Pain

Jai Ganesh · 2023-05-05 00:31:41

Pain

Summary

Pain is a signal in your nervous system that something may be wrong. It is an unpleasant feeling, such as a prick, tingle, sting, burn, or ache. Pain may be sharp or dull. It may come and go, or it may be constant. You may feel pain in one area of your body, such as your back, abdomen, chest, pelvis, or you may feel pain all over.

Pain can be helpful in diagnosing a problem. If you never felt pain, you might seriously hurt yourself without knowing it, or you might not realize you have a medical problem that needs treatment.

There are two types of pain: acute and chronic. Acute pain usually comes on suddenly, because of a disease, injury, or inflammation. It can often be diagnosed and treated. It usually goes away, though sometimes it can turn into chronic pain. Chronic pain lasts for a long time, and can cause severe problems.

Pain is not always curable, but there are many ways to treat it. Treatment depends on the cause and type of pain. There are drug treatments, including pain relievers. There are also non-drug treatments, such as acupuncture, physical therapy, and sometimes surgery.

Details

Pain is a distressing feeling often caused by intense or damaging stimuli. The International Association for the Study of Pain defines pain as "an unpleasant sensory and emotional experience associated with, or resembling that associated with, actual or potential tissue damage."

Pain motivates us to withdraw from damaging situations, to protect a damaged body part while it heals, and to avoid similar experiences in the future. Most pain resolves once the noxious stimulus is removed and the body has healed, but it may persist despite removal of the stimulus and apparent healing of the body. Sometimes pain arises in the absence of any detectable stimulus, damage or disease.

Pain is the most common reason for physician consultation in most developed countries. It is a major symptom in many medical conditions, and can interfere with a person's quality of life and general functioning. People in pain experience impaired concentration, working memory, mental flexibility, problem solving and information processing speed, and are more likely to experience irritability, depression and anxiety.

Simple pain medications are useful in 20% to 70% of cases. Psychological factors such as social support, cognitive behavioral therapy, excitement, or distraction can affect pain's intensity or unpleasantness.

Etymology

First attested in English in 1297, the word peyn comes from the Old French peine, in turn from Latin poena meaning "punishment, penalty" (also meaning "torment, hardship, suffering" in Late Latin) and that from Greek (poine), generally meaning "price paid, penalty, punishment".

Classification

The International Association for the Study of Pain recommends using specific features to describe a patient's pain:

* region of the body involved (e.g. abdomen, lower limbs),
* system whose dysfunction may be causing the pain (e.g., nervous, gastrointestinal),
* duration and pattern of occurrence,
* intensity, and
* cause

Chronic versus acute

Pain is usually transitory, lasting only until the noxious stimulus is removed or the underlying damage or pathology has healed, but some painful conditions, such as rheumatoid arthritis, peripheral neuropathy, cancer and idiopathic pain, may persist for years. Pain that lasts a long time is called "chronic" or "persistent", and pain that resolves quickly is called "acute". Traditionally, the distinction between acute and chronic pain has relied upon an arbitrary interval of time between onset and resolution; the two most commonly used markers being 3 months and 6 months since the onset of pain, though some theorists and researchers have placed the transition from acute to chronic pain at 12 months. Others apply "acute" to pain that lasts less than 30 days, "chronic" to pain of more than six months' duration, and "subacute" to pain that lasts from one to six months. A popular alternative definition of "chronic pain", involving no arbitrarily fixed duration, is "pain that extends beyond the expected period of healing". Chronic pain may be classified as "cancer-related" or "benign."

Allodynia

Allodynia is pain experienced in response to a normally painless stimulus. It has no biological function and is classified by stimuli into dynamic mechanical, punctate and static.

Phantom

Phantom pain is pain felt in a part of the body that has been amputated, or from which the brain no longer receives signals. It is a type of neuropathic pain.

The prevalence of phantom pain in upper limb amputees is nearly 82%, and in lower limb amputees is 54%. One study found that eight days after amputation, 72% of patients had phantom limb pain, and six months later, 67% reported it. Some amputees experience continuous pain that varies in intensity or quality; others experience several bouts of pain per day, or it may reoccur less often. It is often described as shooting, crushing, burning or cramping. If the pain is continuous for a long period, parts of the intact body may become sensitized, so that touching them evokes pain in the phantom limb. Phantom limb pain may accompany urination or defecation.

