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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">The increasing body of knowledge of chronic obstructive pulmonary disease acquired in recent decades has helped experts draw up more patient-focused treatment strategies&#46; The latest versions of the Global Initiative for Chronic Obstructive Lung Disease &#40;GOLD&#41; document have moved toward a more multidimensional assessment&#44; while in Spain&#44; the assessment of COPD in the Spanish guidelines &#40;GesEPOC&#41; has evolved with the adoption of clinical phenotypes&#46; Although both strategies have their advantages and disadvantages&#44;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a> they exemplify the progress made in patient classification as a step on the path toward personalized treatment&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">This year has seen the publication of the new version of the GOLD 2017 proposal&#44; which introduces important changes in several aspects of the disease&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">2</span></a> And now&#44; this edition of <span class="elsevierStyleItalic">Archivos de Bronconeumolog&#237;a</span> publishes the executive summary of the major GesEPOC 2017 recommendations for the pharmacological treatment of stable COPD&#46;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">3</span></a> This new version of the guidelines describes an approach with several features that bring it closer to the GOLD document&#44; while maintaining its distinct philosophy in several areas&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">In the diagnostic section&#44; GesEPOC 2017 establishes a new patient classification&#44; in which it replaces the term &#8220;severity&#8221;&#44; measured by BODE&#8211;BODEx&#44; with the concept of high or low risk&#46; This is similar to the GOLD approach&#44; but with 2 important differences&#46; Firstly&#44; a different cutoff point for dyspnea measured by the mMRC scale has been selected&#58; GesEPOC defines the cutoff as more than 2 points for patients without treatment&#46; This new cutoff point may have a lower degree of concordance with the CAT&#44;<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">4</span></a> but it has been proposed as a limit for identifying a patient with a high disease burden&#46;<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">5</span></a> Secondly&#44; GesEPOC maintains lung function as a variable to be taken into account in the classification of risk&#46; This difference with GOLD 2017 is a clear indication of the controversy surrounding the role of spirometry in monitoring patients&#46; While it is true that lung function remains stable over time in some patients&#44; and in these patients repeat spirometry during monitoring will provide little new prognostic information&#44; spirometric data can be of value in patients with progressively deteriorating lung function&#46; We understand by this that the need for regular lung function assessments could be personalized&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">Another significant change in the diagnostic recommendations of GesEPOC is the incorporation of the asthma-COPD overlap &#40;ACO&#41;&#46; In this new version&#44; GesEPOC adopts the term ACO as used in GOLD&#46; However&#44; diagnostic criteria have changed considerably since the previous version of GesEPOC&#44; and are based on the SEPAR consensus published by the Asthma and COPD interest areas&#46;<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">6</span></a> Major and minor criteria that appeared in the previous version have been dropped&#44; probably after the results of observational studies were examined&#46;<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">7</span></a> To date&#44; GOLD 2017 has not yet published the annex mentioned in its section on ACO&#44; so we do not know if the diagnostic approach will change&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">Regarding treatment&#44; GesEPOC proposes a stepwise approach to the gradual intensification of therapy according to risk stratification and clinical phenotype&#46; If we use the same type of figure that appears in the GOLD document&#44; the GesEPOC treatment strategy would be similar to that of <a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#46; We need to make 2 points here&#46; Firstly&#44; regarding the impact of long-term double bronchodilation&#44; GesEPOC 2017&#44; like GOLD 2017&#44; proposes starting with one long-acting bronchodilator in patients with a low disease burden&#44; and later stepping up to 2 bronchodilators&#46; This approach makes good clinical sense&#44; and for now it is the most logical approach&#46; However&#44; it should be remembered that disease onset is a good time to modify FEV<span class="elsevierStyleInf">1</span> decline&#44;<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">8</span></a> making it a window of opportunity for delaying functional progression of the disease&#46; If it were confirmed that 2 bronchodilators could reduce FEV<span class="elsevierStyleInf">1</span> decline&#44; the strategy should be reversed&#44; and it would make more sense to administer 2 bronchodilators at the beginning of the disease&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0030" class="elsevierStylePara elsevierViewall">Secondly&#44; the current proposals assume that the indications for the use of inhaled corticosteroids are frequent exacerbations despite bronchodilator treatment and ACOS&#46; This assumption needs to be clarified&#46; First&#44; the so-called persistent exacerbator&#44;<a class="elsevierStyleCrossRef" href="#bib0095"><span class="elsevierStyleSup">9</span></a> a patient who continues to present exacerbations despite receiving correct inhaled therapy&#44; does not necessarily need inhaled corticosteroids&#46; Several comorbidities have been identified that might influence the rate of exacerbations&#44; and which cannot be treated with inhaled