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Hospital Universitario de Guadalajara, Instituto de Investigación Sanitaria de Castilla la Mancha (IDISCAM), Universidad de Alcalá, Madrid, Spain" "etiqueta" => "j" "identificador" => "aff0045" ] 10 => array:3 [ "entidad" => "Servei de Medicina Intensiva, Parc Taulí Hospital Universitari, Institut de Recerca Parc Taulí–I3PT, Departament de Medicina, Universitat Autònoma de Barcelona, Bellaterra, Spain" "etiqueta" => "k" "identificador" => "aff0050" ] 11 => array:3 [ "entidad" => "Servicio de Anestesiología, UCI Quirúrgica y U. Dolor. H. U. Puerta de Hierro, Madrid, Spain" "etiqueta" => "l" "identificador" => "aff0055" ] 12 => array:3 [ "entidad" => "Servicio Urgencias, Hospital Universitario Central de Asturias, Spain" "etiqueta" => "m" "identificador" => "aff0060" ] 13 => array:3 [ "entidad" => "Unidad de Corta Estancia, Hospital Universitario Dr. Peset, Valencia, Spain" "etiqueta" => "n" "identificador" => "aff0065" ] 14 => array:3 [ "entidad" => "Servicio de Medicina Intensiva, Hospital Universitari Son Llàtzer, Palma de Mallorca, Spain" "etiqueta" => "o" "identificador" => "aff0070" ] 15 => array:3 [ "entidad" => "Servicio de Medicina Intensiva, Hospital Virgen de la Salud, Toledo, Spain" "etiqueta" => "p" "identificador" => "aff0075" ] 16 => array:3 [ "entidad" => "Servicio de Medicina Intensiva Hospital Universitario Son Espases, Facultad de Medicina de las Islas Baleares, Spain" "etiqueta" => "q" "identificador" => "aff0080" ] 17 => array:3 [ "entidad" => "UVIIR, Servei de Pneumologia, Institut de Respiratori, Clínic Barcelona, IDIBAPS. Universitat de Barcelona, Barcelona, Spain" "etiqueta" => "r" "identificador" => "aff0085" ] 18 => array:3 [ "entidad" => "Servicio de Neumologia, Hospital Universitario de Araba, Spain" "etiqueta" => "s" "identificador" => "aff0090" ] ] "correspondencia" => array:1 [ 0 => array:3 [ "identificador" => "cor0005" "etiqueta" => "⁎" "correspondencia" => "Corresponding author." ] ] ] ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0005" "etiqueta" => "Fig. 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 2883 "Ancho" => 2508 "Tamanyo" => 266288 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Recommendations for NIV withdrawal in COVID-19 patients. *Respiratory stability considered as pH<span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>7.35, FiO<span class="elsevierStyleInf">2</span> requirement<span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>40%, Kelly–Mattahy 1–2, FR<span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>25<span class="elsevierStyleHsp" style=""></span>rpm, PEEP<span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>5<span class="elsevierStyleHsp" style=""></span>cmH<span class="elsevierStyleInf">2</span>O.</p>" ] ] ] "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Introduction</span><p id="par0005" class="elsevierStylePara elsevierViewall">Acute respiratory failure (ARF) secondary to SARS-CoV2 infection (COVID-19) may require a variety of non-invasive respiratory support (NIRS) strategies in addition to conventional oxygen therapy (COT), including high-flow therapy (HFT), continuous positive airway pressure (CPAP), non-invasive mechanical ventilation (NIV) or awake proning (AP). During the early phase of the pandemic, guidelines were published based on previous experience in non-COVID patients.<a class="elsevierStyleCrossRef" href="#bib0560"><span class="elsevierStyleSup">1</span></a> Four years later, the recommendations should be updated based on the evidence. To achieve this goal, four scientific societies (SEDAR, SEMES, SEMICYUC, SEPAR) with a total of 25 experts in the field participated in this document.</p><p id="par0010" class="elsevierStylePara elsevierViewall">Despite the same societies published previously a specific document about ARF in non-COVID patients,<a class="elsevierStyleCrossRef" href="#bib0565"><span class="elsevierStyleSup">2</span></a> some concepts of the current recommendations may be applicable, with some exceptions, to other infectious entities, such as viral or bacterial pneumonia with single organ failure. However, there are some discrepancies regarding the NIRS strategy to be used, with HFT being the modality of choice in non-COVID ARF.<a class="elsevierStyleCrossRef" href="#bib0570"><span class="elsevierStyleSup">3</span></a> Obviously, these recommendations do not apply to other etiologies of ARF such as cardiogenic acute pulmonary edema.</p><p id="par0015" class="elsevierStylePara elsevierViewall">The full document is available in the <a class="elsevierStyleCrossRef" href="#sec0020">online supplement</a>.<span class="elsevierStyleVsp" style="height:0.5px"></span><ul class="elsevierStyleList" id="lis0005"><li class="elsevierStyleListItem" id="lsti0005"><span class="elsevierStyleLabel">1.</span><p id="par0020" class="elsevierStylePara elsevierViewall">What should be the clinical picture to consider initiation of NIRS?</p></li></ul></p><p id="par0025" class="elsevierStylePara elsevierViewall">COT was clearly the most important initial supportive technique in ARF after COVID-19.<a class="elsevierStyleCrossRef" href="#bib0575"><span class="elsevierStyleSup">4</span></a> However, this technique was not sufficient in many patients.<a class="elsevierStyleCrossRef" href="#bib0580"><span class="elsevierStyleSup">5</span></a> One of the key questions is the ideal time to initiate NIRS. The intense inspiratory during spontaneous ventilation in patients with ARF may generate elevated transpulmonary pressures and ultimately exacerbate self-induced lung injury (P-SILI).<a class="elsevierStyleCrossRef" href="#bib0585"><span class="elsevierStyleSup">6</span></a> Therefore, initiation of NIRS could have a preventive effect.</p><p id="par0030" class="elsevierStylePara elsevierViewall">During the first wave, some societies recommended initiating NIRS from a cut-off FiO<span class="elsevierStyleInf">2</span> of 0.4 under COT in addition to clinical criteria.<a class="elsevierStyleCrossRef" href="#bib0590"><span class="elsevierStyleSup">7</span></a> The stratification system proposed in Italy, with four categories of patients, was one of the most followed.<a class="elsevierStyleCrossRef" href="#bib0595"><span class="elsevierStyleSup">8</span></a> In this classification,<a class="elsevierStyleCrossRef" href="#bib0600"><span class="elsevierStyleSup">9</span></a> the indication for initiation corresponded to the third degree of ARF severity. The German position paper suggested initiating HFT when PaO<span class="elsevierStyleInf">2</span><span class="elsevierStyleHsp" style=""></span>≤<span class="elsevierStyleHsp" style=""></span>55<span class="elsevierStyleHsp" style=""></span>mm Hg and FR<span class="elsevierStyleHsp" style=""></span>≥<span class="elsevierStyleHsp" style=""></span>30/min on room air.<a class="elsevierStyleCrossRef" href="#bib0605"><span class="elsevierStyleSup">10</span></a> In the English guidelines, the proposed criteria for initiating CPAP and O<span class="elsevierStyleInf">2</span> were the inability to maintain SpO<span class="elsevierStyleInf">2</span> between 92 and 94% at an FiO<span class="elsevierStyleInf">2</span> between 0.4 and 0.6.<a class="elsevierStyleCrossRef" href="#bib0610"><span class="elsevierStyleSup">11</span></a> With these recommendations, the experts proposed two different scenarios for starting NIRS: early start (PaO<span class="elsevierStyleInf">2</span>: FiO<span class="elsevierStyleInf">2</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>300 or SpO<span class="elsevierStyleInf">2</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>93% at O<span class="elsevierStyleInf">2</span><span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>5<span class="elsevierStyleHsp" style=""></span>L/min or SpO<span class="elsevierStyleInf">2</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>94% at FiO<span class="elsevierStyleInf">2</span> 0.4%) or late start (SpO<span class="elsevierStyleInf">2</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>92% under O<span class="elsevierStyleInf">2</span> at 15<span class="elsevierStyleHsp" style=""></span>L).<a class="elsevierStyleCrossRef" href="#bib0615"><span class="elsevierStyleSup">12</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">Two retrospective studies<a class="elsevierStyleCrossRefs" href="#bib0620"><span class="elsevierStyleSup">13,14</span></a> compared the use of early versus late HFT and found significant differences in the rate of intubation, which was lower in the early group. Of course, both studies may have a selection bias, since patients in the late onset groups were selected if they presented with respiratory progression on COT. The only high-quality randomized trial designed to answer the question of early HFT showed no benefit of early administration on final prognosis.