Literature DB >> 32616600

Building the house of CARDS by phenotyping on the fly.

Rajkumar Rajendram1,2.   

Abstract

Entities:  

Mesh:

Year:  2020        PMID: 32616600      PMCID: PMC7450144          DOI: 10.1183/13993003.02429-2020

Source DB:  PubMed          Journal:  Eur Respir J        ISSN: 0903-1936            Impact factor:   16.671


× No keyword cloud information.
To the Editor: Some patients with coronavirus disease 2019 (COVID-19), fulfilling the Berlin criteria for acute respiratory distress syndrome (ARDS), do not respond well to the current treatment paradigm [1]. The perspective by Rello et al. [2] on phenotypes of COVID-19, and the editorial by Bos et al. [3], are therefore of great interest. The “responsible” phenotyping of COVID-19 ARDS (CARDS) recommended by Bos et al. [3] may be expedited by re-evaluating the existing literature on refractory hypoxia. In 2000, the landmark ARDS Network (ARDSNet) trial demonstrated that ventilation with low tidal volumes (VT; 6–8 mL·kg−1 predicted body weight (PBW)), titration of positive end-expiratory pressure (PEEP) to inspiratory oxygen fraction and maintaining plateau pressure under 30 cmH2O significantly reduced mortality [4]. The mortality in the group that received ARDSNet ventilation (31.0%) was significantly lower than that of the control group (39.8%) who were ventilated with a “traditional” high VT strategy (12 mL·kg−1 PBW) [4]. Absolute risk reduction was 8.8%, so the number needed to treat (NNT) to prevent one death is 11.4. So, for the past 20 years, the ARDSNet protocol has set the standard for ventilation of patients with ARDS. Bos et al. [3] essentially say that this is rightly so, and suggest that the ARDSNet protocol should also be rigorously applied to CARDS. Indeed, the Surviving Sepsis Campaign guidelines for the management of COVID-19 [5] support Bos et al. [3]. However, in the ARDSNet trial, approximately 30% of patients receiving ARDSNet ventilation died, and just over 60% of controls survived [4]. Thus, although the NNT is low, of every 11.4 patients with ARDS, 10.4 do not benefit from this ventilatory strategy and 60% can tolerate high VT. In 2015, Amato et al. [6] reported a multilevel mediation reanalysis of pooled data from four randomised controlled trials of ventilatory strategies for ARDS. This showed that driving pressure (i.e. plateau pressure minus total PEEP; ΔP) was the ventilator variable most strongly associated with survival. Any change in VT or PEEP only improved outcomes if associated with a fall in ΔP [6]. Thus, while the net effect of the ARDSNet protocol is beneficial at the level of the study population, theoretically it may harm select patients, particularly when not associated with a fall in ΔP. Therefore, contrary to the opinions of the Surviving Sepsis Campaign [5] and Bos et al. [3], the ARDSNet protocol is not a panacea. Unfortunately, the subgroup of patients with ARDS who do not benefit from the ARDSNet protocol is a “known unknown”. So individualising ventilatory support is currently extremely challenging. To improve outcomes, further research is required to determine which patients benefit from the ARDSNet protocol (i.e. phenotyping). This will allow consideration of alternative strategies for patients who are unlikely to benefit from the ARDSNet protocol. Sadly, the literature on ARDS is littered with promising interventions that were associated with improved outcomes in case reports, case series and observational studies but were subsequently discarded after large randomised controlled trials. This may reflect the shortcomings of previous research on ARDS. Indiscriminate recruitment of heterogeneous cohorts of patients generated significant noise, which may have drowned out any potential benefits in specific subgroups of patients. The COVID-19 pandemic provides the unique opportunity to rectify this deplorable situation by responsibly phenotyping “on the fly”. The evidence-base for the management of refractory hypoxia could be significantly advanced by analysing the effect of interventions such as nitric oxide and prone positioning on multiple phenotypes of ARDS with a unique aetiology. Observations in CARDS may be relevant to other respiratory diseases. However, to increase generalisability, future studies should, a priori, explore outcomes in clinically, pathophysiologically and immunologically defined subgroups. This one-page PDF can be shared freely online. Shareable PDF ERJ-02429-2020.Shareable
  6 in total

1.  Ventilation with lower tidal volumes as compared with traditional tidal volumes for acute lung injury and the acute respiratory distress syndrome.

