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Although present in only 50&#37; of patients&#44; the recent demonstration of its impact on the evolution and prognosis of ARDS provides strong evidence to consider DAD as the gold standard of ARDS&#46;<a class="elsevierStyleCrossRefs" href="#bib0015"><span class="elsevierStyleSup">3&#44;4</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">From the epidemiological perspective&#44; a definition is a set of criteria considered by a group of experts to be necessary to characterize a condition or disease&#46; Usually&#44; there are at least two levels of decision &#8211; one clinical and one definitive &#8211; usually referred to as the &#34;gold standard&#34;&#46; In the case of ARDS&#44; there is no general agreement on the gold standard&#44; with histology &#40;DAD&#41; and&#47;or the conceptual framework of the disease being proposed&#46; The relationship between the clinical definition and the gold standard can be assessed in terms of sensitivity&#44; specificity&#44; precision and validity &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; Sensitivity is the proportion of patients who have a positive gold standard and meet the clinical definition&#46; As sensitivity increases&#44; the proportion of individuals with a positive gold standard but who do not meet the definition &#40;false-negative cases&#41; decreases&#46; Specificity is the proportion of patients with a negative gold standard who do not meet the definition&#46; As specificity increases&#44; the proportion of individuals with a negative gold standard who meet the definition &#40;false-positive cases&#41; decreases&#46; Precision refers to how reproducible the result is under similar conditions&#46; For example&#44; two people evaluating the same patient at the same time should reach the same conclusion&#46; Validity refers to the ability of a test to correctly measure what it is intended to measure&#44; i&#46;e&#46; &#34;how close the clinical definition is to the gold standard&#34;&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">The recent global definition of ARDS incorporates clinical modifications that make it much more sensitive&#46; For example&#44; it includes lung ultrasound&#44; which is more sensitive than conventional radiography and tomography&#46; Two new categories are included&#58; non-intubated patients with ARDS and ARDS in resource-constrained settings&#46; The non-intubated category includes patients on high-flow nasal cannula &#40;HFNC&#41; oxygen therapy&#44; which is characterized by a more indolent course of the disease&#46; For ARDS in resource- constrained settings&#44; the Kigali modification is used&#44; which employs the Sp0<span class="elsevierStyleInf">2</span>&#47;Fi0<span class="elsevierStyleInf">2</span> ratio&#46;<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a> This parameter shows good correlation with Pa0<span class="elsevierStyleInf">2</span>&#47;Fi0<span class="elsevierStyleInf">2</span> but is influenced by several factors &#40;e&#46;g&#46;&#44; hemoglobin concentration&#44; skin color&#44; tissue hypoperfusion&#41;&#44; which inevitably leads to increased measurement error&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">Regarding the precision and validity of the global definition&#44; given the increase in sensitivity and the consequent decrease in specificity&#44; it can be expected that precision will increase and validity will decrease&#44; i&#46;e&#46;&#44; there will be more interobserver agreement and more patients will be diagnosed with ARDS&#44; but the proportion of them presenting the gold standard will decrease&#46; This aspect is not a simple academic issue&#44; because for a therapeutic intervention to be effective&#44; it must have a therapeutic target&#46; The changes introduced by the global definition will facilitate the identification of patients with ARDS and&#44; consequently&#44; their enrollment in clinical trials<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">6</span></a>&#59; however&#44; the inclusion of heterogeneous patient groups will make it more difficult to demonstrate beneficial results&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">7</span></a> In line with these assertions&#44; the term &#34;therapeutic paradox&#34; was introduced 10 years ago to refer to the success of interventions in preclinical research &#40;where diagnoses are usually made on the basis of the gold standard&#41; and their failure when transferred to clinical practice &#40;where diagnoses are made on the basis of surrogate biomarkers or syndromes&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">8</span></a> Incorporating the new definition could exacerbate this phenomenon and slow down the transfer of basic research to the clinical setting&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">Finally&#44; it is clear that intensive care medicine is moving towards personalization of treatment&#44; seeking to identify homogeneous groups of patients who will benefit from specific therapies&#46; The identification of sub-phenotypes is an attractive&#44; feasible and effective strategy in this regard&#44; as it can pinpoint groups of patients with common clinical&#44; laboratory test&#44; prognostic and interventional response characteristics&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">9</span></a> Such strategies are based on the use of mathematical techniques and algorithms to identify groupings in observable variables that may reflect the presence of one or more latent &#40;i&#46;e&#46;&#44; unobservable&#41; variables&#46; Several studies have shown the existence of different sub-phenotypes within the same syndrome&#44; which may reflect the existence of different latent variables&#44; the fact that different samples were involved in the analysis of different observable variables&#44; the effect of different environmental stimuli &#40;e&#46;g&#46;&#44; treatments applied&#41;&#44; variations in the statistical techniques used&#44; or &#8211; most likely &#8211; the effect of the combination of all these factors&#46; The new global definition is in clear contradiction with the concept of personalized medicine since it simplifies several of the diagnostic criteria &#8211; most of which were already arbitrary and questionable<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">10</span></a> &#8211; and practically eliminates all traces of pathophysiological variables&#44; tending to generate a definition where &#34;one size fits all&#34;&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">11</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">In summary&#44; the new global definition increases the sensitivity of the definition&#44; allowing for the diagnosis to be made in virtually any setting&#46; However&#44; this comes at the cost of sacrificing specificity&#46; As a result&#44; a global increase in the incidence of the syndrome can be expected&#46; All this will make clinical investigators very happy and those trying to develop specific treatments very sad&#46; It seems that the goal of providing personalized medicine has receded a bit&#46; Only time will tell whether this definition will be universally accepted or whether it will be just another bold initiative that fails to pass the filter of clinical practice&#46;</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Conflicts of interest</span><p id="par0035" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest&#46;</p></span></span>"
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Editorial
Available online 21 October 2024
Global definition of acute respiratory distress syndrome: An epidemiology perspective
Definición global del síndrome de distrés respiratorio agudo: una visión epidemiológica
Pablo Cardinal-Fernándeza,b,
Corresponding author
pablocardinal@hotmail.com

Corresponding author.
, Guillermo Ortizc,d, Luis Blanche,f,g,h
a Hospital Universitario HM Torrelodones, Madrid, Spain
b Universidad Camilo José Cela, Madrid, Spain
c Pulmonary Medicine, Universidad El Bosque, Bogotá, Colombia
d Unidad de Cuidados Intensivos, Hospital Santa Clara Bogotá, Bogotá, Colombia
e Critical Care Department, Parc Taulí University Hospital, Sabadell, Barcelona, Spain
f Institut d'Investigació i Innovació Parc Taulí (I3PT-CERCA), Sabadell, Barcelona, Spain
g CIBER de Enfermedades Respiratorias, ISCIII, Madrid, Spain
h Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain
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