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IASP TaxonomyThe following pain terminology is updated from "Part III: Pain Terms, A Current List with Definitions and Notes on Usage" (pp 209-214) Classification of Chronic Pain, Second Edition, IASP Task Force on Taxonomy, edited by H. Merskey and N. Bogduk, IASP Press, Seattle, ©1994. To request permission to use, reprint or translate any IASP Publications, complete the Copyright Permissions Request form. Changes in the 2011 ListThe work of the Task Force on Taxonomy in the era of 1979 to 1994 has been continued by the Committee on Taxonomy that has worked to update both pain terms and the classification of pain syndromes. All of the terms have been carefully reviewed and their utility assessed in reference to new knowledge about both clinical and basic science aspects of pain. The Committee conducted its business primarily by e-mail, but face-to-face meetings were held at each of the annual Congresses of IASP. We now present the 2011 version of IASP Pain Terminology. Members of the Taxonomy Committee in this era included: David Boyd, Michael Butler, Daniel Carr, Milton Cohen, Marshall Devor, Robert Dworkin, Joel Greenspan, Troels Jensen, Steven King, Martin Koltzenburg, John Loeser, Harold Merskey, Akiko Okifuji, Judy Paice, Jordi Serra, Rolf-Detlef Treede, and Alain Woda. The Chair would like to acknowledge the continuous contributions that Harold Merskey has made to taxonomy since the founding of IASP. As stated in prior publications of the IASP taxonomy, we do not see this listing of terms as immutable. As we learn more about pain, we will need to update terminology. John D. Loeser, M.D. Changes in the 1994 List Read 1994 Notes > There was substantial correspondence from 1986 to 1993 among members of the Task Force and other colleagues. The previous definitions all remain unchanged, except for very slight alterations in the wording of the definitions of Central Pain and Hyperpathia. Two new terms have been introduced here: Neuropathic Pain and Peripheral Neuropathic Pain. The terms Sympathetically Maintained Pain and Sympathetically Independent Pain have also been employed; however, these terms are used in connection with syndromes 1–4 and 1–5, now called Complex Regional Pain Syndromes, Types I and II. These were formerly labeled Reflex Sympathetic Dystrophy and Causalgia, and the discussion of Sympathetically Maintained Pain and Sympathetically Independent Pain is found with those categories. Changes have been made in the notes on Allodynia to clarify the fact that it may refer to a light stimulus on damaged skin, as well as on normal skin. Also, in the tabulation of the implications of some of the definitions, the words lowered threshold have been removed from the features of Allodynia because it does not occur regularly. Small changes have been made to better describe Hyperpathia in the definition and note. A sentence has been added to the note on Hyperalgesia to refer to current views on its physiology, although as with other definitions, that for Hyperalgesia remains tied to clinical criteria. Last, the note on neuropathy has been expanded. Introduction to the 1986 List Read 1986 Introduction > A list of pain terms was first published in 1979 (Pain 1979;6:249–52). Many of the terms were already established in the literature. One, allodynia, quickly came into use in the columns of Pain and other journals. The terms have been translated into Portuguese (Rev Bras Anest 1980;30(5):349–51), into French (H. Dehen, Lexique de la douleur, La Presse Medicale 1983;12(23):1459–60), and into Turkish (as Agri Terimleri, translated by T. Aldemir, J Turkish Soc Algology 1989;1:45–6). A supplementary note was added to these pain terms in Pain (1982;14:205–6). The original list was adopted by the first Subcommittee on Taxonomy of IASP. Subsequent revisions and additions were prepared by a subgroup of the Committee, particularly Drs. U. Lindblom, P.W. Nathan, W. Noordenbos, and H. Merskey. In 1984, in particular response to some observations by Dr. M. Devor, a further review was undertaken both by correspondence and during the 4th World Congress on Pain of IASP. Those taking part in that review included Dr. Devor, the other colleagues just mentioned, and Dr. J.M. Mumford, Sir Sydney Sunderland, and Dr. P.W. Wall. Following that review, it was agreed to take advantage of the publication of the draft collection of syndromes and their system for classification, to issue an updated list of terms with definitions and notes on usage. The versions now presented are based upon some subsequent discussions by correspondence. The form of the definitions and notes at this point has been the responsibility of the editor (H.M.). It would be difficult now to single out individual contributions, but the editor remains heavily indebted to those five members of the original Subcommittee on Taxonomy who sustained this work in the form of an Ad Hoc group and whose names are listed at the