1. Comparison between thoracic epidural analgesia VS patient controlled analgesia on chronic postoperative pain after video-assisted thoracoscopic surgery: A prospective randomized controlled study.
- Author
-
Jiang L, Wang C, Tong J, Han X, Miao C, and Liang C
- Subjects
- Humans, Male, Female, Middle Aged, Prospective Studies, Single-Blind Method, Aged, Adult, Pain Measurement statistics & numerical data, Anesthesia, General adverse effects, Anesthesia, General methods, Treatment Outcome, Follow-Up Studies, Thoracic Surgery, Video-Assisted adverse effects, Thoracic Surgery, Video-Assisted methods, Pain, Postoperative prevention & control, Pain, Postoperative etiology, Analgesia, Patient-Controlled methods, Analgesia, Patient-Controlled statistics & numerical data, Analgesia, Epidural methods, Analgesia, Epidural adverse effects, Chronic Pain prevention & control, Chronic Pain etiology
- Abstract
Study Objective: To test the hypothesis that thoracic epidural anesthesia and analgesia (TEA) reduces the incidence of chronic postoperative pain (CPSP) after video-assisted thoracoscopic surgery (VATS)., Design: A single-center, single-blind, randomized controlled trial was conducted., Setting: The study was conducted in the operating room, with follow-up assessments performed in the ward. Telephone was used to follow the long-term outcomes., Patients: 231 patients ≥18 years of age and scheduled for VATS., Interventions: Patients were randomized into two groups, including an epidural block (EPI) group (general anesthesia with patient-controlled epidural analgesia) and a general anesthesia with patient-controlled intravenous analgesia (PCIA) group., Measurements: The primary endpoint was the incidence of CPSP at 3 months postoperatively. CPSP data, including acute pain, neuropathic pain, depression, and side effects, were collected at 3 and 6 months postoperatively through telephone follow-up., Main Results: A total of 231 patients were analyzed, including 114 in the PCIA group and 117 in the EPI group. Sixty-six patients (56.4 %) in the PCIA group and 33 patients (28.9 %) in the EPI group experienced chronic pain at 3 months postoperatively. The odds ratio (OR) was 0.31 (95 % confidence interval [CI], 0.18 to 0.54; P < 0.0001). After adjusting for confounding factors, the adjusted OR was 0.28 (95 % CI, 0.16 to 0.50, P < 0.001). Six months postoperatively, 50 (42.7 %) and 17 (14.9 %) patients in the PCIA and EPI groups, respectively, were diagnosed with CPSP (P < 0.0001)., Competing Interests: Declaration of competing interest None., (Copyright © 2024 Elsevier Inc. All rights reserved.)
- Published
- 2025
- Full Text
- View/download PDF