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Saavedra" "apellidos" => "Lozano" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">j</span>" "identificador" => "aff0050" ] ] ] 10 => array:2 [ "colaborador" => "representing the Sociedad Española de Infectología Pediátrica (SEIP), Sociedad Española de Neumología Pediátrica (SENP) and the Comité Asesor de Vacunas de la Asociación Española de Pediatría (CAV-AEP)" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">1</span>" "identificador" => "fn0005" ] ] ] ] "afiliaciones" => array:10 [ 0 => array:3 [ "entidad" => "Infectología Pediátrica e Inmunodeficiencias, Unidad de Gestión Clínica de Pediatría, Hospital Materno-Infantil, Hospital Regional Universitario de Málaga, Grupo de Investigación IBIMA, Departamento de Pediatría y Farmacología, Facultad de Medicina, Universidad de Málaga, Málaga, Spain" "etiqueta" => "a" "identificador" => "aff0005" ] 1 => array:3 [ "entidad" => "Sección de Neumología Pediátrica, Servicio de Pediatría, Hospital Universitario Virgen Macarena, Departamento de Farmacología, Pediatría y Radiología, Facultad de Medicina, Universidad de Sevilla, Sevilla, Spain" "etiqueta" => "b" "identificador" => "aff0010" ] 2 => array:3 [ "entidad" => "Servicio de Pediatría, Hospital Infanta Sofía, San Sebastián de los Reyes, Madrid, Spain" "etiqueta" => "c" "identificador" => "aff0015" ] 3 => array:3 [ "entidad" => "Unidad de Neumología Pediátrica y Fibrosis Quística, Servicio de Pediatría, Hospital Clínico Universitario, Universitat de València, Valencia, Spain" "etiqueta" => "d" "identificador" => "aff0020" ] 4 => array:3 [ "entidad" => "Unidad de Neumología y Alergia Pediátrica, Servicio de Pediatría, Hospital Universitario Son Espases, Palma de Mallorca, Islas Baleares, Spain" "etiqueta" => "e" "identificador" => "aff0025" ] 5 => array:3 [ "entidad" => "Servicio de Pediatría, Hospital San Joan de Dèu, Universitat de Barcelona, Barcelona, Spain" "etiqueta" => "f" "identificador" => "aff0030" ] 6 => array:3 [ "entidad" => "Sección de Neumología Pediátrica y Fibrosis Quística, Hospital Universitario Vall d¿Hebron, Barcelona, Universitat Autònoma de Barcelona, Barcelona, Spain" "etiqueta" => "g" "identificador" => "aff0035" ] 7 => array:3 [ "entidad" => "Unidad de Enfermedades Infecciosas e Inmunología Clínica, Servicio de Pediatría, Hospital Universitario Germans Trias i Pujol, Badalona, Universitat Autònoma de Barcelona, Barcelona, Spain" "etiqueta" => "h" "identificador" => "aff0040" ] 8 => array:3 [ "entidad" => "Servicio de Pediatría, Hospital 12 de Octubre, Departamento de Pediatría, Facultad de Medicina, Universidad Complutense de Madrid, Madrid, Spain" "etiqueta" => "i" "identificador" => "aff0045" ] 9 => array:3 [ "entidad" => "Unidad de Infectología Pediátrica, Servicio de Pediatría, Hospital General Universitario Gregorio Marañón, Madrid, Spain" "etiqueta" => "j" "identificador" => "aff0050" ] ] "correspondencia" => array:1 [ 0 => array:3 [ "identificador" => "cor0005" "etiqueta" => "⁎" "correspondencia" => "Corresponding author." ] ] ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Neumonía adquirida en la comunidad: tratamiento ambulatorio y prevención" ] ] "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Introduction</span><p id="par0005" class="elsevierStylePara elsevierViewall">Community acquired pneumonia (CAP) is the single main cause of child mortality worldwide. It is estimated to be responsible for 1.2 annual million deaths in children under 5 years of age, which accounts for 18% of all deaths at this age, 99% of them in developing countries.<a class="elsevierStyleCrossRef" href="#bib0195"><span class="elsevierStyleSup">1</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">In developed countries and regions, such as North America, Europe, Oceania and Japan, there are estimated to be up to 2.6 million annual cases of CAP in children under 5 years of age, causing 1.5 million hospitalisations and, approximately, 3000 deaths,<a class="elsevierStyleCrossRef" href="#bib0200"><span class="elsevierStyleSup">2</span></a> more than the number of deaths for meningitis.</p><p id="par0015" class="elsevierStylePara elsevierViewall">In the last decade, the aetiology, clinical presentation and evolution of CAP in the paediatric population have changed significantly with the introduction of vaccines against pathogens involved in its aetiology (such as <span class="elsevierStyleItalic">Haemophilus influenzae</span> [<span class="elsevierStyleItalic">H. influenzae</span>] type b and <span class="elsevierStyleItalic">Streptococcus pneumoniae</span> [<span class="elsevierStyleItalic">S. pneumoniae</span>]), the better use of antibiotics, as well as other factors which have not yet been explained but are probably associated with independent epidemiological trends.</p><p id="par0020" class="elsevierStylePara elsevierViewall">As already explained in the document on the aetiology and diagnosis of CAP agreed by these two paediatric associations,<a class="elsevierStyleCrossRef" href="#bib0205"><span class="elsevierStyleSup">3</span></a> the main aetiological agents are viruses and <span class="elsevierStyleItalic">S. pneumoniae</span>. Viruses affect mainly children under 4–5 years of age, while <span class="elsevierStyleItalic">S. pneumoniae</span> affects children of any age. However, in the last 10–15 years the incidence of complicated pneumonias, manifesting as either pleural effusion or necrotising pneumonia, has steadily increased. Changes have also been observed in the age of onset of complicated pneumonias. Where previously it was more frequent in children under the age of 2–3 years, it now predominates in children 2–5 years of age. There has also been a slight increase in the number of cases caused by <span class="elsevierStyleItalic">Staphylococcus aureus</span> (<span class="elsevierStyleItalic">S. aureus</span>), some caused by strains produced by certain virus factors which make them more serious.</p><p id="par0025" class="elsevierStylePara elsevierViewall">Paediatricians treating children with CAP<a class="elsevierStyleCrossRef" href="#bib0210"><span class="elsevierStyleSup">4</span></a> have access to a huge range of therapies, and in many countries clinical guidelines are not followed.<a class="elsevierStyleCrossRefs" href="#bib0215"><span class="elsevierStyleSup">5,6</span></a> Therefore, one of the most ambitious goals of this consensus is to harmonise therapeutic measures against this disease in Spain and improve control measures.