Please use this identifier to cite or link to this item: https://covid-19.conacyt.mx/jspui/handle/1000/3115
The Randomized Embedded Multifactorial Adaptive Platform for Community-acquired Pneumonia (REMAP-CAP) Study: Rationale and Design.
Angus Derek C.
Berry Scott.
Lewis Roger J.
Al-Beidh Farah.
Arabi Yaseen.
van Bentum-Puijk Wilma.
Bhimani Zahra.
Bonten Marc.
Broglio Kristine.
Brunkhorst Frank.
Cheng Allen C.
Chiche Jean-Daniel.
De Jong Menno.
Detry Michelle.
Goossens Herman.
Gordon Anthony.
Green Cameron.
Higgins Alisa M.
Hullegie Sebastiaan J.
Kruger Peter.
Lamontagne Francois.
Litton Edward.
Marshall John.
McGlothlin Anna.
McGuinness Shay.
Mouncey Paul.
Murthy Srinivas.
Nichol Alistair.
O'Neill Genevieve K.
Parke Rachael.
Parker Jane.
Rohde Gernot.
Rowan Kathryn.
Turner Anne.
Young Paul.
Derde Lennie.
McArthur Colin.
Webb Steven A.
Acceso Abierto
Atribución-NoComercial-SinDerivadas
10.1513/annalsats.202003-192sd
There is broad interest in improved methods to generate robust evidence regarding best practice, especially in settings where patient conditions are heterogenous and require multiple concomitant therapies. Here, we present the rationale and design of a large, international trial that combines features of adaptive platform trials with pragmatic point-of-care trials to determine best treatment strategies for patients admitted to an intensive care unit with severe community-acquired pneumonia (CAP). The trial uses a novel design entitled a randomized embedded multifactorial adaptive platform (REMAP). The design has 5 key features: i.) randomization, allowing robust causal inference; ii.) embedding of study procedures into routine care processes, facilitating enrollment, trial efficiency, and generalizability; iii.) a multifactorial statistical model comparing multiple interventions across multiple patient subgroups; iv.) response-adaptive randomization with preferential assignment to those interventions that appear most favorable, and v.) a platform structured to permit continuous, potentially perpetual enrollment beyond the evaluation of the initial treatments. The trial randomizes patients to multiple interventions within 4 treatment domains: antibiotics, antiviral therapy for influenza, host immunomodulation with extended macrolide therapy, and alternative corticosteroid regimens, representing 240 treatment regimens. The trial generates estimates of superiority, inferiority and equivalence between regimens on the primary outcome of 90-day mortality, stratified by presence or absence of concomitant shock and proven or suspected influenza infection. The trial will also compare ventilatory and oxygenation strategies and has capacity to address additional questions rapidly during pandemic respiratory infections. As of January 2020, REMAP-CAP was approved and enrolling patients in 52 ICUs in 13 countries in 3 continents. In February, it transitioned into pandemic mode with several design adaptations for COVID-19 disease. Lessons learned from the design and conduct of this trial should aid in dissemination of similar platform initiatives in other disease areas. Clinical trial registered with ClinicalTrials.gov (NCT02735707).
Annals of the American Thoracic Society
2020
Artículo
http://www.atsjournals.org/doi/pdf/10.1513/AnnalsATS.202003-192SD
Inglés
VIRUS RESPIRATORIOS
Appears in Collections:Artículos científicos

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