|
|
Continuum,
Neuropathic Pain, October 2009,
Volume 15,
Issue 5
| Issue Overview |
| Key Points for Issue. (pdf) |
|
faculty.
(PDF only)
|
|
editor's preface.
- Miller, Aaron
|
|
painful peripheral neuropathy: diagnosis and assessment.
- Freeman, Roy
>
Show/Hide Abstract
Neuropathic pain is more prevalent in neuropathies associated with prominent involvement of the small unmyelinated and lightly myelinated nerve fibers (the C and A[delta] nerve fibers). However, it is not unusual to find neuropathic pain in patients with mixed large-fiber and small-fiber neuropathies and even in neuropathies with predominantly large-fiber involvement. Peripheral neuropathic pain may occur in generalized polyneuropathies, focal peripheral neuropathies (eg, postherpetic neuralgia), mononeuritis multiplex, segmental neuropathies (eg, brachial neuritis), and radiculopathies. Pain results in a substantial proportion of the morbidity associated with a generalized polyneuropathy. This chapter will cover the diagnosis and assessment of the most common and clinically important generalized polyneuropathies that cause neuropathic pain.(C) 2009 American Academy of Neurology
|
|
imaging the cns correlates of neuropathic pain.
- Barad, Meredith, Greicius, Michael, Mackey, Sean
>
Show/Hide Abstract
In recent years, there has been considerable growth in the use of imaging to understand, define, and-to a lesser extent, treat-neuropathic pain. This review seeks to summarize the newfound focus on neuroimaging and to put this research in the context of the existing definitions of neuropathic pain and the pain matrix. The research described herein is leading to an expanded definition of neuropathic pain at a time when some in the scientific community have sought to narrow the definition. The research also is helping us understand the role of central neural systems in the development, diagnosis, and treatment of chronic neuropathic pain. However, much of this early research on imaging has been based on relatively small studies and/or heterogenous patient populations, suggesting that further research needs to be done to validate them.(C) 2009 American Academy of Neurology
|
|
complex regional pain syndrome: evolving understanding of pathogenesis and implications for treament.
- Naleschinski, Dennis, Baron, Ralf
>
Show/Hide Abstract
Complex regional pain syndrome (CRPS) is clinically characterized by pain, abnormal regulation of blood flow and sweating, edema of skin and subcutaneous tissues, active and passive movement disorders, and trophic changes. It is classified as type I (reflex sympathetic dystrophy) and type II (causalgia). CRPS cannot be reduced to one system or to one mechanism only. Changes in somatosensory systems processing afferent information in sympathetic systems and in the somatomotor system indicate that the central representations are altered. Edema, inflammation, and sympathetic-afferent interaction (sympathetically maintained pain) point to peripheral abnormalities. Treatment of the individual patient is empiric, mainly using evidence-based techniques that have been proven to be effective in other neuropathic conditions. Treatment should be immediate and most importantly directed toward restoration of full function of the extremity. This objective is best attained in a comprehensive interdisciplinary setting with particular emphasis on pain management and functional restoration.(C) 2009 American Academy of Neurology
|
|
evidence-based treatment of chronic neuropathic pain using nonopioid pharmacotherapy.
- O'Connor, Alec, Dworkin, Robert
>
Show/Hide Abstract
Chronic neuropathic pain may be more challenging to treat than other forms of chronic pain. However, several nonopioid medications have demonstrated efficacy in patients with neuropathic pain. This chapter will summarize the evolving evidence base supporting nonopioid pharmacotherapy for neuropathic pain. Three classes of medications are consistently considered first-line treatments for neuropathic pain: certain antidepressants, including tricyclics, duloxetine, and venlafaxine; calcium channel [alpha]2[delta] ligands (ie, gabapentin and pregabalin); and topical lidocaine for localized, peripheral neuropathic pain. Several additional medications have been studied in neuropathic pain but have produced less favorable results. This chapter also will summarize a recommended approach to the management of patients with chronic neuropathic pain. Continuum Lifelong Learning Neurol 2009;15(5):70-83.(C) 2009 American Academy of Neurology
|
|
the role of opioid therapy in the treatment of neuropathic pain.
- Backonja, Miroslav
>
Show/Hide Abstract
Opioids have demonstrated efficacy in relieving neuropathic pain. Familiarity with the pharmacology and adverse effect profile of this class of medication is essential for its safe and optimal use, as is knowledge of the regulatory requirements related to opioid prescribing. Opioids are versatile and can be effective as part of a rational multidrug therapeutic approach. As such, they are an integral part of the multimodal and multidisciplinary treatment of neuropathic pain.(C) 2009 American Academy of Neurology
|
|
the role of interventional therapy in the treatment of neuropathic pain.
