Randomised crossover trial of transdermal fentanyl and sustained release oral morphine for treating chronic non-cancer
Top Cited Papers
- 12 May 2001
- Vol. 322 (7295) , 1154
- https://doi.org/10.1136/bmj.322.7295.1154
Abstract
Objectives: To compare patients' preference for transdermal fentanyl or sustained release oral morphine, their level of pain control, and their quality of life after treatment. Design: Randomised, multicentre, international, open label, crossover trial. Setting: 35 centres in Belgium, Canada, Denmark, Finland, the United Kingdom, the Netherlands, and South Africa. Participants: 256 patients (aged 26-82 years) with chronic non-cancer pain who had been treated with opioids. Main outcome measures: Patients' preference for transdermal fentanyl or sustained release oral morphine, pain control, quality of life, and safety assessments. Results: Of 212 patients, 138 (65%) preferred transdermal fentanyl, whereas 59 (28%) preferred sustained release oral morphine and 15 (7%) expressed no preference. Better pain relief was the main reason for preference for fentanyl given by 35% of patients. More patients considered pain control as being “good” or “very good” with fentanyl than with morphine (35% v 23%, P=0.002). These results were reflected in both patients' and investigators' opinions on the global efficacy of transdermal fentanyl. Patients receiving fentanyl had on average higher quality of life scores than those receiving morphine. The incidence of adverse events was similar in both treatment groups; however, more patients experienced constipation with morphine than with fentanyl (48% v 29%, Pv 5%). However, within the subgroup of patients naive to both fentanyl and morphine, similar numbers of patients withdrew owing to adverse effects (11% v 10%, respectively). Conclusion: Transdermal fentanyl was preferred to sustained release oral morphine by patients with chronic non-cancer pain previously treated with opioids. The main reason for preference was better pain relief, achieved with less constipation and an enhanced quality of life. What is already known on this topic The clinical use of potent opioids in the treatment of chronic non-cancer pain is supported by retrospective, survey data and small randomised controlled trials showing efficacy and safety Studies with transdermal fentanyl have shown efficacy and preference over sustained release oral morphine in the treatment of cancer pain What this study adds This is the first study to provide comparative data supporting treatment options with potent opioids for chronic non-cancer pain Both transdermal fentanyl and sustained release oral morphine provided effective and well tolerated pain relief During fentanyl treatment patients experienced superior pain relief, higher quality of life, and less constipation; fentanyl was preferred to morphine by 65% of patientsKeywords
This publication has 37 references indexed in Scilit:
- Size is everything – large amounts of information are needed to overcome random effects in estimating direction and magnitude of treatment effectsPain, 1998
- Transdermal fentanyl versussustained-release oral morphine in cancer pain: Preference, efficacy, and quality of lifeJournal of Pain and Symptom Management, 1997
- Transdermal fentanyl in the long-term treatment of cancer pain: a prospective study of 50 patients with advanced cancer of the gastrointestinal tract or the head and neck regionPain, 1997
- Transdermal FentanylDrugs, 1997
- Opioid therapy for chronic nonmalignant pain: a review of the critical issuesJournal of Pain and Symptom Management, 1996
- Randomised trial of oral morphine for chronic non-cancer painThe Lancet, 1996
- Transdermal fentanyl therapy: system design, pharmacokinetics and efficacyAnti-Cancer Drugs, 1995
- Transdermal fentanyl and initial dose-finding with patient-controlled analgesia in cancer pain. A pilot study with 20 terminally ill cancer patientsPain, 1992
- The MOS 36-ltem Short-Form Health Survey (SF-36)Medical Care, 1992
- Treatment Principles for the Use of Opioids in Pain of Nonmalignant OriginDrugs, 1991