Escalating Pain in the Adult with Cancer
TERMS
epidural
fibrosis
intractable
intrathecal
morphine sulfate sustained release (MSSR)
myoclonus
neuroablative procedures
neurostimulation
plexopathy
regional plexus
regional infusion
QUICK LOOK AT THE CHAPTER AHEAD
Individuals with cancer are at risk for a variety of physiological problems capable of causing pain. Comprehensive assessments for the etiology of the pain, appropriate treatment, and ongoing monitoring of pain are essential to achieve relief of pain and improve quality of life. Knowledge of the patterns of metastasis for cancer and the characteristics of pain are tools the physician and nurse use to identify the etiology of pain and subsequent treatment.
Changes in the nature and intensity of chronic cancer pain are critical assessment findings that require prompt medical treatment. Neuropathic pain often requires high doses of opioids along with adjunct medications to achieve relief and control of the pain. Although oral opioids and adjunct analgesics may effectively relieve neuropathic pain in some individuals, escalation of pain intensity may require rapid titration of IV opioids in a clinical setting that allows for close monitoring of side effects. Morphine continues to be the drug of choice for severe cancer pain, but high doses of morphine along with high doses of adjuvant analgesics are often required for pain relief and control.
CASE STUDY
J. T. is a 50-year-old patient with a 3-year history of lung cancer with metastasis to the bone. For several months, she has been experiencing pain that until recently has been well controlled with morphine sulfate sustained release (MSSR) (for example, MS Contin®) 90 mg PO every 12 hours and occasional morphine sulfate immediate release (MSIR) 20 mg q 2 hours PRN.
Two days ago, J. T. began to have more frequent pain in her right shoulder, which she rated a “7” on a scale of 0 to 10. Throughout the day she took six doses of MSIR 20 mg with good effect. The home health nurse contacted J. T.’s physician to request an increase in her MSSR to provide better pain control. The doctor ordered an increase in J. T.’s MSSR to 150 mg every 12 hours, and an increase in the morphine sulfate immediate release (MSIR) to 40 mg every 2 hours as needed. He also instructed the client to contact him if the pain continued or got worse.
One day after increasing her MSSR to 150 mg every 12 hours, J. T. rates her pain as “2” at rest. But the following day, J. T.’s pain rating increases to a “10” despite the increase in MSSR and increased use of MSIR. Today’s assessment of pain indicates that the pain in J. T.’s shoulder is now associated with painful sensations shooting down to her thumb and index finger. The nurse recognizes that J. T.’s pain is out of control, that it meets the definition for pain crisis as defined by National Comprehensive Cancer Network (NCCN) guidelines, that it is likely neuropathic, and that J. T. needs more aggressive treatment to control her pain. The nurse instructs J. T. to take a dose of MSIR 40 mg, and she contacts the physician, who agrees to have J. T. admitted directly to the oncology unit with a diagnosis of uncontrolled pain related to metastatic lung cancer.
THE PROBLEM OF CANCER PAIN
Surveys in the early 1990s indicated that pain was experienced by approximately one-third of individuals treated for cancer and more than two-thirds with advanced cancer. At that time is was estimated that in
almost all cases (98% and 99%, respectively), clients should have had their pain adequately relieved. Instead, 40% to 50% of these clients failed to achieve adequate pain relief.
almost all cases (98% and 99%, respectively), clients should have had their pain adequately relieved. Instead, 40% to 50% of these clients failed to achieve adequate pain relief.
Since that time, there have been advances in the scientific understanding of pain, therapeutic options, and training of healthcare providers. Despite this, current estimates suggest that worldwide, as many as 50% of patients with cancer pain are inadequately treated. Table 6-1 addresses the steps required to improve cancer pain management.
The purpose of this chapter is to educate current and future healthcare providers about clinical problems in the management of pain that they may not encounter in traditional curricula. Hopefully it will enlighten providers in such a way that improvements in the management of cancer pain occur and more relief is achieved.
TYPES OF CANCER PAIN
Etiologies of Cancer Pain
Pain related to cancer can be classified according to its etiology, its origin and character, and its duration. Cancer pain can be secondary to:
1. Tumor involvement;
2. Cancer-related procedures and treatment effects; or
3. Causes unrelated to cancer or its treatment.
Pain associated with a tumor is responsible for the majority of pain related to cancer. An example of this type of pain would be abdominal pain related to a colorectal tumor obstructing the large colon. Nerve damage secondary to chemotherapy resulting in peripheral neuropathy is an example of pain related to cancer therapy. Pain related to appendicitis is an example of pain unrelated to cancer or the treatment.
