Yim 1996.
| Methods | Single centre RCT of talc insufflation versus talc slurry for symptomatic MPE (Hong Kong) | |
| Participants | Inclusion: established, symptomatic MPE (all cell types); dyspnoea improved after tube thoracostomy or large volume thoracentesis Exclusion: Karnofsky score < 30%; FEV1 < 0.5 L; trapped lung; chemotherapy or radiotherapy within six months 57 participants randomised |
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| Interventions | Talc insufflation group: all participants underwent a GA with one lung ventilation in the lateral decubitus position. 10 mm port inserted. Adehsions and loculations broken down. 5 g talc insufflated into the chest. 28 Fr tube at end of procedure, connected to suction. Drain removed when < 50 ml/24 hours drainage Talc slurry group: chest tube. 5 g talc in 50 ml saline and 10 ml 2% lidocaine instilled through the drain. Drain clamped for two hours and participant turned Drain reconnected to suction and removed when output < 50 ml/24hours |
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| Outcomes | Radiological recurrence of effusion Complications of the procedure Post‐procedure chest drain duration Length of hospital stay Parenteral meperidine use |
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| Notes | People with trapped lung excluded from trial entry Included in network meta‐analysis for pleurodesis efficacy and mortality |
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| Risk of bias | ||
| Bias | Authors' judgement | Support for judgement |
| Random sequence generation (selection bias) | Unclear risk | Not stated |
| Allocation concealment (selection bias) | Unclear risk | Not stated |
| Blinding of participants and personnel (performance bias) All outcomes | High risk | Unable to blind due to nature of the interventions |
| Blinding of outcome assessment (detection bias) All outcomes | High risk | Adverse event reporting and length of stay may be biased by lack of blinding. Not stated whether radiology was reported blindly |
| Incomplete outcome data (attrition bias) All outcomes | Low risk | All data reported. Survial data not entirely clear |
| Selective reporting (reporting bias) | Low risk | All outcomes reported on |
| Other bias | Low risk | Unclear how many patients in the poudrage arm had a drain in situ at the time of trial entry. Pleurodesis success only defined using radiology |