<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>2182-5173</journal-id>
<journal-title><![CDATA[Revista Portuguesa de Medicina Geral e Familiar]]></journal-title>
<abbrev-journal-title><![CDATA[Rev Port Med Geral Fam]]></abbrev-journal-title>
<issn>2182-5173</issn>
<publisher>
<publisher-name><![CDATA[Associação Portuguesa de Medicina Geral e Familiar]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S2182-51732015000600006</article-id>
<title-group>
<article-title xml:lang="pt"><![CDATA[Erradicação do Helicobacter pylori: fim de linha para a terapêutica tripla standard?]]></article-title>
<article-title xml:lang="en"><![CDATA[Eradication of Helicobacter pylori: the end of the line for standard triple therapy?]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Silva]]></surname>
<given-names><![CDATA[António Assunção]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Macedo]]></surname>
<given-names><![CDATA[Rui]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Fernandes]]></surname>
<given-names><![CDATA[Dina Novais]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Sousa]]></surname>
<given-names><![CDATA[Luís]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Miranda]]></surname>
<given-names><![CDATA[Adriana]]></given-names>
</name>
<xref ref-type="aff" rid="A03"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,USF MaxiSaúde  ]]></institution>
<addr-line><![CDATA[Braga ]]></addr-line>
</aff>
<aff id="A02">
<institution><![CDATA[,USF +Carandá  ]]></institution>
<addr-line><![CDATA[Braga ]]></addr-line>
</aff>
<aff id="A03">
<institution><![CDATA[,USF Pró-Saúde  ]]></institution>
<addr-line><![CDATA[Vilaverde ]]></addr-line>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>12</month>
<year>2015</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>12</month>
<year>2015</year>
</pub-date>
<volume>31</volume>
<numero>6</numero>
<fpage>392</fpage>
<lpage>400</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_arttext&amp;pid=S2182-51732015000600006&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_abstract&amp;pid=S2182-51732015000600006&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_pdf&amp;pid=S2182-51732015000600006&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="pt"><p><![CDATA[Objetivo: Rever a evidência sobre a eficácia da terapêutica tripla (TT) e da terapêutica sequencial (TS) na erradicação da infeção por Helicobacter pylori (H. pylori). Fontes de Dados: MEDLINE e sítios de medicina baseada na evidência. Métodos: Pesquisa de normas de orientação clínica (NOC), revisões sistemáticas (RS), meta-análises (MA) e ensaios clínicos aleatorizados e controlados (EAC), publicados entre junho/2004 e junho/2014, utilizando os termos MeSH Helicobacter pylori, Drug therapy e Disease eradication. Para atribuição do nível de evidência (NE) e da força de recomendação (FR) foi utilizada a Strenght of Recomendation Taxonomy (SORT). Resultados: Foram selecionados 15 de entre 227 artigos encontrados: três NOC, oito MA, duas RS e dois ECA. As NOC recomendam a TT como principal tratamento a ser utilizado. As oito MA e as duas RS evidenciaram superioridade da TS na erradicação do H. pylori (variando entre 81-95,6%) comparativamente à TT (principalmente de 7-10 dias, consistentemente <80%). Os dois EAC obtiveram dados sobreponíveis às MA e RS. Conclusões: A TS apresenta uma eficácia superior comparativamente à TT e deve ser considerada, atualmente, como terapêutica de 1.ª linha na erradicação da infeção por H. pylori (FR A). Se comparada com a TT-14d, a TS convencional parece apresentar taxas de erradicação sobreponíveis embora, quando aumentada para 14 dias, a TS apresente superioridade terapêutica (FR B). Nas áreas de elevada resistência à claritromicina, metronidazol ou ambos, como é o caso de Portugal, aumenta a superioridade da TS face à TT (FR A).]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Objectives: To review the evidence for the effectiveness of triple therapy (TT) and sequential therapy (TS) in the eradication of Helicobacter pylori infection (H. pylori). Data sources: MEDLINE and evidence-based medicine websites. Methods: We conducted a search for clinical practice guidelines (CPG), systematic reviews (SR), meta-analyses (MA) and randomized clinical trials (RCT), published between June, 2004 and June, 2014, using the MeSH terms &#8216;Helicobacter pylori', &#8216;Drug therapy' and &#8216;Disease eradication'. The Strength of Recommendation Taxonomy (SORT) was used for the assignment of levels of evidence and the strength of recommendations. Results: A total of 15 articles were selected out of 227 articles found. These included 3 CPG, 8 MA, 2 RS and 2 RCT. The CPG recommend TT as the preferred treatment. The 8 MA and 2 RS showed the superiority of ST in the eradication of Helicobacter pylori (ranging from 81 to 95.6%) compared to the TT (for 7-10 days, consistently <80%). The 2 EAC had overlapping findings with the MA and RS. Conclusions: TS has superior efficacy compared to TT and should be considered as the first line of therapy for eradication of H. pylori infection (SOR A). When compared to TT for 14 days, conventional TS appears to have a similar rate of eradication. When given for more 14 days, TS is better than TT (SOR B). In areas of high resistance to clarithromycin, metronidazole or both, as in Portugal, TS is better than TT (SOR A).]]></p></abstract>
