Goodman 2006.
Methods | Single centre RCT evaluating duration of chest tube drainage after a talc slurry pleurodesis (UK) | |
Participants | Inclusion criteria: confirmed MPE requiring palliation of breathlessness due to the effusion (all cell types) Exclusion criteria: expected survival < 3 months; Karnofsky score < 40; previous unsuccessful pleurodesis; ipsilateral endobronchial obstruction; evidence of trapped lung 41 participants randomised |
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Interventions | All participants had 8 ‐ 14 Fr intercostal drain inserted under ultrasound guidance. 4 g talc slurry when effusion fully drained and trapped lung excluded on CXR In one group, drain removed after 24 hours. In the other group, drain removed at 72 hours. Drains removed regardless of fluid drainage |
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Outcomes | Pleurodesis failure at one month (defined according to fluid recurrence requiring repeat aspiration). Length of hospital stay. Mortality | |
Notes | People with trapped lung excluded from the study. Study didn't complete recruitment numbers required by the power calculation Participants who died in first month after randomisation excluded from the analysis Not included in network meta‐analysis |
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Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Sealed envelopes in random blocks of 10 |
Allocation concealment (selection bias) | Low risk | Sealed envelopes in random blocks of 10 |
Blinding of participants and personnel (performance bias) All outcomes | High risk | Not possible to blind due to nature of interventions (drain removal after 24 or 48 hours) |
Blinding of outcome assessment (detection bias) All outcomes | High risk | Need for repeat pleural interventions, length of stay may be biased by lack of blinding. Mortality data not biased |
Incomplete outcome data (attrition bias) All outcomes | Low risk | Deaths within the first month well matched between the two arms (3 patients in each arm). No other LTFU |
Selective reporting (reporting bias) | Low risk | All predefined outcomes reported. Unpublished data on complications provided by the authors |
Other bias | Low risk | No other biases identified |