TY - JOUR
T1 - Custom-made capsules and suppositories of methadone for patients on high-dose opioids for cancer pain
AU - Bruera, Eduardo
AU - Watanabe, Sharon
AU - Fainsinger, Robin L.
AU - Spachynski, Kathy
AU - Suarez-Almazor, Maria
AU - Inturrisi, Charles
PY - 1995/8
Y1 - 1995/8
N2 - In a prospective, open study, 37 advanced cancer patients in poor pain control receiving high doses of subcutaneous hydromorphone (mean daily dose: 276 ± 163 mg) were switched to methadone by use of custom-made capsules (21 patients) or suppositories (16 patients). The change in opioid took place over 6.5 ± 3.6 days (oral) and 3.2 ± 2.7 days (rectal). The methadone/ hydromorphone dose ratios were 1.2 ± 1.3 and 3 ± 2 for the oral and rectal routes, respectively (P = 0.03) as compared to an expected ratio of 5-7, based on single dose available data. Pain intensity (VAS 0-100 mm) and the number of extra doses of analgesic per day were 51 ± 22 and 3.2 ± 2.7 with hydromorphone, versus 34 ± 21 (P < 0.001) and 2.1 ± 1.9 (P = 0.03) with methadone, respectively. The total cost of treatment was Canadian $148 ± 202 with methadone as compared to Canadian $2135 ± 472 with hydromorphone (P < 0.001). Toxicity was limited to mild sedation in all patients and proctitis in 2 patients on suppositories (one of whom required discontinuation of methadone). Plasma levels obtained in 6 patients on suppositories revealed large inter-individual variation in methadone level (ng/ ml) to dose (mg/ day) ratio (range: 0.8-8.5). Within individuals, the ratio remained constant over a range of doses. We conclude that a slow switch-over to methadone is a safe, effective and low cost alternative in selected cancer patients receiving high doses of opioids for poor prognostic pain syndromes.
AB - In a prospective, open study, 37 advanced cancer patients in poor pain control receiving high doses of subcutaneous hydromorphone (mean daily dose: 276 ± 163 mg) were switched to methadone by use of custom-made capsules (21 patients) or suppositories (16 patients). The change in opioid took place over 6.5 ± 3.6 days (oral) and 3.2 ± 2.7 days (rectal). The methadone/ hydromorphone dose ratios were 1.2 ± 1.3 and 3 ± 2 for the oral and rectal routes, respectively (P = 0.03) as compared to an expected ratio of 5-7, based on single dose available data. Pain intensity (VAS 0-100 mm) and the number of extra doses of analgesic per day were 51 ± 22 and 3.2 ± 2.7 with hydromorphone, versus 34 ± 21 (P < 0.001) and 2.1 ± 1.9 (P = 0.03) with methadone, respectively. The total cost of treatment was Canadian $148 ± 202 with methadone as compared to Canadian $2135 ± 472 with hydromorphone (P < 0.001). Toxicity was limited to mild sedation in all patients and proctitis in 2 patients on suppositories (one of whom required discontinuation of methadone). Plasma levels obtained in 6 patients on suppositories revealed large inter-individual variation in methadone level (ng/ ml) to dose (mg/ day) ratio (range: 0.8-8.5). Within individuals, the ratio remained constant over a range of doses. We conclude that a slow switch-over to methadone is a safe, effective and low cost alternative in selected cancer patients receiving high doses of opioids for poor prognostic pain syndromes.
KW - Cancer pain
KW - Hydromorphone
KW - Methadone
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U2 - 10.1016/0304-3959(94)00257-F
DO - 10.1016/0304-3959(94)00257-F
M3 - Article
C2 - 8545138
AN - SCOPUS:0029125290
SN - 0304-3959
VL - 62
SP - 141
EP - 146
JO - Pain
JF - Pain
IS - 2
ER -