<a class="elsevierStyleCrossRef" href="#bib0225"><span class="elsevierStyleSup">7</span></a> In this document, based on the scientific information available and the experience of the authors, initial measures are proposed which we believe are more adequate for the therapeutic treatment of CAP. Also, the prevention measures available against CAP in the population of children are summarised. In another document, soon to be published in this journal the therapeutic approach to complicated cases and special circumstances will be presented.</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Current status of resistances to antimicrobial drugs</span><p id="par0030" class="elsevierStylePara elsevierViewall">Drug-resistant bacteria that can potentially cause CAP include <span class="elsevierStyleItalic">S. pneumoniae</span>, <span class="elsevierStyleItalic">S. aureus</span>, <span class="elsevierStyleItalic">Streptococcus pyogenes</span> (<span class="elsevierStyleItalic">S. pyogenes</span>) and <span class="elsevierStyleItalic">H. influenzae</span> type b. In Spain, other causal agents of CAP, such as <span class="elsevierStyleItalic">Mycoplasma pneumoniae</span> (<span class="elsevierStyleItalic">M. pneumoniae</span>) or <span class="elsevierStyleItalic">Chlamydophila pneumoniae</span> (<span class="elsevierStyleItalic">C. pneumoniae</span>), or viruses, are not drug-resistant. <span class="elsevierStyleItalic">M. pneumoniae</span> and <span class="elsevierStyleItalic">C. pneumoniae</span> are usually sensitive to macrolides and the only virus to be treated with antiviral drugs, the flu virus, so far does not present resistance to oseltamivir in our area.</p><p id="par0035" class="elsevierStylePara elsevierViewall">The most reliable data on the drug-resistance of the main respiratory pathogens in our area are periodically provided by the multi-centre study known as Sensitivity to Antibiotic Drugs Used in the Community in Spain (SAUCE in Spanish). The latest, published in 2010 as the SAUCE-4 study,<a class="elsevierStyleCrossRef" href="#bib0230"><span class="elsevierStyleSup">8</span></a> offers results on sensitivity and resistance according to official cutoff points (<span class="elsevierStyleItalic">CLSI cutoff points</span>). It contains a total of 2559 isolations of <span class="elsevierStyleItalic">S. pneumoniae</span>, 2287 of <span class="elsevierStyleItalic">S. pyogenes</span> and 2287 of <span class="elsevierStyleItalic">H. influenzae</span>, and these are compared to those recorded in the previous 11 years. In summary, the most relevant data are described in <a class="elsevierStyleCrossRef" href="#tbl0010">Table 1</a>. For <span class="elsevierStyleItalic">S. pneumoniae</span>, as regards sensitivity to β-lactams, currently almost all strains circulating in Spain are sensitive to oral amoxicillin and intravenous penicillin and ampicillin, and also cefuroxime, if we wish to broaden the spectrum. They are all sensitive to cephotaxime. In recent years, the percentage of penicillin-resistant strains (intermediate sensitivity or total resistance) have risen from 60.0% to 22.9%. The proportion of strains with total resistance to oral penicillin (MIC<span class="elsevierStyleHsp" style=""></span>≥<span class="elsevierStyleHsp" style=""></span>2) has decreased drastically from 36.5% to 0.9%. Also, 0% presents total resistance (MIC<span class="elsevierStyleHsp" style=""></span>≥<span class="elsevierStyleHsp" style=""></span>8) for parenteral penicillin and only 0.2% intermediate sensitivity (MIC<span class="elsevierStyleHsp" style=""></span>≥<span class="elsevierStyleHsp" style=""></span>4). There are still high rates of resistance to macrolides (21–25%).</p><elsevierMultimedia ident="tbl0010"></elsevierMultimedia><p id="par0040" class="elsevierStylePara elsevierViewall">For <span class="elsevierStyleItalic">H. influenzae</span>, 15.7% are producers of β-lactamases and, therefore, resistant to penicillin, ampicillin or amoxicillin. This percentage has decreased, from the previous level of 25.7%.</p><p id="par0045" class="elsevierStylePara elsevierViewall">These data, based on samples from children and adults taken 6–7 years ago, can be combined with the findings of a recent study by Heracles in the Community of Madrid (May 2011–April 2013),<a class="elsevierStyleCrossRefs" href="#bib0235"><span class="elsevierStyleSup">9,10</span></a> where 100% of <span class="elsevierStyleItalic">S. pneumoniae</span> strains isolated in children under 15 years old with invasive pneumococci disease outside the central nervous system—including bacteraemia pneumonias and empyema—are sensitive to penicillin and cephotaxime.</p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Adjuvant support treatment</span><p id="par0050" class="elsevierStylePara elsevierViewall">In children with CAP, antibiotic therapy at times needs to be complemented with other strategies, although this is less frequent in patients not requiring hospitalisation.</p><p id="par0055" class="elsevierStylePara elsevierViewall">Children with pneumonia usually feel associated pain (pleuritic, abdominal, headache) and discomfort or pain due to inflammation of upper airways (otalgia, odynophagia). Analgesia is recommended for relief, especially in cases of pleuritic pain, because it interferes with coughing and breathing.<a class="elsevierStyleCrossRefs" href="#bib0245"><span class="elsevierStyleSup">11,12</span></a> Paracetamol can be used (15<span class="elsevierStyleHsp" style=""></span>mg/kg/6<span class="elsevierStyleHsp" style=""></span>h; up to a maximum of 75<span class="elsevierStyleHsp" style=""></span>mg/kg/day) or ibuprofen (5–10<span class="elsevierStyleHsp" style=""></span>mg/kg/6–8<span class="elsevierStyleHsp" style=""></span>h). Fever must be controlled with these same agents, as oxygen requirements increase. There is insufficient evidence that mucolytic and cough suppressants are beneficial, and in theory, medications with codeine or antihistamines should not be used in young children.<a class="elsevierStyleCrossRef" href="#bib0255"><span class="elsevierStyleSup">13</span></a></p><p id="par0060" class="elsevierStylePara elsevierViewall">Increased effort of breathing and fever increase the requirement for fluids. The ideal way to provide them is orally, in small amounts and frequently.</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">Ambulatory treatment of non-complicated CAP with antibiotics</span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">Indication for the use of antibiotics</span><p id="par0065" class="elsevierStylePara elsevierViewall">Empirical treatment of CAP is based on the pathogens most frequently involved. However, one of the most important problems is correct distinction between probable viral aetiology and probable bacterial aetiology. Clinicians tend, mistakenly, to use antibiotics in excess, which leads to an increase in antimicrobial resistances. In patients aged less than 2 years, with mild clinical lower airway manifestations and a history of correct immunisation according to age against <span class="elsevierStyleItalic">H. influenzae</span> type b and <span class="elsevierStyleItalic">S. pneumoniae</span> bacterial aetiology is unlikely.