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Multicenter Study Clinical Trial
Titration with oxymorphone extended release to achieve effective long-term pain relief and improve tolerability in opioid-naive patients with moderate to severe pain.
- Richard Rauck, Tina Ma, Rosemary Kerwin, and Harry Ahdieh.
- Carolinas Pain Institute, Wake Forest University, Winston-Salem, North Carolina 27103, USA. rrauck@ccrpain.com
- Pain Med. 2008 Oct 1;9(7):777-85.
ObjectiveAssess the effectiveness and tolerability of a program of gradual dose titration with oxymorphone extended release (ER) for treatment of moderate to severe chronic pain in opioid-naive patients.DesignOpen-label, nonrandomized 6-month study with a titration/stabilization period of
SettingMultidisciplinary pain centers in the United States.PatientsAdult opioid-naive patients with moderate to severe chronic pain.InterventionsPatients were gradually titrated from a 5-mg dose of oxymorphone ER (taken every 12 hours) to a stabilized dose that provided effective pain relief and was well tolerated.Outcome MeasuresBrief Pain Inventory Short Form questions 5 and 9, patient and physician global assessments of pain relief, adverse events (AEs), and discontinuations.ResultsThe majority (94/126; 75%) of patients were stabilized on a dose of oxymorphone ER that provided effective pain relief with tolerable AEs. Most (81/94; 86%) required <24 days to reach a stable dose. Sixteen percent of patients in the titration period and 17% of patients in the maintenance period discontinued because of AEs possibly or probably related to oxymorphone ER. Patients completing the entire 5-month maintenance period experienced effective pain relief with significant (>50%) reductions of pain interference with quality-of-life measures. There was minimal dose escalation over the 5 months and low use of rescue medication.ConclusionsOxymorphone ER provided effective pain relief from moderate to severe chronic pain in opioid-naive patients. Gradual titration was well tolerated, with a low rate of discontinuations caused by AEs. Notes
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