Local anesthetic injections into the nerves or sensitive areas of the stump may relieve pain for days, weeks, or sometimes permanently, despite the drug wearing off in a matter of hours; and small injections of hypertonic saline into the soft tissue between vertebrae produces local pain that radiates into the phantom limb for ten minutes or so and may be followed by hours, weeks or even longer of partial or total relief from phantom pain. Vigorous vibration or electrical stimulation of the stump, or current from electrodes surgically implanted onto the spinal cord, all produce relief in some patients.

Mirror box therapy produces the illusion of movement and touch in a phantom limb which in turn may cause a reduction in pain.

Paraplegia, the loss of sensation and voluntary motor control after serious spinal cord damage, may be accompanied by girdle pain at the level of the spinal cord damage, visceral pain evoked by a filling bladder or bowel, or, in five to ten per cent of paraplegics, phantom body pain in areas of complete sensory loss. This phantom body pain is initially described as burning or tingling but may evolve into severe crushing or pinching pain, or the sensation of fire running down the legs or of a knife twisting in the flesh. Onset may be immediate or may not occur until years after the disabling injury. Surgical treatment rarely provides lasting relief.

Breakthrough

Breakthrough pain is transitory pain that comes on suddenly and is not alleviated by the patient's regular pain management. It is common in cancer patients who often have background pain that is generally well-controlled by medications, but who also sometimes experience bouts of severe pain that from time to time "breaks through" the medication. The characteristics of breakthrough cancer pain vary from person to person and according to the cause. Management of breakthrough pain can entail intensive use of opioids, including fentanyl.

Asymbolia and insensitivity

The ability to experience pain is essential for protection from injury, and recognition of the presence of injury. Episodic analgesia may occur under special circumstances, such as in the excitement of sport or war: a soldier on the battlefield may feel no pain for many hours from a traumatic amputation or other severe injury.

Although unpleasantness is an essential part of the IASP definition of pain, it is possible to induce a state described as intense pain devoid of unpleasantness in some patients, with morphine injection or psychosurgery. Such patients report that they have pain but are not bothered by it; they recognize the sensation of pain but suffer little, or not at all. Indifference to pain can also rarely be present from birth; these people have normal nerves on medical investigations, and find pain unpleasant, but do not avoid repetition of the pain stimulus.

Insensitivity to pain may also result from abnormalities in the nervous system. This is usually the result of acquired damage to the nerves, such as spinal cord injury, diabetes mellitus (diabetic neuropathy), or leprosy in countries where that disease is prevalent. These individuals are at risk of tissue damage and infection due to undiscovered injuries. People with diabetes-related nerve damage, for instance, sustain poorly-healing foot ulcers as a result of decreased sensation.

A much smaller number of people are insensitive to pain due to an inborn abnormality of the nervous system, known as "congenital insensitivity to pain". Children with this condition incur carelessly-repeated damage to their tongues, eyes, joints, skin, and muscles. Some die before adulthood, and others have a reduced life expectancy. Most people with congenital insensitivity to pain have one of five hereditary sensory and autonomic neuropathies (which includes familial dysautonomia and congenital insensitivity to pain with anhidrosis). These conditions feature decreased sensitivity to pain together with other neurological abnormalities, particularly of the autonomic nervous system. A very rare syndrome with isolated congenital insensitivity to pain has been linked with mutations in the SCN9A gene, which codes for a sodium channel (Nav1.7) necessary in conducting pain nerve stimuli.

Additional Information

Pain is complex experience consisting of a physiological and a psychological response to a noxious stimulus. Pain is a warning mechanism that protects an organism by influencing it to withdraw from harmful stimuli; it is primarily associated with injury or the threat of injury.

Pain is subjective and difficult to quantify, because it has both an affective and a sensory component. Although the neuroanatomic basis of pain reception develops before birth, individual pain responses are learned in early childhood and are affected by social, cultural, psychological, cognitive, and genetic factors, among others. Those factors account for differences in pain tolerance among humans. Athletes, for example, may be able to withstand or ignore pain while engaged in a sport, and certain religious practices may require participants to endure pain that seems intolerable to most people.

