Analgesic Consumption, Postoperative Pain, Postoperative Pain After Total Knee Arthroplasty
Conditions
Keywords
Total Knee Arthroplasty, Postoperative Pain, Anesthesia Techniques, Analgesic Consumption, Epidural Analgesia, Opioid Use, General Anesthesia, Spinal Anesthesia, Pain Management
Brief summary
This prospective observational study evaluates postoperative pain intensity and analgesic consumption in patients undergoing total knee arthroplasty (TKA) under different anesthesia techniques. Patients receive either general anesthesia with peripheral nerve block, spinal anesthesia with peripheral nerve block, spinal anesthesia alone, or general anesthesia with an epidural catheter. Pain scores (NRS), analgesic use, adverse effects, patient satisfaction, and the need for therapeutic interventions are assessed during the first 48 hours after surgery. The study aims to identify differences in postoperative pain control and factors associated with hypotension and other complications.
Detailed description
This prospective, monocentric observational study evaluates postoperative pain intensity and analgesic consumption in adult patients undergoing primary total knee arthroplasty (TKA). The study focuses on anesthesia techniques routinely used in clinical practice, including general anesthesia with peripheral nerve block, general anesthesia with an epidural catheter, spinal anesthesia with peripheral nerve block, and spinal anesthesia alone. The primary methodological aim is to compare postoperative pain trajectories (NRS) and total analgesic use during the first 48 hours after surgery across anesthesia strategies. Secondary observations include adverse effects related to analgesia, patient satisfaction, and the need for therapeutic interventions such as fluid administration, vasopressors, antiemetics, or adjustments in analgesic regimen. Independent variables include type of anesthesia, ASA physical status, age, sex, BMI, type of peripheral nerve block, and duration of surgery. Dependent variables include postoperative pain scores, analgesic consumption, adverse events, and patient-reported satisfaction. The study is designed to identify clinically relevant differences in postoperative pain control and to explore factors associated with hypotension and other perioperative complications. Findings may support optimization of perioperative analgesia and guide clinical decision-making in anesthesia management for TKA.
Interventions
None listed
Sponsors
Tomas Bata Hospital, Czech Republic
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
Yes
Inclusion criteria
* Age 18-100 years * Primary total knee arthroplasty (TKA) * ASA physical status I-III * Glasgow Coma Scale (GCS) score of 15 * Ability to understand study procedures and provide informed consent * Ability to cooperate during pre-anesthetic evaluation * No severe sensory impairment (e.g., blindness, deafness)
Exclusion criteria
* Revision or reoperation of TKA * ASA score IV or higher * Refusal to participate or inability to provide informed consent * GCS ≤ 14 * Limited legal capacity * Active psychiatric disorder * Chronic use of strong opioid analgesics * Neurological disease affecting pain perception or cooperation * Cognitive impairment or language barrier preventing questionnaire completion * Use of anesthesia techniques other than GA + PNB or SA + PNB (e.g., epidural anesthesia, local infiltration without PNB)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Postoperative pain intensity | 6 hours, 24 hours, and 48 hours after surgery | Pain intensity will be assessed using the Visual Analog Scale (VAS) or Numerical Rating Scale (NRS) at predefined postoperative intervals. Both scales range from 0 to 10, where 0 indicates no pain and 10 indicates the worst pain imaginable. Higher scores represent worse pain intensity. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Analgesic consumption | First 48 hours after surgery | Total opioid and non-opioid analgesic dose administered within 48 hours postoperatively. |
| Adverse effects | First 48 hours after surgery | Incidence of nausea, vomiting, urinary retention, hypotension, and other analgesia-related adverse events. |
| Patient satisfaction | 48 hours after surgery | Patient satisfaction with pain control and overall care will be assessed using a 5-point Likert scale, ranging from 1 to 5, where 1 indicates very low satisfaction and 5 indicates very high satisfaction. Higher scores represent better satisfaction. |
| Length of hospital stay | From the day of surgery (Day 0) through hospital discharge (typically 3-14 days). | Length of hospital stay will be measured as the number of days from the date of surgery until the date of hospital discharge |
| Number of participants requiring therapeutic interventions | Up to 48 hours after surgery. | The need for therapeutic interventions will be recorded, including additional analgesia, intravenous fluids, vasopressors, or other supportive measures administered due to insufficient pain control or hemodynamic instability. |
Countries
Czechia
Contacts
CONTACTKlára Nekvindová, MD, Ph.D.
Outcome results
None listed