anesthesia

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also an·aes·the·sia (ăn'ĭs-thē'zhə) pronunciation
n.
  1. Total or partial loss of sensation, especially tactile sensibility, induced by disease, injury, acupuncture, or an anesthetic, such as chloroform or nitrous oxide.
  2. Local or general insensibility to pain with or without the loss of consciousness, induced by an anesthetic.
  3. A drug, administered for medical or surgical purposes, that induces partial or total loss of sensation and may be topical, local, regional, or general, depending on the method of administration and area of the body affected.

[New Latin anaesthēsia, from Greek anaisthēsiā, insensibility : an-, without; see a-1 + aisthēsis, feeling (from aisthanesthai, aisthē-, to feel).]

WORD HISTORY   The following passage, written on November 21, 1846, by Oliver Wendell Holmes, a physician-poet and the father of the Supreme Court justice of the same name, allows us to pinpoint the entry of anesthesia and anesthetic into English: "Every body wants to have a hand in a great discovery. All I will do is to give you a hint or two as to names-or the name-to be applied to the state produced and the agent. The state should, I think, be called 'Anaesthesia' [from the Greek word anaisthēsia, "lack of sensation"]. This signifies insensibility-=@ellipsis4=- The adjective will be 'Anaesthetic.' Thus we might say the state of Anaesthesia, or the anaesthetic state." This citation is taken from a letter to William Thomas Green Morton, who in October of that year had successfully demonstrated the use of ether at Massachusetts General Hospital in Boston. Although anaesthesia is recorded in Nathan Bailey's Universal Etymological English Dictionary in 1721, it is clear that Holmes really was responsible for its entry into the language. The Oxford English Dictionary has several citations for anesthesia and anesthetic in 1847 and 1848, indicating that the words gained rapid acceptance.


Loss of sensation with or without loss of consciousness. There are several ways of producing anesthesia, with the choice dependent on the type of surgery and the medical condition and preference of the patient.

During general anesthesia a state of complete insensitivity or unconsciousness is produced when anesthetic gases are inhaled; adjuvant drugs are often given intravenously. Although the mechanism of general anesthesia is unknown, the anesthetics act on the upper reticular formation of neurons in the thalamus and midbrain (neuronal structures necessary for activating the cerebral cortex and maintaining an active, attentive state).

Analgesia, without loss of consciousness, results from injecting a solution of local anesthetic drug either into the cerebrospinal fluid surrounding the spinal cord (spinal anesthesia) or into the epidural space surrounding the cerebrospinal fluid (epidural anesthesia). The local anesthetic acts by blocking the conduction of nerve impulses. Narcotic opioids are injected postoperatively into either the epidural space or cerebrospinal fluid for pain relief.

Analgesia can be localized to a small area, for example, the forearm, by injecting a local anesthetic solution around nerves supplying the area (the bracheal plexus in the upper arm and chest supplies the forearm). Large peripheral nerves may also be blocked individually by using this method.

Acupuncture is an ancient procedure, once used only in China but now practiced in the United States and elsewhere. It involves inserting needles into specific points around the body, as determined from historical charts, and manipulation of the needles; sometimes electric current is applied. Weak analgesia results through alteration of pain perception. Although sometimes helpful for chronic pain, acupuncture generally has not been found satisfactory for surgical anesthesia. See also Central nervous system; Pain.


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anesthesia (ănĭsthē'zhə) [Gr.,=insensibility], loss of sensation, especially that of pain, induced by drugs, especially as a means of facilitating safe surgical procedures. Early modern medical anesthesia dates to experiments with nitrous oxide (laughing gas) by Sir Humphry Davy of England and the dentist Horace Wells of the United States. Ether came into general use as an anesthetic after a demonstration at the Massachusetts General Hospital in Boston by William T. G. Morton in 1846.

General anesthetics, administered by inhalation or intravenous injection, cause unconsciousness as well as insensibility to pain, and are used for major surgical procedures. In the past, ether was the most commonly used general anesthetic. Today, safer anesthetics include Halothane and Isoflurane, both of which are administered through inhalation. Short-acting anesthetic agents, such as pentothal, Diprivan, and Midazolam, are generally given through intravenous or intramuscular routes. Inhaled nitrous oxide is used for light anesthesia in minor surgical procedures and in dentistry. Ultra-short-acting analgesics can also be given intranasally for pre-medication prior to the induction of general anesthesia. Anesthetics such as Brevital may be administered rectally, primarily among children.

Local anesthetics affect sensation only in the region where they are injected, and are used regularly in dentistry and minor surgery. Spinal and epidural anesthesia involves the injection of an anesthetic agent into a space adjacent to the spinal cord, a technique frequently employed for surgical procedures below the waist (e.g., obstetrics) where total unconsciousness is not necessary. Such anesthetics are known as regional blocks. Muscle relaxants may be used in conjunction with general anesthetics, particularly to reduce the amount of anesthetic required. Body temperatures are generally lowered in conjunction with the use of anesthetics in heart and brain surgery, reducing the body's metabolic rate so that cells are not damaged by the lack of circulating blood and reduced oxygenation. Several forms of anesthesia may be used in combination. Safer and more efficient anesthetics are constantly researched, in the hopes of perfecting new ways of combining and administering them.

See also acupuncture, analgesic, anesthesiology, and surgery.

Bibliography

See J. Rupreht et al., ed., Anesthesia: Essays on Its History (1985); J. Tolmie and A. Birch, Anesthesia for the Uninterested (2d ed. 1986); J. M. Fenster, Ether Day: The Strange Tale of America's Greatest Medical Discovery and the Haunted Men Who Made It (2001).


(an-is-thee-zhuh)

Loss of sensation or consciousness. Anesthesia can be induced by an anesthetic, by acupuncture, or as the result of injury or disease.

Anaesthesia may be described as a reversible loss of consciousness produced by a drug, from which arousal does not take place even with painful stimuli such as setting a fracture or surgical operation. In this latter respect it differs from sleep or the change in consciousness following sensory deprivation, and it is this that made it so revolutionary a discovery, opening the gateway to modern surgery and safer childbirth. The name is not quite exact, since loss of consciousness is not the same as loss of feeling, and a good anaesthetic in clinical practice should exert other actions, such as some analgesia (to diminish reflex responses to what would be very painful stimuli) and muscular relaxation (to facilitate the surgeon's work). When an anaesthetic such as ether or chloroform is given, there is a characteristic progression of effects, first described by Guedel in 1937: first analgesia, some loss of memory, and perhaps euphoria; then consciousness is lost, but the patient may struggle, breathe irregularly, is sweating and flushed; in the third stage, the patient becomes quieter with regular breathing, but the eyeballs move rhythmically and a good many reflexes are still present. As anaesthesia deepens, and the patient passes through the successive planes of the third stage, various reflexes progressively fall away, the breathing becomes shallower, and eventually death may ensue (the fourth stage). In modern practice anaesthesia is induced with a suitable barbiturate (such as thiopentone) injected intravenously: the patient then passes through the early stages within seconds; once 'under', anaesthesia is usually maintained by some other substance.

