Advocacy

Pediatric Chronic Pain

A Position Statement from the American Pain Society

Significance of the problem

Chronic pain is a significant problem in the pediatric population, conservatively estimated to affect 15% to 20% of children (Goodman & McGrath, 1991). Children* and their families experience significant emotional and social consequences as a result of pain and disability. The financial costs of childhood pain also may be significant in terms of healthcare utilization as well as other indirect costs, such as lost wages due to time off work to care for the child (Li & Balint, in press). In addition, the physical and psychological sequelae associated with chronic pain may have an impact on overall health and may predispose for the development of adult chronic pain (Campo et al., 1999; Walker, Garber, Van Slyke, & Greene, 1995).

* This term refers to all individuals in the pediatric age range (i.e., neonates, infants, and adolescents).

Definition of chronic pain

Acute pain follows injury to the body and generally disappears when the bodily injury heals. It is often, but not always, associated with objective physical signs of autonomic nervous system activity. Chronic pain, in contrast to acute pain, rarely is accompanied by signs of sympathetic nervous system arousal. The lack of objective signs may prompt the inexperienced clinician to say the patient does not "look" like he or she is in pain. (American Pain Society, 1999, p. 4)

Chronic pain can be differentiated from acute pain in that acute pain signals a specific nociceptive event and is self-limited. Chronic pain may begin as acute pain, but it continues beyond the normal time expected for resolution of the problem or persists or recurs for other reasons.

Chronic pain in children is the result of a dynamic integration of biological processes, psychological factors, and sociocultural context, considered within a developmental trajectory. This category of pain includes persistent (ongoing) and recurrent (episodic) pain with possible fluctuations in severity, quality, regularity, and predictability. Chronic pain can occur in single or multiple body regions and can involve single or multiple organ systems. Ongoing nociception can result in a sensitization of the peripheral and central nervous systems to produce neuroanatomical, neurochemical, and neurophysiological changes. It is important that assessment and treatment strategies be based on this definition and related dimensions.

To evaluate and treat chronic childhood pain efficiently and effectively, the mind-body dualism must be abandoned. It is meaningless to dichotomize chronic pain as organic versus nonorganic, because all pain is associated with, at minimum, neurosensory changes. Maintaining this dichotomy is harmful because such faulty thinking leads to over-medicalization (inappropriate investigations, procedures, and interventions) or insufficient acknowledgment of the child's multidimensional experience and underlying neurophysiology.

The International Association for the Study of Pain (IASP) characterized chronic pain as less than 1 month, 1 to 6 months, and greater than 6 months (Task Force on Taxonomy, 1994). Formerly chronic pain was defined as having pain for longer than 6 months. It is now recognized that key elements of chronic pain can be evident much earlier. Definitions also are influenced by developmental factors. For example, recurrent migraine headache that lasts 1 hour in a 4-year-old is typical, whereas headache of this length in adolescents would not likely be classified as a migraine.

Chronic pain may include varying amounts of disability, from none to severe, and may be independent of the amount of tissue damage and perceived severity (Melzack & Wall, 1965). Biological, psychological, social, cultural, and developmental factors can impact pain-related functioning.

Assessment

An evaluation of a child with chronic pain should include consideration of the biological, psychological, and sociocultural factors in a developmental context (Bursch, Walco, & Zeltzer, 1998).

The evaluation should begin with a history of the current problem, including a careful description of the pain, detailing the sensory characteristics, intensity, quality, location, duration, variability, predictability, exacerbating and alleviating factors, and impact of pain on daily life (e.g., sleeping, eating, school, social and physical activities, family and peer interactions). The history, evaluation, and treatment of the current pain problem in terms of its onset and development should be detailed. Inquiry should include the magnitude of distress for the child and family attributed to the pain, and the impact of the pain on cognitive functioning, anxiety, depression, and feelings of hopelessness. Assessment also should include what the child and family members perceive as the cause of the pain and how they respond to it. History of past pain problems in the child and in other family members also should be elicited. A review with the family of current treatments for the pain should include inquiry about home remedies and alternative and complementary therapies (Zeltzer, Bush, Chen, & Riveral, 1997a, 1997b).

In addition to the pain history, a typical pediatric history should include medical-surgical history, birth and early childhood history, developmental milestones, social history (i.e., school, friends, interests), and family medical and social history. Particular attention should be paid to recent stressful events, such as deaths, marital disruption, moves, and other changes in life circumstances (e.g., new school).

