Intravenous saline administration in patients with severe acquired brain injury and orthostatic intolerance for tilt-table mobilization

Christian Riberholt*, Niels Olesen, Peter Hovind, Jesper Mehlsen, Tue Hvass Petersen

*Corresponding author for this work
    2 Citations (Scopus)

    Abstract

    Primary objective: This study aimed to investigate the effect of intravenous saline administration on orthostatic hypotension (OH) during head up tilt (HUT) and the change in the renin–angiotensin–aldosterone system before and after HUT in patients with severe acquired brain injury (ABI). Research design: The study is designed as an observational study. Methods and procedures: Fourteen patients with ABI, low level of consciousness and OH were monitored before, during and after HUT with non-invasive beat-to-beat blood pressure measurement, and transcranial Doppler determination of middle cerebral artery blood flow velocity. Blood samples were collected before and after two HUT sessions separated by 1 hour and saline was administered in between. Main outcomes and results: Patients’ ability to stand upright did not change after saline administration due to OH. The patients showed signs of reduced cerebral autoregulation at both HUT sessions. The patients had a significant lower level of renin and angiotensin II but not aldosterone. Conclusions: Patients with severe ABI and OH demonstrate no improvement in standing time with reduced plasma renin and angiotensin II after two HUT sessions and 1 hour fluid administration. Research focusing on the ability to retain fluid after bed rest is warranted.

    Original languageEnglish
    JournalBrain Injury
    Volume32
    Issue number2
    Pages (from-to)252-256
    Number of pages5
    ISSN0269-9052
    DOIs
    Publication statusPublished - Jan 2018

    Keywords

    • Cerebral autoregulation
    • head up tilt
    • rehabilitation
    • renin–angiotensin–aldosterone system

    Fingerprint

    Dive into the research topics of 'Intravenous saline administration in patients with severe acquired brain injury and orthostatic intolerance for tilt-table mobilization'. Together they form a unique fingerprint.

    Cite this