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https://wslhd.intersearch.com.au/wslhdjspui/handle/1/9603
Title: | Australasian Malignant PLeural Effusion (AMPLE)-4 trial: study protocol for a multi-centre randomised trial of topical antibiotics prophylaxis for infections of indwelling pleural catheters |
Authors: | Lau, E. P. M.;Ing, M.;Vekaria, S.;Tan, A. L.;Charlesworth, C.;Fysh, E.;Shrestha, R.;Yap, E. L. C.;Smith, N. A.;Kwan, B. C. H.;Saghaie, T.;Roy, Bapti;Goddard, J.;Muruganandan, S.;Badiei, A.;Nguyen, P.;Hamid, M. F. A.;George, V.;Fitzgerald, D.;Maskell, N.;Feller-Kopman, D.;Murray, K.;Chakera, A.;Lee, Y. C. G. |
WSLHD Author: | Roy, Bapti |
Subjects: | Pleural Effusion, Malignant;Quality of Life;Mupirocin;Pleurodesis;Talc;Catheters, Indwelling;Catheter-Related Infections |
Issue Date: | 2024 |
Citation: | Trials [Electronic Resource] 25(1):249, 2024 |
Abstract: | BACKGROUND: Malignant pleural effusion (MPE) is a debilitating condition as it commonly causes disabling breathlessness and impairs quality of life (QoL). Indwelling pleural catheter (IPC) offers an effective alternative for the management of MPE. However, IPC-related infections remain a significant concern and there are currently no long-term strategies for their prevention. The Australasian Malignant PLeural Effusion (AMPLE)-4 trial is a multicentre randomised trial that evaluates the use of topical mupirocin prophylaxis (vs no mupirocin) to reduce catheter-related infections in patients with MPE treated with an IPC. METHODS: A pragmatic, multi-centre, open-labelled, randomised trial. Eligible patients with MPE and an IPC will be randomised 1:1 to either regular topical mupirocin prophylaxis or no mupirocin (standard care). For the interventional arm, topical mupirocin will be applied around the IPC exit-site after each drainage, at least twice weekly. Weekly follow-up via phone calls or in person will be conducted for up to 6 months. The primary outcome is the percentage of patients who develop an IPC-related (pleural, skin, or tract) infection between the time of catheter insertion and end of follow-up period. Secondary outcomes include analyses of infection (types and episodes), hospitalisation days, health economics, adverse events, and survival. Subject to interim analyses, the trial will recruit up to 418 participants. DISCUSSION: Results from this trial will determine the efficacy of mupirocin prophylaxis in patients who require IPC for MPE. It will provide data on infection rates, microbiology, and potentially infection pathways associated with IPC-related infections. |
URI: | https://wslhd.intersearch.com.au/wslhdjspui/handle/1/9603 |
DOI: | https://dx.doi.org/10.1186/s13063-024-08065-1 |
Journal: | Trials [Electronic Resource] |
Type: | Journal Article |
Department: | Respiratory and Sleep Medicine |
Facility: | Westmead |
Appears in Collections: | Westmead Hospital 2019 - 2024 |
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