An Intervention to Reduce Delirium After Cardiac Surgery
Primary Purpose
Delirium, Congenital Heart Disease, Coronary Artery Disease
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Remote ischemic pre-conditioning
Delirium Assessment
Sponsored by
About this trial
This is an interventional treatment trial for Delirium focused on measuring delirium, heart, valve, graft, surgery, coronary
Eligibility Criteria
Inclusion Criteria:
- ≥65 years old
- Undergoing coronary artery bypass and/or valve surgery
Exclusion Criteria:
- Mini mental state exam < 23
- Delirium at baseline
- Inability to speak and understand English
- Severe hearing impairment, resulting in inability to converse
- Planned use of intraoperative ketamine
- Inability to place or tolerate upper extremity tourniquet
- Hemoglobinopathy (e.g. sickle cell disease)
Sites / Locations
- The Johns Hopkins Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Experimental
Arm Label
Control: Usual care
Treatment: Ischemic Pre-conditioning
Arm Description
This group will receive usual care and delirium assessments.
Remote Ischemic pre-conditioning before cardiac surgery and delirium assessments.
Outcomes
Primary Outcome Measures
Incident Delirium
Delirium will be assessed using the Confusion Assessment Method (CAM) on three of the first four postoperative days. The primary outcome will be positive if delirium occurs by CAM criteria at any of these assessments
Secondary Outcome Measures
Levels of novel cerebral injury biomarkers
Biomarkers include inflammatory proteins, and markers of neuronal damage or change in homeostasis, including glial fibrillary acidic protein and neurotrophic factors
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT02587039
Brief Title
An Intervention to Reduce Delirium After Cardiac Surgery
Official Title
An Intervention to Reduce Delirium After Cardiac Surgery
Study Type
Interventional
2. Study Status
Record Verification Date
August 2016
Overall Recruitment Status
Completed
Study Start Date
June 2014 (undefined)
Primary Completion Date
December 2015 (Actual)
Study Completion Date
December 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Johns Hopkins University
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Patients that have cardiac surgery may suffer from unrecognized cerebral ischemia or loss of blood flow to the brain temporarily during surgery. This temporary loss of blood flow to the brain may result in a condition called delirium. Delirium is a type temporary confusion. There are some strategies that can help reduce cerebral ischemia during cardiac surgery which can help lead to a reduction in the incidence of delirium. The investigator believes that a strategy called remote ischemic preconditioning will help to reduce the incidence of delirium incidence after cardiac surgery.
Remote ischemic preconditioning is a brief exposure to ischemia. This brief exposure to ischemia occurs in an area of the body that is not undergoing a procedure. This brief exposure to ischemia is not long enough to cause any damage to the body and it has been demonstrated to help protect against more severe ischemic injury that may occur later during surgery. In this study the investigator will use remote ischemic preconditioning to see if it can reduce the incidence delirium after cardiac surgery.
Detailed Description
Delirium is common after cardiac surgery, occurring in 45-55% of patients, and is independently associated with increased postoperative complications, reduced functional capacity, cognitive decline, and increased mortality. Although the pathophysiology of delirium is unclear, a leading hypothesis is that delirium results from unrecognized cerebral ischemia during surgery. In preliminary data from the investigators group, delirium was reduced in patients randomized to optimal blood pressure control during cardiopulmonary bypass, using novel technology that determines an individual patient's lower limit of cerebral autoregulation. Thus, patients undergoing cardiac surgery may suffer from unrecognized cerebral ischemia that contributes to delirium, and strategies to attenuate the effects of cerebral ischemia may reduce the incidence of delirium.
Ischemic preconditioning represents a novel strategy to attenuate the effects of cerebral ischemia during cardiac surgery. Exposure to a brief period of ischemia, below the threshold for tissue injury, has been demonstrated to protect against the harmful effects of a subsequent more severe ischemic insult, in both animal and human studies. The protection provided by ischemic preconditioning may also be effective when the preconditioning is applied to a location remote from the organ of interest (i.e. a limb). Recently, a large randomized trial in patients undergoing cardiac surgery demonstrated a survival benefit among patients randomized to remote ischemic preconditioning vs. placebo. Remote ischemic preconditioning was achieved by simple inflation of a blood pressure cuff to supra-systolic pressures for 5 minutes, repeated for 3 cycles. However, neurological outcomes were not assessed in this trial, although animal models support potential neurological protection following remote ischemic preconditioning.
