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Reconsidering injection volume for caudal epidural block in young pediatric patients: a dynamic flow tracking experimental study
  1. Ha-Jung Kim1,
  2. Hyungtae Kim1,
  3. Sooho Lee2,
  4. Won Uk Koh1,
  5. Soo-Sung Park3 and
  6. Youngjin Ro1
  1. 1 Department of Anesthesiology and Pain Medicine, Asan Medical Center, University of Ulsan College of Medicine, Songpa-gu, Seoul, Korea (the Republic of)
  2. 2 Department of Anesthesiology and Pain Medicine, International Saint Mary's Hospital, Catholic Kwandong University, Incheon, Korea (the Republic of)
  3. 3 Department of Orthopedic Surgery, Asan Medical Center, University of Ulsan College of Medicine, Songpa-gu, Seoul, Korea (the Republic of)
  1. Correspondence to Dr Hyungtae Kim, Department of Anesthesiology and Pain Medicine, University of Ulsan College of Medicine, Songpa-gu, Seoul 05505, Korea (the Republic of); ingwei2475{at}gmail.com

Abstract

Introduction Caudal epidural block is a commonly used analgesic technique in pediatric patients. Ultrasound could be used to increase the accuracy of the block by visual confirmation of the drug-spreading. Therefore, we aimed to estimate the cephalad spread of injection volume by caudal route using dynamic ultrasound imaging in young pediatric patients.

Methods Forty patients, aged 6–24 months, undergoing foot surgery were included. After inducing general anesthesia, an angiocatheter was inserted into the sacral canal under ultrasound guidance. Thereafter, the probe was placed in the paramedian sagittal oblique position, and prepared 0.15% ropivacaine was injected, 1 mL at a time, up to 1.0 mL.kg−1. The ultrasound probe was moved cranially following the bulk flow of local anesthetics. Our primary outcome was the required volume of local anesthetics to reach each level of interlaminar space.

Results The dynamic flow tracking was available in 39 patients, and the required volume of the injectate to reach L5–S1, L4–L5, L3–L4, L2–L3, L1–L2, T12–L1, and T11–T12 was 0.125, 0.223, 0.381, 0.591, 0.797, 0.960, and 1.050 mL.kg−1, respectively. The required volume to reach the immediate upper spinal level was inconsistent across various spinal levels.

Conclusions Local anesthetics of 0.223, 0.591, and 0.797 mL.kg−1 could provide sufficient analgesia for localized foot, knee, and hip surgeries, respectively. However, since the required volume of the local anesthetics could not be calculated linearly, the real-time dynamic flow tracking technique for the caudal epidural block is recommended in young pediatric patients.

Trial registrations ClinicalTrials.gov (NCT04039295).

  • pediatrics
  • ultrasonography
  • pain, postoperative
  • analgesia

Data availability statement

Data are available upon reasonable request. The datasets used and analyzed in the current study are available from the corresponding author on reasonable request.

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Data availability statement

Data are available upon reasonable request. The datasets used and analyzed in the current study are available from the corresponding author on reasonable request.

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Footnotes

  • Contributors H-JK: data curation, formal analysis, investigation, project administration, writing–original draft and writing–review and editing. HK (guarantor): conceptualization, formal analysis, investigation, writing–original draft and writing–review and editing. SL: data curation and investigation. WUK: formal analysis, methodology, and investigation. S-SP: investigation and supervision. YR: investigation and supervision.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Competing interests None declared.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.