beginning of this report. Their knowledge and patience was repeatedly provided freely and with good will. The revised current list follows. The original comments provided as an introduction to the terms are given in the following two paragraphs, which indicate both the process by which the terms were first delivered and the justification for them. "The usage of individual terms in medicine often varies widely. That need not be a cause of distress provided that each author makes clear precisely how he employs a word. Nevertheless, it is convenient and helpful to others if words can be used which have agreed technical meanings. Following correspondence and meetings during the period 1976–1978, the present committee agreed on the definitions which follow, and the notes have been prepared by the chairman in the light of members' comments. The definitions are intended to be specific and explanatory and to serve as an operational framework, not as a constraint on future development. They represent agreement between diverse specialties including anesthesiology, dentistry, neurology, neurosurgery, neurophysiology, psychiatry, and psychology. A starting point for some of these definitions was provided by the reports of a workshop on Orofacial Pain held at the U.S. National Institute of Dental Research in November 1974. "The terms and definitions are not meant to provide a comprehensive glossary but rather a minimum standard vocabulary for members of different disciplines who work in the field of pain. We hope that they will prove acceptable to all those in the health professions who deal with pain. Not only are they a limited selection from available terms, but it is emphasized that except for pain itself, they are defined primarily in relation to the skin and the special senses are excluded. They may be used when appropriate for responses to somatic stimulation elsewhere or to the viscera. Except for Pain, the arrangement is in alphabetical order." It is important to emphasize something that was implicit in the previous definitions but was not specifically stated: that the terms have been developed for use in clinical practice rather than for experimental work, physiology, or anatomical purposes.
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| The implications of some of the above definitions may be summarized for convenience as follows: | ||
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| Allodynia | lowered threshold | stimulus and response mode differ |
| Hyperalgesia | increased response | stimulus and response mode are the same |
| Hyperpathia | raised threshold: increased response | stimulus and response mode may be the same or different |
| Hypoalgesia | raised threshold: lowered response | stimulus and response mode are the same |
The above essentials of the definitions do not have to be symmetrical and are not symmetrical at present. Lowered threshold may occur with allodynia but is not required. Also, there is no category for lowered threshold and lowered response—if it ever occurs.
Hypoesthesia
Decreased sensitivity to stimulation, excluding the special senses.
Note: Stimulation and locus to be specified.
Neuralgia
Pain in the distribution of a nerve or nerves.
Note: Common usage, especially in Europe, often implies a paroxysmal quality, but neuralgia should not be reserved for paroxysmal pains.
Neuritis
Inflammation of a nerve or nerves.
Note: Not to be used unless inflammation is thought to be present.
Neuropathic pain*
Pain caused by a lesion or disease of the somatosensory nervous
system.
Note: Neuropathic pain is a clinical description (and not a diagnosis) which requires a demonstrable lesion or a disease that satisfies established neurological diagnostic criteria. The term lesion is commonly used when diagnostic investigations (e.g. imaging, neurophysiology, biopsies, lab tests) reveal an abnormality or when there was obvious trauma. The term disease is commonly used when the underlying cause of the lesion is known (e.g. stroke, vasculitis, diabetes mellitus, genetic abnormality). Somatosensory refers to information about the body per se including visceral organs, rather than information about the external world (e.g., vision, hearing, or olfaction). The presence of symptoms or signs (e.g., touch-evoked pain) alone does not justify the use of the term neuropathic. Some disease entities, such as trigeminal neuralgia, are currently defined by their clinical presentation rather than by objective diagnostic testing. Other diagnoses such as postherpetic neuralgia are normally based upon the history. It is common when investigating neuropathic pain that diagnostic testing may yield inconclusive or even inconsistent data. In such instances, clinical judgment is required to reduce the totality of findings in a patient into one putative diagnosis or concise group of diagnoses.
Central neuropathic
pain*
Pain caused by a lesion or disease of the central somatosensory nervous
system. See neuropathic pain note.
