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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Pryce<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a> described pulmonary sequestration &#40;PS&#41; as a spectrum of abnormalities in which part of the lung&#44; with or without bronchial communication&#44; receives aberrant systemic arterial vascularization&#46; The extralobar type is covered by the pleura itself and drains into the systemic veins&#44; while the intralobar type shares the pleura with the rest of the lung and drains into the pulmonary veins&#59; it accounts for 0&#46;15&#37;&#8211;6&#46;4&#37; of all congenital pulmonary malformations&#46; Treatment has conventionally been surgical&#44; although nowadays a less invasive option is available in the form of percutaneous treatment&#46;<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">2&#8211;4</span></a> Very few series of children with PS treated with embolization have been published&#44; so we would like to report our experience in the percutaneous treatment of PS in a pediatric hospital in the Ecuadorian Andes&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">This was a cross-sectional study with consecutive sampling performed between March 2014 and April 2016&#46; Data in common &#40;<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>&#41;&#58; single artery feeding PS&#59; vascular access via the femoral artery&#46; No complications occurred&#44; except in the first patient&#46; Check-up with tomography was performed in patients 1&#44; 2&#44; and 3&#46; Informed consent was obtained for all patients&#46;</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">In the first case&#44; PS was suspected on radiograph&#44; so we requested a tomography that confirmed a large PS&#46; The procedure was complicated by reduced femoral pulse&#44; treated with enoxaparin&#59; the patient then developed systemic inflammatory response syndrome &#40;SIRS&#41; requiring intensive care&#46; During follow-up&#44; femoral pulses remained symmetric&#44; pulmonary scintigraphy was normal&#44; and the tomography showed full resolution of the PS&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">In the other cases&#44; PS was detected during catheterization&#46; The second patient was catheterized due to suspected pulmonary hypertension on echocardiography&#46; The third patient underwent catheterization due to poor progress after intervention for tetralogy of Fallot&#46; Dilated bronchial arteries were detected and occluded with a 6<span class="elsevierStyleHsp" style=""></span>mm Amplatzer&#8482; vascular plug &#40;AVP&#41;-II&#44; and an AVP-I was implanted in the vessel feeding the PS&#46; Residual flow was observed&#44; so a Gianturco coil &#40;GC&#41; was implanted&#44; completing occlusion of the aberrant artery&#46; The fourth patient underwent catheterization after developing cyanosis&#46; The last patient had a diagnosis of tetralogy of Fallot and collateral vessels on echocardiography&#44; so catheterization was indicated&#44; during which the diagnosis was ruled out&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">The essential component for diagnosing PS is angio-MRI&#44; angio-tomography&#44; or systemic artery angiogram of abnormal feeding of the pulmonary region&#46; It is not yet clearly defined whether PS should be treated percutaneously or surgically&#44; and the situation is even less clear if the patient is asymptomatic&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">3</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">Surgical treatment might require lobectomy&#44; cause bleeding&#44; infection or pneumothorax&#44; and hospital stay is extended&#46; Percutaneous treatment involves less risk of bleeding&#44; is less incapacitating&#44; and reduces length of hospital stay&#46; However&#44; complications&#44; such as vascular events and SIRS&#44; may occur&#44; particularly in small children with large PS&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">Several types of devices have been used for PS embolization<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">2&#44;4</span></a>&#58; we use AVP and GC because of their availability&#44; safety and proven effectiveness in vascular occlusion&#44; and their accessible&#44; state-funded cost&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">Patients were followed up with tomography 6 months after the procedure&#44; and in all cases it was confirmed that the aberrant vessel had not rechanneled&#44; the PS had resolved&#44; and the residual lung had expanded&#46; Resolution and expansion were particularly evident in the first patient&#44; who had presented a very large PS&#59; in this patient&#44; the pulmonary scintigraphy also showed normal uptake in the right lung&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">Although no significant differences have been identified between surgery and percutaneous intervention in terms of mortality&#44; series with large numbers of patients undergoing surgery report 7&#8211;14 days of hospitalization&#44; chest tube for 4 days&#44; and lobectomy in most cases&#44; particularly if the PS was intralobar&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">3&#44;5</span></a> We did not make a comparative study of the 2 techniques&#44; but these comorbidities are avoided with the use of percutaneous treatment&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">To our knowledge&#44; this is the second report of percutaneous treatment for PS in children in South America&#44;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">4</span></a> and while endovascular was safe and effective in our series&#44; it is still early to recommend it as an initial treatment choice&#44; because more experience is required&#46; However&#44; thanks to the growing body of information about its effectiveness&#44;<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">2&#8211;4</span></a> it can be considered as a first treatment option in places where resources are limited in terms of intensive care beds or the availability of pediatric surgeons trained in the correction of congenital pulmonary disorders&#46;</p></span>"
