Evidence map›Paper›PMID 36648084›Full record

SynthesisClinical cardiology2023

Efficacy and safety of low-dose sacubitril/valsartan in heart failure patients: A systematic review and meta-analysis.

Wen-Wen Chen, Juan Jiang, Jie Gao, Xiu-Zhen Zhang, Yuan-Min Li, Yan-Lin Liu, He-Qin Dang

Open access · goldFull text readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in Clinical cardiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
1.8field-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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
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

7 authors at 1 institution in 1 country.

Wen-Wen ChenDepartment of Pharmacy, The Second Affiliated Hospital of Shandong First Medical University, Tai'an, China.ORCID http://orcid.org/0000-0003-0975-0839
Juan JiangDepartment of Stomatology, The Second Affiliated Hospital of Shandong First Medical University, Tai'an, China.
Jie GaoDepartment of Pharmacy, The Second Affiliated Hospital of Shandong First Medical University, Tai'an, China.
Xiu-Zhen ZhangDepartment of Pharmacy, The Second Affiliated Hospital of Shandong First Medical University, Tai'an, China.
Yuan-Min LiDepartment of Cardiology, The Second Affiliated Hospital of Shandong First Medical University, Tai'an, China.ORCID http://orcid.org/0000-0002-3385-3734
Yan-Lin LiuDepartment of Pharmacy, The Second Affiliated Hospital of Shandong First Medical University, Tai'an, China.
He-Qin DangDepartment of Pharmacy, The Second Affiliated Hospital of Shandong First Medical University, Tai'an, China.
Affiliated Hospital of Taishan Medical University · CN

Funding

Academic promotion programme of Shandong First Medical University 2019QL017Tai'an City Science and technology Innovation development Project 2020NS226
6 · The paper itself

Abstract

backgroundControversy has persisted over the clinical benefits of low-dose sacubitril/valsartan in patients with heart failure (HF). HYPOTHESIS: Low-dose sacubitril/valsartan might also be effective and safe in HF patients.

methodsElectronic databases including PubMed, Ovid, and Cochrane Library were systematically retrieved from inception to August 5, 2021. Review manager 5.4 and Stata 15.1 were employed in this systematic review and meta-analysis. Key efficacy outcomes of interest included HF hospitalization, all-cause mortality, left ventricular ejection fraction (LVEF), N-terminal pro-B-type natriuretic peptide (NT-proBNP), together with New York Heart Association (NYHA) functional class. The safety outcome was systolic blood pressure (SBP). The grading of recommendations assessment, development, and evaluation approach was conducted to evaluate the quality of evidence for each outcome.

resultsA total of 1269 studies were screened and 9 real-world studies met the inclusion criteria were included in the meta-analysis, with 1697 participants. Compared with low-dose sacubitril/valsartan, high-dose sacubitril/valsartan significantly reduced the risk of HF hospitalization (odds ratio [OR]: 0.4, 95% confidence interval [CI]: 0.27-0.61, p < .0001) and the risk of all-cause mortality (OR: 0.23, 95% CI: 0.11-0.47, p < .0001). However, there were no appreciable differences in improvements of NYHA (OR: 0.59, 95% CI: 0.15-2.35, p = .45), changes of LVEF (mean difference [MD]: 2.73%, 95% CI: -2.24% to 7.7%, p = .28), changes of NT-proBNP (MD: 43.09, 95% CI: -28.41 to 114.59, p = .24) and changes of SBP (MD: 3.01, 95% CI: -4.62 to 10.64, p = .44) between groups with low-dose and high-dose sacubitril/valsartan.

conclusionsCompared with high-dose sacubitril/valsartan, low-dose sacubitril/valsartan was associated with increased risks of HF hospitalization and all-cause mortality. However, no distinct between-group differences in improvements of NYHA, changes of LVEF, changes of NT-proBNP and changes of SBP were observed.

Indexed as

Heart FailureVentricular Function, LeftAminobutyratesAngiotensin Receptor AntagonistsBiphenyl CompoundsDrug CombinationsHumansStroke VolumeTetrazolesValsartanAminobutyratesAngiotensin Receptor AntagonistsBiphenyl CompoundsDrug CombinationssacubitrilTetrazolesValsartandoseefficacyheart failuremeta-analysissacubitril/valsartansafety

Identifiers

PMID36648084
PMCPMC10018087
OpenAlexW4316928475

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read77
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.