<a class="elsevierStyleCrossRef" href="#bib0630"><span class="elsevierStyleSup">15</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">Non-targeted randomized controlled trials showed heterogeneity in defining the criteria for initiating NIRS. For example, the RECOVERY trial defined the clinical condition for randomization as patients with an FiO<span class="elsevierStyleInf">2</span> requirement equal to or greater than 0.4 and an SpO<span class="elsevierStyleInf">2</span><span class="elsevierStyleHsp" style=""></span>≤<span class="elsevierStyleHsp" style=""></span>94%,<a class="elsevierStyleCrossRef" href="#bib0635"><span class="elsevierStyleSup">16</span></a> whereas the HENIVOT study<a class="elsevierStyleCrossRef" href="#bib0640"><span class="elsevierStyleSup">17</span></a> required a PaO<span class="elsevierStyleInf">2</span>/FiO<span class="elsevierStyleInf">2</span><span class="elsevierStyleHsp" style=""></span>≤<span class="elsevierStyleHsp" style=""></span>200 as a criterion for initiating NIRS. The PaO<span class="elsevierStyleInf">2</span>/FiO<span class="elsevierStyleInf">2</span> index may not reflect the severity of exchange because it does not take into account baseline PaCO<span class="elsevierStyleInf">2</span>, which is often decreased in patients with ARF secondary to COVID-19.<a class="elsevierStyleCrossRef" href="#bib0645"><span class="elsevierStyleSup">18</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">Therefore, there is insufficient evidence to support early initiation of NIRS (mainly HFT) as a preventive measure against deterioration of respiratory status in patients with severe ARF secondary to COVID-19.</p><p id="par0050" class="elsevierStylePara elsevierViewall">The criteria for starting NIRS would be the following:<ul class="elsevierStyleList" id="lis0010"><li class="elsevierStyleListItem" id="lsti0010"><span class="elsevierStyleLabel">-</span><p id="par0055" class="elsevierStylePara elsevierViewall">Moderate to severe dyspnea and evidence of increased work of breathing (use of accessory muscles or tachypnea<span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>25<span class="elsevierStyleHsp" style=""></span>rpm) or</p></li><li class="elsevierStyleListItem" id="lsti0015"><span class="elsevierStyleLabel">-</span><p id="par0060" class="elsevierStylePara elsevierViewall">PaO<span class="elsevierStyleInf">2</span>/FiO<span class="elsevierStyleInf">2</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>200 o (SpO<span class="elsevierStyleInf">2</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>92% at FiO<span class="elsevierStyleInf">2</span> of 0.4) o PaCO<span class="elsevierStyleInf">2</span><span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>45<span class="elsevierStyleHsp" style=""></span>mmHg and pH<span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>7.35.<a class="elsevierStyleCrossRefs" href="#bib0650"><span class="elsevierStyleSup">19–21</span></a></p></li></ul><span class="elsevierStyleVsp" style="height:0.5px"></span><ul class="elsevierStyleList" id="lis0015"><li class="elsevierStyleListItem" id="lsti0020"><span class="elsevierStyleLabel">2.</span><p id="par0065" class="elsevierStylePara elsevierViewall">What should be the first line NIRS therapy?</p></li></ul><span class="elsevierStyleVsp" style="height:0.5px"></span></p><p id="par0070" class="elsevierStylePara elsevierViewall"><ul class="elsevierStyleList" id="lis0020"><li class="elsevierStyleListItem" id="lsti0025"><span class="elsevierStyleLabel">2.1</span><p id="par0075" class="elsevierStylePara elsevierViewall">Considering age and comorbidity</p></li></ul></p><p id="par0080" class="elsevierStylePara elsevierViewall">An expert consensus<a class="elsevierStyleCrossRef" href="#bib0650"><span class="elsevierStyleSup">19</span></a> recommended the initial use of NIV only in the presence of global ARF (hypoxemia and hypercapnia) and in selected patients with increased work of breathing. It can be considered as a first option in patients with underlying respiratory comorbidity, secondary to chronic obstructive pulmonary disease (COPD), neuromuscular involvement or chest disease. In hypoxemic ARF, the use of CPAP would be the first choice in the presence of heart failure or acute pulmonary edema. In addition, CPAP has been used as one of the main treatment alternatives in selected patients with a therapeutic ceiling (no intubation order).<a class="elsevierStyleCrossRef" href="#bib0665"><span class="elsevierStyleSup">22</span></a></p><p id="par0085" class="elsevierStylePara elsevierViewall">There is no scientific evidence to support a device type based on age. However, it seems logical that HFT may be recommended in particularly frail patients or those with compromised baseline conditions due to better tolerability and fewer side effects. A retrospective study showed a reduction in mortality in the elderly population when the therapy was used in patients with PaO<span class="elsevierStyleInf">2</span>/FiO<span class="elsevierStyleInf">2</span> between 200 and 300).<a class="elsevierStyleCrossRef" href="#bib0625"><span class="elsevierStyleSup">14</span></a><span class="elsevierStyleVsp" style="height:0.5px"></span><ul class="elsevierStyleList" id="lis0025"><li class="elsevierStyleListItem" id="lsti0030"><span class="elsevierStyleLabel">2.2</span><p id="par0090" class="elsevierStylePara elsevierViewall">Based on clinics and pulmonary gas exchange</p></li></ul></p><p id="par0095" class="elsevierStylePara elsevierViewall">The pre-pandemic FLORALI study<a class="elsevierStyleCrossRef" href="#bib0670"><span class="elsevierStyleSup">23</span></a> showed that in hypoxemic ARF, mortality and ventilator-free days were significantly lower in the HFT-treated group than in the NIV-treated group. The same strategy was also applied in the early phases of the pandemic.<a class="elsevierStyleCrossRef" href="#bib0575"><span class="elsevierStyleSup">4</span></a> However, in the RECOVERY trial<a class="elsevierStyleCrossRef" href="#bib0675"><span class="elsevierStyleSup">24</span></a> the use of COT versus HFT showed no difference in intubation or 30-day mortality (45.1 vs. 44%), whereas the CPAP-treated group had a significantly lower rate. There were no standardized criteria for the initiation of invasive mechanical ventilation. On the other hand, the results of another recent randomized trial<a class="elsevierStyleCrossRef" href="#bib0680"><span class="elsevierStyleSup">25</span></a> showed that the use of HFT reduced the need for intubation and the time to recovery from mechanical ventilation compared with patients treated with COT. Finally, in a retrospective study involving more than 1000 patients, the use of HFT was an independent factor in reducing the need for mechanical ventilation and mortality.<a class="elsevierStyleCrossRef" href="#bib0685"><span class="elsevierStyleSup">26</span></a></p><p id="par0100" class="elsevierStylePara elsevierViewall">A recent metaanalysis<a class="elsevierStyleCrossRef" href="#bib0690"><span class="elsevierStyleSup">27</span></a> concluded that, despite a significant increase in the PaO<span class="elsevierStyleInf">2</span>/FiO<span class="elsevierStyleInf">2</span> ratio in the positive pressure group, intubation and length of hospital stay were similar between HFT and NIV.</p><p id="par0105" class="elsevierStylePara elsevierViewall">Another interesting option is the combination of therapies (CPAP/HFT; NIV/HFT), which facilitate resting and feeding. CPAP/HFT early combination has been associated with lower intubation and mortality rates in a cohort of patients with a PaO<span class="elsevierStyleInf">2</span>/FiO<span class="elsevierStyleInf">2</span> ratio<span class="elsevierStyleHsp" style=""></span>≤<span class="elsevierStyleHsp" style=""></span>100.<a class="elsevierStyleCrossRef" href="#bib0695"><span class="elsevierStyleSup">28</span></a></p><p id="par0110" class="elsevierStylePara elsevierViewall">Finally, pressure support ventilation (PSV) may worsen ventilator-induced lung injury, and its use was associated with increased mortality in retrospective studies conducted during the early phase of the pandemic.<a class="elsevierStyleCrossRef" href="#bib0700"><span class="elsevierStyleSup">29</span></a></p><p id="par0115" class="elsevierStylePara elsevierViewall">Therefore, initiation with continuous positive airway pressure (CPAP) is recommended. The option of PSV should only be considered in cases of global acute respiratory failure.<a class="elsevierStyleCrossRefs" href="#bib0635"><span class="elsevierStyleSup">16,30</span></a> HFT is a recommended alternative in hypoxemic patients without respiratory acidosis.