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Redefining critical illness

delete2022-06-17
delete170
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OA
AI
D
David M. Maslove *
B
Benjamin Tang
M
Manu Shankar‐Hari
P
Patrick R. Lawler
D
Derek C. Angus
J
J. Kenneth Baillie
R
Rebecca M. Baron
M
Michael Bauer
T
Timothy G. Buchman
C
Carolyn S. Calfee
C
Claúdia C. dos Santos
E
Evangelos J. Giamarellos‐Bourboulis
A
Anthony Gordon
J
John A. Kellum
J
Julian C. Knight
A
Aleksandra Leligdowicz
D
Daniel F. McAuley
A
Anthony S. McLean
D
David Menon
N
Nuala J. Meyer
L
Lyle L. Moldawer
K
Kiran Reddy
J
John P. Reilly
J
James A. Russell
J
Jonathan Sevransky
C
Christopher W. Seymour
N
Nathan I. Shapiro
M
Mervyn Singer
C
Charlotte Summers
T
Timothy E. Sweeney
B
Bruce Thompson
T
Tom van der Poll
B
Balasubramanian Venkatesh
K
Keith R. Walley
T
Timothy Walsh
L
Lorraine B. Ware
H
Hector R. Wong
Z
Zsolt Zádor
J
John C. Marshall
DOI:10.1038/s41591-022-01843-xdelete
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摘要

摘要

En 中文
The authors propose a new conceptual model of critical illness that moves away from the current syndrome-based framework in favor of more precise biological descriptors-spurred by mounting translational evidence and insights from Coronavirus Disease 2019 (COVID-19) research. Research and practice in critical care medicine have long been defined by syndromes, which, despite being clinically recognizable entities, are, in fact, loose amalgams of heterogeneous states that may respond differently to therapy. Mounting translational evidence-supported by research on respiratory failure due to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection-suggests that the current syndrome-based framework of critical illness should be reconsidered. Here we discuss recent findings from basic science and clinical research in critical care and explore how these might inform a new conceptual model of critical illness. De-emphasizing syndromes, we focus on the underlying biological changes that underpin critical illness states and that may be amenable to treatment. We hypothesize that such an approach will accelerate critical care research, leading to a richer understanding of the pathobiology of critical illness and of the key determinants of patient outcomes. This, in turn, will support the design of more effective clinical trials and inform a more precise and more effective practice at the bedside.
Keyword:
SEPTIC SHOCK
PRECISION MEDICINE
STAGING SYSTEM
SEPSIS
DEFINITIONS
OUTCOMES
TRIAL
ARDS
CLASSIFICATION
SUBPHENOTYPES

期刊

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Nature Medicine
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50
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Queen's University Belfast
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Friedrich Schiller University of Jena
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被引数: 25
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western university (university of western ontario)
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queens university - canada
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university of pennsylvania
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Royal Infirmary of Edinburgh
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university health network toronto
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pennsylvania commonwealth system of higher education (pcshe)
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uk research & innovation (ukri)
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peter munk cardiac centre
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