The physical examination will vary depending on previous assessments the child has undergone and the specific symptoms. However, the physical examination always should include observation of the child's general appearance, posture, gait, and emotional and cognitive state. Muscle spasms, trigger points, and areas of somatic sensitivity to light touch should be assessed. Vital signs should include height, weight, blood pressure, heart rate, respiratory rate, and temperature. A complete neurological examination should be conducted. It can be helpful to examine the painful area(s) multiple times during the examination. Somatic pain may be elicited when the child tenses his or her muscles due to fear of the examination. It is common for children with chronic pain to develop secondary myofascial pain because of abnormal body posturing and prolonged inactivity. It is helpful to remember that visceral pain, because of its afferent pathways, may be referred to as somatic dermatomes. If significant findings that have not been previously addressed are identified, referral to the appropriate subspecialist is indicated for more thorough evaluation.

Treatment

Treatment strategies should be based on the findings of the assessment and should address the inciting and contributing factors. A multimodal approach often is more effective than a single sequential treatment approach. This approach includes specific treatment targeting possible underlying pain mechanisms, as well as symptom-focused management addressing pain, sleep disturbance, anxiety, or depressive feelings. For example, a treatment approach for a child with a recalcitrant myofascial shoulder pain might include amitriptyline for facilitating sleep, transcutaneous electrical nerve stimulation (TENS), biofeedback, and massage for pain. Treatment also should address pain-related disability with the goal of maximizing functioning and improving quality of life. For example, partial or complete return to school should often be an early target of treatment for children with pain-related school absenteeism.

Treatment techniques include education about the pain experience and the pain problem, cognitive-behavioral (e.g., self-regulatory behaviors such as hypnosis or biofeedback) strategies, behavioral techniques (e.g., reinforcement), family interventions, physical interventions (e.g., massage, acupuncture, TENS, physical therapy, occupational therapy), and systemic and regional pharmacological interventions (e.g., opioid and non-opioid analgesics, anesthetics, anxiolytics, antidepressants, anticonvulsants, hypnotics, alpha-adrenergic blockers, etc.). Whenever possible, oral routes for medication are preferable. Referral to a pediatric pain program should be considered for children with complex or refractory problems.

Evidence-based treatments should be used whenever available. For example, in adolescent migraine headache, cognitive behavioral interventions have better evidence for efficacy than triptans (Hermann, Kim, & Blanchard, 1995), and ibuprofen seems to be more effective than acetaminophen (Hamalainen, Hoppu, Valkeila, & Santavuori, 1997). Most of the currently employed pharmacological strategies are extrapolated from adult trials without evidence of efficacy in children. Controlled trials are needed to address safety and efficacy in this population.

Specific pain conditions and treatments

Although the previously mentioned treatment strategies apply to all children with chronic pain, more detailed discussion can be found in the references organized by topic at the end of this document.

Education

Pain management should be part of the educational curriculum of all health professionals who care for children. For example, assessment and management of chronic pain in children should be a mandatory part of pediatric residency. Multidisciplinary pediatric pain programs are a particularly valuable resource for this training.

Education of the public will increase community awareness, support of children with chronic pain, and shape appropriate public policy. Mass media coverage of chronic pain in children should be promoted (Kuttner, 1996; McGrath, Finley, & Turner, 1992). School staff may benefit from education to facilitate reintegration and support of children with chronic pain in the classroom.

Research

More research is needed to provide evidence-based treatments in chronic pediatric pain. Targeted government and private funding for research in pediatric chronic pain should be augmented. Such funding would not only benefit children with pain and their families, but also would be relevant, in the long term, for reducing the enormous costs of adult chronic pain (Walco & Harkins, 1999). The treatment of chronic pediatric pain would benefit from the development and support of cooperative pediatric chronic pain research consortia.

Examples of key scientific areas that need to be developed include epidemiology, nosology, clinical science (including clinical trials), developmental neurobiology, health services research, sociocultural studies, developmental pharmacology, the developmental psychology of pediatric pain, and the relationship between pediatric and adult chronic pain.

Clinical studies should include detailed attention to definition of populations, measurement of pain and distress, documentation of interventions, family factors, culture, gender, and developmental variables such as pubertal status and cognitive function. Outcome variables should be broad and include measures of pain and distress, function, quality of life, and healthcare utilization.

