全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

The Effect of Intravenous Dexamethasone and Lidocaine on Propofol-Induced Vascular Pain: A Randomized Double-Blinded Placebo-Controlled Trial

DOI: 10.1155/2013/734531

Full-Text   Cite this paper   Add to My Lib

Abstract:

Background. The mechanism for pain associated with intravenous administration of propofol is believed to be related to the release of nitric oxide. We hypothesized that pain following propofol injection would be reduced by pretreatment with dexamethasone. Methods. One hundred fourteen female subjects received 5?mL of preservative-free saline, 0.5?mg·kg?1 of lignocaine hydrochloride 10?mg·mL?1 or 0.25?mg·kg?1 of dexamethasone, intravenously, following exsanguination and occlusion of the veins of the arm. This was followed by a 0.5?mg·kg?1 injection of propofol. Pain scores, facial grimacing, arm withdrawal, and vocalization were recorded prior to and at 15 and 30 seconds following the injection of propofol. Results. The incidence of moderate to severe pain following the injection of propofol was significantly decreased with both lidocaine and dexamethasone. Hand withdrawal was also significantly decreased in comparison to saline. Conclusion. Low dose dexamethasone is commonly used as an antiemetic, and, in larger doses, it has been demonstrated to provide prolonged postoperative analgesia. At higher analgesic doses, dexamethasone may also reduce pain associated with the injection of propofol. This effect is probably related to the effect of the steroid on nitric oxide production associated with intravenous propofol injection. 1. Introduction Propofol (Diprivan, 2,6-di-isopropylphenol) was introduced into clinical use in 1986 and has now become the most widely used intravenous anaesthetic, despite the high incidence of localized pain on injection. In studies of propofol injection into an intravenous catheter in a forearm cephalic vein or vein on the back of the hand, the incidence of pain was 68%–72% [1, 2]. The pain is immediate and can be profound, and it has been ranked the seventh out of the 33 anesthesia outcomes deserving high priority for improvement, by a panel of anaesthesiologists from academic and community practices [3]. In addition, the hyperdynamic cardiovascular response to the pain can precipitate adverse events in high-risk patients with history of coronary artery disease and/or abnormal heart rhythm. Clinical strategies designed to alleviate propofol-related pain have been described in the literature including cooling the extremity, dilution of the propofol solution injecting propofol into a large antecubital vein, and the application of topical nitroglycerin on the skin overlying the tip of the intravenous catheter. Injection of lidocaine to prevent propofol injection pain is the most extensively studied technique and is commonly used

