Cerebral Oximetry in Cardiac Surgery to Reduce Neurological Impairment and Hospital Length-of-stay

Sponsor
Hull University Teaching Hospitals NHS Trust (Other)
Overall Status
Completed
CT.gov ID
NCT04463563
Collaborator
The Hull and East Riding Cardiac Trust Fund (Other)
182
2
43

Study Details

Study Description

Brief Summary

Cerebral oximetry using near-infrared spectroscopy (NIRS) has been shown to reduce the incidence of neurological dysfunction and hospital length-of-stay in adult cardiac surgery though not all studies agree. A previous audit using cerebral saturations at or above baseline showed improved neurological and length-of-stay outcomes.

Condition or Disease Intervention/Treatment Phase
  • Other: Physiological
N/A

Detailed Description

This prospective, single centre, double-blinded controlled study randomized 182 consecutive patients, scheduled for cardiac surgical procedures using cardiopulmonary bypass. Participants were randomized by concealed envelope prior to anaesthesia. NIRS study group were managed perioperatively using our NIRS protocol. The control group had standard management without NIRS. Primary outcomes were post-operative neurological impairment and hospital length-of-stay. Secondary outcomes included ventilation times, intensive care unit length-of-stay, major organ dysfunction and mortality

Study Design

Study Type:
Interventional
Actual Enrollment :
182 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
This prospective, single centre, double-blinded controlled study randomized 182 consecutive patients, scheduled for cardiac surgical procedures using cardiopulmonary bypass. Participants were randomized by concealed envelope.This prospective, single centre, double-blinded controlled study randomized 182 consecutive patients, scheduled for cardiac surgical procedures using cardiopulmonary bypass. Participants were randomized by concealed envelope.
Masking:
Double (Participant, Outcomes Assessor)
Masking Description:
The personnel assessing and collecting the post-operative data were unaware of the patient group in the operating room.
Primary Purpose:
Prevention
Official Title:
Cerebral Oximetry in Adult Cardiac Surgery to Reduce the Incidence of Neurological Impairment and Hospital Length-of-stay: A Prospective, Randomized, Controlled Trial
Actual Study Start Date :
Feb 1, 2011
Actual Primary Completion Date :
Mar 1, 2014
Actual Study Completion Date :
Sep 1, 2014

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: NIRS group. Brain oxygen saturations group.

A monitor by means of non-invasive stickers will display cerebral oximetry (brain oxygen saturations) throughout the heart surgery.This gives a direct reading of brain frontal lobe oxygen levels. The baseline is recorded before the patient goes to sleep (anaesthetised) and throughout the surgery and time on cardiopulmonary bypass if the brain oxygen levels fall below baseline then various physiological changes are made to restore oxygen to baseline.

Other: Physiological
Changes to carbon dioxide, oxygen flow, cardiac output, blood pressure, haemoglobin, surgical surveillance, depth of anaesthesia, patient position.

No Intervention: Standard Patient Monitoring

No cerebral monitoring. Standard patient monitoring according to normal practice at Castle Hill Hospital apply.

Outcome Measures

Primary Outcome Measures

  1. Hospital length-of-stay [Measured in days from the day of operation to the day the patient is discharged from hospital or death in hospital. If neither has occurred within 6 months of participant's operation it will be recorded as 6 months hospital stay.]

    How long before discharge post-operatively.

  2. Physical neurological examination [3 day post-operatively]

    Mobility and conscious control of limbs.

  3. Neurological assessment. [6 months post-operatively]

    Telephone interview to assess patients perception of mobility, function and well being. (see below details)

  4. Neurocognitive test 1 [Day 3 post op.]

    Fluency and cognitive functions: Mini-Mental State Examination (MMSE). This test is conducted as a questionnaire of 11 questions. Questions include 'what is the date?', 'name the town you are in?', spelling-forwards and backwards, counting backwards, copying a picture, follow an instruction, naming objects etc. The test is scored out of 30 and recorded in a table. The test is repeated on the third post op day and the 2 scores compared to give a number which relates to performance.

  5. Neurocognitive Test 2 [Day 3 post op]

    Visual attention and task switching: Trail Making test A and B

  6. Neurocognitive test 3 [Day 3 post op]

    Visual-spatial, frontal lobe: Anti-saccadic eye test

  7. Neurocognitive test 4 [Day 3 post op]

    Executive function/verbal immediate and delayed recall: Hopkins Verbal and Hopkins Delay.

  8. Neurocognitive test 5 [Day 3 post op]

    General well-being HADS (hospital anxiety and depression score) A and D. HADS A -hospital anxiety and depression score relating to Anxiety. HADS D- hospital anxiety and depression score relating to Depression. Patients are asked a question and their response is scored from 0-3. There are 14 questions the score is recorded and compared with the score after the same questions on the 3rd post-op day. The result gives an indication of the patient's mental state and how it may have changed dur to the sugery.

  9. Late neurocognitive test 1.Telephone questionnaire using elements of the previously used questionnaires. [6 months post op]

    General health questions were: how is your overall health, memory, mood, motor function?Designed to be shorter and not require any visual skills. The questions include the patients perception of whether they believe in each domain that their performance is the same, better or worse than before the surgery.

  10. Late neurocognitive test 2. Telephone questionnaire using elements of the previously used questionnaires. [6 months post op]

    Cognition questions were: Date, repeat and recall, serial 7s, spell, recall. Designed to be shorter and not require any visual skills. The questions include the patients perception of whether they believe in each domain that their performance is the same, better or worse than before the surgery.

  11. Late neurocognitive test 3 [6 months post op]

    Functionality questions were: Stairs, driving, cleaning, dressing, eating/cooking.

Secondary Outcome Measures

  1. Intensive Care length-of-stay [The assessment period is every day on ICU until participant moved to ward. Or patient dies on ICU. Total assessment period 6 months.]

    Days on ICU. The time from the day of surgery to the discharge to the ward or death. assessed .

  2. Major organ dysfunction [Before hospital discharge]

    Renal function is assessed measuring creatinine. Gastrointestinal function is assessed by the diagnosis of ileus or ischaemic bowel at laparotomy. Cardiac function is assessed by the requirement for inotropic support. Respiratory function is assessed by the requirement for ventilation. All these outcomes are have clinical relevance during the stay on ICU.

  3. Mortality [Day of surgery to death. If the participant is discharged from hospital alive it is not a mortality. Assessed for 6 months from the day of surgery.]

    Death in hospital at any time following surgery. Death is considered a mortality.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:

Patients undergoing elective cardiac surgery using cardiopulmonary bypass. Patient over 18 years age. -

Exclusion Criteria:

Emergency surgery. Cardiac surgery without cardiopulmonary bypass. Inability to perform test.

Persistent neurological conditions:

Recent stroke. Dementia. Alzheimer's Disease Parkinson's Disease

-

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Hull University Teaching Hospitals NHS Trust
  • The Hull and East Riding Cardiac Trust Fund

Investigators

  • Principal Investigator: Sean R Bennett, MB Chb, Consultant Anaesthetist Hull Hospital Trust

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Hull University Teaching Hospitals NHS Trust
ClinicalTrials.gov Identifier:
NCT04463563
Other Study ID Numbers:
  • REC-10/H0906/72
First Posted:
Jul 9, 2020
Last Update Posted:
Jul 9, 2020
Last Verified:
Jul 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 9, 2020