Authors:  Roy G Brower; Michael A Matthay; Alan Morris; David Schoenfeld; B Taylor Thompson; Arthur Wheeler
Journal:  N Engl J Med       Date:  2000-05-04       Impact factor: 91.245

2.  Driving pressure and survival in the acute respiratory distress syndrome.

Authors:  Marcelo B P Amato; Maureen O Meade; Arthur S Slutsky; Laurent Brochard; Eduardo L V Costa; David A Schoenfeld; Thomas E Stewart; Matthias Briel; Daniel Talmor; Alain Mercat; Jean-Christophe M Richard; Carlos R R Carvalho; Roy G Brower
Journal:  N Engl J Med       Date:  2015-02-19       Impact factor: 91.245

3.  Clinical phenotypes of SARS-CoV-2: implications for clinicians and researchers.

Authors:  Jordi Rello; Enrico Storti; Mirko Belliato; Ricardo Serrano
Journal:  Eur Respir J       Date:  2020-05-21       Impact factor: 16.671

4.  COVID-19 Does Not Lead to a "Typical" Acute Respiratory Distress Syndrome.

Authors:  Luciano Gattinoni; Silvia Coppola; Massimo Cressoni; Mattia Busana; Sandra Rossi; Davide Chiumello
Journal:  Am J Respir Crit Care Med       Date:  2020-05-15       Impact factor: 21.405

5.  Surviving Sepsis Campaign: Guidelines on the Management of Critically Ill Adults with Coronavirus Disease 2019 (COVID-19).

Authors:  Waleed Alhazzani; Morten Hylander Møller; Yaseen M Arabi; Mark Loeb; Michelle Ng Gong; Eddy Fan; Simon Oczkowski; Mitchell M Levy; Lennie Derde; Amy Dzierba; Bin Du; Michael Aboodi; Hannah Wunsch; Maurizio Cecconi; Younsuck Koh; Daniel S Chertow; Kathryn Maitland; Fayez Alshamsi; Emilie Belley-Cote; Massimiliano Greco; Matthew Laundy; Jill S Morgan; Jozef Kesecioglu; Allison McGeer; Leonard Mermel; Manoj J Mammen; Paul E Alexander; Amy Arrington; John E Centofanti; Giuseppe Citerio; Bandar Baw; Ziad A Memish; Naomi Hammond; Frederick G Hayden; Laura Evans; Andrew Rhodes
Journal:  Crit Care Med       Date:  2020-06       Impact factor: 7.598

6.  The perils of premature phenotyping in COVID-19: a call for caution.

Authors:  Lieuwe D J Bos; Pratik Sinha; Robert P Dickson
Journal:  Eur Respir J       Date:  2020-07-23       Impact factor: 16.671

  6 in total
  2 in total

1.  Airway pressure release ventilation in mechanically ventilated patients with COVID-19: a multicenter observational study.

Authors:  John S Zorbas; Kwok M Ho; Edward Litton; Bradley Wibrow; Edward Fysh; Matthew H Anstey
Journal:  Acute Crit Care       Date:  2021-05-04

2.  Management of hospitalised adults with coronavirus disease 2019 (COVID-19): a European Respiratory Society living guideline.

Authors:  James D Chalmers; Megan L Crichton; Pieter C Goeminne; Bin Cao; Marc Humbert; Michal Shteinberg; Katerina M Antoniou; Charlotte Suppli Ulrik; Helen Parks; Chen Wang; Thomas Vandendriessche; Jieming Qu; Daiana Stolz; Christopher Brightling; Tobias Welte; Stefano Aliberti; Anita K Simonds; Thomy Tonia; Nicolas Roche
Journal:  Eur Respir J       Date:  2021-04-15       Impact factor: 33.795

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.