Peripheral neuropathic
pain*
Pain caused by a lesion or disease of the peripheral somatosensory
nervous system. See neuropathic pain note.
Neuropathy*
A disturbance of function or pathological change in a nerve: in one
nerve, mononeuropathy; in several nerves, mononeuropathy multiplex; if
diffuse and bilateral, polyneuropathy.
Note: Neuritis (q.v.) is a special case of neuropathy and is now reserved for inflammatory processes affecting nerves.
Nociception*
The neural process of encoding noxious stimuli.
Note: Consequences of encoding may be autonomic (e. g. elevated blood pressure) or behavioral (motor withdrawal reflex or more complex nocifensive behavior). Pain sensation is not necessarily implied.
Nociceptive neuron*
A central or peripheral neuron of the somatosensory nervous system that
is capable of encoding noxious stimuli.
Nociceptive pain*
Pain that arises from actual or threatened damage to non-neural tissue
and is due to the activation of nociceptors.
Note: This term is designed to contrast with neuropathic pain. The term is used to describe pain occurring with a normally functioning somatosensory nervous system to contrast with the abnormal function seen in neuropathic pain.
Nociceptive stimulus*
An actually or potentially tissue-damaging event transduced and encoded
by nociceptors.
Nociceptor*
A high-threshold sensory receptor of the peripheral somatosensory
nervous system that is capable of transducing and encoding noxious
stimuli.
Noxious stimulus*
A stimulus that is damaging or threatens damage to normal tissues.
Pain threshold*
The minimum intensity of a stimulus that is perceived as painful.
Note: Traditionally the threshold has often been defined, as we defined it formerly, as the least stimulus intensity at which a subject perceives pain. Properly defined, the threshold is really the experience of the patient, whereas the intensity measured is an external event. It has been common usage for most pain research workers to define the threshold in terms of the stimulus, and that should be avoided. However, the threshold stimulus can be recognized as such and measured. In psychophysics, thresholds are defined as the level at which 50% of stimuli are recognized. In that case, the pain threshold would be the level at which 50% of stimuli would be recognized as painful. The stimulus is not pain (q.v.) and cannot be a measure of pain.
Pain tolerance level*
The maximum intensity of a pain-producing stimulus that a subject is
willing to accept in a given situation.
Note: As with pain threshold, the pain tolerance level is the subjective experience of the individual. The stimuli which are normally measured in relation to its production are the pain tolerance level stimuli and not the level itself. Thus, the same argument applies to pain tolerance level as to pain threshold, and it is not defined in terms of the external stimulation as such.
Paresthesia
An abnormal sensation, whether spontaneous or evoked.
Note: Compare with dysesthesia. After much discussion, it has been agreed to recommend that paresthesia be used to describe an abnormal sensation that is not unpleasant while dysesthesia be used preferentially for an abnormal sensation that is considered to be unpleasant. The use of one term (paresthesia) to indicate spontaneous sensations and the other to refer to evoked sensations is not favored. There is a sense in which, since paresthesia refers to abnormal sensations in general, it might include dysesthesia, but the reverse is not true. Dysesthesia does not include all abnormal sensations, but only those that are unpleasant.
Sensitization*
Increased responsiveness of nociceptive neurons to their normal input,
and/or recruitment of a response to normally subthreshold inputs.
Note: Sensitization can include a drop in threshold and an increase in suprathreshold response. Spontaneous discharges and increases in receptive field size may also occur. This is a neurophysiological term that can only be applied when both input and output of the neural system under study are known, e.g., by controlling the stimulus and measuring the neural event. Clinically, sensitization may only be inferred indirectly from phenomena such as hyperalgesia or allodynia.
Central sensitization*
Increased responsiveness of nociceptive neurons in the central nervous
system to their normal or subthreshold afferent input.
Note: See note for sensitization and nociceptive neuron above. This may include increased responsiveness due to dysfunction of endogenous pain control systems. Peripheral neurons are functioning normally; changes in function occur in central neurons only.
Peripheral
sensitization*
Increased responsiveness and reduced threshold of nociceptive neurons in
the periphery to the stimulation of their receptive fields.
Note: See note for sensitization above.
Last Updated: 22·May·2012