Biomarkers Associated With Postoperative Cognitive Dysfunction

NCT05464355 — Active not recruiting, 45 participants, University of Oxford

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Feasibility Study of the Use of Biomarkers to Detect Perioperative Brain Injury: the Association Between Serum Neurofilament Light Chains, Tau Proteins, Continuous Intra-operative Electroencephalography, and the Development of Post Operative Cognitive Dysfunction After Surgery

RegistryNCT05464355
StatusActive not recruiting
Study typeObservational
Enrollment45 (Estimated)
SponsorUniversity of Oxford (Other); collaborators: Oxford University Hospitals NHS Trust
ConditionsDelirium, Postoperative Cognitive Dysfunction, Cognitive Decline, Cognitive Impairment
InterventionsIntraoperative electroencephalography recording, Neurofilament light chain measurement, Tau protein measurement (Procedure)
Datesstart 2023-01-05, primary completion 2026-01-01 (estimated), completion 2030-01-01 (estimated), first posted 2022-07-19, last updated 2025-06-22
Locations1 site in United Kingdom

Related Papers Related Patents Related Grants Related Experts
All trials for Delirium All trials for Postoperative Cognitive Dysfunction All trials of Intraoperative electroencephalography recording All trials of Neurofilament light chain measurement

-Summary

Loss of cognitive function after major surgery is a significant risk in older people. It can occur acutely in the days after surgery as delirium or in months to years later as a persistent reduction in brain function termed neurocognitive decline. Together these conditions are called post operative cognitive dysfunction (POCD). They can be acutely distressing for patients and are associated with other problems after surgery.

The causes of post operative cognitive dysfunction are poorly understood. Studies have been limited by a lack of biomarkers to predict which patients are at high risk of developing POCD. Research suggests silent strokes occurring during surgery and different sensitivities to anaesthetic medicines are associated with POCD.

The project consists of a feasibility study to investigate markers that might predict people over 65 years old getting POCD. The first biomarker is a non-invasive monitor of anaesthetics effects on brain function called electroencephalography (EEG): The investigators will identify which EEG patterns predict delirium within five days surgery. The second set of biomarkers are two blood tests of proteins that increase after strokes: these are neurofilament light chains and tau proteins. The investigators will establish if these can be used to predict having POCD up to one year after surgery and long term cognitive impairment up to 5 years after surgery.

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+Arms and interventions

ArmTypeInterventionsDescription
Biomarker monitoringProcedure: Intraoperative electroencephalography recording; Procedure: Neurofilament light chain measurement; Procedure: Tau protein measurement
  • Intraoperative electroencephalography recording (Procedure), also known as EEG recording: Intraoperative electroencephalography measurements, a non-invasive routine monitoring device used during anaesthesia to measure the brain's electrical activity
  • Neurofilament light chain measurement (Procedure), also known as NfL: Measurement of the level of neurofilament light chain in a blood sample
  • Tau protein measurement (Procedure): Measurement of the level of tau protein in a blood sample

+Outcome measures

Primary outcomes

  • Feasibility to conduct the study [1 year after surgery]: The total number of participants who are successfully recruited, receive the study procedures and complete both 90 day and 1 year follow up after surgery.

Secondary outcomes

  • Postoperative delirium incidence and severity [Up to 5 days after surgery]: Postoperative delirium identified as being present according to a positive result using 3-Minute Diagnostic Interview for Confusion Assessment Method (3D-CAM) and severity according to the absolute value on the 3D-CAM-Severity which is a scale converting the 3-Minute Diagnostic Interview for Confusion Assessment Method into a scale from 0-7. Higher scores are associated with worse outcome.
  • Days alive and at home up to 90 days after surgery [90 days after surgery]: The number of days a participant is alive and how many are spent at home after surgery
  • Change in neurofilament light chains and tau proteins levels pre- to post operatively [Up to 2 days after surgery]: Measurements of the level of the biomarkers neurofilament light chain and tau protein in plasma
  • Postoperative neurocognitive dysfunction and severity [Up to 1 year after surgery]: Cognitive impairment measured on Montreal Objective Cognitive Assessment administered by telephone. The scale is 0-22 with higher scores representing better outcome.
  • Long term cognitive impairment [Up to 5 years after surgery]: Incidence of new diagnosis in primary or secondary care of dementia or mild cognitive impairment

+Eligibility

Sex: All, ages: 65 Years to any

Inclusion Criteria:

* Greater than or equal to 65 years of age
* Having elective non-cardiac surgery under general anaesthesia
* Anticipated to have at least 48 hours of inpatient admission
* Able \& willing to give informed consent

Exclusion Criteria:

* Unable to participate in neurocognitive assessments
* Presence of delirium prior to surgery
* Contraindication to use of EEG electrodes (e.g. known allergy to a component of the electrodes)
* Known history of severe traumatic brain injury
* Learning disability specifically with a known structural brain lesion
* Known history of dementia
* Participants undergoing operations on the carotid artery

+Locations (1)

FacilityCityCountryStatus
Royal Berkshire NHS Foundation TrustReading, BerkshireUnited Kingdom

+Investigators

  • Martyn Ezra, Principal investigator, University of Oxford