<a class="elsevierStyleCrossRefs" href="#bib0710"><span class="elsevierStyleSup">31–34</span></a></p><p id="par0120" class="elsevierStylePara elsevierViewall">Patients with more severe hypoxemia (PaO<span class="elsevierStyleInf">2</span>/FiO<span class="elsevierStyleInf">2</span> less than 150<span class="elsevierStyleHsp" style=""></span>mmHg) should be closely monitored when starting NIRS, as there is a higher risk of failure.<a class="elsevierStyleCrossRefs" href="#bib0640"><span class="elsevierStyleSup">17,35</span></a><span class="elsevierStyleVsp" style="height:0.5px"></span><ul class="elsevierStyleList" id="lis0030"><li class="elsevierStyleListItem" id="lsti0035"><span class="elsevierStyleLabel">3.</span><p id="par0125" class="elsevierStylePara elsevierViewall">Parameterization and adaptation of NIRS</p></li></ul><span class="elsevierStyleVsp" style="height:0.5px"></span></p><p id="par0130" class="elsevierStylePara elsevierViewall"><ul class="elsevierStyleList" id="lis0035"><li class="elsevierStyleListItem" id="lsti0040"><span class="elsevierStyleLabel">3.1</span><p id="par0135" class="elsevierStylePara elsevierViewall">Parameter choice</p></li></ul></p><p id="par0140" class="elsevierStylePara elsevierViewall">In HFT, it is recommended to start therapy at the maximum tolerated flow with an adequate FiO<span class="elsevierStyleInf">2</span> to maintain SpO<span class="elsevierStyleInf">2</span><span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>92%.<a class="elsevierStyleCrossRefs" href="#bib0710"><span class="elsevierStyleSup">31,36,37</span></a> Some studies have suggested using peak flow during spontaneous ventilation as a reference to titrate HFT.<a class="elsevierStyleCrossRef" href="#bib0745"><span class="elsevierStyleSup">38</span></a> The temperature should be set in the range of 31–37<span class="elsevierStyleHsp" style=""></span>°C, with preference given to higher values. It has also been shown that the use of a surgical mask not only reduces aerosol spread to the environment, but also improves oxygenation without increasing the risk of CO2 rebreathing.<a class="elsevierStyleCrossRef" href="#bib0750"><span class="elsevierStyleSup">39</span></a></p><p id="par0145" class="elsevierStylePara elsevierViewall">In CPAP, it is usually initiated at 10<span class="elsevierStyleHsp" style=""></span>cmH<span class="elsevierStyleInf">2</span>O, not exceeding 12–13<span class="elsevierStyleHsp" style=""></span>cmH<span class="elsevierStyleInf">2</span>O to avoid barotrauma or negative hemodynamic effects, and FiO<span class="elsevierStyleInf">2</span> to achieve SpO<span class="elsevierStyleInf">2</span><span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>92% or PaO<span class="elsevierStyleInf">2</span><span class="elsevierStyleHsp" style=""></span>≥<span class="elsevierStyleHsp" style=""></span>60<span class="elsevierStyleHsp" style=""></span>mmHg. An improvement in oxygenation of ≥15% or ≥30% is equivalent to lung recruitment, which can be confirmed by ultrasound.<a class="elsevierStyleCrossRef" href="#bib0755"><span class="elsevierStyleSup">40</span></a></p><p id="par0150" class="elsevierStylePara elsevierViewall">In NIV, PEEP between 10 and 12<span class="elsevierStyleHsp" style=""></span>cmH<span class="elsevierStyleInf">2</span>O (similar to CPAP) and moderate PSV is recommended, with a target VT of 4–6<span class="elsevierStyleHsp" style=""></span>ml/kg<a class="elsevierStyleCrossRef" href="#bib0760"><span class="elsevierStyleSup">41</span></a> avoiding overassistance.<a class="elsevierStyleCrossRef" href="#bib0765"><span class="elsevierStyleSup">42</span></a><span class="elsevierStyleVsp" style="height:0.5px"></span><ul class="elsevierStyleList" id="lis0040"><li class="elsevierStyleListItem" id="lsti0045"><span class="elsevierStyleLabel">3.2</span><p id="par0155" class="elsevierStylePara elsevierViewall">Interface selection</p></li></ul></p><p id="par0160" class="elsevierStylePara elsevierViewall">The interface with the best reported results would be the helmet with High Efficiency Particulate Air (HEPA) filters, both in CPAP mode and for NIV.<a class="elsevierStyleCrossRefs" href="#bib0770"><span class="elsevierStyleSup">43–46</span></a> If a helmet is not available, full-face or oronasal masks can be used, although they carry a higher risk of aerosol dispersion due to increased leakage.<a class="elsevierStyleCrossRef" href="#bib0790"><span class="elsevierStyleSup">47</span></a></p><p id="par0165" class="elsevierStylePara elsevierViewall">The use of interfaces with the leak port built into the mask itself is not recommended.<a class="elsevierStyleCrossRef" href="#bib0795"><span class="elsevierStyleSup">48</span></a> Nasal masks should also be avoided.</p><p id="par0170" class="elsevierStylePara elsevierViewall">For nasal cannulas, it is recommended to seal more than 50% of the nostril diameter.<a class="elsevierStyleCrossRef" href="#bib0800"><span class="elsevierStyleSup">49</span></a></p><p id="par0175" class="elsevierStylePara elsevierViewall">The use of oils with hyperoxygenated fatty acids is recommended to protect the skin.<a class="elsevierStyleCrossRef" href="#bib0805"><span class="elsevierStyleSup">50</span></a><span class="elsevierStyleVsp" style="height:0.5px"></span><ul class="elsevierStyleList" id="lis0045"><li class="elsevierStyleListItem" id="lsti0050"><span class="elsevierStyleLabel">4.</span><p id="par0180" class="elsevierStylePara elsevierViewall">How should the response to NIRS be monitored?</p></li></ul></p><p id="par0185" class="elsevierStylePara elsevierViewall">Monitoring of NIRS should include a combination of clinical and oxygenation parameters. The important role of intermediate care units during the different phases of the pandemic should be highlighted.<a class="elsevierStyleCrossRef" href="#bib0810"><span class="elsevierStyleSup">51</span></a></p><p id="par0190" class="elsevierStylePara elsevierViewall">The criteria for a positive response to NIRS are the following.<ul class="elsevierStyleList" id="lis0050"><li class="elsevierStyleListItem" id="lsti0055"><span class="elsevierStyleLabel">•</span><p id="par0195" class="elsevierStylePara elsevierViewall">Improvement in clinical signs of work of breathing, with decreased respiratory rate (RF) and accessory muscle use, and improvement in dyspnea.</p></li><li class="elsevierStyleListItem" id="lsti0060"><span class="elsevierStyleLabel">•</span><p id="par0200" class="elsevierStylePara elsevierViewall">Improvement of oxygenation:<ul class="elsevierStyleList" id="lis0055"><li class="elsevierStyleListItem" id="lsti0065"><span class="elsevierStyleLabel">∘</span><p id="par0205" class="elsevierStylePara elsevierViewall">ROX index: The combination of SpO<span class="elsevierStyleInf">2</span> and RR ((SpO<span class="elsevierStyleInf">2</span>/FiO<span class="elsevierStyleInf">2</span>)/RR) has been proposed as an index that may be useful in predicting the success or failure of HFT treatment.<a class="elsevierStyleCrossRef" href="#bib0815"><span class="elsevierStyleSup">52</span></a> The cut-off points described for predicting the success of HFT in COVID patients were very similar to those previously described in non-COVID patients.<a class="elsevierStyleCrossRefs" href="#bib0820"><span class="elsevierStyleSup">53,54</span></a></p></li><li class="elsevierStyleListItem" id="lsti0070"><span class="elsevierStyleLabel">∘</span><p id="par0210" class="elsevierStylePara elsevierViewall">Exhaled tidal volume should also be monitored in patients on NIV or CPAP. Persistent intense inspiratory effort<a class="elsevierStyleCrossRef" href="#bib0590"><span class="elsevierStyleSup">7</span></a> and high exhaled tidal volume (>9–9.5<span class="elsevierStyleHsp" style=""></span>ml/kg ideal body weight) have been associated with NIRS failure.<a class="elsevierStyleCrossRefs" href="#bib0760"><span class="elsevierStyleSup">41,55</span></a></p></li></ul></p></li></ul><span class="elsevierStyleVsp" style="height:0.5px"></span><ul class="elsevierStyleList" id="lis0060"><li class="elsevierStyleListItem" id="lsti0075"><span class="elsevierStyleLabel">5.</span><p id="par0215" class="elsevierStylePara elsevierViewall">When should we consider NIRS failure?</p></li></ul></p><p id="par0220" class="elsevierStylePara elsevierViewall">The definition of NIRS failure and when it occurs in hypoxemic ARF in COVID-19 is controversial. The risk-benefit trade-off between avoiding unnecessary intubation and delaying intubation needs to be carefully considered. Therefore, it may be useful to adopt the criteria defined in the most relevant clinical trials.