Journal
INTERNATIONAL JOURNAL OF CLINICAL PRACTICE
Volume 61, Issue 10, Pages 1671-1676Publisher
WILEY
DOI: 10.1111/j.1742-1241.2007.01500.x
Keywords
-
Ask authors/readers for more resources
Background: The use of opioid analgesics for patients with chronic nonmalignant pain is becoming more widely accepted, and long-acting formulations are an important treatment option. Aim: To assess conversion to extended-release OROS (R) hydromorphone from previous stable opioid agonist therapy in patients with chronic nonmalignant pain of moderate-to-severe intensity. Methods: In this open-label multicentre trial, patients were stabilised on their previous opioid therapy before being switched to OROS (R) hydromorphone at a ratio of 5 : 1 (morphine sulphate equivalent to hydromorphone hydrochloride). The OROS (R) hydromorphone dose was titrated over 3-16 days to achieve effective analgesia, and maintenance treatment continued for 14 days. Results: Study medication was received by 336 patients; 66% completed all study phases. Stabilisation of OROS (R) hydromorphone was achieved by 94.6% of patients, the majority in two or fewer titration steps (mean time, 4.2 days). Mean pain intensity scores, as determined by the Brief Pain Inventory, decreased during OROS (R) hydromorphone treatment (p <= 0.001). The percentage of patients rating their pain relief as 'good' or 'complete' increased, and the use of rescue analgesics for breakthrough pain decreased. The interference of pain with everyday activities (e.g. walking or work), and the effects on mood and enjoyment of life, also improved during the study (all p < 0.001). OROS (R) hydromorphone was well tolerated, and adverse events were those expected for opioid agonist therapy. Conclusion: Patients with chronic nonmalignant pain who had been receiving opioid therapy easily underwent conversion to OROS (R) hydromorphone, with no loss of efficacy or increase in adverse events.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available