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 inPain medicine (Malden, Mass.) Vol. 8; no. 5; pp. 410 - 418
Main Authors Armstrong, David G., Chappell, Amy S., Le, Trong K., Kajdasz, Daniel K., Backonja, Miroslav, D'Souza, Deborah N., Russell, James M.
Format Journal Article
LanguageEnglish
Published 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.
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
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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
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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
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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
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Snippet ABSTRACT 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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StartPage 410
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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https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1526-4637.2007.00276.x
https://www.ncbi.nlm.nih.gov/pubmed/17661854
https://www.proquest.com/docview/20527862
https://www.proquest.com/docview/68101400
Volume 8
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