Literature DB >> 20662557

Changes in opioid use and healthcare costs among U.S. patients with diabetic peripheral neuropathic pain treated with duloxetine compared with other therapies.

Y Zhao1, N Wu, S Chen, L Boulanger, R L Police, K Fraser.   

Abstract

OBJECTIVE: To examine changes in opioid use and healthcare costs among commercially insured patients with diabetic peripheral neuropathic pain (DPNP) who initiated duloxetine versus other standard of care (SOC) medications (tricyclic antidepressants, venlafaxine, gabapentin, pregabalin). RESEARCH DESIGN AND METHODS: Using an administrative claims database, patients with DPNP aged 18-64 who initiated duloxetine or SOC between March 1, 2005 and December 31, 2005 were identified. Initiation was defined as a 90-day clean period without the available study medication. Selected patients had 12 months of continuous enrollment before and after the index date, and at least one opioid dispensed in the prior 90 days. Duloxetine and SOC patients were further classified into continuous and non-continuous users based on whether the medication possession ratio was > or =0.8. Total opioid days, number of opioid prescriptions dispensed, and cumulative morphine equivalents were examined over the 12-month pre- and post-index periods. Multivariate regressions were applied to assess the changes (pre-index minus post-index) in opioid use (total, short-acting vs. long-acting) and healthcare costs, controlling for demographic and clinical characteristics.
RESULTS: The study sample included 1281 patients: 98 duloxetine continuous, 243 duloxetine non-continuous, 195 SOC continuous, and 745 SOC non-continuous users. Controlling for demographic and clinical characteristics, duloxetine non-continuous and SOC (continuous and non-continuous) patients had significantly less reduction in total opioid days (-24.4, -23.7, -18.5, respectively, all p < 0.05) from the 12-month pre-index to the post-index period than duloxetine continuous patients. Compared with duloxetine non-continuous, SOC continuous, and SOC non-continuous users, duloxetine continuous users had a greater reduction in short-acting hydrocodone use (difference between the 12 month pre-index and post-index periods) in terms of the total number of prescriptions dispensed (adjusted differences: 1.5, 1.7, 1.7, respectively, all p < 0.05), total supply days (adjusted differences: 28.1, 27.3, 29.7, respectively, all p < 0.05), and morphine equivalent dosage (adjusted differences: 1290 mg, 1132 mg, 1127 mg, respectively, all p < 0.05). Duloxetine non-continuous patients had significantly higher adjusted total ($12,729, p < 0.05) and inpatient costs ($14,993, p < 0.05) than duloxetine continuous patients. LIMITATIONS: Due to the use of a retrospective administrative claims database, this study is subject to selection bias between study cohorts, misidentification of DPNP and/or other comorbidities, and an inability to confirm adherence to therapy or assess indirect costs and costs of over-the-counter medications.
CONCLUSIONS: Among commercially insured patients with DPNP, continuous treatment with duloxetine was associated with a reduction in opioid use between the 12-month pre- and post-index periods compared with treatment with SOC or non-continuous treatment with duloxetine. Duloxetine continuous patients also incurred lower subsequent healthcare costs than non-continuous duloxetine patients.

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Year:  2010        PMID: 20662557     DOI: 10.1185/03007995.2010.503140

Source DB:  PubMed          Journal:  Curr Med Res Opin        ISSN: 0300-7995            Impact factor:   2.580


  8 in total

1.  Opioid use in the management of diabetic peripheral neuropathy (DPN) in a large commercially insured population.

Authors:  Pravinkumar R Patil; Jonathan Wolfe; Qayyim Said; Jeremy Thomas; Bradley C Martin
Journal:  Clin J Pain       Date:  2015-05       Impact factor: 3.442

Review 2.  Epidemiology of Peripheral Neuropathy and Lower Extremity Disease in Diabetes.

Authors:  Caitlin W Hicks; Elizabeth Selvin
Journal:  Curr Diab Rep       Date:  2019-08-27       Impact factor: 4.810

3.  Duloxetine in the management of diabetic peripheral neuropathic pain.

Authors:  Michelle J Ormseth; Beth A Scholz; Chad S Boomershine
Journal:  Patient Prefer Adherence       Date:  2011-07-19       Impact factor: 2.711

4.  Endomorphin-2 Inhibition of Substance P Signaling within Lamina I of the Spinal Cord Is Impaired in Diabetic Neuropathic Pain Rats.

Authors:  Fa-Ping Wan; Yang Bai; Zhen-Zhen Kou; Ting Zhang; Hui Li; Ya-Yun Wang; Yun-Qing Li
Journal:  Front Mol Neurosci       Date:  2017-01-10       Impact factor: 5.639

5.  Efficacy of interventions to reduce long term opioid treatment for chronic non-cancer pain: systematic review and meta-analysis.

Authors:  Nicholas Avery; Amy G McNeilage; Fiona Stanaway; Claire E Ashton-James; Fiona M Blyth; Rebecca Martin; Ali Gholamrezaei; Paul Glare
Journal:  BMJ       Date:  2022-04-04

Review 6.  A review of the clinical utility of duloxetine in the treatment of diabetic peripheral neuropathic pain.

Authors:  Jordan B King; Marisa B Schauerhamer; Brandon K Bellows
Journal:  Ther Clin Risk Manag       Date:  2015-08-10       Impact factor: 2.423

7.  Real-world treatment patterns and opioid use in chronic low back pain patients initiating duloxetine versus standard of care.

Authors:  Jeffrey Scott Andrews; Ning Wu; Shih-Yin Chen; Xia Yu; Xiaomei Peng; Diego Novick
Journal:  J Pain Res       Date:  2013-11-26       Impact factor: 3.133

8.  Decreased Endomorphin-2 and μ-Opioid Receptor in the Spinal Cord Are Associated with Painful Diabetic Neuropathy.

Authors:  Zhen-Zhen Kou; Fa-Ping Wan; Yang Bai; Chun-Yu Li; Jia-Chen Hu; Guo-Tao Zhang; Ting Zhang; Tao Chen; Ya-Yun Wang; Hui Li; Yun-Qing Li
Journal:  Front Mol Neurosci       Date:  2016-09-07       Impact factor: 5.639

  8 in total

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