<kwd-group>
<kwd lng="pt"><![CDATA[Helicobacter pylori]]></kwd>
<kwd lng="pt"><![CDATA[Drug Therapy]]></kwd>
<kwd lng="pt"><![CDATA[Disease Eradication]]></kwd>
<kwd lng="en"><![CDATA[Helicobacter pylori]]></kwd>
<kwd lng="en"><![CDATA[Drug Therapy]]></kwd>
<kwd lng="en"><![CDATA[Disease Eradication]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p align="right"><b>REVIS&#213;ES</b></p>     <p><font size="4"><b>Erradica&#231;&#227;o do Helicobacter pylori: fim de linha para a terap&#234;utica tripla     standard?</b></font></p>     <p><font size="3"><b>Eradication   of Helicobacter pylori: the end of the line for standard triple therapy?</b></font></p>       <p><b>Ant&#243;nio Assun&#231;&#227;o Silva,<sup>1</sup> Rui     Macedo,<sup>2</sup> Dina Novais Fernandes,<sup>3</sup> Lu&#237;s Sousa,<sup>3</sup> Adriana Miranda<sup>4</sup></b></p>       <p><sup>1</sup>M&#233;dico     interno de Medicina Geral e Familiar. na USF MaxiSa&#250;de, Braga. </p>       <p><sup>2</sup>M&#233;dico     Especialista em Medicina Geral e Familiar e orientador de forma&#231;&#227;o na USF     MaxiSa&#250;de, Braga. </p>       <p><sup>3</sup>M&#233;dicos     internos de Medicina Geral e Familiar na USF +Carand&#225;, Braga. </p>       <p><sup>4</sup>M&#233;dica     interna de Medicina Geral e Familiar na USF Pr&#243;-Sa&#250;de, Vilaverde.</p>       <p><a href="#c0">Endere&ccedil;o para correspond&ecirc;ncia</a> | <a href="#c0">Direcci&oacute;n para correspondencia</a> | <a href="#c0">Correspondence</a><a name="topc0"></a></p> <hr/>     <p>&nbsp;</p>     ]]></body>
<body><![CDATA[<p><b>RESUMO</b></p>       <p><b>Objetivo:</b> Rever a evid&#234;ncia sobre a     efic&#225;cia da terap&#234;utica tripla (TT) e da terap&#234;utica sequencial (TS) na     erradica&#231;&#227;o da infe&#231;&#227;o por<i> Helicobacter     pylori (H. pylori).</i></p>       <p><b>Fontes de Dados:</b> MEDLINE e s&#237;tios de     medicina baseada na evid&#234;ncia. </p>       <p><b>M&#233;todos:</b> Pesquisa de normas de     orienta&#231;&#227;o cl&#237;nica (NOC), revis&#245;es sistem&#225;ticas (RS), meta-an&#225;lises (MA) e     ensaios cl&#237;nicos aleatorizados e controlados (EAC), publicados entre junho/2004     e junho/2014, utilizando os termos <i>MeSH     Helicobacter pylori, Drug therapy</i> e <i>Disease     eradication.</i> Para atribui&#231;&#227;o do n&#237;vel de evid&#234;ncia (NE) e da for&#231;a de     recomenda&#231;&#227;o (FR) foi utilizada a <i>Strenght     of Recomendation Taxonomy</i> (SORT). </p>       <p><b>Resultados:</b> Foram selecionados 15 de     entre 227 artigos encontrados: tr&#234;s NOC, oito MA, duas RS e dois ECA. As NOC     recomendam a TT como principal tratamento a ser utilizado. As oito MA e as duas     RS evidenciaram superioridade da TS na erradica&#231;&#227;o do <i>H. pylori</i> (variando entre 81-95,6%) comparativamente &#224; TT     (principalmente de 7-10 dias, consistentemente &lt;80%). Os dois EAC obtiveram     dados sobrepon&#237;veis &#224;s MA e RS. </p>       <p><b>Conclus&#245;es:</b> A TS apresenta uma efic&#225;cia     superior comparativamente &#224; TT e deve ser considerada, atualmente, como     terap&#234;utica de 1.<sup>a</sup> linha na erradica&#231;&#227;o da infe&#231;&#227;o por <i>H. pylori</i> (FR A). Se comparada com a TT-14d,     a TS convencional parece apresentar taxas de erradica&#231;&#227;o sobrepon&#237;veis embora,     quando aumentada para 14 dias, a TS apresente superioridade terap&#234;utica (FR B).     Nas &#225;reas de elevada resist&#234;ncia &#224; claritromicina, metronidazol ou ambos, como     &#233; o caso de Portugal, aumenta a superioridade da TS face &#224; TT (FR A). </p>       <p><b>Termos MeSH:</b> <i>Helicobacter pylori; </i>Drug Therapy; Disease Eradication.</p>   <hr/>     <p>&nbsp;</p>       <p><b>ABSTRACT</b></p>       <p><b>Objectives:</b> To review the evidence for     the effectiveness of triple therapy (TT) and sequential therapy (TS) in the     eradication of Helicobacter pylori infection (H. pylori).</p>       ]]></body>
<body><![CDATA[<p><b>Data sources:</b> MEDLINE and     evidence-based medicine websites. </p>       <p><b>Methods:</b> We conducted a search for     clinical practice guidelines (CPG), systematic reviews (SR), meta-analyses (MA)     and randomized clinical trials (RCT), published between June, 2004 and June,     2014, using the MeSH terms &#8216;Helicobacter pylori&#8217;, &#8216;Drug therapy&#8217; and &#8216;Disease     eradication&#8217;. The Strength of Recommendation Taxonomy (SORT) was used for the     assignment of levels of evidence and the strength of recommendations. </p>       <p><b>Results:</b> A total of 15 articles were     selected out of 227 articles found. These included 3 CPG, 8 MA, 2 RS and 2 RCT.     The CPG recommend TT as the preferred treatment. The 8 MA and 2 RS showed the     superiority of ST in the eradication of Helicobacter pylori (ranging from 81 to     95.6%) compared to the TT (for 7-10 days, consistently &lt;80%). The 2 EAC had     overlapping findings with the MA and RS.</p>       <p><b>Conclusions:</b> TS has superior efficacy     compared to TT and should be considered as the first line of therapy for     eradication of H. pylori infection (SOR A). When compared to TT for 14 days,     conventional TS appears to have a similar rate of eradication. When given for     more 14 days, TS is better than TT (SOR B). In areas of high resistance to     clarithromycin, metronidazole or both, as in Portugal, TS is better than TT     (SOR A).