About this trial
The study aims to test the relationship between the preoperative pain threshold and the intraoperative need for opioids.
The objective of the study is to try to predict a patient's analgesic needs based on their objectively determined preoperative pain threshold.
The investigators will include patients scheduled for elective cardiovascular surgery.
The investigators will investigate the correlation between the preoperative pain threshold and intraoperative/postoperative opioid consumption in a highly standardized anesthesia setting.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
ASA 3 patients with scheduled cardiac surgery by thoracotomy or sternotomy
Disqualifiers
Patient refusal,
A body mass index (BMI) > 30 kg/m²,
Allergies to any medication used in typical cardiac anesthesia,
Chronic pain or regular use of analgesics,
Trial design
Single group
Treatments tested in this trial
Measure of the minimal pain threshold with an algometer
DeviceThe measure of the minimal pain threshold is taken the day before the cardiac surgery
Treatment groups
Trial outcomes
Primary outcomes
Correlation between the pressure pain threshold and the consumption of opioid during and after the surgery
After the measure of the minimal pain threshold the day before the surgery, the investigators look at the quantity of Remifentanil which has been given to the patient during the surgery. Then they will look for a correlation
Secondary outcomes
Correlation between the pain threshold and the consumption of morphine during the post-operative time
After the measure of the minimal pain threshold the day before the surgery, the investigators look at the quantity of morphine which has been administrated by a PCA (Intravenous Patient-Controlled Analgesia (IV-PCA) with morphine) to the patient during the post-operative time. Then they are looking for a correlation.
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