Evidence map›Paper›PMID 40010939›Full record

ArticleShock (Augusta, Ga.)2025

CELL FREE DNA-BASED PREDICTION OF PROGNOSIS FOR PATIENTS ON VENO-ARTERIAL EXTRACORPOREAL MEMBRANE OXYGENATION.

Jin Li, ChengLong Li, Liangshan Wang, Xiaomeng Wang, Bo Xu, Chunjing Jiang, Meng Xin, Dong Guo, Jing Chen, Zhongtao Du and 3 more

Abstract read
In one paragraph

Article in Shock (Augusta, Ga.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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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

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

13 authors.

Jin LiCenter for Cardiac Intensive Care, Beijing Anzhen Hospital, Capital Medical University, Beijing, People's Republic of China.
ChengLong Li
Liangshan Wang
Xiaomeng Wang
Bo Xu
Chunjing Jiang
Meng Xin
Dong Guo
Jing Chen
Zhongtao Du
Hong Wang
Xing Hao

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

abstractIntroduction : Elevated cell-free DNA (cfDNA) was observed in patients receiving venoarterial (VA) extracorporeal membrane oxygenation (ECMO), but the clinical relevance of cfDNA is still not clear. We aimed to establish a predictive model based on the cfDNA to predict the prognosis for patients on ECMO, and reveal the values of cfDNA for complications of limb ischemia and bleeding/thromboembolic events. Methods : Single-center, retrospective evaluation of patients with ECMO support from 2018 through 2023. The derivation cohort included 133 adults diagnosed with cardiogenic shock who received VA-ECMO for circulatory support. We developed three independent features and combined them with a logistic model to predict mortality. Predictive performance was assessed through Bootstrap analysis and validated by another cohort of 27 patients. The values of cfDNA for complications were analyzed by restricted cubic spline analysis, receiver-operating characteristic curves and multivariate regression analyses. Results : A total of 133 adults who underwent VA-ECMO for refractory cardiogenic shock were entered into the derivation cohort. The logistic model, consisted of cfDNA, the worst mean arterial pressure (MAP) before ECMO and the worst lactate within 24 h of VA-ECMO implantation was predictive and performed similarly for validation cohorts (area under the receiver operating characteristic curve: 0.768 vs. 0.747). Restricted cubic spline analysis revealed a positive linear relationship for the risk of limb ischemia (linear, P = 0.006; area under the receiver operating characteristic curve of 0.75 [95% CI, 0.656-0.848]), a U-shaped trend for bleeding events (nonlinear, P = 0.214), and a negative trend for thrombotic events (linear, P = 0.552). Conclusions: In addition to MAP and lactate levels, elevated cfDNA levels within 48 h of ECMO support were highly associated with mortality for patients. Additionally, cfDNA is predictive of limb ischemia.

Indexed as

Cell-Free Nucleic AcidsExtracorporeal Membrane OxygenationShock, CardiogenicAdultAgedFemaleHumansMaleMiddle AgedPrognosisRetrospective StudiesCell-Free Nucleic AcidsBiomarkercomplicationECMOmortalityprediction

Identifiers

PMID40010939
PMCPMC12105943

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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.