Effects of warmed carrier fluid on nefopam injection-induced pain
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Background: Nefopam is a non-opioid, non-steroidal analgesic drug with fewer adverse effects than narcotic analgesics and nonsteroidal anti-inflammatory drugs, and is widely used for postoperative pain control. Because nefopam sometimes causes side effects such as nausea, vomiting, somnolence, hyperhidrosis and injection-related pain, manufacturers are advised to infuse it slowly, over a duration of 15 minutes. Nevertheless, pain at the injection site is very common. Therefore, we investigated the effect of warmed carrier fluid on nefopam injection-induced pain.Methods: A total of 48 patients were randomly selected and allocated to either a control or a warming group. Warming was performed by diluting 40 mg of nefopam in 100 ml of normal saline heated to 31–32°C using two fluid warmers. The control group was administered 40 mg of nefopam dissolved in 100 ml of normal saline stored at room temperature (21–22°C) through the fluid warmers, but the fluid warmers were not activated.Results: The pain intensity was lower in the warming group than in the control group (P < 0.001). The pain severity and tolerance measurements also showed statistically significant differences between groups (P < 0.001). In the analysis of vital signs before and after the injection, the mean blood pressure after the injection differed significantly between the groups (P = 0.005), but the heart rate did not. The incidence of hypertension also showed a significant difference between groups (P = 0.017).Conclusions: Use of warmed carrier fluid for nefopam injection decreased injection-induced pain compared to mildly cool carrier fluid. (Korean J Pain 2018; 31: 102-8)
Abstract
Background: Nefopam is a non-opioid, non-steroidal analgesic drug with fewer adverse effects than narcotic analgesics and nonsteroidal anti-inflammatory drugs, and is widely used for postoperative pain control. Because nefopam sometimes causes side effects such as nausea, vomiting, somnolence, hyperhidrosis and injection-related pain, manufacturers are advised to infuse it slowly, over a duration of 15 minutes. Nevertheless, pain at the injection site is very common. Therefore, we investigated the effect of warmed carrier fluid on nefopam injection-induced pain.Methods: A total of 48 patients were randomly selected and allocated to either a control or a warming group. Warming was performed by diluting 40 mg of nefopam in 100 ml of normal saline heated to 31–32°C using two fluid warmers. The control group was administered 40 mg of nefopam dissolved in 100 ml of normal saline stored at room temperature (21–22°C) through the fluid warmers, but the fluid warmers were not activated.Results: The pain intensity was lower in the warming group than in the control group (P < 0.001). The pain severity and tolerance measurements also showed statistically significant differences between groups (P < 0.001). In the analysis of vital signs before and after the injection, the mean blood pressure after the injection differed significantly between the groups (P = 0.005), but the heart rate did not. The incidence of hypertension also showed a significant difference between groups (P = 0.017).Conclusions: Use of warmed carrier fluid for nefopam injection decreased injection-induced pain compared to mildly cool carrier fluid. (Korean J Pain 2018; 31: 102-8)
참고문헌 (27)
- Girard P, "Nefopam analgesia and its role in multimodal analgesia: a review of preclinical and clinical studies", Clin Exp Pharmacol Physiol, 43, pp.3~12 (2016)[DOI]
- Kim YM, "Slow injection of nefopam reduces pain intensity associated with intravenous injection: a prospective randomized trial", J Anesth, 28, pp.399~406 (2014)[DOI]
