About this trial
This study aims to better understand 3 crucial questions:
1. Why do some patients experience more severe complications after heart surgery than others? 2. Are there markers on our genetic makeup (called epigenetic modifications) that can predict complications after major surgery? 3. How do epigenetic modifications lead to overactive inflammation that causes harm to patients after heart surgery?
Over 270,000 patients undergo major surgery in Scotland each year. Major surgery is associated with increased risk of complications, particularly in older patients with multiple health conditions. Complications are a leading cause of death, delayed recovery, long-term illness and increased healthcare cost to the NHS. Significant complications occur in up to 57% of patients after heart surgery. In response to major surgery, the body stimulates an inflammatory response as part of a complex repair mechanism, however, in some cases inflammation can become exaggerated, becoming harmful and contributing to the development of complications.
The investigators believe that a patient's risk of overactive inflammation, which can lead to complications after surgery, is heavily influenced by a patient-specific system of biological markers, layered upon their DNA; a scientific field known as epigenetics. Where a patient's DNA (their 'genetics') may be considered as an instruction manual for each cell's molecular processes, these 'epigenetic' markers work as if someone has highlighted sections of the manual to be read (and actioned). The pattern of these markers on immune system cells can therefore dictate the extent of the inflammatory response, especially after a major insult such as surgery. While the DNA itself cannot be modified, epigenetic markers can be modified, through strategies including diet, exercise, and medication.
The aim of this study is to evaluate whether the modifiable epigenetic code of key immune-system cells dictates the extent of post-operative inflammation, contributing to organ damage and complications.
With patients' permission, the investigators will:
1. Obtain blood samples before and after major heart surgery, to test for epigenetic markers and inflammation. 2. Observe patients after surgery and collect routine data from laboratory tests and patient observations which assess for organ dysfunction and inflammation. 3. Conduct patient questionnaires before and after surgery to assess physical fitness and patient-centred quality of life measures. 4. Analyse patterns between patients who have severe organ dysfunction after surgery and those patients who have minimal organ dysfunction after similar surgery, to better understand which patients are at greatest risk, according to their epigenetic makeup.
This study may improve understanding of which patients are likely to suffer organ damage and complications after major surgery, and which patients may have a protective epigenetic makeup which reduces complications. With this knowledge, the investigators aim is that future patients could receive personalised treatment plans before surgery, to modify their epigenetic makeup, reduce harm from complications and improve outcomes for patients. The investigators are not testing any new treatments in this study.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Provision of informed consent
Age >18 years
Planned elective coronary artery bypass grafting (CABG) surgery with cardiopulmonary bypass
Disqualifiers
Pregnancy.
On-going participation in any investigational research which could undermine the scientific basis of the study.
Previous major surgery (as per PQIP procedures list) within three months prior to recruitment, or previous midline sternotomy.
Patients receiving immunosuppressive therapies for a chronic inflammatory condition or cancer.
Trial population
Elective coronary artery bypass grafting (CABG) surgery with cardiopulmonary bypass at the Golden Jubilee National Hospital (NHS).
Trial design
Cohort
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Post-operative organ dysfunction quantified by measurement of mean Sequential Organ Failure Assessment (SOFA) score over the first seven postoperative days.
Sponsors and contacts
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University of Glasgow
Lead sponsor
European Association of Cardiothoracic Anaesthesiologists
Collaborator
NHS National Waiting Times Centre Board
Collaborator
This trial is not recruiting at the moment. You can still explore other options: