Median effective concentration of ropivacaine for preoperative analgesia under ultrasound-guided supra-inguinal fascia Iliaca compartment block in hip fracture patients
Ultrasound-guided supra-inguinal fascia iliaca compartment block (FICB) is increasingly used for preoperative analgesia in elderly hip fracture patients. However, the median effective concentration (50% effective concentration, EC<sub>50</sub>) of ropivacaine required for supra-inguinal FICB for preoperative analgesia has not been determined. This study was designed to evaluate the EC<sub>50</sub> of 30 mL ropivacaine to maintain preoperative analgesia for at least 24 h. Twenty-eight consecutive patients aged 75 years or older with acute hip fracture were enrolled. All patients received 30 mL ropivacaine for preoperative analgesia. Dixon's up-and-down sequential method was used to determine the concentration of ropivacaine. The initial concentration was 0.35%. Successful analgesia was defined as a Numerical Rating Scale (NRS) score for pain less than 4 during movement within the first 24 h after the block. The concentration in each subsequent patient was determined by the response of the previous patient, and concentrations were adjusted at 0.025% intervals. The 50% and 95% effective concentrations (EC<sub>50</sub>, and EC<sub>95</sub>) of ropivacaine were calculated using probit regression. The EC<sub>50</sub> and EC<sub>95</sub> of 30 mL ropivacaine for at least 24-hours effective preoperative analgesia via ultrasound-guided supra-inguinal FICB were 0.248% (95% confidence interval [CI], 0.233-0.262%) and 0.276% (95% CI, 0.262-0.343%), respectively. No adverse events occurred. A single dose of ropivacaine was found to provide effective preoperative analgesia via ultrasound-guided supra-inguinal FICB in elderly patients with hip fracture. The EC<sub>50</sub> (95% CI) of 30 mL ropivacaine for preoperative analgesia lasting at least 24 h was 0.248% (0.233-0.262%).Trial Registration: This trial was registered on UMIN Center Clinical Trials Register (registration number UMIN000050676, date of first trial registration 25/03/2023).
Authors
- Tinghua Li
- Di-jiao Ruan
- Haiwen Chen (ORCID: https://orcid.org/0000-0002-3836-9845)
- T. Chen
- Jie Chen (ORCID: https://orcid.org/0000-0002-6808-1076)
- Yan Chen (ORCID: https://orcid.org/0000-0001-6258-082X)
- Chunhong Liu (ORCID: https://orcid.org/0000-0003-4354-9151)
- Ke Qian (ORCID: https://orcid.org/0000-0003-2418-8450)
Institutions
- University of Science and Technology of China (CN)
- Army Medical University (CN)
- University of Illinois Urbana-Champaign (US)
- Southwest Hospital (CN)
- Chongqing Emergency Medical Center (CN)
- Chongqing Medical University (CN)
Publication Details
- Journal
- Scientific Reports
- Published
- 2025-09-29
- DOI
- https://doi.org/10.1038/s41598-025-18616-4
- Primary Topic
- Anesthesia and Pain Management
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Chongqing Medical University