How do anaesthetics work? It is paradoxical that more is known at the molecular level than at any other. A remarkable feature is the astonishing range of substances that can produce anaesthesia: in addition to the classical anaesthetics and the barbiturates, nitrogen in the air (if given at high pressure) and many other gases, alcohols, dry cleaning fluids (such as trichloroethene), industrial solvents, and certain steroids can all produce typical anaesthesia. There is no common chemical structure such as would suggest a specific action on some particular part of the brain. Instead, as two pharmacologists, Overton and Meyer, pointed out over 80 years ago, anaesthetics all share the property of dissolving in fats and it is remarkable that one can predict the potency of an anaesthetic quite accurately by measuring the pressure of a gas or the concentration of a vapour that will produce a given concentration (about 0.05 moles per litre) of the substance concerned in olive oil. Modern work has revealed the significance of this: the cell membrane, which defines the cell's limits, and across which an electric potential is maintained, consists of an ordered array of fatty molecules (mostly phospholipids and cholesterol); the anaesthetic dissolves in it, and slightly expands and disorders the membrane. Since the membrane also carries large protein molecules (enzymes, ion channels, receptors, transport mechanisms) which mediate its 'traffic' with its environment and with other cells, disturbance of their normal function becomes possible. A fascinating aspect is that very high pressures (which compress and reorder the membrane) cause recovery from anaesthesia. Conversely, a suitable amount of an anaesthetic can be used to neutralize the adverse effects of high pressure. The 'high-pressure nervous syndrome', which includes tremor, bursts of 'micro-sleep', and convulsions, threatened to limit the depth to which divers could go, but the addition of nitrogen (using it as a small dose of anaesthetic) to the diver's helium–oxygen mixture has extended that limit.

But if one asks, 'On what synapses, or on what cell groups of the brain, is this molecular action particularly exerted?', no satisfactory answer exists. The simple fact of surgical anaesthesia shows that higher brain functions are particularly sensitive, while respiration and simple reflexes, as well as other bodily processes like the heartbeat, are relatively resistant. Detailed analysis yields a bewildering variety of effects, with actions both pre- and post-synaptically, varying with the synapse and with the anaesthetic. A simple view is that the anaesthetic picks out any delicately poised nervous activity, and that the pattern of anaesthetic activity is simply that of reduced activity in the most vulnerable nervous pathways — particularly complex nervous functions rather than (for example) simple reflex movement. Theories include the idea of a specific effect on the 'ascending reticular activating system', in the absence of whose activity the cerebral cortex is believed to relapse into a sleeping state, or on cortical cells generally. Some recent drugs (such as ketamine), which produce the so-called 'dissociative anaesthesia', may help to throw light on the problem; these differ, both in having a specific chemical structure and in producing a rather different pattern of anaesthesia.

There is an abundant literature on the effects of anaesthetics on mental function, short of anaesthesia, and Humphry Davy's description (in 1800) of the effect of nitrous oxide (laughing gas) on himself and his friends (including Southey, Coleridge, Roget, and Wedgwood) reveals the salient features recorded many times subsequently: considerable variation with the individual; excitement; euphoria or sometimes dysphoria; compulsive movements or laughter; 'thrilling' sensations in the limbs; feelings of deep significance; rush of ideas; synaesthesiae; drowsiness; warmth, rapid breathing, palpitations, giddiness; and often a strong desire to repeat the performance. This last characteristic brings the risk of addiction in its train, particularly for those (such as anaesthetists and nurses) with easy access to the drugs; and it shows itself again in 'glue-sniffing' in children, or with workers using some solvents in industry.

An important feature with all these volatile substances is the speed with which effects are produced by inhalation, by which the vapour passes very quickly into the circulation. More familiar to most people will be the effect of anaesthetics such as alcohol or barbiturates taken orally, with an onset delayed by circulatory absorption, and the fact that by this route some of the more dramatic effects are lacking (although euphoria and the risk of addiction remain) suggests that these effects are largely due to especially rapid access to, and uptake by, particular parts of the brain, producing a selective action which fades as distribution of the drug becomes general. With sustained exposure to any anaesthetic, the adaptation known as 'tolerance' develops, by which an increasing dose is required to produce the effect. 'Cross-tolerance' occurs between different anaesthetics — hence the difficulty often encountered of anaesthetizing an alcoholic! When exposure stops and the drug is withdrawn, characteristic symptoms appear: for example, insomnia after a short course of any sleeping pill, or delirium tremens (DTs) after prolonged high exposure to alcohol, or convulsions after chronic barbiturate use. While some of the adaptive changes may be biochemical, some of them certainly represent a change in nerve cell function, and there are interesting indications that the composition of the cell membrane changes so as to reduce the effect of the anaesthetic.

One would like to think that experience with anaesthetics would deepen our understanding of consciousness, mood, sensation, pain, memory. Yet it is still impossible to move convincingly from the subjective phenomena to physiological understanding. Perhaps it is unreasonable to expect to do so until our knowledge of normal neurophysiology is more satisfactory, or perhaps pharmacology and physiology need to proceed, collaboratively, in parallel. Some areas may be picked out as potentially fruitful.

