Evidence map›Paper›PMID 28878047›Full record

ArticleNeurology2017

Long-term risk of seizures in adult survivors of sepsis.

Michael E Reznik, Alexander E Merkler, Ali Mahta, Santosh B Murthy, Jan Claassen, Hooman Kamel

Open access · bronzeAbstract read
In one paragraph

Article in Neurology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

13 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Article
  3. Neuroinflammation and Disease: Pathways and Opportunities.Annual review of pharmacology and toxicology · 2026
    Review
  4. Article
  5. Review
  6. Article
  7. Seizures and Sepsis: A Narrative Review.Journal of clinical medicine · 2021
    Review
  8. Article
  9. Article
  10. Review
  11. Septic Encephalopathy.Current neurology and neuroscience reports · 2018
    Review
  12. Article
  13. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Michael E ReznikFrom the Clinical and Translational Neuroscience Unit, Feil Family Brain and Mind Research Institute (M.E.R., A.E.M., A.M., S.B.M., H.K.), and Division of Neurocritical Care, Department of Neurology (M.E.R., A.E.M., A.M., S.B.M., H.K.), Weill Cornell Medical College; and Department of Neurology (M.E.R., A.M., J.C.), Columbia University Medical Center, New York, NY.
Alexander E MerklerFrom the Clinical and Translational Neuroscience Unit, Feil Family Brain and Mind Research Institute (M.E.R., A.E.M., A.M., S.B.M., H.K.), and Division of Neurocritical Care, Department of Neurology (M.E.R., A.E.M., A.M., S.B.M., H.K.), Weill Cornell Medical College; and Department of Neurology (M.E.R., A.M., J.C.), Columbia University Medical Center, New York, NY.
Ali MahtaFrom the Clinical and Translational Neuroscience Unit, Feil Family Brain and Mind Research Institute (M.E.R., A.E.M., A.M., S.B.M., H.K.), and Division of Neurocritical Care, Department of Neurology (M.E.R., A.E.M., A.M., S.B.M., H.K.), Weill Cornell Medical College; and Department of Neurology (M.E.R., A.M., J.C.), Columbia University Medical Center, New York, NY.
Santosh B MurthyFrom the Clinical and Translational Neuroscience Unit, Feil Family Brain and Mind Research Institute (M.E.R., A.E.M., A.M., S.B.M., H.K.), and Division of Neurocritical Care, Department of Neurology (M.E.R., A.E.M., A.M., S.B.M., H.K.), Weill Cornell Medical College; and Department of Neurology (M.E.R., A.M., J.C.), Columbia University Medical Center, New York, NY.
Jan ClaassenFrom the Clinical and Translational Neuroscience Unit, Feil Family Brain and Mind Research Institute (M.E.R., A.E.M., A.M., S.B.M., H.K.), and Division of Neurocritical Care, Department of Neurology (M.E.R., A.E.M., A.M., S.B.M., H.K.), Weill Cornell Medical College; and Department of Neurology (M.E.R., A.M., J.C.), Columbia University Medical Center, New York, NY.
Hooman KamelFrom the Clinical and Translational Neuroscience Unit, Feil Family Brain and Mind Research Institute (M.E.R., A.E.M., A.M., S.B.M., H.K.), and Division of Neurocritical Care, Department of Neurology (M.E.R., A.E.M., A.M., S.B.M., H.K.), Weill Cornell Medical College; and Department of Neurology (M.E.R., A.M., J.C.), Columbia University Medical Center, New York, NY. hok9010@med.cornell.edu.
Cornell University · US

Funding

AtRial Cardiopathy and Antithrombotic Drugs In prevention After cryptogenicstroke (ARCADIA)U01NS095869 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI BRODERICK, JOSEPH PAUL, KAMEL, HOOMAN · 2017 to 2022
$22.0M
Left Atrial abNormality, ThromboEmbolism, and Race: Novel risk factors for stroke (LANTERN)R01NS097443 · NINDS · WEILL MEDICAL COLL OF CORNELL UNIV · PI KAMEL, HOOMAN · 2016 to 2019
$1.5M
Atrial Fibrillation Precursors May Be Novel Stroke Risk FactorsK23NS082367 · NINDS · WEILL MEDICAL COLL OF CORNELL UNIV · PI KAMEL, HOOMAN · 2013 to 2017
$937k
NINDS NIH HHS K23 NS082367NINDS NIH HHS R01 NS097443NINDS NIH HHS U01 NS095869
6 · The paper itself

Abstract

objectiveTo examine the association between sepsis and the long-term risk of seizures.

methodsWe conducted a retrospective population-based cohort study using administrative claims data from all emergency department visits and hospitalizations at nonfederal acute care hospitals in California, Florida, and New York from 2005 to 2013. Using previously validated diagnosis codes, we identified all adult patients hospitalized with sepsis. Our outcome was any emergency department visit or hospitalization for seizure. Poisson regression and demographic data were used to calculate age-, sex-, and race-standardized incidence rate ratios (IRR). To confirm our findings, we used a matched cohort of hospitalized patients without sepsis for comparison and additionally assessed claims data from a nationally representative 5% sample of Medicare beneficiaries.

resultsWe identified 842,735 patients with sepsis. The annual incidence of seizure was 1.29% (95% confidence interval [CI] 1.27%-1.30%) in patients with sepsis vs 0.16% (95% CI 0.16%-0.16%) in the general population (IRR 4.98; 95% CI 4.92-5.04). A secondary analysis using matched hospitalized patients confirmed these findings (IRR 4.33; 95% CI 4.13-4.55), as did a separate analysis of Medicare beneficiaries, in whom we found a similar strength of association (IRR 2.72; 95% CI 2.60-2.83), as we did in patients ≥65 years of age in our primary statewide data (IRR 2.83; 95% CI 2.78-2.88).

conclusionsWe found that survivors of sepsis faced a significantly higher long-term risk of seizures than both the general population and other hospitalized patients. Our findings suggest that sepsis is associated with pathways that lead to permanent neurologic sequelae.

Indexed as

AdultAgedAge FactorsCaliforniaCohort StudiesFemaleFloridaHospitalizationHumansIncidenceMaleMedicareMiddle AgedNew YorkRisk FactorsSeizures

Identifiers

PMID28878047
PMCPMC5631168
OpenAlexW2752181382

What OpenQuestion holds

Textmetadata
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.