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J Thomas
Dr J Thomas, San Diego Hospice and Palliative Care, San Diego, CA, USA; jthomas@sdhospice.org
STUDY DESIGN
Design:
randomised placebo controlled trial.
Allocation:
unclear allocation concealment.*
Blinding:
blinded (patients, healthcare providers, and outcome assessors).*
STUDY QUESTION
Setting:
27 nursing homes, hospice sites, and palliative care centres in the USA and Canada.
Patients:
133 patients ⩾18 years of age (median age 71 y, 57% women) who had terminal illness with life expectancy ⩾1 month, were receiving opioids for analgesia, and had opioid-induced constipation (<3 laxations in the previous wk or no laxation in the previous 48 h, despite having taken laxatives for ⩾3 d).
Intervention:
subcutaneous methylnaltrexone, 0.15 mg/kg body weight (n = 62), or placebo (n = 71) every other day for 2 weeks. Laxatives could be taken as needed but not within 4 hours of the study drug. …
Footnotes
Source of funding: Progenics Pharmaceuticals.