Personalized medicine for ARDS: the 2035 research agenda

被引:59
作者
Beitler, Jeremy R. [1 ]
Goligher, Ewan C. [2 ]
Schmidt, Matthieu [3 ]
Spieth, Peter M. [4 ]
Zanella, Alberto [5 ]
Martin-Loeches, Ignacio [6 ]
Calfee, Carolyn S. [7 ,8 ,9 ]
Cavalcanti, Alexandre B. [10 ]
机构
[1] Univ Calif San Diego, Div Pulm & Crit Care Med, 200 West Arbor Dr 8409, San Diego, CA 92103 USA
[2] Univ Toronto, Dept Physiol, Interdept Div Crit Care Med, Toronto, ON, Canada
[3] Hop La Pitie Salpetriere, iCAN Inst Cardiometab & Nutr, Serv Reanimat Med, Paris, France
[4] Tech Univ Dresden, Univ Hosp Carl Gustav Carus, Dept Anesthesiol & Crit Care Med, D-01062 Dresden, Germany
[5] Osped Maggiore Policlin, Fdn IRCCS Ca Granda, Dipartimento Anestesia Rianimaz & Emergenza Urgen, Milan, Italy
[6] St James Univ Hosp, Trinity Ctr Hlth Sci, Dept Clin Med, MICRO Wellcome Trust HRB Clin Res, Dublin, Ireland
[7] Univ Calif San Francisco, Div Pulm & Crit Care Med, San Francisco, CA 94143 USA
[8] Univ Calif San Francisco, Cardiovasc Res Inst, Dept Med, San Francisco, CA 94143 USA
[9] Univ Calif San Francisco, Dept Anesthesia, San Francisco, CA 94143 USA
[10] Hosp Coracao, HCor, Res Inst, Sao Paulo, Brazil
关键词
Acute respiratory distress syndrome; Acute lung injury; Ventilator-induced lung injury; Positive-pressure respiration; Respiratory mechanics; Clinical trials; RESPIRATORY-DISTRESS-SYNDROME; ACUTE LUNG INJURY; END-EXPIRATORY PRESSURE; EXTRACORPOREAL MEMBRANE-OXYGENATION; CARBON-DIOXIDE REMOVAL; PROTECTIVE-VENTILATION; MECHANICAL VENTILATION; INTENSIVE-CARE; TIDAL VOLUMES; RECRUITMENT MANEUVERS;
D O I
10.1007/s00134-016-4331-6
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
In the last 20 years, survival among patients with acute respiratory distress syndrome (ARDS) has increased substantially with advances in lung-protective ventilation and resuscitation. Building on this success, personalizing mechanical ventilation to patient-specific physiology for enhanced lung protection will be a top research priority for the years ahead. However, the ARDS research agenda must be broader in scope. Further understanding of the heterogeneous biology, from molecular to mechanical, underlying early ARDS pathogenesis is essential to inform therapeutic discovery and tailor treatment and prevention strategies to the individual patient. The ARDSne(x)t research agenda for the next 20 years calls for bringing personalized medicine to ARDS, asking simultaneously both whether a treatment affords clinically meaningful benefit and for whom. This expanded scope necessitates standard acquisition of highly granular biological, physiological, and clinical data across studies to identify biologically distinct subgroups that may respond differently to a given intervention. Clinical trials will need to consider enrichment strategies and incorporate long-term functional outcomes. Tremendous investment in research infrastructure and global collaboration will be vital to fulfilling this agenda.
引用
收藏
页码:756 / 767
页数:12
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