<a class="elsevierStyleCrossRef" href="#bib0260"><span class="elsevierStyleSup">14</span></a></p><p id="par0070" class="elsevierStylePara elsevierViewall">Antibiotics are indicated in typical CAP where bacterial aetiology is suspected. In cases of atypical CAP they should only be used in children over 4–5 years old and in certain younger patients if the infection is serious.</p><p id="par0075" class="elsevierStylePara elsevierViewall">For treatment under special circumstances (allergy to β-lactams, base disease, immunodepressed, etc.), or patients requiring hospitalisation, more information will be available in the specific document that will be published in a subsequent issue of this journal.</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0050">Selection of the antibiotic, route, dosage and duration</span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0055">Typical CAP</span><p id="par0080" class="elsevierStylePara elsevierViewall">If it has been decided to initiate ambulatory antibiotic treatment in typical CAP with no criteria for hospital admission, considering that most are caused by pneumococci and that, currently, almost all are sensitive to penicillin and amoxicillin,<a class="elsevierStyleCrossRef" href="#bib0230"><span class="elsevierStyleSup">8</span></a> the antibiotic of choice is 80–90<span class="elsevierStyleHsp" style=""></span>mg/kg/day oral amoxicillin, every 8<span class="elsevierStyleHsp" style=""></span>h (<a class="elsevierStyleCrossRef" href="#tbl0015">Table 2</a>). This recommendation is consistent with current international guidelines.<a class="elsevierStyleCrossRefs" href="#bib0250"><span class="elsevierStyleSup">12,15</span></a> The maximum recommended dose, according to the package leaflet, is 2<span class="elsevierStyleHsp" style=""></span>g every 8<span class="elsevierStyleHsp" style=""></span>h, given the good tolerance of this antibiotic.</p><elsevierMultimedia ident="tbl0015"></elsevierMultimedia><p id="par0085" class="elsevierStylePara elsevierViewall">There may be some controversy regarding the recommended dose. Given the good absorption of this drug and its good penetration at a pulmonary level, as well as the low rates of resistances of <span class="elsevierStyleItalic">S. pneumoniae</span>, doses of 40–50<span class="elsevierStyleHsp" style=""></span>mg/kg/day will suffice in most cases. This consensus recommends, however, higher doses (80–90<span class="elsevierStyleHsp" style=""></span>mg/kg/day) due to the following reasons:<a class="elsevierStyleCrossRef" href="#bib0270"><span class="elsevierStyleSup">16</span></a><ul class="elsevierStyleList" id="lis0005"><li class="elsevierStyleListItem" id="lsti0005"><span class="elsevierStyleLabel">–</span><p id="par0090" class="elsevierStylePara elsevierViewall">The use of low doses (40–50<span class="elsevierStyleHsp" style=""></span>mg/kg/day) may lead to reappearance of resistant strains.</p></li><li class="elsevierStyleListItem" id="lsti0010"><span class="elsevierStyleLabel">–</span><p id="par0095" class="elsevierStylePara elsevierViewall">Children with respiratory infections frequently vomit, which may cause infradosage scenarios, especially if low doses are used.</p></li><li class="elsevierStyleListItem" id="lsti0015"><span class="elsevierStyleLabel">–</span><p id="par0100" class="elsevierStylePara elsevierViewall">In pneumococcal infections of the upper airways (acute otitis media and sinusitis), it is necessary to continue to use high doses due to lower penetration of drugs in these locations. It is preferable to harmonise the dosage of this oral antibiotic for all pneumococcal infections, for the purpose of minimising prescription errors.</p></li></ul></p><p id="par0105" class="elsevierStylePara elsevierViewall">The use of clavulanic acid together with amoxicillin in children with typical CAP with no underlying disease and vaccinated against <span class="elsevierStyleItalic">H. influenzae</span> type b, is not justified if there is suspicion of probable pneumococci aetiology, since <span class="elsevierStyleItalic">S. pneumoniae</span> drug-resistance through the production of β-lactamases is still unclear. Furthermore, their use is associated, relatively frequently, with gastrointestinal symptomatology, particularly diarrhoea, which can decrease absorption of amoxicillin.</p><p id="par0110" class="elsevierStylePara elsevierViewall">Macrolides should not be used for the treatment of typical CAP for many reasons, the most important being current resistance of <span class="elsevierStyleItalic">S. pneumoniae</span> to these antibiotics and the risk of bacteraemia in these patients.<a class="elsevierStyleCrossRef" href="#bib0275"><span class="elsevierStyleSup">17</span></a> Despite that, they are often incorrectly prescribed for CAP.<a class="elsevierStyleCrossRef" href="#bib0215"><span class="elsevierStyleSup">5</span></a></p><p id="par0115" class="elsevierStylePara elsevierViewall">The recommended duration of treatment in a patient with typical CAP with no complications and not requiring admission is 7 days. There are several meta-analyses, based mainly on trials carried out in developing countries, which showed that 3 days of oral amoxicillin will be effective in treating children of 2–59 months of age with CAP that do not require hospitalisation. Although this strategy reduces costs,<a class="elsevierStyleCrossRefs" href="#bib0280"><span class="elsevierStyleSup">18,19</span></a> it is associated with a high rate of therapeutic failure, and therefore should not be used in Spain.</p></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0060">Atypical CAP</span><p id="par0120" class="elsevierStylePara elsevierViewall">In the case of atypical CAP in children under 4–5 years old, the aetiology is usually viral, and therefore no antibiotics are prescribed. In children over 4–5 years old, in whom <span class="elsevierStyleItalic">M. pneumoniae</span> aetiology is more frequent (up to 40% of CAP in this age group)<a class="elsevierStyleCrossRef" href="#bib0290"><span class="elsevierStyleSup">20</span></a> and, to a lesser extent, <span class="elsevierStyleItalic">C. pneumoniae</span>, the use of oral macrolides is recommended,<a class="elsevierStyleCrossRefs" href="#bib0265"><span class="elsevierStyleSup">15,20</span></a> although there is no clear evidence of its effectiveness in resolving CAP in this population.