Autonomic Cardiovascular Control for Elderly Surgery Patients
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Details and patient eligibility
About
The purpose of this study is to study aspects of autonomic cardiovascular control and the level of stress hormones and inflammatory markers in saliva or serum, in elderly patients exposed to elective, major abdominal surgery, with or without postoperative delirium, to explore the hypothesis that delirium may be the result of aberrant stress responses.
Full description
Patients admitted for elective, major, abdominal surgery will be tested with a head-up tilting to 20 degrees for 15 minutes preoperatively and again on the second postoperative day. Haemodynamic variables will be registered by the device TaskForceMonitor which monitors heart rate (HR), electrocardiography (ECG), blood pressure and stroke volume continuously and non-invasively.
Background variables (including demographics, comorbidity and simple cognitive tests) and daily variables (including delirium assessments) will be registered.
Blood and saliva samples will be drawn preoperatively and postoperatively to measure levels of stress hormones and inflammatory markers.
Enrollment
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Volunteers
Inclusion criteria
- Patients 65 years or older scheduled for abdominal surgery at Oslo University Hospital
Exclusion criteria
- Absence of a valid informed consent or assent, or consent from a legal proxy
- Patients with atrial fibrillation or a pacemaker rhythm
- Polyneuropathy
- Current treatment with beta-blockers, calcium-blockers or cholinesterase inhibitors
- Competing research project
Trial design
3 participants in 1 patient group
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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