<a class="elsevierStyleCrossRefs" href="#bib0635"><span class="elsevierStyleSup">16,17,56</span></a> Failure of NIRS should be defined as the presence of 2 or more of the criteria in <a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>.</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><p id="par0225" class="elsevierStylePara elsevierViewall">Studies agree that the final decision to intubate for NIRS failure should be at the discretion of the clinician and that objective criteria should simply guide the decision. It is also advisable to closely monitor patients treated with NIRS for more than 72<span class="elsevierStyleHsp" style=""></span>h who do not improve or show signs of late deterioration, as well as those who show acute deterioration after a previously stable situation, to proceed with intubation and invasive ventilation.<a class="elsevierStyleCrossRefs" href="#bib0840"><span class="elsevierStyleSup">57,58</span></a><span class="elsevierStyleVsp" style="height:0.5px"></span><ul class="elsevierStyleList" id="lis0065"><li class="elsevierStyleListItem" id="lsti0080"><span class="elsevierStyleLabel">6.</span><p id="par0230" class="elsevierStylePara elsevierViewall">What should be done if NIRS fails?</p></li></ul></p><p id="par0235" class="elsevierStylePara elsevierViewall">Although NIRS failure often is followed by tracheal intubation and initiation of invasive mechanical ventilation (IMV), in the event of failure of treatment with HFT, rescue treatment with CPAP or NIV may be considered in selected cases (reversible condition and do-not-intubate orders), although mortality is very high.<a class="elsevierStyleCrossRef" href="#bib0850"><span class="elsevierStyleSup">59</span></a></p><p id="par0240" class="elsevierStylePara elsevierViewall">Finally, if NIRS fails in patients with a therapeutic ceiling, it should be replaced by COT and symptomatic management of dyspnea should be optimized. These last steps should ideally be carried out in collaboration with hospital palliative care teams.<span class="elsevierStyleVsp" style="height:0.5px"></span><ul class="elsevierStyleList" id="lis0070"><li class="elsevierStyleListItem" id="lsti0085"><span class="elsevierStyleLabel">7.</span><p id="par0245" class="elsevierStylePara elsevierViewall">What is the role of awake prone positioning in non-intubated patients?</p></li></ul></p><p id="par0250" class="elsevierStylePara elsevierViewall">Prone positioning has been shown to improve oxygenation and mortality in intubated patients with moderate to severe acute respiratory distress syndrome (ARDS).<a class="elsevierStyleCrossRefs" href="#bib0855"><span class="elsevierStyleSup">60,61</span></a> Since the publication of the PROSEVA study, it should be considered the standard of care in the management of ARDS.<a class="elsevierStyleCrossRef" href="#bib0865"><span class="elsevierStyleSup">62</span></a> The prone position in ARDS patients favors lung recruitment, improving homogeneity and reducing lung stress and strain. The homogeneous distribution of ventilation reduces overdistension of the ventral areas. Improved ventilation of the dorsal regions also improves the <span class="elsevierStyleItalic">V</span>/<span class="elsevierStyleItalic">Q</span> ratio by reducing the shunt.<a class="elsevierStyleCrossRef" href="#bib0860"><span class="elsevierStyleSup">61</span></a></p><p id="par0255" class="elsevierStylePara elsevierViewall">The same mechanisms described for the prone position of the patient in IMV also occur in awake pronated patients with NIRS (mainly HFT).<a class="elsevierStyleCrossRef" href="#bib0870"><span class="elsevierStyleSup">63</span></a> However, the experience is much more limited. The only pre-pandemic study published included 20 patients, of whom 9 (45%) required intubation; of the 11 non-intubated patients, 8 received HFT and awake prone, and 6 of these required escalation to NIV.<a class="elsevierStyleCrossRef" href="#bib0875"><span class="elsevierStyleSup">64</span></a> Since the early stages of the pandemic, AP has been recommended by several scientific societies for its potential benefits, but without clear evidence.<a class="elsevierStyleCrossRefs" href="#bib0650"><span class="elsevierStyleSup">19,65</span></a> The results of a meta-trial involving more than 1000 patients showed that the AP in patients with COVID-19 requiring HFT reduced the need for intubation.<a class="elsevierStyleCrossRef" href="#bib0835"><span class="elsevierStyleSup">56</span></a> In addition, a recent systematic review and meta-analysis confirmed that the AP reduces the need for intubation in patients with acute hypoxemic respiratory failure secondary to COVID-19.<a class="elsevierStyleCrossRef" href="#bib0885"><span class="elsevierStyleSup">66</span></a> AP may be beneficial in patients with COVID-19-related hypoxemic acute respiratory failure who require admission to the ICU and receive NIRS treatment.<span class="elsevierStyleVsp" style="height:0.5px"></span><ul class="elsevierStyleList" id="lis0075"><li class="elsevierStyleListItem" id="lsti0090"><span class="elsevierStyleLabel">8.</span><p id="par0260" class="elsevierStylePara elsevierViewall">NIRS de-escalation protocols</p></li></ul></p><p id="par0265" class="elsevierStylePara elsevierViewall">Patients with global ARF: There are few randomized trials evaluating different NIRS weaning strategies, and none specifically in COVID-19. No relevant differences have been shown between a sudden NIV withdraw and a progressive weaning strategy.<a class="elsevierStyleCrossRefs" href="#bib0890"><span class="elsevierStyleSup">67,68</span></a> However, it is suggested a gradual withdrawal of NIV sessions<a class="elsevierStyleCrossRef" href="#bib0900"><span class="elsevierStyleSup">69</span></a> and/or set PSV<a class="elsevierStyleCrossRef" href="#bib0905"><span class="elsevierStyleSup">70</span></a> in difficult-to-wean patients.</p><p id="par0270" class="elsevierStylePara elsevierViewall">Considering the different characteristics of COVID-19 involvement in patients with hypercapnic failure (mainly COPD),<a class="elsevierStyleCrossRef" href="#bib0910"><span class="elsevierStyleSup">71</span></a> the proposed withdrawal may be more conservative than in situations of exacerbation due to other etiologies. <a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a> shows the proposal for hypercapnic ARF.</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0275" class="elsevierStylePara elsevierViewall">In hypoxemic ARF, the approach will be different depending on whether HFT or CPAP have been used. A pragmatic strategy could be to gradually reduce FiO<span class="elsevierStyleInf">2</span> with the aim of maintaining SpO<span class="elsevierStyleInf">2</span> between 92 and 98%.<a class="elsevierStyleCrossRefs" href="#bib0570"><span class="elsevierStyleSup">3,18</span></a> Once an FiO<span class="elsevierStyleInf">2</span> of 40% or less is reached, flow reduction would be initiated.<a class="elsevierStyleCrossRef" href="#bib0915"><span class="elsevierStyleSup">72</span></a> An ongoing study is comparing sequential FiO<span class="elsevierStyleInf">2</span> and flow reduction strategies or vice versa.<a class="elsevierStyleCrossRef" href="#bib0920"><span class="elsevierStyleSup">73</span></a><a class="elsevierStyleCrossRef" href="#fig0010">Fig. 2</a> shows the proposal for withdrawal for patients with HFT. A special situation would be the combined use of CPAP/HFT, in which a progressive increase of HFT periods and a progressive decrease in FiO<span class="elsevierStyleInf">2</span> would be recommended. When FiO<span class="elsevierStyleInf">2</span> is below 50%, a reduction in CPAP level can be considered.</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0280" class="elsevierStylePara elsevierViewall">In CPAP patients, when clinical stability is achieved (RR<span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>25<span class="elsevierStyleHsp" style=""></span>rpm, absence of accessory muscle use, good level of consciousness) with a CPAP level<span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>5<span class="elsevierStyleHsp" style=""></span>cmH<span class="elsevierStyleInf">2</span>O and FiO<span class="elsevierStyleInf">2</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>50%, a CPAP weaning trial could be considered. If PaO<span class="elsevierStyleInf">2</span>/FiO<span class="elsevierStyleInf">2</span><span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>240 under COT and FiO<span class="elsevierStyleInf">2</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.4 is maintained for 24<span class="elsevierStyleHsp" style=""></span>hours, the patient can be considered as “successfully weaned”.<a class="elsevierStyleCrossRefs" href="#bib0925"><span class="elsevierStyleSup">74,75</span></a><a class="elsevierStyleCrossRef" href="#fig0015">Fig. 3</a> reflects this strategy.