Policy

Children with chronic pain should have access to appropriate services, and children with complex or refractory chronic pain should be referred directly to pediatric pain programs when possible. Many pain approaches validated on adults that lack a developmental and family focus may be inappropriate or even potentially harmful for children with chronic pain.

Reimbursement policies should reflect the multidisciplinary complexity and efforts required to assess and treat children with chronic pain. Comprehensive, integrated treatment of medical, psychological, and social factors may be the most cost-effective approach in the treatment of complex and refractory pediatric pain problems.

References

American Pain Society. (1999). Principles of analgesic use in the treatment of acute pain and cancer pain (4th ed.). Glenview, IL: Author.

Bursch, B., Walco, G.A., & Zeltzer, L. (1998). Clinical assessment and management of chronic pain and pain-associated disability syndrome. Journal of Developmental and Behavioral Pediatrics, 19, 45–53.

Campo, J.V., Di Lorenzo, C., Bridge, J., Chiappetta, L., Colborn, D.K., Gartner, J.C., Gaffney, P., Kocoshis, S., & Brent, D. (1999). Adult outcomes of recurrent abdominal pain: Preliminary results. Orlando, FL: American Gastroenterological Association.

Goodman, J.E., & McGrath, P.J. (1991). The epidemiology of pain in children and adolescents: A review. Pain, 46, 247–264.

Hamalainen, M.L., Hoppu, K., Valkeila, E., & Santavuori, P.R. (1997). Ibuprofen or acetaminophen for the acute treatment of migraine in children: A double-blind, randomized, placebo-controlled, crossover study. Neurology, 48, 103–107.

Hermann, C., Kim, M., & Blanchard, E.B. (1995). Behavioral and prophylactic pharmacological intervention studies of pediatric migraine: An exploratory meta-analysis. Pain, 60, 239–255.

Kuttner, L. (1996). A child in pain: How to help, what to do. Point Roberts, WA: Hartly & Marks Publishers.

Li, B., & Balint, J.P. (in press). Cyclic vomiting syndrome: The evolution of understanding of a brain-gut disorder. Advances in Pediatrics.

McGrath, P.J., Finley, G.A., & Turner, C.J. (1992). Making cancer less painful: A handbook for parents. Halifax, NS, Canada: IWK Hospital for Children.

Melzack, R., & Wall, P.D. (1965). Pain mechanisms: A new theory. Science, 150, 971–979.

Task Force on Taxonomy. (1994). Classification of chronic pain: Descriptions of chronic pain syndromes and definitions of pain terms. Seattle: IASP Press.

Walco, G.A., & Harkins, S. (1999). Life-span developmental approaches to pain. In R.J. Gatchel & D.C. Turk (Eds.), Psychosocial factors in pain: Critical perspectives (pp. 107–117). New York: Guilford Publications.

Walker, L.S., Garber, J., Van Slyke, D.A., & Greene, J.W. (1995). Long-term health outcomes in patients with recurrent abdominal pain. Journal of Pediatric Psychology, 20, 233–245.

Zeltzer, L.K., Bush, J.P., Chen, E., & Riveral, A. (1997a). A psychobiologic approach to pediatric pain: Part I. History, physiology, and assessment strategies. Current Problems in Pediatrics, 27, 223–253.

Zeltzer, L.K., Bush, J.P., Chen, E., & Riveral, A. (1997b). Psychobiologic approach to pediatric pain: Part II. Prevention and treatment. Current Problems in Pediatrics, 27, 263–284.

Further Reading

Assessment/measurement

Finley, G.A., & McGrath, P.J. (1998). Measurement of pain in infants and children. Progress in pain research and management (Vol. 10). Seattle: IASP Press.

McGrath, P.J., Rosmus, C., Camfield, C., Campbell, M.A., & Hennigar, A. (1998). Behaviours caregivers use to determine pain in non-verbal, cognitively impaired individuals. Developmental Medicine and Child Neurology, 40, 340–343.

Burns

Sheridan, R.L., Hinson, M., Nackel, A., Blaquiere, M., Daley, W., Querzoli, B., Spezzafaro, J., Lybarger, P., Martyn, J., Szyfelbein, S., & Tompkins, R. (1997). Development of a pediatric burn pain and anxiety management program. Journal of Burn Care & Rehabilitation, 18, 455–459; discussion 453–454.

