Evidence map›Paper›PMID 33302892›Full record

ArticleBMC nephrology2020

Combination of biomarker with clinical risk factors for prediction of severe acute kidney injury in critically ill patients.

Lan Jia, Xiaohua Sheng, Anna Zamperetti, Yun Xie, Valentina Corradi, Shikha Chandel, Massimo De Cal, Diego Pomarè Montin, Carlotta Caprara, Claudio Ronco

Open access · goldAbstract read
In one paragraph

Article in BMC nephrology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 26% of its field
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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
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

10 authors at 6 institutions in 2 countries.

Lan JiaDepartment of Kidney Disease and Blood Purification, Institute of Urology & Key Laboratory of Tianjin, The Second Hospital of Tianjin Medical University, Tianjin, 300211, China. langirl1989@sina.com.ORCID 0000-0003-2622-4208
Xiaohua ShengInternational Renal Research Institute of Vicenza, San Bortolo Hospital, 36100, Vicenza, Italy.
Anna ZamperettiInternational Renal Research Institute of Vicenza, San Bortolo Hospital, 36100, Vicenza, Italy.
Yun XieInternational Renal Research Institute of Vicenza, San Bortolo Hospital, 36100, Vicenza, Italy.
Valentina CorradiInternational Renal Research Institute of Vicenza, San Bortolo Hospital, 36100, Vicenza, Italy.
Shikha ChandelInternational Renal Research Institute of Vicenza, San Bortolo Hospital, 36100, Vicenza, Italy.
Massimo De CalInternational Renal Research Institute of Vicenza, San Bortolo Hospital, 36100, Vicenza, Italy.
Diego Pomarè MontinInternational Renal Research Institute of Vicenza, San Bortolo Hospital, 36100, Vicenza, Italy.
Carlotta CapraraInternational Renal Research Institute of Vicenza, San Bortolo Hospital, 36100, Vicenza, Italy.
Claudio RoncoInternational Renal Research Institute of Vicenza, San Bortolo Hospital, 36100, Vicenza, Italy.
International Renal Research Institute of Vicenza · ITOspedale San Bortolo · ITSecond Hospital of Tianjin Medical University · CNShanghai Jiao Tong University · CNUniversità degli Studi del Piemonte Orientale “Amedeo Avogadro” · ITXinHua Hospital · CN

Funding

National Natural Science Foundation of China 81600591Science and Technology Project of Tianjin Health Committee QN20016
6 · The paper itself

Abstract

backgroundAcute kidney injury (AKI) occurs commonly in the intensive care unit (ICU). Insulin-like growth factor-binding protein 7 (IGFBP7) and tissue inhibitor of metalloproteinase-2 (TIMP-2), known as [TIMP-2] x [IGFBP7] (NephroCheck), have been identified as novel biomarkers for the prediction of AKI risk. However, the effective use of disease biomarkers is indispensable from an appropriate clinical context. We conducted a retrospective cohort study to find risk factors and assess the performance of the combination of NephroCheck with risk factors, so as to provide feasible information for AKI prediction.

methodsAll patients who were admitted in the ICU (from June 2016 to July 2017) participated in the study. The primary outcome was the detection of severe AKI within the first 7 days after patients being admitted to the ICU. The predictors were separated into three categories: chronic risk factors, acute risk factors and biochemical indicators.

resultsThe study included 577 patients. 96 patients developed to severe AKI (16.6%) within 7 days. In addition to NephroCheck (+) (OR = 2.139, 95% CI (1.260-3.630), P = 0.005), age > 65 years (OR = 1.961, 95% CI (1.153-3.336), P = 0.013), CKD (OR = 2.573, 95% CI (1.319-5.018), P = 0.006) and PCT (+)(OR = 3.223, 95% CI (1.643-6.321), P = 0.001) were also the independent predictors of severe AKI within 7 days. Compared to NephroCheck (+) only (AUC = 0.66, 95% CI:0.60-0.72), the combination of NephroCheck (+) and risk factors (age > 65 years, CKD and PCT positive) (AUC = 0.75, 95% CI:0.70-0.81) led to a significant increase in the area under ROC curve for severe AKI prediction within 7 days.

conclusionsAlthough NephroCheck is an effective screening tool for recognizing high-risk patients, we found that combination with biomarker and risk factors (age > 65 years, CKD, procalcitonin positive) for risk assessment of AKI has the greatest significance to patients with uncertain disease trajectories.

Indexed as

Critical IllnessAcute Kidney InjuryAgedAged, 80 and overAge FactorsBiomarkersClinical Decision RulesContinuous Renal Replacement TherapyCreatinineFemaleHospital MortalityHumansInsulin-Like Growth Factor Binding ProteinsIntensive Care UnitsLactic AcidLength of StayBiomarkersCreatinineinsulin-like growth factor binding protein-related protein 1Insulin-Like Growth Factor Binding ProteinsLactic AcidProcalcitoninTIMP2 protein, humanTissue Inhibitor of Metalloproteinase-2Acute kidney injuryClinical predictionInsulin-like growth factor-binding protein 7Intensive careRisk factorsTissue inhibitor of metalloproteinase-2

Identifiers

PMID33302892
PMCPMC7731753
OpenAlexW3112865526

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.