Abstract
Background
The effects of early renal replacement therapy (RRT) on mortality and renal recovery in patients with acute kidney injury (AKI) remain controversial. A systematic review and meta-analysis of randomized-controlled trials (RCTs) was performed.
Methods
MEDLINE, EMBASE and the Cochrane Library database (Cochrane Central Register of Controlled Trials) were searched to identify RCTs, investigating the effects of early RRT on patients with AKI.
Results
Six studies with a total of 1257 participants were included in this meta-analysis. Compared to late RRT, early RRT did not reduce the risk of mortality (RR 0.93, 95 % CI 0.68–1.26) or affect renal recovery (RR 0.88, 95 % CI 0.48–1.62) or composite endpoint (death or dialysis dependence) (RR 0.91, 95 % CI 0.71–1.17). There was no significant difference in adverse events in the analysis, between the early RRT and late RRT arms.
Conclusions
Early initiation of RRT for patients with AKI is not associated with decreased overall mortality or a delayed renal recovery rate. The optimal time to initiate RRT remains uncertain. Large scale and adequately powered RCTs are needed to detect the effects of early initiation of RRT in AKI patients.
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Acknowledgments
This study was supported in part by Twelfth Five-Year Plan Medical Science Development Foundation of the Chinese People’s Liberation Army (AWS11J013) and the Army Medical Science Youth Development Project (13QNP088).
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All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. This article does not contain any studies with animals performed by any of the authors. Informed consent was not involved.
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Yongxing Xu and Jianjun Gao contributed equally to this work.
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Xu, Y., Gao, J., Zheng, X. et al. Timing of initiation of renal replacement therapy for acute kidney injury: a systematic review and meta-analysis of randomized-controlled trials. Clin Exp Nephrol 21, 552–562 (2017). https://doi.org/10.1007/s10157-016-1316-2
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DOI: https://doi.org/10.1007/s10157-016-1316-2