Evidence map›Paper›PMID 34151546›Full record

Observational studyESC heart failure2021

Prognostic impact of Clinical Frailty Scale in patients with heart failure with preserved ejection fraction.

Akihiro Sunaga, Shungo Hikoso, Takahisa Yamada, Yoshio Yasumura, Masaaki Uematsu, Shunsuke Tamaki, Haruhiko Abe, Yusuke Nakagawa, Yoshiharu Higuchi, Hisakazu Fuji and 16 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in ESC heart failure, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 3 pooled it
–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

24 citing papers in PubMed, 3 syntheses or guidelines pooled it.

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  15. β-blockers may be detrimental in frail patients with heart failure with preserved ejection fraction.Clinical research in cardiology : official journal of the German Cardiac Society · 2024
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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

26 authors.

Akihiro SunagaDepartment of Cardiovascular Medicine, Graduate School of Medicine, Osaka University, Suita, Japan.
Shungo HikosoDepartment of Cardiovascular Medicine, Graduate School of Medicine, Osaka University, Suita, Japan.
Takahisa YamadaDivision of Cardiology, Osaka General Medical Center, Osaka, Japan.
Yoshio YasumuraDivision of Cardiology, Amagasaki Chuo Hospital, Amagasaki, Japan.
Masaaki UematsuCardiovascular Division, National Hospital Organization Osaka National Hospital, Osaka, Japan.
Shunsuke TamakiDivision of Cardiology, Osaka General Medical Center, Osaka, Japan.
Haruhiko AbeCardiovascular Division, National Hospital Organization Osaka National Hospital, Osaka, Japan.
Yusuke NakagawaDivision of Cardiology, Kawanishi City Hospital, Kawanishi, Japan.
Yoshiharu HiguchiCardiovascular Division, Osaka Police Hospital, Osaka, Japan.
Hisakazu FujiDivision of Cardiology, Kobe Ekisaikai Hospital, Kobe, Japan.
Toshiaki ManoCardiovascular Center, Kansai Rosai Hospital, Amagasaki, Japan.
Hiroyuki KurakamiDepartment of Medical Innovation, Osaka University Hospital, Suita, Japan.
Tomomi YamadaDepartment of Medical Innovation, Osaka University Hospital, Suita, Japan.
Tetsuhisa KitamuraDepartment of Social and Environmental Medicine, Graduate School of Medicine, Osaka University, Suita, Japan.
Taiki SatoDepartment of Cardiovascular Medicine, Graduate School of Medicine, Osaka University, Suita, Japan.
Bolrathanak OeunDepartment of Cardiovascular Medicine, Graduate School of Medicine, Osaka University, Suita, Japan.
Hirota KidaDepartment of Cardiovascular Medicine, Graduate School of Medicine, Osaka University, Suita, Japan.
Takayuki KojimaDepartment of Cardiovascular Medicine, Graduate School of Medicine, Osaka University, Suita, Japan.
Yohei SotomiDepartment of Cardiovascular Medicine, Graduate School of Medicine, Osaka University, Suita, Japan.
Tomoharu DohiDepartment of Cardiovascular Medicine, Graduate School of Medicine, Osaka University, Suita, Japan.
Katsuki OkadaDepartment of Cardiovascular Medicine, Graduate School of Medicine, Osaka University, Suita, Japan.
Shinichiro SunaDepartment of Cardiovascular Medicine, Graduate School of Medicine, Osaka University, Suita, Japan.
Hiroya MizunoDepartment of Cardiovascular Medicine, Graduate School of Medicine, Osaka University, Suita, Japan.
Daisaku NakataniDepartment of Cardiovascular Medicine, Graduate School of Medicine, Osaka University, Suita, Japan.
Yasushi SakataDepartment of Cardiovascular Medicine, Graduate School of Medicine, Osaka University, Suita, Japan.
OCVC-Heart Failure Investigators

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsFrailty is associated with prognosis of cardiovascular diseases. However, the significance of frailty in patients with heart failure with preserved ejection fraction (HFpEF) remains to be elucidated. The purpose of this study was to examine the prognostic significance of the Clinical Frailty Scale (CFS) in real-world patients with HFpEF using data from a prospective multicentre observational study of patients with HFpEF (PURSUIT-HFpEF study). METHOD AND

resultsWe classified 842 patients with HFpEF enrolled in the PURSUIT-HFpEF study into two groups using CFS. The registry enrolled patients hospitalized with a diagnosis of decompensated heart failure. Median age was 82 [interquartile range: 77, 87], and 45% of the patients were male. Of 842 patients, 406 were classified as high CFS (CFS ≥ 4, 48%) and 436 as low CFS (CFS ≤ 3, 52%). The primary endpoint was the composite of all-cause mortality and heart failure admission. Secondary endpoints were all-cause mortality and heart failure admission. Patients with high CFS were older (85 vs. 79 years, P < 0.001), predominantly female (65% vs. 46%, P < 0.001) and more likely to have New York Heart Association (NYHA) ≥ 2 (75% vs. 53%, P < 0.001) and a higher level of NT-proBNP (1360 vs 838 pg/mL, P < 0.001) than those with low CFS. Patients with high CFS had a significantly greater risk of composite endpoint (Kaplan-Meier estimated 1-year event rate 39% vs. 23%, log-rank P < 0.001), all-cause mortality (Kaplan-Meier estimated 1-year event rate 17% vs. 7%, log-rank P < 0.001) and heart failure admission (Kaplan-Meier estimated 1-year event rate 28% vs. 19%, log-rank P = 0.002) than those with low CFS. Multivariable Cox regression analysis revealed that high CFS was significantly associated with composite endpoint (adjusted HR 1.92, 95% CI 1.35-2.73, P < 0.001), all-cause mortality (adjusted HR 2.54, 95% CI 1.39-4.66, P = 0.003) and heart failure admission (adjusted HR 1.55, 95% CI 1.03-2.32, P = 0.035) even after adjustment for covariates. Moreover, change in CFS grade was also significantly associated with composite endpoint (adjusted HR 1.23, 95% CI 1.11-1.36, P < 0.001), all-cause mortality (adjusted HR 1.32, 95% CI 1.13-1.55, P = 0.001) and heart failure admission (adjusted HR 1.15, 95% CI 1.02-1.30, P = 0.021).

conclusionsFrailty assessed by the CFS was associated with poor prognosis in patients with HFpEF.

Indexed as

FrailtyHeart FailureAged, 80 and overFemaleHumansMalePrognosisProspective StudiesStroke VolumeFrailty; Heart failure with preserved ejection fraction; Clinical Frailty Scale

Identifiers

PMID34151546
PMCPMC8318468

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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.