An important function of pain is to alert the body to potential damage. That is accomplished through nociception, the neural processing of harmful stimuli. The pain sensation, however, is only one part of the nociceptive response, which may include an increase in blood pressure, an increase in heart rate, and a reflexive withdrawal from the noxious stimulus. Acute pain can arise from breaking a bone or touching a hot surface. During acute pain, an immediate intense feeling of short duration, sometimes described as a sharp pricking sensation, is followed by a dull throbbing sensation. Chronic pain, which is often associated with diseases such as cancer or arthritis, is more difficult to locate and treat. If pain cannot be alleviated, psychological factors such as depression and anxiety can intensify the condition.

Early conceptions of pain

Pain is a physiological and psychological element of human existence, and thus it has been known to humankind since the earliest eras, but the ways in which people respond to and conceive of pain vary dramatically. In certain ancient cultures, for example, pain was deliberately inflicted on individuals as a means of pacifying angry gods. Pain was also seen as a form of punishment, inflicted on humans by gods or demons. In ancient China, pain was thought to arise from an imbalance between the two complementary forces of life, yin and yang. Ancient Greek physician Hippocrates believed that pain is associated with too much or too little of one of the four humours (blood, phlegm, yellow bile, or black bile). Muslim physician Avicenna believed that pain is a sensation that originated with a change in the physical condition of the body.

Theories of pain

Medical understanding of the physiological basis of pain is a comparatively recent development, having emerged in earnest in the 19th century. At that time, various British, German, and French physicians recognized the problem of chronic “pains without lesion” and attributed them to a functional disorder or persistent irritation of the nervous system. German physiologist and comparative anatomist Johannes Peter Müller’s concept of Gemeingefühl, or “cenesthesis,” an individual’s ability to correctly perceive internal sensations, was another of the creative etiologies proposed for pain. American physician and author S. Weir Mitchell observed Civil War soldiers afflicted with causalgia (constant burning pain; later known as complex regional pain syndrome), phantom limb pain, and other painful conditions long after their original wounds had healed. Despite the odd and often hostile behaviour of his patients, Mitchell was convinced of the reality of their physical suffering.

By the late 1800s the development of specific diagnostic tests and the identification of specific signs of pain were beginning to redefine the practice of neurology, leaving little room for chronic pains that could not be explained in the absence of other physiological symptoms. At the same time, practitioners of psychiatry and the emerging field of psychoanalysis found that “hysterical” pains offered potential insights into mental and emotional disease. The contributions of individuals such as English physiologist Sir Charles Scott Sherrington supported the concept of specificity, according to which “real” pain was a direct one-to-one response to a specific noxious stimulus. Sherrington introduced the term nociception to describe the pain response to such stimuli. Specificity theory suggested that individuals who reported pain in the absence of an evident cause were delusional, neurotically obsessed, or malingering (often the conclusion of military surgeons or those treating workmen’s compensation cases). Another theory, which was popular with psychologists at the time but was soon after abandoned, was intensive pain theory, in which pain was considered to be an emotional state, incited by unusually intense stimuli.

In the 1890s German neurologist Alfred Goldscheider endorsed Sherrington’s insistence that the central nervous system integrates inputs from the periphery. Goldscheider proposed that pain is a result of the brain’s recognition of spatial and temporal patterns of sensation. French surgeon René Leriche, who worked with injured soldiers during World War I, suggested that a nerve injury that damages the myelin sheath surrounding the sympathetic nerves (the nerves involved in the fight-or-flight response) might lead to sensations of pain in response to normal stimuli and internal physiological activity. American neurologist William K. Livingston, who worked with patients with industrial injuries in the 1930s, diagrammed a feedback loop within the nervous system, which he described as a “vicious circle.” Livingston theorized that severe lasting pain induces functional and organic changes in the nervous system, thereby producing a chronic pain state.