<a class="elsevierStyleCrossRefs" href="#bib0295"><span class="elsevierStyleSup">21,22</span></a></p><p id="par0125" class="elsevierStylePara elsevierViewall">The macrolides most used currently (azithromycin and clarithromycin) and their recommended dosage are described in <a class="elsevierStyleCrossRef" href="#tbl0015">Table 2</a>.<a class="elsevierStyleCrossRef" href="#bib0265"><span class="elsevierStyleSup">15</span></a> Erythromycin is clearly not used due to its adverse effects (mainly gastrointestinal) and complicated dosing regimen (every 6<span class="elsevierStyleHsp" style=""></span>h, 10–14 days), which limits its effectiveness.</p></span></span></span><span id="sec0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0065">Evolution and follow-up</span><p id="par0130" class="elsevierStylePara elsevierViewall">Once CAP has been diagnosed and treatment has started a clinical assessment by the paediatrician is recommended after 48<span class="elsevierStyleHsp" style=""></span>h. In non-complicated cases, 90% of patients are afebrile 48–72<span class="elsevierStyleHsp" style=""></span>h after starting antibiotic treatment, and do not need further blood tests or radiological follow-up.<a class="elsevierStyleCrossRef" href="#bib0205"><span class="elsevierStyleSup">3</span></a></p><p id="par0135" class="elsevierStylePara elsevierViewall">Only a small proportion need hospital admission. The management of therapeutic failure and the assessment of the hospital admission will be addressed in the second part of this document.</p></span><span id="sec0050" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0070">Preventive measures. Vaccines</span><p id="par0140" class="elsevierStylePara elsevierViewall">Vaccination against certain microorganisms has proven to have an impact on the incidence and mortality of CAP worldwide. The aetiological agents for which there are vaccines available are <span class="elsevierStyleItalic">S. pneumoniae</span>, <span class="elsevierStyleItalic">H. influenzae</span> type b and the flu virus.</p><span id="sec0055" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0075">Vaccination against <span class="elsevierStyleItalic">S. pneumoniae</span></span><p id="par0145" class="elsevierStylePara elsevierViewall">The release of the heptavalent conjugate vaccine led to a global reduction of invasive pneumococcal disease (IPD) in children, given its effect on nasopharyngeal colonisation by the serotypes included in the vaccine and, consequently, in its clinical forms.<a class="elsevierStyleCrossRef" href="#bib0305"><span class="elsevierStyleSup">23</span></a> However, incidence of IPD has increased in recent years, mainly complicated CAP especially in children over 2 years,<a class="elsevierStyleCrossRef" href="#bib0310"><span class="elsevierStyleSup">24</span></a> produced by serotypes not included in the vaccine.<a class="elsevierStyleCrossRef" href="#bib0305"><span class="elsevierStyleSup">23</span></a> In Spain, the most frequent are: 1, 19A, 7F, 3, 6A, 19F. Serotype 1 mainly affects children over 24 months of age and causes, in particular, bacterial pneumonia and pleural empyema. Serotypes 1, 19A and 3 caused 85% of pleural empyema of children in Spain, before the development of new vaccines, according to a study carried out by Laboratorio Español de Referencia de Neumococo del Instituto Carlos III.<a class="elsevierStyleCrossRef" href="#bib0315"><span class="elsevierStyleSup">25</span></a> Most serotypes noted are uniformly sensitive to penicillin, except serotype 19A, associated more frequently with resistance, including cephotaxime.</p><p id="par0150" class="elsevierStylePara elsevierViewall">Two conjugated antipneumococcal vaccines are currently authorised in children: decavalent vaccine (VNC10) (Synflorix<span class="elsevierStyleSup">®</span>, GSK), up to 5 years of age, and tridecavalent (VNC13) (Prevenar 13<span class="elsevierStyleSup">®</span>, Pfizer), authorised in children up to 17 years of age. Systematic antipneumococcal vaccination is still recommended by the Advisory Committee of Vaccines of the Spanish Paediatric Association in its annual immunisation report.<a class="elsevierStyleCrossRef" href="#bib0320"><span class="elsevierStyleSup">26</span></a></p><span id="sec0060" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0080">13-valent pneumococcal conjugate vaccine</span><p id="par0155" class="elsevierStylePara elsevierViewall">PCV13 has the 7 serotypes of the VNC7 and the following 6 additional serotypes: 1, 3, 5, 6A, 7F and 19A, and is approved for the prevention of CAP. Currently, PCV13 offers the widest coverage against pneumococcal disease worldwide,<a class="elsevierStyleCrossRef" href="#bib0305"><span class="elsevierStyleSup">23</span></a> including Spain,<a class="elsevierStyleCrossRefs" href="#bib0235"><span class="elsevierStyleSup">9,10,25</span></a> and therefore, it is recommended for all children under 5 years of age, both healthy and at risk for disease.<a class="elsevierStyleCrossRef" href="#bib0325"><span class="elsevierStyleSup">27</span></a></p><p id="par0160" class="elsevierStylePara elsevierViewall">In Madrid, as of July 2012, PCV13 is no longer subsidised, and therefore coverage has decreased to approximately 70%. Still, the data are very good so far, with a decrease in bacterial CAP (87%), pleural pneumococcal empyema (61%) and meningitis (72%), compared with 2007–2010.<a class="elsevierStyleCrossRef" href="#bib0235"><span class="elsevierStyleSup">9</span></a></p><p id="par0165" class="elsevierStylePara elsevierViewall">In the United Kingdom, one year after starting vaccination, PCV13 was shown to be effective against additional serotypes (1, 3, 5, 6A, 7F and 19A) in over 50% in children under 2 years of age.<a class="elsevierStyleCrossRef" href="#bib0330"><span class="elsevierStyleSup">28</span></a></p><p id="par0170" class="elsevierStylePara elsevierViewall">In France, where there has been systematic vaccination with PCV13 since 2010 (previously with PCV7) recent studies in children under 15 years of age have shown a 16% decrease in CAP overall, and 63% decrease in pneumococcal CAP. This is in addition to a 53% decrease in cases with pleural effusion.<a class="elsevierStyleCrossRef" href="#bib0335"><span class="elsevierStyleSup">29</span></a></p><p id="par0175" class="elsevierStylePara elsevierViewall">In the USA, with systematic vaccination with PCV13 since 2010 (previously with PCV7) a 50% overall reduction In IPD has been reported, and a 70% reduction in cases attributed to PCV13, while hospitalisation for CAP in children under 2 years of age fell by 65% in 2012.