- Markman, John, Hanson, Ross
>
Show/Hide Abstract
Understanding the complementary role of interventional approaches in the treatment of chronic neuropathic pain is essential to optimizing analgesic benefit. Only a minority of patients experience both a significant reduction in pain intensity with tolerable side effects from drug therapy and behavioral approaches alone. Targeting the localized site of altered nociceptive processing along the neuraxis is a longstanding strategy adapted from the acute pain context. The myriad techniques range from reversible ion channel blockade of a peripheral nerve with a local anesthetic to continuous modulation of spinal cord signaling with electrical stimulation. The three principal domains of interventional techniques are: (1) ablation, (2) augmentation, and (3) anatomic modification. The risks and benefits must be assessed in both a condition-specific and technology-specific fashion. This chapter will also consider the improvement in therapeutic index potentially offered by neuraxial delivery of drugs through the intrathecal, epidural, and perineural routes of administration.(C) 2009 American Academy of Neurology
|
|
multimodal analgesia for chronic pain.
- Argoff, Charles, Albrecht, Phillip, Rice, Frank
>
Show/Hide Abstract
Chronic pain is a multifaceted disease requiring multimodal treatment. Clinicians frequently prescribe various combinations of pharmacologic, interventional, cognitive-behavioral, rehabilitative, and other nonmedical therapies, even in the absence of high-quality evidence in support of such an approach. Therapies are often selected consistent with the biopsychosocial model of chronic pain, reflecting the complex nature of the patient's report of pain and the myriad factors that influence it. Elucidating mechanisms that govern normal sensation in the periphery has provided insights into the biochemical, molecular, and neuroanatomic correlates of chronic pain, an understanding of which is leading increasingly to efforts to provide mechanism-specific multidrug therapies. Peripheral and central neuroplastic reorganization underlying the disease of chronic pain is influenced by patient-specific emotions, cognition, and memories, further impairing function and idiosyncratically defining the illness of chronic pain. Clinical perceptions of these and related subjective elements associated with the suffering of chronic pain drive psychosocial treatments, including, among other options, relaxation therapies, coping skills development, and cognitive-behavioral therapy. Treatment selection is thus guided by comprehensive assessment of the phenomenology and inferred pathophysiology of the pain syndrome; patient goals, preferences, and expectations; behavioral, cognitive, and physical function; and level of risk. Experiential, practice-based evidence may be necessary for improving patient care but is insufficient; well-designed studies are needed to support therapeutic decision making. This review will discuss the biochemical basis of pain, factors that govern its severity and chronicity, and foundational elements for current and emerging multimodal treatment strategies.(C) 2009 American Academy of Neurology
|
|
patient management problem.
- Walk, David
|
|
ethical perspectives in neurology.
- Russell, James
|
|
practice issues in neurology.
- Collins, Timothy
|
|
appendix a: an evidence-based guideline for clinicians: treatment of postherpetic neuralgia.
|
|
appendix b: managing a pain flare.
|
|
appendix c: brief pain inventory (short form).
|
|
appendix d: neuropathic pain questionnaire.
|
|
appendix e.
|
|
appendix f: long-term controlled substances therapy for chronic pain: sample agreement.
|
|
appendix g: consent for chronic opioid therapy.
|
|
appendix h: an evidence-based guideline for clinicians: trigeminal neuralgia.
|
|
index.
(PDF only)
|
|
Take Continuum Online CME for this issue
.
|
The AAN is accredited by the Accreditation Council for Continuing Medical Education (ACCME) to provide continuing medical
education (CME) for physicians.
The AAN designates this educational activity for a maximum of 10 American Medical Association (AMA) Physician Recognition Award
(PRA) Category 1 Credits™. Physicians should claim only those hours of credit that they actually spend in the educational activity.
Per AMA PRA guidelines, only US and licensed international physicians may be awarded AMA PRA Category 1 Credit certificates. The
AAN will issue certificates of participation to non-MD/DO health professionals indicating that the activity was designated
for AMA PRA Category 1 Credit.
The American Board of Psychiatry and Neurology has reviewed
Continuum: Lifelong Learning in Neurology® and has approved the product as part of a
comprehensive lifelong learning program, which is mandated by the American Board of Medical Specialties
as a necessary component of maintenance of certification.
Andrea Weiss
Associate Publisher, AAN Enterprises, Inc.
Managing Editor, Continuum and Quintessentials
aweiss@aan.com
(651) 695-2742
|
|