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中心夜间血液透析与常规血液透析的比较:证据的系统评价。

In-Center Nocturnal Hemodialysis Versus Conventional Hemodialysis: A Systematic Review of the Evidence.

机构信息

Division of Nephrology and Transplant Immunology, University of Alberta, Edmonton, AB, Canada; Headwaters Health Care Centre, Orangeville, ON, Canada.

University of Manitoba, Winnipeg, MB, Canada.

出版信息

Am J Kidney Dis. 2017 Aug;70(2):218-234. doi: 10.1053/j.ajkd.2017.01.047. Epub 2017 Mar 27.

Abstract

BACKGROUND

Owing to its longer treatment duration-up to 8 hours per dialysis treatment-in-center thrice-weekly nocturnal hemodialysis (HD) is receiving greater attention. To better understand the evidence for in-center nocturnal HD, we sought to systematically review the literature to determine the effects of in-center nocturnal HD versus conventional HD on clinically relevant outcomes.

STUDY DESIGN

We searched MEDLINE, Embase, Evidence-Based Medicine Reviews (EBMR), Web of Science, and Scopus from the earliest date in the database to November 2016.

SETTING & POPULATION: Adults receiving in-center nocturnal HD compared with those receiving conventional HD.

SELECTION CRITERIA FOR STUDIES

All quasi-experimental and observational studies were considered; randomized trials were sought but not found.

PREDICTOR

Nocturnal vs conventional in-center HD.

OUTCOMES

Indexes of blood pressure and left ventricular hypertrophy, markers of anemia, measures of bone mineral metabolism, nutrition, quality of life, sleep quality, episodes of intradialytic hypotension, hospitalization, and mortality.

RESULTS

Of 2,086 identified citations, 21 met the inclusion criteria, comprising a total of 1,165 in-center nocturnal HD patients and 15,865 conventional HD patients. Although there was substantial heterogeneity in reporting of outcomes, we pooled data for measures of blood pressure, anemia, and mineral metabolism. Though heterogeneity was generally high, in-center nocturnal HD was associated with improved systolic blood pressure (-3.18 [95% CI, -5.58 to -0.78) mm Hg, increased hemoglobin levels (0.53 [95% CI, 0.11-0.94] g/dL), and lower serum phosphate levels (-0.97 [95% CI, -1.48 to -0.46] mg/dL).

LIMITATIONS

No randomized trials have been conducted to address the clinical effects of in-center nocturnal HD. The quality of the observational literature contributing to the results of this review was generally poor to moderate. Confounded outcomes are a significant concern. Publication bias and outcome reporting bias remain possibilities.

CONCLUSIONS

Relative to conventional HD, in-center nocturnal HD was associated with improvements in several clinically relevant outcomes. Other benefits may not have been detected due to small sample sizes of included studies; no prespecified outcome was worse with in-center nocturnal HD.

摘要

背景

由于治疗时间较长——每次透析治疗长达 8 小时——中心夜间血液透析(HD)正在受到更多关注。为了更好地了解中心夜间 HD 的证据,我们系统地回顾了文献,以确定中心夜间 HD 与常规 HD 对临床相关结局的影响。

研究设计

我们检索了 MEDLINE、Embase、循证医学评价(EBMR)、Web of Science 和 Scopus,最早检索到数据库中的日期为 2016 年 11 月。

研究场所和人群

在中心接受夜间 HD 治疗的成年人与接受常规 HD 治疗的成年人进行比较。

研究选择标准

所有准实验和观察性研究都被考虑在内;虽然寻找了但未发现随机试验。

预测因子

夜间与常规中心 HD。

结局

血压和左心室肥厚指数、贫血标志物、骨矿物质代谢标志物、营养状况、生活质量、睡眠质量、透析中低血压发作、住院和死亡率。

结果

在 2086 篇被识别的引文,21 篇符合纳入标准,共纳入 1165 例中心夜间 HD 患者和 15865 例常规 HD 患者。尽管结局报告存在很大的异质性,但我们对血压、贫血和矿物质代谢的测量值进行了数据合并。尽管异质性通常很高,但中心夜间 HD 与收缩压降低(-3.18[95%CI,-5.58 至-0.78)mmHg、血红蛋白水平升高(0.53[95%CI,0.11-0.94]g/dL)和血清磷酸盐水平降低(-0.97[95%CI,-1.48 至-0.46]mg/dL)相关。

局限性

尚未进行随机试验来解决中心夜间 HD 的临床效果。对本综述结果有贡献的观察性文献的质量普遍较差到中等。混杂结局是一个重大关注点。发表偏倚和结局报告偏倚仍然是可能的。

结论

与常规 HD 相比,中心夜间 HD 与多项临床相关结局的改善相关。由于纳入研究的样本量较小,其他益处可能未被检测到;没有预设的结局在中心夜间 HD 治疗下更差。

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