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).

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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

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article

Median effective concentration of ropivacaine for preoperative analgesia under ultrasound-guided supra-inguinal fascia Iliaca compartment block in hip fracture patients

Tinghua Li, Di-jiao Ruan, Haiwen Chen, T. Chen et al.
Scientific Reports
Anesthesia and Pain Management
article

Median effective concentration of ropivacaine for preoperative analgesia under ultrasound-guided supra-inguinal fascia Iliaca compartment block in hip fracture patients

Tinghua Li, Di-jiao Ruan, Haiwen Chen, T. Chen, Jie Chen, Yan Chen, Chunhong Liu, Ke Qian
article en

Abstract

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).

Scientific ReportsVol. 15(1)
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)
Chongqing Medical University
Openalex Percentile: Top 57%
Anesthesia and Pain Management
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