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Program and patient characteristics for the United States Expanded Access Program to COVID-19 convalescent plasma
Jonathon W Senefeld; Patrick W Johnson; Katie L Kunze; Noud van Helmond; Stephen A Klassen; Chad C Wiggins; Katelyn A Bruno; Michael A Golafshar; Molly M Petersen; Matthew R Buras; Allan M Klompas; Matthew A Sexton; Juan C Diaz Soto; Sarah E Baker; John R.A. Shepherd; Nicole C Verdun; Peter Marks; Camille M van Buskirk; Jeffrey L Winters; James R Stubbs; Robert F Rea; Vitaly Herasevich; Emily R Whelan; Andrew J Clayburn; Kathryn F Larson; Juan G Ripoll; Kylie J Andersen; Matthew N.P. Vogt; Joshua J Dennis; Riley J Regimbal; Philippe R Bauer; Janis E Blair; Katherine Wright; Joel T Greenshields; Nigel S Paneth; DeLisa Fairweather; R. Scott Wright; Arturo Casadevall; Rickey E Carter; Michael J Joyner.
Afiliación
  • Jonathon W Senefeld; Mayo Clinic
  • Patrick W Johnson; Mayo Clinic
  • Katie L Kunze; Mayo Clinic
  • Noud van Helmond; Cooper Medical School of Rowan University
  • Stephen A Klassen; Mayo Clinic
  • Chad C Wiggins; Mayo Clinic
  • Katelyn A Bruno; Mayo Clinic
  • Michael A Golafshar; Mayo Clinic
  • Molly M Petersen; Mayo Clinic
  • Matthew R Buras; Mayo Clinic
  • Allan M Klompas; Mayo Clinic
  • Matthew A Sexton; Mayo Clinic
  • Juan C Diaz Soto; Mayo Clinic
  • Sarah E Baker; Mayo Clinic
  • John R.A. Shepherd; Mayo Clinic
  • Nicole C Verdun; U.S. Food and Drug Administration
  • Peter Marks; U.S. Food and Drug Administration
  • Camille M van Buskirk; Mayo Clinic
  • Jeffrey L Winters; Mayo Clinic
  • James R Stubbs; Mayo Clinic
  • Robert F Rea; Mayo Clinic
  • Vitaly Herasevich; Mayo Clinic
  • Emily R Whelan; Mayo Clinic
  • Andrew J Clayburn; Mayo Clinic
  • Kathryn F Larson; Mayo Clinic
  • Juan G Ripoll; Mayo Clinic
  • Kylie J Andersen; Mayo Clinic
  • Matthew N.P. Vogt; Mayo Clinic
  • Joshua J Dennis; Mayo Clinic
  • Riley J Regimbal; Mayo Clinic
  • Philippe R Bauer; Mayo Clinic
  • Janis E Blair; Mayo Clinic
  • Katherine Wright; Arizona State University
  • Joel T Greenshields; Indiana University
  • Nigel S Paneth; Michigan State University
  • DeLisa Fairweather; Mayo Clinic
  • R. Scott Wright; Mayo Clinic
  • Arturo Casadevall; Johns Hopkins University
  • Rickey E Carter; Mayo Clinic
  • Michael J Joyner; Mayo Clinic
Preprint en En | PREPRINT-MEDRXIV | ID: ppmedrxiv-21255115
ABSTRACT
BackgroundThe United States (US) Expanded Access Program (EAP) to COVID-19 convalescent plasma was initiated in response to the rapid spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative agent of coronavirus disease-2019 (COVID-19). While randomized clinical trials were in various stages of development and enrollment, there was an urgent need for widespread access to potential therapeutic agents particularly for vulnerable racial and ethnic minority populations who were disproportionately affected by the pandemic. The objective of this study is to report on the demographic, geographic, and chronological access to COVID-19 convalescent plasma in the US via the EAP. Methods and findingsMayo Clinic served as the central IRB for all participating facilities and any US physician could participate as local physician-principal investigator. Registration occurred through the EAP central website. Blood banks rapidly developed logistics to provide convalescent plasma to hospitalized patients with COVID-19. Demographic and clinical characteristics of all enrolled patients in the EAP were summarized. Temporal trends in access to COVID-19 convalescent plasma were investigated by comparing daily and weekly changes in EAP enrollment in response to changes in infection rate on a state level. Geographical analyses on access to convalescent plasma included assessing EAP enrollment in all national hospital referral regions as well as assessing enrollment in metropolitan and less populated areas which did not have access to COVID-19 clinical trials. From April 3 to August 23, 2020, 105,717 hospitalized patients with severe or life-threatening COVID-19 were enrolled in the EAP. A majority of patients were older than 60 years of age (57.8%), male (58.4%), and overweight or obese (83.8%). There was substantial inclusion of minorities and underserved populations, including 46.4% of patients with a race other than White, and 37.2% of patients were of Hispanic ethnicity. Severe or life-threatening COVID-19 was present in 61.8% of patients and 18.9% of patients were mechanically ventilated at time of convalescent plasma infusion. Chronologically and geographically, increases in enrollment in the EAP closely followed confirmed infections across all 50 states. Nearly all national hospital referral regions enrolled patients in the EAP, including both in metropolitan and less populated areas. ConclusionsThe EAP successfully provided widespread access to COVID-19 convalescent plasma in all 50 states, including for underserved racial and ethnic minority populations. The efficient study design of the EAP may serve as an example framework for future efforts when broad access to a treatment is needed in response to a dynamic disease affecting demographic groups and areas historically underrepresented in clinical studies.
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Texto completo: 1 Colección: 09-preprints Base de datos: PREPRINT-MEDRXIV Tipo de estudio: Experimental_studies / Prognostic_studies / Rct Idioma: En Año: 2021 Tipo del documento: Preprint
Texto completo: 1 Colección: 09-preprints Base de datos: PREPRINT-MEDRXIV Tipo de estudio: Experimental_studies / Prognostic_studies / Rct Idioma: En Año: 2021 Tipo del documento: Preprint