- Dordoni PL, "Effect of ketorolac, ketoprofen and nefopam on platelet function", Anaesthesia, 49, pp.1046~1049 (1994)[DOI]
- Bhatt AM, "Respiratory and metabolic effects of oral nefopam in human volunteers", Br J Clin Pharmacol, 11, pp.209~211 (1981)
- Evans MS, "Nefopam for the prevention of postoperative pain: quantitative systematic review", Br J Anaesth, 101, pp.610~617 (2008)[DOI]
- Piercey MF, "Spinal and supraspinal sites for morphine and nefopam analgesia in the mouse", Eur J Pharmacol, 74, pp.135~140 (1981)[DOI]
- Heel RC, "Nefopam: a review of its pharmacological properties and therapeutic efficacy", Drugs, 19, pp.249~267 (1980)[DOI]
- Durrieu G, "Overview of adverse reactions to nefopam: an analysis of the French Pharmacovigilance database", Fundam Clin Pharmacol, 21, pp.555~558 (2007)[DOI]
- 정기태, "Effects of lidocaine, ketamine, and remifentanil on withdrawal response of rocuronium", Korean Journal of Anesthesiology, 67(3), pp.175~180 (2014), 대한마취통증의학회
- Polat R, "The effects of remifentanil, lidocaine, metoclopramide, or ketamine pretreatment on propofol injection pain", Middle East J Anaesthesiol, 21, pp.673~677 (2012)
- Alipour M, "Paracetamol, ondansetron, granisetron, magnesium sulfate and lidocaine and reduced propofol injection pain", Iran Red Crescent Med J, 16, pp.e16086~ (2014)
- Mahajan C, "Local warming at injection site helps alleviate pain after rocuronium administration", J Anesth, 24, pp.845~848 (2010)[DOI]
- Jeong M, "Comparison of the effects of lidocaine pre-administration and local warming of the intravenous access site on propofol injection pain: randomized, doubleblind controlled trial", Int J Nurs Stud, 61, pp.209~218 (2016)[DOI]
- 윤앤미선, "Heated carrier fluids in decreasing propofol injection pain: a randomized, controlled trial", Korean Journal of Anesthesiology, 70(1), pp.33~38 (2017), 대한마취통증의학회
- 김동준, "Mega Acer KitⓇ is more effective for warming the intravenous fluid than RangerTM and ThermoSensⓇ at 440 ml", h of infusion rate: an experimental performance study, 2017, pp.70(4), 456~461[DOI]
- Klement W, "injection of some anaesthetic agents is evoked by the unphysiological osmolality or pH of their formulations", Br J Anaesth, 66, pp.189~195 (1991)[DOI]
- Gregori-Puigjane E, "Identifying mechanism-of-action targets for drugs and probes", Proc Natl Acad Sci U S A, 109, pp.11178~11183 (2012)[DOI]
- Raote I, "Serotonin receptors in neurobiology", pp.105~132 (2007), CRC Press
- Kaplanski G, "Activated platelets induce endothelial secretion of interleukin-8 in vitro via an interleukin-1-mediated event", Blood, 81, pp.2492~2495 (1993)
- Neumann FJ, "Induction of cytokine expression in leukocytes by binding of thrombin-stimulated platelets", Circulation, 95, pp.2387~2394 (1997)
- Christen S, "Dose-dependent vasodilatory effects of acetylcholine and local warming on skin microcirculation", J Cardiovasc Pharmacol, 44, pp.659~664 (2004)
- Minson CT, "Nitric oxide and neurally mediated regulation of skin blood flow during local heating", J Appl Physiol (1985), 91, pp.1619~1626 (2001)[DOI]
- Taylor WF, "Effect of high local temperature on reflex cutaneous vasodilation", J Appl Physiol Respir Environ Exerc Physiol, 57, pp.191~196 (1984)
- Elstad M, "Responses in acral and non-acral skin vasomotion and temperature during lowering of ambient temperature", J Therm Biol, 45, pp.168~174 (2014)[DOI]
- Bergersen TK, "Cold-induced sympathetic tone modifies the impact of endothelium-dependent vasodilation in the finger pulp", Auton Neurosci, 203, pp.97~102 (2017)[DOI]
- Hagemann K, "Haemodynamic effects of nefopam (author's transl)", Dtsch Med Wochenschr, 103, pp.1040~1043 (1978)[DOI]
- Sacco M, "The relationship between blood pressure and pain", J Clin Hypertens (Greenwich), 15, pp.600~605 (2013)[DOI]
