Nerve Block Techniques for Pain Relief in Total Knee Replacement
This study observes the effectiveness of different nerve block techniques in providing pain relief after total knee replacement surgery.
Data Collection
Collected from past medical records and data - RetrospectiveAgnosia+5
+ Nervous System Diseases
+ Neurologic Manifestations
Cohort
Tracking disease incidence in order to identify risk factors and understand disease progression over time.Summary
Study start date: June 26, 2024
Actual date on which the first participant was enrolled.Protocol title: Analysis of postoperative analgesic effect and complications among different approaches of nerve block for total knee replacement surgery Objectives: There is no consensus on the optimal nerve block choice for knee joint replacement. Therefore, the aim of this study is to conduct a retrospective analysis using data from patients who underwent total knee replacement (TKR) and received nerve blocks at our hospital. This study will investigate the postoperative analgesic consumption, duration of pain relief, motor function block, complications, and patient satisfaction for different nerve block techniques. The goal of this project is to identify the optimal nerve block choice to benefit future patients undergoing knee joint replacement. Background: After undergoing total knee replacement (TKR), patients need rehabilitation to restore knee function and reduce postoperative adhesions. However, pain often prevents them from achieving this goal. Clinically, nerve block anesthesia is gradually becoming mainstream, as it achieves intraoperative anesthesia and postoperative analgesia by infiltrating local anesthetics into the nerves supplying the knee joint. According to a study by Allen et al. (1998), patients receiving nerve blocks such as femoral and sciatic nerve blocks experienced better pain relief within the first 8 hours postoperatively and had a 50% reduction in total morphine consumption on the second postoperative day compared to those who received spinal anesthesia alone. Carli et al. (2010) found that patients who received femoral nerve blocks used less postoperative patient-controlled analgesia (PCA) and had better postoperative motor function recovery compared to those who received periarticular anesthetic infiltration. Currently, there are various types of nerve block techniques, including femoral nerve, obturator nerve, adductor canal nerve, and sciatic nerve blocks. Different nerve block techniques result in varying analgesic efficacy, duration, functional impact, motor block, and complications. Sharma et al. (2010) indicated that femoral nerve blocks might cause quadriceps muscle weakness and patient falls. Kinghorn et al. (2012) also reported that sciatic nerve blocks might result in foot drop. Study Design: This study is a retrospective analysis using the accumulated clinical database from 2017/09-2023/11 to analyze patients who underwent total knee arthroplasty and received nerve blocks. The aim is to compare the analgesic effects, incidence of nerve injury, and rate of chronic pain under different nerve block techniques. Methods: A. Evaluation Methods: Data is collected in a patient registry called "acute pain service" (APS), which is the medical record for documenting the dose of patient controlled analgesia and side effects of PCA or nerve blocks. 1. Duration of Pain Relief: Ask patients when they started to feel pain (duration). 2. Quantitative Assessment of Analgesic Effectiveness: Patients receiving nerve blocks will also use intra-venous patient-controlled analgesia (PCA) for 2 days postoperatively. The total amount of medication used in the PCA machine over these 2 days will reflect the patient's pain level. i. Pain: VAS score ii. Motor Block Assessment: The motor function of patients who received nerve blocks will be evaluated for abnormalities the day after surgery. Motor block will be assessed using the Modified Bromage Motor Blockade Score. c. Complication Statistics: Defined as conditions like foot drop, quadriceps muscle weakness, or any situation requiring special medical treatment.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.94 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Cohort
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 20 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Study Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Fu Jen Catholic University Hospital
New Taipei City, TaiwanOpen Fu Jen Catholic University Hospital in Google Maps