<?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>0034-8910</journal-id>
<journal-title><![CDATA[Revista de Saúde Pública]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. Saúde Pública]]></abbrev-journal-title>
<issn>0034-8910</issn>
<publisher>
<publisher-name><![CDATA[Faculdade de Saúde Pública da Universidade de São Paulo]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0034-89102009000400017</article-id>
<article-id pub-id-type="doi">10.1590/S0034-89102009005000038</article-id>
<title-group>
<article-title xml:lang="pt"><![CDATA[Suplementação com vitamina A no puerpério: revisão sistemática]]></article-title>
<article-title xml:lang="en"><![CDATA[Vitamin A supplementation during puerperium: systematic review]]></article-title>
<article-title xml:lang="es"><![CDATA[Suplementación con vitamina A en el puerperio: revisión sistemática]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Caminha]]></surname>
<given-names><![CDATA[Maria de Fátima Costa]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Batista Filho]]></surname>
<given-names><![CDATA[Malaquias]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Fernandes]]></surname>
<given-names><![CDATA[Taciana Fernanda dos Santos]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Arruda]]></surname>
<given-names><![CDATA[Ilma Kruze Grande de]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Diniz]]></surname>
<given-names><![CDATA[Alcides da Silva]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Instituto de Medicina Integral Prof. Fernando Figueira  ]]></institution>
<addr-line><![CDATA[Recife PE]]></addr-line>
<country>Brasil</country>
</aff>
<aff id="A02">
<institution><![CDATA[,Universidade Federal de Pernambuco  ]]></institution>
<addr-line><![CDATA[Recife PE]]></addr-line>
<country>Brasil</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>08</month>
<year>2009</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>08</month>
<year>2009</year>
</pub-date>
<volume>43</volume>
<numero>4</numero>
<fpage>699</fpage>
<lpage>706</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielosp.org/scielo.php?script=sci_arttext&amp;pid=S0034-89102009000400017&amp;lng=en&amp;nrm=iso&amp;tlng=en"></self-uri><self-uri xlink:href="http://www.scielosp.org/scielo.php?script=sci_abstract&amp;pid=S0034-89102009000400017&amp;lng=en&amp;nrm=iso&amp;tlng=en"></self-uri><self-uri xlink:href="http://www.scielosp.org/scielo.php?script=sci_pdf&amp;pid=S0034-89102009000400017&amp;lng=en&amp;nrm=iso&amp;tlng=en"></self-uri><abstract abstract-type="short" xml:lang="pt"><p><![CDATA[Realizou-se revisão sistemática de estudos avaliativos da aplicação de megadoses de vitamina A nas concentrações de retinol no sangue e no leite maternos como medida de curto prazo para a prevenção de hipovitaminose A. Com base na estratégia do Centro Cochrane do Brasil para ensaios clínicos aleatórios foram identificadas 115 publicações no PubMed, entre as quais, por um conjunto de critérios de inclusão/exclusão, foram selecionados 14 artigos publicados entre 1993 a 2007. O efeito das intervenções com três esquemas posológicos (200.000, 300.000 e 400.000 UI) de vitamina A foram analisados. Dos 11 experimentos realizados em leite materno, nove apresentaram elevação dos níveis de retinol em comparação com o grupo controle; dos nove que avaliaram sangue materno, quatro mostraram elevação após tempos variados de aplicação de megadoses de vitamina A. Conclui-se que a administração de vitamina A em elevadas doses foi positiva em 82% dos ensaios com leite materno, mas menos notáveis em comparação ao sangue materno. Não foram observadas diferenças significativas quanto à posologia aplicada.