Pijnbehandeling discomfort Postoperative pain
Conditions
Interventions
The proposed intervention in this study constitutes an organizational change.
Research subjects randomized to *fast-track recovery* participate in a novel
perioperative treatment pathway. In the int
Sponsors
Academisch Medisch Centrum
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: Scheduled for elective, inpatient lower limb surgery Aged eighteen years or older Willing and able to provide written informed consent Able to handle cPNB and equipment
Exclusion criteria
Exclusion criteria: Polytrauma patients Emergency surgery Surgery for (bone) infections Severe renal and/or hepatic insufficiency Allergy to local anesthetics (Suspected) pregnancy Daycare surgery ASA 4 or higher Chronic use of opioids (> 3 months)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Patient-reported overall benefit of analgesia, as measured by the Overall Benefit of Analgesic Score (OBAS). | — |
Secondary
| Measure | Time frame |
|---|---|
| Healthcare costs, productivity costs, postoperative opioid consumption, length of hospital stay, incidence of CPSP, postoperative pain, quality of recovery, and adverse events. | — |
Countries
Netherlands
Outcome results
None listed