JOURNAL TRANSCRIPT

---

Consensus Panel Recommendations for the Assessment and Management of Breakthrough Pain PART 1 ASSESSMENT Daniel Bennett, MD, Allen W. Burton, MD, Scott Fishman, MD, Barr y Fortner, PhD, Bill McCarberg, MD, Chris Miaskowski, PhD, RN, David B. Nash, MD, MBA, Marco Pappagallo, MD, Richard Payne, MD, James Ray, PharmD, Eugene R. Viscusi, MD, and Winston Wong, PharmD

INTRODUCTION: DEVELOPMENT OF THE CONSENSUS PANEL RECOMMENDATIONS The consensus recommendations detailed in this article are intended to guide clinicians in the assessment and effective management of breakthrough pain (BTP). Although BTP can occur in patients with acute as well as chronic pain syndromes, these recommendations focus on BTP associated with chronic cancer-related and non–cancer-related pain, with an emphasis on pharmacological management. Several approaches were taken to survey the medical literature. PubMed, a search engine for selected peer-reviewed journal articles and which is part of the National Library of Medicine, was examined for the period from 1990 through October 2004. The search for management-related references

Breakthrough Pain Consensus Panel: Dr. Bennett is Medical Director of Integrative Treatment Centers in Denver, Colorado. Dr. Burton is Associate Professor, Section Chief of Cancer Pain Management at the University of Texas–M. D. Anderson Cancer Center in Houston, Texas. Dr. Fishman is Chief of the Division of Pain Medicine at the University of California–Davis in Sacramento, California. Dr. Fortner is Chief Operating Officer and Chief Scientific Officer of Supportive Oncology Services, Inc., in Memphis, Tennessee. Dr. McCarberg is Founder of the Chronic Pain Management Program of Kaiser Permanente in San Diego, California. Dr. Miaskowski is Professor of Physiological Nursing at the University of California–San Francisco in San Francisco, California. Dr. Nash is the Dr. Raymond C. and Doris N. Grandon Professor of Health Policy at Jefferson Medical College at Thomas Jefferson University in Philadelphia, Pennsylvania. Dr. Pappagallo is Director of the Division of Chronic Pain at Beth Israel University Hospital in New York, New York. Dr. Payne is Director and Esther Colliflower Professor at Duke University in Durham, North Carolina. Dr. Ray is Director of Pain and Palliative Care at Hamot Medical Center in Erie, Pennsylvania. Dr. Viscusi is Director of the Acute Pain Management Service in the Department of Anesthesiology at Thomas Jefferson University Hospital in Philadelphia. Dr. Wong is Director of Pharmacy Management at CareFirst Blue Cross Blue Shield in Baltimore, Maryland.

296 P&T®

• May 2005 • Vol. 30 No. 5

was initiated after all references with pain (as a major focus) and drug therapy were identified. References related to headache were excluded. All articles with the terms breakthrough or episodic or flare or incident or transient or rescue were identified. These two searches were combined to identify the references common to both. This subset was then limited to those in English and human and clinical trial or meta-analysis or practice guideline. A similar approach was also used for assessment-related references in PubMed. The Cumulative Index to Nursing & Allied Health Literature (CINAHL) database was also searched via a strategy similar to that used for PubMed. Relevant references were identified by searching guidelines and summaries from the following sources: Agency for Health Care Research and Quality Clinical Guidelines and Evidence Reports, Bandolier, Cochrane Database of Systematic Reviews, American College of Physicians (ACP) Journal Club, Database of Abstracts of Reviews of Effects, Cochrane Central Register of Controlled Trials, Institute for Clinical Systems Improvement, National Guideline Clearinghouse, and U.S. Preventive Services Task Force. The abstract of each reference was reviewed; if the abstract was considered potentially relevant, the complete reference was obtained and reviewed in detail. The Consensus Panel members, who provided recommendations based on the review of the literature and their experience in pain management, prepared and evaluated a summary of each reference as it related to BTP. Two teleconferences were held on September 30, 2004, and November 5, 2004, to discuss the scope of the project and to search for terms and key words, definitions, outlines, sections, and subsections, par ticularly the assessment and management of BTP. From these findings, the Consensus Panel developed and subsequently reviewed a draft of the manuscript prior to the live meeting on December 4, 2004, in Orlando, Florida. During the live meeting, the Expert Panel achieved consensus recommendations for the assessment and management of BTP. This article was based on two teleconferences and a live Consensus Panel meeting held on December 4, 2004, in Orlando, Florida, and was supported by an educational grant from Cephalon, Inc.

