4.5 Article

Increased plasma morphine metabolites in terminally ill cancer patients with delirium: An intra-individual comparison

Journal

JOURNAL OF PAIN AND SYMPTOM MANAGEMENT
Volume 23, Issue 2, Pages 107-113

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/S0885-3924(01)00392-X

Keywords

palliative care; delirium; morphine; morphine-6-glucuronide; morphine-3-glucuronide; neoplasms

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Delirium often causes severe distress for terminally ill cancer patients, and treatment of underlying pathologies is important to achieve symtom alleviation. Although accumulation of morphine metabolites may play an important role in development of delirium, empirical findings are conflicting due to a large inter-individual variation in morphine-related concentrations. To explore intra-individual changes of morphine metabolite concentrations before and after occurrence of terminal delirium, a prospective observational study was performed on terminally ill cancer patients. Among 131 consecutive hospice inpatients, 16 samples from 8 patients who received two blood samples before and after development of delirium were analyzed. Delirium developed a median of 5 days before death, and clinical causes were attributed to multi-organ failure. Plasma concentrations of morphine-6-glucuronide glucuronide (M-6-G) and morphine-3-glucuronide (M-3-G) significantly increased after development of delirium within the same patient. Mean normalized concentrations of M-6-G and M-3-G elevated from 1.24 +/- 1.06 to 2.94 +/- 3.52 ng/mL/mg (P = 0.016), and from 7,46 +/- 4.75 to 15.4 +/- 13.2 ng/mL/mg (P = 0.016), respectively. Normalized morphine concentration increased with a marginal statistical significance from 0.54 +/- 0.27 to 0.83 +/- 0.22 ng/mL/mg (P = 0.055). In conclusion, plasma concentrations of M-6-G and M-3-G were significantly higher after development of terminal delirium than before. It is suggested that accumulations of morphine metabolites can contribute to develolpment of delirium in cancer patients whose death is impending. (C) U.S. Cancer Pain Relief Committee, 2002.

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