</p>       <p><b>Keywords:</b> Helicobacter pylori; Drug     Therapy; Disease Eradication.</p>   <hr/>     <p>&nbsp;</p>       <p><b>Introdu&#231;&#227;o</b></p>       <p>A infe&#231;&#227;o     por <i>Helicobacter pylori (H. pylori)</i> &#233;     certamente a mais comum a n&#237;vel global, prevendo-se que metade da popula&#231;&#227;o     mundial esteja infetada.<sup>1</sup> A sua tend&#234;ncia para causar doen&#231;a e morte     &#233; uma preocupa&#231;&#227;o ao n&#237;vel da sa&#250;de p&#250;blica em todo o mundo.<sup>1-2</sup> &#201; a     principal causa de gastrite cr&#243;nica, &#250;lcera p&#233;ptica, adenocarcinoma g&#225;strico e     linfoma MALT g&#225;strico.<sup>3</sup></p>       <p>O principal     objetivo terap&#234;utico na infe&#231;&#227;o por <i>H.     pylori</i> &#233; a sua erradica&#231;&#227;o completa. Por conseguinte, a efic&#225;cia do regime     terap&#234;utico deve ser o principal fator decisivo aquando da sua prescri&#231;&#227;o.<sup>1</sup> As principais <i>guidelines</i> ainda     recomendam a terap&#234;utica tripla (TT) convencional (inibidor da bomba de prot&#245;es     (IBP) + claritromicina + amoxicilina ou metronidazol, durante 7-14 dias) como     tratamento de 1.<sup>a</sup> linha.<sup>2,4-6</sup></p>       <p>No entanto,     a preval&#234;ncia da resist&#234;ncia deste agente patog&#233;nico &#224; claritromicina e ao     metronidazol aumentou substancialmente nos &#250;ltimos anos. J&#225; na d&#233;cada de 90,     num estudo realizado por Cabrita <i>et al.</i> verificou-se que, em Portugal, nomeadamente no distrito de Lisboa, as taxas de     resist&#234;ncia ao metronidazol e &#224; claritromicina eram de 30,6% e 19,0%,     respetivamente.<sup>7</sup> Um estudo mais recente, publicado em maio de 2012,     revelou uma taxa de resist&#234;ncia &#224; claritromicina de 31,3% em Portugal, sendo     este o 3.<sup>o</sup> maior valor da Europa, logo a seguir &#224; &#193;ustria e Hungria.<sup>8</sup></p>       ]]></body>
<body><![CDATA[<p>O aumento     das resist&#234;ncias conduziu, inevitavelmente, a uma diminui&#231;&#227;o da taxa de     erradica&#231;&#227;o do <i>H. pylori,</i> a qual     declinou para valores insatisfat&#243;rios em Portugal,<sup>9</sup> bem como na     maioria dos pa&#237;ses ocidentais,<sup>10</sup> encontrando-se agora, comummente,     abaixo dos 80%.<sup>8,11</sup> Nos EUA, as taxas de erradica&#231;&#227;o rondam os 75%;<sup>12-13</sup> na R&#250;ssia e na Mal&#225;sia os 60%;<sup>9</sup> e em Portugal, Alemanha, Isl&#226;ndia e     Turquia rondam os 50%.<sup>9</sup> Por este motivo &#233;, hoje, globalmente aceite     que novas estrat&#233;gias s&#227;o necess&#225;rias para o seu tratamento.<sup>2-3,11</sup></p>       <p>A     terap&#234;utica sequencial (TS) tem demonstrado resultados promissores     comparativamente com a TT,<sup>1-3,14-15</sup> quer em adultos quer em idade     pedi&#225;trica.<sup>2</sup> Na TS, os f&#225;rmacos efetivos contra a bact&#233;ria s&#227;o     utilizados numa combina&#231;&#227;o diferente, sendo o regime sequencial mais     frequentemente utilizado o que consta de IBP + amoxicilina nos primeiros cinco     dias, seguido de IBP + claritromicina + metronidazol ou tinidazol<sup>3,11,14,16</sup> ou amoxicilina<sup>1</sup> nos cinco dias seguintes.</p>       <p>Esta revis&#227;o     tem como objetivo rever a evid&#234;ncia dispon&#237;vel sobre a efic&#225;cia da TS na     erradica&#231;&#227;o do <i>H. pylori,</i> comparativamente com a TT convencional.</p>       <p><b>M&#233;todos</b></p>       <p>Foi     realizada uma pesquisa de normas de orienta&#231;&#227;o cl&#237;nica (NOC), ensaios cl&#237;nicos     aleatorizados e controlados (ECA), revis&#245;es sistem&#225;ticas (RS) e meta-an&#225;lises     (MA), publicados entre junho de 2004 e junho de 2014, em portugu&#234;s, ingl&#234;s e     espanhol, nas bases de dados da <i>National     Guideline Clearing House, Guidelines Finder, CMA Infobase, Cochrane Library,     DARE, Bandolier, Evidence Based Medicine Online, TRIP Database</i> e MEDLINE,     utilizando os termos MeSH: <i>Helicobacter     pylori, Drug therapy</i> e <i>Disease     eradication.</i> Os crit&#233;rios de inclus&#227;o dos artigos consistiram em: popula&#231;&#227;o     alvo constitu&#237;da por adultos ou crian&#231;as com diagn&#243;stico de infe&#231;&#227;o por <i>H. pylori</i> estabelecido por, pelo menos,     um de entre o exame histol&#243;gico, teste r&#225;pido da urease, teste respirat&#243;rio da     ureia ou pesquisa de antig&#233;nio fecal do <i>H.     pylori;</i> interven&#231;&#227;o terap&#234;utica com TS com dois per&#237;odos de tratamento; em     compara&#231;&#227;o com a TT convencional; e outcome baseado na taxa de efic&#225;cia da     erradica&#231;&#227;o do <i>H. pylori,</i> avaliada     por teste de confirma&#231;&#227;o. Foram utilizados como crit&#233;rios de exclus&#227;o: estudos     que inclu&#237;ssem doentes com fal&#234;ncia no tratamento pr&#233;vio para a erradica&#231;&#227;o do <i>H. pylori</i> ou a realizar outra     terap&#234;utica antibi&#243;tica concomitante; artigos duplicados; artigos de opini&#227;o;     artigos de revis&#227;o cl&#225;ssica de tema; e artigos discordantes com o objetivo da     revis&#227;o.</p>       <p>Para estratificar     o n&#237;vel de evid&#234;ncia (NE) dos estudos e a for&#231;a de recomenda&#231;&#227;o (FR) foi     utilizada a <i>Strenght of Recomendation     Taxonomy</i> (SORT), da <i>American Academy     of Family Physicians.</i><sup>17</sup></p>       <p><b>Resultados</b></p>       <p>A pesquisa     efetuada resultou na identifica&#231;&#227;o de 227 artigos e na sele&#231;&#227;o de 15 que     respeitavam todos os crit&#233;rios de inclus&#227;o e de exclus&#227;o: tr&#234;s NOC, dois ECA,     duas RS e oito MA. A <a href="#f1">Figura 1</a> representa o fluxograma da sele&#231;&#227;o dos estudos.</p>       <p>&nbsp;</p>    <p align="center"><a name="f1"></a><img src="/img/revistas/rpmgf/v31n6/31n6a06f1.jpg"/></p>    
