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16 - Sedation and Analgesia Medications

from PART II - SYSTEMIC PAIN CONTROL

Published online by Cambridge University Press:  04 September 2009

Charles E. Ray, Jr.
Affiliation:
Denver Health Medical Center
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Summary

INTRODUCTION

The performance of minimally invasive interventional radiology procedures has increased in a significant fashion over the past 20 years. The trend in modern medicine has definitely moved toward solving medical problems with minimally invasive techniques. This trend toward minimally invasive techniques has made it extremely important for the interventionalist to be able to provide adequate sedation and analgesia during interventional procedures. Providing effective and safe sedation and analgesia has become part of the standards of care for any interventional radiology practice.

Selected patients undergoing very simple procedures may not require any sedation or analgesia; however, most of the therapeutic procedures currently performed in interventional radiology suites require the patient to be under moderate sedation and analgesia, which is also known as “conscious sedation” or, more appropriately, “sedation and analgesia.”

The purpose of this chapter is to provide an overview of the most important components of sedation that an interventional radiologist should know about sedation and analgesia. The chapter will address the use of medications, mechanisms of action, doses, and antagonists, as well as the appropriate ways to monitor the patient.

DEFINITIONS

The terms sedation and analgesia refer to a fluctuant state of conscious depression induced by pharmacological agents (1). In 2002, the American Society of Anesthesiologists (ASA) published well-defined guidelines for sedation and analgesia by nonanesthesiologists. The document specifies the spectrum of sedation/analgesia and provides qualitative parameters for the classification of stages of sedation (Table 1).

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Publisher: Cambridge University Press
Print publication year: 2008