<span class="elsevierStyleVsp" style="height:0.5px"></span><ul class="elsevierStyleList" id="lis0080"><li class="elsevierStyleListItem" id="lsti0095"><span class="elsevierStyleLabel">9.</span><p id="par0285" class="elsevierStylePara elsevierViewall">Other supportive measures in the NIV patient: nutrition, hydration and skin protection</p></li></ul></p><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0290" class="elsevierStylePara elsevierViewall">Interface pressure ulcers (IPU) occur in 5–50% of patients after the first 2<span class="elsevierStyleHsp" style=""></span>h of NIV therapy, particularly at the bridge of the nose, and using oronasal masks. On the other hand, hospitalized patients with COVID-19 have a high prevalence of malnutrition (14–70%), which worsens their prognosis. <a class="elsevierStyleCrossRef" href="#tbl0010">Table 2</a> reflects the supportive recommendations for both conditions.<a class="elsevierStyleCrossRefs" href="#bib0935"><span class="elsevierStyleSup">76–85</span></a><span class="elsevierStyleVsp" style="height:0.5px"></span><ul class="elsevierStyleList" id="lis0085"><li class="elsevierStyleListItem" id="lsti0100"><span class="elsevierStyleLabel">10.</span><p id="par0295" class="elsevierStylePara elsevierViewall">What measures should be taken to prevent the spread of the virus to healthcare workers?</p></li></ul></p><elsevierMultimedia ident="tbl0010"></elsevierMultimedia><p id="par0300" class="elsevierStylePara elsevierViewall">The aerosol generating procedures (AGP) with higher risk of transmission of SARS-CoV-2 infection to healthcare workers are endotracheal intubation, NIV and nebulization. Other AGP, such as secretion aspiration or bronchoscopy, have not shown such conclusive results.<a class="elsevierStyleCrossRef" href="#bib0985"><span class="elsevierStyleSup">86</span></a></p><p id="par0305" class="elsevierStylePara elsevierViewall">Intubation is considered a high-risk practice for COVID-19 transmission. <a class="elsevierStyleCrossRef" href="#tbl0015">Table 3</a> reflects the strategy to reduce the SARS-CoV-2 transmission during endotracheal intubation.<a class="elsevierStyleCrossRefs" href="#bib0990"><span class="elsevierStyleSup">87,88</span></a></p><elsevierMultimedia ident="tbl0015"></elsevierMultimedia><p id="par0310" class="elsevierStylePara elsevierViewall">Aspiration of secretions in patients with an artificial airway is considered a high-risk APG<a class="elsevierStyleCrossRef" href="#bib1000"><span class="elsevierStyleSup">89</span></a> and although their ability to infect healthcare workers with COVID-19 has not been demonstrated,<a class="elsevierStyleCrossRef" href="#bib0985"><span class="elsevierStyleSup">86</span></a> the use of closed versus open suction systems is recommended.<a class="elsevierStyleCrossRef" href="#bib1005"><span class="elsevierStyleSup">90</span></a></p><p id="par0315" class="elsevierStylePara elsevierViewall">Regarding the spontaneous breathing test before extubation, it is suggested to perform the test with the CPAP/PSV method instead of the T-tube to avoid disconnection of the patient. If the T-tube test is used, a filter should be placed on the expiratory limb.<a class="elsevierStyleCrossRef" href="#bib0995"><span class="elsevierStyleSup">88</span></a></p><p id="par0320" class="elsevierStylePara elsevierViewall">It is recommended that the extubation procedure is performed by two professionals, with the ventilator connected to the orotracheal tube and the closed suction system aspirating while the orotracheal tube is removed.<a class="elsevierStyleCrossRef" href="#bib0995"><span class="elsevierStyleSup">88</span></a></p><p id="par0325" class="elsevierStylePara elsevierViewall">During NIV, exhaled air is dispersed up to 1<span class="elsevierStyleHsp" style=""></span>m around the patient.<a class="elsevierStyleCrossRefs" href="#bib1010"><span class="elsevierStyleSup">91,92</span></a> This distance may be greater if the mask is not properly fitted<a class="elsevierStyleCrossRef" href="#bib1010"><span class="elsevierStyleSup">91</span></a> and is proportional to the set pressures.<a class="elsevierStyleCrossRef" href="#bib0995"><span class="elsevierStyleSup">88</span></a> In addition, the use of intentionally leak systems with single-limb circuits has been shown to increase exhaled air dispersion.<a class="elsevierStyleCrossRef" href="#bib1015"><span class="elsevierStyleSup">92</span></a> Oral masks are preferable to nasal masks. If there is no good seal with the oral mask, the use of full-face masks or helmet may be considered.</p><p id="par0330" class="elsevierStylePara elsevierViewall">Although aerosol therapy has not been shown to increase the likelihood of infection risk to healthcare workers, it is recommended that protective measures be taken.<a class="elsevierStyleCrossRefs" href="#bib1020"><span class="elsevierStyleSup">93–95</span></a> The dispersion of particles into the environment is related to the transmission capacity, and jet systems are therefore discouraged because of their higher dispersion.<a class="elsevierStyleCrossRef" href="#bib1035"><span class="elsevierStyleSup">96</span></a></p><p id="par0335" class="elsevierStylePara elsevierViewall">For patients with spontaneous breathing or HFT, inhaled therapy with an MDI device and spacer chamber is recommended.<a class="elsevierStyleCrossRef" href="#bib1030"><span class="elsevierStyleSup">95</span></a> For patients requiring aerosol therapy, vibrating mesh devices with mouthpiece and filter are recommended,<a class="elsevierStyleCrossRef" href="#bib1040"><span class="elsevierStyleSup">97</span></a> although the deposited drug doses may be higher, requiring dose adjustment. If inhaled therapy is used with NIV, an adapter in inspiratory limb is recommended (in metered-dose inhalers). Vibrating mesh systems should be fitted to the elbow of the mask when nebulizing.<a class="elsevierStyleCrossRefs" href="#bib1020"><span class="elsevierStyleSup">93–95,98,99</span></a></p><p id="par0340" class="elsevierStylePara elsevierViewall">Finally, the following general measures should be taken:<ul class="elsevierStyleList" id="lis0090"><li class="elsevierStyleListItem" id="lsti0105"><span class="elsevierStyleLabel">•</span><p id="par0345" class="elsevierStylePara elsevierViewall">Design of a dual circuit (clean and dirty area), separating COVID-positive from COVID-negative patients.</p></li><li class="elsevierStyleListItem" id="lsti0110"><span class="elsevierStyleLabel">•</span><p id="par0350" class="elsevierStylePara elsevierViewall">Use of PPE, FFP2 or FFP3 individual masks, hydroalcoholic gel and safety distance.</p></li><li class="elsevierStyleListItem" id="lsti0115"><span class="elsevierStyleLabel">•</span><p id="par0355" class="elsevierStylePara elsevierViewall">Implement physical segregation barriers, equipment and surface hygiene and respiratory protection measures.</p></li><li class="elsevierStyleListItem" id="lsti0120"><span class="elsevierStyleLabel">•</span><p id="par0360" class="elsevierStylePara elsevierViewall">Adaptation of working conditions: use of common areas, organization of workstations and shifts.<a class="elsevierStyleCrossRefs" href="#bib1055"><span class="elsevierStyleSup">100,101</span></a></p></li></ul><span class="elsevierStyleVsp" style="height:0.5px"></span><ul class="elsevierStyleList" id="lis0095"><li class="elsevierStyleListItem" id="lsti0125"><span class="elsevierStyleLabel">11.</span><p id="par0365" class="elsevierStylePara elsevierViewall">Indications for NIRS after weaning from mechanical ventilation</p></li></ul><span class="elsevierStyleVsp" style="height:0.5px"></span></p><p id="par0370" class="elsevierStylePara elsevierViewall"><ul class="elsevierStyleList" id="lis0100"><li class="elsevierStyleListItem" id="lsti0130"><span class="elsevierStyleLabel">11.1</span><p id="par0375" class="elsevierStylePara elsevierViewall">Following extubation</p></li></ul></p><p id="par0380" class="elsevierStylePara elsevierViewall">Positive evidences on the usefulness of NIRS have been reported mainly in patients with hypercapnic ARF.<a class="elsevierStyleCrossRef" href="#bib1065"><span class="elsevierStyleSup">102</span></a> However, in recent years, studies conducted in patients with hypoxemic ARF, in specific groups at high risk of reintubation, have also shown its usefulness. Vaschetto et al.<a class="elsevierStyleCrossRef" href="#bib1070"><span class="elsevierStyleSup">103</span></a> showed that early extubation followed by immediate NIV is safe and effective in selected patients (<a class="elsevierStyleCrossRef" href="#tbl0020">Table 4</a>), with a reduction in the duration of mechanical ventilation and hospital stay.