]]></body>
<body><![CDATA[<p>&nbsp;</p>       <p>As     principais NOC atuais - de <i>Maastricht,</i><sup>4</sup> da <i>American College of Gastroenterology</i> (ACG)<sup>6</sup> e da <i>Asia-Pacific     guidelines</i><sup>5</sup> - recomendam a TT como principal tratamento a     ser utilizado, a n&#237;vel mundial, para a erradica&#231;&#227;o do <i>H. pylori</i> (<a href="#q1">Quadro I</a>). Esta consiste na associa&#231;&#227;o de IBP 2id +     claritromicina 500mg 2id + amoxicilina 1g 2id ou metronidazol 500mg 2id,     durante 7-14 dias. As duas primeiras NOC recomendam a TS como terap&#234;utica     alternativa, embora a de Maastricht restrinja essa indica&#231;&#227;o &#224;s &#225;reas com taxa     de resist&#234;ncia &#224; claritromicina superior a 15-20%, se os sais de bismuto para terap&#234;utica     qu&#225;drupla n&#227;o estiverem dispon&#237;veis (FR A).<sup>4</sup> Quer a <i>Asia-Pacific Guidelines</i> quer a ACG     relatam a necessidade de valida&#231;&#227;o da TS, atrav&#233;s de mais estudos     multic&#234;ntricos, randomizados e de boa qualidade antes de poderem recomendar a     TS como terap&#234;utica de 1.a linha na erradica&#231;&#227;o do <i>H. pylori</i> (FR C).<sup>5-6</sup></p>          <p>&nbsp;</p>    <p align="center"><a name="q1"></a><img src="/img/revistas/rpmgf/v31n6/31n6a06q1.jpg"/></p>    
<p>&nbsp;</p>       <p>Kim <i>et al.</i> realizaram, em 2014, uma MA     (<a href="#q2">Quadro II</a>) em que foram inclu&#237;dos nove ECA, todos asi&#225;ticos.<sup>3</sup> Nesta, a TS revelou-se superior &#224; TT de 7, 10 e 14 dias, embora sem     signific&#226;ncia estat&#237;stica no &#250;ltimo grupo (<i>p</i>=0,000, <i>p</i>=0,004 e <i>p</i>=0,148, respetivamente). A taxa de erradica&#231;&#227;o agrupada da TS por     an&#225;lise <i>Intention-to-treat</i> (ITT) e <i>Per Protocol</i> (PP) (81,3% e 87,6%) foi     superior &#224; da TT (70,8% e 77,1%), assim como o valor de <i>odds-ratio</i> <i>(OR)</i> na     an&#225;lise <i>ITT</i> e <i>PP</i> (1,768 e 1,997, respetivamente, ambos com <i>p</i>&lt;0,001). Em tr&#234;s dos estudos utilizou-se tinidazol e, nos     restantes, metronidazol como parte da TS revelando, ambos os esquemas,     superioridade face &#224; TT. N&#227;o se observaram diferen&#231;as entre as duas     terap&#234;uticas quanto aos efeitos laterais. Os autores conclu&#237;ram que a TS parece     ser superior &#224; TT, pelo que pode ser considerada uma op&#231;&#227;o como tratamento de     1.<sup>a</sup> linha.</p>       <p>&nbsp;</p>    <p align="center"><a name="q2"></a><img src="/img/revistas/rpmgf/v31n6/31n6a06q2.jpg"/></p>    
<p>&nbsp;</p>       <p>A MA de     Gatta <i>et al.,</i> publicada em 2013     (<a href="#q2">Quadro II</a>), incluiu 43 ECA, sendo que se comparou a efic&#225;cia da TS com a TT-7d     em 22 deles, com a TT-10d em 14 e com a TT-14d em sete estudos.<sup>11</sup> A     taxa de erradica&#231;&#227;o da TS foi superior &#224; TT-7d e TT-10d (risco relativo     (RR)=1,21 e 1,11, respetivamente), mas n&#227;o comparativamente com a TT-14d     (RR=0,99). Em dois dos estudos comparou-se a TS-10d com a TS-14d, n&#227;o tendo     sido constatada diferen&#231;a estatisticamente significativa entre ambos os     regimes. Nos indiv&#237;duos infetados por estirpes de <i>H. pylori</i> resistentes &#224; claritromicina e ao metronidazol, detetados     por testes de sensibilidade antimicrobiana pr&#233;-tratamento, a TS obteve melhores     taxas de erradica&#231;&#227;o, mas apenas em compara&#231;&#227;o com a TT de sete e de 10 dias. A     taxa de erradica&#231;&#227;o global com a TS foi de 84,3%, o que levou os autores a     concluir que as taxas de erradica&#231;&#227;o s&#227;o sub&#243;timas com qualquer dos regimes     terap&#234;uticos. N&#227;o se observaram diferen&#231;as entre as duas terap&#234;uticas quanto     aos efeitos laterais.</p>       ]]></body>
