Evidence map›Paper›PMID 35118813›Full record

ArticleESC heart failure2022

Effect of carperitide on the 1 year prognosis of patients with acute decompensated heart failure.

Kazutaka Nogi, Tomoya Ueda, Yuya Matsue, Maki Nogi, Satomi Ishihara, Yasuki Nakada, Rika Kawakami, Nobuyuki Kagiyama, Takeshi Kitai, Shogo Oishi and 6 more

Open access · goldAbstract read
In one paragraph

Article in ESC heart failure, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
4.3field-weighted citation impact, top 5% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Pooled it
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  7. Article
  8. Neurohumoral Activation in Heart Failure.International journal of molecular sciences · 2023
    Review
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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

16 authors at 10 institutions in 1 country.

Kazutaka NogiDepartment of Cardiovascular Medicine, Nara Medical University, 840 Shijo-cho, Kashihara, 634-8522, Japan.
Tomoya UedaDepartment of Cardiovascular Medicine, Nara Medical University, 840 Shijo-cho, Kashihara, 634-8522, Japan.
Yuya MatsueDepartment of Cardiovascular Biology and Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Maki NogiDepartment of Cardiovascular Medicine, Nara Medical University, 840 Shijo-cho, Kashihara, 634-8522, Japan.
Satomi IshiharaDepartment of Cardiovascular Medicine, Nara Medical University, 840 Shijo-cho, Kashihara, 634-8522, Japan.
Yasuki NakadaDepartment of Cardiovascular Medicine, Nara Medical University, 840 Shijo-cho, Kashihara, 634-8522, Japan.
Rika KawakamiDepartment of Cardiovascular Medicine, Nara Medical University, 840 Shijo-cho, Kashihara, 634-8522, Japan.
Nobuyuki KagiyamaDepartment of Cardiovascular Biology and Medicine, Juntendo University Faculty of Medicine, Tokyo, Japan.
Takeshi KitaiDepartment of Cardiovascular Medicine, National Cerebral and Cardiovascular Center, Osaka, Japan.
Shogo OishiDepartment of Cardiology, Himeji Cardiovascular Center, Himeji, Japan.
Eiichi AkiyamaDivision of Cardiology, Yokohama City University Medical Center, Yokohama, Japan.
Satoshi SuzukiDepartment of Cardiovascular Medicine, Fukushima Medical University, Fukushima, Japan.
Masayoshi YamamotoCardiovascular Division, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
Keisuke KidaDepartment of Pharmacology, St. Marianna University School of Medicine, Kawasaki, Japan.
Takahiro OkumuraDepartment of Cardiology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Yoshihiko SaitoDepartment of Cardiovascular Medicine, Nara Medical University, 840 Shijo-cho, Kashihara, 634-8522, Japan.
Nara Medical University · JPFukushima Medical University · JPHimeji High School · JPJuntendo University · JPKobe City Medical Center General Hospital · JPNagoya University · JPSakakibara Hospital · JPSt. Marianna University School of Medicine · JPUniversity of Tsukuba · JPYokohama City University Medical Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsAcute heart failure (AHF) is a clinical syndrome with a poor prognosis and a major public health concern worldwide. The aim of this study was to investigate whether carperitide administration improves the 1 year prognosis of patients with AHF and to check whether there is an optimal dose of the drug. METHODS AND

resultsWe analysed the data of COOPERATE-HF-J (the Consortium for Pooled Data Analysis regarding Hospitalized Patients with Heart Failure in Japan), combining two cohorts (NARA-HF and REALITY-AHF), which included 2435 patients with acute decompensated heart failure. The patients were divided into no carperitide (NO-ANP, n = 1098); very low-dose carperitide (VLD-ANP, <0.02 μg/kg/min, n = 593); and low-dose carperitide groups (LD-ANP, ≥0.02 μg/kg/min, n = 744). The primary endpoint was cardiovascular mortality within 1 year after admission. The secondary endpoints were all-cause mortality and rehospitalization due to worsening heart failure within 1 year after admission. The median carperitide doses in the VLD-ANP and LD-ANP groups were 0.013 and 0.025 μg/kg/min, respectively. Kaplan-Meier analysis showed that cardiovascular mortality and all-cause mortality were significantly lower in the LD-ANP group than in the NO-ANP and VLD-ANP groups (P < 0.001 and P = 0.002, respectively). Multivariable Cox regression analysis for cardiovascular and all-cause mortality revealed that LD-ANP was significantly associated with lower cardiovascular and all-cause mortality within 1 year after admission, even after adjusting other covariates (hazard ratio: 0.696 and 0.791, 95% confidence interval: 0.513-0.944 and 0.628-0.997, P = 0.020 and 0.047, respectively).

conclusionsLow-dose carperitide was significantly associated with lower cardiovascular and all-cause mortality within 1 year after admission. Our results suggest the necessity for well-designed randomized controlled trials to determine the doses of carperitide that could improve clinical outcomes in patients with AHF.

Indexed as

Atrial Natriuretic FactorHeart FailureAcute DiseaseHumansPrognosisAtrial Natriuretic FactorNPPA protein, humanAcute heart failureAtrial natriuretic peptideCarperitideDosing

Identifiers

PMID35118813
PMCPMC8934945
OpenAlexW4210531987

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

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.