Study Results
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Basic Information
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RECRUITING
40 participants
OBSERVATIONAL
2019-12-20
2025-12-30
Brief Summary
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Detailed Description
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One potentially treatable cause of cerebral injury during cardiac surgery is hypoperfusion related infarct/ischemia. 7 Watershed, or boundary zone, are situated along border zones between the territories of two major cerebral arteries (e.g., the middle and posterior, or the anterior and middle cerebral arteries) where terminal arteriolar anastomoses exist which are more susceptible to hypoperfusion related infarct/ischemia. 8 These hypoperfusion related injuries are potentially treatable by increasing systematic blood pressure if those injuries are being identified early. Previous study has used electroencephalography to detect intraoperative brain injury at the watershed area9, but the clinical utility of electroencephalography is limited because of its cumbersome set-up and complex logistics. As such, this study aims to use a novel multichannel fNIRS to detect and monitor cerebral oxygenation at multiple brain regions simultaneously for adult patients undergoing during cardiac surgery. This study will increase the experiences of using fNIRS as a monitoring tool in cardiac surgery and improve the understandings to the cerebral injury pattern during cardiac surgery.
Multichannel functional near infrared spectroscopy (fNIRS) is an emerging brain-imaging technique to measure hemodynamic changes at the cortical surface. During the acquisition of fNIRS data light (600-900 nm) is emitted from light sources that can pass through the skull and reach cortex. Photons reflected from the cortex can be detected and quantified by detectors placed in close proximity to the sources. Light is mainly absorbed by oxygenated hemoglobin and deoxygenated hemoglobin, which have distinct absorption spectra. Alterations in the concentrations of oxy- and deoxy-hemoglobin derived from neuronal activation can be quantified using two or more wavelengths. The early studies has showed that the use of two channels cerebral near-infrared spectroscopy can avoid profound cerebral desaturation and is associated with significantly fewer incidences of major organ dysfunction. 10 However, one major limitation of two channels NIRS is that sensor placement is currently limited to forehead that only the frontal lobes are being monitored. Such placement prevents monitoring the critical posterior watershed at the juncture of the anterior, middle, and posterior cerebral arteries, and results in undetected stroke despite the patients having normal cerebral oxygenation throughout the surgery. The lack of comprehensive cortical coverage of the important brain regions such as water-shed area also limit the utility of two channels NIRS as a research tool to assess regional cerebral flow and metabolism during cardiac surgery. The multichannel fNIRS offers a number of advantages for assessing surgical patients intraoperatively including its high temporal resolution (\~100ms), low-cost and portability. The multichannel fNIRS allows up to 64 channels of real-time data acquisition and interpretation, which allows adequate spatial and temporal resolutions to assess the brain regions at risk intraoperatively. In this study, only 16 channels will be used to assess the brain oxygenation.
The fNIRS system in this study is a class I Health Canada approved device (NIRx NIRScout 64x32 Laser/LED 4-wavelength fNRIS system, info:https://nirx.net/nirscout). It does not heat up nor can it damage eyesight. This commercially available device has been used safely in previous studies in neonatal population at Western (WREM #: 111168, 113443) and other studies published in the literature. This device is approved for brain oxygenation monitoring in humans.
Single site, prospective, observational study where patients undergoing cardiac surgical procedures will be monitored using multichannel fNIRS monitoring to assess cerebral oxygenation in regions of the brain that are susceptible to injury during cardiac surgery. No intervention will be used in this study. 40 patients total will be included in the study and receive this monitoring during surgery. There will be no randomization and no additional changes to standard of care.
Patients who agree to participate in this study will receive brain monitoring in the form of multichannel fNIRS monitoring that is not standard of care. This consists of wearing the NIRS cap that will be positioned on the patient's head according to international operational guidelines and will be secured to the temporal region of the patient's forehead. The NIRS cap is entirely non-invasive and does not pose any additional risk to the patient. Monitoring will be commenced prior to the induction of anesthesia.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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multichannel fNIRS monitoring
Patients who will be enrolled in this study will be monitored during cardiac surgery using multichannel fNIRS monitoring. This consists of wearing the NIRS cap during surgery. The patient's surgery and subsequent medical care will not be altered.
multichannel fNIRS monitoring
Patients who will be enrolled in this study will be monitored during cardiac surgery using multichannel fNIRS monitoring. This consists of wearing the NIRS cap that will be positioned on the patient's head according to international operational guidelines and will be secured to the temporal region of the patient's forehead. The NIRS cap is entirely non-invasive and does not pose any additional risk to the patient. Monitoring will be commenced prior to the induction of anesthesia. Subsequent surgical and medical care will not be affected.
