Patient due for elective, ambulatory gynaecological laparoscopy will be screened peri-operatively for known and potential risk factors of postoperative pain and nausea/vomiting. The actual incidence and severity of pain and nausea/vomiting will be recorded during th 0-24 hr intervall after end of surgery, as well as the doses of all drugs, given for either prophylaxis or treatment
Study Type
OBSERVATIONAL
Enrollment
300
Patient will be interviewed pre-operatively and at 24 hrs post-opartively
Oslo University Hospital
Oslo, Norway
RECRUITINGpostoperative pain
Numerical Ratings Score (NRS) Scale 0-10, 10 is worst
Time frame: 0-24 hours
postoperative nausea
yes/no, Numerical Rating Score (NRS), Scale 0-10, 10 is worst
Time frame: 0-24 hours
Peri-operative nausea risk score
Apfel score, 0-4 (4 is maximal risk).Based on a number of registrations, such as: smoking status, postoperative opioid effects, smoking status, travel sickness, previous nause or vomiting after surgery/anaesthesia
Time frame: preop, 0-24 hours post-operatively
Peri-operative pain risk score
Based on a number of registrations, such as: age, sosio-economic status, pre-op pain, pre-op use of opioids, pre-op anxiety or depression, pre-op catastrophizing, pre-op expectations, type of surgery, type of anaesthesia, lenght/ivasive ness of surgery, peri-op drug consumtion
Time frame: preop, 0-24 hours
Post-op fatigue
Christensen score, 0-10, 10 is maximal fatigue
Time frame: 0-24 hrs
Post-op function
Everyday function
Time frame: 0-24hr
Post-op analgesia consumption
number of opioid equivalents consumed
Time frame: 0-24hr
Post-op anti-emetic drug consumption
type and dose of ante-emetic medication
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Time frame: 0-24hr