In this study the investigator will examine whether remote ischemic preconditioning can reduce delirium, functional decline, and biomarkers of cerebral injury after cardiac surgery. The investigator will explore the mechanism of preconditioning by examining proteomic analyses in a subset of patients. These results will provide data to support an NIH trial to examine the protective effects of remote ischemic preconditioning in cardiac surgery, identify potential mechanisms of action and potential targets for therapeutic pharmacologic interventions.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Delirium, Congenital Heart Disease, Coronary Artery Disease, Heart Valve Disease
Keywords
delirium, heart, valve, graft, surgery, coronary
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
53 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Control: Usual care
Arm Type
Placebo Comparator
Arm Description
This group will receive usual care and delirium assessments.
Arm Title
Treatment: Ischemic Pre-conditioning
Arm Type
Experimental
Arm Description
Remote Ischemic pre-conditioning before cardiac surgery and delirium assessments.
Intervention Type
Procedure
Intervention Name(s)
Remote ischemic pre-conditioning
Intervention Description
Remote ischemic preconditioning is exposure to a brief period ischemia to an area or limb that is not involved in surgery. This intervention is believed to reduce the incidence of cerebral (brain) ischemia during cardiac surgery.
Intervention Type
Behavioral
Intervention Name(s)
Delirium Assessment
Intervention Description
The Delirium assessment consist of a validated psychiatric screening tool called the Confusion Assessment Method. We will use this tool to determine if patients have any confusion after surgery.
Primary Outcome Measure Information:
Title
Incident Delirium
Description
Delirium will be assessed using the Confusion Assessment Method (CAM) on three of the first four postoperative days. The primary outcome will be positive if delirium occurs by CAM criteria at any of these assessments
Time Frame
First four postoperative days
Secondary Outcome Measure Information:
Title
Levels of novel cerebral injury biomarkers
Description
Biomarkers include inflammatory proteins, and markers of neuronal damage or change in homeostasis, including glial fibrillary acidic protein and neurotrophic factors
Time Frame
Within 1 hour before the surgical incision, immediately after cardiopulmonary bypass, 2 hours after cardiopulmonary bypass, and 20 hours after skin closure
Other Pre-specified Outcome Measures:
Title
Instrumental Activities of Daily Living
Time Frame
1 month and 6 months after surgery
10. Eligibility
Sex
All
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
≥65 years old
Undergoing coronary artery bypass and/or valve surgery
Exclusion Criteria:
Mini mental state exam < 23
Delirium at baseline
Inability to speak and understand English
Severe hearing impairment, resulting in inability to converse
Planned use of intraoperative ketamine
Inability to place or tolerate upper extremity tourniquet
Hemoglobinopathy (e.g. sickle cell disease)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Charles Brown, MD
Organizational Affiliation
Johns Hopkins University
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Johns Hopkins Hospital
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21287
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
32384343
Citation
Nakano M, Nomura Y, Suffredini G, Bush B, Tian J, Yamaguchi A, Walston J, Hasan R, Mandal K, Schena S, Hogue CW, Brown CH 4th. Functional Outcomes of Frail Patients After Cardiac Surgery: An Observational Study. Anesth Analg. 2020 Jun;130(6):1534-1544. doi: 10.1213/ANE.0000000000004786.
Results Reference
derived
PubMed Identifier
30540612
Citation
Nomura Y, Nakano M, Bush B, Tian J, Yamaguchi A, Walston J, Hasan R, Zehr K, Mandal K, LaFlam A, Neufeld KJ, Kamath V, Hogue CW, Brown CH 4th. Observational Study Examining the Association of Baseline Frailty and Postcardiac Surgery Delirium and Cognitive Change. Anesth Analg. 2019 Aug;129(2):507-514. doi: 10.1213/ANE.0000000000003967.
Results Reference
derived
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An Intervention to Reduce Delirium After Cardiac Surgery
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