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                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">24&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">Abdominal&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">Abdominal&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">RIB&nbsp;\t\t\t\t\t\t\n
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Scientific Letter
Short-term Outcome of Percutaneous Treatment of Pulmonary Sequestration in a Pediatric Hospital in the Andes: A Case Series
Resultados a corto plazo del tratamiento percutáneo de secuestro pulmonar en hospital pediátrico ubicado en la región andina: serie de casos
Raúl E. Ríos-Méndeza,
Corresponding author
riosmendez@intramed.net.ar

Corresponding author.
, Jimena N. Andrade-Herrerab, María E. Aráuz-Martínezc
a Servicio de Cardiología y Hemodinamia, Hospital Pediátrico Baca Ortiz, Ministerio de Salud Pública, Quito, Ecuador
b Servicio de Imagenología, Hospital Pediátrico Baca Ortiz, Ministerio de Salud Pública, Quito, Ecuador
c Servicio de Neumología, Hospital Pediátrico Baca Ortiz, Ministerio de Salud Pública, Quito, Ecuador
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Pryce<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a> described pulmonary sequestration &#40;PS&#41; as a spectrum of abnormalities in which part of the lung&#44; with or without bronchial communication&#44; receives aberrant systemic arterial vascularization&#46; The extralobar type is covered by the pleura itself and drains into the systemic veins&#44; while the intralobar type shares the pleura with the rest of the lung and drains into the pulmonary veins&#59; it accounts for 0&#46;15&#37;&#8211;6&#46;4&#37; of all congenital pulmonary malformations&#46; Treatment has conventionally been surgical&#44; although nowadays a less invasive option is available in the form of percutaneous treatment&#46;<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">2&#8211;4</span></a> Very few series of children with PS treated with embolization have been published&#44; so we would like to report our experience in the percutaneous treatment of PS in a pediatric hospital in the Ecuadorian Andes&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">This was a cross-sectional study with consecutive sampling performed between March 2014 and April 2016&#46; Data in common &#40;<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>&#41;&#58; single artery feeding PS&#59; vascular access via the femoral artery&#46; No complications occurred&#44; except in the first patient&#46; Check-up with tomography was performed in patients 1&#44; 2&#44; and 3&#46; Informed consent was obtained for all patients&#46;</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">In the first case&#44; PS was suspected on radiograph&#44; so we requested a tomography that confirmed a large PS&#46; The procedure was complicated by reduced femoral pulse&#44; treated with enoxaparin&#59; the patient then developed systemic inflammatory response syndrome &#40;SIRS&#41; requiring intensive care&#46; During follow-up&#44; femoral pulses remained symmetric&#44; pulmonary scintigraphy was normal&#44; and the tomography showed full resolution of the PS&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">In the other cases&#44; PS was detected during catheterization&#46; The second patient was catheterized due to suspected pulmonary hypertension on echocardiography&#46; The third patient underwent catheterization due to poor progress after intervention for tetralogy of Fallot&#46; Dilated bronchial arteries were detected and occluded with a 6<span class="elsevierStyleHsp" style=""></span>mm Amplatzer&#8482; vascular plug &#40;AVP&#41;-II&#44; and an AVP-I was implanted in the vessel feeding the PS&#46; Residual flow was observed&#44; so a Gianturco coil &#40;GC&#41; was implanted&#44; completing occlusion of the aberrant artery&#46; The fourth patient underwent catheterization after developing cyanosis&#46; The last patient had a diagnosis of tetralogy of Fallot and collateral vessels on echocardiography&#44; so catheterization was indicated&#44; during which the diagnosis was ruled out&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">The essential component for diagnosing PS is angio-MRI&#44; angio-tomography&#44; or systemic artery angiogram of abnormal feeding of the pulmonary region&#46; It is not yet clearly defined whether PS should be treated percutaneously or surgically&#44; and the situation is even less clear if the patient is asymptomatic&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">3</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">Surgical treatment might require lobectomy&#44; cause bleeding&#44; infection or pneumothorax&#44; and hospital stay is extended&#46; Percutaneous treatment involves less risk of bleeding&#44; is less incapacitating&#44; and reduces length of hospital stay&#46; However&#44; complications&#44; such as vascular events and SIRS&#44; may occur&#44; particularly in small children with large PS&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">Several