<body><![CDATA[<p>Outra MA de     Gatta <i>et al.,</i> de 2009, incluiu 10 ECA     envolvendo 3.006 adultos e tr&#234;s ECA envolvendo 260 crian&#231;as e adolescentes     (<a href="#q2">Quadro II</a>).<sup>2</sup> Do total dos estudos, 10 foram realizados em It&#225;lia e     os restantes na Rom&#233;nia, China e Coreia. Em ambos os grupos et&#225;rios, a TS foi     superior em rela&#231;&#227;o &#224; TT (adultos: <i>OR</i> agrupado=2,99; crian&#231;as e adolescentes: <i>OR</i> agrupado=1,98), apesar de, no grupo das crian&#231;as, o resultado estatisticamente     significativo ter sido alcan&#231;ado apenas na compara&#231;&#227;o com a TT-7d (12% mais     eficaz, com <i>p</i>=0,014). A taxa de     erradica&#231;&#227;o global ascendeu aos 91,0% nos adultos e a 90,7% nas crian&#231;as com a     TS, ficando pelos 75,7% e 82,9%, respetivamente, com a TT. Nos casos detetados     de infe&#231;&#227;o por estirpes de <i>H. pylori</i> resistentes &#224; claritromicina, a diferen&#231;a na efic&#225;cia da erradica&#231;&#227;o entre os     dois regimes dilatou-se, favorecendo a TS (83,3% <i>vs.</i> 25,9%, com OR=10,21).<sup>18-19</sup> Os autores conclu&#237;ram que     a TS &#233; uma terapia promissora, aparentemente superior &#224; TT na erradica&#231;&#227;o do <i>H. pylori.</i> Todavia, alegaram a     necessidade de mais estudos de elevada qualidade antes de poder ser recomendada     como terap&#234;utica de 1.<sup>a</sup> linha.</p>       <p>Na MA de     Yoon <i>et al.,</i> publicada em 2013     (<a href="#q2">Quadro II</a>), foram inclu&#237;dos 17 ECA, todos realizados em pa&#237;ses asi&#225;ticos.<sup>14</sup> A taxa de erradica&#231;&#227;o, por an&#225;lise <i>ITT,</i> foi significativamente superior na TS (81,8%) em compara&#231;&#227;o com a TT-7d     (74,3%), com um RR de 1,10 (<i>p</i>=0,0005).     N&#227;o obstante, essa superioridade n&#227;o se fez notar de forma estatisticamente     significativa em compara&#231;&#227;o com a TT-10d e TT-14d (<i>p</i>=0,11 e <i>p</i>=0,73,     respetivamente). O metronidazol fez parte da TS em nove dos estudos e o     tinidazol nos oito restantes. Ambos os regimes se mostraram superiores &#224; TT (RR     1,10; <i>p</i>=0,03 e RR 1,09; <i>p</i>=0,002, respetivamente). Os autores     conclu&#237;ram que a TS parece ser superior &#224; TT na erradica&#231;&#227;o da infe&#231;&#227;o por <i>H. pylori,</i> apesar de apresentar taxas de     efic&#225;cia aparentemente inferiores nos pa&#237;ses asi&#225;ticos. Os autores atribuem     esses resultados &#224; maior taxa de resist&#234;ncia concomitante &#224; claritromicina e     metronidazol presente nesses pa&#237;ses, em rela&#231;&#227;o a outros pa&#237;ses da Europa, onde     algumas MA pr&#233;vias obtiveram taxas de erradica&#231;&#227;o de 91,0-93,5%.<sup>2,15,20-21</sup></p>       <p>A MA de     Chung <i>et al.,</i> datada de 2013, incluiu     seis ECA, todos com popula&#231;&#227;o adulta da Coreia (<a href="#q2">Quadro II</a>).<sup>22</sup> As     taxas de erradica&#231;&#227;o agrupadas da TS (<i>ITT</i>=79,7%     e <i>PP</i>=86,4%) revelaram-se superiores     em rela&#231;&#227;o &#224; TT (<i>ITT</i>=68,1% e <i>PP</i>=76,0%). O valor do OR por an&#225;lise <i>ITT</i> e <i>PP</i> foi de 1,84 e 1,97, respetivamente, favorecendo a TS (<i>p</i>&lt;0,001). Os autores relataram tamb&#233;m     uma rela&#231;&#227;o custo-efic&#225;cia favor&#225;vel &#224; TS, uma vez que a claritromicina,     relativamente dispendiosa, &#233; usada durante menos tempo nesse regime. N&#227;o houve     diferen&#231;as significativas entre as duas terap&#234;uticas quanto aos efeitos     laterais. Estes resultados levaram os autores a concluir que a TS apresenta     taxas de erradica&#231;&#227;o superiores &#224;s da TT, embora inferiores ao esperado e que,     neste momento, &#233; a op&#231;&#227;o terap&#234;utica prefer&#237;vel. No entanto, consideram ser     necess&#225;rio o desenvolvimento de regimes terap&#234;uticos mais efetivos.</p>       <p>A MA de     Horvath, Dziechciarz e Szajewska, realizada em 2012, englobou 10 ECA,     envolvendo 857 crian&#231;as dos 3-18 anos (<a href="#q2">Quadro II</a>).<sup>23</sup> A TS apresentou     melhores taxas de erradica&#231;&#227;o do <i>H.     pylori</i> em compara&#231;&#227;o com a TT-7d (RR=1,17; <i>p</i>=0,0006). A TS melhorou moderadamente a taxa de erradica&#231;&#227;o (78% <i>vs.</i> 71%), sendo o NNT=15. N&#227;o houve     diferen&#231;as significativas quanto &#224; <i>compliance</i> (&#8805;95%) ou aos efeitos adversos entre ambos os regimes. Os autores     conclu&#237;ram que a TS pode ser considerada uma op&#231;&#227;o para aumentar a taxa de     erradica&#231;&#227;o na faixa et&#225;ria pedi&#225;trica, embora o seu benef&#237;cio n&#227;o seja t&#227;o     evidente como o &#233; na popula&#231;&#227;o adulta.</p>       <p>Na MA de     Jafri, Hornung e Howden,<sup>15</sup> publicada em 2008 (<a href="#q2">Quadro II</a>), foram     inclu&#237;dos 10 ECA, todos realizados em It&#225;lia, embora, em dois deles,<sup>18-19</sup> se tenham recrutado pacientes atrav&#233;s de um <i>site</i> americano. Um dos estudos debru&#231;ou-se somente sobre a popula&#231;&#227;o pedi&#225;trica<sup>24</sup> e outro utilizou ranitidina em substitui&#231;&#227;o do IBP.<sup>25</sup> Nenhum dos     estudos comparou a TS com a TT-14d. A taxa de erradica&#231;&#227;o global da TS alcan&#231;ou     o valor de 93,4%, enquanto a da TT registou 76,9% de efic&#225;cia (redu&#231;&#227;o do     RR=71% e redu&#231;&#227;o do Risco Absoluto (RA)=16%). A <i>compliance</i> foi semelhante em ambos os grupos (97,4% na TS e 96,8%     na TT), assim como a taxa de efeitos laterais. A TS foi superior &#224; TT em todos     os subgrupos analisados, nomeadamente presen&#231;a de h&#225;bitos tab&#225;gicos, doen&#231;a     ulcerosa ou dispepsia n&#227;o ulcerosa, resist&#234;ncia &#224; claritromicina, imidaz&#243;is ou     ambos, dura&#231;&#227;o da TT, entre outros, levando os autores a concluir que a TS &#233;     superior em rela&#231;&#227;o &#224; TT de 7-10 dias na erradica&#231;&#227;o da infe&#231;&#227;o por <i>H. pylori.