1. The effect on sense of time. There is a puzzle here: nitrous oxide and alcohol appear to reduce 'felt' time compared with 'clock' time, whereas ketamine (like cannabis) prolongs it. With the latter drugs, one can readily suggest, as William James suggested, that 'disinhibition' in the brain, allowing a greater than normal sensory input, could give rise to an experience of more numerous mental impressions than usual per unit of 'clock' time, and hence a greater 'felt' time. But why should other anaesthetics differ?
2. The effect on pain sense. There is some evidence that enkephalins or endorphins may play a part in analgesia produced by anaesthetics. (See neuropeptides.) But there remain remarkable differences between anaesthetics, some with pronounced analgesic action, some potentiating the response to a painful stimulus. Bearing in mind its practical relevance, as well as the recent advances in our knowledge of the neuroanatomy and neurochemistry of the nociceptive pathways, and the successful application of decision theory to the study of pain, a systematic study of the action of a range of anaesthetics on pain discrimination and pain report seems well worth while.
3. The effect on sensation generally. An intriguing but neglected observation is that anaesthetics facilitate the generation of impulses in the vagal nerve fibres registering the inflation of the lung, which accounts for the ability of many anaesthetics to produce what is known as 'rapid shallow breathing'. It is an intriguing action and, exerted peripherally on the proprioceptive endings in muscles, it might account for the 'thrilling' sensation described by Davy. But more generally there might also be an important effect both on the pattern of sensory input to the brain and on subsequent processing.
4. Effect on memory. With the recent advances in our knowledge of registration, consolidation, and retrieval, systematic study of the effect of a range of anaesthetics on memory is overdue, although the problem is complicated by 'state dependence'. An old method of anaesthesia for childbirth, 'twilight sleep', exploited the effect of the drug hyoscine on memory, so that, even if pain was felt, it was not remembered. The method has been abandoned because of the effect on the baby, but the approach is still interesting.
5. The concept of disinhibition is constantly, and plausibly, invoked to account for phenomena such as the rush of ideas, synaesthesia, and electroencephalographic synchronization. The underlying idea is that the great complexity of mental activity does not merely need some neurons to be active, but also needs others to be actively 'switched off' (inhibited): if the latter process were interfered with (disinhibition), then differential activity and 'gating' of information transfer could become progressively impaired. Simple model systems exist, illustrating how depression of an inhibitory pathway can lead to release phenomena, but no serious attempt has been made to extend the idea to more complex systems. Yet if certain inhibitory mechanisms are particularly vulnerable, it should be possible, by careful choice of systems sharing common elements, to identify them more closely.
6. A tedious but necessary development is that of knowledge about the kinetics of anaesthetic distribution in the brain. Some knowledge exists of the rise and fall of the concentration of an anaesthetic during and after an exposure, for samples of brain containing thousands or millions of neurons. But this is merely a gross average, telling us nothing of local concentration in synaptic detail. Equilibrium with an anaesthetic is virtually never reached in clinical practice, and rarely in experimental work, so that (as mentioned earlier) there is ample scope for differential effects arising, not from the properties of the drug itself, but from varying access and uptake. For instance, evidence is accumulating that if any part of the brain becomes particularly active it consumes more energy, with a corresponding increase in blood flow, which would at once open the way to differential access by an anaesthetic.
7. Finally one must recall that, despite all the advances in neuroanatomy, it is only a tiny minority of nervous pathways that can be precisely and completely described in anatomical and neurochemical detail, with the specific neurons and their connections specified. But some beautiful techniques now exist for mapping out these pathways, for recording the activity of single or groups of neurons, and for neurochemical analysis (see neuroanatomical techniques): the new methods of anaesthesia that a deeper understanding will provide are not far away.

(Published 1987)

— Sir Willam Patron

    Bibliography
  • Miller, K. W. (1986). 'General anaesthetics'. In Feldman, S. A., Scurr, C. F., and Paton, W. D. M. (eds.), Mechanisms of Action of Drugs in Anaesthetic Practice.
  • Paton, W. D. M. (1984). 'How far do we understand the mechanism of anaesthesia?' European Journal of Anaesthesiology, 1.


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anesthesia

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pronunciation

IN BRIEF: A condition or substance that results in the lack of feeling.

pronunciation Carla insisted on having anesthesia before the dentist began to drill.

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Loss of feeling or sensation. Artificial anesthesia may be produced by a number of agents capable of bringing about partial or complete loss of sensation. It is induced to permit the performance of surgery or other painful procedures. See also anesthetic.

  • balanced a. — anesthesia that balances the depressing effects on the motor, sensory, reflex and mental aspects of nervous system function by the anesthetic agents. The philosophy encourages the use of several agents, each designed to affect one of the functions.
  • basal a. — narcosis produced by preliminary medication so that the inhalation of anesthetic necessary to produce surgical anesthesia is greatly reduced.
  • block a. — regional anesthesia. See also block.
  • caudal a. — injection of an anesthetic into the sacral canal. See also caudal anesthesia.
  • central a. — lack of sensation caused by disease of the nerve centers.
  • closed a. — that produced by continuous rebreathing of a small amount of anesthetic gas in a closed system with an apparatus for removing carbon dioxide.
  • crossed a. — loss of sensation on one side of the face and loss of pain and temperature sense on the opposite side of the body.
  • dissociated a., dissociation a. — loss of perception of certain stimuli while that of others remains intact.
  • electric a. — anesthesia induced by passage of an electric current.
  • endotracheal a. — anesthesia produced by introduction of a gaseous mixture through a tube inserted into the trachea.
  • epidural a. — see epidural anesthesia.
  • field block a. — the anesthetic agent is injected around the boundaries of the area to be anesthetized, with no attempt to locate specific nerves.
  • frost a. — abolition of feeling or sensation as a result of topical refrigeration produced by a jet of a highly volatile liquid.
  • general a. — a state of unconsciousness produced by anesthestic agents, with absence of pain sensation over the entire body and a greater or lesser degree of muscular relaxation; the drugs producing this state can be administered by inhalation, intravenously, intramuscularly, or rectally, or via the gastrointestinal tract.
  • infiltration a. — local anesthesia produced by injection of the anesthetic solution directly into the area of terminal nerve endings.
  • inhalation a. — anesthesia produced by the respiration of a volatile liquid or gaseous anesthetic agent. Halothane, methoxyflurane, isoflurane, and a combination of nitrous oxide and oxygen are the common agents in veterinary use.
  • insufflation a. — anesthesia produced by introduction of a gaseous mixture into the trachea through a slender tube.
  • intrasynovial a. — injection of a local anesthetic agent into a joint or tendon sheath.
  • intrathecal a. — introduction of local anesthetic agent into the spinal fluid by penetration of the spinal dura. Causes anesthesia in the tissues supplied by the nerves in the spinal cord zone that has been anesthetized. There is danger of injury to the cord and the technique is litte used in veterinary surgery. Called also subarachnoid, subdural or intradural anesthesia/analgesia.
  • intravenous a. — the anesthetic agent, e.g. a barbiturate, is administered intravenously to effect. If an intravenous catheter is used, ‘topping-up’ amounts can also be administered as required.
  • intravenous regional a. — see bier technique.
  • irreversible a. — the loss of sensory and motor function of the part is permanent. The local injection of isopropyl alcohol has this effect.
  • local a. — that produced in a limited area, as by injection of a local anesthetic or by freezing with ethyl chloride. Includes infiltration, nerve block, field block, surface, regional, retrograde regional, spinal, epidural.
  • mixed a. — that produced by use of more than one anesthetic agent.
  • nerve block a. — the anesthetic agent is deposited from a syringe and needle as close to the target nerve as possible. Several injections are often made if the landmarks for the location of the nerve are not outstanding.
  • obstetrical a. — see obstetrical anesthesia.
  • open a. — general inhalation anesthesia in which there is no rebreathing of the expired gases.
  • parasacral a. — regional anesthesia produced by injection of a local anesthetic around the sacral nerves as they emerge from the sacral foramina.
  • paravertebral a. — regional anesthesia produced by the injection of a local anesthetic around the spinal nerves at their exit from the spinal column, and outside the spinal dura.
  • parenteral a. — anesthesia induced by the injection of the agent, either intravenously, intraperitoneally, subcutaneously or intramuscularly.
  • peripheral a. — lack of sensation due to changes in the peripheral nerves.
  • permeation a. — analgesia of a body surface produced by application of a local anesthetic, most commonly to the mucous membranes. Called also surface anesthesia.
  • rectal a. — anesthesia produced by introduction of the anesthetic agent into the rectum.
  • refrigeration a. — local anesthesia produced by applying a tourniquet and chilling the part to near freezing temperature. Called also cryoanesthesia.
  • regional a. — insensibility caused by interrupting the sensory nerve conductivity of any region of the body: produced by (1) field block, encircling the operative field by means of injections of a local anesthetic; or (2) nerve block, making injections in close proximity to the nerves supplying the area.
  • saddle block a. — the production of anesthesia in the region of the body corresponding roughly with the areas of the buttocks, perineum and inner aspects of the thighs, by introducing the anesthetic agent low in the dural sac.
  • segmental a. — loss of sensation in a segment of the body due to a lesion of a nerve root.
  • spinal a. — 1. anesthesia due to a spinal lesion.
  • — 2. anesthesia produced by injection of the agent beneath the membrane of the spinal cord.
  • splanchnic a. — block anesthesia for visceral operation by injection of the anesthetic agent into the region of the celiac ganglia.
  • subarachnoid a. — see intrathecal anesthesia (above).
  • surface a. — the application of a local anesthetic agent in solution, as in eye drops, or as a jelly, cream or ointment. The use of cold materials which freeze the superficial layers of skin is not much used in veterinary surgery. See also permeation anesthesia (above).
  • surgical a. — that degree of anesthesia at which operation may safely be performed. There is muscular relaxation, and coordinated movements, consciousness and pain sensations disappear; many of the spinal neuromuscular reflexes are abolished.
  • topical a. — that produced by application of a local anesthetic directly to the area involved.
(an′esthē′zē-ə, an′esthē′zhə)
n

