Abstract
Objective: This study aims to determine the effectiveness of converting patients from high doses of full-opioid agonists to sublingual (SL) buprenorphine. Design: An observational report of outcomes assessment. Setting: An interventional pain management practice setting in the United States. Subjects: Thirty-five chronic pain patients (age 24-66) were previously treated with high-dose opioid-agonist drugs and converted to SL buprenorphine. Patients' daily morphine equivalents ranged from 200mg to 1,370mg preconversion, with a mean daily dose of 550mg. Methods: A retrospective chart analysis examined numerical pain levels and quality of life scores before and 2 months after conversion to SL buprenorphine. Results: After continuation of SL buprenorphine therapy for 2 months, the mean pain score decreased from 7.2 to 3.5 (P
Original language | English (US) |
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Pages (from-to) | 2087-2094 |
Number of pages | 8 |
Journal | Pain Medicine |
Volume | 15 |
Issue number | 12 |
DOIs | |
State | Published - Dec 1 2014 |
Keywords
- Analgesia
- Buprenorphine
- Opioid conversion
- Opioid tolerance
- Opioid-iNDUCED hYperalgesia
- Sublingual buprenorphine
ASJC Scopus subject areas
- Clinical Neurology
- Anesthesiology and Pain Medicine
- Medicine(all)