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Pain on injection with microemulsion propofol
Ji-Yeon Sim1, Soo-Han Lee, Do-Yang Park
1Department of Anesthesiology and Pain Medicine, Asan Medical Centre, University of Ulsan College of Medicine, Seoul, Korea.
Aims:
To evaluate the incidence and severity of injection pain caused by microemulsion propofol and lipid emulsion propofol in relation to plasma bradykinin generation and aqueous free propofol concentrations.
Methods:
Injection pain was evaluated in 147 patients. Aqueous free propofol concentrations in each formulation, and in formulation mixtures containing agents that reduce propofol-induced pain, were measured by high-performance liquid chromatography. Plasma bradykinin concentrations in both formulations and in their components mixed with blood sampled from six volunteers were measured by radioimmunoassays. Injection pain caused by 8% polyethylene glycol 660 hydroxystearate (PEG660 HS) was evaluated in another 10 volunteers.
Results:
The incidence of injection pain [visual analogue scale (VAS) >30 mm] caused by microemulsion and lipid emulsion propofol was 69.7 and 42.3% (P < 0.001), respectively. The median VAS scores for microemulsion and lipid emulsion propofol were 59 and 24 mm, respectively (95% confidence interval for the difference 12.5, 40.0). The aqueous free propofol concentration of microemulsion propofol was seven times higher than that of lipid emulsion propofol. Agents that reduce injection pain did not affect aqueous free propofol concentrations. Microemulsion propofol and 8% PEG660 HS enhanced plasma bradykinin generation, whereas lipid emulsion propofol and lipid solvent did not. PEG660 HS did not cause injection pain.
Conclusions:
Higher aqueous free propofol concentrations of microemulsion propofol produce more frequent and severe pain. The plasma kallikrein-kinin system may not be involved, and the agents that reduce injection pain may not act by decreasing aqueous free propofol concentrations.
Insights
Microemulsion propofol causes more injection pain than lipid emulsion propofol due to higher free propofol concentrations. Pain reduction agents may not work by lowering free propofol levels.
Area of Science:
- Anesthesiology
- Pharmacology
Background:
- Propofol is a widely used anesthetic agent.
- Injection pain is a common side effect of propofol administration.
- Different propofol formulations exist, including microemulsion and lipid emulsion.
Purpose of the Study:
- To compare the incidence and severity of injection pain between microemulsion propofol and lipid emulsion propofol.
- To investigate the relationship between injection pain, plasma bradykinin generation, and aqueous free propofol concentrations.
Main Methods:
- 147 patients were evaluated for injection pain.
- Aqueous free propofol concentrations were measured using high-performance liquid chromatography.
- Plasma bradykinin concentrations were measured by radioimmunoassays.
Main Results:
- Microemulsion propofol caused significantly more frequent (69.7% vs 42.3%) and severe injection pain (median VAS 59 mm vs 24 mm) compared to lipid emulsion propofol.
- Aqueous free propofol concentration was seven times higher in microemulsion propofol.
- Microemulsion propofol and PEG660 HS increased plasma bradykinin, while lipid emulsion propofol did not.
Conclusions:
- Higher aqueous free propofol concentrations in microemulsion propofol are associated with increased injection pain.
- The plasma kallikrein-kinin system may not be the primary mediator of propofol-induced pain.
- Agents reducing injection pain may not function by decreasing aqueous free propofol concentrations.
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