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Updated: Aug 15, 2026

An Experimental Paradigm for the Prediction of Post-Operative Pain (PPOP)
Published on: January 28, 2010
Back pain after epidural anesthesia with chloroprocaine
R A Stevens1, W F Urmey, B L Urquhart
1Hospital for Special Surgery, Cornell University Medical College, New York, New York.
Large volumes of chloroprocaine, particularly those containing EDTA, are linked to increased deep back pain after epidural anesthesia. Lower doses (≤25 ml) of chloroprocaine showed similar back pain rates to lidocaine.
Area of Science:
- Anesthesiology
- Pain Management
- Pharmacology
Background:
- Chloroprocaine use in epidural anesthesia is associated with severe back pain.
- Potential contributing factors include EDTA preservative, large anesthetic volumes, low pH, and local infiltration.
Purpose of the Study:
- To investigate the relationship between chloroprocaine characteristics and post-epidural anesthesia back pain.
- To compare the incidence and severity of back pain across different chloroprocaine formulations and volumes versus lidocaine.
Main Methods:
- A randomized study involving 100 outpatients undergoing knee surgery with continuous epidural anesthesia.
- Patients received one of five local anesthetics: lidocaine control, chloroprocaine with EDTA, higher volume chloroprocaine, chloroprocaine without EDTA, or pH-adjusted chloroprocaine.
- Pain was assessed using visual analog and verbal analog scales post-anesthesia and via telephone interview at 24 hours.
Main Results:
- Two types of back pain were identified: superficial (Type 1) and deep, aching, burning lumbar pain (Type 2).
- Type 2 pain incidence was significantly higher in the group receiving 30 ml of chloroprocaine (Group III) compared to lidocaine and other chloroprocaine groups.
- Group III also reported significantly higher overall pain scores.
Conclusions:
- Large doses (≥40 ml) of chloroprocaine containing EDTA are associated with a higher incidence of deep, burning lumbar back pain.
- Using 25 ml or less of chloroprocaine resulted in back pain incidence comparable to the lidocaine control group.
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