Evidence map›Paper›PMID 39433425›Full record

ArticleOpen heart2024

Risk stratification by renal function and NYHA class in patients with hypotension initiated on sacubitril/valsartan: a retrospective cohort study from 17 centres in Japan.

Koshiro Kanaoka, Takahito Nasu, Atsushi Kikuchi, Takeshi Ijichi, Tatsuhiro Shibata, Keisuke Kida, Nobuyuki Kagiyama, Wataru Fujimoto, Syunsuke Ishii, Yoshitaka Iwanaga and 2 more

Abstract readMulticenter Study
In one paragraph

Article in Open heart, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

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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

12 authors.

Koshiro KanaokaDepartment of Medical and Health Information Management, National Cerebral and Cardiovascular Center, Suita, Osaka, Japan kanaokak@ncvc.go.jp.ORCID 0000-0001-7900-7835
Takahito NasuDepartment of Internal Medicine, Iwate Medical University, Shiwa-gun, Iwate, Japan.
Atsushi KikuchiOsaka General Medical Center, Osaka, Japan.
Takeshi IjichiDepartment of Cardiology, Tokai University School of Medicine, Isehara, Kanagawa, Japan.
Tatsuhiro ShibataDepartment of Internal Medicine, Kurume University School of Medicine, Kurume, Japan.
Keisuke KidaCardiology, St. Marianna University School of Medicine, Kawasaki, Kanagawa, Japan.
Nobuyuki KagiyamaDepartment of Cardiovascular Biology and Medicine, Juntendo University Faculty of Medicine, Tokyo, Japan.
Wataru FujimotoDepartment of Internal Medicine, Kobe University Graduate School of Medicine, Kobe, Japan.
Syunsuke IshiiCardiovascular Medicine, Kitasato University School of Medicine, Sagamihara, none, Japan.
Yoshitaka IwanagaDepartment of Medical and Health Information Management, National Cerebral and Cardiovascular Center, Suita, Osaka, Japan.
Yoshihiro MiyamotoDepartment of Medical and Health Information Management, National Cerebral and Cardiovascular Center, Suita, Osaka, Japan.
Shingo MatsumotoCardiovascular Medicine, Toho University Graduate School of Medicine, Ota-ku, Japan.ORCID 0000-0002-2000-1954

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPatients with heart failure exhibiting low systolic blood pressure (SBP) have a poor prognosis. Sacubitril/valsartan reduces cardiovascular events; however, its use in patients with low SBP has not been fully examined. Therefore, in this study, we aimed to investigate the association between baseline SBP and adverse events (AEs) in patients starting sacubitril/valsartan therapy using data from a real-world registry in Japan.

methodsWe analysed data from a multicentre retrospective study, including patients who initiated sacubitril/valsartan between August 2020 and August 2021. The patients were categorised into five groups based on their baseline SBP (<100, 100-109, 110-119, 120-129 and ≥130 mm Hg). The composite of AEs occurring within 3 months according to baseline SBP and the patient characteristics associated with AEs in a baseline SBP <110 mm Hg were analysed.

resultsAmong the 964 patients newly prescribed sacubitril/valsartan, the median (IQR) age was 73 (61-80) years, and 388 (40.2%) patients had a baseline SBP <110 mm Hg. AEs occurred in 24% (n=232) of patients. The adjusted ORs for all AEs were 1.91 (95% CI (CI) 1.13-3.23; p=0.02) for the SBP <100 mm Hg group and 3.33 (95% CI 1.98 to 5.59; p<0.001) for the SBP 100-109 mm Hg group, compared with the SBP 110-119 mm Hg group. In patients with a baseline SBP <110 mm Hg, factors associated with an increased risk of AEs included a higher New York Heart Association class (II, III or IV) and a lower estimated glomerular filtration rate <30 mL/min/1.73 m

conclusionsCaution is needed when initiating sacubitril/valsartan in patients with lower baseline SBP. The severity of heart failure and kidney function may be useful for risk stratification in these high-risk patients.

Indexed as

AminobutyratesBiphenyl CompoundsDrug CombinationsHeart FailureHypotensionValsartanAgedAged, 80 and overAngiotensin Receptor AntagonistsBlood PressureFemaleFollow-Up StudiesGlomerular Filtration RateHumansJapanKidneyAminobutyratesAngiotensin Receptor AntagonistsBiphenyl CompoundsDrug Combinationssacubitril and valsartan sodium hydrate drug combinationTetrazolesValsartanHeart FailureHEART FAILUREHeart Failure, DiastolicHeart Failure, Systolic

Identifiers

PMID39433425
PMCPMC11499766

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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.