Practical Considerations for the Use of Tapentadol Prolonged Release for the Management of Severe Chronic Pain
Abstract Purpose Chronic pain is often challenging to address appropriately. Although patients with severe chronic pain may respond to treatment with an opioid analgesic, opioids are often associated with adverse effects that may lead patients to disrupt or discontinue therapy. In addition, opioid a...
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description | Abstract Purpose Chronic pain is often challenging to address appropriately. Although patients with severe chronic pain may respond to treatment with an opioid analgesic, opioids are often associated with adverse effects that may lead patients to disrupt or discontinue therapy. In addition, opioid analgesics alone may not be effective for all types of chronic pain, including neuropathic pain. Tapentadol prolonged release (PR), a centrally acting analgesic with 2 mechanisms of action (μ-opioid receptor agonism and noradrenaline reuptake inhibition), provides strong and reliable analgesia across a range of indications, including nociceptive, neuropathic, and mixed types of chronic pain, and is associated with an improved tolerability profile relative to classic opioid analgesics. The purpose of this article was to review the recent literature on different aspects related to the clinical use of tapentadol PR. Methods A review was conducted of the current literature and relevant unpublished data on initiation and titration of tapentadol PR, switching from classic strong opioids, risk of withdrawal after discontinuation, long-term treatment, coadministration with other medications, and risk of abuse and diversion. Findings Tapentadol PR may provide clinically meaningful benefits over classic opioid analgesics, including ease of initiating and titrating tapentadol PR treatment in opioid-naive and opioid-experienced patients, low risk of withdrawal after cessation of tapentadol PR therapy, a favorable pharmacokinetic profile (allowing for coadministration with other medications) of tapentadol PR, and low potential for tapentadol PR abuse. Implications The broad analgesic efficacy of tapentadol PR may simplify chronic pain management by allowing for the treatment of different types of pain with a single analgesic. In addition, tapentadol is associated with a low risk of pharmacokinetic interactions, which permits its use in patients taking multiple medications. Furthermore, the favorable tolerability profile of tapentadol PR may result in improved patient compliance and allow for easy titration and rotation from previous strong opioids. |
doi_str_mv | 10.1016/j.clinthera.2014.07.005 |
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Although patients with severe chronic pain may respond to treatment with an opioid analgesic, opioids are often associated with adverse effects that may lead patients to disrupt or discontinue therapy. In addition, opioid analgesics alone may not be effective for all types of chronic pain, including neuropathic pain. Tapentadol prolonged release (PR), a centrally acting analgesic with 2 mechanisms of action (μ-opioid receptor agonism and noradrenaline reuptake inhibition), provides strong and reliable analgesia across a range of indications, including nociceptive, neuropathic, and mixed types of chronic pain, and is associated with an improved tolerability profile relative to classic opioid analgesics. The purpose of this article was to review the recent literature on different aspects related to the clinical use of tapentadol PR. Methods A review was conducted of the current literature and relevant unpublished data on initiation and titration of tapentadol PR, switching from classic strong opioids, risk of withdrawal after discontinuation, long-term treatment, coadministration with other medications, and risk of abuse and diversion. Findings Tapentadol PR may provide clinically meaningful benefits over classic opioid analgesics, including ease of initiating and titrating tapentadol PR treatment in opioid-naive and opioid-experienced patients, low risk of withdrawal after cessation of tapentadol PR therapy, a favorable pharmacokinetic profile (allowing for coadministration with other medications) of tapentadol PR, and low potential for tapentadol PR abuse. Implications The broad analgesic efficacy of tapentadol PR may simplify chronic pain management by allowing for the treatment of different types of pain with a single analgesic. In addition, tapentadol is associated with a low risk of pharmacokinetic interactions, which permits its use in patients taking multiple medications. Furthermore, the favorable tolerability profile of tapentadol PR may result in improved patient compliance and allow for easy titration and rotation from previous strong opioids.</description><identifier>ISSN: 0149-2918</identifier><identifier>EISSN: 1879-114X</identifier><identifier>DOI: 10.1016/j.clinthera.2014.07.005</identifier><identifier>PMID: 25108647</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Analgesics ; Analgesics, Opioid - administration & dosage ; Analgesics, Opioid - therapeutic use ; Arthritis ; Chronic Pain - diagnosis ; Chronic Pain - drug therapy ; Constipation ; Delayed-Action Preparations - administration & dosage ; Delayed-Action Preparations - therapeutic use ; Humans ; Internal Medicine ; Medical Education ; Pain management ; Pain Measurement ; Phenols - administration & dosage ; Phenols - therapeutic use ; prolonged release ; severe chronic pain ; Studies ; tapentadol</subject><ispartof>Clinical therapeutics, 2015-01, Vol.37 (1), p.94-113</ispartof><rights>The Authors</rights><rights>2015 The Authors</rights><rights>Copyright © 2015 The Authors. Published by Elsevier Inc. All rights reserved.