1Influence of Opioids on Cardiovascular Dynamics
1Hemodynamic responses to painful/noxious stimulation can be completely suppressed by the action of potent volatile anesthetics.
The difficulty in this approach is that the amount of a volatile anesthetic needed to suppress such hemodynamic responses would also be sufficient to result in significant hypotension.
Accordingly, opioids may be used to provide greater hemodynamic stability, suppressing hemodynamic responses to pain.
The proposition that high-does opioids representing the primary/only anesthetic results in hemodynamic stability remains controversial.
Nevertheless, the role of opioids as an adjunct to other agents is well established as is the ability of opioids to suppress hemodynamic responses to events commonly occurring intraoperatively.
Excursion from a stable hemodynamic profile can be associated with anesthesia induction, intubation, as well as events occurring during surgery. The qualitative and quantitative aspects of these excursions can be influenced by other factors which include:
Extent of -adrenergic receptor blockade as well as the possibility of Ca2+ channel blockade
Preoperative status of ventricular function
Hydration state of the patient
Administration of premedication
Presence or absence of patient awareness.
1The specific opioid used to modify hemodynamic excursions is also likely to have an effect.
This consideration is another example of lack of conclusive resolution in that some research indicates limited difference between fentanyl and sufentanil when used as principal anesthetics and cardiac surgery; whereas other results suggest that sufentanil might provide better intraoperative hemodynamic management.
Sufentanil administration appears to limit the need for vasodilators during cardiopulmonary bypass procedures as well as during the post-bypass period and the post-operative period.
|
1Bailey, PL, Egan, TD, Stanley, TH, "Intravenous Opioid Anesthetics", in Anesthesia 5th edition, Miller, R.D., editor, Churchill Livingstone, Philadelphia, 2000, 273-377 (references secondarily sourced from this primary reference are noted below in the indented references)
1aLowenstein, E, Hallowell P, Levine FH et al.: Cardiovascular response to large doses of intravenous morphine in man.N. Engl J Med 281:13 89, 1969
1b Stanley, TH, Webster LR; Anesthetic requirements and cardiovascular effects of fentanyl-oxygen and fentanyl-diazepam-oxygen anesthesia in man. Anesth Analg 51:901, 1972.
1c Arens, JR, Benbow, BP, Ochsner JL et al: Morphine anesthesia for the aorto-coronary bypass procedures. Anesth Analg 57: 411, 1978
1d Stanley, TH, Gray NJ, Staford W. et al: The effects of high-dose morphine on fluid and blood requirements in open-heart operations. Anesthesiology 38:536, 1973.
1e Stoelting, RK, Gibbs PS, Creasser CW et al: Hemodynamic in ventilatory response to fentanyl, fentanyl-droperidol, and nitrous oxide in patients with acquired valvular heart disease. Anesthesiology 42:319, 1975.
1f Bowdle, TA, Ward, RJ: Induction of anesthesia with small doses of sufentanil or fentanyl: Dose versus EEG response, speed of onset and thiopental requirement. Anesthesiology 70:26, 1989
1gHecker BR, Lake CL, DiFazio CA et al: The decrease of the minimum alveolar anesthetic concentration produced by sufentanil in rats. Anesth Anal 62:987, 1983.
1hGoldstein,A: Opiate receptors. Life Sci. 14:615, 1974.
1iSnyder SH: Opiate receptors in the brain. N Engl. J Med to 96:266, 1977.
1jMayer, DJ, Wolfle, TL, Akil H et al: Analgesia from electrical stimulation in the brainstem of the rat. Science 174:13 51, 1971.
1kFields, HL: Brainstem mechanisms of pain modulation: Anatomy and physiology. In Herz, A (ed): Opioids II: Handbook of Experimental Pharmacology. Berlin, Springer-Verlag, 1993, p.3.
1lKissin I, Vinik HR, Castillo R et al:Alfentanil potentiates midazolam-induced unconsciousness in subanalgesic doses. Anesth Analg 71:65, 1990
1mMcEwan AI, Smith C, Dyar O et al: Isoflurane minimum alveolar concentration reduction by fentanyl. Anesthesiology 78:864, 1993.
1nBailey, PL, Wilbrink J, Zwanikken P et al: in Anesthetic induction with fentanyl. Anesth. Analg 64:45, 1985.
1oHeier, T, Steen, PA: Assessment of anesthesia depth.Acta Anaesthesiol Scand 40:10 87, 1996.