corticosteroids&#46; GesEPOC 2017 establishes the use of inhaled corticosteroids as yet another option among a number of preventive treatments&#46; It seems&#44; then&#44; that before debating the best way of scaling up to triple therapy&#44;<a class="elsevierStyleCrossRef" href="#bib0100"><span class="elsevierStyleSup">10</span></a> we should conduct a study on the factors that trigger these exacerbations&#44; in order to determine the best preventive treatment&#46; We also need to identify a marker for ACOS&#46; GesEPOC 2017 proposes a definition based on the concomitant diagnosis of asthma&#44; bronchoreversibility&#44; and eosinophils in blood&#46; The debate surrounding these criteria goes beyond the objectives of this editorial&#44; but this proposal seems appropriate in the light of current knowledge&#46; However&#44; it must be mentioned that&#44; while there is a correlation between these parameters and markers of response to inhaled corticosteroids&#44; the degree of concordance between criteria associated with response to inhaled corticosteroids in individual patients is poor&#46;<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">7</span></a> We need&#44; therefore&#44; to identify candidate markers of response to these drugs that will allow us to take decisions at the patient level in the future&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">Finally&#44; other topics currently generating controversy in COPD should be addressed in the future&#44; including&#44; but not limited to&#44; treatment of patients with few symptoms&#44; classification of symptomatic patients with no spirometric obstruction&#44; or the evaluation of comorbidities in patient management&#46; Remembering rock and roll band Status Quo&#39;s hit &#8220;Cross that Bridge&#8221; from their 1988 studio album &#8220;Ain&#8217;t Complaining&#8221;&#44; we will have to cross that bridge when we come to it&#44; insofar as scientific progress permits&#46; Meanwhile&#44; the new GesEPOC 2017 document brings us closer to personalized&#44; evidence-based treatment of COPD supported by a multidisciplinary committee of experts showing the best evidence available to date&#46;</p></span>"
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Editorial
Major Changes in the Spanish COPD Guidelines (GesEPOC) 2017: Crossing Bridges
Cambios mayores en la Guía española de la EPOC (GesEPOC) 2017: cruzando puentes
José Luis Lopez-Camposa,b,
Corresponding author
lopezcampos@separ.es

Corresponding author.
, Eduardo Marquez-Martína, Francisco Ortega-Ruiza,b
a Unidad Médico-Quirúrgica de Enfermedades Respiratorias, Instituto de Biomedicina de Sevilla (IBiS), Hospital Universitario Virgen del Rocío, Universidad de Sevilla, Spain
b CIBER de Enfermedades Respiratorias (CIBERES), Instituto de Salud Carlos III, Madrid, Spain
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">The increasing body of knowledge of chronic obstructive pulmonary disease acquired in recent decades has helped experts draw up more patient-focused treatment strategies&#46; The latest versions of the Global Initiative for Chronic Obstructive Lung Disease &#40;GOLD&#41; document have moved toward a more multidimensional assessment&#44; while in Spain&#44; the assessment of COPD in the Spanish guidelines &#40;GesEPOC&#41; has evolved with the adoption of clinical phenotypes&#46; Although both strategies have their advantages and disadvantages&#44;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a> they exemplify the progress made in patient classification as a step on the path toward personalized treatment&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">This year has seen the publication of the new version of the GOLD 2017 proposal&#44; which introduces important changes in several aspects of the disease&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">2</span></a> And now&#44; this edition of <span class="elsevierStyleItalic">Archivos de Bronconeumolog&#237;a</span> publishes the executive summary of the major GesEPOC 2017 recommendations for the pharmacological treatment of stable COPD&#46;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">3</span></a> This new version of the guidelines describes an approach with several features that bring it closer to the GOLD document&#44; while maintaining its distinct philosophy in several areas&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">In the diagnostic section&#44; GesEPOC 2017 establishes a new patient classification&#44; in which it replaces the term &#8220;severity&#8221;&#44; measured by BODE&#8211;BODEx&#44; with the concept of high or low risk&#46; This is similar to the GOLD approach&#44; but with 2 important differences&#46; Firstly&#44; a different cutoff point for dyspnea measured by the mMRC scale has been selected&#58; GesEPOC defines the cutoff as more than 2 points for patients without treatment&#46; This new cutoff point may have a lower degree of concordance with the CAT&#44;<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">4</span></a> but it has been proposed as a limit for identifying a patient with a high disease burden&#46;<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">5</span></a> Secondly&#44; GesEPOC maintains lung function as a variable to be taken into account in the classification of risk&#46; This difference with GOLD 2017 is a clear indication of the controversy surrounding the role of spirometry in monitoring patients&#46; While it is true that lung function remains stable over time in some patients&#44; and in these patients repeat spirometry during monitoring will provide little new prognostic information&#44; spirometric data can be of value in patients with progressively deteriorating lung function&#46; We understand by this that the need for regular lung function assessments could be personalized&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">Another significant change in the diagnostic recommendations of GesEPOC is the incorporation of the asthma-COPD overlap &#40;ACO&#41;&#46; In this new