Publications by authors named "Sandra Magnoni"

Article Synopsis
  • - The study explores the complex pathophysiology and outcomes of Traumatic Brain Injury (TBI), highlighting that current classifications do not adequately reflect the underlying biological processes involved.
  • - Using advanced proteomic techniques, researchers analyzed plasma samples from 88 participants to identify 16 proteins with significant expression differences in TBI patients compared to non-injured controls, focusing on various markers related to neurons, astrocytes, and inflammation.
  • - Their findings indicated correlations between specific plasma proteins and brain injury measures, suggesting that certain biomarkers like UCH-L1 and total tau could serve as potential indicators for TBI severity and progression.
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Article Synopsis
  • Traumatic brain injury (TBI) does not significantly increase plasma levels of phosphorylated tau at serine-181 (p-tau181) within a year post-injury, unlike Alzheimer's disease where p-tau181 is elevated.* -
  • In contrast, other biomarkers like total-tau (t-tau), neurofilament light (NfL), and glial fibrillary acidic protein (GFAP) were significantly elevated following TBI and were predictive of brain atrophy rates.* -
  • The study highlights that while p-tau181 is a relevant marker in Alzheimer's, it doesn't serve as an indicator of neurodegeneration after moderate-to-severe TBI.*
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Article Synopsis
  • Traumatic brain injury (TBI) is linked to chronic neurodegeneration, potentially due to systemic inflammation signaling the brain and activating microglia, which can lead to widespread brain damage.
  • The study, TBI-braINFLAMM, will analyze data from two major TBI research projects—CREACTIVE and BIO-AX-TBI—to assess the relationship between systemic inflammation, injury severity, and ongoing neurodegeneration.
  • Ethical approval has been obtained, and findings will be shared through peer-reviewed publications and conferences to enhance understanding and inform future research in this area.
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To assess the prevalence of symptoms of Post-Traumatic Stress Disorder (PTSD) in survivors of COVID-19 Acute Respiratory Distress Syndrome that needed ICU care; to investigate risk factors and their impact on the Health-Related Quality of life (HR-QoL). This multicenter, prospective, observational study included all patients who were discharged from the ICU. Patients were administered the European Quality of Life 5 Dimensions 5 Level Version (EQ-5D-5L) questionnaire, the Short-Form Health Survey 36Version 2 (SF-36v2), a socioeconomic question set and the Impact of Event Scale-Revised (IES-R) to assess PTSD.

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Background: Investigating the health-related quality of life (HRQoL) after intensive care unit (ICU) discharge is necessary to identify possible modifiable risk factors. The primary aim of this study was to investigate the HRQoL in COVID-19 critically ill patients one year after ICU discharge.

Methods: In this multicenter prospective observational study, COVID-19 patients admitted to nine ICUs from 1 March 2020 to 28 February 2021 in Italy were enrolled.

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Following traumatic brain injury (TBI), cerebral metabolic dysfunction, characterized by an elevated cerebral microdialysis (CMD) lactate/pyruvate (LP) ratio, is associated with poor outcome. However, the exact pathophysiological mechanisms underlying this association are not entirely established. In this pre-planned analysis of the BIOmarkers of AXonal injury after Traumatic Brain Injury (BIO-AX-TBI) prospective study, we investigated any associations of LP ratio with brain structure volume change rates at 1 year.

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Background: Recent reports of patients with severe, late-stage COVID-19 ARDS with reduced respiratory system compliance described paradoxical decreases in plateau pressure and increases in respiratory system compliance in response to anterior chest wall loading. We aimed to assess the effect of chest wall loading during supine and prone position in ill patients with COVID-19-related ARDS and to investigate the effect of a low or normal baseline respiratory system compliance on the findings.

Methods: This is a single-center, prospective, cohort study in the intensive care unit of a COVID-19 referral center.

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Purpose: Assess long-term quality of life (HR-QoL) and socio-economic impact in COVID-19-related ARDS (C-ARDS) survivors.

Methods: C-ARDS survivors were followed up at 6 months in this prospective, cohort study. HR-QoL was assessed using SF-36 and EQ-5D-5L, and the socio-economic burden of COVID-19 was evaluated with a dedicated questionnaire.

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Axonal injury is a key determinant of long-term outcomes after traumatic brain injury (TBI) but has been difficult to measure clinically. Fluid biomarker assays can now sensitively quantify neuronal proteins in blood. Axonal components such as neurofilament light (NfL) potentially provide a diagnostic measure of injury.

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Introduction: Critical illness from SARS-CoV-2 infection (COVID-19) is associated with a high burden of pulmonary embolism (PE) and thromboembolic events despite standard thromboprophylaxis. Available guidance is discordant, ranging from standard care to the use of therapeutic anticoagulation for enhanced thromboprophylaxis (ET). Local ET protocols have been empirically determined and are generally intermediate between standard prophylaxis and full anticoagulation.

