section name header

Information

Pain-producing (nociceptive) sensory stimuli in skin and viscera activate peripheral nerve endings of primary afferent neurons, which synapse on second-order neurons in spinal cord or medulla (Fig. 6-1. Pain Transmission and Modulatory Pathways). These second-order neurons form crossed ascending pathways that reach the thalamus and project to the somatosensory cortex. Parallel ascending neurons, connecting with brainstem and thalamic nuclei, project to the limbic system and underlie the emotional aspect of pain. Pain transmission is regulated at the dorsal horn level by descending bulbospinal pathways that utilize serotonin, norepinephrine, and several neuropeptides as neurotransmitters.

Agents that modify pain perception may act by reducing tissue inflammation (NSAIDs, prostaglandin synthesis inhibitors), interfering with pain transmission (narcotics), or enhancing descending modulation (narcotics and antidepressants). Anticonvulsants (gabapentin, carbamazepine) may be effective for aberrant pain sensations arising from peripheral nerve injury.

TREATMENT

ACUTE SOMATIC PAIN

  • Mild to moderate pain: Usually treated effectively with nonnarcotic analgesics, e.g., aspirin, acetaminophen, and NSAIDs, which inhibit cyclooxygenase (COX) and, except for acetaminophen, have anti-inflammatory actions, especially at high dosages. Particularly effective for headache and musculoskeletal pain.
  • Parenteral NSAIDs: Ketorolac and diclofenac are sufficiently potent and rapid in onset to supplant opioids for many pts with acute severe pain.
  • Narcotic analgesics in oral or parenteral form can be used for more severe pain. These are the most effective drugs available; the opioid antagonist naloxone should be readily available when narcotics are used in high doses or in unstable pts.
  • Pt-controlled analgesia (PCA) permits infusion of a baseline dose plus self-administered boluses (activated by press of a button) as needed to control pain.

CHRONIC PAIN

  • Develop an explicit treatment plan including specific and realistic goals for therapy, e.g., getting a good night's sleep, being able to go shopping, or returning to work.
  • A multidisciplinary approach that utilizes medications, counseling, physical therapy, nerve blocks, and even surgery may be required to improve quality of life.
  • Psychological evaluation is key; behaviorally based treatment paradigms are frequently helpful.
  • Some pts may require referral to a pain clinic; for others, pharmacologic management alone can provide significant help.
  • Tricyclic antidepressants are useful in management of chronic pain from many causes, including headache, diabetic neuropathy, postherpetic neuralgia, chronic low back pain, cancer, and central post-stroke pain.
  • Anticonvulsants or antiarrhythmics benefit pts with neuropathic pain (e.g., diabetic neuropathy, trigeminal neuralgia).
  • The long-term use of opioids is accepted for pain due to malignant disease, but is controversial for chronic pain of nonmalignant origin.

Pain (Table 6-2 Drugs for Relief of Pain)

Outline

Section 1. Care of the Hospitalized Patient