types of devices have been used for PS embolization<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">2&#44;4</span></a>&#58; we use AVP and GC because of their availability&#44; safety and proven effectiveness in vascular occlusion&#44; and their accessible&#44; state-funded cost&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">Patients were followed up with tomography 6 months after the procedure&#44; and in all cases it was confirmed that the aberrant vessel had not rechanneled&#44; the PS had resolved&#44; and the residual lung had expanded&#46; Resolution and expansion were particularly evident in the first patient&#44; who had presented a very large PS&#59; in this patient&#44; the pulmonary scintigraphy also showed normal uptake in the right lung&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">Although no significant differences have been identified between surgery and percutaneous intervention in terms of mortality&#44; series with large numbers of patients undergoing surgery report 7&#8211;14 days of hospitalization&#44; chest tube for 4 days&#44; and lobectomy in most cases&#44; particularly if the PS was intralobar&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">3&#44;5</span></a> We did not make a comparative study of the 2 techniques&#44; but these comorbidities are avoided with the use of percutaneous treatment&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">To our knowledge&#44; this is the second report of percutaneous treatment for PS in children in South America&#44;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">4</span></a> and while endovascular was safe and effective in our series&#44; it is still early to recommend it as an initial treatment choice&#44; because more experience is required&#46; However&#44; thanks to the growing body of information about its effectiveness&#44;<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">2&#8211;4</span></a> it can be considered as a first treatment option in places where resources are limited in terms of intensive care beds or the availability of pediatric surgeons trained in the correction of congenital pulmonary disorders&#46;</p></span>"
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                  \t\t\t\t\tvoid\n
                  \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><th class="td" title="table-head  " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">Case&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">2 years&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">RIB&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">3<span class="elsevierStyleHsp" style=""></span>mm&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">AVP-II 6<span class="elsevierStyleHsp" style=""></span>mm&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">Abdominal&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">No&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">1 day&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">Scimitar syndrome&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">20&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">3&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">8<span class="elsevierStyleHsp" style=""></span>m&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">RIB&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">5<span class="elsevierStyleHsp" style=""></span>mm&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">AVP-I 8<span class="elsevierStyleHsp" style=""></span>mm&#43;GC 3<span class="elsevierStyleHsp" style=""></span>mm&#215;4<span class="elsevierStyleHsp" style=""></span>mm&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">Abdominal&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">No&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">2 days&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">After intervention for tetralogy of Fallot&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">11&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">4&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">8 years&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">LIB&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">1&#46;8<span class="elsevierStyleHsp" style=""></span>mm&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">GC 3<span class="elsevierStyleHsp" style=""></span>mm&#215;4<span class="elsevierStyleHsp" style=""></span>mm&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">Abdominal&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">No&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">1 day&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">Trisomy 21&#43;unbalanced CAVC&#43;PAT banding&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">3&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">5&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">4 years&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">RIB&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">2<span class="elsevierStyleHsp" style=""></span>mm&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">AVP-II 3<span class="elsevierStyleHsp" style=""></span>mm&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">Abdominal&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">No&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">1 day&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">Tetralogy of Fallot&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">1&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr></tbody></table>
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ISSN: 15792129
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