</i> Os autores alegaram     igualmente que, a confirmar a superioridade da TS em rela&#231;&#227;o &#224; TT em futuros     ECA de boa qualidade, inclusivamente comparando com a TT-14d (amplamente     utilizada nos EUA), a TS pode ser considerada o tratamento <i>standard</i> na erradica&#231;&#227;o do <i>H.     pylori.</i></p>       <p>A MA de Tong <i>et al.,</i> de 2009 (<a href="#q2">Quadro II</a>),     incorporou 11 ECA, dos quais sete compararam a efic&#225;cia da TS com a TT-7d, dois     com a TT-10d e outros dois com ambas as dura&#231;&#245;es de TT.20 A TS foi associada a     uma taxa de erradica&#231;&#227;o do <i>H. pylori</i> superior &#224; TT-7d (93,5% <i>vs.</i> 76,1%;     RR=1,23) e &#224; TT-10d (92,4% <i>vs.</i> 79,2%;     RR=1,16). A TS foi igualmente mais eficaz do que a TT nos doentes com dispepsia     com &#250;lcera p&#233;ptica ou sem &#250;lcera p&#233;ptica (RR=1,24 e RR=1,26, respetivamente). A     superioridade da TS tornou-se ainda mais evidente em indiv&#237;duos resistentes &#224;     claritromicina (RR=2,01) ou metronidazol (RR=2,07). N&#227;o foram observadas     diferen&#231;as significativas quanto aos efeitos colaterais. Os autores conclu&#237;ram     que a TS &#233; um regime terap&#234;utico promissor para a erradica&#231;&#227;o do <i>H. pylori.</i> Tamb&#233;m nesta MA os autores     sugerem a realiza&#231;&#227;o futura de mais ECA de boa qualidade, comparando     diretamente TS com a TT-14d, de modo a averiguar qual dever&#225; ser, de facto, o     regime terap&#234;utico de 1.<sup>a</sup> linha.</p>       <p>A RS de     Zullo <i>et al.,</i> realizada em 2012     (<a href="#q3">Quadro III</a>), englobou 21 ECA, sendo um dos crit&#233;rios de inclus&#227;o neste estudo     a avalia&#231;&#227;o de um padr&#227;o modificado de TS, em compara&#231;&#227;o com a TT e TS     convencionais.<sup>26</sup> O esquema modificado mais frequentemente utilizado     inclu&#237;a 7d + 7d de um regime contendo tetraciclina, alcan&#231;ando taxas de     erradica&#231;&#227;o de 73,3%, superiores aos 63,6% da TT-14d. A taxa de erradica&#231;&#227;o dos     esquemas de TS modificada contendo levofloxacina 250mg ou 500mg, 2id (&gt;95%)     revelou-se superior, quer em compara&#231;&#227;o com a TS convencional contendo     claritromicina (80,8%) quer com a TT convencional (71,7%). Um dos estudos     constatou uma superioridade not&#243;ria entre o esquema modificado, de 14 dias,     contendo levofloxacina em rela&#231;&#227;o &#224; TT-14d (86,6% <i>vs.</i> 45,3%).<sup>27</sup> Os restantes esquemas modificados n&#227;o     alcan&#231;aram taxas de erradica&#231;&#227;o aceit&#225;veis. Os autores conclu&#237;ram que, tanto a     TS modificada contendo levofloxacina como a TS modificada contendo     tetraciclina, parecem ser mais efetivas na erradica&#231;&#227;o do <i>H. pylori</i> quando comparadas com a TT <i>standard.</i> No entanto, os autores alertam para o facto de a     tetraciclina necessitar de ser administrada quatro vezes por dia neste esquema,     podendo limitar a <i>compliance</i> do     doente.</p>       <p>&nbsp;</p>    <p align="center"><a name="q3"></a><img src="/img/revistas/rpmgf/v31n6/31n6a06q3.jpg"/></p>    
<p>&nbsp;</p>       ]]></body>
<body><![CDATA[<p>A outra     revis&#227;o, de Kate <i>et al.,</i> realizada em     2013 (<a href="#q3">Quadro III</a>), incluiu 17 ECA, dos quais 12 reportaram melhores taxas de     erradica&#231;&#227;o com a TS, um evidenciou melhores resultados com a TT e quatro n&#227;o     encontraram diferen&#231;as entre os dois regimes.<sup>1</sup> O maior ECA realizado     na Am&#233;rica Latina (<i>n</i>=974) foi um     desses quatro estudos.<sup>28</sup> Na Europa foram realizados tr&#234;s estudos que     constataram superioridade da TS em rela&#231;&#227;o &#224; TT, embora de forma     estatisticamente significativa em apenas dois.<sup>29-30</sup> Tr&#234;s ECA     compararam a efic&#225;cia de ambas as terap&#234;uticas em idade pedi&#225;trica<sup>30-32</sup> e dois deles reportaram melhores taxas de erradica&#231;&#227;o com a TS, enquanto o     outro ECA n&#227;o demonstrou diferen&#231;as entre os regimes. Tamb&#233;m em tr&#234;s estudos se     efetuou uma an&#225;lise de custos e, em todos, se demonstrou que a TS-10d era mais     econ&#243;mica que a TT-10d.<sup>27,33-34</sup> Quatro estudos compararam regimes de     TS modificada-14d (dois contendo tetraciclina e dois contendo levofloxacina)     com TT-14d e em todos se verificou superioridade estatisticamente significativa     dos regimes de TS modificada-14d (<i>p</i>&lt;0,01).     N&#227;o houve diferen&#231;as significativas em rela&#231;&#227;o aos efeitos adversos, &#224; exce&#231;&#227;o     de um artigo.<sup>35</sup> Os autores conclu&#237;ram que a TS apresenta uma boa     efic&#225;cia, aparenta ser mais econ&#243;mica e n&#227;o condiciona um aumento nos efeitos     adversos em rela&#231;&#227;o &#224; TT.</p>       <p>Relativamente     aos ensaios cl&#237;nicos, o de Liou <i>et al.,</i> de 2013 (<a href="#q4">Quadro IV</a>), publicado na <i>Lancet,</i> englobou 900 pacientes, com mais de 20 anos e com diagn&#243;stico documentado de     infe&#231;&#227;o por<i> H. pylori</i> (sem tratamento     pr&#233;vio), de seis diferentes cl&#237;nicas de gastroenterologia tailandesas.