<a class="elsevierStyleCrossRefs" href="#bib1065"><span class="elsevierStyleSup">102,104</span></a></p><elsevierMultimedia ident="tbl0020"></elsevierMultimedia><p id="par0385" class="elsevierStylePara elsevierViewall">In COVID-19 patients, Cammarota et al. showed that early extubation followed by immediate use of NIV, shortened the duration of MV and reduced the rate of failure and reintubation.<a class="elsevierStyleCrossRef" href="#bib1080"><span class="elsevierStyleSup">105</span></a> Given the few data available in COVID-19 patients, the recommendation would be to use NIRS (NIV or HFT) in patients of high-risk groups displayed in <a class="elsevierStyleCrossRef" href="#tbl0020">Table 4</a>.<span class="elsevierStyleVsp" style="height:0.5px"></span><ul class="elsevierStyleList" id="lis0105"><li class="elsevierStyleListItem" id="lsti0135"><span class="elsevierStyleLabel">11.2</span><p id="par0390" class="elsevierStylePara elsevierViewall">In tracheostomized patients</p></li></ul></p><p id="par0395" class="elsevierStylePara elsevierViewall">The conditioning of medical gases applied directly to the tracheostomy is supported by scientific evidence.<a class="elsevierStyleCrossRef" href="#bib1085"><span class="elsevierStyleSup">106</span></a> The use of home humidification systems is recommended when the oxygen flow exceeds 4<span class="elsevierStyleHsp" style=""></span>L/min.<a class="elsevierStyleCrossRef" href="#bib1090"><span class="elsevierStyleSup">107</span></a> These recommendations are old and were developed before the technical development of HFT, which meant that COT was systematically applied to these patients.<a class="elsevierStyleCrossRef" href="#bib1095"><span class="elsevierStyleSup">108</span></a> Recent studies have shown that high-flow systems, can help to reduce ventilator weaning and decannulation times.<a class="elsevierStyleCrossRefs" href="#bib1100"><span class="elsevierStyleSup">109,110</span></a> These studies do not compare the specific effect of HFT as it is applied across the board to all patients. There is no clear effect beyond gas conditioning.<a class="elsevierStyleCrossRef" href="#bib1110"><span class="elsevierStyleSup">111</span></a> The tracheostomized patient therefore has the option of HFT supplementation directly through the tracheostomy tube.</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Conclusions</span><p id="par0400" class="elsevierStylePara elsevierViewall">Several years after the pandemic, the management of patients with COVID-19 pneumonia and ARF remains a challenge for supportive care with NIRS. Several recommendations, summarized in <a class="elsevierStyleCrossRef" href="#tbl0025">Table 5</a>, have been agreed to address clinically relevant issues in daily practice.</p><elsevierMultimedia ident="tbl0025"></elsevierMultimedia></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Conflict of interests</span><p id="par0405" class="elsevierStylePara elsevierViewall">The authors state that they have no conflict of interests</p></span></span>" "textoCompletoSecciones" => array:1 [ "secciones" => array:7 [ 0 => array:3 [ "identificador" => "xres2138962" "titulo" => "Abstract" "secciones" => array:1 [ 0 => array:1 [ "identificador" => "abst0005" ] ] ] 1 => array:2 [ "identificador" => "xpalclavsec1816046" "titulo" => "Keywords" ] 2 => array:2 [ "identificador" => "xpalclavsec1816047" "titulo" => "Abbreviations" ] 3 => array:2 [ "identificador" => "sec0005" "titulo" => "Introduction" ] 4 => array:2 [ "identificador" => "sec0010" "titulo" => "Conclusions" ] 5 => array:2 [ "identificador" => "sec0015" "titulo" => "Conflict of interests" ] 6 => array:1 [ "titulo" => "References" ] ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "fechaRecibido" => "2024-02-19" "fechaAceptado" => "2024-02-27" "PalabrasClave" => array:1 [ "en" => array:2 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Keywords" "identificador" => "xpalclavsec1816046" "palabras" => array:6 [ 0 => "COVID-19" 1 => "Non invasive support" 2 => "High flow therapy" 3 => "Non invasive ventilation" 4 => "Continuous positive airway pressure" 5 => "Awake proning" ] ] 1 => array:4 [ "clase" => "abr" "titulo" => "Abbreviations" "identificador" => "xpalclavsec1816047" "palabras" => array:15 [ 0 => "ARF" 1 => "NIRS" 2 => "COT" 3 => "HFT" 4 => "HEPA" 5 => "CPAP" 6 => "NIV" 7 => "AP" 8 => "P-SILI" 9 => "PSV" 10 => "RR" 11 => "IMV" 12 => "ARDS" 13 => "IPU" 14 => "APG" ] ] ] ] "tieneResumen" => true "resumen" => array:1 [ "en" => array:2 [ "titulo" => "Abstract" "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Acute respiratory failure due to COVID-19 pneumonia often requires a comprehensive approach that includes non-pharmacological strategies such as non-invasive support (including positive pressure modes, high flow therapy or awake proning) in addition to oxygen therapy, with the primary goal of avoiding endotracheal intubation.</p><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Clinical issues such as determining the optimal time to initiate non-invasive support, choosing the most appropriate modality (based not only on the acute clinical picture but also on comorbidities), establishing criteria for recognition of treatment failure and strategies to follow in this setting (including palliative care), or implementing de-escalation procedures when improvement occurs are of paramount importance in the ongoing management of severe COVID-19 cases. Organizational issues, such as the most appropriate setting for management and monitoring of the severe COVID-19 patient or protective measures to prevent virus spread to healthcare workers in the presence of aerosol-generating procedures, should also be considered.</p><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">While many early clinical guidelines during the pandemic were based on previous experience with acute respiratory distress syndrome, the landscape has evolved since then. Today, we have a wealth of high-quality studies that support evidence-based recommendations to address these complex issues. This document, the result of a collaborative effort between four leading scientific societies (SEDAR, SEMES, SEMICYUC, SEPAR), draws on the experience of 25 experts in the field to synthesize knowledge to address pertinent clinical questions and refine the approach to patient care in the face of the challenges posed by severe COVID-19 infection.</p></span>" ] ] "apendice" => array:1 [ 0 => array:1 [ "seccion" => array:1 [ 0 => array:4 [ "apendice" => "<p id="par0415" class="elsevierStylePara elsevierViewall">The following are the supplementary data to this article:<elsevierMultimedia ident="upi0005"></elsevierMultimedia></p>" "etiqueta" => "Appendix A" "titulo" => "Supplementary data" "identificador" => "sec0025" ] ] ] ] "multimedia" => array:9 [ 0 => array:7 [ "identificador" => "fig0005" "etiqueta" => "Fig. 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 2883 "Ancho" => 2508 "Tamanyo" => 266288 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Recommendations for NIV withdrawal in COVID-19 patients. *Respiratory stability considered as pH<span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>7.35, FiO<span class="elsevierStyleInf">2</span> requirement<span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>40%, Kelly–Mattahy 1–2, FR<span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>25<span class="elsevierStyleHsp" style=""></span>rpm, PEEP<span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>5<span class="elsevierStyleHsp" style=""></span>cmH<span class="elsevierStyleInf">2</span>O.</p>" ] ] 1 => array:7 [ "identificador" => "fig0010" "etiqueta" => "Fig. 2" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr2.jpeg" "Alto" => 4232 "Ancho" => 2508 "Tamanyo" => 415904 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">Proposed withdrawal of NIRS in case of using HFT.</p>" ] ] 2 => array:7 [ "identificador" => "fig0015" "etiqueta" => "Fig. 3" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr3.jpeg" "Alto" => 3427 "Ancho" => 2508 "Tamanyo" => 348840 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">Proposed CPAP withdrawal.</p>" ] ] 3 => array:8 [ "identificador" => "tbl0005" "etiqueta" => "Table 1" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at1" "detalle" => "Table " "rol" => "short" ] ] "tabla" => array:2 [ "leyenda" => "<p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">The presence of two or more of the conditions suggests NIRS failure.