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Outcome of reaching end stage renal failure in children under 2 years of age.

机译:2岁以下儿童达到终末期肾衰竭的结果。

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AIMS: To determine the outcome of children who reach end stage renal failure before the age of 2 years. METHODS: Using a retrospective questionnaire, 10 years' data were collected from the paediatric nephrology units in Britain and Ireland (1988 to 1997, follow up 1.3-11.5 years). RESULTS: A total of 192 children were identified; 0.31/million/year. Most had congenital or inherited conditions, and there were more boys. Latterly, half were diagnosed antenatally. Ninety per cent were dialysed initially, most using home peritoneal cyclers, some by haemodialysis through central lines. Five per cent recovered sufficient function to come off dialysis. Most required tube feeding (often gastrostomy) and erythropoietin; some needed growth hormone. A total of 56% received a transplant (2% without prior dialysis) at (medians) 2.6 years and 12.3 kg. The 2 and 10 year survival of first kidneys was 78%. Growth improved following transplantation. Fourteen per cent died because treatment was not started or was withdrawn. Most had particularly complex renal conditions, or additional major non-renal diagnoses. Typically, decisions not to treat were made mutually between clinicians and families. When treatment was continued, 71% survived, and few had serious non-renal conditions. Most attended normal schools, and by 6 years of age, less than 10% still required dialysis. Infants starting treatment under and over 1 month of age fared equally well. CONCLUSIONS: By school age, most infants treated for end stage renal failure will have a functioning transplant, reasonable growth, and will attend a normal class, regardless of the age at which they commence treatment. Treatment is seldom sustained in children who have serious additional medical conditions. It is reasonable to treat infants with uncomplicated renal failure.
机译:目的:确定在2岁之前达到末期肾衰竭的儿童的结局。方法:使用回顾性调查表,从英国和爱尔兰的儿科肾脏病科收集了10年的数据(1988年至1997年,随访1.3-11.5年)。结果:总共鉴定出192名儿童; 0.31百万/年。大多数患有先天性或遗传性疾病,男孩更多。后来,有一半被诊断为产前。最初有90%的患者进行了透析,大部分使用了家用腹膜循环仪,其中一些通过中心管路进行了血液透析。百分之五的人恢复了足够的功能以摆脱透析。最需要的管饲(通常是胃造口术)和促红细胞生成素;一些需要的生长激素。共有56%的患者接受了中位2.6年和12.3公斤的移植手术(其中2%的患者未经事先透析)。首个肾脏的2年和10年生存率为78%。移植后生长得到改善。 14%的人死于未开始治疗或被撤回治疗。大多数患者的肾脏疾病特别复杂,或者还有其他重大的非肾脏诊断。通常,不治疗的决定是临床医生和家庭之间共同做出的。继续治疗时,有71%存活,很少有严重的非肾脏疾病。大多数人上过正规学校,到6岁时,仍不到10%的人需要透析。 1个月以下及1个月以上开始治疗的婴儿情况也一样。结论:到学龄期,接受终末期肾衰竭治疗的大多数婴儿都将具有正常的移植功能,合理的生长,并且无论他们开始治疗的年龄如何,都将参加正常班级。对于患有严重其他疾病的儿童,很少维持治疗。治疗无并发症肾功能衰竭的婴儿是合理的。

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