The various theories on pain, however, were largely ignored until World War II, when organized teams of clinicians began to observe and treat large numbers of individuals with similar injuries. In the 1950s American anesthesiologist Henry K. Beecher, using his experiences of treating civilian patients and wartime casualties, found that soldiers with serious wounds frequently seemed to be in much less pain than civilian surgical patients. Beecher concluded that pain is the result of a fusion of physical sensation with a cognitive and emotional “reaction component.” Thus, the mental context of pain is important. Pain for the surgical patient meant a disruption of normal life and fears of serious illness, whereas pain for the wounded soldier meant release from the battlefield and an increased chance of survival. Therefore, the assumptions of specificity theory, which were based on laboratory experiments in which the reaction component was relatively neutral, could not be applied to the understanding of clinical pain. Beecher’s conclusions were supported by the work of American anesthesiologist John Bonica, who in his book 'The Management of Pain' (1953) considered clinical pain to include both physiological and psychological components.

Dutch neurosurgeon Willem Noordenbos extended the theory of pain as an integration of multiple inputs into the nervous system in his short but classic book, 'Pain' (1959). Noordenbos’s ideas appealed to Canadian psychologist Ronald Melzack and British neuroscientist Patrick David Wall. Melzack and Wall combined the ideas of Goldscheider, Livingston, and Noordenbos with available research evidence and in 1965 proposed the so-called gate control theory of pain. According to gate control theory, the perception of pain depends on a neural mechanism in the substantia gelatinosa layer of the dorsal horn of the spinal cord. The mechanism acts as a synaptic gate that modulates the pain sensation from myelinated and unmyelinated peripheral nerve fibres and the activity of inhibitory neurons. Thus, stimulation of nearby nerve endings can inhibit the nerve fibres that transmit pain signals, which explains the relief that can occur when an injured area is stimulated by pressure or rubbing. Although the theory itself proved to be incorrect, the implication that laboratory and clinical observations together could demonstrate the physiological basis of a complex neural integration mechanism for pain perception inspired and challenged a young generation of researchers.

In 1973, drawing on the upsurge of interest in pain generated by Wall and Melzack, Bonica organized a meeting among interdisciplinary pain researchers and clinicians. Under Bonica’s leadership, the conference, which was held in the United States, gave birth to an interdisciplinary organization known as the International Association for the Study of Pain (IASP) and a new journal titled Pain, initially edited by Wall. The formation of IASP and the launch of the journal marked the emergence of pain science as a professional field.

In the following decades, research on the problem of pain expanded significantly. From that work, two major findings emerged. First, severe pain from an injury or other stimulus, if continued over some period, was found to alter the neurochemistry of the central nervous system, thereby sensitizing it and giving rise to neuronal changes that endure after the initial stimulus is removed. That process is perceived as chronic pain by the affected individual. The involvement of neuronal changes in the central nervous system in the development of chronic pain was demonstrated across multiple studies. In 1989, for example, American anesthesiologist Gary J. Bennett and Chinese scientist Xie Yikuan demonstrated the neural mechanism underlying the phenomenon in rats with constrictive ligatures placed loosely around the sciatic nerve. In 2002 Chinese-born neuroscientist Min Zhuo and colleagues reported the identification of two enzymes, adenylyl cyclase types 1 and 8, in the forebrains of mice that play an important role in sensitizing the central nervous system to pain stimuli.

The second finding that emerged was that pain perception and response differ with gender and ethnicity and with learning and experience. Women appear to suffer pain more often and with greater emotional stress than do men, but some evidence shows that women may cope with severe pain more effectively than men. African Americans show a higher vulnerability to chronic pain and a higher level of disability than do white patients. Those observations have been borne out by neurochemical research. For example, in 1996 a team of researchers led by American neuroscientist Jon D. Levine reported that different types of opioid drugs produce different levels of pain relief in women and men. Other research conducted in animals suggested that pain experiences early in life can produce neuronal changes at the molecular level that influence an individual’s pain response as an adult. A significant conclusion from those studies is that no two individuals experience pain the same way.

Physiology of pain

In spite of its subjective nature, most pain is associated with tissue damage and has a physiological basis. Not all tissues, however, are sensitive to the same type of injury. For example, although skin is sensitive to burning and cutting, the visceral organs can be cut without generating pain. Overdistension or chemical irritation of the visceral surface, however, will induce pain. Some tissues do not give rise to pain, no matter how they are stimulated; the liver and the alveoli of the lungs are insensitive to almost every stimulus. Thus, tissues respond only to the specific stimuli that they are likely to encounter and generally are not receptive to all types of damage.

