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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Published in | Pain medicine (Malden, Mass.) Vol. 8; no. 5; pp. 410 - 418 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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Malden, USA
Blackwell Publishing Inc
01.07.2007
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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. |
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AbstractList | 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).OBJECTIVETo 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).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.METHODSThe 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.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 <or= 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.RESULTSIn 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 <or= 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.Acute treatment with duloxetine was associated with significant improvement in functional outcomes in persons with DPNP.CONCLUSIONSAcute treatment with duloxetine was associated with significant improvement in functional outcomes in persons with DPNP. 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). 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. 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 <or= 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. Acute treatment with duloxetine was associated with significant improvement in functional outcomes in persons with DPNP. 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. 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 less than or equal to 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. |
Author | Le, Trong K. Kajdasz, Daniel K. D'Souza, Deborah N. Russell, James M. Chappell, Amy S. Armstrong, David G. Backonja, Miroslav |
Author_xml | – sequence: 1 givenname: David G. surname: Armstrong fullname: Armstrong, David G. organization: Scholl's Center for Lower Extremity Ambulatory Research (CLEAR) at Rosalind Franklin University of Medicine and Science, North Chicago, Illinois, USA – sequence: 2 givenname: Amy S. surname: Chappell fullname: Chappell, Amy S. email: aschappell@lilly.com organization: Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, Indiana, USA – sequence: 3 givenname: Trong K. surname: Le fullname: Le, Trong K. organization: Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, Indiana, USA – sequence: 4 givenname: Daniel K. surname: Kajdasz fullname: Kajdasz, Daniel K. organization: Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, Indiana, USA – sequence: 5 givenname: Miroslav surname: Backonja fullname: Backonja, Miroslav organization: University of Wisconsin Medical School, Madison, Wisconsin, USA – sequence: 6 givenname: Deborah N. surname: D'Souza fullname: D'Souza, Deborah N. organization: Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, Indiana, USA – sequence: 7 givenname: James M. surname: Russell fullname: Russell, James M. organization: Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, Indiana, USA |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/17661854$$D View this record in MEDLINE/PubMed |
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Hum Psychopharmacol 2005;20:327-41. 2002; 58 2002; 36 2005; 293 2002; 18 2000; 47 2000; 25 1990; 16 2002; 50 1997; 20 2005; 116 2004; 45 2004; 24 1993, 2000 1994; 23 2005; 20 1996 1995 1994 1993 2003; 19 1999; 7 2005; 28 1998; 21 1992; 30 1998; 59 2005; 19 2006; 67 2002; 63 2002; 20 2000 1989; 262 1997; 14 2000; 55 1999; 173 2003; 26 2005; 6 2003; 5 1998; 91 2001; 17 2003; 60 2001; 57 2004; 20 2016012020385996000_8.5.410.20 2016012020385996000_8.5.410.21 2016012020385996000_8.5.410.22 2016012020385996000_8.5.410.16 Wong (2016012020385996000_8.5.410.17) 2002; 58 2016012020385996000_8.5.410.18 2016012020385996000_8.5.410.19 2016012020385996000_8.5.410.12 2016012020385996000_8.5.410.13 2016012020385996000_8.5.410.14 2016012020385996000_8.5.410.15 Vileikyte (2016012020385996000_8.5.410.11) 2004; 20 2016012020385996000_8.5.410.10 2016012020385996000_8.5.410.50 2016012020385996000_8.5.410.51 2016012020385996000_8.5.410.49 2016012020385996000_8.5.410.45 2016012020385996000_8.5.410.46 2016012020385996000_8.5.410.47 Nash (2016012020385996000_8.5.410.5) 1999; 173 Vileikyte (2016012020385996000_8.5.410.48) 1999; 7 2016012020385996000_8.5.410.41 2016012020385996000_8.5.410.42 2016012020385996000_8.5.410.43 2016012020385996000_8.5.410.44 2016012020385996000_8.5.410.40 2016012020385996000_8.5.410.38 2016012020385996000_8.5.410.39 2016012020385996000_8.5.410.34 2016012020385996000_8.5.410.36 2016012020385996000_8.5.410.37 Amos (2016012020385996000_8.5.410.2) 1997; 14 Sheehan (2016012020385996000_8.5.410.30) 1998; 59 2016012020385996000_8.5.410.31 Nemeroff (2016012020385996000_8.5.410.25) 2002; 36 2016012020385996000_8.5.410.32 2016012020385996000_8.5.410.33 2016012020385996000_8.5.410.27 2016012020385996000_8.5.410.28 2016012020385996000_8.5.410.29 Mallinckrodt (2016012020385996000_8.5.410.26) 2003; 5 2016012020385996000_8.5.410.23 2016012020385996000_8.5.410.9 2016012020385996000_8.5.410.24 2016012020385996000_8.5.410.8 Cleeland (2016012020385996000_8.5.410.35) 1994; 23 2016012020385996000_8.5.410.7 2016012020385996000_8.5.410.6 2016012020385996000_8.5.410.4 2016012020385996000_8.5.410.3 2016012020385996000_8.5.410.1 Pain Med. 2007 Nov-Dec;8(8):690 |
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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... To assess the effectiveness of duloxetine, compared with placebo, on patient-reported health outcomes over a 12-week period, in the management of diabetic... Objective. To assess the effectiveness of duloxetine, compared with placebo, on patient-reported health outcomes over a 12-week period, in the management of... |
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SubjectTerms | 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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