Evidence map›Paper›PMID 37056709›Full record

ArticleFrontiers in cellular and infection microbiology2023

Effect of β-blockers on mortality in patients with sepsis: A propensity-score matched analysis.

Cheng-Long Ge, Li-Na Zhang, Yu-Hang Ai, Wei Chen, Zhi-Wen Ye, Yu Zou, Qian-Yi Peng

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.1field-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

15 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
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  6. Targeting sepsis through inflammation and oxidative metabolism.World journal of critical care medicine · 2025
    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

7 authors at 2 institutions in 1 country.

Cheng-Long GeDepartment of Critical Care Medicine, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Li-Na ZhangDepartment of Critical Care Medicine, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Yu-Hang AiDepartment of Critical Care Medicine, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Wei ChenDepartment of Critical Care Medicine, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Zhi-Wen YeDepartment of Critical Care Medicine, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Yu ZouDepartment of Anesthesia, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Qian-Yi PengDepartment of Critical Care Medicine, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Xiangya Hospital Central South University · CNCentral South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: We aimed to evaluate the association between β-blocker therapy and mortality in patients with sepsis. Methods: Patients with sepsis were selected from the Medical Information Mart for Intensive Care (MIMIC)-III. Propensity score matching (PSM) was used to balance the baseline differences. A multivariate Cox regression model was used to assess the relationship between β-blocker therapy and mortality. The primary outcome was the 28-day mortality. Results: A total of 12,360 patients were included in the study, involving 3,895 who received β-blocker therapy and 8,465 who did not. After PSM, 3,891 pairs of patients were matched. The results showed that β-blockers were associated with improved 28- (hazards ratio (HR) 0.78) and 90-day (HR 0.84) mortality. Long-acting β-blockers were associated with improved 28-day survival (757/3627 [20.9%] vs. 583/3627 [16.1%], Conclusions: β-blockers were associated with improved 28- and 90-day mortality in patients with sepsis and septic shock. Long-acting β-blocker therapy may have a protective role in patients with sepsis, reducing the 28-day and 90-day mortality. However, short-acting β-blocker (esmolol) treatment did not reduce the mortality in sepsis.

Indexed as

SepsisShock, SepticAdrenergic beta-AntagonistsHumansPropensity ScoreRetrospective StudiesAdrenergic beta-AntagonistsMIMICmortalitypropensity score matchingsepsisβ-blockers

Identifiers

PMID37056709
PMCPMC10086225
OpenAlexW4361218370

What OpenQuestion holds

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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.