<a class="elsevierStyleCrossRefs" href="#bib0340"><span class="elsevierStyleSup">30,27</span></a></p><p id="par0180" class="elsevierStylePara elsevierViewall">In Latin America, several countries have published good results after the introduction of PCV13 in their vaccination calendars, including Argentina, with a 41% reduction in cases of CAP in children under 5 years old.<a class="elsevierStyleCrossRef" href="#bib0345"><span class="elsevierStyleSup">31</span></a> In Uruguay, hospitalisation for CAP in the under-14 age group has decreased by 78% overall, and by 92% in cases of pneumococcal origin.<a class="elsevierStyleCrossRef" href="#bib0350"><span class="elsevierStyleSup">32</span></a></p></span><span id="sec0065" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0085">10-valent pneumococcal conjugated vaccine</span><p id="par0185" class="elsevierStylePara elsevierViewall">PCV10 in addition to the serotypes contained in PCV7 incorporates another 3 serotypes: 1, 5 and 7F, and is approved for the prevention of CAP. In a randomised clinical trial (COMPAS study), carried out in approximately 24,000 infants in 3 Latin American countries, a 22% efficacy over typical CAP was reported (95% CI, 7.7–34.2).<a class="elsevierStyleCrossRef" href="#bib0355"><span class="elsevierStyleSup">33</span></a></p><p id="par0190" class="elsevierStylePara elsevierViewall">In Brazil, a country with low incidence of serotype 19A since the introduction of systematic vaccination with PCV10 there has been a 15% decrease in mortality from pneumonia in children under 24 months.<a class="elsevierStyleCrossRef" href="#bib0360"><span class="elsevierStyleSup">34</span></a></p></span><span id="sec0070" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0090">23-valent pneumococcal polysaccharide vaccine</span><p id="par0290" class="elsevierStylePara elsevierViewall">The 23-valent pneumococcal polysaccharide vaccine is still recommended in children over 2 years of age at risk for infection, although it probably has little impact on the prevention of CAP.</p></span></span><span id="sec0075" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0095">Vaccination against <span class="elsevierStyleItalic">H. influenzae</span> type b</span><p id="par0200" class="elsevierStylePara elsevierViewall">Since the introduction of the vaccine against Hib in the late 90s, there has been a drastic decrease of CAP caused by this microorganism. In some reports, a reduction of up to 30% of NACs has radiologically confirmed.<a class="elsevierStyleCrossRefs" href="#bib0365"><span class="elsevierStyleSup">35,36</span></a></p><p id="par0205" class="elsevierStylePara elsevierViewall">Since non-typifiable <span class="elsevierStyleItalic">H. influenzae</span> is a very infrequent cause of CAP in previously healthy children, the PCV10 vaccine (due to its non-typifiable Hi component) probably has little impact.</p></span></span><span id="sec0080" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0100">Flu vaccine</span><p id="par0210" class="elsevierStylePara elsevierViewall">The flu virus is a cause <span class="elsevierStyleItalic">per se</span> of CAP in the epidemic season. Also, in the cases of bacterial CAP co-infection with this virus is associated with a higher incidence of complicated forms,<a class="elsevierStyleCrossRef" href="#bib0375"><span class="elsevierStyleSup">37</span></a> especially in cases where <span class="elsevierStyleItalic">S. aureus</span> is isolated, or no micro-organism is isolated.</p><p id="par0215" class="elsevierStylePara elsevierViewall">According to current guidelines, the flu vaccine is recommended, for patients over 6 months of age with risk factors of complications, or for those living in the same household.<a class="elsevierStyleCrossRef" href="#bib0380"><span class="elsevierStyleSup">38</span></a> Currently, the trivalent inactivated vaccine, which can be administered intramuscularly, is usually used in children. Some countries, such as the USA and the United Kingdom, have introduced the intranasal live attenuated influenza vaccine for children over 2 years of age with no history of bronchialhyperresponsiveness or asthma. This formulation will probably be available in Spain in the 2015–2016 vaccination campaign.</p></span><span id="sec0085" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0105">Funding</span><p id="par0220" class="elsevierStylePara elsevierViewall">The authors declare they have not received any type of funding for this study.</p></span><span id="sec0090" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0110">Conflict of interests</span><p id="par0225" class="elsevierStylePara elsevierViewall">Conflict of interests of the authors as regards the document (in the last 5 years):<ul class="elsevierStyleList" id="lis0010"><li class="elsevierStyleListItem" id="lsti0020"><span class="elsevierStyleLabel">–</span><p id="par0230" class="elsevierStylePara elsevierViewall">DMP has collaborated in teaching activities funded by GlaxoSmithKline, Pfizer and Sanofi Pasteur MSD, as a researcher in a clinical study conducted by Novartis and as a consultant on the Advisory Board of Astra-Zeneca and Pfizer.</p></li><li class="elsevierStyleListItem" id="lsti0025"><span class="elsevierStyleLabel">–</span><p id="par0235" class="elsevierStylePara elsevierViewall">AAM presents no conflict of interests.</p></li><li class="elsevierStyleListItem" id="lsti0030"><span class="elsevierStyleLabel">–</span><p id="par0240" class="elsevierStylePara elsevierViewall">ATG has collaborated in research activities funded by Pfizer.</p></li><li class="elsevierStyleListItem" id="lsti0035"><span class="elsevierStyleLabel">–</span><p id="par0245" class="elsevierStylePara elsevierViewall">AEM has collaborated in teaching activities funded by Novartis, as a researcher in a multicentre study sponsored by GlaxoSmithKline and as a consultant in an Advisory Board of Gilead.</p></li><li class="elsevierStyleListItem" id="lsti0040"><span class="elsevierStyleLabel">–</span><p id="par0250" class="elsevierStylePara elsevierViewall">JFM has collaborated in teaching activities funded by Gilead and Abbvie.</p></li><li class="elsevierStyleListItem" id="lsti0045"><span class="elsevierStyleLabel">–</span><p id="par0255" class="elsevierStylePara elsevierViewall">JGG has collaborated in teaching activities funded by Pfizer and Sanofi Pasteur MSD.</p></li><li class="elsevierStyleListItem" id="lsti0050"><span class="elsevierStyleLabel">–</span><p id="par0260" class="elsevierStylePara elsevierViewall">AMG has participated as a consultant in the Advisory Board of Abbvie and Gilead, has received institutional investigation grants from Abbvie and grants to attend congresses organised by Abbvie, Actelion, Ferrer, GlaxoSmithKline and Novartis.