Cancer

American Academy of Pediatrics. (1990). Report of the subcommittee on disease-related pain in childhood cancer. Pediatrics, 86, 818–825.

Collins, J.J., Grier, H.E., Kinney, H.C., & Berde, C.B. (1995). Control of severe pain in children with terminal malignancy. Journal of Pediatrics, 126, 653–657.

Steif, B.L., & Heiligenstein, E,L. (1989). Psychiatric symptoms of pediatric cancer pain. Journal of Pain & Symptom Management, 4, 191–196.

Tao, M., Zeltzer, P.M., & Zeltzer, L.K. (in press). Cancer: Children and survivors. In M. Green, R.J. Haggerty, & M. Weitzman (Eds.), Ambulatory pediatrics (5th ed.). Philadelphia: W.B. Saunders Co.

Zeltzer, L.K. (1994). Pain and symptom management. In D. Bearison & R. Mulhern (Eds.), Pediatric psychooncology: Psychological research in children with cancer (pp. 61–83). New York: Oxford University Press.

Chronic fatigue syndrome

Krilov, L.R., Fisher, M., Friedman, S.B., Reitman, D., Mandel, F.S. (1998). Course and outcome of chronic fatigue in children and adolescents. Pediatrics, 102, 360–366.

Marshall, G.S. (1999). Report of a workshop on the epidemiology, natural history, and pathogenesis of chronic fatigue syndrome in adolescents. Journal of Pediatrics, 134, 395–405.

Fibromyalgia

Bennett, R.M. (1999). Emerging concepts in the neurobiology of chronic pain: Evidence of abnormal sensory processing in fibromyalgia. Mayo Clinic Proceedings, 74, 385–398.

Mikkelsson, M. (1999). One year outcome of preadolescents with fibromyalgia. Journal of Rheumatology, 26, 674–682.

Schanberg, L.E., Keefe, F.J., Lefebvre, J.C., Kredich, D.W., & Gil, K.M. (1998). Social context of pain in children with juvenile primary fibromyalgia syndrome: Parental pain history and family environment. Clinical Journal of Pain, 14, 107–115.

Siegel, D.M., Janeway, D., & Baum, J. (1998). Fibromyalgia syndrome in children and adolescents: Clinical features at presentation and status at follow-up. Pediatrics, 101, 377–382.

General

Barr, R.G., Boyce, T., & Zeltzer, L.K. (1994). The stress and illness connection in children: A perspective from the biobehavioral interface. In N. Garmezy & M. Rutter (Eds.), Risk and resilience in children (3rd ed.), 182–224.

Finley, G.A., & McGrath, P.J.(1999). Chronic and recurrent pain in children and adolescents. Progress in pain research and management (Vol. 13). Seattle: IASP Press.

Schechter, N.L., Berde, C.B., & Yaster, M. (1993). Pain in infants, children, and adolescents. Baltimore: Williams and Wilkins.

Zeltzer, L. K., Bursch, B., & Walco, G. (1997). Pain responsiveness and chronic pain: A psychobiological perspective. Journal of Developmental & Behavioral Pediatrics, 18, 402–412.

Zeltzer, L.K., & Feldman, S. (in press). Soothing and chronic pain. In M. Lewis & D. Ramsey (Eds.), Stress and soothing. Mahwah, NJ: Lawrence Erlbaum Associates, Inc.

Headache

Larsson, B., & Carlsson, J. (1996). A school-based, nurse-administered relaxation training for children with chronic tension-type headache. Journal of Pediatric Psychology, 21, 603–614.

McGrath, P.J., Humphreys, P., Keene, D., Goodman, J.T., Lascelles, M.A., Cunningham, S.J., & Firestone, P. (1992). The efficacy and efficiency of a self-administered treatment for adolescent migraine. Pain, 49, 321–324.

Juvenile rheumatoid arthritis

Lovell, D.J., & Walco, G.A. (1989). Pain associated with juvenile rheumatoid arthritis. Pediatric Clinics of North America, 36, 1015–1027.

van Rossum, M.A., Fiselier, T.J., Franssen, M.J., Zwinderman, A.H., ten Cate, R., van Suijlekom-Smit, L.W., et al. (1998). Sulfasalazine in the treatment of juvenile chronic arthritis: A randomized, double-blind, placebo-controlled, multicenter study. Dutch Juvenile Chronic Arthritis Study Group. Arthritis & Rheumatism, 41, 808–816.

