Evidence map›Paper›PMID 40221700›Full record

SynthesisBMC neurology2025

Bilirubin as a predictor of severity and adverse clinical outcomes of acute ischemic stroke: a systematic review and meta-analysis.

Ying Zhong, Lei Li

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in BMC neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. 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

2 authors.

Ying ZhongGeriatrics Department, Huzhou Third Municipal Hospital, the Affiliated Hospital of Huzhou University, Huzhou, Zhejiang, China.
Lei LiGeriatrics Department, Huzhou Third Municipal Hospital, the Affiliated Hospital of Huzhou University, Huzhou, Zhejiang, China. chenjinshijin1@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis review aims to comprehensively examine the role of bilirubin in predicting severity and adverse clinical outcomes in patients with acute ischemic stroke (AIS).

methodsWe searched the electronic PubMed, Embase, Scopus, and Web of Science repositories for articles published in English available before the 15th of June 2024. The outcomes assessed were stroke severity, haemorrhagic transformation, symptomatic intracranial haemorrhage (sICH), mortality, and poor functional results.

resultsWe analysed data from 13 studies. Our meta-analysis showed that both total bilirubin (RR, 1.10; 95% CI, 1.01-1.19) and direct bilirubin (RR, 1.79; 95% CI, 1.33-2.42) were independently associated with the severity of AIS. Higher quartiles of total bilirubin were associated with an increased risk of haemorrhagic transformation, but without statistical significance (RR, 2.34; 95% CI, 0.90-6.07). In addition, each unit increase in direct (RR, 1.25; 95% CI, 1.09-1.43) and indirect (RR, 1.09; 95% CI, 1.02-1.17) bilirubin levels was significantly associated with a higher risk of haemorrhagic transformation. Moreover, each unit increases in total (RR, 1.08; 95% CI, 1.04-1.12), direct (RR, 1.28; 95% CI, 1.13-1.44), and indirect (RR, 1.10; 95% CI, 1.03-1.18) bilirubin levels was significantly associated with a higher risk of sICH. Data on mortality and poor functional outcomes were insufficient.

conclusionSerum bilirubin levels were positively associated with the severity of AIS. The evidence suggests that bilirubin may be a potential indicator for haemorrhagic transformation and sICH after AIS.

Indexed as

BilirubinIschemic StrokeBiomarkersHumansIntracranial HemorrhagesPrognosisSeverity of Illness IndexBilirubinBiomarkersCerebrovascular accidentHaemorrhagic transformationLiver functionStroke

Identifiers

PMID40221700
PMCPMC11992745

What Socratic holds

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LicenceCC BY-NC-ND
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Registered trials

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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 Socratic graph.