References

[1]  C.-L. Huang, Y.-P. Wang, Y.-J. Cheng, L. Susetio, and C.-C. Liu, “The effect of carrier intravenous fluid speed on the injection pain of propofol,” Anesthesia and Analgesia, vol. 81, no. 5, pp. 1087–1088, 1995.
[2]  G. Gehan, P. Karoubi, F. Quinet, A. Leroy, C. Rathat, and J. L. Pourriat, “Optimal dose of lignocaine for preventing pain on injection of propofol,” British Journal of Anaesthesia, vol. 66, no. 3, pp. 324–326, 1991.
[3]  A. Macario, M. Weinger, P. Truong, and M. Lee, “Which clinical anesthesia outcomes are both common and important to avoid? The perspective of a panel of expert anesthesiologists,” Anesthesia and Analgesia, vol. 88, no. 5, pp. 1085–1091, 1999.
[4]  P. Picard and M. R. Tramèr, “Prevention of pain on injection with propofol: a quantitative systematic review,” Anesthesia and Analgesia, vol. 90, no. 4, pp. 963–969, 2000.
[5]  G. S. De Oliveira Jr., L. J. Castro-Alves, S. Ahmad, M. C. Kendall, and R. J. McCarthy, “Dexamethasone to prevent postoperative nausea and vomiting: an updated meta-analysis of randomized,” Anesthesia & Analgesia, vol. 116, pp. 58–74, 2013.
[6]  G. S. De Oliveira Jr., S. Ahmad, P. C. Fitzgerald et al., “Dose ranging study on the effect of preoperative dexamethasone on postoperative quality of recovery and opioid consumption after ambulatory gynaecological surgery,” British Journal of Anaesthesia, vol. 107, no. 3, pp. 362–371, 2011.
[7]  C. S. Bolac, A. H. Wallace, G. Broadwater, L. J. Havrilesky, and A. S. Habib, “The impact of postoperative nausea and vomiting prophylaxis with dexamethasone on postoperative wound complications in patients undergoing laparotomy for endometrial cancer,” Anesthesia & Analgesia, vol. 116, pp. 1041–1047, 2013.
[8]  B. B. Abdelmalak, A. M. Bonilla, D. Yang et al., “The hyperglycemic response to major noncardiac surgery and the added effect of steroid administration in patients with and without diabetes,” Anesthesia & Analgesia, vol. 116, pp. 1116–1122, 2013.
[9]  W. K. Park, C. Lynch III, and R. A. Johns, “Effects of propofol and thiopental in isolated rat aorta and pulmonary artery,” Anesthesiology, vol. 77, no. 5, pp. 956–963, 1992.
[10]  L. Moreno, M. A. Martínez-Cuesta, V. Muedra, B. Beltrán, and J. Esplugues, “Role of the endothelium in the relaxation induced by propofol and thiopental in isolated arteries from man,” Journal of Pharmacy and Pharmacology, vol. 49, no. 4, pp. 430–432, 1997.
[11]  D. Kindgen-Milles and J. O. Arndt, “Nitric oxide as a chemical link in the generation of pain from veins in humans,” Pain, vol. 64, no. 1, pp. 139–142, 1996.
[12]  S. A. Kharitonov, D. H. Yates, and P. J. Barnes, “Inhaled glucocorticoids decrease nitric oxide in exhaled air of asthmatic patients,” American Journal of Respiratory and Critical Care Medicine, vol. 153, no. 1, pp. 454–457, 1996.
[13]  P. S. Grabowski, H. Macpherson, and S. H. Ralston, “Nitric oxide production in cells derived from the human joint,” British Journal of Rheumatology, vol. 35, no. 3, pp. 207–212, 1996.
[14]  Y. Huo, P. Rangarajan, E.-A. Ling, and S. T. Dheen, “Dexamethasone inhibits the Nox-dependent ROS production via suppression of MKP-1-dependent MAPK pathways in activated microglia,” BMC Neuroscience, vol. 12, article 49, 2011.
[15]  R. Aras-López, F. E. Xavier, M. Ferrer, and G. Balfagón, “Dexamethasone decreases neuronal nitric oxide release in mesenteric arteries from hypertensive rats through decreased protein kinase C activation,” Clinical Science, vol. 117, no. 8, pp. 305–312, 2009.
[16]  T. Morishima, K. Sobue, H. Arima et al., “Profound pain due to propofol injection triggered myocardial ischemia in a patient with a suspected pheochromocytoma,” Anesthesia & Analgesia, vol. 96, no. 2, p. 631, 2003.
[17]  G. S. De Oliveira Jr., P. Fitzgerald, L. F. Streicher, R. J. Marcus, and R. J. McCarthy, “Systemic lidocaine to improve postoperative quality of recovery after ambulatory laparoscopic surgery,” Anesthesia & Analgesia, vol. 115, pp. 262–267, 2012.
[18]  A. J. Petros, R. G. Bogle, and J. D. Pearson, “Propofol stimulates nitric oxide release from cultured porcine aortic endothelial cells,” British Journal of Pharmacology, vol. 109, no. 1, pp. 6–7, 1993.
[19]  F. S. Gragasin, S. L. Bourque, and S. T. Davidge, “Propofol increases vascular relaxation in aging rats chronically treated with the angiotensin-converting enzyme inhibitor captopril,” Anesthesia & Analgesia, vol. 116, pp. 775–783, 2013.
[20]  T. R. L. Romero, G. S. Galdino, G. C. Silva et al., “Ketamine activates the l-arginine/nitric oxide/cyclic guanosine monophosphate pathway to induce peripheral antinociception in rats,” Anesthesia and Analgesia, vol. 113, no. 5, pp. 1254–1259, 2011.
[21]  M. Nakane and H. Iwama, “A potential mechanism of propofol-induced pain on injection based on studies using nafamostat mesilate,” British Journal of Anaesthesia, vol. 83, no. 3, pp. 397–404, 1999.
[22]  T. Shimizu, S. Inomata, and M. Tanaka, “Rapid injection of propofol reduces vascular pain and facilitates Laryngeal Mask Airway insertion,” Journal of Clinical Anesthesia, vol. 23, no. 7, pp. 540–543, 2011.
[23]  X. Feng, J. J. Liu, X. Zhou et al., “Single sevoflurane exposure decreases neuronal nitric oxide synthase levels in the hippocampus of developing rats,” British Journal of Anaesthesia, vol. 109, pp. 225–233, 2012.
[24]  K. Hama-Tomioka, H. Kinoshita, K. Nakahata et al., “Roles of neuronal nitric oxide synthase, oxidative stress, and propofol in N-methyl-D-aspartate-induced dilatation of cerebral arterioles,” British Journal of Anaesthesia, vol. 108, no. 1, pp. 21–29, 2012.
[25]  R. Holt, P. Rask, K. P. Coulthard et al., “Tropisetron plus dexamethasone is more effective than tropisetron alone for the prevention of postoperative nausea and vomiting in children undergoing tonsillectomy,” Paediatric Anaesthesia, vol. 10, no. 2, pp. 181–188, 2000.
[26]  J.-J. Wang, S.-T. Ho, J.-I. Tzeng, and C.-S. Tang, “The effect of timing of dexamethasone administration on its efficacy as a prophylactic antiemetic for postoperative nausea and vomiting,” Anesthesia and Analgesia, vol. 91, no. 1, pp. 136–139, 2000.
[27]  G. Del Priore, K. J. Gurski, D. P. Warshal, C. Angel, and B. Dubeshter, “Adrenal function following high-dose steroids in ovarian cancer patients,” Gynecologic Oncology, vol. 59, no. 1, pp. 102–104, 1995.

Full-Text

comments powered by Disqus

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133