Table 6-1 What is Needed to Improve Management of Cancer Pain | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
|
Origins of Cancer Pain
Cancer pain can also be classified according to its origin and character. Nociceptive pain refers to pain that is directly related to tumor infiltration of either somatic (for example, joint, muscle, bone) or visceral (for example, gastrointestinal tract) structures. Somatic pain is characterized as well-localized, deep, dull, or achy. The underlying cause is usually an inflammatory process. Bone metastasis, incisional pain, and wound pain are examples of somatic pain. Visceral pain originating from gastrointestinal tract structure is characterized as poorly localized, vague pressure that is often constricting or cramping. Visceral pain is often present in clients with advanced colon, pancreatic, ovarian, or uterine cancers secondary to stretching of the mesentery and abdominal organs.
Neuropathic pain applies to a variety of pain syndromes characterized by aberrant or somatosensory processes that originate in the peripheral or central nervous system. It is described as sharp, tingling, burning, shooting, shock-like, or electric. Sources of neuropathic pain involve tumor invasion of nerves, post-herpetic neuralgia, chemical damage to nerves from chemotherapy, surgical interruption of nerves, or spinal nerve root compression.
Duration of Cancer Pain
Cancer pain is also classified in terms of duration, with acute pain generally being defined as lasting less than 6 months and chronic pain lasting longer than 6 months. Pain related to an unresectable or recurrent tumor is generally chronic in duration.
Pain that occurs intermittently in clients with chronic cancer pain may be described as episodic. Episodic pain can be categorized in three distinct ways: incident pain, end-of-dose pain, and breakthrough pain.
Incident pain is related to a particular activity or experience, such as getting out of bed or reacting to emotional stimuli such as fear. End-of-dose pain occurs when the effect of a long-acting analgesic is not sustained over an expected duration. Breakthrough pain is a transitory episode of pain that is rapid in onset and usually of short duration (< 30 minutes). Breakthrough pain may occur despite adequate titration of long-acting opioids or continuous intravenous (IV) opioid drips.
Incident pain is related to a particular activity or experience, such as getting out of bed or reacting to emotional stimuli such as fear. End-of-dose pain occurs when the effect of a long-acting analgesic is not sustained over an expected duration. Breakthrough pain is a transitory episode of pain that is rapid in onset and usually of short duration (< 30 minutes). Breakthrough pain may occur despite adequate titration of long-acting opioids or continuous intravenous (IV) opioid drips.
SEVERITY OF CANCER PAIN
The intensity of chronic cancer pain varies from mild (1-3) to moderate (4-6) to severe or excruciating (7-10). Most clients describe their cancer pain as mild to moderate (1-6). If an increase in the intensity of chronic cancer pain occurs, prompt medical attention is warranted to fully assess the pain and determine its origin. Increased pain often represents progression of cancer, particularly in advanced disease. However, new pain in a person with cancer may also be a sign of infection, fracture, or a neurological problem. It is essential that client reports of a “new” pain be thoroughly explored to ensure that a reversible complication (such as spinal cord compression) is not overlooked. Reports of pain, especially of increased severity or at a new location, must not automatically be attributed to a pre-existent cause or to opioid tolerance. Opioid tolerance is seldom the cause of increased cancer pain.
Knowledge of relationships that certain cancers have with pain patterns and patterns of metastasis helps determine the etiology of new pain. Multiple myeloma and cancers of the breast, prostate, and lung account for the majority of cancers with bone metastasis that frequently is characterized by pain. Pain in bones is caused by direct tumor involvement of bone with activation of nociceptors or from compression of adjacent nerves, vascular structures, and soft tissue. With multiple sites involved, clients with bone metastasis commonly have multiple areas of pain. Complications of bone metastasis, such as pathological fractures or spinal cord compression, can lead to additional sources for pain and morbidity. Spinal cord or epidural compression commonly occurs with cancers of the breast, prostate, lung, and kidney, as well as with multiple myeloma and melanoma.