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[A systematic review on studies evaluating the effect of applying megadoses of vitamin A on the retinol concentrations in maternal milk and blood, as a short-term measure for preventing hypovitaminosis A, was conducted. Based on the strategy of the Brazilian Cochrane Center for randomized trials, 115 published papers were identified in PubMed. From these, through a set of inclusion/exclusion criteria, 14 articles published between 1993 and 2007 were selected. The effects of interventions with three posological regimens (200,000, 300,000 and 400,000 IU) of vitamin A were analyzed. Out of 11 experiments conducted on maternal milk, nine presented elevation of the retinol levels in comparison with the control group; out of nine that evaluated maternal blood, four showed elevation at varying times after applying megadoses of vitamin A. It was concluded that the results from administration of vitamin A at high doses were positive in 82% of the trials on maternal milk, but less notable in relation to maternal blood. No significant differences regarding the posological regimens applied were observed.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[Se realizó revisión sistemática de estudios evaluativos de la aplicación de megadosis de vitamina A en las concentraciones de retinol en la sangre y en la leche maternos como medida de corto plazo para la prevención de hipovitaminosis A. Con base en la estratégia del Centro Cochrane de Brasil para ensayos clínicos aleatorios fueron identificadas 115 publicaciones en el PubMed, entre las cuales, por un conjunto de criterios de inclusión/exclusión, fueron seleccionados 14 artículos publicados entre 1993 a 2007. El efecto de las intervenciones con tres esquemas posológicos (200.000. 300.000 y 400.000 UI) de vitamina A fueron analizados. De los 11 experimentos realizados en leche materna, nueve presentaron elevación de los niveles de retinol en comparación con el grupo control; de los nueve que evaluaron sangre materna, cuatro mostraron elevación posterior a tiempos variados de aplicación de megadosis de vitamina A. Se concluye que la administración de vitamina A en elevadas dosis fue positiva en 82% de los ensayos con leche materna, pero menos notables en comparación a la sangre materna. No fueron observadas diferencias significativas con relación a la posología aplicada.]]></p></abstract>
<kwd-group>
<kwd lng="pt"><![CDATA[Deficiência de Vitamina A]]></kwd>
<kwd lng="pt"><![CDATA[terapia medicamentosa]]></kwd>
<kwd lng="pt"><![CDATA[Suplementos Dietéticos]]></kwd>
<kwd lng="pt"><![CDATA[Vitamina A]]></kwd>
<kwd lng="pt"><![CDATA[Saúde Materno-Infantil]]></kwd>
<kwd lng="pt"><![CDATA[Revisão]]></kwd>
<kwd lng="en"><![CDATA[Vitamin A Deficiency]]></kwd>
<kwd lng="en"><![CDATA[drug therapy]]></kwd>
<kwd lng="en"><![CDATA[Dietary Supplements]]></kwd>
<kwd lng="en"><![CDATA[Vitamin A]]></kwd>
<kwd lng="en"><![CDATA[Maternal and Child Health]]></kwd>
<kwd lng="en"><![CDATA[Review]]></kwd>
<kwd lng="es"><![CDATA[Deficiencia de Vitamina A]]></kwd>
<kwd lng="es"><![CDATA[terapia medicamentosa]]></kwd>
<kwd lng="es"><![CDATA[Suplementos Dietéticos]]></kwd>
<kwd lng="es"><![CDATA[Vitamina A]]></kwd>
<kwd lng="es"><![CDATA[Salud Materno-Infantil]]></kwd>
<kwd lng="es"><![CDATA[Revisión]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p ALIGN="RIGHT"><FONT FACE="Verdana, Arial, Helvetica, sans-serif" SIZE="2"><B>REVIS&Atilde;O</B></FONT></p>    <p>&nbsp;</p>    <p><a name="top"></a><font face="Verdana, Arial, Helvetica, sans-serif" size="4"><b>Suplementa&ccedil;&atilde;o  com vitamina A no puerp&eacute;rio: revis&atilde;o sistem&aacute;tica</b></font></p>     <p>&nbsp;</p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="3 "><b>Suplementaci&oacute;n con vitamina A en el puerperio: revisi&oacute;n sistem&aacute;tica</b></font></p>    <p>&nbsp;</p>    <p>&nbsp;</p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Maria  de F&aacute;tima Costa Caminha<sup>I</sup>; Malaquias Batista Filho<sup>I</sup>;  Taciana Fernanda dos Santos Fernandes<sup>II</sup>; Ilma Kruze Grande de Arruda<sup>II</sup>;  Alcides da Silva Diniz<sup>II</sup></b></font></p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><sup>I</sup>Instituto  de Medicina Integral Prof. Fernando Figueira. Recife, PE, Brasil    <br> <sup>II</sup>Universidade  Federal de Pernambuco. Recife, PE, Brasil</font></p>    ]]></body>