Pain receptors, located in the skin and other tissues, are nerve fibres with endings that can be excited by three types of stimuli—mechanical, thermal, and chemical; some endings respond primarily to one type of stimulation, whereas other endings can detect all types. Chemical substances produced by the body that excite pain receptors include bradykinin, serotonin, and histamine. Prostaglandins are fatty acids that are released when inflammation occurs and can heighten the pain sensation by sensitizing the nerve endings; that increase in sensitivity is called hyperalgesia.

The dual-phase experience of acute pain is mediated by two types of primary afferent nerve fibres that transmit electrical impulses from the tissues to the spinal cord via the ascending nerve tracts. The A delta fibres are the larger and the most rapidly conducting of the two types, because of their thin myelin covering, and, therefore, they are associated with the sharp, well-localized pain that first occurs. A delta fibres are activated by mechanical and thermal stimuli. Smaller, unmyelinated C fibres respond to chemical, mechanical, and thermal stimuli and are associated with the lingering, poorly localized sensation that follows the first quick sensation of pain.

Pain impulses enter the spinal cord, where they synapse primarily on the dorsal horn neurons in the marginal zone and substantia gelatinosa of the gray matter of the spinal cord. That area is responsible for regulating and modulating the incoming impulses. Two different pathways, the spinothalamic and spinoreticular tracts, transmit impulses to the brainstem and thalamus. Spinothalamic input is thought to effect the conscious sensation of pain, and the spinoreticular tract is thought to effect the arousal and emotional aspects of pain.

Pain signals can be selectively inhibited in the spinal cord through a descending pathway, which originates in the midbrain and ends in the dorsal horn. That analgesic (pain-relieving) response is controlled by neurochemicals called endorphins, which are opioid peptides such as enkephalins that are produced by the body. Those substances block the reception of pain stimuli by binding to neural receptors that activate the pain-inhibiting neural pathway. That system can be activated by stress or shock and is probably responsible for the absence of pain associated with a severe injury. It may also explain the differing abilities among individuals to perceive pain.

The origin of pain signals can be unclear to the sufferer. Pain arising from the deep tissues but “felt” in the superficial tissues is called referred pain. Though the precise mechanism is unclear, that phenomenon may result from the convergence of nerve fibres from different tissues onto the same portion of the spinal cord, which could allow nerve impulses from one pathway to pass to other pathways. Phantom limb pain is suffered by an amputee who experiences pain in the missing limb. That phenomenon occurs because the nerve trunks that connected the now absent limb to the brain still exist and are capable of being excited. The brain continues to interpret stimuli from those fibres as arriving from what it had previously learned was the limb.

Psychology of pain

The perception of pain results from the brain’s processing of new sensory input with existing memories and emotions, in the same way that other perceptions are produced. Childhood experiences, cultural attitudes, heredity, and gender are factors that contribute to the development of each individual’s perception of and response to different types of pain. Although some people may be able physiologically to withstand pain better than others, cultural factors rather than heredity usually account for that ability.

The point at which a stimulus begins to become painful is the pain perception threshold; most studies have found that point to be relatively similar among disparate groups of people. However, the pain tolerance threshold, the point at which pain becomes unbearable, varies significantly among those groups. A stoical, nonemotional response to an injury may be a sign of bravery in certain cultural or social groups, but that behaviour can also mask the severity of an injury to an examining physician.

Depression and anxiety can lower both types of pain thresholds. Anger or excitement, however, can obscure or lessen pain temporarily. Feelings of emotional relief can also lessen a painful sensation. The context of pain and the meaning it has for the sufferer also determine how pain is perceived.

Alleviation of pain

Attempts to relieve pain typically address both the physiological and the psychological aspects of pain. The reduction of anxiety, for example, may lessen the amount of medication needed to alleviate pain. Acute pain is generally the easiest to control; medication and rest are often effective treatments. Some pain, however, may defy treatment and persist for years. Such chronic pain can be compounded by hopelessness and anxiety.

