Evidence map›Paper›PMID 33072197›Full record

Trial reportJournal of medicine and life

The Effect of Cerebrolysin on the Predictive Value of Baseline Prognostic Risk Score in Moderate and Severe Traumatic Brain Injury.

Codruta Birle, Dana Slavoaca, Ioana Muresanu, Diana Chira, Vitalie Vacaras, Adina Dora Stan, Constantin Dina, Stefan Strilciuc

Open access · diamondAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of medicine and life. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.3field-weighted citation impact, top 40% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Observational
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 4 institutions in 1 country.

Codruta BirleDepartment of Neurosciences, "Iuliu Hatieganu" University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Dana SlavoacaDepartment of Neurosciences, "Iuliu Hatieganu" University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Ioana MuresanuDepartment of Neurosciences, "Iuliu Hatieganu" University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Diana Chira"RoNeuro" Institute for Neurological Research and Diagnostic, Cluj-Napoca, Romania.
Vitalie VacarasDepartment of Neurosciences, "Iuliu Hatieganu" University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Adina Dora StanDepartment of Neurosciences, "Iuliu Hatieganu" University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Constantin DinaDepartment of Radiology, "Ovidius" University, Faculty of Medicine, Constanta, Romania.
Stefan StrilciucDepartment of Neurosciences, "Iuliu Hatieganu" University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Iuliu Hațieganu University of Medicine and Pharmacy · ROResearch Institute for Analytical Instrumentation · ROOvidius University · ROSpitalul Clinic Județean de Urgență Cluj-Napoca · RO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cognitive dysfunction is a significant complaint among patients after moderate to severe traumatic brain injury (TBI), with devastating consequences on functional recovery and quality of life. Prognostic models allow a better assessment and management of neurotrauma patients. The aim of the study was to demonstrate the predictive value of the Baseline Prognostic Risk Score (BPRS) in moderate to severe TBI, in a sample of patients treated with neurotrophic factors. Eighty patients with moderate-severe TBI from the CAPTAIN II study were included in secondary data analysis. Patients received active treatment with Cerebrolysin, 50 mL per day for ten days, followed by two treatment cycles with 10 mL per day for ten days. BPRS was determined on admission; the age was recorded, and patients were evaluated using the following neurocognitive tests: Mini-Mental State Essay (MMSE), Wechsler Adult Intelligence Scale-Third Edition Processing Speed Index (WAIS-III PSI) and Stroop Colour Word Test-Victoria Version at 10, 30 and 90 days. Hierarchical regression analysis was performed to investigate the unique predictive value of BPRS on cognitive evolution, independent of age. BPRS independently predicted scores on the WAIS-III PSI DSCales and the Word subscale of the Stroop Colour Word Test at 90 days. Age was a significant predictor for all the investigated scales at 10, 30, and 90 days. This study demonstrates the predictive value of a validated prognostic model (BPRS) for medium-term neurocognitive outcomes in a sample of moderate-severe traumatic brain injury treated with neurotrophic factors.

Indexed as

AdultAmino AcidsAttentionBrain Injuries, TraumaticCognitionExecutive FunctionFemaleHumansMaleMental Status and Dementia TestsMiddle AgedPredictive Value of TestsPrognosisQuality of LifeRecovery of FunctionRisk FactorsAmino AcidscerebrolysinAIS - Abbreviated Injury ScaleBPRS - Baseline Prognostic Risk ScoreCerebrolysincognitive outcomeCTT - Colour Trails TestGCS - Glasgow Coma ScaleGOSE - Glasgow Outcome Scale ExtendedHADS - Hospital Anxiety and Depression ScaleIMPACT - The International Mission on Prognosis and Analysis of Clinical Trials in TBIMMSE - Mini Mental State ExaminationMRC CRASH - Medical Research Council Corticosteroid Randomization after Significant Head InjuryprognosticPSI DSC - Processing Speed Index Digit Symbol CodingPSI SS - Processing Speed Index Symbol SearchPTA - post-traumatic amnesiaTBI - Traumatic Brain InjuryTraumatic brain injuryWAIS III - Wechsler Adult Intelligence Scale Third Edition.

Identifiers

PMID33072197
PMCPMC7550150
OpenAlexW3092724095

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.