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Intrathecal Drug Therapy for Spasticity and Pain: Practical Patient Management PDF

217 Pages·1996·6.914 MB·English
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Intrathecal Drug Therapy for Spasticity and Pain Springer New York Berlin Heidelberg Barcelona Budapest Hong Kong London Milan Paris Santa Clara Singapore Tokyo Intrathecal Drug Therapy for Spasticity and Pain Practical Patient Management Janet M. Gianino Michelle M. York Judith A. Paice Rush-Presbyterian-St. Luke's Medical Center, Neuroscience Institute, Neurosurgery Division, Chicago, Illinois Foreword by Richard D. Penn With 88 Illustrations Springer· Janet M. Gianino, MS, RN Michelle M. York. RN Rush -Presbyterian· St. Luke's Rush - Presbyterian -51. Luke's Medical Center Medical Center Neurosurgery Division Neurosurgery Division I72S West Harrison Street I72S West Harrison Street Chicago, lL 60612 Chicago, IL 60612 USA USA Judith A. Paice. PhD, RN Rush -Presbyterian -St. Luke's Medical Center Neurosurgery Division 172S West Harrison Street Chicago, IL 60612 USA Library of Congress Cataloging.in·Publil;lltion Data Gianino. Janet M. Intratheca.l drug therapy for spasticity and pain ; practical patient managflllent I by Janet M. Gianino, Michelle M. York. Judith A. Paice. p. em. Includes biblioaraphical refereJJCe$. ISBN-13: 97S-O-387-94552-1 (he : a1k. paper) I. Antispasmodics. 2. Morphine. 3. Injection •• Spinal. I. Title. [DNLM: I. Mu$Cle Spastictty- drugtherapy. 2. Injections, Spinal. 3. Pain_druj tllerapy. 4. Baclofen-thera~tic use. S. Morphine therap(utic use. WE Ss(! G<t13i 19I1S] RM321.OS2 1995 6IS'.184-dc20 Printed on acid-fret: paper. 01996 SpriJlier-Verlll New York, Inc. Reprinl of the original edition 1996 All riihll reserved. This work may tIOI be translated or copied in whole or in ~ without the written permission of the publisher (Springer·Verlli New York. Inc .. 17S Fifth Avenue, New York. NY 10010. USA), exoept for brief excerpts in connection with reviews or ""holarly analysis. Use in connection with any form of information and retrieval, electronic adaptation. «nnputer software, or by similar or dissimilar methodololY now kl\OwtI Or herealter developed is forbidden. The use of ,meral descriptive names, trade names, trademarks. etc., in this publicatiOQ. even if the former are nO{ especially identified, is nO{ to be taken as a si&n that such names, as understood by the Trade Marts and Merchandise Mark, Act, may acoordinJly be used fret:ly by anyone. While the advice and infonnation in this book are believed 10 be true and accurate at the date of goinJ; to press, neither the authors nor the editors oor the publisher can acupt any legal responsibility for any errors or omlulons that may be made. The publisher makes no warranty. express Or implied. with respect to the material contained herein. Production coordinated by Bill Imbomoni; manufacturinl sUp(rvised by Jacqui Ashri. Typeset by TechType Inc .• Upper Saddle River, NJ. 981654321 ISBN-13: 97S-O-387_94552_1 e-ISBN-13: 978-1-4612_2348_1 001: IQ,IOO7t97S·I-4612-2}4S·1 Foreword The amazing thing about treating spasticity and pain by intrathecal drug infusion is how a minute amount of fluid containing a small amount of drug can have such a significant clinical effect. A typical intrathecal dose of medication is one hundred times less than the oral dose, yet produces a marked reduction in pain or the elimination of rigidity and spasms. To visualize how little fluid is infused, consider the average volume of 1/3 mL given per day by drug pump. A milliliter contains about 20 drops of fluid; therefore a single drop of fluid is infused every 3 to 4 hours. At this slow rate an observer would be unable to see the flow; it is so small that the fluid if in the air would evaporate before accumulating at the tip of the catheter. Infusing the medicine directly to the right area in the nervous system clearly makes a huge difference in how much is needed. The tool for achieving this is equally amazing. The accuracy of the programmable implanted pump is higher than any other drug delivery system used in clinical medicine; it is better than ±50/0, and it can go from a range of a small fraction of 1 mL to 2 mL per hour. Furthermore, the pump is reliable, giving what it is instructed to give and working in a continuous fashion for 3 to 5 years. As would be expected, the pump took many years to engineer and test, but it has been equal to the demands placed on it. Properly using this new technology requires many skills. Though it is simple in concept, it is not necessarily so in application. Knowledge of the mechanics of the pump and the pharmacology of drug delivery, accuracy in the assessment of the patient's pain or spasticity, and correct diagnosis of complications are just a few of the requirements. The nurse practitio ners who wrote this book have developed the necessary skills and, fortunately, taken the time from their busy schedules to write a guide to the successful management of this sometimes difficult but very rewarding new field of medicine. Beyond their technical skills and knowledge they have manifested kindness, concern, meticulousness, and dedication in y vi Foreword working with our patients. Their willingness to share their expertise and experience to teach others the practical management skills they have developed is another example of their energy and generosity. They are models of what medical practitioners should strive to be in the chal lenging world of medicine. RICHARD D. PENN. M.D. Rush -Presbyterian -St. Luke's Medical Center Chicago,IL Contents Foreword by Richard D. Penn, MD ............................. v Introduction ............................................................ . 2 Spinal Cord Anatomy....................... ...... ................... 3 3 Implantable Delivery Systems ...................................... 15 4 The Operative Course............. ................ ................... 33 5 Pharmacology of Baclofen and Morphine.................. .... 55 6 Intrathecal Baclofen for Spasticity................................ 67 Spasticity........ .............. .. ........... ....... ................. 67 Current methods 0/ treatment................ ................ 76 Benefits 0/ reduced spasticity................................. 