The loss of feeling or sensation, especially loss of tactile sensibility, with or without loss of consciousness.

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categories related to 'anesthesia'

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Random House Word Menu by Stephen Glazier
For a list of words related to anesthesia, see:
  • Signs and Symptoms - anesthesia: loss of sensation in part or all of body
  • Procedures - anesthesia: introduction of local or general anesthetic into body, usu. preparatory to surgery


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Anesthesia, or anaesthesia (see spelling differences; from Greek αν-, an-, "without"; and αἴσθησις, aisthēsis, "sensation"), traditionally meant the condition of having sensation (including the feeling of pain) blocked or temporarily taken away. It is a pharmacologically induced and reversible state of amnesia, analgesia, loss of responsiveness, loss of skeletal muscle reflexes or decreased fight-or-flight response, or all simultaneously. This allows patients to undergo surgery and other procedures without the distress and pain they would otherwise experience. An alternative definition is a "reversible lack of awareness," including a total lack of awareness (e.g. a general anesthetic) or a lack of awareness of a part of the body such as a spinal anesthetic. The pre-existing word anesthesia was suggested by Oliver Wendell Holmes, Sr. in 1846 as a word to use to describe this state.[1]

Types of anesthesia include local anesthesia, regional anesthesia, general anesthesia, and dissociative anesthesia. Local anesthesia inhibits sensory perception within a specific location on the body, such as a tooth or the urinary bladder. Regional anesthesia renders a larger area of the body insensate by blocking transmission of nerve impulses between a part of the body and the spinal cord. Two frequently used types of regional anesthesia are spinal anesthesia and epidural anesthesia. General anesthesia refers to inhibition of sensory, motor and sympathetic nerve transmission at the level of the brain, resulting in unconsciousness and lack of sensation.[2] Dissociative anesthesia uses agents that inhibit transmission of nerve impulses between higher centers of the brain (such as the cerebral cortex) and the lower centers, such as those found within the limbic system.

Contents

History

Plant derivatives

Throughout Europe, Asia, and the Americas a variety of Solanum species containing potent tropane alkaloids were used, such as mandrake, henbane, Datura metel, and Datura inoxia. Ancient Greek and Roman medical texts by Hippocrates, Theophrastus, Aulus Cornelius Celsus, Pedanius Dioscorides, and Pliny the Elder discussed the use of opium and Solanum species. In 13th century Italy, Theodoric Borgognoni used similar mixtures along with opiates to induce unconsciousness, and treatment with the combined alkaloids proved a mainstay of anesthesia until the nineteenth century. In the Americas coca was also an important anesthetic used in trephining operations. Incan shamans chewed coca leaves and performed operations on the skull while spitting into the wounds they had inflicted to anesthetize the site.[citation needed] Alcohol was also used, its vasodilatory properties being unknown. Ancient herbal anesthetics have variously been called soporifics, anodynes, and narcotics, depending on whether the emphasis is on producing unconsciousness or relieving pain.

The use of herbal anesthesia had a crucial drawback compared to modern practice—as lamented by Fallopius, "When soporifics are weak, they are useless, and when strong, they kill." To overcome this, production was typically standardized as much as feasible, with production occurring from specific locations (such as opium from the fields of Thebes in ancient Egypt). Anesthetics were sometimes administered in the "spongia somnifera", a sponge into which a large quantity of drug was allowed to dry, from which a saturated solution could be trickled into the nose of the patient. At least in more recent centuries, trade was often highly standardized, with the drying and packing of opium in standard chests, for example. In the 19th century, varying aconitum alkaloids from a variety of species were standardized by testing with guinea pigs. Trumping this method was the discovery of morphine, a purified alkaloid that could be injected by hypodermic needle for a consistent dosage. The enthusiastic reception of morphine led to the foundation of the modern pharmaceutical industry.[citation needed]

The first effective local anesthetic was cocaine. Isolated in 1859, it was first used by Karl Koller, at the suggestion of Sigmund Freud, in eye surgery in 1884.[1] German surgeon August Bier (1861–1949) was the first to use cocaine for intrathecal anesthesia in 1898.[3] Romanian surgeon Nicolae Racoviceanu-Piteşti (1860–1942) was the first to use opioids for intrathecal analgesia; he presented his experience in Paris in 1901.[3] A number of newer local anesthetic agents, many of them derivatives of cocaine, were synthesized in the 20th century, including eucaine (1900), amylocaine (1904), procaine (1905), and lidocaine (1943).

Sweet vitriol and laughing gas

In 1275, Spanish physician Raymond Lullus, while experimenting with chemicals, made a volatile, flammable liquid he called sweet vitriol.[citation needed] In the 16th century, a Swiss-born physician commonly known as Paracelsus made chickens breathe sweet vitriol and noted that they not only fell asleep but also felt no pain. Like Lullus before him, he did not experiment on humans. In 1730, German chemist Frobenius gave this liquid its present name, ether, which is Greek for “heavenly.” But 112 more years would pass before ether’s anesthetic powers were fully appreciated. Meanwhile, in 1772, English scientist Joseph Priestley discovered the gas nitrous oxide. Initially, people thought this gas to be lethal, even in small doses. However, in 1799, British chemist and inventor Humphry Davy decided to find out by experimenting on himself. To his astonishment he found that nitrous oxide made him laugh, so he nicknamed it laughing gas. Davy wrote about the potential anesthetic properties of nitrous oxide, but nobody at that time pursued the matter any further.

