Renal Unit, Department of Medicine, Faculty of Medicine , Ramathibodi Hospital , Mahidol University , Bangkok , Thailand ; UCL Centre for Nephrology, Royal Free Hospital , University College London Medical School , London , UK.
Renal Unit, Department of Medicine, Faculty of Medicine , Ramathibodi Hospital , Mahidol University , Bangkok , Thailand.
Clin Kidney J. 2015 Apr;8(2):202-11. doi: 10.1093/ckj/sfu140. Epub 2015 Jan 13.
Although there have been many advancements in the treatment of patients with chronic kidney disease (CKD) over the last 50 years, in terms of reducing cardiovascular risk, mortality remains unacceptably high, particularly for those patients who progress to stage 5 CKD and initiate dialysis (CKD5d). As mortality risk increases exponentially with progressive CKD stage, the question arises as to whether preservation of residual renal function once dialysis has been initiated can reduce mortality risk. Observational studies to date have reported an association between even small amounts of residual renal function and improved patient survival and quality of life. Dialysis therapies predominantly provide clearance for small water-soluble solutes, volume and acid-base control, but cannot reproduce the metabolic functions of the kidney. As such, protein-bound solutes, advanced glycosylation end-products, middle molecules and other azotaemic toxins accumulate over time in the anuric CKD5d patient. Apart from avoiding potential nephrotoxic insults, observational and interventional trials have suggested that a number of interventions and treatments may potentially reduce the progression of earlier stages of CKD, including targeted blood pressure control, reducing proteinuria and dietary intervention using combinations of protein restriction with keto acid supplementation. However, many interventions which have been proven to be effective in the general population have not been equally effective in the CKD5d patient, and so the question arises as to whether these treatment options are equally applicable to CKD5d patients. As strategies to help preserve residual renal function in CKD5d patients are not well established, we have reviewed the evidence for preserving or losing residual renal function in peritoneal dialysis patients, as urine collections are routinely collected, whereas few centres regularly collect urine from haemodialysis patients, and haemodialysis dialysis patients are at risk of sudden intravascular volume shifts associated with dialysis treatments. On the other hand, peritoneal dialysis patients are exposed to a variety of hypertonic dialysates and episodes of peritonitis. Whereas blood pressure control, using an angiotensin-converting enzyme inhibitor (ACEI) or angiotensin receptor blocker (ARB), and low-protein diets along with keto acid supplementation have been shown to reduce the rate of progression in patients with earlier stages of CKD, the strategies to preserve residual renal function (RRF) in dialysis patients are not well established. For peritoneal dialysis patients, there are additional technical factors that might aggravate the rate of loss of residual renal function including peritoneal dialysis prescriptions and modality, bio-incompatible dialysis fluid and over ultrafiltration of fluid causing dehydration. In this review, we aim to evaluate the evidence of interventions and treatments, which may sustain residual renal function in peritoneal dialysis patients.
尽管在过去的 50 年中,在治疗慢性肾脏病(CKD)患者方面已经取得了许多进展,但就降低心血管风险而言,死亡率仍然高得令人无法接受,尤其是对于那些进展到 CKD5d 并开始透析的患者。由于随着 CKD 阶段的进展,死亡率呈指数级增长,因此出现了这样一个问题,即在开始透析后保留残余肾功能是否可以降低死亡率。迄今为止的观察性研究报告称,即使是少量的残余肾功能与改善患者的生存和生活质量之间存在关联。透析疗法主要提供清除小分子水溶性溶质、容量和酸碱控制的功能,但无法复制肾脏的代谢功能。因此,蛋白质结合的溶质、晚期糖基化终产物、中分子物质和其他氮质毒素会在无尿的 CKD5d 患者中随时间逐渐积累。除了避免潜在的肾毒性损伤外,观察性和干预性试验表明,一些干预和治疗方法可能潜在地减缓 CKD 早期阶段的进展,包括有针对性的血压控制、减少蛋白尿以及使用蛋白质限制与酮酸补充相结合的饮食干预。然而,许多在普通人群中被证明有效的干预措施在 CKD5d 患者中并不同样有效,因此出现了这样一个问题,即这些治疗选择是否同样适用于 CKD5d 患者。由于帮助 CKD5d 患者保留残余肾功能的策略尚未得到充分确立,我们回顾了在腹膜透析患者中保留或丧失残余肾功能的证据,因为常规收集尿液,而很少有中心定期从血液透析患者中收集尿液,并且血液透析患者存在与透析治疗相关的突然血管内容量转移的风险。另一方面,腹膜透析患者暴露于各种高渗透析液和腹膜炎发作中。尽管使用血管紧张素转换酶抑制剂(ACEI)或血管紧张素受体阻滞剂(ARB)控制血压以及低蛋白饮食加上酮酸补充已被证明可以降低早期 CKD 患者的进展速度,但保留透析患者残余肾功能(RRF)的策略尚未得到充分确立。对于腹膜透析患者,还有其他技术因素可能会加速残余肾功能的丧失,包括腹膜透析处方和方式、生物不相容的透析液以及导致脱水的过度超滤。在本综述中,我们旨在评估可能维持腹膜透析患者残余肾功能的干预和治疗措施的证据。