80 Patient selection....................... ........................... 86 Screening procedures........................................... 93 Patient management ....................................... ..... 96 Tolerance .......................................................... 118 7 Intraspinal Morphine for Pain............... ...................... 127 Physiology 0/ pain ........ .................... .................. 128 Intrathecal drug dosing ........................................ 138 Supplemental opioids........................................... 143 Adverse intraspinal drug effects................ ............. 146 Patient education ................................................ 149 Case study ......................................................... 149 8 Mechanical System Complications................................ 155 9 Starting Up a Program............................................... 173 10 Current Controversies and Future Applications ............... 187 vII vIII Contents References ............................................................ 189 Appendixes Baclofen Patient Teaching Booklet............................... 201 2 Intrathecal Baclofen and Morphine: Policy and Procedure (Rush-Presbyterian-St. Luke's Medical Center, Chicago, IL) ............................................................ 207 3 Resources for Spasticity.............................................. 211 3.1 Patient Resources: Spasticity....................................... 211 3.2 Professional Resources: Spasticity................................ 212 3.3 Patient Resources: Travel Assistance for the Disabled........................................................ 212 4 Resources for Pain .................................................... 213 4.1 Patient Resources: Pain.............................................. 213 4.2 Professional Resources: Pain .... ..................... .............. 214 5 Research Organizations .............................................. 215 6 Electronic Support Groups.......................................... 217 1 Introduction Centuries ago, natural products, such as plants, animals, or minerals, were ingested or applied to the skin to treat various disorders. For example, juices from the pods of the plant Papaver somni/erum, a member of the poppy family, were used to relieve pain. It is only since the 1800s that chemically active compounds were synthesized from plants and other products into tablets, liquids, or topical solutions. Morphine, an essential agent used today in the treatment of pain, was first isolated in 1804 by Friedrich Wilhelm Sertiirner. Since that time, pharmacologic advancements have led to the synthesis of many new agents to treat a variety of diseases and symptoms. Methods of drug delivery have also advanced. Injectable compounds have been introduced, expanding the available methods of delivery, and the use of intravenous delivery has become popular in the past 50 years. Although oral, topical, and parenteral routes are useful, these delivery systems have significant limitations. Most of these routes deliver the drug widely throughout the body, leading to the desired effect, as well as possible side effects. As we learn more about the pharmacokinetics and pharmacodynamics of various agents, the specific site or sites of action are being identified. Thus, delivery to the site of action produces a more pronounced desired effect with fewer adverse effects. Local delivery into the spinal cord is especially attractive in the treatment of spasticity and pain. Antispasmodic agents, such as baclofen, may produce significant central effects when given orally. The site of action of baclofen is within the spinal cord; thus delivery into this site would reduce spasticity at much lower doses when compared to oral administration, producing fewer central effects. Most patients in pain can tolerate oral opioids, yet a small percentage develop severe adverse effects to morphine. These patients might also benefit by delivery of drug into the spinal cord, a key anatomical site in pain processing, with fewer side effects. 1 2 1. Introduction The local delivery of drugs into the spinal cord began in 1901 in Japan with the intrathecal bolus injection of morphine by a physician named Kitagawa. The technology to chronically deliver intraspinal drugs pro gressed slowly until the 1960s. Indwelling reservoirs, such as the Ommaya reservoir, were introduced at that time to overcome barriers in chemo therapy administration to the brain. I External catheters, often attached to external pumps, were developed to improve intraspinal delivery. Technology has only recently allowed totally implanted systems to deliver drugs continuously into intraspinal spaces, minimizing complications such as infections.2 Although minimizing the risk associated with intraspinal delivery, the use of these more complex systems requires extensive training of health professionals caring for patients receiving this therapy. Knowledge is necessary of the mechanics of these systems, the pharmacokinetics of drugs intended for intraspinal delivery, and the specific needs of patients with neurologic disorders, cancer, and chronic nonmalignant pain who receive this therapy. The purpose of this book is to provide clinicians with the information necessary to provide safe and effective care to patients being treated with intraspinal agents for spasticity and pain. Where controversies exist in management, we have tried to present alternative views. Additionally, although every effort has been made to be thorough, no text can be completely comprehensive. Therefore, we have included other resources to assist in the care of these patients. The use of intraspinal drug delivery has rapidly expanded with the advent of implantable systems. This expansion is likely to continue with the investigation of new compounds with larger structures, such as peptides and growth factors, for the treatment of spasticity, pain, other neuromuscular disorders, and even neurodegenerative diseases. Knowl edgeable clinicians can make informed judgments while providing care for these patients as well as form collaborative relationships with basic investigators to advance the underlying science of this technique.

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