Breakthrough Pain: Assessment Case Study: T. G. T. G. is a 62-year-old woman with stage IV breast cancer. A recent bone scan has demonstrated several new metastatic bone lesions. On physical examination, the most painful area is her right hip and anterior thigh.This pain is worsened with any weight-bearing activities such as standing and walking. She is being referred to radiation oncology to receive external beam radiation for pain control and to prevent a possible pathological fracture. Her current pain medication is oral sustained-release morphine sulfate 90 mg every 12 hours, which she has been taking for the past six months.

BACKGROUND This case represents a common scenario seen in clinical practice. Almost 50% of all Americans seek medical care each year for pain, making pain the single most frequent reason for a physician consultation in the U.S.1,2 Pain is inadequately controlled in many of these patients. In some patients such as T. G., the pain that was established at the baseline examination persists, affecting her quality of life and functioning, often even with drug therapy. Furthermore, such patients also experience BTP, which affects 19% to 95% of all patients with pain, depending on the population surveyed and the definition of BTP used.3–11 Despite the considerable variability in how BTP is defined, it is clear that BTP is associated with significant patient morbidity, including decreased functioning10,12,13 and increased levels of depression and anxiety.12,13 BTP may also predict a poor medical outcome.3,4,14–16 It is associated with lower patient satisfaction with opioid therapy9,15 and significantly increased utilization of health care compared with patients without BTP.6 BTP is a major component of the public health problem related to the undertreatment of pain, which has become a national quality-of-care issue and is a priority concern of the Agency for Healthcare Research and Quality.17 To help address this situation, we present this two-part series to emphasize the importance of BTP as a clinical entity.

Part 1 describes the definition, clinical spectrum, and assessment of BTP. Part 2 focuses on the management of BTP.

TERMINOLOGY “Breakthrough,” “episodic,” “incidental,” and “transient” pain are some of the terms most commonly used to refer to the pain flares that occur beyond baseline persistent pain. Complicating matters is the fact that no widely accepted definition exists for any of these terms; in fact, several definitions of BTP have been proposed.7,18–22 To be practical, we chose to use the term “breakthrough” pain and have defined it as a transient exacerbation of pain that occurs in patients with otherwise stable, baseline persistent pain. This definition requires the presence of baseline persistent pain and stresses the importance of worsening pain intensity and a transient profile. Although baseline persistent pain might result from an acute pain syndrome, our consensus recommendations relate to persistent chronic pain. The chronic pain may be either cancer-related or non–cancer-related in origin (e.g., arthritis, low back pain, or diabetic neuropathy). Although most of the research on BTP has focused on patients with cancer, we and others believe the limited evidence suggesting that non–cancer-related BTP shares many common features with cancer-related BTP.23 Consequently, we have developed these consensus recommendations to include both cancer-related BTP and non–cancer-related BTP and have based our recommendations on the results of clinical trials and our collective clinical experience. BTP and baseline persistent pain generally share the same etiologic mechanism, but this is not always the case. Furthermore, from our definition, baseline persistent pain must be stable, because unstable baseline persistent pain suggests the need for more aggressive around-the-clock management, which differs from BTP management. Finally, the pharmacological management of baseline persistent pain typically consists of around-the-clock analgesics, and usually an opioid, but the analgesic treatment of baseline persistent pain is not required to satisfy our definition of BTP. Three subtypes of BTP have been defined: (1) incident pain, (2) idiopathic pain, and (3) end-of-dose pain (Table 1).