</p></li><li class="elsevierStyleListItem" id="lsti0055"><span class="elsevierStyleLabel">–</span><p id="par0265" class="elsevierStylePara elsevierViewall">CRGL has collaborated in teaching activities funded by GlaxoSmithKline, Novartis, Pfizer and Sanofi Pasteur MSD, as a researcher in clinical trials conducted by GlaxoSmithKline and as a consultant on the Advisory Board of Astra-Zeneca, Novartis, GlaxoSmithKline and Pfizer.</p></li><li class="elsevierStyleListItem" id="lsti0060"><span class="elsevierStyleLabel">–</span><p id="par0270" class="elsevierStylePara elsevierViewall">JRC has collaborated in teaching activities funded by GlaxoSmithKline, Pfizer and Sanofi Pasteur MSD and as a researcher in clinical trials conducted by GlaxoSmithKline and Pfizer.</p></li><li class="elsevierStyleListItem" id="lsti0065"><span class="elsevierStyleLabel">–</span><p id="par0275" class="elsevierStylePara elsevierViewall">JSL has collaborated as a researcher in clinical trials conducted by GlaxoSmithKline and Roche.</p></li></ul></p></span></span>" "textoCompletoSecciones" => array:1 [ "secciones" => array:14 [ 0 => array:3 [ "identificador" => "xres597293" "titulo" => "Abstract" "secciones" => array:1 [ 0 => array:1 [ "identificador" => "abst0005" ] ] ] 1 => array:2 [ "identificador" => "xpalclavsec612014" "titulo" => "Keywords" ] 2 => array:3 [ "identificador" => "xres597292" "titulo" => "Resumen" "secciones" => array:1 [ 0 => array:1 [ "identificador" => "abst0010" ] ] ] 3 => array:2 [ "identificador" => "xpalclavsec612013" "titulo" => "Palabras clave" ] 4 => array:2 [ "identificador" => "sec0005" "titulo" => "Introduction" ] 5 => array:2 [ "identificador" => "sec0010" "titulo" => "Current status of resistances to antimicrobial drugs" ] 6 => array:2 [ "identificador" => "sec0015" "titulo" => "Adjuvant support treatment" ] 7 => array:3 [ "identificador" => "sec0020" "titulo" => "Ambulatory treatment of non-complicated CAP with antibiotics" "secciones" => array:2 [ 0 => array:2 [ "identificador" => "sec0025" "titulo" => "Indication for the use of antibiotics" ] 1 => array:3 [ "identificador" => "sec0030" "titulo" => "Selection of the antibiotic, route, dosage and duration" "secciones" => array:2 [ 0 => array:2 [ "identificador" => "sec0035" "titulo" => "Typical CAP" ] 1 => array:2 [ "identificador" => "sec0040" "titulo" => "Atypical CAP" ] ] ] ] ] 8 => array:2 [ "identificador" => "sec0045" "titulo" => "Evolution and follow-up" ] 9 => array:3 [ "identificador" => "sec0050" "titulo" => "Preventive measures. Vaccines" "secciones" => array:2 [ 0 => array:3 [ "identificador" => "sec0055" "titulo" => "Vaccination against S. pneumoniae" "secciones" => array:3 [ 0 => array:2 [ "identificador" => "sec0060" "titulo" => "13-valent pneumococcal conjugate vaccine" ] 1 => array:2 [ "identificador" => "sec0065" "titulo" => "10-valent pneumococcal conjugated vaccine" ] 2 => array:2 [ "identificador" => "sec0070" "titulo" => "23-valent pneumococcal polysaccharide vaccine" ] ] ] 1 => array:2 [ "identificador" => "sec0075" "titulo" => "Vaccination against H. influenzae type b" ] ] ] 10 => array:2 [ "identificador" => "sec0080" "titulo" => "Flu vaccine" ] 11 => array:2 [ "identificador" => "sec0085" "titulo" => "Funding" ] 12 => array:2 [ "identificador" => "sec0090" "titulo" => "Conflict of interests" ] 13 => array:1 [ "titulo" => "References" ] ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "fechaRecibido" => "2014-10-01" "fechaAceptado" => "2014-10-29" "PalabrasClave" => array:2 [ "en" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Keywords" "identificador" => "xpalclavsec612014" "palabras" => array:7 [ 0 => "Community acquired pneumonia" 1 => "Children" 2 => "Treatment" 3 => "Prevention" 4 => "<span class="elsevierStyleItalic">Streptococcus pneumoniae</span>" 5 => "Resistances" 6 => "Vaccines" ] ] ] "es" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Palabras clave" "identificador" => "xpalclavsec612013" "palabras" => array:7 [ 0 => "Neumonía adquirida en la comunidad" 1 => "Niños" 2 => "Tratamiento" 3 => "Prevención" 4 => "<span class="elsevierStyleItalic">Streptococcus pneumoniae</span>" 5 => "Resistencias" 6 => "Vacunas" ] ] ] ] "tieneResumen" => true "resumen" => array:2 [ "en" => array:2 [ "titulo" => "Abstract" "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">There have been significant changes in community acquired pneumonia (CAP) in children in the last decade. These changes are related to epidemiology and clinical presentation. Resistance to antibiotics is also a changing issue. These all have to be considered when treating Community acquired pneumonia (CAP). In this document, two of the main Spanish pediatric societies involved in the treatment of CAP in children, propose a consensus concerning therapeutic approach. These societies are the Spanish Society of Paediatric Infectious Diseases and the Spanish Society of Paediatric Chest Diseases. The Advisory Committee on Vaccines of the Spanish Association of Paediatrics (CAV-AEP) has also been involved in the prevention of CAP. An attempt is made to provide up-to-date guidelines to all paediatricians. The first part of the statement presents the approach to ambulatory, previously healthy children. We also review the prevention with currently available vaccines. In a second part, special situations and complicated forms will be addressed.</p></span>" ] "es" => array:2 [ "titulo" => "Resumen" "resumen" => "<span id="abst0010" class="elsevierStyleSection elsevierViewall"><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">La neumonía adquirida en la comunidad (NAC) en la edad pediátrica ha sufrido, en la última década, una serie de cambios epidemiológicos, clínicos, etiológicos y de resistencias a antibióticos, que obligan a replantear su abordaje terapéutico. En este documento, dos de las principales sociedades de especialidades pediátricas involucradas en el diagnóstico y tratamiento de esta entidad, como son la Sociedad Española de Infectología Pediátrica y la Sociedad Española de Neumología Pediátrica, así como el Comité Asesor de Vacunas de la AEP, proponen unas pautas consensuadas de tratamiento y prevención, con el fin de proporcionar a todos los pediatras una guía actualizada. En esta primera parte del consenso, se aborda el tratamiento de los pacientes sin enfermedades de base relevantes con NAC que no precisan ingreso hospitalario, así como la prevención global de esta patología con vacunas. En un siguiente documento se expondrá el abordaje terapéutico tanto de aquellos pacientes en situaciones especiales como de las formas complicadas de la enfermedad.