</rights><rights>Copyright Elsevier Limited Jan 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c664t-a082db8e7ed4b5d1f012d834f2dc9ea1e90b7a4f4d63b259582eb1cfb4c259a93</citedby><cites>FETCH-LOGICAL-c664t-a082db8e7ed4b5d1f012d834f2dc9ea1e90b7a4f4d63b259582eb1cfb4c259a93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/1644505134?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995,64385,64387,64389,72469</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25108647$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sánchez del Águila, Manuel J., FCARCSI</creatorcontrib><creatorcontrib>Schenk, Michael, MD</creatorcontrib><creatorcontrib>Kern, Kai-Uwe, PhD, MD</creatorcontrib><creatorcontrib>Drost, Tanja, MD</creatorcontrib><creatorcontrib>Steigerwald, Ilona, MD</creatorcontrib><title>Practical Considerations for the Use of Tapentadol Prolonged Release for the Management of Severe Chronic Pain</title><title>Clinical therapeutics</title><addtitle>Clin Ther</addtitle><description>Abstract Purpose Chronic pain is often challenging to address appropriately. Although patients with severe chronic pain may respond to treatment with an opioid analgesic, opioids are often associated with adverse effects that may lead patients to disrupt or discontinue therapy. In addition, opioid analgesics alone may not be effective for all types of chronic pain, including neuropathic pain. Tapentadol prolonged release (PR), a centrally acting analgesic with 2 mechanisms of action (μ-opioid receptor agonism and noradrenaline reuptake inhibition), provides strong and reliable analgesia across a range of indications, including nociceptive, neuropathic, and mixed types of chronic pain, and is associated with an improved tolerability profile relative to classic opioid analgesics. The purpose of this article was to review the recent literature on different aspects related to the clinical use of tapentadol PR. Methods A review was conducted of the current literature and relevant unpublished data on initiation and titration of tapentadol PR, switching from classic strong opioids, risk of withdrawal after discontinuation, long-term treatment, coadministration with other medications, and risk of abuse and diversion. Findings Tapentadol PR may provide clinically meaningful benefits over classic opioid analgesics, including ease of initiating and titrating tapentadol PR treatment in opioid-naive and opioid-experienced patients, low risk of withdrawal after cessation of tapentadol PR therapy, a favorable pharmacokinetic profile (allowing for coadministration with other medications) of tapentadol PR, and low potential for tapentadol PR abuse. Implications The broad analgesic efficacy of tapentadol PR may simplify chronic pain management by allowing for the treatment of different types of pain with a single analgesic. In addition, tapentadol is associated with a low risk of pharmacokinetic interactions, which permits its use in patients taking multiple medications. Furthermore, the favorable tolerability profile of tapentadol PR may result in improved patient compliance and allow for easy titration and rotation from previous strong opioids.</description><subject>Analgesics</subject><subject>Analgesics, Opioid - administration & dosage</subject><subject>Analgesics, Opioid - therapeutic use</subject><subject>Arthritis</subject><subject>Chronic Pain - diagnosis</subject><subject>Chronic Pain - drug therapy</subject><subject>Constipation</subject><subject>Delayed-Action Preparations - administration & dosage</subject><subject>Delayed-Action Preparations - therapeutic use</subject><subject>Humans</subject><subject>Internal Medicine</subject><subject>Medical Education</subject><subject>Pain management</subject><subject>Pain Measurement</subject><subject>Phenols - administration & dosage</subject><subject>Phenols - therapeutic use</subject><subject>prolonged release</subject><subject>severe chronic pain</subject><subject>Studies</subject><subject>tapentadol</subject><issn>0149-2918</issn><issn>1879-114X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqNkt9LHDEQx0Npqaf1X2gDfenLbifZ7I-8FORobcHiURV8C9lkVnPdS85kT_C_b5ZTCz75lIT5zHdm8h1CPjEoGbDm67o0o_PTLUZdcmCihLYEqN-QBetaWTAmrt-SRQ7IgkvWHZDDlNYAUMmavycHvGbQNaJdEL-K2kzO6JEug0_OZsXJ5RsdQqS5AL1KSMNAL_UW_aRtGOkqhjH4G7T0D46oc_yJ_a29vsFNBueUC7zHiHR5G4N3hq608x_Iu0GPCY8fzyNy9eP75fJncXZ--mt5claYphFToaHjtu-wRSv62rIBGLddJQZujUTNUELfajEI21Q9r2XdceyZGXph8kvL6oh82etuY7jbYZrUxiWD46g9hl1SrGmgEVxWXUY_v0DXYRd97i5TQtRQs0pkqt1TJoaUIg5qG91GxwfFQM2WqLV6tkTNlihoVbYkZ3581N_1G7TPeU8eZOBkD2D-kHuHUSXj0Bu0LqKZlA3uFUW-vdCYudnWv_iA6f9EKnEF6mLejHkxmADIM7bVP0t8tpw</recordid><startdate>20150101</startdate><enddate>20150101</enddate><creator>Sánchez del Águila, Manuel J., FCARCSI</creator><creator>Schenk, Michael, MD</creator><creator>Kern, Kai-Uwe, PhD, MD</creator><creator>Drost, Tanja, MD</creator><creator>Steigerwald, Ilona, MD</creator><general>Elsevier Inc</general><general>Elsevier