Evidence map›Paper›PMID 42105095›Full record

ArticleActa neurochirurgica2026

ASA class is independently associated with 30-day mortality after mild traumatic brain injury with intracranial injury: a national retrospective cohort study.

Olivia Kiwanuka, Hans Pettersson, Gabriel Sandblom

Abstract read
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Article in Acta neurochirurgica, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Olivia KiwanukaDepartment of Clinical Science and Education, Karolinska Institutet, Södersjukhuset, Stockholm, Sweden. olivia.kiwanuka@ki.se.ORCID 0000-0003-3562-5513
Hans PetterssonDepartment of Clinical Science and Education, Karolinska Institutet, Södersjukhuset, Stockholm, Sweden.ORCID 0000-0002-7674-3711
Gabriel SandblomDepartment of Clinical Science and Education, Karolinska Institutet, Södersjukhuset, Stockholm, Sweden.ORCID 0000-0002-7416-4951

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionOutcome assessment after mild traumatic brain injury (mTBI) has largely focused on acute injury severity, while the role of pre-injury health has received comparatively less attention. The American Society of Anesthesiologists (ASA) physical status classification provides a simple measure of pre-existing health and comorbidity that may be relevant to early outcomes after trauma. This study examined whether pre-injury ASA class is independently associated with short-term mortality after mTBI and compared these associations with those observed in trauma patients without brain injury (NTBI).

methodsWe conducted a nationwide retrospective study using the Swedish Trauma Registry (2018-2023). Adults (≥ 18 years) with Glasgow Coma Scale (GCS) > 12 were included and classified as mTBI (ICD-10 S06.0-S06.9) or NTBI (no S06 diagnosis, AIS head = 0, age-matched). The primary outcome was 30-day all-cause mortality. Associations between clinical variables and mortality were examined using univariable and multivariable logistic regression, with models specified a priori to separate age-ASA effects from injury-related adjustment.

resultsA total of 8,670 patients were included in the mTBI cohort and 26,001 in the age-matched cohort. The mTBI cohort had poorer health (ASA ≥ 3: 27% vs 24%), and more often injured by low-energy falls (28% vs 20%). Mortality was higher in mTBI (5% vs 2.8%), and outcomes poorer (Glasgow Outcome Scale 1-3: 23% vs 17%). Within the mTBI cohort, mortality was strongly associated with increasing age, higher ASA category, and greater intracranial injury severity. After adjustment for age and injury-related variables, ASA class remained independently associated with 30-day mortality. Specifically, compared to ASA 1 patients, those with ASA 2 had 2.8 times higher odds of 30-day mortality, ASA 3 patients had 4.3 times higher odds, and ASA 4 patients had 21 times higher odds. A graded association between ASA class and mortality was also observed in the NTBI cohort, although the pattern of injury-related covariates differed.

conclusionsPre-injury health status, measured by the ASA class, was independently associated with 30-day mortality in patients with mild traumatic brain injury. Comparable associations in non-TBI trauma suggest that comorbidity and baseline health contribute substantially to early post-trauma mortality among awake trauma patients. ASA class may provide complementary information to traditional injury-based assessments, particularly in older patients, although further studies are needed to evaluate how such information can best inform clinical decision-making.

Indexed as

Brain ConcussionHealth StatusAdultAgedFemaleGlasgow Coma ScaleHumansMaleMiddle AgedRegistriesRetrospective StudiesSwedenComorbidityMild traumatic brain injuryMortalityPrognostic validationTrauma, ASA class

Identifiers

PMID42105095
PMCPMC13157432

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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 OpenQuestion graph.