<sup>36</sup> As op&#231;&#245;es terap&#234;uticas testadas consistiram em TS-10d e TS-14d (lansoprazol     30mg + amoxilina 1g na 1.<sup>a</sup> metade do esquema e lansoprazol 30mg +     claritromicina 500mg + metronidazol 500mg na 2.<sup>a</sup> metade do esquema,     todos duas vezes por dia) e TT-14d (lansoprazol 30mg + amoxicilina 1g +     claritromicina 500mg, todos duas vezes por dia). As taxas de erradica&#231;&#227;o foram     de 90,7% para a TS-14d, 87% na TS-10d e de 82,3% na TT-14d. A TS-14d revelou-se     superior &#224; TT-14, quer pela an&#225;lise<i> ITT</i> (NNT=12; p=0,003) quer pela an&#225;lise <i>PP</i> (NNT=13,7; <i>p</i>=0,003). N&#227;o se     observaram diferen&#231;as quanto aos efeitos adversos ou &#224; <i>compliance</i> entre os tr&#234;s grupos. Os resultados obtidos levaram os     autores a concluir que a TS-14d &#233; superior &#224; TT-14d e deve ser recomendada como     terap&#234;utica de 1.<sup>a</sup> linha na erradica&#231;&#227;o do <i>H. pylori.</i> De acordo com os crit&#233;rios da escala SORT trata-se de um     ECA de elevada qualidade, pelo que se atribui um NE 1.</p>        <p>&nbsp;</p>    <p align="center"><a name="q4"></a><img src="/img/revistas/rpmgf/v31n6/31n6a06q4.jpg"/></p>    
<p>&nbsp;</p>       <p>O outro ECA,     de Seddik <i>et al.,</i> levado a cabo em     2013 (<a href="#q4">Quadro IV</a>), envolveu 281 pacientes com infe&#231;&#227;o documentada por <i>H. pylori,</i> de um &#250;nico centro hospitalar     de Marrocos.<sup>37</sup> Os pacientes foram randomizados para receber TS     (omeprazol 20mg + amoxicilina 1g nos primeiros cinco dias, seguido de omeprazol     20mg + claritromicina 500mg + tinidazol 500mg nos cinco dias subsequentes,     todos duas vezes por dia) ou TT (omeprazol 20mg + amoxicilina 1g +     claritromicina 500mg, durante sete dias, todos duas vezes por dia). A taxa de     erradica&#231;&#227;o, por an&#225;lise <i>ITT</i> e <i>PP,</i> da TS (82,9% e 89,9%,     respetivamente) demonstrou ser superior &#224; TT (65,9% e 71%, respetivamente).     Esta diferen&#231;a foi estatisticamente significativa (<i>p</i>&#706;0,001), o     que levou os autores a concluir que a TS-10d &#233; mais efetiva que a TT na     erradica&#231;&#227;o do <i>H. pylori,</i> sendo     igualmente tolerada. De acordo com os crit&#233;rios da escala SORT trata-se de um     ECA de qualidade limitada, pelo que se atribui um NE 2.</p>       <p><b>Conclus&#245;es</b></p>       <p>Esta revis&#227;o     compreende um elevado n&#250;mero de estudos, a maioria de boa qualidade e com     resultados consistentes, proporcionando robustez &#224;s conclus&#245;es retiradas pelos     autores deste trabalho.</p>       <p>De acordo     com a evid&#234;ncia dispon&#237;vel pode concluir-se que a TS &#233; mais eficaz em     compara&#231;&#227;o com a TT, sendo sobrepon&#237;vel em rela&#231;&#227;o &#224; <i>compliance</i> ou ocorr&#234;ncia de efeitos adversos, devendo ser     considerada atualmente como terap&#234;utica de 1.<sup>a</sup> linha na erradica&#231;&#227;o     do <i>H. pylori</i> (FR A).</p>       <p>Os estudos     inclu&#237;dos nesta revis&#227;o demonstraram que a TS &#233; superior em rela&#231;&#227;o &#224; TT-7d e,     somente em dois, n&#227;o se comprovou o mesmo em rela&#231;&#227;o &#224; TT-10d. Quando comparada     com a TT-14d, os resultados foram maioritariamente sobrepon&#237;veis. Estes     resultados podem sugerir que o aumento da dura&#231;&#227;o da TT para 14 dias seja     suficiente para se alcan&#231;ar a mesma taxa de sucesso obtida com a TS de 7-10     dias<sup>3</sup> embora os regimes de 14 dias da TS (7+7) apresentem     superioridade terap&#234;utica (FR B). N&#227;o obstante, o n&#250;mero de estudos a comparar     a TS com a TT-14d &#233; reduzido, pelo que n&#227;o &#233; poss&#237;vel tirar conclus&#245;es s&#243;lidas     a este respeito. O prolongamento da TT para 14 dias abre, todavia, espa&#231;o &#224;     discuss&#227;o de uma nova variante: a econ&#243;mica. O custo do tratamento &#233; um     importante fator a determinar o sucesso terap&#234;utico, principalmente nos pa&#237;ses     em desenvolvimento.<sup>1</sup> A TS revelou-se mais econ&#243;mica nos estudos em     que foi realizada uma an&#225;lise de custos.<sup>33-34</sup> Uma vez que a     claritromicina &#233; o componente de custo mais elevado de entre os utilizados para     erradica&#231;&#227;o do <i>H. pylori,</i><sup>1</sup> a redu&#231;&#227;o da sua dose total presente na TS (cinco dias, 2id) &#233; outro fator a     favorecer este regime, em compara&#231;&#227;o com a TT (7, 10 ou 14 dias, 2id). N&#227;o     obstante, em termos econ&#243;micos latos, n&#227;o podem ser retiradas ila&#231;&#245;es firmes,     uma vez que os custos dependem tamb&#233;m da taxa de sucesso/insucesso dos     diferentes regimes e esse fator n&#227;o foi contabilizado nestes estudos.</p>       ]]></body>
