2019
DOI: 10.31636/pmjua.v4i1.3
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Opioids in the treatment of non-specific acute and chronic pain

Abstract: After reading this article, the reader will be familiar with the general classes of opioid agonists and partial agonists, the basics of the pharmacokinetics and pharmacodynamics of opioids, the risks of opioid therapy and the requirements for the safe and effective use of opioids in acute and chronic pain. The use of opioids during surgical procedures or anesthesia is not discussed. Also, there is no discussion about various available opioid antagonists that are used to treat overdose and the various disorders… Show more

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Cited by 1 publication
(2 citation statements)
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References 47 publications
(51 reference statements)
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“…Nalbuphine is an agonist of -opioid receptors and a partial antagonist of μ-opioid receptors, which can stimulate -receptors and antagonize the acute rewarding effects of morphine, has a short duration of action and rapid clearance compared with other opioids and is less likely to cause side effects [15]. It is widely used either as an analgesic or as an adjuvant with morphine [4,12,19]. For this reason, the number of requests for opioids in Pubmed has traditionally remained the same.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Nalbuphine is an agonist of -opioid receptors and a partial antagonist of μ-opioid receptors, which can stimulate -receptors and antagonize the acute rewarding effects of morphine, has a short duration of action and rapid clearance compared with other opioids and is less likely to cause side effects [15]. It is widely used either as an analgesic or as an adjuvant with morphine [4,12,19]. For this reason, the number of requests for opioids in Pubmed has traditionally remained the same.…”
Section: Discussionmentioning
confidence: 99%
“…It is used to treat moderate to severe pain and provide preoperative and postoperative analgesia and sedation [4,20]. Endothelial cells (human arterial and rat microvascular) contain a high affinity, saturable opiate binding site [22].…”
Section: Introductionmentioning
confidence: 99%