Duloxetine for the Management of Diabetic Peripheral Neuropathic Pain: Evaluation of Functional Outcomes
ABSTRACT Objective. To assess the effectiveness of duloxetine, compared with placebo, on patient‐reported health outcomes over a 12‐week period, in the management of diabetic peripheral neuropathic pain (DPNP). Methods. The results were pooled from three 12‐week multicenter, double‐blind studies....
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| Veröffentlicht in: | Pain medicine (Malden, Mass.) Mass.), 2007-07, Vol.8 (5), p.410-418 |
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| creator | Armstrong, David G. Chappell, Amy S. Le, Trong K. Kajdasz, Daniel K. Backonja, Miroslav D'Souza, Deborah N. Russell, James M. |
| description | ABSTRACT
Objective. To assess the effectiveness of duloxetine, compared with placebo, on patient‐reported health outcomes over a 12‐week period, in the management of diabetic peripheral neuropathic pain (DPNP).
Methods. The results were pooled from three 12‐week multicenter, double‐blind studies. In study 1 (N = 457), patients with DPNP were randomly assigned to treatment with duloxetine 20 mg once daily (QD), 60 mg QD, 60 mg twice daily (BID), or placebo. In studies 2 (N = 334) and 3 (N = 348), patients with DPNP were randomly assigned to treatment with duloxetine 60 mg QD, 60 mg BID, or placebo. Patient‐reported functional outcomes were measured by the Short Form 36 (SF‐36), the interference portion of the Brief Pain Inventory (BPI), and EuroQol 5D Health Questionnaire (EQ‐5D). Results for all functional outcomes from the intent‐to‐treat and completer populations are discussed.
Results. In the SF‐36 health survey and the BPI interference, duloxetine 60 mg QD and 60 mg BID were significantly superior to placebo in all the domains (P ≤ 0.03). In the analysis of the EQ‐5D, duloxetine 60 mg QD (P = 0.004) and 60 mg BID (P |
| doi_str_mv | 10.1111/j.1526-4637.2007.00276.x |
| format | Article |
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Objective. To assess the effectiveness of duloxetine, compared with placebo, on patient‐reported health outcomes over a 12‐week period, in the management of diabetic peripheral neuropathic pain (DPNP).
Methods. The results were pooled from three 12‐week multicenter, double‐blind studies. In study 1 (N = 457), patients with DPNP were randomly assigned to treatment with duloxetine 20 mg once daily (QD), 60 mg QD, 60 mg twice daily (BID), or placebo. In studies 2 (N = 334) and 3 (N = 348), patients with DPNP were randomly assigned to treatment with duloxetine 60 mg QD, 60 mg BID, or placebo. Patient‐reported functional outcomes were measured by the Short Form 36 (SF‐36), the interference portion of the Brief Pain Inventory (BPI), and EuroQol 5D Health Questionnaire (EQ‐5D). Results for all functional outcomes from the intent‐to‐treat and completer populations are discussed.
Results. In the SF‐36 health survey and the BPI interference, duloxetine 60 mg QD and 60 mg BID were significantly superior to placebo in all the domains (P ≤ 0.03). In the analysis of the EQ‐5D, duloxetine 60 mg QD (P = 0.004) and 60 mg BID (P < 0.001) were significantly better than placebo on all items.
Conclusions. Acute treatment with duloxetine was associated with significant improvement in functional outcomes in persons with DPNP.</description><identifier>ISSN: 1526-2375</identifier><identifier>EISSN: 1526-4637</identifier><identifier>DOI: 10.1111/j.1526-4637.2007.00276.x</identifier><identifier>PMID: 17661854</identifier><language>eng</language><publisher>Malden, USA: Blackwell Publishing Inc</publisher><subject>Aged ; Antidepressants ; Diabetic Neuropathies - drug therapy ; Diabetic Neuropathies - physiopathology ; Diabetic Neuropathy ; Dose-Response Relationship, Drug ; Double-Blind Method ; Drug Administration Schedule ; Duloxetine Hydrochloride ; Female ; Humans ; Male ; Middle Aged ; Outcome Assessment (Health Care) - methods ; Pain Measurement - drug effects ; Pain Measurement - methods ; Patient Satisfaction ; Peripheral Nerves - drug effects ; Peripheral Nerves - physiopathology ; Placebos ; Serotonin Uptake Inhibitors - administration & dosage ; Serotonin Uptake Inhibitors - adverse effects ; Surveys and Questionnaires ; Thiophenes - administration & dosage ; Thiophenes - adverse effects ; Treatment Outcome</subject><ispartof>Pain medicine (Malden, Mass.), 2007-07, Vol.8 (5), p.410-418</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5106-d92aac69bfc424353583fe3e421962ccd2fa7f77d470ffb6e7eed8e7a73d66a83</citedby><cites>FETCH-LOGICAL-c5106-d92aac69bfc424353583fe3e421962ccd2fa7f77d470ffb6e7eed8e7a73d66a83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1526-4637.2007.00276.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1526-4637.2007.00276.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17661854$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Armstrong, David G.</creatorcontrib><creatorcontrib>Chappell, Amy S.</creatorcontrib><creatorcontrib>Le, Trong K.</creatorcontrib><creatorcontrib>Kajdasz, Daniel K.</creatorcontrib><creatorcontrib>Backonja, Miroslav</creatorcontrib><creatorcontrib>D'Souza, Deborah N.</creatorcontrib><creatorcontrib>Russell, James M.</creatorcontrib><title>Duloxetine for the Management of Diabetic Peripheral Neuropathic Pain: Evaluation of Functional Outcomes</title><title>Pain medicine (Malden, Mass.)</title><addtitle>Pain Med</addtitle><description>ABSTRACT
Objective. To assess the effectiveness of duloxetine, compared with placebo, on patient‐reported health outcomes over a 12‐week period, in the management of diabetic peripheral neuropathic pain (DPNP).
