A systematic review of hereditary spherocytosis reported in Chinese biomedical journals from 1978 to 2013 and estimation of the prevalence of the disease using a disease model

被引:73
|
作者
Wang, Chao [1 ,2 ]
Cui, Yazhou [1 ]
Li, Yan [1 ,2 ]
Liu, Xiao [1 ,2 ]
Han, Jinxiang [1 ]
机构
[1] Shandong Acad Med Sci, Shandong Med Biotechnol Ctr, Key Lab Biotech Drugs Minist Hlth, Key Lab Rare Dis Shandong Prov, Jinan 250062, Shandong, Peoples R China
[2] Univ Jinan, Shandong Acad Med Sci, Sch Med & Life Sci, Jinan, Shandong, Peoples R China
基金
“十二五”国家科技支撑计划重点项目”;
关键词
Hereditary spherocytosis; Bibliographic study; DisMod-II; China;
D O I
10.5582/irdr.2015.01002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Epidemiological information of hereditary spherocytosis in China is slight. This systematic review summarizes the number of cases of hereditary spherocytosis reported in China Biology Medicine disc from 1978 to 2013. In total, 2,043 cases were reported in the past 36 years. We describe its distribution from time and space. We also estimate the literature reported prevalence of hereditary spherocytosis by DisMod-II software, overall prevalence in China was estimated to be: 1.27 cases per 100,000 people in males and 1.49 cases per 100,000 people in females. All results suggest a stronger network of diagnosis and treatment including all levels of hospitals should be created to improve healthcare for hereditary spherocytosis and even other rare diseases in the future, meanwhile we can obtain more useful information for orphan drug designation purposes and make public health decisions regarding such diseases through the use of the burden of disease models.
引用
收藏
页码:76 / 81
页数:6
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