Myofascial and temporomandibular joint pain

Wahlund, K., List, T., & Dworkin, S.F. (1998). Temporomandibular disorders in children and adolescents: Reliability of a questionnaire, clinical examination, and diagnosis. Journal of Orofacial Pain, 12, 42–51.

Neonates

Anand, K.J.S., Stevens, B., & McGrath, P.J. (Eds.). (1999). Pain in neonates (2nd ed.), Amsterdam: Elsevier

Neuropathic pain

Woolf, C.J., & Mannion, R.J. (1999). Neuropathic pain: Aetiology, symptoms, mechanisms, and management [Review]. Lancet, 353, 1959–1964.

Phantom pain and sensation

Wilkins, K.L., McGrath, P.J., Finley, G.A., & Katz, J. (1998). Phantom limb sensations and phantom limb pain in child and adolescent amputees. Pain, 78, 7–12.

Pharmacology

Berde, C.B., & Sethna, N.F. (in press). Treatment of pain in children. New England Journal of Medicine.

Sethna, N.F. (1999). Pharmacotherapy in long-term pain: Current experience and future direction. In P. McGrath, & G.A. Finley (Eds.), Chronic and recurrent pain in children and adolescents. Progress in pain research and management (pp. 243–266). Seattle: IASP Press.

Reflex sympathetic dystrophy (CRPS I & II)

Stanton, R.P., Malcolm, J.R., Wesdock, K.A., & Singsen, B.H. (1993). Reflex sympathetic dystrophy in children: An orthopedic perspective. Orthopedics, 16, 773–779.

Wilder, R.T., Berde, C.B., Wolohan, M., Vieyra, M.A., Masek, B.J., & Micheli, L.J. (1992). Reflex sympathetic dystrophy in children. Clinical characteristics and follow-up of seventy patients. Journal of Bone & Joint Surgery—American Volume, 74, 910-919.

Sickle-cell disease

Fuggle, P., Shand, P.A., Gill, L.J., & Davies, S.C. (1996). Pain, quality of life, and coping in sickle cell disease. Archives of Disease in Childhood, 75, 199–203.

Gil, K.M., Edens, J.L., Wilson, J.J., Raezer, L.B., Kinney, T.R., Schultz, W.H., et al. (1997). Coping strategies and laboratory pain in children with sickle cell disease. Annals of Behavioral Medicine, 19, 22–29.

Jacobson, S.J., Kopecky, E.A., Joshi, P., & Babul, N. (1997). Randomised trial of oral morphine for painful episodes of sickle-cell disease in children. Lancet, 350, 1358–1361.

Shapiro, B.S. (1989). The management of pain in sickle cell disease. Pediatric Clinics of North America, 36, 1029–1045.

Trauma

Joseph, M.H., Brill, J., & Zeltzer, L.K. (1999). Pediatric pain relief in trauma. Pediatrics in Review, 20, 75–83.

Moront, M.L., Williams, J.A., Eichelberger, M.R., & Wilkinson, J.D. (1994). The injured child. An approach to care [Review]. Pediatric Clinics of North America, 41, 1201–1226.

Treatment

LeBaron, S., & Zeltzer, L.K. (1997). Children in pain: Evaluation and treatment. In J. Barber (Ed.), Hypnosis and suggestion in the treatment of pain. New York: W.W. Norton & Co., Inc.

Visceral pain

Hyams, J.S. (1999). Chronic and recurrent abdominal pain. In P.E. Hyman (Ed.), Pediatric functional bowel disorders. New York: Academy Professional Information Services.

Raghavan, R., Joseph, M., & Zeltzer, L.K. (1999). The development of visceral pain. In P.E. Hyman (Ed.), Pediatric functional bowel disorders. New York: Academy Professional Information Services.


This position statement was prepared by the following members of the Pediatric Chronic Pain Task Force: Brenda Bursch, PhD (chair); Julie Collier, PhD; Michael Joseph, MD; Leora Kuttner, PhD; Patrick McGrath, PhD; Navil Sethna, MB ChB; Gary Walco, PhD; and Lonnie Zeltzer, MD.

American Pain Society Mission: The American Pain Society is a multidisciplinary organization of basic and clinical scientists, practicing clinicians, policy analysts, and others. The mission of the American Pain Society is to advance pain-related research, education, treatment, and professional practice.