<body><![CDATA[<p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><a href="#back">Correspond&ecirc;ncia  | Correspondence</a></font></p>    <p>&nbsp;</p>    <p>&nbsp;</p><hr size="1" noshade>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>RESUMO</b></font></p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Realizou-se  revis&atilde;o sistem&aacute;tica de estudos avaliativos da aplica&ccedil;&atilde;o  de megadoses de vitamina A nas concentra&ccedil;&otilde;es de retinol no sangue  e no leite maternos como medida de curto prazo para a preven&ccedil;&atilde;o  de hipovitaminose A. Com base na estrat&eacute;gia do Centro Cochrane do Brasil  para ensaios cl&iacute;nicos aleat&oacute;rios foram identificadas 115 publica&ccedil;&otilde;es  no PubMed, entre as quais, por um conjunto de crit&eacute;rios de inclus&atilde;o/exclus&atilde;o,  foram selecionados 14 artigos publicados entre 1993 a 2007. O efeito das interven&ccedil;&otilde;es  com tr&ecirc;s esquemas posol&oacute;gicos (200.000, 300.000 e 400.000 UI) de  vitamina A foram analisados. Dos 11 experimentos realizados em leite materno,  nove apresentaram eleva&ccedil;&atilde;o dos n&iacute;veis de retinol em compara&ccedil;&atilde;o  com o grupo controle; dos nove que avaliaram sangue materno, quatro mostraram  eleva&ccedil;&atilde;o ap&oacute;s tempos variados de aplica&ccedil;&atilde;o  de megadoses de vitamina A. Conclui-se que a administra&ccedil;&atilde;o de vitamina  A em elevadas doses foi positiva em 82% dos ensaios com leite materno, mas menos  not&aacute;veis em compara&ccedil;&atilde;o ao sangue materno. N&atilde;o foram  observadas diferen&ccedil;as significativas quanto &agrave; posologia aplicada.</font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Descritores:    </b> Defici&ecirc;ncia de Vitamina A, terapia medicamentosa. Suplementos Diet&eacute;ticos.    Vitamina A. Sa&uacute;de Materno-Infantil. Revis&atilde;o.</font></p> <hr size="1" noshade>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>RESUMEN</b></font></p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Se  realiz&oacute; revisi&oacute;n sistem&aacute;tica de estudios evaluativos de la  aplicaci&oacute;n de megadosis de vitamina A en las concentraciones de retinol  en la sangre y en la leche maternos como medida de corto plazo para la prevenci&oacute;n  de hipovitaminosis A. Con base en la estrat&eacute;gia del Centro Cochrane de  Brasil para ensayos cl&iacute;nicos aleatorios fueron identificadas 115 publicaciones  en el PubMed, entre las cuales, por un conjunto de criterios de inclusi&oacute;n/exclusi&oacute;n,  fueron seleccionados 14 art&iacute;culos publicados entre 1993 a 2007. El efecto  de las intervenciones con tres esquemas posol&oacute;gicos (200.000. 300.000 y  400.000 UI) de vitamina A fueron analizados. De los 11 experimentos realizados  en leche materna, nueve presentaron elevaci&oacute;n de los niveles de retinol  en comparaci&oacute;n con el grupo control; de los nueve que evaluaron sangre  materna, cuatro mostraron elevaci&oacute;n posterior a tiempos variados de aplicaci&oacute;n  de megadosis de vitamina A. Se concluye que la administraci&oacute;n de vitamina  A en elevadas dosis fue positiva en 82% de los ensayos con leche materna, pero  menos notables en comparaci&oacute;n a la sangre materna. No fueron observadas  diferencias significativas con relaci&oacute;n a la posolog&iacute;a aplicada.</font></p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Descriptores:  </b> Deficiencia de Vitamina A, terapia medicamentosa. Suplementos Diet&eacute;ticos.  Vitamina A. Salud Materno-Infantil. Revisi&oacute;n.</font></p><hr size="1" noshade>      <p>&nbsp;</p>    ]]></body>
