Dunlop Joanna L, Vandal Alain C, Marshall Mark R
Department of Medicine, Counties Manukau Health, Orakau Rd, Auckland, New Zealand.
Cochrane Database Syst Rev. 2019 Jan 16;1(1):CD011204. doi: 10.1002/14651858.CD011204.pub2.
Cardiovascular (CV) disease is the leading cause of death in dialysis patients, and strongly associated with fluid overload and hypertension. It is plausible that low dialysate [Na+] may decrease total body sodium content, thereby reducing fluid overload and hypertension, and ultimately reducing CV morbidity and mortality.
This review evaluated harms and benefits of using a low (< 138 mM) dialysate [Na+] for maintenance haemodialysis (HD) patients.
We searched the Cochrane Kidney and Transplant Register of Studies up to 7 August 2018 through contact with the Information Specialist using search terms relevant to this review. Studies in the Register are identified through searches of CENTRAL, MEDLINE, and EMBASE, conference proceedings, the International Clinical Trials Register (ICTRP) Search Portal and ClinicalTrials.gov.
Randomised controlled trials (RCTs), both parallel and cross-over, of low (< 138 mM) versus neutral (138 to 140 mM) or high (> 140 mM) dialysate [Na+] for maintenance HD patients were included.
Two investigators independently screened studies for inclusion and extracted data. Statistical analyses were performed using random effects models, and results expressed as risk ratios (RR) for dichotomous outcomes, and mean differences (MD) or standardised MD (SMD) for continuous outcomes, with 95% confidence intervals (CI). Confidence in the evidence was assessed using GRADE.
We included 12 studies randomising 310 patients, with data available for 266 patients after dropout. All but one study evaluated a fixed concentration of low dialysate [Na+], and one profiled dialysate [Na+]. Three studies were parallel group, and the remaining nine cross-over. Of the latter, only two used a washout between intervention and control periods. Most studies were short-term with a median (interquartile range) follow-up of 3 (3, 8.5) weeks. Two were of a single HD session, and two of a single week's HD. Half of the studies were conducted prior to 2000, and five reported use of obsolete HD practices. Risks of bias in the included studies were often high or unclear, lowering confidence in the results.Compared to neutral or high dialysate [Na+], low dialysate [Na+] had the following effects on "efficacy" endpoints: reduced interdialytic weight gain (10 studies: MD -0.35 kg, 95% CI -0.18 to -0.51; high certainty evidence); probably reduced predialysis mean arterial blood pressure (BP) (4 studies: MD -3.58 mmHg, 95% CI -5.46 to -1.69; moderate certainty evidence); probably reduced postdialysis mean arterial BP (MAP) (4 studies: MD -3.26 mmHg, 95% CI -1.70 to -4.82; moderate certainty evidence); probably reduced predialysis serum [Na+] (7 studies: MD -1.69 mM, 95% CI -2.36 to -1.02; moderate certainty evidence); may have reduced antihypertensive medication (2 studies: SMD -0.67 SD, 95% CI -1.07 to -0.28; low certainty evidence). Compared to neutral or high dialysate [Na+], low dialysate [Na+] had the following effects on "safety" endpoints: probably increased intradialytic hypotension events (9 studies: RR 1.56, 95% 1.17 to 2.07; moderate certainty evidence); probably increased intradialytic cramps (6 studies: RR 1.77, 95% 1.15 to 2.73; moderate certainty evidence).Compared to neutral or high dialysate [Na+], low dialysate [Na+] may make little or no difference to: intradialytic BP (2 studies: MD for systolic BP -3.99 mmHg, 95% CI -17.96 to 9.99; diastolic BP 1.33 mmHg, 95% CI -6.29 to 8.95; low certainty evidence); interdialytic BP (2 studies:, MD for systolic BP 0.17 mmHg, 95% CI -5.42 to 5.08; diastolic BP -2.00 mmHg, 95% CI -4.84 to 0.84; low certainty evidence); dietary salt intake (2 studies: MD -0.21g/d, 95% CI -0.48 to 0.06; low certainty evidence).Due to very low quality of evidence, it is uncertain whether low dialysate [Na+] changed extracellular fluid status, venous tone, arterial vascular resistance, left ventricular mass or volumes, thirst or fatigue. Studies did not examine cardiovascular or all-cause mortality, cardiovascular events, or hospitalisation.
