An unpleasant sensation that can be either acute or chronic and is a consequence of complex neurochemical processes in the peripheral and central nervous systems (CNS)
Pain is subjective, and the clinician must rely on the patient's perception and description of pain
Nociceptive pain
Pain from physical damage or potential damage to the body
Nociceptive pain
Sports injury
Dental procedure
Arthritis
Nociceptive pain is the most common type of pain people experience
Neuropathic pain
Pain that develops when the nervous system is damaged or not working properly due to disease or injury
Neuropathic pain does not develop in response to any specific circumstance or outside stimulus
People can suffer from neuropathic pain even when the aching or injured body part is not actually there
Conditions that can result in neuropathy
Alcoholism
Shingles
Unmanaged diabetes
Stroke
Multiple sclerosis
Cancer treatments
Nonopioid analgesics
Nonsteroidal anti-inflammatory agents (NSAIDs) that are often effective for mild to moderate arthritic pain (nociceptive pain)
Neuropathic pain
Can be treated with opioids (some situations require higher doses) but responds best to anticonvulsants, tricyclic antidepressants, or serotonin/norepinephrine reuptake inhibitors
For severe or chronic malignant or nonmalignant pain, opioids are considered part of the treatment plan in select patients
Opioids
Natural, semisynthetic, or synthetic compounds that produce morphine-like effects
All opioids act by binding to specific opioid receptors in the CNS to produce effects that mimic the action of endogenous peptide neurotransmitters (for example, endorphins, enkephalins, and dynorphins)
Our bodies produce these neurotransmitters in order to produce analgesic effect
Widespread availability of opioids has led to abuse of those agents with euphoric properties (which is why morphine is a controlled substance)
Opioid receptor subtypes, their functions, and their endogenous peptide affinities
μ (mu): Supraspinal and spinal analgesia; sedation; inhibition of respiration; slowed gastrointestinal transit; modulation of hormone and neurotransmitter release. Endorphins > Enkephalins > Dynorphins
δ (delta): Supraspinal and spinal analgesia; modulation of hormone and neurotransmitter release. Enkephalins > Endorphins and Dynorphins
κ (kappa): Supraspinal and spinal analgesia; psychotomimetic effects; slowed gastrointestinal transit. Dynorphins >> Endorphins and enkephalins
Non-narcotic (Non-opioid) analgesics
They can remove pain but they do not produce the effects of morphine or narcotic effects. Generally safer; most of them can be bought OTC.
NSAIDs
Act by inhibiting the synthesis of prostaglandins, which are created from arachidonic acid and are the major mediator of pain and cause inflammation
Do not give aspirin to patients with dengue because dengue fever or virus may affect platelet count. Aspirin is non-selective therefore it would also affect COX-1, which is important in platelet aggregation.
Acetaminophen
Inhibits prostaglandin synthesis in the CNS, which explains its antipyretic and analgesic properties. It has less effect on cyclooxygenase in peripheral tissues, which accounts for its weak anti-inflammatory activity. It is inactivated in our periphery.