<body><![CDATA[<p>As     principais NOC atuais - Maastricht IV, <i>Asia-Pacific Guidelines</i> e ACG - para a erradica&#231;&#227;o do <i>H. pylori</i> ainda recomendam a TT como     terap&#234;utica de 1.<sup>a</sup> linha a n&#237;vel mundial. Todavia, &#233; importante     ressalvar que as &#250;ltimas atualiza&#231;&#245;es das mesmas datam de 2012, 2009 e 2007,     respetivamente. Nas NOC de <i>Maastricht </i>e     da ACG, a TS &#233; recomendada como terap&#234;utica alternativa, embora no primeiro     caso essa indica&#231;&#227;o esteja restringida &#224;s &#225;reas com taxas de resist&#234;ncia &#224;     claritromicina superior a 15-20%, como &#233; o caso de Portugal. Quer a <i>Asia-Pacific Guidelines</i> quer a ACG     relataram a necessidade de valida&#231;&#227;o da TS, atrav&#233;s de mais estudos     multic&#234;ntricos, randomizados e de boa qualidade, antes de poderem recomendar a     TS como terap&#234;utica de 1.<sup>a</sup> linha na erradica&#231;&#227;o do <i>H. pylori.</i> Entretanto, como reportado     neste artigo, muitos ECA foram desenvolvidos desde essa altura, relatando taxas     de erradica&#231;&#227;o da TS superiores &#224; TT tradicional, o que poder&#225; justificar uma     futura revis&#227;o das recomenda&#231;&#245;es pelos peritos.</p>       <p>Pelos dados     obtidos por esta revis&#227;o, os autores real&#231;am ainda dois pontos: o da evid&#234;ncia     de superioridade da TS ser, aparentemente, maior quando se estudam popula&#231;&#245;es     em idade adulta e o facto de ser nas &#225;reas de elevada resist&#234;ncia &#224;     claritromicina, metronidazol ou ambos, como &#233; o caso de Portugal, que a     superioridade da TS se demarca notavelmente face &#224; TT (FR A).<sup>2,11,15,20</sup></p>       <p>N&#227;o     obstante, as taxas de erradica&#231;&#227;o de todos os regimes relatados s&#227;o sub&#243;timas,     uma vez que n&#227;o alcan&#231;am sistematicamente valores de efic&#225;cia aconselh&#225;veis     (&gt;90%) para doen&#231;as infeciosas.<sup>3,10,38</sup> A procura constante por     regimes terap&#234;uticos mais efetivos ou por novos agentes para erradicar o <i>H. pylori</i> deve continuar. Tendo em conta     que a resist&#234;ncia prim&#225;ria aos antibi&#243;ticos se assume como a principal causa de     fal&#234;ncia terap&#234;utica,<sup>39</sup> a escolha do regime terap&#234;utico dever&#225; ser     sempre baseada no conhecimento do padr&#227;o de resist&#234;ncia local, o qual necessita     de ser permanentemente monitorizado.<sup>11</sup> Novos regimes de terap&#234;utica     sequencial, modificada com levofloxacina ou tetraciclinas, t&#234;m sido testados,     geralmente com sucesso, inclusivamente em compara&#231;&#227;o com a TT de 14 dias.<sup>26</sup> No entanto, os estudos que testam esses regimes diferentes de TS s&#227;o escassos     e, portanto, n&#227;o &#233; poss&#237;vel, para j&#225;, tecer recomenda&#231;&#245;es validadas.</p>       <p>Mais estudos     de boa qualidade s&#227;o necess&#225;rios para avaliar qual o regime terap&#234;utico mais     vantajoso e se o principal fator de sucesso terap&#234;utico est&#225; no regime ou na     dura&#231;&#227;o da terap&#234;utica. </p>       <p>&nbsp;</p>       <p><b>REFER&#202;NCIAS     BIBLIOGR&#193;FICAS</b></p>       <!-- ref --><p>1. Kate V,     Kalayarasan R, Ananthakrishnan N. Sequential therapy versus standard     triple-drug therapy for Helicobacter pylori eradication: a systematic review of     recent evidence. Drugs. 2013;73(8):815-24.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1358374&pid=S2182-5173201500060000600001&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --> </p>       <!-- ref --><p>2. Gatta L,     Vakil N, Leandro G, Di Mario F, Vaira D. Sequential therapy or triple therapy     for Helicobacter pylori infection: systematic review and meta-analysis of     randomized controlled trials in adults and children. Am J Gastroenterol.     2009;104(12):3069-79.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1358376&pid=S2182-5173201500060000600002&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>       ]]></body>
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<body><![CDATA[<!-- ref --><p>38. Vakil N,     Megraud F. Eradication therapy for Helicobacter pylori. Gastroenterology.     2007;133(3):985-1001.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1358448&pid=S2182-5173201500060000600038&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>       <!-- ref --><p>39. Hopkins     RJ. In search of the Holy Grail of Heliocobacter pylori remedies. Helicobacter.     2001;6(2):81-3.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1358450&pid=S2182-5173201500060000600039&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <p>&nbsp;</p>     <p><a href="#topc0">Endere&ccedil;o para correspond&ecirc;ncia</a> | <a href="#topc0">Direcci&oacute;n para correspondencia</a> | <a href="#topc0">Correspondence</a><a name="c0"></a></p>        <p>Ant&#243;nio     Assun&#231;&#227;o Silva </p>      <p>E-mail: <a href="mailto:alpasilva18@gmail.com">alpasilva18@gmail.com</a></p>       <p>&nbsp;</p>       <p><b>Agradecimentos</b></p>       ]]></body>
<body><![CDATA[<p>&#192; Dr&#170; M&#243;nica     Oleastro, do Departamento de Doen&#231;as Infecciosas do Instituto Nacional de Sa&#250;de     Dr. Ricardo Jorge, pelo contributo importante e cordialidade na ced&#234;ncia de     artigos e dados estat&#237;sticos sobre o tema.</p>       <p><b>Conflito   de interesses</b></p>       <p>Os autores     declaram n&#227;o ter conflitos de interesses.</p>       <p>&nbsp;</p>       <p><b>Recebido em 16-06-2015</b></p>       <p><b>Aceite para publica&#231;&#227;o em 22-11-2015</b></p>       <p><i>Artigo escrito ao abrigo do novo acordo     ortogr&#225;fico.</i></p>      ]]></body><back>
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