Likar 2008.
Methods | Randomised, double‐blind study | |
Participants | 13 patients: semi‐conscious, terminal cancer with predicted life expectancy of up to 3 days. All had metastatic disease. Primary cancer: bronchial (10), rectal (2), bladder (1). Age: Intervention A = 71.3 + 3.8 years Intervention B = 71.8 + 5.4 years Gender: Intervention A = 5 males, 2 females Intervention B = 5 males, 1 female. |
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Interventions | Intervention A = Hyoscine hydrobromide 0.5 mg every 6 hours intravenously Intervention B = Glycopyrronium bromide 0.4 mg every 6 hours intravenously. Discontinued if no abatement of death rattle after third injection. |
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Outcomes | Death rattle assessed using scale of one to five:
1 = noisy breathing; 2 = minimal rattle; 3 = moderate rattle; 4 = severe rattle; 5 = very severe rattle
Assessment carried out two‐hourly from zero hours till 12 hours. Stronger decrease in death rattle at various time points in those who had Intervention B (i.e. glycopyrronium) compared to those who had Intervention A: statistically significant difference. Mean time from first treatment to death (SD): Intervention A = 19.5 + 5.4 hours Intervention B = 12.8 + 5.0 hours; not statistically significant |
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Notes | Restlessness and expressions of pain also assessed on scale of one to three:
1 = slight; 2 = moderate; 3 = severe Outcome: Restlessness: appeared to be greater with Intervention B at 2 hours, then no statistical difference. Expressions of pain: no difference |
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Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Lack of detailed description: 'envelope method' used |
Allocation concealment (selection bias) | Unclear risk | Lack of detailed description: 'envelope method' used |
Selective reporting (reporting bias) | Unclear risk | Lack of detailed data for secondary outcomes |
Incomplete outcome data addressed | Low risk | All participants accounted for. |
Blinding | Low risk | Injection solutions blinded by hospital pharmacy |