Evidence map›Paper›PMID 32383323›Full record

ArticleESC heart failure2020

Renoprotective effect of tolvaptan in patients with new-onset acute heart failure.

Hiromi Kin, Koichiro Matsumura, Yoshihiro Yamamoto, Kenichi Fujii, Munemitsu Otagaki, Hiroki Takahashi, Haengnam Park, Kei Yoshioka, Mitsuru Yokoi, Tetsuro Sugiura and 1 more

Open access · goldAbstract read
In one paragraph

Article in ESC heart failure, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.6field-weighted citation impact, top 14% 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

11 citing papers in PubMed, 13 citations in OpenAlex.

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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

11 authors at 1 institution in 1 country.

Hiromi KinDepartment of Cardiology, Kansai Medical University Medical Center, Osaka, Japan.
Koichiro MatsumuraDepartment of Cardiology, Kansai Medical University Medical Center, Osaka, Japan.ORCID 0000-0002-9089-3505
Yoshihiro YamamotoDepartment of Cardiology, Kansai Medical University Medical Center, Osaka, Japan.
Kenichi FujiiDivision of Cardiology, Department of Medicine II, Kansai Medical University, Osaka, Japan.
Munemitsu OtagakiDepartment of Cardiology, Kansai Medical University Medical Center, Osaka, Japan.
Hiroki TakahashiDepartment of Cardiology, Kansai Medical University Medical Center, Osaka, Japan.
Haengnam ParkDepartment of Cardiology, Kansai Medical University Medical Center, Osaka, Japan.
Kei YoshiokaDepartment of Cardiology, Kansai Medical University Medical Center, Osaka, Japan.
Mitsuru YokoiDepartment of Cardiology, Kansai Medical University Medical Center, Osaka, Japan.
Tetsuro SugiuraDepartment of Cardiology, Kansai Medical University Medical Center, Osaka, Japan.
Ichiro ShiojimaDivision of Cardiology, Department of Medicine II, Kansai Medical University, Osaka, Japan.
Kansai Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsAlthough tolvaptan has been reported to prevent worsening renal function (WRF) in patients with advanced acute heart failure (AHF), evidence regarding the effect of tolvaptan on renal function in patients with new-onset AHF is not available. This study aimed to investigate the renoprotective effect of tolvaptan in patients hospitalized with new-onset AHF. METHODS AND

resultsA total of 122 consecutive patients hospitalized with new-onset AHF between May 2015 and December 2018 were retrospectively evaluated. WRF was defined as an absolute increase in serum creatinine ≥0.3 mg/dL (≥26.4 μmol/L) within 48 h or a 1.5-fold increase in serum creatinine after hospitalization. The furosemide group (n = 75) and the tolvaptan add-on group (n = 47) were compared. The tolvaptan group consists of patients who received tolvaptan as an individual physicians' decision. The incidence of WRF was significantly lower in the tolvaptan add-on group (8.5%) than in the furosemide group (24.0%, P = 0.03). Multivariate logistic regression analysis revealed that tolvaptan treatment was an independent variable related to the prevention of WRF [odds ratio (OR), 0.20; 95% confidence interval (CI), 0.05-0.85]. Furthermore, subgroup analysis revealed a more favourable effect of tolvaptan in patients with serum creatinine ≥1.1 mg/dL on admission (OR, 0.23; 95% CI, 0.06-0.98) and an ejection fraction <50% (OR, 0.19; 95% CI, 0.04-0.90).

conclusionsA lower incidence of WRF was observed in patients with new-onset AHF who were treated with the tolvaptan add-on therapy, specifically those with left ventricular systolic dysfunction and renal impairment on admission.

Indexed as

DiureticsHeart FailureFurosemideHumansRetrospective StudiesTolvaptanDiureticsFurosemideTolvaptanAcute heart failureTolvaptanWorsening renal function

Identifiers

PMID32383323
PMCPMC7373889
OpenAlexW3023118659

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.