Opiates are potent pain-relieving medications and are used to treat severe pain. Opium, a dried extract obtained from the unripe seedpods of opium poppy (Papaver somniferum), is one of the oldest analgesics. Morphine, a powerful opiate, is an extremely effective analgesic. Those narcotic alkaloids mimic the endorphins produced naturally by the body by binding to their receptors and blocking or reducing the activation of pain neurons. However, the use of opiate pain relievers must be monitored not only because they are addictive substances but also because the patient can develop a tolerance to them and may require progressively greater doses to achieve the desired level of pain relief. Overdose can cause potentially fatal respiratory depression. Other significant side effects, such as nausea and psychological depression upon withdrawal, also limit the usefulness of opiates.

Extracts of the bark of willows (genus Salix) contain the active ingredient salicin and have been used since antiquity to relieve pain. Modern nonnarcotic anti-inflammatory analgesic salicylates, such as aspirin (acetylsalicylic acid), and other anti-inflammatory analgesics, such as acetaminophen, nonsteroidal anti-inflammatory drugs (NSAIDs; e.g., ibuprofen), and cyclooxygenase (COX) inhibitors (e.g., celecoxib), are less potent than opiates but are nonaddictive. Aspirin, NSAIDs, and COX inhibitors either nonselectively or selectively block the activity of COX enzymes. COX enzymes are responsible for the conversion of arachidonic acid (a fatty acid) to prostaglandins, which enhance sensitivity to pain. Acetaminophen also prevents the formation of prostaglandins, but its activity appears to be limited primarily to the central nervous system and to be exerted through multiple mechanisms. Drugs known as N-methyl-D-aspartate receptor (NMDAR) antagonists, examples of which include dextromethorphan and ketamine, may be used in the treatment of certain forms of neuropathic pain, such as diabetic neuropathy. The drugs work by blocking NMDARs, the activation of which is involved in nociceptive transmission.

Psychotropic medications, including antidepressants and tranquilizers, may be used to treat patients with chronic pain who are also suffering from psychological conditions. Those medications help to reduce anxiety and sometimes alter the perception of the pain. Pain seems to be alleviated in a similar manner by hypnosis, placebos, and psychotherapy. Although the reasons why an individual may report pain relief after taking a placebo or following psychotherapy remain unclear, researchers suspect that the expectation of relief is stimulated by dopamine release in the region of the brain known as the ventral striatum. Activity in the ventral striatum is linked to increased dopamine activity and is associated with the placebo effect, in which pain relief is reported following treatment with a placebo.

Specific nerves can be blocked in cases in which pain is restricted to an area that has few sensory nerves. Phenol and alcohol are neurolytics that destroy nerves; lidocaine can be used for temporary pain relief. Surgical severing of nerves is rarely performed, because it can produce serious side effects such as motor loss or relocalized pain.

Some pain may be treated by transcutaneous electrical nerve stimulation (TENS), in which electrodes are placed on the skin above the painful area. The stimulation of additional peripheral nerve endings has an inhibitory effect on the nerve fibres generating the pain. Acupuncture, compresses, and heat treatment may operate by the same mechanism.

Chronic pain, defined generally as pain that has persisted for at least six months, presents the greatest challenge in pain management. Unrelieved chronic discomfort can cause psychological complications such as hypochondriasis, depression, sleep disturbances, loss of appetite, and feelings of helplessness. Many pain clinics offer a multidisciplinary approach to chronic pain treatment. Patients with chronic pain may require unique pain-management strategies. For example, some patients may benefit from the use of a surgical implant. Examples of implants include intrathecal drug delivery, in which a pump implanted beneath the skin delivers pain medication directly to the spinal cord, and a spinal cord stimulation implant, in which an electrical device placed in the body sends electric pulses to the spinal cord to inhibit the transmission of pain signals. Other strategies for the management of chronic pain include alternative therapy, exercise, physical therapy, cognitive behavioral therapy, and TENS. Therapy to identify emotions associated with chronic pain can benefit patients suffering from chronic pain of unknown cause.

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#1 2023-05-05 00:31:41

Pain

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