Limited</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88C</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M0T</scope><scope>M1P</scope><scope>M2O</scope><scope>M7N</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20150101</creationdate><title>Practical Considerations for the Use of Tapentadol Prolonged Release for the Management of Severe Chronic Pain</title><author>Sánchez del Águila, Manuel J., FCARCSI ; Schenk, Michael, MD ; Kern, Kai-Uwe, PhD, MD ; Drost, Tanja, MD ; Steigerwald, Ilona, MD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c664t-a082db8e7ed4b5d1f012d834f2dc9ea1e90b7a4f4d63b259582eb1cfb4c259a93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Analgesics</topic><topic>Analgesics, Opioid - administration & dosage</topic><topic>Analgesics, Opioid - therapeutic use</topic><topic>Arthritis</topic><topic>Chronic Pain - diagnosis</topic><topic>Chronic Pain - drug therapy</topic><topic>Constipation</topic><topic>Delayed-Action Preparations - administration & dosage</topic><topic>Delayed-Action Preparations - therapeutic use</topic><topic>Humans</topic><topic>Internal Medicine</topic><topic>Medical Education</topic><topic>Pain management</topic><topic>Pain Measurement</topic><topic>Phenols - administration & dosage</topic><topic>Phenols - therapeutic use</topic><topic>prolonged release</topic><topic>severe chronic pain</topic><topic>Studies</topic><topic>tapentadol</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sánchez del Águila, Manuel J., FCARCSI</creatorcontrib><creatorcontrib>Schenk, Michael, MD</creatorcontrib><creatorcontrib>Kern, Kai-Uwe, PhD, MD</creatorcontrib><creatorcontrib>Drost, Tanja, MD</creatorcontrib><creatorcontrib>Steigerwald, Ilona, MD</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Healthcare Administration Database (Alumni)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Healthcare Administration Database</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sánchez del Águila, Manuel J., FCARCSI</au><au>Schenk, Michael, MD</au><au>Kern, Kai-Uwe, PhD, MD</au><au>Drost, Tanja, MD</au><au>Steigerwald, Ilona, MD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Practical Considerations for the Use of Tapentadol Prolonged Release for the Management of Severe Chronic Pain</atitle><jtitle>Clinical therapeutics</jtitle><addtitle>Clin Ther</addtitle><date>2015-01-01</date><risdate>2015</risdate><volume>37</volume><issue>1</issue><spage>94</spage><epage>113</epage><pages>94-113</pages><issn>0149-2918</issn><eissn>1879-114X</eissn><abstract>Abstract Purpose Chronic pain is often challenging to address appropriately. Although patients with severe chronic pain may respond to treatment with an opioid analgesic, opioids are often associated with adverse effects that may lead patients to disrupt or discontinue therapy. In addition, opioid analgesics alone may not be effective for all types of chronic pain, including neuropathic pain. Tapentadol prolonged release (PR), a centrally acting analgesic with 2 mechanisms of action (μ-opioid receptor agonism and noradrenaline reuptake inhibition), provides strong and reliable analgesia across a range of indications, including nociceptive, neuropathic, and mixed types of chronic pain, and is associated with an improved tolerability profile relative to classic opioid analgesics. The purpose of this article was to review the recent literature on different aspects related to the clinical use of tapentadol PR. Methods A review was conducted of the current literature and relevant unpublished data on initiation and titration of tapentadol PR, switching from classic strong opioids, risk of withdrawal after discontinuation, long-term treatment, coadministration with other medications, and risk of abuse and diversion. Findings Tapentadol PR may provide clinically meaningful benefits over classic opioid analgesics, including ease of initiating and titrating tapentadol PR treatment in opioid-naive and opioid-experienced patients, low risk of withdrawal after cessation of tapentadol PR therapy, a favorable pharmacokinetic profile (allowing for coadministration with other medications) of tapentadol PR, and low potential for tapentadol PR abuse. Implications The broad analgesic efficacy of tapentadol PR may simplify chronic pain management by allowing for the treatment of different types of pain with a single analgesic. In addition, tapentadol is associated with a low risk of pharmacokinetic interactions, which permits its use in patients taking multiple medications. Furthermore, the favorable tolerability profile of tapentadol PR may result in improved patient compliance and allow for easy titration and rotation from previous strong opioids.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>25108647</pmid><doi>10.1016/j.clinthera.2014.07.005</doi><tpages>20</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analgesics Analgesics, Opioid - administration & dosage Analgesics, Opioid - therapeutic use Arthritis Chronic Pain - diagnosis Chronic Pain - drug therapy Constipation Delayed-Action Preparations - administration & dosage Delayed-Action Preparations - therapeutic use Humans Internal Medicine Medical Education Pain management Pain Measurement Phenols - administration & dosage Phenols - therapeutic use prolonged release severe chronic pain Studies tapentadol |
title | Practical Considerations for the Use of Tapentadol Prolonged Release for the Management of Severe Chronic Pain |
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