Evidence map›Paper›PMID 37168691›Full record

ArticleCritical care explorations2023

Association of Epileptiform Activity With Outcomes in Toxic-Metabolic Encephalopathy.

Patrick M Chen, Sophie Schuurmans Stekhoven, Adnan Haider, Jin Jing, Wendong Ge, Eric S Rosenthal, M Brandon Westover, Sahar F Zafar

Open access · goldAbstract read
In one paragraph

Article in Critical care explorations, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
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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

8 authors at 3 institutions in 1 country.

Patrick M ChenDepartment of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA.
Sophie Schuurmans StekhovenDepartment of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA.
Adnan HaiderDepartment of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA.
Jin JingDepartment of Neurology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA.
Wendong GeDepartment of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA.
Eric S RosenthalDepartment of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA.
M Brandon WestoverDepartment of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA.
Sahar F ZafarDepartment of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA.
Massachusetts General Hospital · USHarvard University · USBeth Israel Deaconess Medical Center · US

Funding

Optimizing anti-epileptic drug treatment in acute brain injuryK23NS114201 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI ZAFAR, SAHAR F · 2019 to 2023
$1.0M
NINDS NIH HHS K23 NS114201
6 · The paper itself

Abstract

The clinical significance of epileptiform abnormalities (EAs) specific to toxic-metabolic encephalopathy (TME) is unknown.

objectivesTo quantify EA burden in patients with TME and its association with neurologic outcomes. DESIGN SETTING AND PARTICIPANT: This is a retrospective study. A cohort of patients with TME and EA (positive) were age, Sequential Organ Failure Assessment Score, Acute Physiology and Chronic Health Evaluation II (APACHE-II) score matched to a cohort of TME patients without EA (control). Univariate analysis compared EA-positive patients against controls. Multivariable logistical regression adjusting for underlying disease etiology was performed to examine the relationship between EA burden and probability of poor neurologic outcome (modified Rankin Score [mRS] 4-6) at discharge. Consecutive admissions to inpatient floors or ICUs that underwent continuous electroencephalography (cEEG) monitoring at a single center between 2012 and 2019. Inclusion criteria were 1) patients with TME diagnosis, 2) age greater than 18 years, and 3) greater than or equal to 16 hours of cEEG. Patients with acute brain injury and cardiac arrest were excluded. MAIN OUTCOMES AND MEASURES: Poor neurologic outcome defined by mRS (mRS 4-6).

resultsOne hundred sixteen patients were included, 58 with EA and 58 controls without EA, where matching was performed on age and APACHE-II score. The median age was 66 (Q1-Q3, 57-75) and median APACHE II score was 18 (Q1-Q3, 13-22). Overall cohort discharge mortality was 22% and 70% had a poor neurologic outcome. Peak EA burden was defined as the 12-hour window of recording with the highest prevalence of EAs. In multivariable analysis adjusted for Charlson Comorbidity Index and primary diagnosis, presence of EAs was associated with poor outcome (odds ratio 3.89; CI [1.05-14.2], CONCLUSIONS AND RELEVANCE: Increasing burden of EA is associated with worse discharge outcomes in patients with TME. Future studies are needed to determine whether short-term treatment with anti-seizure medications while medically treating the underlying metabolic derangement improves outcomes.

Indexed as

electroencephalogramencephalopathyepileptiform abnormalitiestoxic-metabolic encephalopathy

Identifiers

PMID37168691
PMCPMC10166342
OpenAlexW4376223808

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.