Evidence mapPaperPMID 41680652Full record

ArticleBMC anesthesiology2026

Extracranial organ dysfunction in non-traumatic subarachnoid hemorrhage: a retrospective single center cohort study.

Gaia Furlan, Teodora Dragu, Marzia Savi, Julia de Sá Liston, Pedro Cury, Valeria Bianchi, Armin Quispe Cornejo, Fabio Silvio Taccone, Elisa Gouvêa Bogossian

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Article in BMC anesthesiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Gaia Furlan *Department of Intensive Care, Erasme Hospital- Brussels University Hospital, Université Libre de Bruxelles, Brussels, Belgium.
Teodora Dragu *Department of Intensive Care, Erasme Hospital- Brussels University Hospital, Université Libre de Bruxelles, Brussels, Belgium.
Marzia SaviDepartment of Intensive Care, Neurosciences and Trauma Critical Care Unit, Cambridge University Hospitals NHS Foundation Trust - Addenbrooke's Hospital, Cambridge, UK.
Julia de Sá ListonDepartment of Intensive Care, Rede Mater Dei de Saúde, Belo Horizonte, Minas Gerais, Brazil.
Pedro CuryEscola Bahiana de Medicina e Saúde Pública - EBMSP, Salvador, Brazil.
Valeria BianchiDivision of Internal Medicine 2, Department of Medical Science, University of Torino, Torino, Italy.
Armin Quispe CornejoDepartment of Intensive Care, Erasme Hospital- Brussels University Hospital, Université Libre de Bruxelles, Brussels, Belgium.
Fabio Silvio TacconeDepartment of Intensive Care, Erasme Hospital- Brussels University Hospital, Université Libre de Bruxelles, Brussels, Belgium.
Elisa Gouvêa BogossianDepartment of Intensive Care, Erasme Hospital- Brussels University Hospital, Université Libre de Bruxelles, Brussels, Belgium. elisagobog@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionNon-traumatic subarachnoid hemorrhage (SAH) is a potentially devastating type of stroke associated with high morbidity and mortality rates. SAH patients are at risk of systemic complications and extracranial organ dysfunction that may worsen their outcome. The objective of this study was to assess the impact of early onset extracranial organ dysfunction on the outcome of SAH patients.

methodsWe performed a retrospective single center cohort study of consecutive non-traumatic SAH patients admitted to the Intensive Care Unit (ICU) of the Brussels University Hospital (Brussels, Belgium) from January 2012 to December 2022. The modified Sequential Organ Failure Assessment (mSOFA) score, excluding the neurological component, was calculated daily for the first 5 days after ICU admission to assess the presence of extra-cerebral organ dysfunction. Unfavorable Outcome (UO) was defined as a Glasgow Outcome Scale of 1–3 at 3 months.

resultsA total of 387 patients were included; mean age was 55 (±13) years and 240 (62%) patients were female. The median World Federation of Neurosurgical Societies score on admission was 3 (IQR 1–5). At 3 months, 189 (48.8%) patients had UO (n= 125 being non-survivors). The median mSOFA on admission was 2 (0–4). The majority of patients (n = 330, 85.3%) experienced at least on extracranial organ dysfunction in the first 5 days of hospitalization, the most common being respiratory (276/387 patients, 71.3%) and cardiovascular (224/387 patients, 57.9%). In a generalized multilevel mixed model, mSOFA in the first 5 days of ICU admission was independently associated with UO (OR 1.29 95% CI 1.21–1.37).

conclusionIn this cohort, early extracranial organ dysfunction assessed by the mSOFA score was common in SAH patients. Higher SOFA score was significantly associated with a higher risk of unfavorable outcome.

Indexed as

Multiple Organ FailureSubarachnoid HemorrhageAdultAgedBelgiumCohort StudiesFemaleGlasgow Outcome ScaleHumansIntensive Care UnitsMaleMiddle AgedOrgan Dysfunction ScoresRetrospective StudiesOrgan dysfunctionScoreStrokeSystemic complication

Identifiers

PMID41680652
PMCPMC13005430

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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.