Early inhalational anesthetics

Contemporary re-enactment of Morton's 16 October 1846, ether operation; daguerrotype by Southworth & Hawes

American physician Crawford W. Long noticed that his friends felt no pain when they injured themselves while staggering around under the influence of ether. He immediately thought of its potential in surgery. Conveniently, a participant in one of those “ether frolics,” a student named James Venable, had two small tumors he wanted excised. But fearing the pain of surgery, Venable kept putting the operation off. Hence, Long suggested that he have his operation while under the influence of ether. Venable agreed, and on 30 March 1842, he had a painless operation. However, Long did not announce his discovery until 1849.[4]

William Thomas Green Morton, a Boston dentist, conducted the first public demonstration of the inhalational anesthetic. Morton, who was unaware of Long's previous work, was invited to the Massachusetts General Hospital to demonstrate his new technique for painless surgery. After Morton had induced anesthesia, surgeon John Collins Warren removed a tumor from the neck of Edward Gilbert Abbott. This occurred in the surgical amphitheater now called the Ether Dome. The previously skeptical Dr. Warren was impressed and stated "Gentlemen, this is no humbug." In a letter to Morton shortly thereafter, physician and writer Oliver Wendell Holmes, Sr. proposed naming the state produced "anesthesia", and the procedure an "anesthetic".[5]

Morton at first attempted to hide the actual nature of his anesthetic substance, referring to it as Letheon. He received a US patent for his substance, but news of the successful anesthetic spread quickly by late 1846. Respected surgeons in Europe including Liston, Dieffenbach, Pirogov, and Syme, quickly undertook numerous operations with ether. An American-born physician, Boott, encouraged London dentist James Robinson to perform a dental procedure on a Miss Lonsdale. This was the first case of an operator-anesthetist. On the same day, 19 December 1846, in Dumfries Royal Infirmary, Scotland, a Dr. Scott used ether for a surgical procedure.[citation needed] The first use of anesthesia in the Southern Hemisphere took place in Launceston, Tasmania, that same year. Drawbacks with ether such as excessive vomiting and its flammability led to its replacement in England with chloroform.

Discovered in 1831, the use of chloroform in anesthesia is linked to James Young Simpson, who, in a wide-ranging study of organic compounds, found chloroform's efficacy on 4 November 1847. Its use spread quickly and gained royal approval in 1853 when John Snow gave it to Queen Victoria during the birth of Prince Leopold. Unfortunately, chloroform is not as safe an agent as ether, especially when administered by an untrained practitioner (medical students, nurses, and occasionally members of the public were often pressed into giving anesthetics at this time). This led to many deaths from the use of chloroform that (with hindsight) might have been preventable. The first fatality directly attributed to chloroform anesthesia was recorded on 28 January 1848 after the death of Hannah Greener.[citation needed]

John Snow of London published articles from May 1848 onwards "On Narcotism by the Inhalation of Vapours" in the London Medical Gazette. Snow also involved himself in the production of equipment needed for the administration of inhalational anesthetics.

Anesthesia providers

Doctors specializing in perioperative care, development of an anesthetic plan, and the administration of anesthetics are known in the US as anesthesiologists and in the UK, Canada, Australia, and NZ as anaesthetists or anaesthesiologists. All anesthetics in the UK, Australia, New Zealand, Hong Kong and Japan are administered by doctors. Nurse anesthetists also administer anesthesia in 109 nations.[6] In the US, 35% of anesthetics are provided by physicians in solo practice, about 55% are provided by anesthesia care teams (ACTs) with anesthesiologists medically directing anesthesiologist assistants or certified registered nurse anesthetists (CRNAs), and about 10% are provided by CRNAs in solo practice.[7][8][9][10][11]

Physicians

Anesthesia students training with a patient simulator

In the strict sense, the term anesthetist refers to any individual who administers anesthesia. In the US, however, the term is most commonly employed to refer to registered nurses who have completed specialized education and training in anesthesia to become certified registered nurse anesthetists (CRNAs). In the US and Canada, medical doctors who specialize in anesthesiology are called anesthesiologists. Such physicians in the United Kingdom (UK), Australia and New Zealand are called anaesthetists.

In the US, a physician specializing in anesthesiology typically completes four years of college, four years of medical school, and four years of postgraduate medical training or residency[12] According to the American Society of Anesthesiologists, anesthesiologists provide or participate in more than ninety percent of the forty million anesthetics delivered annually.[13] In the UK, this training lasts a minimum of seven years after the awarding of a medical degree and two years of basic residency, and takes place under the supervision of the Royal College of Anaesthetists.[citation needed] In Australia and New Zealand, it lasts five years after the awarding of a medical degree and two years of basic residency, under the supervision of the Australian and New Zealand College of Anaesthetists.[14] Other countries have similar systems, including Ireland (the Faculty of Anaesthetists of the Royal College of Surgeons in Ireland), Canada and South Africa (the College of Anaesthetists of South Africa).

In the US, satisfactory completion of the written and oral Board examinations allows an anesthesiologist to be called a "Diplomate" of the American Board of Anesthesiology (or of the American Osteopathic Board of Anesthesiology, for osteopathic physicians). This is often referred to colloquially as being "Board Certified". In the UK, Fellowship of the Royal College of Anaesthetists (FRCA) is conferred upon medical doctors following satisfactory completion of the written and oral parts of the Royal College's examination.

The role of the anesthesiologist is no longer limited to the operation itself. Many anesthesiologists function as perioperative physicians, ensuring optimal analgesia and maintenance of physiologic homeostasis throughout the preoperative, intraoperative, and postoperative periods. Anesthesiologists may elect to subspecialize in anesthesia for particular types of surgery (cardiothoracic, obstetrical, neurosurgical, pediatric), regional anesthesia, acute or chronic pain medicine, or Intensive Care Medicine.

Anesthesia providers are often trained using full scale human simulators. The field was an early adopter of this technology and has used it to train students and practitioners at all levels for the past several decades. Notable centers in the United States can be found at the Johns Hopkins Medicine Simulation Center,[15] Harvard's Center for Medical Simulation,[16] Stanford,[17] The Mount Sinai School of Medicine HELPS Center in New York,[18] and Duke University.[19]

Nurse anesthetists

In the United States, advanced practice nurses specializing in the provision of anesthesia care are known as certified registered nurse anesthetists (CRNAs). According to the American Association of Nurse Anesthetists, the 39,000 CRNAs in the US administer approximately 30 million anesthetics each year, roughly two thirds of the US total.[20] 34% of nurse anesthetists practice in communities of less than 50,000. CRNAs start school with a bachelors degree in nursing and at least 1 year of acute care nursing experience,[21] and gain a masters degree in nurse anesthesia before passing the mandatory Certification Exam. Masters-level CRNA training programs range in length from 24 to 36 months.

