Evidence map›Paper›PMID 34727955›Full record

Observational studyScandinavian journal of trauma, resuscitation and emergency medicine2021

Hospitals with and without neurosurgery: a comparative study evaluating the outcome of patients with traumatic brain injury.

Aimone Giugni, Lorenzo Gamberini, Greta Carrara, Luca Antiga, Obou Brissy, Virginia Buldini, Italo Calamai, Akos Csomos, Alessandra De Luca, Enrico Ferri and 18 more

Abstract readObservational Study
In one paragraph

Observational study in Scandinavian journal of trauma, resuscitation and emergency medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
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

28 authors.

Aimone Giugni *Anesthesia, Intensive Care and Prehospital Emergency, Maggiore Hospital, Bologna, Italy.
Lorenzo Gamberini *Anesthesia, Intensive Care and Prehospital Emergency, Maggiore Hospital, Bologna, Italy.
Greta CarraraLaboratory of Clinical Epidemiology, Department of Public Health, Istituto Di Ricerche Farmacologiche Mario Negri IRCCS, Villa Camozzi, Via G.B. Camozzi 3, 24020, Ranica, Bergamo, Italy.
Luca AntigaOrobix, Bergamo, Italy.
Obou BrissyLaboratory of Clinical Epidemiology, Department of Public Health, Istituto Di Ricerche Farmacologiche Mario Negri IRCCS, Villa Camozzi, Via G.B. Camozzi 3, 24020, Ranica, Bergamo, Italy.
Virginia BuldiniAnesthesia, Intensive Care and Prehospital Emergency, Maggiore Hospital, Bologna, Italy.
Italo CalamaiAnesthesia and Intensive Care Unit, AUSL Toscana Centro, San Giuseppe Hospital, Empoli, Florence, Italy.
Akos CsomosHungarian Army Medical Center, Budapest, Hungary.
Alessandra De LucaNeurointensive Care Unit, Department of Anesthesia and Intensive Care Unit, AOU Careggi, Florence, Italy.
Enrico FerriAnesthesia, Intensive Care and Prehospital Emergency, Maggiore Hospital, Bologna, Italy.
Joanne M FlemingLaboratory of Clinical Epidemiology, Department of Public Health, Istituto Di Ricerche Farmacologiche Mario Negri IRCCS, Villa Camozzi, Via G.B. Camozzi 3, 24020, Ranica, Bergamo, Italy.
Primoz GradisekClinical Department of Anaesthesiology and Intensive Therapy, University Medical Centre Ljubljana, Ljubljana, Slovenia.
Rafael KapsGeneral Hospital Novo Mesto, Novo Mesto, Slovenia.
Theodoros KyprianouUniversity of Nicosia Medical School, Nicosia, Cyprus.
Silvia LagomarsinoNeurointensive Care Unit, Department of Anesthesia and Intensive Care Unit, AOU Careggi, Florence, Italy.
Isaac LazarPediatric Intensive Care Unit, Soroka Medical Center and The Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer Sheva, Israel.
Costanza MartinoAnesthesia and Intensive Care Unit, AUSL Romagna, Maurizio Bufalini Hospital, Cesena, Italy.
Malgorzata Mikaszewska-SokolewiczClinic of Anaesthesia and Intensive Care, Medical University of Warsaw, Warsaw, Poland.
Andrea MontisDepartment of Neurorehabilitation, ASSL Oristano, ATS Sardegna, Oristano, Italy.
Gabor NardaiDepartment of Anaesthesiology and Intensive Care, Péterfy Hospital and Trauma Centre, Budapest, Hungary.
Giovanni NattinoLaboratory of Clinical Epidemiology, Department of Public Health, Istituto Di Ricerche Farmacologiche Mario Negri IRCCS, Villa Camozzi, Via G.B. Camozzi 3, 24020, Ranica, Bergamo, Italy. giovanni.nattino@marionegri.it.ORCID http://orcid.org/0000-0002-3034-6251
Giuseppe NattinoIntensive Care Unit, Azienda Socio Sanitaria Territoriale di Lecco, Lecco, Italy.
Giulia PaciLaboratory of Clinical Epidemiology, Department of Public Health, Istituto Di Ricerche Farmacologiche Mario Negri IRCCS, Villa Camozzi, Via G.B. Camozzi 3, 24020, Ranica, Bergamo, Italy.
Laila PortolaniAnesthesia and Intensive Care Unit, AUSL Romagna, Maurizio Bufalini Hospital, Cesena, Italy.
Nektaria XirouchakiUniversity Hospital of Heraklion, Crete, Greece.
Arturo ChieregatoNeurointensive Care Unit, Grande Ospedale Metropolitano Niguarda, Milan, Italy.
Guido BertoliniLaboratory of Clinical Epidemiology, Department of Public Health, Istituto Di Ricerche Farmacologiche Mario Negri IRCCS, Villa Camozzi, Via G.B. Camozzi 3, 24020, Ranica, Bergamo, Italy.
CREACTIVE consortium

Funding

FP7 Health 602714
6 · The paper itself

Abstract

backgroundWe leveraged the data of the international CREACTIVE consortium to investigate whether the outcome of traumatic brain injury (TBI) patients admitted to intensive care units (ICU) in hospitals without on-site neurosurgical capabilities (no-NSH) would differ had the same patients been admitted to ICUs in hospitals with neurosurgical capabilities (NSH).

methodsThe CREACTIVE observational study enrolled more than 8000 patients from 83 ICUs. Adult TBI patients admitted to no-NSH ICUs within 48 h of trauma were propensity-score matched 1:3 with patients admitted to NSH ICUs. The primary outcome was the 6-month extended Glasgow Outcome Scale (GOS-E), while secondary outcomes were ICU and hospital mortality.

resultsA total of 232 patients, less than 5% of the eligible cohort, were admitted to no-NSH ICUs. Each of them was matched to 3 NSH patients, leading to a study sample of 928 TBI patients where the no-NSH and NSH groups were well-balanced with respect to all of the variables included into the propensity score. Patients admitted to no-NSH ICUs experienced significantly higher ICU and in-hospital mortality. Compared to the matched NSH ICU admissions, their 6-month GOS-E scores showed a significantly higher prevalence of upper good recovery for cases with mild TBI and low expected mortality risk at admission, along with a progressively higher incidence of poor outcomes with increased TBI severity and mortality risk.

conclusionsIn our study, centralization of TBI patients significantly impacted short- and long-term outcomes. For TBI patients admitted to no-NSH centers, our results suggest that the least critically ill can effectively be managed in centers without neurosurgical capabilities. Conversely, the most complex patients would benefit from being treated in high-volume, neuro-oriented ICUs.

Indexed as

Brain Injuries, TraumaticNeurosurgeryAdultGlasgow Coma ScaleGlasgow Outcome ScaleHospitalsHumansIntensive Care UnitsBrain injuriesGOS-EOutcome assessmentProspective studiesRehabilitationTraumatic

Identifiers

PMID34727955
PMCPMC8561979

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Registered trials

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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.