Methods. The results were pooled from three 12‐week multicenter, double‐blind studies. In study 1 (N = 457), patients with DPNP were randomly assigned to treatment with duloxetine 20 mg once daily (QD), 60 mg QD, 60 mg twice daily (BID), or placebo. In studies 2 (N = 334) and 3 (N = 348), patients with DPNP were randomly assigned to treatment with duloxetine 60 mg QD, 60 mg BID, or placebo. Patient‐reported functional outcomes were measured by the Short Form 36 (SF‐36), the interference portion of the Brief Pain Inventory (BPI), and EuroQol 5D Health Questionnaire (EQ‐5D). Results for all functional outcomes from the intent‐to‐treat and completer populations are discussed.
Results. In the SF‐36 health survey and the BPI interference, duloxetine 60 mg QD and 60 mg BID were significantly superior to placebo in all the domains (P ≤ 0.03). In the analysis of the EQ‐5D, duloxetine 60 mg QD (P = 0.004) and 60 mg BID (P < 0.001) were significantly better than placebo on all items.
Conclusions. Acute treatment with duloxetine was associated with significant improvement in functional outcomes in persons with DPNP.</description><subject>Aged</subject><subject>Antidepressants</subject><subject>Diabetic Neuropathies - drug therapy</subject><subject>Diabetic Neuropathies - physiopathology</subject><subject>Diabetic Neuropathy</subject><subject>Dose-Response Relationship, Drug</subject><subject>Double-Blind Method</subject><subject>Drug Administration Schedule</subject><subject>Duloxetine Hydrochloride</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Outcome Assessment (Health Care) - methods</subject><subject>Pain Measurement - drug effects</subject><subject>Pain Measurement - methods</subject><subject>Patient Satisfaction</subject><subject>Peripheral Nerves - drug effects</subject><subject>Peripheral Nerves - physiopathology</subject><subject>Placebos</subject><subject>Serotonin Uptake Inhibitors - administration & dosage</subject><subject>Serotonin Uptake Inhibitors - adverse effects</subject><subject>Surveys and Questionnaires</subject><subject>Thiophenes - administration & dosage</subject><subject>Thiophenes - adverse effects</subject><subject>Treatment Outcome</subject><issn>1526-2375</issn><issn>1526-4637</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkUtP3DAURi1UxKv9C8ir7hL8SOxM1U0FM4DES2iqLi2Pc814msRTOynDv8dhRrDFG1_5fude6RghTElO0zlb5bRkIisElzkjROaEMCnyzR46em982dWMy_IQHce4IoSKouIH6JBKIWhVFkdoeTE0fgO96wBbH3C_BHyrO_0ELXQ99hZfOL1IfYMfILj1EoJu8B0Mwa91vxyftet-4Ol_3Qy6d74bmdnQmbFO0fuhN76F-BXtW91E-La7T9Dv2XR-fpXd3F9en_-6yUxJicjqCdPaiMnCmoIVvORlxS1wKBidCGZMzayWVsq6kMTahQAJUFcgteS1ELriJ-j7du46-H8DxF61LhpoGt2BH6JipGSyEiwFq23QBB9jAKvWwbU6vChK1GhZrdQoUI0y1WhZvVlWm4Se7nYMixbqD3CnNQV-bgPProGXTw9WD7fTVCQ82-Iu9rB5x3X4q4RM36n-3F2q2aOg_HHO1Zy_Andxm70</recordid><startdate>200707</startdate><enddate>200707</enddate><creator>Armstrong, David G.</creator><creator>Chappell, Amy S.</creator><creator>Le, Trong K.</creator><creator>Kajdasz, Daniel K.</creator><creator>Backonja, Miroslav</creator><creator>D'Souza, Deborah N.</creator><creator>Russell, James M.</creator><general>Blackwell Publishing Inc</general><scope>BSCLL</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>7TK</scope></search><sort><creationdate>200707</creationdate><title>Duloxetine for the Management of Diabetic Peripheral Neuropathic Pain: Evaluation of Functional Outcomes</title><author>Armstrong, David G. ; Chappell, Amy S. ; Le, Trong K. ; Kajdasz, Daniel K. ; Backonja, Miroslav ; D'Souza, Deborah N. ; Russell, James M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5106-d92aac69bfc424353583fe3e421962ccd2fa7f77d470ffb6e7eed8e7a73d66a83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Aged</topic><topic>Antidepressants</topic><topic>Diabetic Neuropathies - drug therapy</topic><topic>Diabetic Neuropathies - physiopathology</topic><topic>Diabetic Neuropathy</topic><topic>Dose-Response Relationship, Drug</topic><topic>Double-Blind Method</topic><topic>Drug Administration Schedule</topic><topic>Duloxetine Hydrochloride</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Outcome Assessment (Health Care) - methods</topic><topic>Pain Measurement - drug effects</topic><topic>Pain Measurement - methods</topic><topic>Patient Satisfaction</topic><topic>Peripheral Nerves - drug effects</topic><topic>Peripheral Nerves - physiopathology</topic><topic>Placebos</topic><topic>Serotonin Uptake Inhibitors - administration & dosage</topic><topic>Serotonin Uptake Inhibitors - adverse effects</topic><topic>Surveys and Questionnaires</topic><topic>Thiophenes - administration & dosage</topic><topic>Thiophenes - adverse effects</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Armstrong, David G.