CRNAs may work with podiatrists, dentists, anesthesiologists, surgeons, obstetricians and other professionals requiring their services. CRNAs administer anesthesia in all types of surgical cases, and are able to apply all the accepted anesthetic techniques—general, regional, local, or sedation. 34 states require physician supervision of a CRNA's practice, and hospitals can regulate what CRNAs can or can not do based on local laws.[22]

In the United States, the Centers for Medicare and Medicaid Services (CMS), a federal agency within the United States Department of Health and Human Services, determines the conditions for payment for all anesthesia services provided under the Medicare, Medicaid, and State Children's Health Insurance Program (SCHIP) programs. For the purposes of payment for anesthesiology services, CMS defines an anesthesia practitioner as a physician who performs the anesthesia service alone, a CRNA who is not medically directed, or a CRNA or AA who is medically directed.[23] Under the QZ Anesthesia Claims Modifier, CMS allows payment to a CRNA for anesthesiology services provided under these programs without medical direction by a physician.[23] Furthermore, under CMS regulations, anesthesia must be administered only by:

  • a qualified doctor of medicine or osteopathic medicine, dentist, oral surgeon, or podiatrist;
  • a CRNA who, unless exempted, is under the supervision of the operating practitioner or of an anesthesiologist;
  • an anesthesiologist's assistant who is under the supervision of an anesthesiologist.[24]

The aforementioned exemption for CRNAs is the State exemption (also referred to as an "opt-out"). Under the State exemption, if the State in which the hospital is located submits a letter to CMS requesting exemption from physician supervision of CRNAs, and that letter has been signed by the Governor of that State, then hospitals within that State may be exempted from the requirement for physician supervision of CRNAs.[24] In 2001, CMS established this exemption for CRNAs from the physician supervision requirement by recognizing a Governor's written request to CMS attesting that it is in the best interests of the State's citizens to exercise this exemption.[25] As of September 2010, sixteen states (California, Iowa, Nebraska, Idaho, Minnesota, New Hampshire, New Mexico, Kansas, North Dakota, Washington, Alaska, Oregon, South Dakota, Wisconsin, Montana and Colorado) have chosen to opt-out of the CRNA physician supervision regulation.[25]

Anesthesiologist assistants

In the United States, anesthesiologist assistants (AAs) are graduate-level trained specialists who have undertaken specialized education and training to provide anesthesia care under the direction of an anesthesiologist. AAs typically hold a masters degree and practice under anesthesiologist supervision in 18 states and the District of Columbia through licensing, certification or physician delegation.[26]

In the UK, a similar group of assistants are currently being evaluated. They are referred to as "physician assistant (anaesthesia)" (PAA). Their background can be nursing, operating department practice, another of the allied medical professions, or even one of the natural sciences.[27] Training is in the form of a postgraduate diploma and takes 27 months to complete.[27]

Operating department practitioners

In the United Kingdom, operating department practitioners provide assistance and support to the anesthetist or anesthesiologist. They can also assist the surgeon with surgical procedures and provide postoperative care to patients emerging from anesthesia. ODPs can be found in the operating department, accident and emergency department, intensive care unit, high dependency unit and in radiology, cardiology and endoscopy suites which require anesthesia support. They may also work with organ transplantation teams, as well as provide pre-hospital care to trauma victims. They are state-registered in the UK. The ODP is a mid-level practitioner of perioperative medicine. ODPs also function as lecturers and trainers in cardiopulmonary resuscitation, and work in management positions in operating departments.

Veterinary anesthetists and anesthesiologists

Much of the equipment and drugs utilized by veterinary anesthetists is similar or identical to that used in anesthesia for human patients. There are vast differences in the physiology of different animal species, which may influence the choice of anesthetic agents and delivery systems in organisms ranging in diversity from (for example) annelids to elephants. For many wild animals, anesthetic drugs must often be delivered from a distance by means of remote projector systems ("dart guns") before the animal can even be approached. Large domestic livestock can often be anesthetized for certain types of surgery in the standing position using only local anesthetics and sedative drugs. While most clinical veterinarians and veterinary technicians routinely function as anesthetists in the course of their professional duties, veterinary anesthesiologists in the U.S. are veterinarians who have completed a three year residency in anesthesia and have qualified for certification by the American College of Veterinary Anesthesiologists.

Other personnel

Anesthesia technicians are specially trained Anaesthetic Assistants,equivalent to Operating Department Practitioners in Great Britain. They do not administer anesthesia, but rather they assist anesthesia providers similar to the way in which scrub technicians assist surgeons. Commonly these services are collectively called perioperative services, and thus the term perioperative service technician (PST) is used interchangeably with anesthesia technician. In the United States, an anesthesia technician can become a Certified Anesthesia Technician (Cer.A.T.), followed by becoming a Certified Anesthesia Technologist (Cer.A.T.T.) through American Society of Anesthesia Technologists & Technicians (ASATT).[28] In New Zealand, an anesthetic technician completes a course of study recognized by the New Zealand Anaesthetic Technicians Society.[29]

Anesthetic agents

An anesthetic agent is a drug that brings about a state of anesthesia. A wide variety of drugs are used in modern anesthetic practice. Many are rarely used outside of anesthesia, although others are used commonly by all disciplines. Anesthetics are categorized in to two categories: general anesthetics cause a reversible loss of consciousness (general anesthesia), while local anesthetics cause reversible local anesthesia and a loss of nociception.

Anesthetic equipment

In modern anesthesia, a wide variety of medical equipment is desirable depending on the necessity for portable field use, surgical operations or intensive care support, and the type(s) of anesthetic(s) to be administered. Anesthesia practitioners must possess a comprehensive and intricate knowledge of the production and use of various medical gases, anesthetic agents and vapors, medical breathing circuits and the variety of anesthetic machines (including vaporizers, ventilators and pressure gauges) and their corresponding safety features, hazards and limitations of each piece of equipment, for the safe, clinical competence and practical application for day to day practice. The risk of transmission of infection by anesthetic equipment has been a problem since the beginnings of anesthesia. Although most equipment that comes into contact with patients is disposable, there is still a risk of contamination from the anesthetic machine itself[30] or because of bacterial passage through protective filters.[31]

Anesthetic monitoring

Patients under general anesthesia must undergo continuous physiological monitoring to ensure safety. In the US, the American Society of Anesthesiologists (ASA) have established minimum monitoring guidelines for patients receiving general anesthesia, regional anesthesia, or sedation. This includes electrocardiography (ECG), heart rate, blood pressure, inspired and expired gases, oxygen saturation of the blood (pulse oximetry), and temperature.[32] In the UK the Association of Anaesthetists (AAGBI) have set minimum monitoring guidelines for general and regional anesthesia. For minor surgery, this generally includes monitoring of heart rate, oxygen saturation, blood pressure, and inspired and expired concentrations for oxygen, carbon dioxide, and inhalational anesthetic agents. For more invasive surgery, monitoring may also include temperature, urine output, blood pressure, central venous pressure, pulmonary artery pressure and pulmonary artery occlusion pressure, cardiac output, cerebral activity, and neuromuscular function. In addition, the operating room environment must be monitored for ambient temperature and humidity, as well as for accumulation of exhaled inhalational anesthetic agents, which might be deleterious to the health of operating room personnel.

