TY - JOUR
T1 - Australasian Malignant PLeural Effusion (AMPLE)-4 trial
T2 - study protocol for a multi-centre randomised trial of topical antibiotics prophylaxis for infections of indwelling pleural catheters
AU - Lau, Estee P.M.
AU - Ing, Matthew
AU - Vekaria, Sona
AU - Tan, Ai Ling
AU - Charlesworth, Chloe
AU - Fysh, Edward
AU - Shrestha, Ranjan
AU - Yap, Elaine L.C.
AU - Smith, Nicola A.
AU - Kwan, Benjamin C.H.
AU - Saghaie, Tajalli
AU - Roy, Bapti
AU - Goddard, John
AU - Muruganandan, Sanjeevan
AU - Badiei, Arash
AU - Nguyen, Phan
AU - Hamid, Mohamed Faisal Abdul
AU - George, Vineeth
AU - Fitzgerald, Deirdre
AU - Maskell, Nick
AU - Feller-Kopman, David
AU - Murray, Kevin
AU - Chakera, Aron
AU - Lee, Y. C.Gary
N1 - Publisher Copyright:
© The Author(s) 2024.
PY - 2024/4/10
Y1 - 2024/4/10
N2 - 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. Ethics and dissemination: Sir Charles Gairdner and Osborne Park Health Care Group Human Research Ethics Committee has approved the study (RGS0000005920). Results will be published in peer-reviewed journals and presented at scientific conferences. Trial registration: Australia New Zealand Clinical Trial Registry ACTRN12623000253606. Registered on 9 March 2023.
AB - 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. Ethics and dissemination: Sir Charles Gairdner and Osborne Park Health Care Group Human Research Ethics Committee has approved the study (RGS0000005920). Results will be published in peer-reviewed journals and presented at scientific conferences. Trial registration: Australia New Zealand Clinical Trial Registry ACTRN12623000253606. Registered on 9 March 2023.
KW - Indwelling catheter
KW - Infection
KW - Mupirocin; Prophylaxis
KW - Pleural
KW - Topical antibiotic
UR - http://www.scopus.com/inward/record.url?scp=85190119580&partnerID=8YFLogxK
U2 - 10.1186/s13063-024-08065-1
DO - 10.1186/s13063-024-08065-1
M3 - Article
C2 - 38594766
AN - SCOPUS:85190119580
SN - 1745-6215
VL - 25
JO - Trials
JF - Trials
M1 - 249
ER -