Table 1 Subtypes of Breakthrough Pain (BTP) Characteristics

Usual Management

Incident, predictable

Consistent temporal causal relationship with predictable motor activity, such as movement, defecation, micturition, breathing, or coughing

Immediate-release opioid, acetaminophen, tramadol on an as-needed basis prophylactically; rest; ice; patient education

Incident, unpredictable

Inconsistent temporal causal relationship with motor activity, such as sneezing, bladder spasm, or coughing

Immediate-release opioid on an as-needed basis

Idiopathic

Not associated with a known cause; generally of longer duration than incident pain

Immediate-release opioid on an as-needed basis

End-of-dose

Occurring before a scheduled dose of an aroundthe-clock analgesic; more gradual onset and longer duration than incident or idiopathic BTP

Increase in dose and/or frequency of around-theclock analgesia

Vol. 30 No. 5 • May 2005 •

P&T® 297

Breakthrough Pain: Assessment Incident pain (pain with activity or movement) appears to be somewhat more common than idiopathic or end-of-dose pain.5,7,11,12,24 Most causes of incident pain are predictable and are relatively responsive to pretreatment with pharmacological therapy or other treatments. Unpredictable incident pain (pain occurring spontaneously) is less responsive to pharmacological therapy because of its rapid escalation and its inability to be pretreated.15,16 Idiopathic pain is not associated with any known cause. Pain that rapidly intensifies is sometimes called crescendo pain. Idiopathic pain generally lasts longer than incident pain.11 Idiopathic BTP that worsens in a patient with cancer often suggests progressive disease, because analgesic tolerance is not generally the cause of progressive pain.25 End-of-dose pain occurs before a scheduled dose of an around-the-clock analgesic.7,12 Characteristically, this form of pain has a more gradual onset of intensity and a longer duration than the other types of BTP. Because end-of-dose pain occurs as a result of an inadequate dose of analgesic or a dosing interval that is too long, the analgesic regimen used to treat baseline persistent pain should be reassessed and modified as necessary.

the same as that of the baseline persistent pain.12 Neuropathic BTP (e.g., postherpetic neuralgia, reflex sympathetic dystrophy) is often of shorter duration, but it occurs more frequently than nociceptive BTP (e.g., sprains, fractures, bruises, burns, inflammation).9,28 Approximately 50% of BTP episodes are incident in nature.

ASSESSMENT The assessment of pain begins with an attempt to find a correctable cause of BTP, such as an unrecognized vertebral compression fracture. The pain must be thoroughly assessed and the pattern must be understood as much as possible so that baseline persistent pain can be differentiated from BTP. Because the management of each type of pain differs significantly from the other, the dual focus of the pain assessment is an important determinant of effective long-term pain management. Case Study (continued) T. G. is having difficulty sleeping at night and has been experiencing at least two or three episodes of waking resulting from pain. The patient is the best source of information about BTP. The most important step a clinician can take is to ask the patient specific questions about BTP. Because some patients might not understand the term “breakthrough pain,” it may be helpful to initiate the discussion by asking the patient to describe a recent episode of severe pain.

Case Study (continued) T. G. has predictable, severe incident BTP upon any movement from a supine position or with attempts at ambulation. Sometimes she also has idiopathic BTP. She has begun experiencing sharp, shooting pains in her right hip and down her leg, which seem to have no specific precipitating cause. BTP encompasses a wide spectrum of characteristics, with no apparent significant differences between cancer-related and non–cancer-related BTP (Table 2).26,27 Typically, the onset of BTP is abrupt, with a time to peak pain severity of 3 to 5 minutes, and then resolving within 15 to 30 minutes. Patients with baseline persistent pain often have a higher median peak pain level and a longer duration of BTP than people without baseline persistent pain.5,10,12,24 Several episodes of BTP can occur on a daily basis; more than four episodes per day may warrant reassessment of the cause as well as the approach to management of the baseline persistent pain. The cause of the BTP is often, but not always,