AUTHORS' CONCLUSIONS: It is likely that low dialysate [Na+] reduces intradialytic weight gain and BP, which are effects directionally associated with improved outcomes. However, the intervention probably also increases intradialytic hypotension and reduces serum [Na+], effects that are associated with increased mortality risk. The effect of the intervention on overall patient health and well-being is unknown. Further evidence is needed in the form of longer-term studies in contemporary settings, evaluating end-organ effects in small-scale mechanistic studies using optimal methods, and clinical outcomes in large-scale multicentre RCTs.
心血管疾病是透析患者的主要死因,与液体过载和高血压密切相关。低透析液[Na⁺]可能会降低总体钠含量,从而减轻液体过载和高血压,并最终降低心血管疾病的发病率和死亡率,这似乎是合理的。
本综述评估了使用低(<138 mM)透析液[Na⁺]对维持性血液透析(HD)患者的危害和益处。
我们通过与信息专家联系,使用与本综述相关的检索词,检索了截至2018年8月7日的Cochrane肾脏与移植研究注册库。注册库中的研究通过检索CENTRAL、MEDLINE、EMBASE、会议论文集、国际临床试验注册平台(ICTRP)检索入口和ClinicalTrials.gov来识别。
纳入针对维持性HD患者,比较低(<138 mM)与中性(138至140 mM)或高(>140 mM)透析液[Na⁺]的平行和交叉随机对照试验(RCT)。
两名研究者独立筛选纳入研究并提取数据。采用随机效应模型进行统计分析,结果以二分结局的风险比(RR)以及连续结局的均值差(MD)或标准化均值差(SMD)表示,并给出95%置信区间(CI)。使用GRADE评估证据的可信度。
我们纳入了12项研究,共随机分配310例患者,剔除后有266例患者的数据可用。除一项研究外,所有研究均评估了固定浓度的低透析液[Na⁺],一项研究分析了透析液[Na⁺]的变化情况。三项研究为平行组设计,其余九项为交叉设计。在交叉设计的研究中,只有两项在干预期和对照期之间设置了洗脱期。大多数研究为短期研究,中位(四分位间距)随访时间为3(3, 8.5)周。两项研究为单次HD治疗,两项研究为单周HD治疗。一半的研究在2000年之前进行,五项研究报告采用了过时的HD治疗方法。纳入研究中的偏倚风险通常较高或不明确,降低了对结果的可信度。与中性或高透析液[Na⁺]相比,低透析液[Na⁺]对“疗效”终点有以下影响:减少透析间期体重增加(10项研究:MD -0.35 kg,95%CI -0.18至-0.51;高确定性证据);可能降低透析前平均动脉血压(BP)(4项研究:MD -3.58 mmHg,95%CI -5.46至-1.69;中等确定性证据);可能降低透析后平均动脉血压(MAP)(4项研究:MD -3.26 mmHg,95%CI -1.70至-4.82;中等确定性证据);可能降低透析前血清[Na⁺](7项研究:MD -1.69 mM,95%CI -2.36至-1.02;中等确定性证据);可能减少抗高血压药物的使用(2项研究:SMD -0.67 SD,95%CI -1.07至-0.28;低确定性证据)。与中性或高透析液[Na⁺]相比,低透析液[Na⁺]对“安全性”终点有以下影响:可能增加透析中低血压事件(9项研究:RR 1.56,95% 1.17至2.07;中等确定性证据);可能增加透析中痉挛(6项研究:RR 1.77,95% 1.15至2.73;中等确定性证据)。与中性或高透析液[Na⁺]相比,低透析液[Na⁺]对以下方面可能影响很小或无影响:透析中血压(2项研究:收缩压MD -3.99 mmHg,95%CI -17.96至9.99;舒张压MD 1.33 mmHg,95%CI -6.29至8.95;低确定性证据);透析间期血压(2项研究:收缩压MD 0.17 mmHg,95%CI -5.42至5.08;舒张压MD -2.00 mmHg,95%CI -4.84至0.84;低确定性证据);饮食盐摄入量(2项研究:MD -0.21g/d,95%CI -0.48至0.06;低确定性证据)。由于证据质量极低,尚不确定低透析液[Na⁺]是否会改变细胞外液状态、静脉张力、动脉血管阻力、左心室质量或容积、口渴或疲劳。研究未考察心血管或全因死亡率、心血管事件或住院情况。
低透析液[Na⁺]可能会减少透析中体重增加和血压,这些效应在方向上与改善结局相关。然而,该干预措施可能还会增加透析中低血压并降低血清[Na⁺],这些效应与死亡风险增加相关。该干预措施对患者整体健康和幸福感的影响尚不清楚。需要通过当代环境下的长期研究、使用最佳方法的小规模机制研究来评估终末器官效应以及大规模多中心RCT的临床结局等形式获取进一步的证据。