Prevention of Pain on Propofol Injection: A Comparative, Randomized, Double Blind Study between Lignocaine, Pethidine, Dexamethasone and Placebo

摘要

Background: Propofol is wonderful drug for short duration procedures. However, pain on injection of propofol, which has been reported to occur in 28-90% of patients, is a major drawback to its use. Different methods have been used to decrease this pain but intravenous lignocaine is most commonly used pretreatment.Methods : A comparative, randomized, double blind study was undertaken to compare the efficacy of three drugs for prevention of pain on propofol injection on induction of anaesthesia 100 female patients of ASA status 1 and 2 posted for intracavitary radiotherapy were allocated randomly in four groups of 25 each, using computer- generated table of random numbers. Venous occlusion was made with tourniquet for one minute. The study drug intravenous lignocaine 1% 2ml (group 1), pethidine 25mg in 2 ml (group2), dexamethasone 4mg in 2ml (group 3), or normal saline 2ml (group 4) was administered over 10 seconds according to random number. There after occlusion was released and intravenous propofol was given. After the first 25% of propofol given, patients were asked for intensity of pain she experienced. Results: Lignocaine, pethidine and dexamethasone significantly reduces the pain on propofol injection in comparison to placebo (p 0.002), but there was no significant difference in pain score among groups 1, 2, 3 (p 0.28). There was no significant difference in recall of pain among groups 1, 2, and 3 (p 0.43). Although there was significant difference between placebo group and other three groups (p 0.009).Conclusion: It was concluded that lignocaine, pethidine and dexamethasone significantly reduces the pain induced by propofol injection pain as compared to placebo but there is no difference in efficacy for prevention of pain among these three groups. Introduction Propofol is frequently used intravenous anaesthetic induction agent, especially for brief cases, day care surgery or when a laryngeal mask airway is to be used. Pain on injection with propofol is a common problem and can be very distressing to the patient. Incidence of pain varies between 28% and 90 %( Stark RD et al 1955 & Mangar D et al 1992) in adults and 28% -85% in children (Valtonen M et al 1988 & 1989) .The younger the child, the higher is the incidence and severity of propofol injection pain (Cameron E et al 1992). This could be due to small veins in hand. Many factors appear to affect the incidence of pain, which includes site of injection, size of vein, speed of injection, buffering effect of blood, temperature of propofol and concomitant use of drugs such as local anaesthetics and opiates. Pain on injection of propofol can be immediate or delayed. Immediate pain probably results from a direct irritant effect whereas delayed pain probably results from an indirect effect via the kinin cascade. Delayed pain has latency of between 10 and 20 s (Briggs LP et al 1981). The sensation produced is usually described as tingling, cold, or numbing or, at its worst, a severe burning pain proximal to the site of injection. This sensation tends to occur within 10-20 s of injection and lasts only for the duration of injection. Despite this discomfort, the incidence of venous sequelae, such as phlebitis, is less than 1 % (Mattila MAK et al 1985).Different methods have been used to decrease this discomfort, including cooling, adding lignocaine, applying nitroglycerine ointment to the venepuncture site, injecting cold saline prior to the injection of propofol, and diluting the propofol with 5% dextrose or intralipid. Intravenous lignocaine is the most commonly used pretreatment, but has a failure rate of 13% to 32% (Scott RPF et al 1988 & Kingsy 1992 et al). Pethidine is synthetic opioid analgesic with proven local anaesthetic effects (Power I et al 1991 & Famewo et al 1985). Dexamethasone is a steroid it also used for postoperative vomiting and pain after pediatric tonsillectomy (Mokhtar E et al 2003). We had done a double-blind comparison of lignocaine, pethidine, Dexamet