Case Study (continued) To facilitate the discussion with T. G., the clinician should ask various questions to establish the presence (or absence) of BTP and its characteristics (Table 3).29 It is important to know the duration and intensity, as well as the onset, of BTP in selecting the appropriate pharmacological option and the route of administration for treating BTP (see Part 2 in the forthcoming June issue of P&T). Similarly, knowing the character, location, and pathophysiology of the BTP helps to differentiate the causes of nociceptive, neuropathic, and mixed pain (e.g., migraine), which can affect the choice of an analgesic or adjuvant analgesic. Understanding the

Table 2 Characteristics of Breakthrough Pain Average

Range

Time to peak severity

3–5 minutes

10 seconds to 180 minutes

Severity

Severe or excruciating

Mild to excruciating

Duration

15–30 minutes

1 second to more than 24 hours

Number of episodes per day

1–5

Less than 1 to 3,600

Precipitated by event

55%–60%

52%–77%

Predictable

50%–60%

41%–81%

Data from references 5–11, 18, 24, 26, and 27.

298 P&T®

• May 2005 • Vol. 30 No. 5

Breakthrough Pain: Assessment The presence of end-of-dose pain should generally lead to a reassessment of the etiology and the management of the baseline persistent pain. For incident pain, the use of an analgesic or an ad• Do you have episodes of severe pain or BTP? juvant analgesic with a slower onset, taken in ad• How many episodes of BTP do you have each week? Each day? vance of the pain-provoking event, may be possi• How long is it from the time the pain first occurs to when the pain is at ble. Similarly, preventive measures are its worst? sometimes helpful, especially when the pain is • How long does each episode of BTP last (minutes, hours)? caused by predictable precipitating factors. For • On a scale of 0 to 10, with 0 being no pain and 10 being the worst pain example, cough-induced BTP that results from alyou can imagine, how much does an episode of BTP hurt when it occurs? lergic rhinitis should be aggressively managed • Describe where the BTP occurs.What does it feels like? with antiallergy therapies, such as nasal steroids • Is the BTP similar to or different from your baseline persistent pain? and antihistamines. • Does your BTP occur with movement or other activity, spontaneously In addition to the history and physical exami(not associated with any activity), or just before you are supposed to nation, computed tomography or magnetic resotake your next dose of pain medicine? nance imaging may be helpful in providing a de• What impact does the BTP have on your daily responsibilities at tailed assessment of the ner vous system and home/work? Are you able to do the things that you want/need to do? soft-tissue structures. However, because these • Are there any things that you avoid doing or that you are able to do only imaging studies do not provide information about with severe pain? the functional status of the structure or its role in • What do you do to relieve the BTP? the pain syndrome, these findings must be care• What types of treatments have you used? How long did you use them? fully evaluated. Were they effective? Are they still effective? Several assessment tools have been used to • What drugs have you used to relieve the BTP? What were the doses? evaluate BTP, although none has been validated Were they effective? Are they still effective? for this type of pain. Because the patient is the best source of information, assessment tools that quantify the patient’s perception of pain may be the most useful. impact of BTP on the patient’s functional status and quality of life is especially important in determining the goals of treatUnidimensional instruments such as the Numerical Ratment because complete resolution of BTP is rarely possible. ing Scale, the Visual Analogue Scale, and the Wong-Baker The clinician should identify the source as well as the subFACES Pain Rating Scale, may be helpful. The Wong-Baker type of BTP, which will help determine the appropriate pharScale (Figure 1) is suitable for patients of all ages (except macological and nonpharmacological management options the very young), for those of all cultures, and for those who (see Table 2, Part 2, in the forthcoming June issue of P&T). are cognitively impaired. A shortcoming of these and simCorrective measures, such as bracing, vertebroplasty, and ilar unidimensional scales is that they assess only pain radiation therapy, should be implemented as appropriate. severity.

