The impact of outpatient<i>versus</i>inpatient management on health-related quality of life outcomes for patients with malignant pleural effusion: the OPTIMUM randomised clinical trial

Parthipan Sivakumar(Guy's and St Thomas' NHS Foundation Trust), Deirdre Fitzgerald(The University of Western Australia), Hugh Ip(The Royal Free Hospital), Deepak Rao(Princess Royal University Hospital), Alex West(Guy's and St Thomas' NHS Foundation Trust), Farinaz Noorzad(St George's Hospital), Deirdre Wallace(Guy's and St Thomas' NHS Foundation Trust), Mohamed Haris(University Hospitals of North Midlands NHS Trust), Benjamin Prudon(North Tees and Hartlepool NHS Foundation Trust), Gihan Hettiarachchi(Medway NHS Foundation Trust), Deepak Jayaram(Surrey and Sussex Healthcare NHS Trust), James Goldring(The Royal Free Hospital), Nick Maskell(University of Bristol), Jayne Holme(Manchester University NHS Foundation Trust), Neel Sharma(East Sussex Healthcare NHS Trust), Iyad Ismail(University Hospitals Birmingham NHS Foundation Trust), Owais Kadwani(Guy's and St Thomas' NHS Foundation Trust), S. J. Simpson(Guy's and St Thomas' NHS Foundation Trust), Catherine Read(The University of Western Australia), Xiaohui Sun(King's College London), Abdel Douiri(The University of Western Australia), Gary Lee(The University of Western Australia), Liju Ahmed(Guy's and St Thomas' NHS Foundation Trust)
European Respiratory Journal
November 23, 2023
Cited by 25Open Access
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Abstract

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.


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