1pSebel PS Lang E Rampil IJ White PF Cork R Jopling M Smith NT Glass PSA Manberg A multicenter study of bispectral electroencephalogram analysis for monitoring anesthetic effect Anesth. Analg. 84(4) 1997 891-899.
1qJones, JG: Use of evoked responses in the EEG to measure depth of anesthesia. In Lunn J, Rosen M (eds): Consciousness, Awareness and Pain and General Anesthesia. Boston, Butterworth, 1987, p 99.
1rEgan TD, Minto CF, Hermann DJ et al: Remifentanil versus alfentanil: Comparative pharmacokinetics and pharmacodynamics. Anesthesiology 84: 821, 1996.
1sKalkman CJ, Rheineck AR, Bovill JG: of high-does opioid anesthesia on posterior tibial nerve somatosensory cortical evoked potentials: Effects of fentanyl, sufentanil, and alfentanil J Cardiothorrac Anesth 2:758, 1998.
1tAdler, LJ, Fyuulai F, Diehl D, Mintun, M, Winter, PM, Firestone, L Regional brain activity changes associated with fentanyl analgesia elucidated by positron emission tomography. Anesth Analg 1997; 84:120-126.
2Coda, BA, "Opioids" in Clinical Anesthesia, 4th edition, Barash, PG, Cullen, BF, Stoelting, RK, editors, Lipincott Williams & Wilkins, Philadelphia, 2001, 345-375
2a Thorpe, DH: Opiate structures and activity: a guide to underlying opioid actions. Anesth Analg 63:143, 1984.
3Gottschalk, A and Smith DS, New Concepts in Acute Pain Therapy: Preemptive Analgesia, American Family Physician, May, 2001 http://www.aafp.org/afp/20010515/1979.html
First figure redrawn with permission by Gottschalk and Smith from: Kehlet H, Dahl JB. The value of "multimodal" or "balanced analgesia" in postoperative pain treatment. Anesth Analg 1993;77:1049.
Second figure redrawn with permission by Gottschalk and Smith from: Woolf CJ, Chong MS. Preemptive analgesia--treating postoperative pain by preventing the establishment of central sensitization. Anesth Analg 1993;77:368.
4Dickenson, AH Spinal cord pharmacology of pain. Br. J. Anaesth. 75: 193, 1995. (references secondarily sourced from this primary reference are noted below in the indented references)
4aBattaglia, G, Rustioni A. Coexistence of glutamate and substance P. and dorsal root ganglion cells of the rat and monkey. Journal of Comparative Neurology 1988; 277:302-312.
4bHaley, JE, Sullivan, AF, Dickenson, AH. Evidence for spinal N-methyl-D-aspartate receptor involvement in prolonged chemical nociception in the rent. Brain Research 1990; 518:218-222.
4cSchiable, HG, Grubb BD, Neugebauer, V, Oppmann M. The effects of NMDA antagonists on neuronal activity in cat spinal cord evoked by acute inflammation in the knee joint. European Journal of Neuroscience, 1991; 3:981-991.
4dWoolf CJ, Thompson, SWN. The induction and maintenance of central sensitization is dependent on N--methyl-D-aspartic acid receptor activation; implications for the treatment of post-injury hypersensitivity states. Pain 1991; 44:293-299.
4eMao, J, Price DD, Hayes, RL, Lu, J, Mayer DJ, Frank H. Intrathecal treatment with dextrophan or ketamine publicly reduces pain-related behaviors in a rat model of peripheral mononeuropathy. Brain Research 1993; 605:164-168.
4fPrice, DD, Mao, J, Mayer DJ. Central neural mechanisms of normal in abnormal pain states. In: Fields, HL, Lebeskind, JC, eds. Progress in Pain Research and Management. Seattle:IASP Press, 1994; 61-84.
4gRogawaki MA. Therapeutic potential of excitatory amino acid antagonists; channel blocks and 2,3 benzodiazepines. Trends in Pharmacological Sciences 1993; 14:325-331
4hEide PK, Jorum E, Stubhaug, A, Bremnes J, Breivik H. Relief of post-herpetic neuralgia with the N-methyl-D-aspartate receptor antagonist ketamine: a double-blind, cross-over comparison with morphine and placebo. Pain 1994; 58:347-354.
4iPrice DD, Mao J, Frenk H, Mayer, DF. Central neural mechanisms of normal in abnormal pain states. In:Fields HL, Lebeskind JC, eds. Progress in Pain Research and Management. Seattle:IASP Press, 1994; 61-84.
