2014Clinical Orthopaedics and Related ResearchOpen access

Reply to the Letter to the Editor: Single-injection or Continuous Femoral Nerve Block for Total Knee Arthroplasty?

Éric Albrecht, Dorothea Morfey, Richard Brull

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Abstract

To the editor, We would like to thank Dr. Byrne for his comments regarding our recent publication exploring the effects of a single injection versus two types of continuous infusion for femoral nerve block [1]. We agree that Brodner and colleagues [3] previously have concluded that ropivacaine 0.2% and ropivacaine 0.3% were equivalent in terms of pain outcomes compared to ropivacaine 0.1% when used as continuous infusion for femoral nerve blocks. However, Brodner and colleagues designed their study to test the hypothesis that ropivacaine 0.3% was superior to ropivacaine 0.2% or 0.1%, and the authors’ conclusion that 0.1% was ineffective was based on an interim statistical analysis of only 20 patients. Although their study demonstrated that increasing the concentration of ropivacaine above 0.2% did not confer any advantage, we relied on another study, that of Paauwe et al [4], to address the effect of decreasing the concentration of ropivacaine below 0.2%. Indeed, Paauwe and colleagues [4] found no advantage in using concentrations of ropivacaine less than 0.1%. In designing our protocol, we were also mindful that Brodner and colleagues had not used a comprehensive multimodal analgesia strategy. The lack of benefits associated with increased concentrations of ropivacaine (ie greater than 0.1%) recently has been confirmed in another study [2]. We recognize that we used a lower total mass of local anesthetic for both the priming injection and for the continuous infusion compared to what has been published recently by Spangehl and colleagues [5]. Such differences in postoperative therapeutic regimens may explain the discrepancy in reported pain scores between institutions.

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What this paper is about

To the editor, We would like to thank Dr. Byrne for his comments regarding our recent publication exploring the effects of a single injection versus two types of continuous infusion for femoral nerve block [1]. We agree that Brodner and colleagues [3] previously have concluded that ropivacaine 0.2% and ropivacaine 0.3% were equivalent in terms of pain outcomes compared to ropivacaine 0.1% when used as continuous infusion for femoral nerve blocks. However, Brodner and colleagues designed their study to test the hypothesis that ropivacaine 0.3% was superior to ropivacaine 0.2% or 0.1%, and the authors’ conclusion that 0.1% was ineffective was based on an interim statistical analysis of only 20 patients. Although their study demonstrated that increasing the concentration of ropivacaine above 0.2% did not confer any advantage, we relied on another study, that of Paauwe et al [4], to address the effect of decreasing the concentration of ropivacaine below 0.2%. Indeed, Paauwe and colleagues [4] found no advantage in using concentrations of ropivacaine less than 0.1%. In designing our protocol, we were also mindful that Brodner and colleagues had not used a comprehensive multimodal analgesia strategy. The lack of benefits associated with increased concentrations of ropivacaine (ie greater than 0.1%) recently has been confirmed in another study [2]. We recognize that we used a lower total mass of local anesthetic for both the priming injection and for the continuous infusion compared to what has been published recently by Spangehl and colleagues [5]. Such differences in postoperative therapeutic regimens may explain the discrepancy in reported pain scores between institutions.

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Available abstract

To the editor, We would like to thank Dr. Byrne for his comments regarding our recent publication exploring the effects of a single injection versus two types of continuous infusion for femoral nerve block [1]. We agree that Brodner and colleagues [3] previously have concluded that ropivacaine 0.2% and ropivacaine 0.3% were equivalent in terms of pain outcomes compared to ropivacaine 0.1% when used as continuous infusion for femoral nerve blocks. However, Brodner and colleagues designed their study to test the hypothesis that ropivacaine 0.3% was superior to ropivacaine 0.2% or 0.1%, and the authors’ conclusion that 0.1% was ineffective was based on an interim statistical analysis of only 20 patients. Although their study demonstrated that increasing the concentration of ropivacaine above 0.2% did not confer any advantage, we relied on another study, that of Paauwe et al [4], to address the effect of decreasing the concentration of ropivacaine below 0.2%. Indeed, Paauwe and colleagues [4] found no advantage in using concentrations of ropivacaine less than 0.1%. In designing our protocol, we were also mindful that Brodner and colleagues had not used a comprehensive multimodal analgesia strategy. The lack of benefits associated with increased concentrations of ropivacaine (ie greater than 0.1%) recently has been confirmed in another study [2]. We recognize that we used a lower total mass of local anesthetic for both the priming injection and for the continuous infusion compared to what has been published recently by Spangehl and colleagues [5]. Such differences in postoperative therapeutic regimens may explain the discrepancy in reported pain scores between institutions.

Key concepts: Ropivacaine, Medicine, Femoral nerve block, Femoral nerve, Anesthesia, Nerve block, Local anesthetic

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