Effective 1 July 2011, the ASA implemented updated standards for patient monitoring.[33]

Anesthesia record

The anesthesia record is the medical and legal documentation of events while a patient is under anesthesia.[34] It should contain a detailed and continuous account of all drugs, fluids, and blood products administered and procedures undertaken, and also includes the observation of cardiovascular responses, estimated blood loss, urine output and data from physiologic monitors (see "Anesthetic monitoring" section above) while a patient is under anesthesia.

Traditionally handwritten on paper, the anesthesia record is increasingly being replaced by an electronic record as part of an Anesthesia Information Management System (AIMS), especially since 2007.[35] An AIMS is any information system that is used as an automated electronic anesthesia record keeper (i.e., connection to patient physiologic monitors and/or the anesthetic machine) and which also may allow the collection and analysis of anesthesia-related perioperative patient data gathered from monitors and/or the anesthesia machine. These systems typically run on medical-grade hardware in the operating room. AIMS can be stand-alone systems or integrated modules of a hospital information system. AIMS have several benefits to the anesthesia departments as well to the hospital administration as documented in the scientific literature:

  • Reducing anesthesia-related drug costs[36]
  • Increased anesthesia billing and capture of anesthesia-related charges[37]
  • Increased hospital reimbursement through improved hospital coding[38][39]
  • Improvement of the data quality of the intraoperative anesthesia record[40][41]
  • Support training and education of the anesthesia workforce[42]
  • Support of clinical decision-making[43]
  • Support of patient care and safety[44]
  • Enhancement of clinical studies[45]
  • Enhancement of clinical quality improvement programs[46]
  • Support of clinical risk management[47]
  • Monitoring for diversion of controlled substances[48]