version&#44; GesEPOC adopts the term ACO as used in GOLD&#46; However&#44; diagnostic criteria have changed considerably since the previous version of GesEPOC&#44; and are based on the SEPAR consensus published by the Asthma and COPD interest areas&#46;<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">6</span></a> Major and minor criteria that appeared in the previous version have been dropped&#44; probably after the results of observational studies were examined&#46;<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">7</span></a> To date&#44; GOLD 2017 has not yet published the annex mentioned in its section on ACO&#44; so we do not know if the diagnostic approach will change&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">Regarding treatment&#44; GesEPOC proposes a stepwise approach to the gradual intensification of therapy according to risk stratification and clinical phenotype&#46; If we use the same type of figure that appears in the GOLD document&#44; the GesEPOC treatment strategy would be similar to that of <a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#46; We need to make 2 points here&#46; Firstly&#44; regarding the impact of long-term double bronchodilation&#44; GesEPOC 2017&#44; like GOLD 2017&#44; proposes starting with one long-acting bronchodilator in patients with a low disease burden&#44; and later stepping up to 2 bronchodilators&#46; This approach makes good clinical sense&#44; and for now it is the most logical approach&#46; However&#44; it should be remembered that disease onset is a good time to modify FEV<span class="elsevierStyleInf">1</span> decline&#44;<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">8</span></a> making it a window of opportunity for delaying functional progression of the disease&#46; If it were confirmed that 2 bronchodilators could reduce FEV<span class="elsevierStyleInf">1</span> decline&#44; the strategy should be reversed&#44; and it would make more sense to administer 2 bronchodilators at the beginning of the disease&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0030" class="elsevierStylePara elsevierViewall">Secondly&#44; the current proposals assume that the indications for the use of inhaled corticosteroids are frequent exacerbations despite bronchodilator treatment and ACOS&#46; This assumption needs to be clarified&#46; First&#44; the so-called persistent exacerbator&#44;<a class="elsevierStyleCrossRef" href="#bib0095"><span class="elsevierStyleSup">9</span></a> a patient who continues to present exacerbations despite receiving correct inhaled therapy&#44; does not necessarily need inhaled corticosteroids&#46; Several comorbidities have been identified that might influence the rate of exacerbations&#44; and which cannot be treated with inhaled corticosteroids&#46; GesEPOC 2017 establishes the use of inhaled corticosteroids as yet another option among a number of preventive treatments&#46; It seems&#44; then&#44; that before debating the best way of scaling up to triple therapy&#44;<a class="elsevierStyleCrossRef" href="#bib0100"><span class="elsevierStyleSup">10</span></a> we should conduct a study on the factors that trigger these exacerbations&#44; in order to determine the best preventive treatment&#46; We also need to identify a marker for ACOS&#46; GesEPOC 2017 proposes a definition based on the concomitant diagnosis of asthma&#44; bronchoreversibility&#44; and eosinophils in blood&#46; The debate surrounding these criteria goes beyond the objectives of this editorial&#44; but this proposal seems appropriate in the light of current knowledge&#46; However&#44; it must be mentioned that&#44; while there is a correlation between these parameters and markers of response to inhaled corticosteroids&#44; the degree of concordance between criteria associated with response to inhaled corticosteroids in individual patients is poor&#46;<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">7</span></a> We need&#44; therefore&#44; to identify candidate markers of response to these drugs that will allow us to take decisions at the patient level in the future&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">Finally&#44; other topics currently generating controversy in COPD should be addressed in the future&#44; including&#44; but not limited to&#44; treatment of patients with few symptoms&#44; classification of symptomatic patients with no spirometric obstruction&#44; or the evaluation of comorbidities in patient management&#46; Remembering rock and roll band Status Quo&#39;s hit &#8220;Cross that Bridge&#8221; from their 1988 studio album &#8220;Ain&#8217;t Complaining&#8221;&#44; we will have to cross that bridge when we come to it&#44; insofar as scientific progress permits&#46; Meanwhile&#44; the new GesEPOC 2017 document brings us closer to personalized&#44; evidence-based treatment of COPD supported by a multidisciplinary committee of experts showing the best evidence available to date&#46;</p></span>"
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        "nota" => "<p class="elsevierStyleNotepara" id="npar0005">Please cite this article as&#58; Lopez-Campos JL&#44; Marquez-Mart&#237;n E&#44; Ortega-Ruiz F&#46; Cambios mayores en la Gu&#237;a espa&#241;ola de la EPOC &#40;GesEPOC&#41; 2017&#58; cruzando puentes&#46; Arch Bronconeumol&#46; 2017&#59;53&#58;291&#8211;292&#46;</p>"
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          "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">GesEPOC treatment strategy&#46; Exacerb&#46;&#58; exacerbation&#59; FEV<span class="elsevierStyleInf">1</span>&#58; forced expiratory volume in 1<span class="elsevierStyleHsp" style=""></span>s&#59; ICS&#58; inhaled corticosteroids&#59; LABA&#58; long-acting beta-agonists&#59; LAMA&#58; long-acting muscarinic receptor agonists&#59; SABD&#58; short-acting bronchodilators&#46;</p>"
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ISSN: 15792129
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Archivos de Bronconeumología

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