Table 3 Assessing the Presence of Breakthrough Pain (BTP)

Explain to the person that each face is for a person who feels happy because he has no pain (hurt) or sad because he has some or a lot of pain. Face 0 is very happy because he doesn’t hurt at all. Face 1 hurts just a little bit. Face 2 hurts a little more. Face 3 hurts even more. Face 4 hurts a whole lot. Face 5 hurts as much as you can imagine, although you don’t have to be crying to feel this bad. Ask the person to choose the face that best describes how he is feeling. The rating scale is recommended for persons age 3 and older. Brief word instructions: Point to each face using the words to describe the pain intensity. Ask the child to choose the face that best describes own pain and record the appropriate number.

Figure 1 Wong-Baker FACES Pain Rating Scale. (From Wong DL, Hockenberry-Eaton M,Wilson D, et al. Wong’s Essentials of Pediatric Nursing, 6th ed. St. Louis: Mosby, 2001:31. Courtesy of Elsevier.)

Vol. 30 No. 5 • May 2005 •

P&T® 299

Breakthrough Pain: Assessment

Figure 2 Pain diary. (From the American Pain Foundation. Available at: www.painfoundation.org/downloads/Notebook.pdf.31)

Multidimensional scales, such as the Brief Pain Inventory, may be more useful because they characterize BTP more extensively; however, they are time-consuming and a health care provider must usually be involved for their completion.30 A pain diary, in contrast, can be used to collect multidimensional information and is designed for completion by the patient over the course of a day or longer. Consequently, a patient’s pain diary is probably more reliable than memory for accurately reflecting the pattern of symptoms in relation to activities and other variables. The diary is useful both in the initial patient evaluation and as an ongoing guide to modify treatment. Figure 2 shows a sample of a completed pain diary, developed by the American Pain Foundation.31 A blank copy of a pain diary is available at the Foundation’s Web site (www.painfoundation.org). A disadvantage of this diary is the time necessary to interpret the relatively large amount of information. Following initiation or changes in the management of BTP, particularly with an opioid, it is critical that the patient be reassessed using the “four A’s” of chronic pain medicine: (1) analgesia, (2) activities of daily living, (3) adverse events, and (4) aberrant drug-related behavior.32 In addition to the tools used in the initial assessment of BTP, the Pain Assessment and Documentation Tool, developed by the National Pain Education Council, may be helpful in guiding further changes to therapy.

300 P&T®

• May 2005 • Vol. 30 No. 5

Case Study (continued) An assessment of T. G.’s pain reveals that her baseline persistent pain, especially at night, is not being adequately controlled. Her pain intensity upon waking from sleep is a 5 or 6 (on a scale of 1 to 10) during the night. She has great difficulty returning to sleep because of the pain. She has not demonstrated any morphine-related adverse drug effects, so the choice is made to schedule her evening dose of morphine closer to her bedtime and to increase the dose to 120 mg.The morning dose is continued at 90 mg. T. G. says that her pain increases to 8 or 9 (on a scale of 1 to 10) whenever she tries to walk.This is especially difficult for her when she is trying to prepare a meal. She also experiences intense sharp, shooting pains three or four times a day while sitting and not moving (e.g., while she is reading or watching television).This pain becomes severe within a matter of minutes and lasts for 10 to 15 minutes; sometimes it lasts as long as 45 minutes. Both types of BTP are related to her baseline persistent pain. T. G.’s pain-management plan must address the predictable incident BTP with movement as well as the idiopathic BTP that has no precipitating cause.

