1983
DOI: 10.1002/ana.410130213
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Central nervous system excitatory effects of meperidine in cancer patients

Abstract: The analgesic meperidine has been reported to produce signs of central nervous system excitation in human beings. To determine the relationship between signs and symptoms of central nervous system excitation and plasma levels of meperidine and normeperidine, we studied 67 patients receiving meperidine for the relief of postoperative or chronic pain. In 48 patients, excitatory effects ranging from mild nervousness to tremors, twitches, multifocal myoclonus, and seizures were directly correlated with accumulatio… Show more

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Cited by 377 publications
(116 citation statements)
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“…Meperidine, the prototypic 4-phenylpiperidine, is a widely used clinical analgesic, although its utility is limited by the toxicity and epileptic actions of its N-demethylated metabolite normeperidine (Kaiko et al, 1983;Inturrisi, 2002). Methadone is another muselective analgesic, and is the major drug in the acyclic analgesic class.…”
Section: Othermentioning
confidence: 99%
“…Meperidine, the prototypic 4-phenylpiperidine, is a widely used clinical analgesic, although its utility is limited by the toxicity and epileptic actions of its N-demethylated metabolite normeperidine (Kaiko et al, 1983;Inturrisi, 2002). Methadone is another muselective analgesic, and is the major drug in the acyclic analgesic class.…”
Section: Othermentioning
confidence: 99%
“…The opioid-induced euphoria experienced by addicts occurs rarely among patients who receive an opioid for pain (179)(180)(181). Indeed, the usual experience of patients is dysphoria.…”
Section: Portenoymentioning
confidence: 99%
“…However, prolonged use of morphine may lead to tolerance and, subsequently, withdrawal symptoms (Fernández-Dueñ as et al, 2007;Ledeboer et al, 2007;Noble and Roques, 2007). In trauma, rat model compounds, such as butorphanol, nalbuphine, meperidine, pentazocine, and codeine, can be used to alleviate acute pain, but buprenorphine is the analgesic recommended by veterinarians due to its potency and long-lasting duration (Kaiko et al, 1983;Gear et al, 1999;Katzung, 2001;Roughan and Flecknell, 2002). Moreover, subcutaneously administration of 0.05 mg=kg reduces pain sensitivity after postoperative surgeries (Curtin et al, 2009).…”
mentioning
confidence: 99%