients develop complications due to inadequate transfusions and due to multiple transfusions. These complications vary from metabolic complications such as diabetes mellitus and clinical complications such as growth retardation, transfusion-transmitted infections (TTI), and iron overload. We selected Balasore district in Odisha which is a satellite center of AIIMS Bhubaneshwar and has a huge population of hemoglobinopathy patients especially thalassemia and this district in Odisha lags in terms of healthcare and health awareness.

MATERIALS AND METHOD

In all, 123 patients with thalassemia major were included in this study for the evaluation of metabolic and clinical complications. Anthropometric measurements such as height and weight with age and gender were used for evaluation of growth parameters as per World Health Organization (WHO) reference data. Children were termed wasted and stunted if the values were below 2 standard deviation of the reference WHO median. Blood samples were collected for TTI status and fasting blood sugar levels.

RESULT

A total of 118 (95.9%) were detected to have under nutrition, 73 (59.3%) of the patients were HCV-positive, and 54 (48.6%) had high fasting blood sugar levels. Based on the HCV status, they were classified as HCV-positive and HCV-negative to compare the anthropometric and growth status in these patients. About 98.6% of the HCV-positive cases were undernutrition and 83.6% were stunted.

CONCLUSION

There is an increasing trend of associated metabolic derangements in patients with thalassemia. The district-level health services have an urgent need for improvement in chelation regimes and screening technologies.

摘要

背景

地中海贫血患者输血是一把双刃剑,因为患者会因输血不足以及多次输血而出现并发症。这些并发症包括代谢并发症,如糖尿病,以及临床并发症,如生长发育迟缓、输血传播感染(TTI)和铁过载。我们选择了奥里萨邦的巴拉索尔地区,该地区是布巴内什瓦尔全印医学科学研究所的卫星中心,有大量血红蛋白病患者,尤其是地中海贫血患者,而且奥里萨邦的这个地区在医疗保健和健康意识方面较为落后。

材料与方法

本研究共纳入123例重型地中海贫血患者,以评估其代谢和临床并发症。根据世界卫生组织(WHO)的参考数据,使用身高、体重等人体测量指标以及年龄和性别来评估生长参数。如果数值低于WHO参考中位数的2个标准差,则儿童被判定为消瘦和发育迟缓。采集血样检测TTI状况和空腹血糖水平。

结果

总共检测出118例(95.9%)存在营养不良,73例(59.3%)患者丙肝病毒呈阳性,54例(48.6%)空腹血糖水平较高。根据丙肝病毒感染状况,将患者分为丙肝病毒阳性和丙肝病毒阴性,以比较这些患者的人体测量和生长状况。约98.6%的丙肝病毒阳性病例存在营养不良,83.6%发育迟缓。

结论

地中海贫血患者并发代谢紊乱的趋势呈上升态势。地区级卫生服务机构迫切需要改进螯合疗法和筛查技术。

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本文引用的文献

1
Thalassemias in South Asia: clinical lessons learnt from Bangladesh.南亚的地中海贫血症:从孟加拉国汲取的临床经验教训。
Orphanet J Rare Dis. 2017 May 18;12(1):93. doi: 10.1186/s13023-017-0643-z.
2
Current growth patterns in children and adolescents with thalassemia major.重型地中海贫血患儿及青少年的当前生长模式。
Blood. 2016 Nov 24;128(21):2580-2582. doi: 10.1182/blood-2016-05-712695. Epub 2016 Oct 13.
3
A Cross-Sectional Study on Burden of Hepatitis C, Hepatitis B, HIV and Syphilis in Multi-Transfused Thalassemia Major Patients Reporting to a Government Hospital of Central India.一项针对印度中部一家政府医院收治的多次输血重型地中海贫血患者丙型肝炎、乙型肝炎、艾滋病毒和梅毒负担的横断面研究。
Indian J Hematol Blood Transfus. 2015 Sep;31(3):367-73. doi: 10.1007/s12288-014-0462-5. Epub 2014 Oct 12.
4
Prevalence of Hepatitis C among Multi-transfused Thalassaemic Patients in Oman: Single centre experience.阿曼多次输血地中海贫血患者丙型肝炎的患病率:单中心经验
Sultan Qaboos Univ Med J. 2015 Feb;15(1):e46-51. Epub 2015 Jan 21.
5
Prevalence of deletional alpha thalassemia and sickle gene in a tribal dominated malaria endemic area of eastern India.印度东部部落主导的疟疾流行地区缺失型α地中海贫血和镰状基因的患病率
ISRN Hematol. 2014 Mar 11;2014:745245. doi: 10.1155/2014/745245. eCollection 2014.
6
The prevention of thalassemia.地中海贫血症的预防。
Cold Spring Harb Perspect Med. 2013 Feb 1;3(2):a011775. doi: 10.1101/cshperspect.a011775.
7
Infectivity of human immunodeficiency virus-1, hepatitis C virus, and hepatitis B virus and risk of transmission by transfusion.人类免疫缺陷病毒1型、丙型肝炎病毒和乙型肝炎病毒的传染性及输血传播风险。
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8
Chronic illness management: what is the role of primary care?慢性病管理:初级保健的作用是什么?
Ann Intern Med. 2003 Feb 4;138(3):256-61. doi: 10.7326/0003-4819-138-3-200302040-00034.