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References

Gross, JB, Bailey, PL, Connis, RT, et al. American Society of Anesthesiologists Task Force on Sedation and Analgesia by Non-Anesthesiologists. Practice guidelines for sedation and analgesia by non-anesthesiologists. Anesthesiology 2002;96:1004– 17.Google Scholar
Practice guidelines for preoperative fasting and the use of pharmacologic agents to reduce the risk of pulmonary aspiration: application to healthy patients undergoing elective procedures: a report by the American Society of Anesthesiologist Task Force on Preoperative Fasting. Anesthesiology 1999;90:896–905.
Hoffman, GM, Nowakski, R, Troshynski, TJ, Bereas, RJ, Weisman, SJ. Risk reduction in pediatric procedural sedation by application of an American Academy of Pediatrics/American Society of Anesthesiologists process model. Pediatrics 2002;109:236–43.CrossRefGoogle Scholar
Agrawal, D, Manzi, SF, Gupta, R, Krauss, B. Preprocedural fasting state and adverse events in children undergoing procedural sedation and analgesia in a pediatric emergency department. Ann Emerg Med 2003;42:636–46.CrossRefGoogle Scholar
American College of Emergency Physicians. Clinical policy for procedural sedation and analgesia in the emergency department. Ann Emerg Med 1998;31:663–77.CrossRef
Bailey, PL, Pace, NL, Ashburn, MA, Moll, JW, East, KA, Stanley, TH. Frequent hypoxemia and apnea after sedation with midazolam and fentanyl. Anesthesiology 1990;73:826–30.CrossRefGoogle ScholarPubMed
Goodchild, CS. GABA receptors and benzodiazepines. Br J Anaesth 1993;71:127–33.CrossRefGoogle ScholarPubMed
Buhrer, M, Maitre, PO, Crevoisier, C, Stanski, DR. Electroencephalographic effects of benzodiazepines. II. Pharmacodynamic modeling of the electroencephalographic effects of midazolam and diazepam. Clin Pharmacol Ther 1990;48:555–67.CrossRefGoogle ScholarPubMed
Kanto, J, Aaltonen, L, Himberg, JJ, Houi-Viander, M. Midazolam as an intravenous induction agent in the elderly: a clinical and pharmacokinetic study. Anesth Analg 1986;65:15–20.CrossRefGoogle ScholarPubMed
Oldenhof, H, deJong, M, Steenhoek, A, Janknegt, R. Clinical pharmacokinetics of midazolam in intensive care patients, a wide interpatient variability?Clin Pharmacol Ther 1988;43:263–9.CrossRefGoogle ScholarPubMed
Meyer, BR. Benzodiazepines in the elderly. Med Clin North Am 1982;66:1017–35.CrossRefGoogle ScholarPubMed
Handal, KA, Schauben, JL, Salamone, FR. Naloxone. Ann Emerg Med 1983;12:438–45.CrossRefGoogle ScholarPubMed
Wilder-Smith, OH. Borgeat, A. Propofol and pharmacokinetic modeling. Anesth Analg 1992;74:316–7.CrossRefGoogle ScholarPubMed
Schnider, TW, Minto, CF, Shafer, SL, et al. The influence of age on propofol pharmacodynamics. Anesthesiology 1999;90:1502–16.CrossRefGoogle ScholarPubMed
Veselis, RA, Reinsel, RA, Feshchenko Va, Va, Wronski, M. The comparative amnestic effects of midazolam, propofol, thiopental, and fentanyl at equisedative concentrations. Anesthesiology 1997;87:749–64.CrossRefGoogle ScholarPubMed
Vargo, JJ, Zuccaro, G Jr, Dumot, JA, et al. Gastroenterologist-administered propofol versus meperidine and midazolam for advanced upper endoscopy: a prospective, randomized trial. Gastroenterology 2002;123:8–16.CrossRefGoogle ScholarPubMed
Rex, DK, Overley, C, Kinser, K, et al. Safety of propofol administered by registered nurses with gastroenterologist supervision in 2000 endoscopic cases. Am J Gastroenterol 2002;97:1159–63.CrossRefGoogle ScholarPubMed
Borgeat, A, Wilder-Smith, OH, Saiah, M, Rifat, K. Subhypnotic doses of propofol possess direct antiemetic properties. Anesth Analg 1992;74:539–41.CrossRefGoogle ScholarPubMed
Gehan, G, Karoubi, P, Quiret, F, Leroy, A, Rathat, C, Pourriat, JL. Optimal dose of lignocaine for preventing pain on injection of propofol. Br J Anaesth 1991;66:324–6.CrossRefGoogle ScholarPubMed
Paakkari, H. Epidemiological and financial aspects of the use of non-steroidal anti-inflammatory analgesics. Pharmacol Toxicol 1994;75(2):56–9.CrossRefGoogle ScholarPubMed
Lichtenstein, DR, Syngal, S, Wolfe, MM. Nonsteroidal antiinflammatory drugs and the gastrointestinal tract. The double-edged sword. Arthritis Rheum 1995;38:5–18.CrossRefGoogle ScholarPubMed
DeWitt, DL, Meade, EA, Smith, WL. PGH synthase isoenzyme selectivity: the potential for safer nonsteroidal antiinflammatory drugs. Am J Med 1993;95:40S–4S.CrossRefGoogle ScholarPubMed
Marnett, LJ, Rowlinson, SW, Goodwin, DC, Kalgutkar, AS, Lanzo, CA. Arachidonic acid oxygenation by COX-1 and COX-2. Mechanisms of catalysis and inhibition. J Biol Chem 1999;274:22903–6.CrossRefGoogle Scholar
Ito, S, Okuda-Ashitaka, E, Minami, T. Central and peripheral roles of prostaglandins in pain and their interactions with novel neuropeptides nociceptin and nocistatin. Neurosci Res 2001;41:299–332.CrossRefGoogle ScholarPubMed
Vane, JR, Botting, RM. Mechanism of action of anti-inflammatory drugs. Adv Exp Med Biol 1997;433:131–8.CrossRefGoogle ScholarPubMed
Rodnan, GP, Benedek, TG. The early history of antirheumatic drugs. Arthritis Rheum 1970;13:145–65.CrossRefGoogle ScholarPubMed
Lee, YS, Kim, H, Wu, TX, Wang, KM, Dionne, RA. Genetically mediated interindividual variation in analgesic responses to cyclooxygenase inhibitory drugs. Clin Pharmacol Ther 2006;79:407–18.CrossRefGoogle ScholarPubMed
Cryer, B. A COX-2-specific inhibitor plus a proton-pump inhibitor: is this a reasonable approach to reduction in NSAIDs' GI toxicity?Am J Gastroenterol 2006;101:711–3.CrossRefGoogle Scholar
Wolfe, MM, Lichenstein, DR, Singh, G. Gastrointestinal toxicity of nonsteroidal antiinflammatory drugs. N Engl J Med 1999;340:1888–99.CrossRefGoogle ScholarPubMed
Scheiman, JM. Pathogenesis of gastroduodenal injury due to nonsteroidal antiinflammatory drugs: implications for prevention and therapy. Semin Arthritis Rheum 1992;21:201–10.CrossRefGoogle ScholarPubMed
Graham, DY, Agrawal, NM, Roth, SH. Prevention of NSAID-induced gastric ulcer with misoprostol: multicentre, double-blind, placebo-controlled trial. Lancet 1988;2(8623):1277–80.CrossRefGoogle ScholarPubMed
Chan, FK, Huang, LC, Suen, BY, et al. Celecoxib versus diclofenac and omeprazole in reducing the risk of recurrent ulcer bleeding in patients with arthritis. N Engl J Med 2002;347:2104–10.CrossRefGoogle ScholarPubMed
Silverstein, FE, Grahan, DY, Senior, JR, et al. Misoprostol reduces serious gastrointestinal complications in patients with rheumatoid arthritis receiving nonsteroidal anti-inflammatory drugs. A randomized, double-blind, placebo-controlled trial. Ann Intern Med 1995;123:241–9.CrossRefGoogle ScholarPubMed
Antithrombotic Trialists' Collaboration. Collaborative meta-analysis of randomised trials of antiplatelet therapy for prevention of death, myocardial infarction, and stroke in high risk patients. BMJ 2002;324:71–86.CrossRef
Brater, DC. Anti-inflammatory agents and renal function. Semin Arthritis Rheum, 2002;32:33–42.CrossRefGoogle ScholarPubMed
Brater, DC, Harris, C, Redfern, JS, Gertz, BJ. Renal effects of COX-2-selective inhibitors. Am J Nephrol 2001;21:1–15.CrossRefGoogle ScholarPubMed
Harris, ED Jr., Budd, RC, Firestein, GS, et al. (eds). Kelley's Textbook of Rheumatology, 7th Edition – Text with Continually Updated Online Reference, 2-Volume Set. Philadelphia: WB Saunders, 2005, pp. 845– 6.Google Scholar

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