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英国肾脏注册处第11次年度报告(2008年12月):第13章 英国儿童肾脏替代治疗人群的人口统计学

UK Renal Registry 11th Annual Report (December 2008): Chapter 13 Demography of the UK paediatric renal replacement therapy population.

作者信息

Lewis Malcolm A, Shaw Joanne, Sinha Manish, Adalat Shazia, Hussain Farida, Inward Carol

机构信息

Manchester Childrens Hospital, Manchester, UK.

出版信息

Nephron Clin Pract. 2009;111 Suppl 1:c257-67. doi: 10.1159/000210002. Epub 2009 Mar 26.

Abstract

AIMS

To describe the demographics of the paediatric RRT population in the UK and analyse changes in demographics with time.

METHODS

Extraction and analysis of data from the UK paediatric Renal Registry.

RESULTS

The UK paediatric established renal failure (ERF) population in April 2008 was 875 patients. The prevalence under the age of 16 years was 55 per million age related population (pmp) and the incidence 7.92 pmp. The incidence and prevalence for South Asian and Other ethnic groups were 3 times that of the White and Black populations. Renal dysplasia was the most common cause of ERF accounting for 33% of prevalent cases. Diseases with autosomal recessive inheritance were more common in patients from ethnic minority groups. The spectrum of diseases seen has changed over a generation. Overall 5 year survival for children with ERF was 91.8%. Five year survival of infants starting dialysis was just 62%. Transplanted patients accounted for 74% of the current population. The proportion with grafts from living donors has steadily risen to 34%. Children from ethnic minority groups were less likely to have an allograft and living donation was less frequent in this population. For those on dialysis, 57% were receiving peritoneal dialysis. This was the main treatment modality for patients under 4 years of age.

CONCLUSIONS

The paediatric ERF population continued to expand slowly. Incidence and prevalence rates were stable and similar to other developed nations. The high incidence in patients from ethnic minority groups will lead to a greater proportion of the population being from these groups in time. To maintain the high proportion of engrafted patients it will be necessary to encourage living donation in the ethnic minority population. The spectrum of diseases seen has already changed over a generation with the treatment of young children with diseases such as congenital nephrosis. The incidence of cystinosis causing ERF was reduced, probably reflecting better early treatment.

摘要

目的

描述英国儿科肾脏替代治疗(RRT)人群的人口统计学特征,并分析其随时间的变化。

方法

从英国儿科肾脏登记处提取并分析数据。

结果

2008年4月英国儿科确诊肾衰竭(ERF)人群为875例患者。16岁以下患病率为每百万年龄相关人口55例(pmp),发病率为7.92 pmp。南亚和其他种族群体的发病率和患病率是白人和黑人的3倍。肾发育不良是ERF最常见的病因,占现患病例的33%。常染色体隐性遗传疾病在少数民族患者中更为常见。一代以来所见疾病谱已发生变化。ERF患儿的总体5年生存率为91.8%。开始透析的婴儿5年生存率仅为62%。移植患者占当前人群的74%。来自活体供者的移植物比例稳步上升至34%。少数民族儿童接受同种异体移植的可能性较小,该人群中活体捐赠也较少。对于接受透析的患者,57%正在接受腹膜透析。这是4岁以下患者的主要治疗方式。

结论

儿科ERF人群继续缓慢扩大。发病率和患病率稳定,与其他发达国家相似。少数民族患者的高发病率将导致该群体在未来占更大比例。为维持高移植患者比例,有必要鼓励少数民族人群进行活体捐赠。随着对先天性肾病等疾病幼儿的治疗,一代以来所见疾病谱已经发生变化。导致ERF的胱氨酸病发病率降低,可能反映了早期治疗的改善。

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