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dc.contributor.authorLarvin, J
dc.contributor.authorEdwards, M
dc.contributor.authorMartin, DS
dc.contributor.authorFeelisch, M
dc.contributor.authorGrocott, MPW
dc.contributor.authorCumpstey, AF
dc.date.accessioned2024-05-01T11:35:21Z
dc.date.available2024-05-01T11:35:21Z
dc.date.issued2024-06
dc.identifier.issn2772-6096
dc.identifier.issn2772-6096
dc.identifier.other100277
dc.identifier.urihttps://pearl.plymouth.ac.uk/handle/10026.1/22401
dc.description.abstract

Oxygen is the most used drug in anaesthesia. Despite such widespread use, optimal perioperative oxygen administration remains highly controversial because of concerns about the competing harms of both hyperoxia and hypoxia. Notwithstanding a Cochrane review concluding that routinely administering a fractional inspired oxygen concentration (FiO2) >0.6 intraoperatively might increase postoperative morbidity and mortality, the World Health Organization (WHO) currently recommends all anaesthetised patients receive 0.8 FiO2 during and immediately after surgery to reduce surgical site infections. Results from the largest trial available at the time of these two reviews (suggesting long-term survival may be worse with high FiO2, particularly in patients with malignant disease) were considered 'biologically implausible' by the WHO's Guideline Development Group. In addition, the integrity of some perioperative oxygen studies has been challenged. Resolving these controversies is of fundamental importance to all perioperative clinicians. This narrative review is based on the inaugural BJA William Mapleson lecture delivered by the senior author (AC) at the 2023 annual meeting of the Royal College of Anaesthetists in Birmingham. We present the current evidence for perioperative oxygen administration and contrast this with how oxygen therapy is targeted in other specialties (e.g. intensive care medicine). We will explore whether anaesthetists follow the WHO recommendations and consider how oxygen administration affects the stress response to surgery. We reason that novel clinical trial designs in combination with targeted experimental medicine studies will be required to improve our understanding of how best to optimise individualised perioperative oxygenation-a cornerstone of anaesthesia.

dc.format.extent100277-100277
dc.format.mediumElectronic-eCollection
dc.languageeng
dc.publisherElsevier BV
dc.subjecthyperoxia
dc.subjecthypoxia
dc.subjectoxidative stress
dc.subjectoxygen therapy
dc.subjectsurgical site infections
dc.titlePerioperative oxygenation-what's the stress?
dc.typejournal-article
dc.typeJournal Article
dc.typeReview
plymouth.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/38545565
plymouth.volume10
plymouth.publisher-urlhttp://dx.doi.org/10.1016/j.bjao.2024.100277
plymouth.publication-statusAccepted
plymouth.journalBJA Open
dc.identifier.doi10.1016/j.bjao.2024.100277
plymouth.organisational-group|Plymouth
plymouth.organisational-group|Plymouth|Faculty of Health
plymouth.organisational-group|Plymouth|REF 2021 Researchers by UoA
plymouth.organisational-group|Plymouth|Users by role
plymouth.organisational-group|Plymouth|Users by role|Current Academic staff
plymouth.organisational-group|Plymouth|REF 2021 Researchers by UoA|UoA01 Clinical Medicine
plymouth.organisational-group|Plymouth|Faculty of Health|Peninsula Medical School
plymouth.organisational-group|Plymouth|REF 2029 Researchers by UoA
plymouth.organisational-group|Plymouth|REF 2029 Researchers by UoA|UoA01 Clinical Medicine
dc.publisher.placeEngland
dcterms.dateAccepted2024-03-01
dc.date.updated2024-05-01T11:35:19Z
dc.rights.embargodate2024-5-2
dc.identifier.eissn2772-6096
dc.rights.embargoperiod
rioxxterms.versionofrecord10.1016/j.bjao.2024.100277


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