TY - JOUR
T1 - The impact of outpatient versus inpatient management on health-related quality of life outcomes for patients with malignant pleural effusion
T2 - the OPTIMUM randomised clinical trial
AU - Sivakumar, Parthipan
AU - Fitzgerald, Deirdre B.
AU - Ip, Hugh
AU - Rao, Deepak
AU - West, Alex
AU - Noorzad, Farinaz
AU - Wallace, Deirdre
AU - Haris, Mohamed
AU - Prudon, Benjamin
AU - Hettiarachchi, Gihan
AU - Jayaram, Deepak
AU - Goldring, James
AU - Maskell, Nick
AU - Holme, Jayne
AU - Sharma, Neel
AU - Ismail, Iyad
AU - Kadwani, Owais
AU - Simpson, Sanchez
AU - Read, Catherine A.
AU - Sun, Xiaohui
AU - Douiri, Abdel
AU - Lee, Y. C.Gary
AU - Ahmed, Liju
PY - 2024/2/1
Y1 - 2024/2/1
N2 - BACKGROUND: The principal aim of malignant pleural effusion (MPE) management is to improve health-related quality of life (HRQoL) and symptoms. METHODS: In this open-label randomised controlled trial, patients with symptomatic MPE were randomly assigned to either indwelling pleural catheter (IPC) insertion with the option of talc pleurodesis or chest drain and talc pleurodesis. The primary end-point was global health status, measured with the 30-item European Organisation for Research and Treatment of Cancer Quality of Life Core Questionnaire (EORTC QLQ-C30) at 30 days post-intervention. 142 participants were enrolled from July 2015 to December 2019. RESULTS: Of participants randomly assigned to the IPC (n=70) and chest drain (n=72) groups, primary outcome data were available in 58 and 56 patients, respectively. Global health status improved in both groups at day 30 compared with baseline: IPC (mean difference 13.11; p=0.001) and chest drain (mean difference 10.11; p=0.001). However, there was no significant between-group difference at day 30 (mean intergroup difference in baseline-adjusted global health status 2.06, 95% CI -5.86-9.99; p=0.61), day 60 or day 90. No significant differences were identified between groups in breathlessness and chest pain scores. All chest drain arm patients were admitted (median length of stay 4 days); seven patients in the IPC arm required intervention-related hospitalisation. CONCLUSIONS: While HRQoL significantly improved in both groups, there were no differences in patient-reported global health status at 30 days. The outpatient pathway using an IPC was not superior to inpatient treatment with a chest drain.
AB - BACKGROUND: The principal aim of malignant pleural effusion (MPE) management is to improve health-related quality of life (HRQoL) and symptoms. METHODS: In this open-label randomised controlled trial, patients with symptomatic MPE were randomly assigned to either indwelling pleural catheter (IPC) insertion with the option of talc pleurodesis or chest drain and talc pleurodesis. The primary end-point was global health status, measured with the 30-item European Organisation for Research and Treatment of Cancer Quality of Life Core Questionnaire (EORTC QLQ-C30) at 30 days post-intervention. 142 participants were enrolled from July 2015 to December 2019. RESULTS: Of participants randomly assigned to the IPC (n=70) and chest drain (n=72) groups, primary outcome data were available in 58 and 56 patients, respectively. Global health status improved in both groups at day 30 compared with baseline: IPC (mean difference 13.11; p=0.001) and chest drain (mean difference 10.11; p=0.001). However, there was no significant between-group difference at day 30 (mean intergroup difference in baseline-adjusted global health status 2.06, 95% CI -5.86-9.99; p=0.61), day 60 or day 90. No significant differences were identified between groups in breathlessness and chest pain scores. All chest drain arm patients were admitted (median length of stay 4 days); seven patients in the IPC arm required intervention-related hospitalisation. CONCLUSIONS: While HRQoL significantly improved in both groups, there were no differences in patient-reported global health status at 30 days. The outpatient pathway using an IPC was not superior to inpatient treatment with a chest drain.
UR - http://www.scopus.com/inward/record.url?scp=85184673566&partnerID=8YFLogxK
U2 - 10.1183/13993003.01215-2022
DO - 10.1183/13993003.01215-2022
M3 - Article
C2 - 37996243
AN - SCOPUS:85184673566
SN - 0903-1936
VL - 63
JO - The European Respiratory Journal
JF - The European Respiratory Journal
IS - 2
M1 - 2201215
ER -