4jBesse, D, Lomabard, MC, Zajac, JM, Roques, BP, Besson, JM Pre- and and postsynaptic distribution of mu, delta, and kappa opioid receptors in the superficial layers of the cervical dorsal horn of the rat spinal cord, Brain Research 521 (1-2), June 1990 pp 15-22.
4kKangrga I and Randic M Outflow of endogenous aspartate in glutamate from the rat spinal dorsal horn in vitro by activation of low-and high-threshold primary afferent fibers. Modulation by mu-opioids Brain research 553, 2, July 1991,pp. 347-352.
5Substantia Gelatinosa Image: Courtesy of
The Digital Slice of Life, a cooperative project with the Slice
of Life office, KUED
Media Solutions, and the Knowledge
Weavers Project.
Ross, AF, Gomez, MK, Tinker, JH "Anesthesia for Adult
Cardiac Procedures in Principles and Practice of Anesthesiology, 2nd
edition, Longnecker, DE, Tinker, JH, Morgan, GE, eds, Mosby, St. Louis,
1998, pp. 1659-1698.
6Two-dimensional & Three Dimensional Images courtesy of CORD Center for Opioid Research and Design http://www.opioid.umn.edu/
7Jaffe, CC, Stewart, WB, Lynch, PJ, Hines, S., Cranial Nerves, Yale University School of Medicine, Center for Advanced Instructional media, (c) 1998 http://info.med.yale.edu/caim/cnerves/contents.html
8Kauffman, AM & Patel M, Center for Cranial Nerve Disorders http://www.umanitoba.ca/cranial_nerves/trigeminal_neuralgia/manuscript/index.html
9Chakrabarti, S, Oppermann, M Gintzler AR Chronic morphine induces the concomitant phosphorylation and altered Association of multiple signaling proteins: A novel mechanism for modulating cell signaling PNAS 98 (7) 4009, 2001
10Brookoff, D Chronic Pain: 1. A New Disease? Hospital Practice July, 2000 http://www.hosppract.com/issues/2000/07/brook.htm
11Protein Structure Study Guide http://www.princeton.edu/~actin/chm543_info.html#Study%20guide%201
12MRC Center for Synaptic Plasticity, University of Bristol, used with permission for non-commercial applications
13Breeze AL, Harvey, TS, Bazzo, R, Campbell ID Solution structure of Human Calcitonin Gene-Related Peptide by H NMR and Distance Geometry with Restrained Molecular Dynamics Biochemistry 30:575-582 (1991)
14Heish, JC, Carr, DB "Choosing a Therapeutic Approach: Opioids" in The Massachusetts General Hospital Handbook of Pain Management (Borsook D, LeBel, AA, McPeek, B, eds) Little, Brown and Company, Boston, 1996, pp 47-75.
15Anwari, J. S. & Iqbal, S. (2003)Antihistamines and potentiation of opioid induced sedation and respiratory depression. Anaesthesia 58 (5), 494-495
3aGustafsson LL, Schildt B, Jacobsen KJ. Adverse effects of extradural and intrathecal opiates: Reports of a nationwide survey in Sweden. British Journal of Anaesthesia 1982; 54:479-486.
3bBrockways MS, Nobel DW, Sharwood-smith GH, McClure JH. Are found respiratory depression after extradural fentanyl. British Journal of Anaesthesia 1990; 64:243-245.
3cHolmstrom, B, Rawal N, Axelsson K, Nydahl P. Risk of catheter migration during combined spinal epidural block. Percutaneous epiduroscopy study. Anesthesia and Analgesia 1995; 80:747-753.
16Yli-Hankala,A Will enough isoflurane during surgery replace morphine after surgery? Acta Anaesthesiologica Scandinavica Volume 47 Issue 7 Page 785 - August 2003)
17Gurman GM, Weksler N, Steiner O, Popescu M, Avinoah E, Porath A. The influence of cortical electrical activity level during general anaesthesia on the severity of immediate postoperative pain in the morbidly obese. Acta Anaesthesiol Scand 2003; 47:804-8
17Soliman E Legatt, AD Somatosensory Evoked Potentials: General Principles eMedicine, http://www.emedicine.com/neuro/topic640.htm, 8/2001.
18Black,
S, Sloan T., SOMATOSENSORY (SSEP) AND MOTOR EVOKED POTENTIALS (MEP) THE
SOCIETY FOR NEUROANESTHESIA AND CRITICAL CARE - 1998 ANNUAL MEETING