</creatorcontrib><creatorcontrib>Chappell, Amy S.</creatorcontrib><creatorcontrib>Le, Trong K.</creatorcontrib><creatorcontrib>Kajdasz, Daniel K.</creatorcontrib><creatorcontrib>Backonja, Miroslav</creatorcontrib><creatorcontrib>D'Souza, Deborah N.</creatorcontrib><creatorcontrib>Russell, James M.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><jtitle>Pain medicine (Malden, Mass.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Armstrong, David G.</au><au>Chappell, Amy S.</au><au>Le, Trong K.</au><au>Kajdasz, Daniel K.</au><au>Backonja, Miroslav</au><au>D'Souza, Deborah N.</au><au>Russell, James M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Duloxetine for the Management of Diabetic Peripheral Neuropathic Pain: Evaluation of Functional Outcomes</atitle><jtitle>Pain medicine (Malden, Mass.)</jtitle><addtitle>Pain Med</addtitle><date>2007-07</date><risdate>2007</risdate><volume>8</volume><issue>5</issue><spage>410</spage><epage>418</epage><pages>410-418</pages><issn>1526-2375</issn><eissn>1526-4637</eissn><abstract>ABSTRACT
Objective. To assess the effectiveness of duloxetine, compared with placebo, on patient‐reported health outcomes over a 12‐week period, in the management of diabetic peripheral neuropathic pain (DPNP).
Methods. The results were pooled from three 12‐week multicenter, double‐blind studies. In study 1 (N = 457), patients with DPNP were randomly assigned to treatment with duloxetine 20 mg once daily (QD), 60 mg QD, 60 mg twice daily (BID), or placebo. In studies 2 (N = 334) and 3 (N = 348), patients with DPNP were randomly assigned to treatment with duloxetine 60 mg QD, 60 mg BID, or placebo. Patient‐reported functional outcomes were measured by the Short Form 36 (SF‐36), the interference portion of the Brief Pain Inventory (BPI), and EuroQol 5D Health Questionnaire (EQ‐5D). Results for all functional outcomes from the intent‐to‐treat and completer populations are discussed.
Results. In the SF‐36 health survey and the BPI interference, duloxetine 60 mg QD and 60 mg BID were significantly superior to placebo in all the domains (P ≤ 0.03). In the analysis of the EQ‐5D, duloxetine 60 mg QD (P = 0.004) and 60 mg BID (P < 0.001) were significantly better than placebo on all items.
Conclusions. Acute treatment with duloxetine was associated with significant improvement in functional outcomes in persons with DPNP.</abstract><cop>Malden, USA</cop><pub>Blackwell Publishing Inc</pub><pmid>17661854</pmid><doi>10.1111/j.1526-4637.2007.00276.x</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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| ispartof | Pain medicine (Malden, Mass.), 2007-07, Vol.8 (5), p.410-418 |
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| source | Wiley-Blackwell Journals; Oxford University Press Journals; MEDLINE |
| subjects | Aged Antidepressants Diabetic Neuropathies - drug therapy Diabetic Neuropathies - physiopathology Diabetic Neuropathy Dose-Response Relationship, Drug Double-Blind Method Drug Administration Schedule Duloxetine Hydrochloride Female Humans Male Middle Aged Outcome Assessment (Health Care) - methods Pain Measurement - drug effects Pain Measurement - methods Patient Satisfaction Peripheral Nerves - drug effects Peripheral Nerves - physiopathology Placebos Serotonin Uptake Inhibitors - administration & dosage Serotonin Uptake Inhibitors - adverse effects Surveys and Questionnaires Thiophenes - administration & dosage Thiophenes - adverse effects Treatment Outcome |
| title | Duloxetine for the Management of Diabetic Peripheral Neuropathic Pain: Evaluation of Functional Outcomes |
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