Literature DB >> 21797962

Current considerations for the treatment of severe chronic pain: the potential for tapentadol.

Joseph Pergolizzi1, Cayetano Alegre, David Blake, Jaime Calvo Alén, Roberto Caporali, Hans-Raimund Casser, Gerardo Correa-Illanes, Pedro Fernandes, Eugenio Galilea, Richard Jany, Anthony Jones, Othmane Mejjad, Jadranka Morovic-Vergles, Ángel Oteo-Álvaro, Ángel Oteo Álvaro, Francisco J Radrigán Araya, Maria Eugénia C Simões, Generoso Uomo.   

Abstract

Studies suggest that around 20% of adults in Europe experience chronic pain, which not only has a considerable impact on their quality of life but also imposes a substantial economic burden on society. More than one-third of these people feel that their pain is inadequately managed. A range of analgesic drugs is currently available, but recent guidelines recommend that NSAIDs and COX-2 inhibitors should be prescribed cautiously. Although the short-term efficacy of opioids is good, adverse events are common and doses are frequently limited by tolerability problems. There is a perceived need for improved pharmacological treatment options. Currently, many treatment decisions are based solely on pain intensity. However, chronic pain is multifactorial and this apaproach ignores the fact that different causative mechanisms may be involved. The presence of more than one causative mechanism means that chronic pain can seldom be controlled by a single agent. Therefore, combining drugs with different analgesic actions increases the probability of interrupting the pain signal, but is often associated with an increased risk of drug/drug interactions, low compliance and increased side effects. Tapentadol combines μ-opioid receptor agonism and noradrenaline reuptake inhibition in a single molecule, with both mechanisms contributing to its analgesic effects. Preclinical testing has shown that μ-opioid agonism is primarily responsible for analgesia in acute pain, whereas noradrenaline reuptake inhibition is more important in chronic pain. In clinical trials in patients with chronic pain, the efficacy of tapentadol was similar to that of oxycodone, but it produced significantly fewer gastrointestinal side-effects and treatment discontinuations. Pain relief remained stable throughout a 1-year safety study. Thus, tapentadol could possibly overcome some of the limitations of currently available analgesics for the treatment of chronic pain.
© 2011 The Authors. Pain Practice © 2011 World Institute of Pain.

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Year:  2011        PMID: 21797962     DOI: 10.1111/j.1533-2500.2011.00487.x

Source DB:  PubMed          Journal:  Pain Pract        ISSN: 1530-7085            Impact factor:   3.183


  11 in total

Review 1.  Tapentadol extended release: in adults with chronic pain.

Authors:  Sheridan M Hoy
Journal:  Drugs       Date:  2012-02-12       Impact factor: 9.546

Review 2.  Differences between opioids: pharmacological, experimental, clinical and economical perspectives.

Authors:  Asbjørn M Drewes; Rasmus D Jensen; Lecia M Nielsen; Joanne Droney; Lona L Christrup; Lars Arendt-Nielsen; Julia Riley; Albert Dahan
Journal:  Br J Clin Pharmacol       Date:  2013-01       Impact factor: 4.335

Review 3.  The mu-opioid receptor agonist/noradrenaline reuptake inhibition (MOR-NRI) concept in analgesia: the case of tapentadol.

Authors:  Thomas M Tzschentke; Thomas Christoph; Babette Y Kögel
Journal:  CNS Drugs       Date:  2014-04       Impact factor: 5.749

4.  μ-Opioid receptor activation and noradrenaline transport inhibition by tapentadol in rat single locus coeruleus neurons.

Authors:  Mahsa Sadeghi; Thomas M Tzschentke; MacDonald J Christie
Journal:  Br J Pharmacol       Date:  2014-07-01       Impact factor: 8.739

5.  Lasting Prolonged-Release Tapentadol for Moderate/Severe Non-Cancer Musculoskeletal Chronic Pain.

Authors:  Boaz G Samolsky Dekel; Sivia Ghedini; Alberto Gori; Alessio Vasarri; GianFranco Di Nino; Rita M Melotti
Journal:  Pain Ther       Date:  2015-01-06

Review 6.  Tapentadol Extended Release in the Treatment of Severe Chronic Low Back Pain and Osteoarthritis Pain.

Authors:  Joseph V Pergolizzi; Robert Taylor; Jo Ann LeQuang; Robert B Raffa; John Bisney
Journal:  Pain Ther       Date:  2018-04-05

7.  Antinociceptive Effect of the Essential Oil from Croton conduplicatus Kunth (Euphorbiaceae).

Authors:  Raimundo Gonçalves de Oliveira Júnior; Christiane Adrielly Alves Ferraz; Juliane Cabral Silva; Ana Paula de Oliveira; Tâmara Coimbra Diniz; Mariana Gama E Silva; Lucindo José Quintans Júnior; Ana Valéria Vieira de Souza; Uiliane Soares Dos Santos; Izabel Cristina Casanova Turatti; Norberto Peporine Lopes; Vitor Prates Lorenzo; Jackson Roberto Guedes da Silva Almeida
Journal:  Molecules       Date:  2017-05-30       Impact factor: 4.411

Review 8.  Do All Opioid Drugs Share the Same Immunomodulatory Properties? A Review From Animal and Human Studies.

Authors:  Silvia Franchi; Giorgia Moschetti; Giada Amodeo; Paola Sacerdote
Journal:  Front Immunol       Date:  2019-12-12       Impact factor: 7.561

9.  Investigation of the presence and antinociceptive function of muscarinic acetylcholine receptors in the African naked mole-rat (Heterocephalus glaber).

Authors:  Kristine B Jørgensen; Karen Krogh-Jensen; Darryl S Pickering; Titus I Kanui; Klas S P Abelson
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2015-10-31       Impact factor: 1.836

10.  Does 'Strong Analgesic' Equal 'Strong Opioid'? Tapentadol and the Concept of 'µ-Load'.

Authors:  Robert B Raffa; Christian Elling; Thomas M Tzschentke
Journal:  Adv Ther       Date:  2018-09-11       Impact factor: 3.845

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