Interventions
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multichannel fNIRS monitoring
Patients who will be enrolled in this study will be monitored during cardiac surgery using multichannel fNIRS monitoring. This consists of wearing the NIRS cap that will be positioned on the patient's head according to international operational guidelines and will be secured to the temporal region of the patient's forehead. The NIRS cap is entirely non-invasive and does not pose any additional risk to the patient. Monitoring will be commenced prior to the induction of anesthesia. Subsequent surgical and medical care will not be affected.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* have skin lesions or other conditions that preclude the application of fNIRS to the head
* lack of written consent
* emergency surgery
18 Years
ALL
No
Sponsors
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London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
OTHER
Responsible Party
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Principal Investigators
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Jason Chui, MD
Role: PRINCIPAL_INVESTIGATOR
Western University
Locations
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London Health Sciences Centre
London, Ontario, Canada
Countries
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Central Contacts
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Facility Contacts
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References
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McKhann GM, Grega MA, Borowicz LM Jr, Baumgartner WA, Selnes OA. Stroke and encephalopathy after cardiac surgery: an update. Stroke. 2006 Feb;37(2):562-71. doi: 10.1161/01.STR.0000199032.78782.6c. Epub 2005 Dec 22.
Roach GW, Kanchuger M, Mangano CM, Newman M, Nussmeier N, Wolman R, Aggarwal A, Marschall K, Graham SH, Ley C. Adverse cerebral outcomes after coronary bypass surgery. Multicenter Study of Perioperative Ischemia Research Group and the Ischemia Research and Education Foundation Investigators. N Engl J Med. 1996 Dec 19;335(25):1857-63. doi: 10.1056/NEJM199612193352501.
Rankin JM, Silbert PL, Yadava OP, Hankey GJ, Stewart-Wynne EG. Mechanism of stroke complicating cardiopulmonary bypass surgery. Aust N Z J Med. 1994 Apr;24(2):154-60. doi: 10.1111/j.1445-5994.1994.tb00551.x.
Salazar JD, Wityk RJ, Grega MA, Borowicz LM, Doty JR, Petrofski JA, Baumgartner WA. Stroke after cardiac surgery: short- and long-term outcomes. Ann Thorac Surg. 2001 Oct;72(4):1195-201; discussion 1201-2. doi: 10.1016/s0003-4975(01)02929-0.
Tufo HM, Ostfeld AM, Shekelle R. Central nervous system dysfunction following open-heart surgery. JAMA. 1970 May 25;212(8):1333-40. No abstract available.
Gardner TJ, Horneffer PJ, Manolio TA, Pearson TA, Gott VL, Baumgartner WA, Borkon AM, Watkins L Jr, Reitz BA. Stroke following coronary artery bypass grafting: a ten-year study. Ann Thorac Surg. 1985 Dec;40(6):574-81. doi: 10.1016/s0003-4975(10)60352-9.
Sun LY, Chung AM, Farkouh ME, van Diepen S, Weinberger J, Bourke M, Ruel M. Defining an Intraoperative Hypotension Threshold in Association with Stroke in Cardiac Surgery. Anesthesiology. 2018 Sep;129(3):440-447. doi: 10.1097/ALN.0000000000002298.
Gottesman RF, Sherman PM, Grega MA, Yousem DM, Borowicz LM Jr, Selnes OA, Baumgartner WA, McKhann GM. Watershed strokes after cardiac surgery: diagnosis, etiology, and outcome. Stroke. 2006 Sep;37(9):2306-11. doi: 10.1161/01.STR.0000236024.68020.3a. Epub 2006 Jul 20.
Malone M, Prior P, Scholtz CL. Brain damage after cardiopulmonary by-pass: correlations between neurophysiological and neuropathological findings. J Neurol Neurosurg Psychiatry. 1981 Oct;44(10):924-31. doi: 10.1136/jnnp.44.10.924.
Murkin JM, Adams SJ, Novick RJ, Quantz M, Bainbridge D, Iglesias I, Cleland A, Schaefer B, Irwin B, Fox S. Monitoring brain oxygen saturation during coronary bypass surgery: a randomized, prospective study. Anesth Analg. 2007 Jan;104(1):51-8. doi: 10.1213/01.ane.0000246814.29362.f4.
Other Identifiers
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FNIRS
Identifier Type: -
Identifier Source: org_study_id
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