Journal ArticleDOI
Buprenorphine: a review of its pharmacological properties and therapeutic efficacy.
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TLDR
Buprenorphine appears to produce side effects which are similar to those seen with other morphine- like compounds, including respiratory depression, and animal studies and a direct addiction study in a few volunteers suggest that the dependence liability of buprenorphines may be lower than that of other older morphine-like drugs.Abstract:
Synopsis: Buprenorphine1, a derivative of the morphine alkaloid thebaine, is a strong analgesic with marked narcotic antagonist activity. In studies in relatively small groups of postoperative patients with moderate to severe pain, one or a few doses of buprenorphine parenterally (by intramuscular or slow intravenous injection) or sublingually2 were at least as effective as standard doses of other strong analgesics such as morphine, pethidine or pentazocine, and buprenorphine was longer acting than these agents. Only a small number of patients with chronic pain have received repeated doses, but in such patients there was no need for increased doses during several weeks to months of treatment.read more
Citations
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Opioids and the management of chronic severe pain in the elderly: Consensus statement of an international expert panel with focus on the six clinically most often used world health organization step III opioids (Buprenorphine, Fentanyl, Hydromorphone, Methadone, Morphine, Oxycodone)
Joseph V. Pergolizzi,Rainer H. Böger,Keith Budd,Albert Dahan,Serdar Erdine,Guy Hans,Hans G. Kress,Richard M. Langford,Rudolf Likar,Robert B. Raffa,Paola Sacerdote +10 more
TL;DR: The criteria for selecting analgesics for pain treatment in the elderly include, but are not limited to, overall efficacy, overall side‐effect profile, onset of action, drug interactions, abuse potential, and practical issues, such as cost and availability of the drug, as well as the severity and type of pain.
Journal ArticleDOI
Incidence, Reversal, and Prevention of Opioid-induced Respiratory Depression.
TL;DR: The clinical approach to severe opioid-induced respiratory depression is to titrate naloxone to effect and continue treatment by continuous infusion until chances for renarcotization have diminished.
Journal ArticleDOI
Growth hormone and the heart
TL;DR: Several lines of evidence have suggested that the cardiovascular abnormalities can be partially reversed by suppressing GH and IGF‐I levels in acromegaly or after GH replacement therapy in GHD patients.
Journal ArticleDOI
Buprenorphine maintenance treatment of opiate dependence: a multicenter, randomized clinical trial.
Walter Ling,Charles Charuvastra,Joseph Collins,Steve Batki,Lawrence S. Brown,Prudencia C. Kintaudi,Donald R. Wesson,Laura McNicholas,Donald J. Tusel,Usha Malkerneker,John A. Renner,Erick Santos,Paul Casadonte,Carol Fye,Susan M. Stine,Richard I. H. Wang,Doralie Segal +16 more
TL;DR: It is suggested that an adequate dose of buprenorphine will be a useful addition to pharmacotherapy and safety outcome measures provided by clinical monitoring and by analysis of the reported adverse events.
Journal ArticleDOI
Buprenorphine: a unique drug with complex pharmacology.
Kabirullah Lutfy,Alan Cowan +1 more
TL;DR: Evidence is provided demonstrating that the ORL-1 receptor plays a functional role not only in the antinociceptive effect of buprenorphine but also in other actions of the drug as well.
References
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Journal Article
The effects of morphine- and nalorphine- like drugs in the nondependent and morphine-dependent chronic spinal dog.
TL;DR: It has been shown that buprenorphine is a partial agonist of the mu type which both suppressed and precipitated abstinence in the morphine-dependent dog while morphine and propoxyphene are stronger agonists.
Journal ArticleDOI
Human Pharmacology and Abuse Potential of the Analgesic Buprenorphine: A Potential Agent for Treating Narcotic Addiction
TL;DR: Buprenorphine has potential for treating narcotic addiction since it is acceptable to addicts, is long-acting, produces a low level of physical dependence such that patients may be easily detoxified, is less toxic than drugs used for maintenance therapy, and blocks the effects of narcotics.
Journal ArticleDOI
Agonist and antagonist properties of buprenorphine, a new antinociceptive agent
TL;DR: In rodent antinociceptive assays (writhing, tail pressure), buprenorphine had an action which was rapid in onset and of long duration; it was 25‐40 timesMore potent than morphine after parenteral injection and 7‐10 times more potent after oral administration.
Journal Article
The measurement of pain; prototype for the quantitative study of subjective responses.
TL;DR: This review covers 106 years of experimental work and finds strong evidence has been presented to direct future therapeutic research to modification of the psychic reaction to the original sensation and Quantitative work with pain is possible and rewarding.