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標(biāo)題: Titlebook: Non-Opioid Analgesics in the Treatment of Acute Pain; Johannesbergs Slott, M. J. Parnham Conference proceedings 1997 Springer Basel AG 1997 [打印本頁(yè)]

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Non-Opioid Analgesics in the Treatment of Acute Pain978-3-0348-8869-1
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Routines, practice and needs for analgesics in out-patient surgery in Sweden, to maintain alertness, ambulation, analgesia and alimentation. In a recent national survey of over 1000 patients it was found that 64% of post-operative patients interviewed had mild pain, 25% moderate pain and 11% severe pain (mainly after inguinal hernia, skeletal surgery or breast surgery) on re
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Conference proceedings 1997ime over the last 75 years in many clinical settings throughout the world. Some 20 years ago, however, concern arose over the implications of isolat- ed reports of agranulocytosis following use of dipyrone. Based on these initial cases the Swedish authorities ordered the withdrawal of the drug from
作者: Obscure    時(shí)間: 2025-3-24 14:45

作者: 贊成你    時(shí)間: 2025-3-24 18:39
Non-opioid analgesics in the treatment of acute pain,s directly related to their mechanism of action. An average of 50– 60% of patients suffer from nausea or vomiting with opioids. Respiratory depression can be reduced with patient-controlled analgesia, though it always remains a risk. Local anaesthetics must also be administered by skilled physicians, but are very useful for post-operative pain.
作者: MIR    時(shí)間: 2025-3-24 22:25
978-3-7643-5680-4Springer Basel AG 1997
作者: 陰謀    時(shí)間: 2025-3-25 00:46
Clinical pharmacokinetics of dipyrone and its metabolites,ipyrine (MAA), following oral administration. Recent studies have shown that oral bioavailability of dipyrone tablets is 85%. Maximal plasma concentrations of MAA after oral dipyrone (0.75 g –1.5 g) are achieved in 1–1.5 h and these kinetics are little affected by food.
作者: Psa617    時(shí)間: 2025-3-25 05:03
Perspectives,aracetamol, with a central site of action, dipyrone does not exhibit the adverse events typical of opioids (e.g. respiratory depression). It is also much less deleterious to the gastrointestinal mucosa than NSAIDs. Its unique direct spasmolytic activity is of additional advantage in colic pain.
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