Application of Innovative Non-Invasive Neuroprotective Technology in Cardiac Surgery and Ophthalmology

NCT ID: NCT04943458

Last Updated: 2022-04-05

Basic Information

• Recruitment Status: UNKNOWN
• Total Enrollment: 270 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2021-09-01
• Study Completion Date: 2022-10-01

Brief Summary

Postoperative cognitive dysfunction (POCD) and delirium (incidence up to 42 %) after cardiac surgery with cardiopulmonary bypass (CPB) are common postoperative complications that impair the patient's quality of life and increase the risk of death. Our previous studies confirm that postoperative POCD are associated with impaired cerebral autoregulation (CA) and momentary increased intracranial pressure (ICP) during surgery. The upper and lower limits of CA are individual and variable. In the elderly, CA is already partially impaired due to decreased cerebral vascular elasticity. What should be the optimal mean arterial pressure for each of these patients individually is not known. In order to individualize the boundaries of CA and prevent postoperative neurological complications, it would be ideal to objectify the condition of cerebral blood vessels. Direct studies of cerebrovascular and vascular status (CT angiography) are invasive and complex, and are therefore not routinely performed prior to cardiac surgery. However, cerebral blood flow and vascular condition can be assessed by retinal blood vessels, which can be considered as a direct biomarker of cerebrovascular disorders and can be visualized by ophthalmoscopy and objectively assessed by optical coherent tomography with angiography.

In this biomedical study, individual patient CA will be monitored in a non-invasive manner during cardiac surgery with CPB. These data would allow real-time adjustments to physiological parameters while keeping them within normal limits. This is expected to reduce the risk of CA impairment and reduce the incidence of neurological complications following such surgery.

Glaucoma is one of the leading causes of irreversible blindness in the world. As the population ages, the number of people with glaucoma increases as the prevalence of glaucoma increases with age. Recently, the influence of ICP on glaucoma optic neuropathy has been highlighted. It is thought that the pressure difference in the optic nerve area may be related to damage to the axons of the ganglion cells passing through the porous plate. Noninvasive ICP measurement is useful in explaining the pathophysiology of glaucoma, assessing translaminar pressure differentials, and seeking new guidelines for the treatment and prevention of glaucoma. Retinal blood flow, like cerebral blood flow, is autoregulated, autoregulation is maintained only within certain limits of perfusion pressure. Decreased ocular perfusion pressure impairs retinal autoregulation and may lead to the development or progression of glaucoma neuropathy. And the activity of neurons in the brain and retina causes local changes in blood circulation. Disruption of this neurovascular interaction during glaucoma neuropathy has not been adequately studied.The introduction of modern technologies into clinical practice enables the qualitative and quantitative assessment of autoregulatory disorders and the selection of optimal treatment.

Conditions

Postoperative Cognitive Disorder; Glaucoma

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

Cardiac surgery group

Monitoring of cerebral autoregulation

Intervention Type: OTHER

Patients will be monitored for cerebral autoregulation using a Vittamed 505 monitor to identify the dynamics of the autoregulation index VRx (t). Intracranial pressure (ICP) will also be measured by non-invasive ultrasound using a robotic TCD device, Dolphin4D (Israel), which simultaneously records MCA blood flow in both hemispheres of the brain. APAs will be assessed using mathematical models.

Glaucoma group

Monitoring of cerebral autoregulation

Intervention Type: OTHER

Patients will be monitored for cerebral autoregulation using a Vittamed 505 monitor to identify the dynamics of the autoregulation index VRx (t). Intracranial pressure (ICP) will also be measured by non-invasive ultrasound using a robotic TCD device, Dolphin4D (Israel), which simultaneously records MCA blood flow in both hemispheres of the brain. APAs will be assessed using mathematical models.

Control group

Monitoring of cerebral autoregulation

Intervention Type: OTHER

Patients will be monitored for cerebral autoregulation using a Vittamed 505 monitor to identify the dynamics of the autoregulation index VRx (t). Intracranial pressure (ICP) will also be measured by non-invasive ultrasound using a robotic TCD device, Dolphin4D (Israel), which simultaneously records MCA blood flow in both hemispheres of the brain. APAs will be assessed using mathematical models.

Interventions

Monitoring of cerebral autoregulation

Patients will be monitored for cerebral autoregulation using a Vittamed 505 monitor to identify the dynamics of the autoregulation index VRx (t). Intracranial pressure (ICP) will also be measured by non-invasive ultrasound using a robotic TCD device, Dolphin4D (Israel), which simultaneously records MCA blood flow in both hemispheres of the brain. APAs will be assessed using mathematical models.

Intervention Type: OTHER

Other Intervention Names

Non invasive ICP monitoring

Eligibility Criteria

Inclusion Criteria

I. Criteria for the inclusion of the CA monitoring method in cardiac surgery:

1. Age 18-90 years.

2. The patient, after reading the personal information form, confirms in writing his / her consent to participate in the study.

3. An AVJS operation is planned.

4. No ophthalmological or neurological disorders have been identified prior to surgery.

II. Criteria for the inclusion of the CA monitoring method in ophthalmology:

1. Age 18-90 years.

2. The patient, after reading the personal information form, confirms in writing his / her consent to participate in the study.

3. Patients with glaucoma changes in the optic disc and eye area shall be included in the study group.

4. The control group shall include volunteers who are free from glaucoma, acute or chronic uncompensated disease that may affect the results of the studies, and age and anthropometric data from other study groups.

Exclusion Criteria

1. No written consent of a person to participate in a biomedical research has been obtained;

2. Persons under 18 years of age.

3. A woman who may become pregnant, be pregnant or breastfeeding.

4. The patient is allergic or sensitive to local anesthetics.

5. Patients with an eye disease that may distort the results of the test, if so decided by the researcher.

6. The patient had an orbital or eye injury.

7. Has an acute or chronic but currently exacerbated respiratory disease.

8. Patients with uncompensated cardiovascular diseases (II-III AV block or cardiogenic shock).

9. Diabetes mellitus treated with more than one hypoglycaemic agent and / or insulin injections.

10. Cognitive impairment diagnosed before surgery

11. History of neurological diseases

12. It is not possible to perform a qualitative neuropsychological examination due to other reasons (hearing, vision, etc. disorders)

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 99 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Kaunas University of Technology

OTHER

Sponsor Role: collaborator

Milda Svagzdiene

OTHER

Sponsor Role: lead

Responsible Party

Milda Svagzdiene

dr, assoc. prof.

Responsibility Role: SPONSOR_INVESTIGATOR

Locations

Milda Svagzdiene

Kaunas, , Lithuania

Site Status: RECRUITING

Countries

Lithuania

Facility Contacts

Svagzdiene

Role: primary

milda.svagzdiene@lsmuni.lt

+37061203924

Other Identifiers

Nr.1

Identifier Type: -

Identifier Source: org_study_id