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Purpose: The COVID-19-related shortage of ICU beds magnified the need of tools to properly titrate the ventilator assistance. We investigated whether bedside-available indices such as the ultrasonographic changes in diaphragm thickening ratio (TR) and the tidal swing in central venous pressure (ΔCVP) are reliable estimates of inspiratory effort, assessed as the tidal swing in esophageal pressure (ΔPes).

Methods: Prospective, observational clinical investigation in the intensive care unit of a tertiary care Hospital.

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Article Synopsis
  • The study focuses on understanding and predicting cognitive impairments caused by traumatic brain injury (TBI) through biomarkers of axonal injury.
  • It involves a prospective longitudinal analysis across multiple European centers, aiming to recruit at least 250 patients and assess various fluid and neuroimaging biomarkers related to clinical outcomes.
  • Ethical approvals have been secured from various ethics committees across different European locations to ensure the study meets regulatory standards.
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Background: Whilst there has been progress in supportive treatment for traumatic brain injury (TBI), specific neuroprotective interventions are lacking. Models of ischaemic heart and brain injury show the therapeutic potential of argon gas, but it is still not known whether inhaled argon (iAr) is protective in TBI. We tested the effects of acute administration of iAr on brain oedema, tissue micro-environmental changes, neurological functions, and structural outcome in a mouse model of TBI.

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Article Synopsis
  • - Traumatic brain injury (TBI) involves a complex interaction between the initial injury, secondary damage, and the body's response, making it a varied and complicated condition that warrants targeted interventions.
  • - Current therapies based on biological understanding have not successfully transitioned into effective clinical treatments, partly due to the limitations in accurately characterizing the biological aspects of TBI.
  • - The review discusses advanced technologies, like cerebral microdialysis and multiplex proteomic techniques, that can enhance the understanding of TBI by allowing for detailed biochemical analysis, while also addressing the challenges in managing the resulting large-scale data.
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Neuroprotection after traumatic brain injury (TBI) is an important goal pursued strenuously in the last 30 years. The acute cerebral injury triggers a cascade of biochemical events that may worsen the integrity, function, and connectivity of the brain cells and decrease the chance of functional recovery. A number of molecules acting against this deleterious cascade have been tested in the experimental setting, often with preliminary encouraging results.

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Lactic acidosis during metformin intoxication is classically mainly attributed to diminished lactate clearance through liver gluconeogenesis. Here we studied 6 healthy, sedated and mechanically ventilated pigs to clarify whether high dose of metformin also increases skeletal muscle lactate production. Each animal had two microdialysis catheters inserted in gluteus muscles, one per side.

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Prognostic models for traumatic brain injury (TBI) are important tools both in clinical practice and research if properly validated, preferably by external validation. Prognostic models also offer the possibility of monitoring performance by comparing predicted outcomes with observed outcomes. In this study, we applied the prognostic models developed by the International Mission on Prognosis and Analysis of Clinical Trials in TBI (IMPACT) in an Italian multi-center database (Neurolink) with two aims: to compare observed with predicted outcomes and to check for a possible improvement of clinical outcome over the 11 years of patient inclusion in Neurolink.

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Introduction: Intracranial pressure (ICP) measurement is used to tailor interventions and to assist in formulating the prognosis for traumatic brain injury patients. Accurate data are therefore essential. The aim of this study was to verify the accuracy of ICP monitoring systems on the basis of a literature review.

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Microdialysis enables the chemistry of the extracellular interstitial space to be monitored. Use of this technique in patients with acute brain injury has increased our understanding of the pathophysiology of several acute neurological disorders. In 2004, a consensus document on the clinical application of cerebral microdialysis was published.

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Article Synopsis
  • Acute brain injuries mainly stem from trauma or cerebrovascular issues like ischemic strokes or hemorrhages, leading to harmful cellular processes triggered by an initial injury.
  • Subarachnoid hemorrhage, a severe type of intracranial hemorrhage, exhibits axonal injury similar to that seen in traumatic brain injury, suggesting underlying commonalities in their mechanisms.
  • Research shows that this axonal injury seen in experimental models of subarachnoid hemorrhage presents with similar markers and patterns as traumatic brain injury, hinting at the need to reconsider how these injuries are understood and managed in clinical settings.
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Axonal injury is a major contributor to adverse outcomes following brain trauma. However, the extent of axonal injury cannot currently be assessed reliably in living humans. Here, we used two experimental methods with distinct noise sources and limitations in the same cohort of 15 patients with severe traumatic brain injury to assess axonal injury.

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Introduction: Posterior reversible encephalopathy syndrome (PRES) is a largely reversible disease with long-term favorable outcome. A minority of patients, however, may develop progressive cerebral edema and ischemia resulting in severe disability or death. We report a case of severe intracranial hypertension associated with PRES that was successfully treated according to intracranial pressure (ICP)- and cerebral perfusion pressure (CPP)-driven therapy.

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Objective: To clarify the dynamics of glucose delivery to the brain and the effects of changes in blood glucose after severe traumatic brain injury.

Design: Retrospective analysis of a prospective observational cohort study.

Setting: Neurosurgical intensive care unit of a university hospital.

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