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Objective real-time epidural pressure measurement using the CompuFlo® device, a mono-center observational study - 17/06/25

Doi : 10.1016/j.accpm.2025.101530 
Laurent Hertz a, , Chrystelle Sola a, b, Julien Pico a, b, Juliette Aros a, Christopher Scott a, Philippe Pirat a, Olivier Choquet d, Sophie Bringuier c, d, Christophe Dadure a, b
a Department of Pediatric Anesthesia, Montpellier University Hospital, 34295 Montpellier Cedex 5, France 
b Institute of Functional Genomics (IGF), University of Montpellier, CNRS, INSERM, 34094 Montpellier, France 
c Biostatistics and Clinical Research Department, Montpellier University Hospital, 34295 Montpellier Cedex 5, France 
d Department of Anesthesia and Critical Care Medicine, Montpellier University Hospital, 34295 Montpellier Cedex 5, France 

Corresponding author at: Hopital Lapeyronie - Département d'Anesthésie-Réanimation FME, 371, Avenue du Doyen Gaston Giraud, 34295 Montpellier Cedex 5, France.Hopital Lapeyronie - Département d'Anesthésie-Réanimation FME371Avenue du Doyen Gaston GiraudMontpellier Cedex 534295France

Highlights

Question — What is the level of pressure just before loss of resistance during an epidural anesthesia procedure in children?
Findings — It was correlated with the weight which may in part explain the classically described difficulties in detecting the epidural space in infants.
Meaning — Tools like the CompuFlo® device, in addition to ultrasound guidance, could give more certainty about the correct position of the epidural catheter under general anesthesia and its use for postoperative analgesia.

Il testo completo di questo articolo è disponibile in PDF.

Abstract

Background

Epidural anesthesia (EA) is particularly relevant in the cases of expected intense and lasting postoperative pain. Yet, this technique is considered challenging in young children because of the difficulty in perceiving the loss of resistance (LOR) required to detect the epidural space. The CompuFlo® device is a computerized injection pump that accurately detects real-time pressure at the tip of a needle. This prospective observational study aimed to describe pressure levels during EA in children. Therefore, we hypothesized that pressures would be lower in smaller children.

Methods

All surgical patients requiring an EA were eligible for inclusion. During the procedure, pressures before LOR were measured in real-time using both modes (manual and automatic) of the CompuFlo® device. Factors that may influence pressure levels, such as weight, were also investigated.

Results

We analyzed the last pressures just before LOR during 56 procedures performed on 47 patients. Median pressures (quartiles) were 174 (120; 314) mmHg. The pressure before LOR was correlated to the weight (r = 0.61 in the automatic group), with values significantly lower in the group of children under 5 kg (p = 0.02) compared to the other weight groups.

Conclusion

The CompuFlo® device allowed a pressure measurement prior to obtaining LOR during EA catheter placement in children. Younger children appear to have lower pressure levels. This could partly explain the difficulty in detecting the epidural space in infants. This observational study describes initial results that could be used as a basis for future hypotheses.

Registration

ClinicalTrial.gov, NCT03672526.

Il testo completo di questo articolo è disponibile in PDF.

Abbreviations : EA, LOR

Keywords : Injection pressure, Loss-of-resistance device, Epidural anesthesia technique, Postoperative pain, Children


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© 2025  Société Française d'Anesthésie et de Réanimation (SFAR). Pubblicato da Elsevier Masson SAS. Tutti i diritti riservati.
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Vol 44 - N° 4

Articolo 101530- agosto 2025 Ritorno al numero
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