Evidence map›Paper›PMID 39756821›Full record

Observational studyOpen heart2025

Acute kidney injury recovery status predicts mortality and cardiorenal outcomes in patients admitted with acute decompensated heart failure.

Sumita Barua, Sanjay Chavali, Albert Vien, Shehane Mahendran, David Makarious, Phillip Lo, Kirsty Pringle, James Chong, Kavitha Muthiah, Christopher Hayward

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Open heart, 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

10 authors.

Sumita BaruaCardiology, St Vincent's Hospital Sydney, Darlinghurst, New South Wales, Australia sbarua88@gmail.com.ORCID http://orcid.org/0000-0001-9091-6773
Sanjay ChavaliCardiology, St Vincent's Hospital Sydney, Darlinghurst, New South Wales, Australia.
Albert VienCardiology, Westmead Hospital, Westmead, New South Wales, Australia.
Shehane MahendranCardiology, Westmead Hospital, Westmead, New South Wales, Australia.
David MakariousCardiology, Westmead Hospital, Westmead, New South Wales, Australia.
Phillip LoCardiology, St Vincent's Hospital Sydney, Darlinghurst, New South Wales, Australia.
Kirsty PringleThe University of Newcastle Hunter Medical Research Institute, New Lambton, New South Wales, Australia.
James ChongCardiology, Westmead Hospital, Westmead, New South Wales, Australia.
Kavitha MuthiahCardiology, St Vincent's Hospital Sydney, Darlinghurst, New South Wales, Australia.
Christopher HaywardCardiology, St Vincent's Hospital Sydney, Darlinghurst, New South Wales, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAcute kidney injury (AKI) in the context of acute decompensated heart failure (ADHF) encompasses a broad spectrum of phenotypes with associated disparate outcomes. We evaluate the impact of 'ongoing AKI' on prognosis and cardiorenal outcomes and describe predictors of 'ongoing AKI'.

methodsA prospective multicentre observational study of patients admitted with ADHF requiring intravenous furosemide was completed, with urinary angiotensinogen (uAGT) measured at baseline. AKI was defined using Kidney Disease Improving Global Outcomes (KDIGO) AKI criteria. AKI recovery status was defined as 'no AKI', 'recovered AKI' or 'ongoing AKI' based on renal function at hospital discharge. Event-free survival analysis was performed to predict death and cardiorenal outcomes at hospital discharge and 6-month follow-up. Multinomial logistic regression was performed to identify predictors of ongoing AKI. Multiclass receiver operator curve analysis was performed to evaluate the relationship between renin-angiotensin system (RAS) blockers and uAGT in predicting ongoing AKI.

resultsAmong 271 enrolled patients, 121 (44.6%) patients developed AKI, of whom 62 patients had ongoing AKI. Ongoing AKI was associated with increased risk of death (HR 6.89, p<0.001), in-hospital end-stage kidney disease (HR 44.39, p<0.001), 6-month composite of death, transplant, left ventricular assist device and heart failure hospitalisation (HR 3.09, p<0.001), and 6-month composite major adverse kidney events (HR 5.71, p<0.001). Elevated baseline uAGT levels, chronic beta-blocker and thiazide diuretic therapy, and lack of RAS blocker prescription at recruitment were associated with ongoing AKI. While uAGT levels were lower with RAS blocker prescription, in patients with ongoing AKI, uAGT levels were elevated regardless of RAS blocker status.

conclusionPatients experiencing ongoing AKI during ADHF admission were at increased risk of death and other adverse cardiorenal outcomes. Differential uAGT response in patients receiving RAS blockers with ongoing AKI suggests biomarkers may be helpful in predicting treatment responses and cardiorenal outcomes.

Indexed as

Acute Kidney InjuryBiomarkersCardio-Renal SyndromeHeart FailureRecovery of FunctionAcute DiseaseAgedAged, 80 and overAngiotensinogenDiureticsFemaleFollow-Up StudiesFurosemideHumansMaleMiddle AgedAngiotensinogenBiomarkersDiureticsFurosemideBiomarkersHeart-Assist DevicesHEART FAILUREHeart Transplantation

Identifiers

PMID39756821
PMCPMC11751981

What OpenQuestion holds

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Registered trials

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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.