Breakthrough Pain: Assessment REFERENCES 1. Gureje O, Von Korff M, Simon GE, Gater R. Persistent pain and well-being: A World Health Organization Study in Primary Care. JAMA 1998;280(2):147–151. 2. Abbott FV, Fraser MI. Use and abuse of over-the-counter analgesic agents. J Psychiatry Neurosci 1998;23(1):13–34. 3. Ashby MA, Fleming BG, Brooksbank M, et al. Description of a mechanistic approach to pain management in advanced cancer: Preliminary report. Pain 1992;51(2):153–161. 4. Bruera E, Fainsinger R, MacEachern T, Hanson J. The use of methylphenidate in patients with incident cancer pain receiving regular opiates: A preliminary report. Pain 1992;50(1):75–77. 5. Swanwick M, Haworth M, Lennard RF. The prevalence of episodic pain in cancer: A survey of hospice patients on admission. Palliat Med 2001;15(1):9–18. 6. Fortner BV, Okon TA, Portenoy RK. A survey of pain-related hospitalizations, emergency department visits, and physician office visits reported by cancer patients with and without history of breakthrough pain. J Pain 2002;3(1):38–44. 7. Portenoy RK, Hagen NA. Breakthrough pain: Definition, prevalence and characteristics. Pain 1990;41(3):273–281. 8. Zeppetella G, O’Doherty CA, Collins S. Prevalence and characteristics of breakthrough pain in patients with non-malignant terminal disease admitted to a hospice. Palliat Med 2001;15(3):243–246. 9. Zeppetella G, O’Doherty CA, Collins S. Prevalence and characteristics of breakthrough pain in cancer patients admitted to a hospice. J Pain Symptom Manage 2000;20(2):87–92. 10. Caraceni A, Martini C, Zecca E, et al. Breakthrough pain characteristics and syndromes in patients with cancer pain: An international survey. Palliat Med 2004;18(3):177–183. 11. Gomez-Batiste X, Madrid F, Moreno F, et al. Breakthrough cancer pain: Prevalence and characteristics in patients in Catalonia, Spain. J Pain Symptom Manage 2002;24(1):45–52. 12. Portenoy RK, Payne D, Jacobsen P. Breakthrough pain: Characteristics and impact in patients with cancer pain. Pain 1999; 81(1–2):129–134. 13. Bruns D, Bennett DS, Simon S, et al. Degree of pain intolerance and adverse outcomes in chronic noncancer pain patients. Presented at the American Pain Society annual meeting, Boston, March 30–April 2, 2005. 14. Mercadante S, Armata M, Salvaggio L. Pain characteristics of advanced lung cancer patients referred to a palliative care service. Pain 1994;59(1):141–145. 15. Mercadante S, Maddaloni S, Roccella S, Salvaggio L. Predictive factors in advanced cancer pain treated only by analgesics. Pain 1992;50(2):151–155. 16. Bruera E, Schoeller T, Wenk R, et al. A prospective multicenter assessment of the Edmonton staging system for cancer pain. J Pain Symptom Manage 1995;10(5):348–355. 17. Agency for Healthcare Research and Quality. Priority areas for national action. Transforming health care quality. Available at: www.ahrq.gov/qual/iompriorities.htm#FinalList. Accessed December 28, 2004. 18. Fine PG, Busch MA. Characterization of breakthrough pain by hospice patients and their caregivers. J Pain Symptom Manage 1998;16(3):179–183. 19. National Comprehensive Cancer Network and American Cancer Society. Cancer pain. Treatment guidelines for patients. Version 1. Available at: www.nccn.org/patients/patient_gls/_english/pdf. Accessed November 12, 2004. 20. Roth SH. Efficacy and safety of tramadol HCl in breakthrough musculoskeletal pain attributed to osteoarthritis. J Rheumatol 1998;25(7):1358–1363. 21. Portenoy RK. Treatment of temporal variations in chronic cancer pain. Semin Oncol 1997;24(5 Suppl 16):S16-7–S16-12. 22. U.S. National Institutes of Health. National Cancer Institute. Pain (PDQ). Available at: www.nci.nih.gov/cancer topics/pdq/ supportivecare/pain/healthprofessional. Accessed November 12, 2004. 23. Svendsen KB, Andersen S, Arnason S, et al. Breakthrough pain in malignant and non-malignant diseases: A review of prevalence, characteristics and mechanisms. Eur J Pain 2005;9(2):195–206.

