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Advancing precision medicine for acute respiratory distress syndrome.
Beitler, Jeremy R; Thompson, B Taylor; Baron, Rebecca M; Bastarache, Julie A; Denlinger, Loren C; Esserman, Laura; Gong, Michelle N; LaVange, Lisa M; Lewis, Roger J; Marshall, John C; Martin, Thomas R; McAuley, Daniel F; Meyer, Nuala J; Moss, Marc; Reineck, Lora A; Rubin, Eileen; Schmidt, Eric P; Standiford, Theodore J; Ware, Lorraine B; Wong, Hector R; Aggarwal, Neil R; Calfee, Carolyn S.
  • Beitler JR; Center for Acute Respiratory Failure and Division of Pulmonary, Allergy, and Critical Care Medicine, Columbia University College of Physicians and Surgeons and New York-Presbyterian Hospital, New York, NY, USA.
  • Thompson BT; Division of Pulmonary and Critical Care Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
  • Baron RM; Division of Pulmonary and Critical Care Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.
  • Bastarache JA; Division of Allergy, Pulmonary, and Critical Care Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Denlinger LC; Division of Allergy, Pulmonary and Critical Care Medicine, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
  • Esserman L; Department of Surgery, University of California San Francisco, San Francisco, CA, USA.
  • Gong MN; Division of Pulmonary and Critical Care Medicine, Montefiore Medical Center and Albert Einstein College of Medicine, Bronx, NY, USA.
  • LaVange LM; Department of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
  • Lewis RJ; Department of Emergency Medicine, Harbor-UCLA Medical Center, Torrance, CA; Berry Consultants, LLC, Austin, TX; Department of Emergency Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
  • Marshall JC; Departments of Surgery and Critical Care Medicine, University of Toronto, Toronto, Canada.
  • Martin TR; Division of Pulmonary, Critical Care and Sleep Medicine, University of Washington, Seattle, WA, USA.
  • McAuley DF; Wellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast and Regional Intensive Care Unit, Royal Victoria Hospital, Belfast, Northern Ireland.
  • Meyer NJ; Division of Pulmonary, Allergy, and Critical Care Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Moss M; Division of Pulmonary Sciences and Critical Care, University of Colorado School of Medicine, Aurora, CO, USA.
  • Reineck LA; Division of Lung Diseases, National Heart, Lung, and Blood Institute, Bethesda, MD, USA.
  • Rubin E; ARDS Foundation, Northbrook, IL, USA.
  • Schmidt EP; Division of Pulmonary Sciences and Critical Care, University of Colorado School of Medicine, Aurora, CO, USA.
  • Standiford TJ; Division of Pulmonary & Critical Care Medicine, University of Michigan, Ann Arbor, MI, USA.
  • Ware LB; Division of Allergy, Pulmonary, and Critical Care Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Wong HR; Division of Critical Care Medicine, Cincinnati Children's Hospital Medical Center and Cincinnati Children's Research Foundation, and Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
  • Aggarwal NR; Division of Lung Diseases, National Heart, Lung, and Blood Institute, Bethesda, MD, USA. Electronic address: neil.aggarwal@nih.gov.
  • Calfee CS; Division of Pulmonary, Critical Care, Allergy and Sleep Medicine, Department of Medicine, and Department of Anesthesia, University of California San Francisco, San Francisco, CA, USA.
Lancet Respir Med ; 10(1): 107-120, 2022 01.
Article in English | MEDLINE | ID: covidwho-1591647
ABSTRACT
Acute respiratory distress syndrome (ARDS) is a heterogeneous clinical syndrome. Understanding of the complex pathways involved in lung injury pathogenesis, resolution, and repair has grown considerably in recent decades. Nevertheless, to date, only therapies targeting ventilation-induced lung injury have consistently proven beneficial, and despite these gains, ARDS morbidity and mortality remain high. Many candidate therapies with promise in preclinical studies have been ineffective in human trials, probably at least in part due to clinical and biological heterogeneity that modifies treatment responsiveness in human ARDS. A precision medicine approach to ARDS seeks to better account for this heterogeneity by matching therapies to subgroups of patients that are anticipated to be most likely to benefit, which initially might be identified in part by assessing for heterogeneity of treatment effect in clinical trials. In October 2019, the US National Heart, Lung, and Blood Institute convened a workshop of multidisciplinary experts to explore research opportunities and challenges for accelerating precision medicine in ARDS. Topics of discussion included the rationale and challenges for a precision medicine approach in ARDS, the roles of preclinical ARDS models in precision medicine, essential features of cohort studies to advance precision medicine, and novel approaches to clinical trials to support development and validation of a precision medicine strategy. In this Position Paper, we summarise workshop discussions, recommendations, and unresolved questions for advancing precision medicine in ARDS. Although the workshop took place before the COVID-19 pandemic began, the pandemic has highlighted the urgent need for precision therapies for ARDS as the global scientific community grapples with many of the key concepts, innovations, and challenges discussed at this workshop.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Respiratory Distress Syndrome / Precision Medicine Type of study: Cohort study / Observational study / Prognostic study Limits: Humans Language: English Journal: Lancet Respir Med Year: 2022 Document Type: Article Affiliation country: S2213-2600(21)00157-0

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Respiratory Distress Syndrome / Precision Medicine Type of study: Cohort study / Observational study / Prognostic study Limits: Humans Language: English Journal: Lancet Respir Med Year: 2022 Document Type: Article Affiliation country: S2213-2600(21)00157-0