Hall Yoshio N, Chertow Glenn M
Division of Nephrology, Department of Medicine, Univeristy of Washington, Veterans Affairs Puget Sound Health Care System, Seattle, Washington, USA.
BMJ Clin Evid. 2007 Oct 17;2007:2002.
End stage renal disease (ESRD) affects over 1500 people per million population in countries with a high prevalence, such as the USA and Japan. Approximately two thirds of people with ESRD receive haemodialysis, a quarter have kidney transplants, and a tenth receive peritoneal dialysis.
We conducted a systematic review and aimed to answer the following clinical questions: What are the effects of different doses and osmotic agents for peritoneal dialysis? What are the effects of different doses and membrane fluxes for haemodialysis? What are the effects of interventions aimed at preventing secondary complications? We searched: Medline, Embase, The Cochrane Library and other important databases up to April 2007 (Clinical Evidence reviews are updated periodically, please check our website for the most up-to-date version of this review). We included harms alerts from relevant organisations such as the US Food and Drug Administration (FDA) and the UK Medicines and Healthcare products Regulatory Agency (MHRA).
We found 20 systematic reviews, RCTs, or observational studies that met our inclusion criteria. We performed a GRADE evaluation of the quality of evidence for interventions.
In this systematic review we present information relating to the effectiveness and safety of the following interventions: cinacalcet, darbepoetin, dextrose solutions, erythropoietin, haemodialysis (standard-dose, increased-dose), high-membrane-flux haemodialysis, icodextrin, increased-dose peritoneal dialysis, low-membrane-flux haemodialysis, mupirocin, sevelamer, and standard-dose dialysis.
在诸如美国和日本等患病率较高的国家,终末期肾病(ESRD)影响着每百万人口中超过1500人。大约三分之二的ESRD患者接受血液透析,四分之一接受肾移植,十分之一接受腹膜透析。
我们进行了一项系统评价,旨在回答以下临床问题:不同剂量和渗透剂用于腹膜透析的效果如何?不同剂量和膜通量用于血液透析的效果如何?旨在预防继发性并发症的干预措施的效果如何?我们检索了:截至2007年4月的医学文献数据库(Medline)、荷兰医学文摘数据库(Embase)、考克兰图书馆及其他重要数据库(《临床证据》综述会定期更新,请查看我们的网站获取本综述的最新版本)。我们纳入了来自美国食品药品监督管理局(FDA)和英国药品及医疗保健产品监管局(MHRA)等相关组织的危害警示。
我们找到了20项符合我们纳入标准的系统评价、随机对照试验或观察性研究。我们对干预措施证据的质量进行了GRADE评估。
在本系统评价中,我们提供了有关以下干预措施有效性和安全性的信息:西那卡塞、达比泊汀、葡萄糖溶液、促红细胞生成素、血液透析(标准剂量、增加剂量)、高膜通量血液透析、艾考糊精、增加剂量腹膜透析、低膜通量血液透析、莫匹罗星、司维拉姆和标准剂量透析。