PAICOD: Peri-Anesthetic Imaging of Cognitive Dysfunction

Sponsor
Vanderbilt University (Other)
Overall Status
Completed
CT.gov ID
NCT01322672
Collaborator
(none)
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1
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Study Details

Study Description

Brief Summary

Recent data suggests that anesthetics can have prolonged effects on gene expression, protein synthesis and processing as well as cellular function in ways that the investigators are only beginning to understand, especially in the very young and the elderly. Within moments to days of emerging from anesthesia - cardiac or non-cardiac - some patients experience mild to very severe disorientation and changes in memory and thinking ability without apparent cause. For the vast majority of patients, this Post-Operative Cognitive Dysfunction (POCD), generally subsides, but for some with "diminished cognitive reserve" - especially the elderly, those with less education or prior CNS events such as stroke or early dementia - changes in memory and executive function may persist. If prolonged for more than three months, POCD has been linked to an increased risk of death. In 1-2% of elderly patients, the problem may ultimately continue for more than a year, leading to a loss of ability to care for themselves and early demise. Though this may seem like a small percentage, seniors will comprise up to 40% of the 50-75 million surgical procedures performed annually over the next 20-30 years. This amounts to 70,000 - 200,000 elder affected, and for them and their families, the cost of POCD in longer-term care, lost wages, and extended suffering will remain very high.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    For more than 160 years, "modern" anesthesia has provided immense benefit to patients of all ages. However, over the past several years, concern has been growing that for patients at the extremes of age, some anesthetic agents may harbor subtle, previously minimally examined, serious neurotoxic effects which can cause lasting decline in the function of the central nervous system (CNS). For the elderly, these effects may manifest in lasting post-operative deterioration of memory and the capacity for normal information processing that can result in the inability to perform the activities of daily living (ADLs) with eventual early demise. Unfortunately, even though our ability to evaluate anesthetic risk has grown asymptotically for virtually every organ system, the brain remains neglected. And even though we know a good deal about effect sites for general anesthetic agents, we still have an incomplete understanding of the potential toxic effects of anesthetics on the brain. Therefore, employing a human surgical model (endoscopic prostatectomy), we propose a pilot study of 15 otherwise neurologically intact, ASA I - III, males, 65+ year of age. After pre-enrollment screening (MMSE & BDI) and standard pre-op evaluation, subjects will undergo both anatomic and functional MRI studies plus a battery of neurocognitive tests (NCT) at two time points approximately 2-3 weeks apart prior to surgery. These pre-op studies will establish both a "non-surgical control" for the study as well as a baseline for post-op studies. 2-3 weeks after surgery, MRI and NCT will be repeated. The study aims to determine if MRI can demonstrate changes in the CNS pre-op vs post-op that relate to anesthesia and surgery and how those changes might correlate with NCT over the same interval.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    6 participants
    Observational Model:
    Case-Only
    Time Perspective:
    Prospective
    Official Title:
    Peri-Anesthetic Imaging Compared With Neurocognitive Testing: A Pilot Study
    Actual Study Start Date :
    Mar 1, 2011
    Actual Primary Completion Date :
    Aug 27, 2015
    Actual Study Completion Date :
    Aug 27, 2015

    Outcome Measures

    Primary Outcome Measures

    1. Comparison of preoperative vs postoperative Brain MRI changes [2 months]

      Anesthetics can have prolonged effects on gene expression, protein synthesis and processing as well as cellular function, especially in the very young and the elderly. After anesthesia, some patients experience mild to very severe disorientation and even delirium without apparent cause. In the elderly, this Post-Operative Cognitive Dysfunction (POCD) - including changes in memory and executive function may persist and has been linked to an increased risk of death. Over the next 20-30 years, 40% of 65+ year-olds will undergo surgery; the cost of POCD in longer-term care, lost wages, and extended suffering of patients and families will remain high.

    Secondary Outcome Measures

    1. Preoperative vs Postoperative Neurocognitive Testing [2 Months]

      Pre- vs postoperative Neurocognitive Testing (NCT) is currently the primary method used to quantify changes in cognitive indices, including memory, processing speed, motor function, etc. This study will compare such pre- and post-op NCT with pre-and post-op MRI and fMRI to determine relationships between changes in each of these modalities.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    65 Years to 95 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Age 65+ years; ASA I - III; capable and willing to consent

    • Scheduled for 3+ hour Endoscopic Prostatectomy under general anesthesia

    • Baseline MMSE > 20 (exclude dementia)

    • All suitable for MRI testing

    Exclusion Criteria:
    • Hx Autoimmune Disease

    • Severe visual or auditory disorder/handicaps

    • Unable to read or understand English

    • Pre-existing cognitive impairment; e.g., MS, AD or Parkinson's Disease, etc.

    • Patients not expected to be able to complete the 2-3 week postoperative testing

    • Major psychiatric condition such as bipolar disorder, schizophrenia

    • Severe Panic Disorder

    • Any implanted ferrous metal

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Vanderbilt University Medical Center Nashville Tennessee United States 37232

    Sponsors and Collaborators

    • Vanderbilt University

    Investigators

    • Principal Investigator: James L Blair, DO, Vanderbilt University Medical Center

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    James L. Blair, Assistant Professor, Vanderbilt University
    ClinicalTrials.gov Identifier:
    NCT01322672
    Other Study ID Numbers:
    • IRB#100885
    First Posted:
    Mar 24, 2011
    Last Update Posted:
    Feb 5, 2019
    Last Verified:
    Feb 1, 2019
    Keywords provided by James L. Blair, Assistant Professor, Vanderbilt University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 5, 2019