Evidence map›Paper›PMID 31932209›Full record

Observational studyJournal of stroke and cerebrovascular diseases : the official journal of National Stroke Association2020

Elevated Cerebrospinal Fluid Protein Is Associated with Unfavorable Functional Outcome in Spontaneous Subarachnoid Hemorrhage.

Neil A Nadkarni, Matthew B Maas, Ayush Batra, Minjee Kim, Edward M Manno, Farzaneh A Sorond, Shyam Prabhakaran, Andrew M Naidech, Eric M Liotta

Open access · greenAbstract readObservational Study
In one paragraph

Observational study in Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 2 pooled it
0.7field-weighted citation impact, top 26% 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

9 citing papers in PubMed, 2 syntheses or guidelines pooled it, 16 citations in OpenAlex.

  1. 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

9 authors at 1 institution in 2 countries.

Neil A NadkarniDivision of Stroke and Neurocritical Care, Department of Neurology, Northwestern University, Chicago, Illinois.
Matthew B MaasDivision of Stroke and Neurocritical Care, Department of Neurology, Northwestern University, Chicago, Illinois.
Ayush BatraDivision of Stroke and Neurocritical Care, Department of Neurology, Northwestern University, Chicago, Illinois.
Minjee KimDivision of Stroke and Neurocritical Care, Department of Neurology, Northwestern University, Chicago, Illinois.
Edward M MannoDivision of Stroke and Neurocritical Care, Department of Neurology, Northwestern University, Chicago, Illinois.
Farzaneh A SorondDivision of Stroke and Neurocritical Care, Department of Neurology, Northwestern University, Chicago, Illinois.
Shyam PrabhakaranDivision of Stroke and Neurocritical Care, Department of Neurology, Northwestern University, Chicago, Illinois.
Andrew M NaidechDivision of Stroke and Neurocritical Care, Department of Neurology, Northwestern University, Chicago, Illinois.
Eric M LiottaDivision of Stroke and Neurocritical Care, Department of Neurology, Northwestern University, Chicago, Illinois. Electronic address: eric.liotta@northwestern.edu.
Northwestern University · US

Funding

Northwestern University Clinical and Translational Science Institute (NUCATS)UL1TR001422 · NCATS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI D'AQUILA, RICHARD · 2015 to 2023
$56.8M
Multidisciplinary Clinical and Translational Science (MCTS) Program (UL1)UL1TR000150 · NCATS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LLOYD-JONES, DONALD M · 2012 to 2013
$10.1M
Northwestern University Clinical and Translational Science Institute (NUCATS)KL2TR001424 · NCATS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SHARMA, LEENA · 2015 to 2023
$8.1M
Hemostasis, Hematoma Expansion, and Outcomes After Intracerebral HemorrhageR01NS110779 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI NAIDECH, ANDREW M · 2019 to 2023
$3.3M
Research Education Program for Trainees in NeurologyR25NS070695 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI KESSLER, JOHN A, SIMUNI, TANYA · 2010 to 2023
$1.4M
Circadian Dysfunction, Encephalopathy, and Cognitive Outcomes after Critical IllnessK23NS092975 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI MAAS, MATTHEW BRANDON · 2015 to 2019
$886k
Health related quality of life and seizure medications after hemorrhagic strokeK18HS023437 · AHRQ · NORTHWESTERN UNIVERSITY AT CHICAGO · PI NAIDECH, ANDREW M · 2015 to 2016
$357k
AHRQ HHS K18 HS023437NCATS NIH HHS KL2 TR001424NCATS NIH HHS UL1 TR000150NCATS NIH HHS UL1 TR001422NINDS NIH HHS K23 NS092975NINDS NIH HHS L30 NS098427NINDS NIH HHS R01 NS110779NINDS NIH HHS R25 NS070695
6 · The paper itself

Abstract

BACKGROUND/

objectiveSubarachnoid hemorrhage (SAH) is a devastating neurologic event for which markers to assess poor outcome are needed. Elevated cerebrospinal fluid (CSF) protein may result from inflammation and blood-brain barrier (BBB) disruption that occurs during SAH. We sought to determine if CSF protein level is associated with functional outcome after SAH.

methodsWe prospectively collected single-center demographic and clinical data for consecutive patients admitted with spontaneous SAH. Inclusion required an external ventricular drain and daily CSF protein and cellular counts starting within 48 hours of symptom onset and extending through 7 days after onset. Seven-day average CSF protein was determined from daily measured values after correcting for contemporaneous CSF red blood cell (RBC) count. Three-month functional outcome was assessed by telephone interview with good outcome defined as modified Rankin score 0-3. Variables univariately associated with outcome at P less than .25 and measures of hemorrhage volume were included for binary logistic regression model development.

resultsThe study included 130 patients (88% aneurysmal SAH, 69% female, 54.8 ± 14.8 years, Glasgow Coma Scale [GCS] 14 [7-15]). Three-month outcome assessment was complete in 112 (86%) patients with good functional outcome in 74 (66%). CSF protein was lower in good outcome (35.3 [20.4-49.7] versus 80.5 [40.5-115.5] mg/dL; P < .001). CSF protein was not associated with cerebral vasospasm, but delayed radiographic infarction on 3 to 12-month neuroimaging was associated with higher CSF protein (46.3 [32.0-75.0] versus 30.2 [20.4-47.8] mg/dL; P = .023). Good 3-month outcome was independently associated with lower CSF protein (odds ratios [OR] .39 [.23-.70] for 75th versus 25th percentile of protein; P = .001) and higher admission GCS (OR 1.23 [1.10-1.37] for good outcome per GCS point increase; P < .001). Parenchymal hematoma predicted worse outcome (OR 6.31 [1.58-25.25]; P = .009). Results were similar after excluding nonaneurysmal SAH and after including CSF RBC count, CT score, and intraventricular hemorrhage volume in models.

conclusionsElevated average CSF protein is associated with poor outcome after spontaneous SAH. Further research should investigate if elevated CSF protein identifies patients in whom mechanisms such as BBB disruption contribute to poor outcome.

Indexed as

Disability EvaluationAdultAgedBiomarkersCerebrospinal Fluid ProteinsFemaleHumansMaleMiddle AgedPredictive Value of TestsPrognosisProspective StudiesRecovery of FunctionSubarachnoid HemorrhageTime FactorsUp-RegulationBiomarkersCerebrospinal Fluid Proteinsblood-brain barriercerebrospinal fluidhemorrhagic strokeinflammationoutcomesSubarachnoid hemorrhage

Identifiers

PMID31932209
PMCPMC7066873
OpenAlexW2999484238

What OpenQuestion holds

Textmetadata
LicenceTDM
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.