Evidence map›Paper›PMID 39526333›Full record

ArticleRenal failure2024

Prediction of dialysis adequacy using data-driven machine learning algorithms.

Yi-Chen Liu, Ji-Ping Qing, Rong Li, Juan Chang, Li-Xia Xu

Abstract read
In one paragraph

Article in Renal failure, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Yi-Chen LiuDepartment of Nephrology, Chongming Hospital Affiliated to Shanghai University of Medicine and Health Sciences, Shanghai Municipality, China.
Ji-Ping QingDepartment of Nephrology, Chongming Hospital Affiliated to Shanghai University of Medicine and Health Sciences, Shanghai Municipality, China.
Rong LiDepartment of Nephrology, Chongming Hospital Affiliated to Shanghai University of Medicine and Health Sciences, Shanghai Municipality, China.
Juan ChangDepartment of Nephrology, Chongming Hospital Affiliated to Shanghai University of Medicine and Health Sciences, Shanghai Municipality, China.
Li-Xia XuDepartment of Nephrology, Chongming Hospital Affiliated to Shanghai University of Medicine and Health Sciences, Shanghai Municipality, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAdequate delivery of hemodialysis (HD), measured by the spKt/V derived from urea reduction, is an important determinant of clinical outcomes in chronic hemodialysis patients. However, the need for pre- and postdialysis blood samples prevented the assessment of spKt/V in every session.

methodsThis retrospective single-center study was performed on end-stage renal disease (ESKD) patients aged ≥ 18 years who received standard thrice-weekly chronic HD therapy. Eighty-seven variables, including general, intradialytic, and laboratory variables, were collected from the medical records for analysis. Five steps of preprocessing procedure were deployed to select only the most relevant variables. Six binary classification models were developed to predict whether spKt/V was higher than 1.4.

resultsA total of 1869 HD sessions from 373 ESKD patients were included in this study. The Random Forest model showed the best prediction for dialysis adequacy, with AUROC scores of 0.860 in the validation dataset and 0.873 in the testing dataset. Notably, an accessible model that solely relied on noninvasively collected general and dialysis-related variables maintained high prediction accuracy, with AUROC scores of 0.854 and 0.868 in the validation and testing datasets, respectively. The five most significant predictive variables were vascular access, gender, body mass index, ultrafiltration volume, and dialysis duration.

conclusionThe study results suggest that the development of ML models for accurately predicting dialysis adequacy based on general and intradialytic variables is feasible. These models have the potential to be utilized for noninvasive clinical assessments of dialysis adequacy.

Indexed as

Kidney Failure, ChronicMachine LearningRenal DialysisAdultAgedAlgorithmsFemaleHumansMaleMiddle AgedRetrospective StudiesUreaUreaDialysis adequacyhemodialysisKt/Vmachine learning

Identifiers

PMID39526333
PMCPMC11556278

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.