Endo-CABG
Procedureminimal invasive cardiac intervention
Other names: minimal invasive Coronary Artery Bypass Grafting
NCT Number: NCT02979782
Primary objectives:
Assessment of the incidence of postoperative cognitive dysfunction (POCD), cerebrovascular accident (CVA), and delirium after minimal invasive coronary artery bypass grafting (Endo-CABG).
Secondary objectives:
* Quality of life, three months after endo-CABG * Patient satisfaction with endo-CABG and the tests performed * The influence of various demographic and peri-operative variables on neurological outcome after endo-CABG * Incidence of fear and depression, 3 months after endo-CABG
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Notify Me18 year and older
All sexes
Observational
Jessa Hospital, Hasselt, Limburg, Belgium
Introduction:
Major improvements in surgical techniques, perfusion systems, and perioperative policies have led to improved quality of life of the patient, lower hospitalisation costs, and lower mortality rates in the field of cardiac surgery. However, despite these improvements and improved postoperative care, the neurological outcome after cardiac surgery remains a recurrent issue of interest. The most common neurological disorders after cardiac surgery are postoperative cognitive dysfunction (POCD), cerebrovascular accident (CVA), and delirium. After conventional cardiac surgery (invasive sternotomy procedure) the incidence of these neurological disorders is well studied. POCD has an incidence of 25-50%, CVA has an incidence of 1-5% and delirium has an incidence of 5-15%. These numbers prove that neurological outcome still is a major problem after cardiac surgery.
Postoperative cognitive dysfunction (POCD) is the most common neurological disorder after cardiac surgery. POCD is defined as a disturbance of the brain function, which is causally related to surgery. Due to the multifactorial nature of POCD it is difficult to pinpoint one major cause. testing of POCD is not standardised and is based on the '1995 statement of concensus on assessment of neurobehavioural outcomes after cardiac surgery'. This consensus statement describes the most reliable tests and study design to study POCD in clinical studies.
A battery of tests is described in the consensus statement:
In this study, two additional tests will be performed to assess POCD:
the digit span test to test the short term verbal memory. the digit symbol-coding test to test the processing speed and memory of the patient.
Additional recommendations of the consensus statement to conduct reliable POCD testing are:
Cerebrovascular accident (CVA or stroke) is caused by disturbances of the brain blood supply. The main causes of these disturbances are clotted vessels, hypoperfusion, or ruptured vessels in the brain. The risk of CVA is high in the first few days after cardiac surgery. CVA is diagnosed based on neurological evaluation and signs on CT or MRI scan.
Delirium is characterised by attention disorders and fluctuating changes in the mental state of the patient. Delirium is mainly related to surgery and can be diagnosed with the CAM-ICU (confusion assessment method for the intensive care unit).
These neurological complications have a negative effect on the quality of life, healthcare costs and mortality rate after cardiac surgery.
Recently, new developments in cardiac surgery hav led to the introduction of minimal invasive cardiac procedures into practice. These minimal invasive cardiac procedures are proven to be beneficial for the patient. Neurological outcome after minimal invasive cardiac surgery however, is not well studied.
Therefore, the main goal of this study is to examine the neurological outcome after endoscopic coronary artery bypass grafting (Endo-CABG). Endo-CABG is a minimal invasive cardiac procedure based on the conventional coronary artery bypass grafting (CABG) procedure.
Study design and study tests:
This study will be a single-centre prospective cohort study. The goal of the study is to assess the neurological outcome after endoscopic coronary artery bypass grafting (Endo-CABG). Three study groups will be included (described in section study groups), which will be tested for POCD, CVA and delirium.
Secondary outcomes in this research are quality of life of the patient (EQ-5D-5L), Fear and depression outcomes (VVO; CES-D), and assessment of demographic and peri-operative predictors of poor neurological outcome after endo-CABG.
Study tests:
Baseline tests will be performed in both intervention groups (Endo-CABG and PCI) and the healthy control group.
In the intervention groups the baseline preoperative tests will include:
For the healthy volunteers the same baseline tests will be performed, with exception of the neurological clinical evaluation.
Postoperative tests in the intervention groups will include:
For the healthy volunteers, the following tests will be performed 3 months after baseline testing:
Statistical analysis:
In this study POCD is defined as a decline in score between baseline and follow-up neurophysiological test, which should be higher than the natural variation. In this setting the natural learning effect will also be taken into account. To perform statistical analysis for POCD testing, Z-scores (or reliable change index (RCI)) will be used. The Z-score is a unit which indicates how the difference between the baseline score and the follow-up test behaves compared to the mean scores of the control group.
Thus, the individual RCI scores will be calculated as follows:
The RCI is the sum of the Z-scores of all tests.
We defined POCD in an individual patient as an RCI equal to or less than -1.645 (significance level 5%), or Z-score equal to or less than -1.645 in at least two different tests.
The group RCI scores will be compared using ANOVA or Kruskall-Wallis.
The quality of life will be tested using a mann-whitney U test at significance level 5%.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
minimal invasive cardiac intervention
Other names: minimal invasive Coronary Artery Bypass Grafting
stenting procedure
Other names: percutaneous coronary intervention
Time frame: 3 months after intervention
percentage of total study population
Time frame: 3 months after intervention
percentage of total study population
Time frame: 3 months after intervention
percentage of total study population
Time frame: 3 months after intervention
assessment with the EQ-5D questionnaire
Time frame: 3 months after intervention
assessment of which demographic and peri-operative variables are associated with poor neurological outcome after minimal invasive coronary
Time frame: 3 months after intervention
assessment with the CES-D questionnaire
Time frame: 3 months after intervention
assessment with the Surgical Fear Questionnaire
Jessa Hospital
Other
Neurological Outcome After Minimal Invasive Coronary Artery Bypass Graft: a Single-centre Prospective Cohort Study
Acronym: NOMICS
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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