</p></span>" ] ] "NotaPie" => array:2 [ 0 => array:2 [ "etiqueta" => "☆" "nota" => "<p class="elsevierStyleNotepara" id="npar0015">Please cite this article as: Moreno-Pérez D, Martín AA, García AT, Montaner AE, Mulet JF, García JJG, et al. Neumonía adquirida en la comunidad: tratamiento ambulatorio y prevención. An Pediatr (Barc). 2015;83:439.e1–439.e7.</p>" ] 1 => array:3 [ "etiqueta" => "1" "nota" => "<p class="elsevierStyleNotepara" id="npar0020">Los nombres de los componentes de las Sociedades están relacionados en el anexo.</p>" "identificador" => "fn0005" ] ] "apendice" => array:1 [ 0 => array:1 [ "seccion" => array:1 [ 0 => array:3 [ "apendice" => "<p id="par0295" class="elsevierStylePara elsevierViewall">The affiliation of the authors is as follows:<elsevierMultimedia ident="tbl0005"></elsevierMultimedia></p>" "etiqueta" => "Appendix" "identificador" => "sec0095" ] ] ] ] "multimedia" => array:3 [ 0 => array:7 [ "identificador" => "tbl0010" "etiqueta" => "Table 1" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:2 [ "leyenda" => "<p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Adapted from Pérez-Trallero et al.<a class="elsevierStyleCrossRef" href="#bib0230"><span class="elsevierStyleSup">8</span></a></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=""><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">Bacteria \t\t\t\t\t\t\n \t\t\t\t</th><th class="td" title="table-head " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">Type of antibiotics \t\t\t\t\t\t\n \t\t\t\t</th><th class="td" title="table-head " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">Percentage pf sensitive strains \t\t\t\t\t\t\n \t\t\t\t</th></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td" title="table-entry " align="left" valign="top"><span class="elsevierStyleItalic">Streptococcus pneumoniae</span>, in infections outside the central nervous system \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">β-Lactams \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Amoxicillin (at high doses): 98.8% \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="" valign="top"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="" valign="top"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Ampicillin: 93.4% \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="" valign="top"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="" valign="top"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Parenteral penicillin: 99.8% \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="" valign="top"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="" valign="top"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Cephotaxime: 99.6% \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="" valign="top"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="" valign="top"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Oral cefuroxime: 94.5% \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="" valign="top"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="" valign="top"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Parenteral cefuroxime: 99.3% \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="" valign="top"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Macrolides \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Erythromycin, clarithromycin, azithromycin: 75–79% \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="" valign="top"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Quinolones \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Levofloxacin: 97.7% \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="left" valign="top"><span class="elsevierStyleItalic">Haemophilus influenzae</span> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">β-Lactams \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Amoxicillin, ampicillin, penicillin: 85% \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="" valign="top"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Macrolides \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">100% \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="left" valign="top"><span class="elsevierStyleItalic">Streptococcus pyogenes</span> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">β-lactams \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">100% \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="" valign="top"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Macrolides \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Erythromycin, clarithromycin, azithromycin: 65% \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab976905.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Sensitivity of the main bacteria causing CAP in Spain (data from the SAUCE-4 study).</p>" ] ] 1 => array:7 [ "identificador" => "tbl0015" "etiqueta" => "Table 2" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:2 [ "tablatextoimagen" => array:2 [ 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" title="table-head " colspan="3" align="center" valign="top" scope="col" style="border-bottom: 2px solid black">Typical CAP (with suspected or confirmed aetiology)</th></tr><tr title="table-row"><th class="td" title="table-head " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">Name \t\t\t\t\t\t\n \t\t\t\t</th><th class="td" title="table-head " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">Posology \t\t\t\t\t\t\n \t\t\t\t</th><th class="td" title="table-head " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">Current duration \t\t\t\t\t\t\n \t\t\t\t</th></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td" title="table-entry " align="left" valign="top">Oral amoxicillin \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">80–90<span class="elsevierStyleHsp" style=""></span>mg/kg/day, divided into 3 doses (every 8<span class="elsevierStyleHsp" style=""></span>h)<a class="elsevierStyleCrossRef" href="#tblfn0005"><span class="elsevierStyleSup">a</span></a> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">7 days \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab976904.png" ] ] 1 => 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" title="table-head " colspan="3" align="center" valign="top" scope="col" style="border-bottom: 2px solid black">Atypical CAP with confirmed aetiology or high suspicion of <span class="elsevierStyleItalic">Mycoplasma</span> or <span class="elsevierStyleItalic">Chlamydia.