Evidence map›Paper›PMID 40205353›Full record

ArticleBMC nephrology2025

Development and validation of a prediction model for the risk of citrate accumulation in critically ill patients with citrate anticoagulation for continuous renal replacement therapy: a retrospective cohort study based on MIMIC-IV database.

Zhi-Qing Hu, Zheng-Long Ye, Hui Zou, Shang-Xiang Liu, Cheng-Qing Mei

Abstract readValidation Study
In one paragraph

Article in BMC nephrology, 2025. 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.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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.

  1. Review
  2. Article
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.

Zhi-Qing HuDepartment of Critical Care Medicine, Nanjing Jiangbei Hospital, 552GeGuan Road, Dachang Street, Jiangbei New District, Nanjing, Jiangsu Province, 210048, China.
Zheng-Long YeDepartment of Critical Care Medicine, Nanjing Jiangbei Hospital, 552GeGuan Road, Dachang Street, Jiangbei New District, Nanjing, Jiangsu Province, 210048, China. zlyenj@126.com.
Hui ZouDepartment of Critical Care Medicine, Nanjing Jiangbei Hospital, 552GeGuan Road, Dachang Street, Jiangbei New District, Nanjing, Jiangsu Province, 210048, China.
Shang-Xiang LiuDepartment of Critical Care Medicine, Nanjing Jiangbei Hospital, 552GeGuan Road, Dachang Street, Jiangbei New District, Nanjing, Jiangsu Province, 210048, China.
Cheng-Qing MeiDepartment of Critical Care Medicine, Nanjing Jiangbei Hospital, 552GeGuan Road, Dachang Street, Jiangbei New District, Nanjing, Jiangsu Province, 210048, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAcute kidney injury (AKI) is a common clinical syndrome, especially in the intensive care unit (ICU), with an incidence of more than 50% and in-hospital mortality of 30%. Continuous renal replacement therapy (CRRT) is an important supportive treatment for patients with AKI (Patel in Trauma Surg Acute Care Open e001381, 2024). Citrate is the preferred anticoagulant for critically ill patients requiring CRRT. Unfortunately, such patients may be confronted with citrate accumulation during citrate anticoagulation.

methodsThe MIMIC-IV2.2 database was used to extract data of patients undergoing CRRT who opted for citrate anticoagulation during ICU admission, including 883 critically ill patients. These 883 patients were randomized into training (n = 618) and Internal validation (n = 265) groups at a ratio of 7:3. Least Absolute Shrinkage and Selection Operator(LASSO)-logistic regression was utilized to screen the variables and construct the prediction model, followed by the plotting of the nomogram. Then, Utilizing the retrospective data from the ICU at Jiangbei Hospital in Nanjing, China, from 2014 to 2024 (n = 200) for external model validation, the model was evaluated with discriminant analysis, calibration curves, decision curve analysis, and rationality analysis.

resultsA total of 883 critically ill patients undergoing CRRT were included, consisting of 542 males and 341 females, with a mean age of 65 ± 14 years. Additionally, there were 618 patients in the training set and 265 in the validation set. A total of 47 independent variables were obtained, among which 15 independent variables were screened with LASSO regression and included in the multivariate logistic analysis. The five risk factors ultimately included in the prediction model were height, hepatic insufficiency, mechanical ventilation, prefilter replacement rate, and albumin. The area under the receiver operating characteristic curve (ROC) of the model was 0.758 (0.701-0.816), 0.747 (0.678-0.817), and 0.714 (0.632-0.810) for the training set, internal validation set, and external validation set, respectively. The calibration curves in the training set and internal/external validation sets showed a high degree of consistency between predicted values and observed values (according to the Hosmer-Lemeshow test, the P-values were 0.7673, 0.2401, and 0.4512 for the training set, internal validation set, and external validation set, respectively). In addition, the Decision-Curve(DCA) revealed that the model had good clinical applicability. Nomo-score comparisons exhibited the rationality of the model.

conclusionThe model developed based on LASSO-logistic regression can reliably predict the risk of citrate accumulation in critically ill patients with citrate anticoagulation for CRRT, providing valuable guidance for the application of early measures to prevent the occurrence of citrate accumulation and to improve the prognosis of patients.

Indexed as

Acute Kidney InjuryAnticoagulantsCitric AcidContinuous Renal Replacement TherapyAgedCohort StudiesCritical IllnessDatabases, FactualFemaleHumansIntensive Care UnitsMaleMiddle AgedNomogramsRetrospective StudiesRisk AssessmentAnticoagulantsCitric AcidCitrate accumulationContinuous renal replacement therapyIntensive care unitMIMIC-IVNomogram

Identifiers

PMID40205353
PMCPMC11983910

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.