Evidence map›Paper›PMID 33527152›Full record

ArticleHeart and vessels2021

Clinical effectiveness and adverse events associated with tolvaptan in patients above 90 years of age with acute decompensated heart failure.

Yusuke Morita, Akihiro Endo, Yuzo Kagawa, Kazuto Yamaguchi, Hirotomo Sato, Takeshi Ouchi, Nobuhide Watanabe, Kazuaki Tanabe

Abstract read
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In one paragraph

Article in Heart and vessels, 2021. 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
0.3field-weighted citation impact, top 42% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
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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

8 authors at 1 institution in 1 country.

Yusuke MoritaDivision of Cardiology, Shimane University Faculty of Medicine, Izumo, 693-8501, Japan. morita-y@med.shimane-u.ac.jp.ORCID http://orcid.org/0000-0002-4419-3874
Akihiro EndoDivision of Cardiology, Shimane University Faculty of Medicine, Izumo, 693-8501, Japan.
Yuzo KagawaDivision of Cardiology, Shimane University Faculty of Medicine, Izumo, 693-8501, Japan.
Kazuto YamaguchiDivision of Cardiology, Shimane University Faculty of Medicine, Izumo, 693-8501, Japan.
Hirotomo SatoDivision of Cardiology, Shimane University Faculty of Medicine, Izumo, 693-8501, Japan.
Takeshi OuchiDivision of Cardiology, Shimane University Faculty of Medicine, Izumo, 693-8501, Japan.
Nobuhide WatanabeDivision of Cardiology, Shimane University Faculty of Medicine, Izumo, 693-8501, Japan.
Kazuaki TanabeDivision of Cardiology, Shimane University Faculty of Medicine, Izumo, 693-8501, Japan.
Shimane University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

With the aging society, the number of very-elderly (VE) patients with acute decompensated heart failure (ADHF) is increasing. Although tolvaptan is recommended for patients with ADHF in whom conventional diuretic therapy is ineffective, few reports exist on VE patients over 90 years of age. Therefore, we aimed to evaluate the clinical effectiveness and adverse events associated with tolvaptan in VE patients with ADHF. From January 2011 to December 2018, we retrospectively studied 180 patients with ADHF who were first administered tolvaptan during hospitalization. Patients were divided into two groups, namely, VE patients who were ≥ 90 years of age (n = 32) and not-VE patients (NVE) who were < 90 years of age (n = 148). The primary effective endpoints were the total urine volume and change in body weight. The safety endpoints evaluated were the incidence of hypernatremia (≥ 150 mEq/L) and worsening renal function (WRF) at any time during hospitalization. The median [interquartile range] patient age was 93 [91-94] years in the VE group and 80 [69-85] years in the NVE group. The mean dose of tolvaptan for the first week of administration was similar between groups (7.9 ± 5.0 mg, VE group; 7.3 ± 3.7 mg, NVE group; p = 0.52). There were no significant differences between the two groups in the total urine volume at 24 h (1901 ± 666 mL, VE group; 2101 ± 1167 mL, NVE group; p = 0.33) and that at 48 h (3707 ± 1274 mL, VE group; 4195 ± 1990 mL, NVE group; p = 0.19) and in the mean change in body weight (- 2.5 ± 2.0 kg, VE group; -2.7 ± 2.4 kg, NVE group; p = 0.70). The median duration of hospitalization was 24 [20-9] and 31 [20-42] days in the VE and NVE groups, respectively (p = 0.67). The incidence of hypernatremia (6.3% (2/32), VE group; 3.4% (5/148), NVE group; p = 0.61) and WRF (25.0% (8/32) VE group; 19.6% (29/148), NVE group; p = 0.31) was similar between the groups. In conclusion, tolvaptan has similar clinical effectiveness in increasing urine volume and decreasing body weight, without increased adverse events, in VE patients with ADHF who were ≥ 90 years of age compared to NVE patients with ADHF.

Indexed as

Acute DiseaseAgedAged, 80 and overAge FactorsAntidiuretic Hormone Receptor AntagonistsFemaleFollow-Up StudiesHeart FailureHumansMaleRetrospective StudiesStroke VolumeTolvaptanTreatment OutcomeAntidiuretic Hormone Receptor AntagonistsTolvaptanAcute decompensated heart failureAdverse eventEffectivenessElderly patientTolvaptan

Identifiers

PMID33527152
OpenAlexW3128178166

What OpenQuestion holds

Textmetadata
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.