</p>" "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><tbody title="tbody"><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Absence of improvement or worsening of symptoms or signs on admission, including oxygenation data and increased respiratory rate \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Appearance of signs of respiratory muscle fatigue or the use of accessory muscles \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Presence of acidosis, both respiratory and metabolic \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Inability to properly clear respiratory secretions \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Signs of hemodynamic instability, including hyperlactacidemia \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Deterioration of the level of consciousness or presence of seizures \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Intolerance to the device, especially in mask wearers. \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab3526094.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">Criteria for NIRS failure.</p>" ] ] 4 => array:8 [ "identificador" => "tbl0010" "etiqueta" => "Table 2" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at2" "detalle" => "Table " "rol" => "short" ] ] "tabla" => array:1 [ "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><th class="td-with-role" title="\n \t\t\t\t\ttable-head\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" scope="col">Skin protection \t\t\t\t\t\t\n \t\t\t\t\t\t</th><th class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" scope="col">Nutrition. \t\t\t\t\t\t\n \t\t\t\t\t\t</th></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Check the skin every 4<span class="elsevierStyleHsp" style=""></span>h to keep it clean and dry and to keep the mask in a normal position, avoiding excessive tightening.• In case of prolonged NIRS, either with CPAP or NIV, total face mask (TFM) or helmet should be considered.• When IPU occur with the oronasal mask, change to a TFM or helmet.• Repeated application of hyperoxygenated fatty acids.• If possible, allow for “skin breaks” after 12 hours of NIV. \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Early detection of malnutrition in high-risk patients: elderly patients and/or patients with • 2 or more chronic diseases• Start feeding in the first 48<span class="elsevierStyleHsp" style=""></span>h.• For critically ill patients, start with half the calculated calories and increase every three days until the target (70–80% of requirement) is reached.• In the NIV/CPAP patient with poor tolerance to interruptions, parenteral nutrition should be considered.• If the enteral route is used, the helmet is preferable as it allows nasogastric tube placement.• If a nasogastric tube is used, continuous feeding with a normocaloric-hyperproteic formula is recommended rather than a bolus.• In the HFT patient and during the weaning phase of NIV, oral enteral nutrition, including supplementation, should be prioritized to achieve nutritional goals. \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab3526096.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">Supportive strategies for skin protection and nutrition in COVID-19 patients.<a class="elsevierStyleCrossRefs" href="#bib0935"><span class="elsevierStyleSup">76–85</span></a></p>" ] ] 5 => array:8 [ "identificador" => "tbl0015" "etiqueta" => "Table 3" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at3" "detalle" => "Table " "rol" => "short" ] ] "tabla" => array:1 [ "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><tbody title="tbody"><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Avoid delays or multiple attempts (the most experience professional should perform the intubation).• Pre-oxygenation prior to intubation using manual mask ventilation and an airway mask bag unit should be performed with a HEPA filter placed between the mask and bag.• Pre-oxygenation with HFT may reduce hypoxemia during intubation but increases expiratory air dispersion.• Consider the use of a video laryngoscope as this will allow greater distance between the clinician and the airway.• Consider the use of a fibrobronchoscope if a difficult airway is anticipated.• Rapid sequence intubation. \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab3526095.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0050" class="elsevierStyleSimplePara elsevierViewall">Strategy for avoiding aerosol dispersion during endotracheal intubation.</p>" ] ] 6 => array:8 [ "identificador" => "tbl0020" "etiqueta" => "Table 4" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at4" "detalle" => "Table " "rol" => "short" ] ] "tabla" => array:1 [ "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><tbody title="tbody"><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Over 65 years of age.• APACHE II score greater than 12 (on the day of extubation).• Obesity with BMI<span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>30.• Poor secretion management.• Difficult or prolonged weaning.• More than 1 comorbidity.• Heart failure as the primary cause of ARF.• Moderate to severe COPD.• Airway management problems.• Long-term mechanical ventilation. \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab3526097.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0055" class="elsevierStyleSimplePara elsevierViewall">Groups at risk (hypoxemic ARF) in which NIV after extubation is recommended.<a class="elsevierStyleCrossRefs" href="#bib1065"><span class="elsevierStyleSup">102,104</span></a></p>" ] ] 7 => array:8 [ "identificador" => "tbl0025" "etiqueta" => "Table 5" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at5" "detalle" => "Table " "rol" => "short" ] ] "tabla" => array:1 [ "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><tbody title="tbody"><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">There is insufficient evidence that early initiation of NIRS (mainly HFT) is effective in preventing respiratory deterioration in patients with severe ARF secondary to COVID19 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">NIRS onset criteria:<span class="elsevierStyleHsp" style=""></span>- Moderate to severe dyspnea and evidence of increased work of breathing (accessory muscle use or tachypnoea<span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>30<span class="elsevierStyleHsp" style=""></span>rpm OR<span class="elsevierStyleHsp" style=""></span>- PaO<span class="elsevierStyleInf">2</span>/FiO<span class="elsevierStyleInf">2</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>200 or (SpO<span class="elsevierStyleInf">2</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>92% at FiO<span class="elsevierStyleInf">2</span> of 0.4) or PaCO<span class="elsevierStyleInf">2</span><span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>45<span class="elsevierStyleHsp" style=""></span>mmHg and pH<span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>7.35 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">In frail patients, HFT should be preferred due to better tolerability and fewer side effects. \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Initiation with CPAP is recommended. The option of PSV should only be considered in those with global acute respiratory failure. HFT is a recommended alternative in hypoxemic patients without respiratory acidosis. \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">For HFT, it is recommended to start therapy at the maximum tolerated flow with an adequate FiO<span class="elsevierStyleInf">2</span> to maintain SpO<span class="elsevierStyleInf">2</span><span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>92%.In the case of CPAP, it is usually initiated with values around 10 cmH20, without exceeding 12–13<span class="elsevierStyleHsp" style=""></span>cmH<span class="elsevierStyleInf">2</span>O to avoid barotrauma or negative hemodynamic effects, and FiO<span class="elsevierStyleInf">2</span> to achieve SpO<span class="elsevierStyleInf">2</span><span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>93% or PaO<span class="elsevierStyleInf">2</span><span class="elsevierStyleHsp" style=""></span>≥<span class="elsevierStyleHsp" style=""></span>60<span class="elsevierStyleHsp" style=""></span>mmHg.In the case of PSV NIV, PEEP between 10 and 12<span class="elsevierStyleHsp" style=""></span>cmH<span class="elsevierStyleInf">2</span>O and BP to target VT 4–6<span class="elsevierStyleHsp" style=""></span>ml/kg and FiO<span class="elsevierStyleInf">2</span> to target SpO<span class="elsevierStyleInf">2</span> 90–95% is suggested. \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">The helmet type is the interface of choice. If a helmet is not available, full face or oronasal masks can be used. The use of interfaces with a leak port in the mask is not recommended.It is recommended that nasal cannulas used for high flow therapy seal more than 50% of the nostril diameter. \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Response to NIRS should