Endothelial Injury Mechanism in Elderly Patients Undergoing Major Surgery

Sponsor
The First Affiliated Hospital of Anhui Medical University (Other)
Overall Status
Completed
CT.gov ID
NCT03639896
Collaborator
Hangzhou Cancer Hospital (Other)
464
2
2
16
232
14.5

Study Details

Study Description

Brief Summary

The incidence of postoperative cognitive injury is high in elderly patients, especially after major surgery. The relevant pathophysiological mechanisms are still unclear, and the possible mechanisms that have been proposed so far include inflammation, neurotransmitter imbalance and metabolic disorders. In recent years, clinical studies of acute brain dysfunction after vascular endothelial injury have attracted attention.

Degradation of the endothelial glycocalyx layer and subsequent shedding of its constituents is seen as an early marker of endothelial injury, and may increase vascular permeability.Many preclinical and clinical studies have demonstrated an association between inflammatory cytokines such as TNF-α, IL-1β, IL-6, and IL-10 and glycocalyx degradation biomarkers.

The scholars found evidence of plasma endothelial injury after abdominal open surgery in the elderly. Dexmedetomidine could attenuate stress response such as TNF-α, IL-1β and IL-6. Based on the above evidence, we hypothesize that elderly patients experience inflammatory response secondary to surgical traumatic stress after major surgery, greatly increasing the degree of endothelial injury (heparan sulphate and syndecan-1), reducing brain perfusion while increasing Blood-brain barrier permeability (S100B level), promoting the release of cytokines Interleukin-2(IL-2), Interleukin-6(IL-6), tumor necrosis factor-alpha(TNF-α) ,and vascular endothelial growth factor (VEGF) while reducing brain-derived neurotrophic factor(BDNF) synthesis, then leading to postoperative acute spasm. We would test the hypothesis that can reverse these effects and improve cognitive deficits.

Study Design

Study Type:
Interventional
Actual Enrollment :
464 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Endothelial Injury Mechanism of Cognitive Decline and Intervention Study in Elderly Patients Undergoing Major Surgery
Actual Study Start Date :
Jul 1, 2019
Actual Primary Completion Date :
Oct 30, 2020
Actual Study Completion Date :
Oct 31, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Dexmedetomidine

0.5μg/kg Dexmedetomidine as initial loading dose is given for 15 minutes before induction of anesthesia, followed by a maintenance infusion of 0.4μg/kg/h and stopped 30 minutes before the surgery over.

Drug: Dexmedetomidine
0.5μg/kg Dexmedetomidine as initial loading dose is given for 15 minutes before induction of anesthesia, followed by a maintenance infusion of 0.4μg/kg/h and stopped 30 minutes before the surgery over.

Placebo Comparator: Controlled

0.5μg/kg Saline as initial loading dose is given for 15 minutes before induction of anesthesia, followed by a maintenance infusion of 0.4μg/kg/h and stopped 30 minutes before the surgery over.

Drug: Saline
0.5μg/kg saline as initial loading dose is given for 15 minutes before induction of anesthesia, followed by a maintenance infusion of 0.4μg/kg/h and stopped 30 minutes before the surgery over.

Outcome Measures

Primary Outcome Measures

  1. The change of incidence of postoperative delirium [The 1st, 2nd and 7th day after the surgery.]

    Through CAM-ICU to assess the incidence of the postoperative delirium.

  2. The change of incidence of postoperative cognition dysfunction [1 day Before surgery,the 3rd,7th day after the surgery.]

    The neuropsychological tests performed at the day before the surgery, the 3rd and 7th day after the surgery respectively.Calculate the difference(ΔX) between the score obtained before surgery and 3 or 7 days after the surgery (there are both positive and negative, we use the absolute value), with this difference( ΔX) divided by the standard deviation(SD)of the difference of the normal population, that is ΔX / SD and it is the Z score.If a patient has two or more than two of the absolute value of Z scores ≥1.96, the postoperative cognition dysfunction(POCD) is exist.

Secondary Outcome Measures

  1. endothelial injury levels [1 day Before surgery,the 1st, 2nd, 3rd,7th day after the surgery.]

    Plasma of patients was collected to test heparan sulphate and syndecan-1.

  2. Blood-brain barrier permeability [1 day Before surgery,the 1st, 2nd, 3rd,7th day after the surgery.]

    Plasma of patients was collected to test S100B level

  3. The serum concentrations of BDNF [1 day Before surgery,the 1st, 2nd, 3rd,7th day after the surgery.]

    Serum level of brain-derived neurotrophic factor (BDNF) was measured.

  4. Inflammatory factor [1 day Before surgery,the 1st, 2nd, 3rd,7th day after the surgery.]

    Plasma of patients was collected to test cytokines IL-2, IL-6, TNF-α and VEGF level.

Eligibility Criteria

Criteria

Ages Eligible for Study:
65 Years to 90 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Written informed consent;

  2. Patients undergoing selective major gastrointestinal surgery with laparoscope and general anesthesia;

  3. Age 65-90 yrs;

  4. Anesthesia Society of American (ASA) Scale II~IV;

  5. Anticipated surgery time 2-6 hrs;

Exclusion Criteria:
  1. Dementia patients(Mini-mental state examination< 20)

  2. Factors existed that affect cognition assessment such as language,visual,and auditory dysfunction;

  3. Unstable metal status and mental disease;

  4. A hematocrit value less than 28%in perioperative period;

  5. Patients with abnormal preoperative inflammatory indicators(Higher white blood cell and C-reactive protein);

  6. Patients undergoing cardiac and neural surgery;

  7. Parkinson's Disease;

  8. Sure or suspected abuse of analgesic and sedation drug.

Contacts and Locations

Locations

Site City State Country Postal Code
1 The First Affiliated Hospital of Anhui Medical University Hefei Anhui China
2 Hangzhou cancer hospital Hangzhou Zhejiang China

Sponsors and Collaborators

  • The First Affiliated Hospital of Anhui Medical University
  • Hangzhou Cancer Hospital

Investigators

  • Principal Investigator: Xinqi Cheng, PhD, The First Affiliated Hospital of Anhui Medical University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
The First Affiliated Hospital of Anhui Medical University
ClinicalTrials.gov Identifier:
NCT03639896
Other Study ID Numbers:
  • 7742
First Posted:
Aug 21, 2018
Last Update Posted:
Feb 10, 2021
Last Verified:
Sep 1, 2019
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 10, 2021