44
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Long-term cognitive impairment after acute respiratory distress syndrome: a review of clinical impact and pathophysiological mechanisms

      review-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Acute respiratory distress syndrome (ARDS) survivors experience a high prevalence of cognitive impairment with concomitantly impaired functional status and quality of life, often persisting months after hospital discharge. In this review, we explore the pathophysiological mechanisms underlying cognitive impairment following ARDS, the interrelations between mechanisms and risk factors, and interventions that may mitigate the risk of cognitive impairment. Risk factors for cognitive decline following ARDS include pre-existing cognitive impairment, neurological injury, delirium, mechanical ventilation, prolonged exposure to sedating medications, sepsis, systemic inflammation, and environmental factors in the intensive care unit, which can co-occur synergistically in various combinations. Detection and characterization of pre-existing cognitive impairment imparts challenges in clinical management and longitudinal outcome study enrollment. Patients with brain injury who experience ARDS constitute a distinct population with a particular combination of risk factors and pathophysiological mechanisms: considerations raised by brain injury include neurogenic pulmonary edema, differences in sympathetic activation and cholinergic transmission, effects of positive end-expiratory pressure on cerebral microcirculation and intracranial pressure, and sensitivity to vasopressor use and volume status. The blood-brain barrier represents a physiological interface at which multiple mechanisms of cognitive impairment interact, as acute blood-brain barrier weakening from mechanical ventilation and systemic inflammation can compound existing chronic blood-brain barrier dysfunction from Alzheimer’s-type pathophysiology, rendering the brain vulnerable to both amyloid-beta accumulation and cytokine-mediated hippocampal damage. Although some contributory elements, such as the presenting brain injury or pre-existing cognitive impairment, may be irreversible, interventions such as minimizing mechanical ventilation tidal volume, minimizing duration of exposure to sedating medications, maintaining hemodynamic stability, optimizing fluid balance, and implementing bundles to enhance patient care help dramatically to reduce duration of delirium and may help prevent acquisition of long-term cognitive impairment.

          Related collections

          Most cited references88

          • Record: found
          • Abstract: found
          • Article: not found

          Epidemiology, Patterns of Care, and Mortality for Patients With Acute Respiratory Distress Syndrome in Intensive Care Units in 50 Countries.

          Limited information exists about the epidemiology, recognition, management, and outcomes of patients with the acute respiratory distress syndrome (ARDS).
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            A paravascular pathway facilitates CSF flow through the brain parenchyma and the clearance of interstitial solutes, including amyloid β.

            Because it lacks a lymphatic circulation, the brain must clear extracellular proteins by an alternative mechanism. The cerebrospinal fluid (CSF) functions as a sink for brain extracellular solutes, but it is not clear how solutes from the brain interstitium move from the parenchyma to the CSF. We demonstrate that a substantial portion of subarachnoid CSF cycles through the brain interstitial space. On the basis of in vivo two-photon imaging of small fluorescent tracers, we showed that CSF enters the parenchyma along paravascular spaces that surround penetrating arteries and that brain interstitial fluid is cleared along paravenous drainage pathways. Animals lacking the water channel aquaporin-4 (AQP4) in astrocytes exhibit slowed CSF influx through this system and a ~70% reduction in interstitial solute clearance, suggesting that the bulk fluid flow between these anatomical influx and efflux routes is supported by astrocytic water transport. Fluorescent-tagged amyloid β, a peptide thought to be pathogenic in Alzheimer's disease, was transported along this route, and deletion of the Aqp4 gene suppressed the clearance of soluble amyloid β, suggesting that this pathway may remove amyloid β from the central nervous system. Clearance through paravenous flow may also regulate extracellular levels of proteins involved with neurodegenerative conditions, its impairment perhaps contributing to the mis-accumulation of soluble proteins.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Neurovascular pathways to neurodegeneration in Alzheimer's disease and other disorders.

              The neurovascular unit (NVU) comprises brain endothelial cells, pericytes or vascular smooth muscle cells, glia and neurons. The NVU controls blood-brain barrier (BBB) permeability and cerebral blood flow, and maintains the chemical composition of the neuronal 'milieu', which is required for proper functioning of neuronal circuits. Recent evidence indicates that BBB dysfunction is associated with the accumulation of several vasculotoxic and neurotoxic molecules within brain parenchyma, a reduction in cerebral blood flow, and hypoxia. Together, these vascular-derived insults might initiate and/or contribute to neuronal degeneration. This article examines mechanisms of BBB dysfunction in neurodegenerative disorders, notably Alzheimer's disease, and highlights therapeutic opportunities relating to these neurovascular deficits.
                Bookmark

                Author and article information

                Contributors
                shouri.lahiri@csmc.edu
                Journal
                Crit Care
                Critical Care
                BioMed Central (London )
                1364-8535
                1466-609X
                12 November 2019
                12 November 2019
                2019
                : 23
                : 352
                Affiliations
                [1 ]ISNI 0000000419368710, GRID grid.47100.32, Division of Neurocritical Care and Emergency Neurology, Department of Neurology, , Yale School of Medicine, ; New Haven, CT USA
                [2 ]ISNI 0000 0001 2264 7217, GRID grid.152326.1, Critical Illness, Brain Dysfunction, Survivorship (CIBS) Center, Department of Pulmonary and Critical Care Medicine, Veteran’s Affairs Tennessee Valley Geriatric Research Education and Clinical Center (GRECC), , Vanderbilt University School of Medicine, ; Nashville, TN USA
                [3 ]ISNI 0000 0001 2152 9905, GRID grid.50956.3f, Division of Neurocritical Care, Department of Neurology, , Cedars-Sinai Medical Center, ; 127 S. San Vicente Blvd, AHSP Building, Suite A6600, A8103, Los Angeles, CA 90048 USA
                [4 ]ISNI 0000 0001 2152 9905, GRID grid.50956.3f, Division of Neurocritical Care, Department of Neurosurgery, , Cedars-Sinai Medical Center, ; 127 S. San Vicente Blvd, AHSP Building, Suite A6600, A8103, Los Angeles, CA 90048 USA
                [5 ]ISNI 0000 0001 2152 9905, GRID grid.50956.3f, Division of Neurocritical Care, Department of Biomedical Sciences, , Cedars-Sinai Medical Center, ; 127 S. San Vicente Blvd, AHSP Building, Suite A6600, A8103, Los Angeles, CA 90048 USA
                Author information
                http://orcid.org/0000-0002-5469-6467
                Article
                2626
                10.1186/s13054-019-2626-z
                6852966
                31718695
                172dfc2e-b601-4453-b7a9-e25ad60847d4
                © The Author(s). 2019

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 18 July 2019
                : 27 September 2019
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100000049, National Institute on Aging;
                Award ID: R03AG064106
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100005339, American Academy of Neurology;
                Award ID: Career Development Award
                Award Recipient :
                Categories
                Review
                Custom metadata
                © The Author(s) 2019

                Emergency medicine & Trauma
                ards,cognitive impairment,outcomes,icu delirium,blood-brain barrier,inflammation,mechanical ventilation,pathophysiological mechanisms

                Comments

                Comment on this article