See also

References

  1. ^ a b Morris Fishbein, ed. (1976). "Anesthesia". The New Illustrated Medical and Health Encyclopedia. 1 (Home Library ed.). New York: H. S. Stuttman Co. pp. 87–9. 
  2. ^ Career as an anaesthesiologist. Institute for career research. 2007. p. 1. ISBN 978-1-58511-105-3. http://www.google.com/books?id=vQb5LnDI5CoC&dq=anesthesia+ancient&lr=&as_brr=3&source=gbs_navlinks_s. Retrieved 2010-11-25. 
  3. ^ a b Brill S, Gurman GM and Fisher A (2003). "A history of neuraxial administration of local analgesics and opioids". European Journal of Anaesthesiology 20 (9): 682–9. doi:10.1017/S026502150300111X. ISSN 0265-0215. PMID 12974588. 
  4. ^ Long C. W. (1849). "An account of the first use of Sulphuric Ether by Inhalation as an Anesthetic in Surgical Operations". Southern Medical and Surgical Journal 5: 705–713. 
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  7. ^ "Is Physician Anesthesia Cost-Effective?". Anesthesia and Analgesia. 2007. http://www.anesthesia-analgesia.org/cgi/content/full/98/3/750#R7-138848. Retrieved 2010-11-25. 
  8. ^ Rosenbach, ML; Cromwell, J (2007). "When do anesthesiologists delegate?". Med Care 27 (5): 453–65. doi:10.1097/00005650-198905000-00002. PMID 2725080. 
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  12. ^ ACGME Program Requirements for Graduate Medical Education in Anesthesiology, Effective: 1 July 2008
  13. ^ "ASA Fast Facts: Anesthesiologists Provide Or Participate In 90 Percent Of All Annual Anesthetics". ASA. http://www.asahq.org/PressRoom/homepage.html. Retrieved 2010-11-25. 
  14. ^ "Australian and New Zealand College of Anaesthetists". College website. http://www.anzca.edu.au. 
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  16. ^ "The Center for Medical Simulation". Cambridge, Massachusetts. 2009. http://www.harvardmedsim.org/. Retrieved 2010-11-25. 
  17. ^ "MedSim-Eagle Patient Simulator – Simulation Center". Stanford University School of Medicine. http://med.stanford.edu/VAsimulator/medsim.html. Retrieved 2010-11-25. 
  18. ^ "Mount Sinai Simulation HELPS Center". http://msmc.affinitymembers.net/simulator/intro2.html. Retrieved 2010-11-25. 
  19. ^ "Simcenter". http://simcenter.duke.edu/. Retrieved 2010-11-25. 
  20. ^ About. AANA. Retrieved on 2010-09-29.
  21. ^ Becoming a CRNA. AANA. Retrieved on 2010-09-29.
  22. ^ Fact Sheet: Concerning State Opt Outs. AANA. Retrieved on 2010-09-29.
  23. ^ a b Centers for Medicare and Medicaid Services, Department of Health and Human Services (2010). "Chapter 12, Section 50: Payment for Anesthesiology Services". Medicare Claims Processing Manual. Washington, DC: U.S. Government Printing Office. pp. 116–23. http://www.cms.gov/manuals/downloads/clm104c12.pdf. Retrieved 2010-11-25. 
  24. ^ a b Centers for Medicare and Medicaid Services, Department of Health and Human Services (2002). "IV: 42CFR482.52: Condition of participation: Anesthesia services". Code of Federal Regulations, Title 42. 3. Washington, DC: U.S. Government Printing Office. pp. 490–1. http://edocket.access.gpo.gov/cfr_2002/octqtr/42cfr482.52.htm. Retrieved 2010-11-25. 
  25. ^ a b Centers for Medicare and Medicaid Services (2010). "Conditions for Coverage (CfCs) & Conditions of Participations (CoPs): Spotlight". Washington, DC: Centers for Medicare and Medicaid Services. http://www.cms.gov/CFCsAndCoPs/02_Spotlight.asp. Retrieved 2010-11-25. 
  26. ^ "Five facts about AAs". American Academy of Anesthesiologist Assistants. Archived from the original on 2006-09-26. http://web.archive.org/web/20060926091707/http://www.anesthetist.org/content/view/14/38/. Retrieved 2010-11-25. 
  27. ^ a b http://www.nova.edu/chcs/healthsciences/anesthesia/forms/brochure.pdf
  28. ^ "ASATT Certification Information". American Society of Anesthesia Technologists & Technicians. http://www.asatt.org/cert.html. Retrieved 2010-11-25. 
  29. ^ New Zealand Anaesthetic Technicians Society
  30. ^ Baillie, JK; P. Sultan, E. Graveling, C. Forrest, C. Lafong (2007). "Contamination of anesthetic machines with pathogenic organisms". Anaesthesia 62 (12): 1257–61. doi:10.1111/j.1365-2044.2007.05261.x. PMID 17991263. 
  31. ^ Scott, DHT; S Fraser, P Willson, G B Drummond, J K Baillie (2010). "Passage of pathogenic microorganisms through breathing system filters used in anaesthesia and intensive care". Anaesthesia 65 (7): 670–3. doi:10.1111/j.1365-2044.2010.06327.x. PMID 20374232. 
  32. ^ STANDARDS FOR BASIC ANESTHETIC MONITORING. Committee of Origin: Standards and Practice Parameters (Approved by the ASA House of Delegates on 21 October 1986, and last amended on 20 October 2010 with an effective date of 1 July 2011)
  33. ^ ASA's Standards Revision Focusing on Ventilation Methods Goes Into Effect July 1 | Anesthesia
  34. ^ Stoelting RK, Miller RD: Basics of Anesthesia, 3rd edition, 1994.
  35. ^ . doi:10.1213/​ane.0b013e31818322d2. 
  36. ^ Gillerman, RG; Browning, RA (2000). "Drug use inefficiency: a hidden source of wasted health care dollars". Anesthesia and Analgesia 91 (4): 921–4. doi:10.1097/00000539-200010000-00028. PMID 11004049. 
  37. ^ Reich, DL; Kahn, RA; Wax, D; Palvia, T; Galati, M; Krol, M (2006). "Development of a module for point-of-care charge capture and submission using an anesthesia information management system". Anesthesiology 105 (1): 179–86; quiz 231–2. doi:10.1097/00000542-200607000-00028. PMID 16810010. 
  38. ^ Martin, J; Ederle, D; Milewski, P (2002). "CompuRecord-A perioperative information management-system for anesthesia". Anasthesiologie, Intensivmedizin, Notfallmedizin, Schmerztherapie : AINS 37 (8): 488–91. doi:10.1055/s-2002-33172. PMID 12165922. 
  39. ^ Meyer-Jark, T; Reissmann, H; Schuster, M; Raetzell, M; Rösler, L; Petersen, F; Liedtke, S; Steinfath, M et al (2007). "Realisation of material costs in anaesthesia. Alternatives to the reimbursement via diagnosis-related groups". Der Anaesthesist 56 (4): 353–5. doi:10.1007/s00101-007-1136-6. PMID 17277957. 
  40. ^ Cook, RI; McDonald, JS; Nunziata, E (1989). "Differences between handwritten and automatic blood pressure records". Anesthesiology 71 (3): 385–90. doi:10.1097/00000542-198909000-00013. PMID 2774266. 
  41. ^ Devitt, JH; Rapanos, T; Kurrek, M; Cohen, MM; Shaw, M (1999). "The anesthetic record: accuracy and completeness". Canadian Journal of Anesthesia 46 (2): 122–8. doi:10.1007/BF03012545. PMID 10083991. 
  42. ^ Edsall, DW (1991). "Computerization of anesthesia information management—users' perspective". Journal of Clinical Monitoring 7 (4): 351–8. doi:10.1007/BF01619360. PMID 1744682. 
  43. ^ Merry AF, Webster CS, Mathew DJ (2001). "A new, safety-oriented, integrated drug administration and automated anesthesia record system". Anesthesia and Analgesia 93 (2): 385–90. doi:10.1097/00000539-200108000-00030. http://www.anesthesia-analgesia.org/content/93/2/385.full. Retrieved 2010-11-25. 
  44. ^ O'Reilly, M; Talsma, A; Vanriper, S; Kheterpal, S; Burney, R (2006). "An anesthesia information system designed to provide physician-specific feedback improves timely administration of prophylactic antibiotics". Anesthesia and Analgesia 103 (4): 908–12. doi:10.1213/01.ane.0000237272.77090.a2. PMID 17000802. 
  45. ^ Hollenberg, JP; Pirraglia, PA; Williams-Russo, P; Hartman, GS; Gold, JP; Yao, FS; Thomas, SJ (1997). "Computerized data collection in the operating room during coronary artery bypass surgery: a comparison to the hand-written anesthesia record". Journal of Cardiothoracic and Vascular Anesthesia 11 (5): 545–51. doi:10.1016/S1053-0770(97)90001-X. PMID 9263082. 
  46. ^ Röhrig, R; Junger, A; Hartmann, B; Klasen, J; Quinzio, L; Jost, A; Benson, M; Hempelmann, G (2004). "The incidence and prediction of automatically detected intraoperative cardiovascular events in noncardiac surgery". Anesthesia and Analgesia 98 (3): 569–77. PMID 14980900. 
  47. ^ Feldman, JM (2004). "Do anesthesia information systems increase malpractice exposure? Results of a survey". Anesthesia and Analgesia 99 (3): 840–3. doi:10.1213/01.ANE.0000130259.52838.3B. PMID 15333420. 
  48. ^ Epstein, RH; Gratch, DM; Grunwald, Z (2007). "Development of a scheduled drug diversion surveillance system based on an analysis of atypical drug transactions". Anesthesia and Analgesia 105 (4): 1053–60, table of contents. doi:10.1213/01.ane.0000281797.00935.08. PMID 17898387. 

Further reading

  • Wolf, Jacqueline H. Deliver Me from Pain: Anesthesia and Birth in America (Johns Hopkins University Press, 2009) 277pp; covers 1840s to 21st century; ISBN 978-0-8018-9110-6

External links


Translations:

Anaesthesia

Top

Dansk (Danish)
n. - anæstesi, bedøvelse, narkose

Nederlands (Dutch)
anesthesie, afwezigheid van pijnsensaties

Français (French)
n. - anesthésie

Deutsch (German)
n. - Anästhesie, Betäubung, Empfindungslosigkeit

Ελληνική (Greek)
n. - (ιατρ.) αναισθησία, νάρκωση

Italiano (Italian)
anestesia

Português (Portuguese)
n. - anestesia (f) (Med.)

Русский (Russian)
обезболивание, анестезия

Español (Spanish)
n. - anestesia, narcosis

Svenska (Swedish)
n. - bedövning

中文(简体)(Chinese (Simplified))
麻木, 麻醉法, 失去知觉

中文(繁體)(Chinese (Traditional))
n. - 麻木, 麻醉法, 失去知覺

한국어 (Korean)
n. - 마취[법], 무감각증

日本語 (Japanese)
n. - 麻酔, 知覚麻痺

العربيه (Arabic)
‏(الاسم) خدار, فقدان الإحساس,‏

עברית (Hebrew)
n. - ‮הרדמה, העדר תחושה, אילחוש‬


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