24. Hwang SS, Chang VT, Kasimis B. Cancer breakthrough pain characteristics and responses to treatment at a VA medical center. Pain 2003;101(1–2):55–64. 25. Coluzzi PH. Oral patient-controlled analgesia. Semin Oncol 1997; 24(5 Suppl 16):S16–S42. 26. Portenoy RK, Bennett DS, Simon S, et al. Prevalence and characteristics of breakthrough pain in patients with chronic noncancer pain. Presented at the American Pain Society annual meeting, Boston, March 30–April 2, 2005. 27. Bennett DS, Simon S, Rauck R, et al. Prevalence and characteristics of breakthrough pain in noncancer patients with chronic back pain. Presented at the American Academy of Pain Management annual meeting, Palm Springs, Calif., February 23–27, 2005. 28. Petzke F, Radbruch L, Zech D, et al. Temporal presentation of chronic cancer pain: Transitory pains on admission to a multidisciplinary pain clinic. J Pain Symptom Manage 1999;17(6):391– 401. 29. Miaskowski C, Cleary J, Burney R, et al. Guidelines for the Management of Cancer Pain in Adults and Children. American Pain Society Clinical Practice Guidelines Series, No. 3. Glenview, IL: American Pain Society; 2004. 30. Goodwin J, Bajwa ZH. Evaluating the patient with chronic pain. In: Warfield CA, Bajwa ZH, eds. Principles and Practice of Pain Medicine, 2nd ed. New York: McGraw-Hill; 2004:61–68. 31. American Pain Foundation. Pain notebook. Available at: www. pain foundation.org/downloads/Notebook.pdf. Accessed November 18, 2004. 32. National Pain Education Council. Pain assessment and documentation tool and guidebook. Available at: www.npecweb.org. Accessed December 17, 2004.

Disclosure Dr. Bennett reports no relationships with respect to his participation in this project. Dr. Burton reports that he receives Research Support from Elan, Celgene, and Glaxo; he is on the Speakers’ Bureau of and has been a Consultant for Medtronic, Inc., and Merck. Dr. Fishman reports the following relationships: Consultant for, Speakers’ Bureau of, and Grants/Research Support from Endo, Janssen, Merck, Pfizer, and Purdue Pharma. Dr. Fortner reports no relationships with respect to his participation in this project. Dr. McCarberg reports that he is on the Speakers’ Bureau of Endo, Janssen, Ligand, Ortho-McNeil, Pfizer, and Purdue Pharma. Dr. Miaskowski reports the following relationships: Cephalon: Chair of Nursing Advisory Board; Endo: Speakers’ Bureau, Research Support; Janssen: Advisory Board, Research Support; Merck: Advisory Board; and Purdue Pharma: Advisory Board, Research Support. Dr. Nash reports the following relationships: Research Grants from Aventis, GlaxoSmithKline, Janssen, Johnson & Johnson, Merck, and Pfizer. Dr. Pappagallo reports the following relationships: Research Grants from GlaxoSmithKline and the National Institutes of Health; Consultant, Algorx, Cephalon, Endo, GlaxoSmithKline, National Institutes of Health, and Pfizer. Dr. Payne reports the following relationships: Consultant for AstraZeneca, Eisai, Elan, Endo, Ionix, Janssen, Johnson & Johnson, Merck, Pfizer, Purdue Pharma, Rinat,TheraQuest, and Xanodyne; Speakers’ Bureau of Janssen and Purdue; and Major Shareholder of Rinat and Xanodyne. Dr. Ray reports the following relationships: Consultant for Pharmacia/Pfizer; Speakers’ Bureau for Purdue and Janssen. Dr. Viscusi reports the following relationships: Honorarium: Cephalon; Advisory Boards: Alza, Endo, Ortho-McNeil, and Skye Pharma; Grants: Adolor, Alza, Bristol-Myers Squibb, Endo, OrthoMcNeil, Progenics, and Skye Pharma; Speakers’ Bureau: B. Braun and Pfizer. Dr. Wong reports that he has no relationships with respect to his participation in this project.

Vol. 30 No. 5 • May 2005 •

P&T® 301