Measuring Salivary Cortisol to Assess the Effect of Natural Environments on Stress Level in Acute Patients With Severe Brain Injuries: An Exploratory Study.

acute phase brain injury nature neurorehabilitation salivary cortisol stress

Journal

Cureus
ISSN: 2168-8184
Titre abrégé: Cureus
Pays: United States
ID NLM: 101596737

Informations de publication

Date de publication:
Sep 2023
Historique:
accepted: 07 09 2023
medline: 10 10 2023
pubmed: 10 10 2023
entrez: 10 10 2023
Statut: epublish

Résumé

Salivary cortisol is a safe and non-invasive measure of hypothalamic-pituitary-adrenal axis function and is used as a biomarker of the human stress response. Natural environments are recognized to contribute to help reduce the effect of stress. To determine the feasibility of a salivary cortisol collection protocol for acute severely brain-injured patients, and to explore the influence of exposure to natural settings on salivary cortisol concentration as an index of stress level. An exploratory study on 17 acute patients with severe brain injury was performed. We collected salivary samples in a closed hospital ward and a therapeutic garden at the start of the session and after 30 minutes of rest time. Physiological parameters, level of communication, and subjective well-being were also assessed. The primary objectives regarding the feasibility of the protocol were met overall. We found no significant differences in cortisol values when including the whole population. However, cortisol values were significantly higher in the indoor environment in patients with communication attempts. A salivary collection protocol with brain-injured patients in the acute phase is feasible and safe, and this type of measurement could pave the way for future research supporting the benefits of nature as an additional resource in their neurorehabilitation.

Sections du résumé

BACKGROUND BACKGROUND
Salivary cortisol is a safe and non-invasive measure of hypothalamic-pituitary-adrenal axis function and is used as a biomarker of the human stress response. Natural environments are recognized to contribute to help reduce the effect of stress.
OBJECTIVE OBJECTIVE
To determine the feasibility of a salivary cortisol collection protocol for acute severely brain-injured patients, and to explore the influence of exposure to natural settings on salivary cortisol concentration as an index of stress level.
METHODS METHODS
An exploratory study on 17 acute patients with severe brain injury was performed. We collected salivary samples in a closed hospital ward and a therapeutic garden at the start of the session and after 30 minutes of rest time. Physiological parameters, level of communication, and subjective well-being were also assessed.
RESULTS RESULTS
The primary objectives regarding the feasibility of the protocol were met overall. We found no significant differences in cortisol values when including the whole population. However, cortisol values were significantly higher in the indoor environment in patients with communication attempts.
CONCLUSIONS CONCLUSIONS
A salivary collection protocol with brain-injured patients in the acute phase is feasible and safe, and this type of measurement could pave the way for future research supporting the benefits of nature as an additional resource in their neurorehabilitation.

Identifiants

pubmed: 37814730
doi: 10.7759/cureus.44878
pmc: PMC10560321
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e44878

Informations de copyright

Copyright © 2023, Jöhr et al.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Jane Jöhr (J)

Department of Clinical Neurosciences/Neurology, Lausanne University Hospital and University of Lausanne (CHUV-UNIL), Lausanne, CHE.

Tania Martinez (T)

Department of Clinical Neurosciences/Neurology, Lausanne University Hospital and University of Lausanne (CHUV-UNIL), Lausanne, CHE.

Renaud Marquis (R)

Department of Clinical Neurosciences/Neurology, Lausanne University Hospital and University of Lausanne (CHUV-UNIL), Lausanne, CHE.

Stephen Bruce (S)

Laboratory of Clinical Chemistry/Biomedicine, Lausanne University Hospital and University of Lausanne (CHUV-UNIL), Lausanne, CHE.

Pierre-Alain Binz (PA)

Laboratory of Clinical Chemistry/Biomedicine, Lausanne University Hospital and University of Lausanne (CHUV-UNIL), Lausanne, CHE.

Sabine Rey (S)

Department of Clinical Neurosciences/Neurology, Lausanne University Hospital and University of Lausanne (CHUV-UNIL), Lausanne, CHE.

Gaël Hafner (G)

Department of Clinical Neurosciences/Neurology, Lausanne University Hospital and University of Lausanne (CHUV-UNIL), Lausanne, CHE.

Caroline Attwell (C)

Department of Clinical Neurosciences/Neurology, Lausanne University Hospital and University of Lausanne (CHUV-UNIL), Lausanne, CHE.

Karin Diserens (K)

Department of Clinical Neurosciences/Neurology, Lausanne University Hospital and University of Lausanne (CHUV-UNIL), Lausanne, CHE.

Classifications MeSH