Optical coherence tomography (OCT) in unconscious and systemically unwell patients using a mobile OCT device: a pilot study.


Journal

BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874

Informations de publication

Date de publication:
07 11 2019
Historique:
entrez: 9 11 2019
pubmed: 9 11 2019
medline: 27 10 2020
Statut: epublish

Résumé

This study aims to evaluate the feasibility of retinal imaging in critical care using a novel mobile optical coherence tomography (OCT) device. The Heidelberg SPECTRALIS FLEX module (Heidelberg Engineering, Heidelberg, Germany) is an OCT unit with a boom arm, enabling ocular OCT assessment in less mobile patients. We undertook an evaluation of the feasibility of using the SPECTRALIS FLEX for undertaking ocular OCT images in unconscious and critically ill patients. This study was conducted in the critical care unit of a large tertiary referral unit in the United Kingdom. 13 systemically unwell patients admitted to the critical care unit were purposively sampled to enable evaluation in patients with a range of clinical states. The primary outcome was the feasibility of acquiring clinically interpretable OCT scans on a consecutive series of patients. The standardised scanning protocol included macula-focused OCT, OCT optic nerve head (ONH), OCT angiography (OCTA) of the macula and ONH OCTA. OCT images from 13 patients were attempted. The success rates of each scan type are 84% for OCT macula, 76% for OCT ONH, 56% for OCTA macula and 36% for OCTA ONH. The overall mean success rate of scans per patient was 64% (95% CI 46% to 81%). Clinicians reported clinical value in 100% scans which were successfully obtained, including both ruling in and ruling out relevant ocular complications such as corneal thinning, macular oedema and optic disc swelling. The most common causes of failure to achieve clinically interpretable scans were inadequately sustained OCT alignment in delirious patients and a compromised ocular surface due to corneal exposure. This prospective evaluation indicates the feasibility and potential clinical value of the SPECTRALIS FLEX OCT system on the critical care unit. Portable OCT systems have the potential to bring instrument-based ophthalmic assessment to critically ill patients, enabling detection and micron-level monitoring of ocular complications.

Identifiants

pubmed: 31699727
pii: bmjopen-2019-030882
doi: 10.1136/bmjopen-2019-030882
pmc: PMC6858135
doi:

Types de publication

Clinical Trial Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e030882

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Department of Health
ID : CS-2014-14-023
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_PC_19005
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 200141/Z/15/Z
Pays : United Kingdom

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

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Auteurs

Xiaoxuan Liu (X)

Ophthalmology Department, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
Academic Unit of Ophthalmology, Institute of Inflammation and Ageing, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.
Health Data Research UK, London, United Kingdom.

Aditya Uday Kale (AU)

Academic Unit of Ophthalmology, Institute of Inflammation and Ageing, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.

Nicholas Capewell (N)

Ophthalmology Department, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.

Nicholas Talbot (N)

Ophthalmology Department, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.

Sumiya Ahmed (S)

Ophthalmology Department, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.

Pearse A Keane (PA)

Health Data Research UK, London, United Kingdom.
NIHR Biomedical Research Centre for Ophthalmology, Moorfields Eye Hospital NHS Foundation Trust, London, UK.

Susan Mollan (S)

Ophthalmology Department, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
Centre for Rare Diseases, Institute of Translational Medicine, Birmingham, UK.

Antonio Belli (A)

Ophthalmology Department, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
Institute of Inflammation and Ageing, University of Birmingham, College of Medical and Dental Sciences, Birmingham, UK.
Department of Critical Care Medicine, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.

Richard J Blanch (RJ)

Ophthalmology Department, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
Academic Department of Military Surgery and Trauma, Royal Centre for Defence Medicine, Birmingham, UK.

Tonny Veenith (T)

Ophthalmology Department, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
Department of Critical Care Medicine, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.

Alastair K Denniston (AK)

Ophthalmology Department, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK a.denniston@bham.ac.uk.
Academic Unit of Ophthalmology, Institute of Inflammation and Ageing, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.
Health Data Research UK, London, United Kingdom.
NIHR Biomedical Research Centre for Ophthalmology, Moorfields Eye Hospital NHS Foundation Trust, London, UK.
Centre for Rare Diseases, Institute of Translational Medicine, Birmingham, UK.

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