</span> Most used macrolides</th></tr><tr title="table-row"><th class="td" title="table-head " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">Name \t\t\t\t\t\t\n \t\t\t\t</th><th class="td" title="table-head " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">Posology \t\t\t\t\t\t\n \t\t\t\t</th><th class="td" title="table-head " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">Duration \t\t\t\t\t\t\n \t\t\t\t</th></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td" title="table-entry " align="left" valign="top">Oral azithromycin \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">10<span class="elsevierStyleHsp" style=""></span>mg/kg every 24<span class="elsevierStyleHsp" style=""></span>h (maximum: 500<span class="elsevierStyleHsp" style=""></span>mg/day)<a class="elsevierStyleCrossRef" href="#tblfn0010"><span class="elsevierStyleSup">b</span></a> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">3 days \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="left" valign="top">Oral clarithromycin \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">15<span class="elsevierStyleHsp" style=""></span>mg/kg/day, every 12<span class="elsevierStyleHsp" style=""></span>h (maximum dose: 1<span class="elsevierStyleHsp" style=""></span>g/day) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">7 days \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab976903.png" ] ] ] "notaPie" => array:2 [ 0 => array:3 [ "identificador" => "tblfn0005" "etiqueta" => "a" "nota" => "<p class="elsevierStyleNotepara" id="npar0005">The maximum recommended dose for children is 2<span class="elsevierStyleHsp" style=""></span>g every 8<span class="elsevierStyleHsp" style=""></span>h (6<span class="elsevierStyleHsp" style=""></span>g/day), according to the data sheet.</p>" ] 1 => array:3 [ "identificador" => "tblfn0010" "etiqueta" => "b" "nota" => "<p class="elsevierStyleNotepara" id="npar0010">In the USA the same total dose is used, but distributed along a period of 5 days (first day 10<span class="elsevierStyleHsp" style=""></span>mg/kg; 5<span class="elsevierStyleHsp" style=""></span>mg/kg/24<span class="elsevierStyleHsp" style=""></span>h from days 2–5), because it is the posology approved by the FDA, but provides no advantage over the 3 days approved by the European Medication Agency (EMA).</p>" ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">Ambulatory antibiotic treatment for children with CAP who do not need hospitalisation.</p>" ] ] 2 => array:5 [ "identificador" => "tbl0005" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => false "mostrarDisplay" => true "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" title="table-entry " align="left" valign="top">Respiratory Infections Work Group. Spanish Society for Paediatric Infectious Diseases (SEIP in Spanish): \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>D Moreno-Pérez, J.J. García García, C Rodrigo Gonzalo de Lliria, J Ruiz Contreras and J Saavedra Lozano \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="left" valign="top">Spanish Society of Paediatric Pneumology (SENP in Spanish): \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>A Andrés Martín, A Escribano Montaner, J Figuerola Mulet, A Moreno-Galdó \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="left" valign="top">Advisory Committee of the Paediatric Spanish Association (CAV-AEP in Spanish): \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>D Moreno-Pérez, J Ruiz Contreras \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab976902.png" ] ] ] ] ] ] "bibliografia" => array:2 [ "titulo" => "References" "seccion" => array:1 [ 0 => array:2 [ "identificador" => "bibs0005" "bibliografiaReferencia" => array:38 [ 0 => array:3 [ "identificador" => "bib0195" "etiqueta" => "1" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "for the Severe Acute Lower Respiratory Infections Working Group. 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Year/Month | Html | Total | |
---|---|---|---|
2024 November | 24 | 10 | 34 |
2024 October | 118 | 61 | 179 |
2024 September | 111 | 38 | 149 |
2024 August | 118 | 64 | 182 |
2024 July | 100 | 35 | 135 |
2024 June | 110 | 41 | 151 |
2024 May | 119 | 47 | 166 |
2024 April | 107 | 38 | 145 |
2024 March | 107 | 41 | 148 |
2024 February | 108 | 33 | 141 |
2024 January | 108 | 25 | 133 |
2023 December | 116 | 21 | 137 |
2023 November | 92 | 38 | 130 |
2023 October | 97 | 63 | 160 |
2023 September | 76 | 30 | 106 |
2023 August | 67 | 17 | 84 |
2023 July | 85 | 27 | 112 |
2023 June | 74 | 31 | 105 |
2023 May | 86 | 28 | 114 |
2023 April | 71 | 23 | 94 |
2023 March | 142 | 35 | 177 |
2023 February | 79 | 21 | 100 |
2023 January | 81 | 19 | 100 |
2022 December | 85 | 28 | 113 |
2022 November | 132 | 50 | 182 |
2022 October | 70 | 39 | 109 |
2022 September | 54 | 33 | 87 |
2022 August | 81 | 91 | 172 |
2022 July | 95 | 77 | 172 |
2022 June | 98 | 45 | 143 |
2022 May | 111 | 55 | 166 |
2022 April | 96 | 49 | 145 |
2022 March | 118 | 58 | 176 |
2022 February | 206 | 51 | 257 |
2022 January | 144 | 39 | 183 |
2021 December | 102 | 55 | 157 |
2021 November | 99 | 56 | 155 |
2021 October | 109 | 47 | 156 |
2021 September | 86 | 42 | 128 |
2021 August | 54 | 44 | 98 |
2021 July | 61 | 34 | 95 |
2021 June | 62 | 44 | 106 |
2021 May | 63 | 31 | 94 |
2021 April | 199 | 82 | 281 |
2021 March | 106 | 59 | 165 |
2021 February | 72 | 25 | 97 |
2021 January | 89 | 25 | 114 |
2020 December | 66 | 53 | 119 |
2020 November | 47 | 25 | 72 |
2020 October | 53 | 15 | 68 |
2020 September | 44 | 28 | 72 |
2020 August | 28 | 25 | 53 |
2020 July | 29 | 26 | 55 |
2020 June | 63 | 19 | 82 |
2020 May | 61 | 31 | 92 |
2020 April | 74 | 24 | 98 |
2020 March | 47 | 26 | 73 |
2020 February | 33 | 30 | 63 |
2020 January | 61 | 17 | 78 |
2019 December | 44 | 31 | 75 |
2019 November | 44 | 17 | 61 |
2019 October | 49 | 23 | 72 |
2019 September | 44 | 22 | 66 |
2019 August | 49 | 26 | 75 |
2019 July | 34 | 36 | 70 |
2019 June | 64 | 38 | 102 |
2019 May | 104 | 27 | 131 |
2019 April | 112 | 56 | 168 |
2019 March | 61 | 35 | 96 |
2019 February | 79 | 36 | 115 |
2019 January | 53 | 24 | 77 |
2018 December | 62 | 37 | 99 |
2018 November | 164 | 40 | 204 |
2018 October | 530 | 71 | 601 |
2018 September | 94 | 24 | 118 |
2018 August | 4 | 0 | 4 |
2018 July | 1 | 0 | 1 |
2018 June | 6 | 0 | 6 |
2018 May | 9 | 0 | 9 |
2018 April | 35 | 0 | 35 |
2018 March | 39 | 0 | 39 |
2018 February | 17 | 0 | 17 |
2018 January | 23 | 0 | 23 |
2017 December | 32 | 0 | 32 |
2017 November | 35 | 0 | 35 |
2017 October | 22 | 0 | 22 |
2017 September | 27 | 0 | 27 |
2017 August | 23 | 0 | 23 |
2017 July | 34 | 1 | 35 |
2017 June | 25 | 13 | 38 |
2017 May | 39 | 13 | 52 |
2017 April | 35 | 17 | 52 |
2017 March | 30 | 6 | 36 |
2017 February | 32 | 15 | 47 |
2017 January | 16 | 9 | 25 |
2016 December | 21 | 13 | 34 |
2016 November | 29 | 14 | 43 |
2016 October | 58 | 13 | 71 |
2016 September | 53 | 19 | 72 |
2016 August | 44 | 12 | 56 |
2016 July | 27 | 6 | 33 |