be monitored by monitoring clinical signs of work of breathing and oxygenation using the ROX index. \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Although failure of NIRS often results in the indication of tracheal intubation and initiation of invasive mechanical ventilation (IMV), in selected cases where there is potential for reversibility, rescue treatment with CPAP or NIV may be considered, although mortality is very high. If NIRS fails in patients with a therapeutic ceiling, it should be replaced by conventional oxygen therapy and symptomatic management of dyspnea should be optimized. \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Prone positioning may be beneficial in patients with COVID-19-related acute hypoxemic respiratory failure who require admission to intensive care and receive NIRS treatment. \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">The strategy for weaning from NIRS should be progressive, with differences depending on the modality used. \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Of particular importance is the strategy to prevent skin breakdown due to the interface.Consideration should be given to initiating enteral or parenteral nutrition within 48<span class="elsevierStyleHsp" style=""></span>h. \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Individual protection measures must be implemented for workers in contact with infected patients. Differentiated circuits for infected and non-infected patients should be organized.Vibrating mesh nebulizers should be preferred if aerosol therapy is required.Patient air filtration systems should be established in case of therapy with positive pressure systems. \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">The use of post-extubation NIRS is recommended in groups at risk of failure.In the tracheostomized patient, it is possible to provide HFT directly through the tracheostomy tube. \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab3526093.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0060" class="elsevierStyleSimplePara elsevierViewall">Summary of recommendations.</p>" ] ] 8 => array:5 [ "identificador" => "upi0005" "tipo" => "MULTIMEDIAECOMPONENTE" "mostrarFloat" => false "mostrarDisplay" => true "Ecomponente" => array:2 [ "fichero" => "mmc1.pdf" "ficheroTamanyo" => 756052 ] ] ] "bibliografia" => array:2 [ "titulo" => "References" "seccion" => array:1 [ 0 => array:2 [ "identificador" => "bibs0015" "bibliografiaReferencia" => array:111 [ 0 => array:3 [ "identificador" => "bib0560" "etiqueta" => "1" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Clinical consensus recommendations regarding non-invasive respiratory support in the adult patient with acute respiratory failure secondary to SARS-CoV-2 infection" "autores" => array:1 [ 0 => array:2 [ …2] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1016/j.arbres.2020.03.005" "Revista" => array:7 [ "tituloSerie" => "Arch Bronconeumol" "fecha" => "2020" "volumen" => "56" "numero" => "Suppl. 2" "paginaInicial" => "11" "paginaFinal" => "18" "link" => array:1 [ …1] ] ] ] ] ] ] 1 => array:3 [ "identificador" => "bib0565" "etiqueta" => "2" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Summary of recommendations and key points of the consensus of Spanish Scientific Societies (SEPAR, SEMICYUC, SEMES; SECIP, SENEO, SEDAR, SENP) on the use of non-invasive ventilation and high-flow oxygen therapy with nasal cannulas in adult, pediatric, and neonatal patients with severe acute respiratory failure" "autores" => array:1 [ 0 => array:2 [ …2] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1016/j.arbres.2020.08.013" "Revista" => array:2 [ "tituloSerie" => "Arch Bronconeumol" "fecha" => "2020" ] ] ] ] ] ] 2 => array:3 [ "identificador" => "bib0570" "etiqueta" => "3" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "ERS Clinical Practice Guidelines: high-flow nasal cannula in acute respiratory failure" "autores" => array:1 [ 0 => array:2 [ …2] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1183/13993003.01574-2021" "Revista" => array:3 [ "tituloSerie" => "Eur Respir J" "fecha" => "2021" "paginaInicial" => "2101574" ] ] ] ] ] ] 3 => array:3 [ "identificador" => "bib0575" "etiqueta" => "4" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "International variation in the management of severe COVID-19 patients" "autores" => array:1 [ 0 => array:2 [ …2] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1186/s13054-020-03194-w" "Revista" => array:4 [ "tituloSerie" => "Crit Care Lond Engl" "fecha" => "2020" "volumen" => "24" "paginaInicial" => "486" ] ] ] ] ] ] 4 => array:3 [ "identificador" => "bib0580" "etiqueta" => "5" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Global current practices of ventilatory support management in COVID-19 patients: an international survey" "autores" => array:1 [ 0 => array:2 [ …2] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.2147/JMDH.S279031" "Revista" => array:6 [ "tituloSerie" => "J Multidiscip Healthc" "fecha" => "2020" "volumen" => "13" "paginaInicial" => "1635" "paginaFinal" => "1648" "link" => array:1 [ …1] ] ] ] ] ] ] 5 => array:3 [ "identificador" => "bib0585" "etiqueta" => "6" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Mechanical ventilation to minimize progression of lung injury in acute respiratory failure" "autores" => array:1 [ 0 => array:2 [ …2] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1164/rccm.201605-1081CP" "Revista" => array:6 [ "tituloSerie" => "Am J Respir Crit Care Med" "fecha" => "2017" "volumen" => "195" "paginaInicial" => "438" "paginaFinal" => "442" "link" => array:1 [ …1] ] ] ] ] ] ] 6 => array:3 [ "identificador" => "bib0590" "etiqueta" => "7" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Early inspiratory effort assessment by esophageal manometry predicts noninvasive ventilation outcome in de novo respiratory failure. A pilot study" "autores" => array:1 [ 0 => array:2 [ …2] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1164/rccm.201912-2512OC" "Revista" => array:6 [ "tituloSerie" => "Am J Respir Crit Care Med" "fecha" => "2020" "volumen" => "202" "paginaInicial" => "558" "paginaFinal" => "567" "link" => array:1 [ …1] ] ] ] ] ] ] 7 => array:3 [ "identificador" => "bib0595" "etiqueta" => "8" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Early consensus management for non-ICU acute respiratory failure SARS-CoV-2 emergency in Italy: from ward to trenches" "autores" => array:1 [ 0 => array:2 [ …2] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1183/13993003.00632-2020" "Revista" => array:5 [ "tituloSerie" => "Eur Respir J" "fecha" => "2020" "volumen" => "55" "paginaInicial" => "2000632" "link" => array:1 [ …1] ] ] ] ] ] ] 8 => array:3 [ "identificador" => "bib0600" "etiqueta" => "9" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Feasibility and clinical impact of out-of-ICU noninvasive respiratory support in patients with COVID-19-related pneumonia" "autores" => array:1 [ 0 => array:2 [ …2] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1183/13993003.02130-2020" "Revista" => array:3 [ "tituloSerie" => "Eur Respir J" "fecha" => "2020" "paginaInicial" => "56" ] ] ] ] ] ] 9 => array:3 [ "identificador" => "bib0605" "etiqueta" => "10" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Position paper for the state-of-the-art application of respiratory support in patients with COVID-19" "autores" => array:1 [ 0 => array:2 [ …2] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1159/000509104" "Revista" => array:5 [ "tituloSerie" => "Respir Int Rev Thorac Dis" "fecha" => "2020" "volumen" => "99" "paginaInicial" => "521" "paginaFinal" => "542" ] ] ] ] ] ] 10 => array:3 [ "identificador" => "bib0610" "etiqueta" => "11" "referencia" => array:1 [ 0 => array:1 [ "referenciaCompleta" => "NHS England Speciality Guide: Guidance for the role and use of non-invasive respiratory support in adult patients with COVID-19 (confirmed or suspected). Med Aware Serv n.d. <a target="_blank" href="https://www.medicinesresources.nhs.uk/nhs-england-speciality-guide-guidance-for-the-role-and-use-of-non-invasive-respiratory-support-in-adult-patients-with-covid-19-confirmed-or-suspected.html">https://www.medicinesresources.nhs.uk/nhs-england-speciality-guide-guidance-for-the-role-and-use-of-non-invasive-respiratory-support-in-adult-patients-with-covid-19-confirmed-or-suspected.html</a> [accessed 19.9.21]." ] ] ] 11 => array:3 [ "identificador" => "bib0615" "etiqueta" => "12" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "COVID-19 pandemic and non invasive respiratory management: every Goliath needs a David. 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Journal Information
Vol. 60. Issue 5.
Pages 285-295 (May 2024)
Vol. 60. Issue 5.
Pages 285-295 (May 2024)