Evidence map›Paper›PMID 36164392›Full record

ReviewOxidative medicine and cellular longevity2022

Molecular, Pathological, Clinical, and Therapeutic Aspects of Perihematomal Edema in Different Stages of Intracerebral Hemorrhage.

Chao Jiang, Hengtao Guo, Zhiying Zhang, Yali Wang, Simon Liu, Jonathan Lai, Tom J Wang, Shize Li, Jing Zhang, Li Zhu and 3 more

Abstract readReview
In one paragraph

Review in Oxidative medicine and cellular longevity, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 2 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

27 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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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

13 authors.

Chao JiangDepartment of Neurology, The Fifth Affiliated Hospital of Zhengzhou University, 450052 Zhengzhou, Henan, China.ORCID https://orcid.org/0000-0001-5588-4294
Hengtao GuoDepartment of Neurology, The Fifth Affiliated Hospital of Zhengzhou University, 450052 Zhengzhou, Henan, China.ORCID https://orcid.org/0000-0003-3052-8570
Zhiying ZhangDepartment of Neurology, The Fifth Affiliated Hospital of Zhengzhou University, 450052 Zhengzhou, Henan, China.
Yali WangDepartment of Neurology, The Fifth Affiliated Hospital of Zhengzhou University, 450052 Zhengzhou, Henan, China.
Simon LiuMedical Genomics Unit, National Human Genome Research Institute, Bethesda, MD 20814, USA.ORCID https://orcid.org/0000-0002-1182-5492
Jonathan LaiBaylor University, Waco, Texas 76706, USA.
Tom J WangThe Johns Hopkins University, Baltimore, MD 21218, USA.
Shize LiDepartment of Neurology, Zhengzhou Central Hospital Affiliated to Zhengzhou University, 450001 Zhengzhou, Henan, China.
Jing ZhangDepartment of Neurology, The Fifth Affiliated Hospital of Zhengzhou University, 450052 Zhengzhou, Henan, China.
Li ZhuDepartment of Neurology, The Fifth Affiliated Hospital of Zhengzhou University, 450052 Zhengzhou, Henan, China.
Peiji FuDepartment of Neurology, The Fifth Affiliated Hospital of Zhengzhou University, 450052 Zhengzhou, Henan, China.
Jiewen ZhangDepartment of Neurology, People's Hospital of Zhengzhou University, 450003 Zhengzhou, Henan, China.ORCID https://orcid.org/0000-0001-6784-6658
Jian WangDepartment of Neurology, The Fifth Affiliated Hospital of Zhengzhou University, 450052 Zhengzhou, Henan, China.ORCID https://orcid.org/0000-0003-2291-640X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute intracerebral hemorrhage (ICH) is a devastating type of stroke worldwide. Neuronal destruction involved in the brain damage process caused by ICH includes a primary injury formed by the mass effect of the hematoma and a secondary injury induced by the degradation products of a blood clot. Additionally, factors in the coagulation cascade and complement activation process also contribute to secondary brain injury by promoting the disruption of the blood-brain barrier and neuronal cell degeneration by enhancing the inflammatory response, oxidative stress, etc. Although treatment options for direct damage are limited, various strategies have been proposed to treat secondary injury post-ICH. Perihematomal edema (PHE) is a potential surrogate marker for secondary injury and may contribute to poor outcomes after ICH. Therefore, it is essential to investigate the underlying pathological mechanism, evolution, and potential therapeutic strategies to treat PHE. Here, we review the pathophysiology and imaging characteristics of PHE at different stages after acute ICH. As illustrated in preclinical and clinical studies, we discussed the merits and limitations of varying PHE quantification protocols, including absolute PHE volume, relative PHE volume, and extension distance calculated with images and other techniques. Importantly, this review summarizes the factors that affect PHE by focusing on traditional variables, the cerebral venous drainage system, and the brain lymphatic drainage system. Finally, to facilitate translational research, we analyze why the relationship between PHE and the functional outcome of ICH is currently controversial. We also emphasize promising therapeutic approaches that modulate multiple targets to alleviate PHE and promote neurologic recovery after acute ICH.

Indexed as

Brain EdemaBiomarkersCerebral HemorrhageEdemaHematomaHumansBiomarkers

Identifiers

PMID36164392
PMCPMC9509250

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.