<body><![CDATA[<p>&nbsp;</p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="3"><b>INTRODU&Ccedil;&Atilde;O</b></font></p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">O  ciclo gr&aacute;vido-puerperal e notadamente o per&iacute;odo de lacta&ccedil;&atilde;o  representam um per&iacute;odo biol&oacute;gico de peculiar vulnerabilidade nutricional  para a mulher, principalmente nas popula&ccedil;&otilde;es de baixas condi&ccedil;&otilde;es  socioecon&ocirc;micas. Isto ocorre em fun&ccedil;&atilde;o das elevadas demandas  fisiol&oacute;gicas, altera&ccedil;&otilde;es comportamentais, metab&oacute;licas  e freq&uuml;entes doen&ccedil;as associadas a essas fases. Estimativas mostram  que de um total de 107,4 milh&otilde;es de mulheres no mundo que tiveram filhos  a cada ano e que habitam regi&otilde;es em risco de defici&ecirc;ncia de vitamina  A (DVA), 19,8 milh&otilde;es (18%) apresentam baixas concentra&ccedil;&otilde;es  de retinol no sangue ou leite materno (&lt;1,05&#181;mol/L), das quais 7,2 milh&otilde;es  teriam concentra&ccedil;&otilde;es consideradas como deficientes (&lt;0,70&#181;mol/L).<sup>30</sup></font></p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">A  DVA leva a um dist&uacute;rbio no funcionamento das c&eacute;lulas da retina,  cujo efeito funcional mais conhecido &eacute; a cegueira transit&oacute;ria, freq&uuml;entemente  descrito em estudos sobre o problema durante a gravidez, principalmente no terceiro  trimestre gestacional.<sup>7</sup> A DVA tamb&eacute;m afeta a integridade an&aacute;tomo-funcional  das mucosas gastrointestinais e respirat&oacute;rias, contribuindo para um aumento  significativo da morbimortalidade por doen&ccedil;as infeciosas.<sup>27</sup></font></p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Nessas  condi&ccedil;&otilde;es, a suplementa&ccedil;&atilde;o com vitamina A ou betacaroteno  em mulheres no per&iacute;odo reprodutivo pode reduzir significativamente sintomas  e sinais de co-morbidades relacionadas &agrave; cegueira noturna, com grande impacto  nas estat&iacute;sticas de mortalidade materna.<sup>6,8,15,29,31</sup> Nesse aspecto,  o ensaio comunit&aacute;rio de West Jr et al<sup>29</sup> (1999) com 44.646 mulheres  em idade reprodutiva no Nepal mostrou redu&ccedil;&atilde;o do risco de mortalidade  materna de 44%, o que pode ser considerado uma indica&ccedil;&atilde;o do efeito  protetor da suplementa&ccedil;&atilde;o de vitamina A nesse per&iacute;odo do  ciclo de vida.</font></p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">A  vitamina A &eacute; requerida continuamente pelo concepto durante a gesta&ccedil;&atilde;o.<sup>23</sup>  No entanto, estoques fetais desse micronutriente s&atilde;o habitualmente baixos  ao nascimento, de modo que, para manter e acumular n&iacute;veis org&acirc;nicos  normais at&eacute; que alimentos complementares forne&ccedil;am suficientes quantidades  adicionais de vitamina A, o rec&eacute;m-nascido passa a depender do leite materno,  sobretudo o inicial (colostro), rico em vitamina A (m&eacute;dia de 7,0 &#181;mol/L).<sup>32</sup></font></p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">As  m&eacute;dias de retinol no leite maduro em mulheres de pa&iacute;ses em desenvolvimento  s&atilde;o menores (em torno de 1,0 &#181;mol/L) em rela&ccedil;&atilde;o aquelas  observadas em mulheres de pa&iacute;ses desenvolvidos (m&eacute;dia de 2,3 &#181;mol/L).  Em regi&otilde;es de pobreza, os teores encontrados no leite materno seriam suficientes  apenas para atender os requerimentos metab&oacute;licos basais da crian&ccedil;a,  sem permitir a forma&ccedil;&atilde;o de reservas org&acirc;nicas dessa vitamina,<sup>23</sup>  tornando assim os lactentes mais suscet&iacute;veis ao problema.<sup>21</sup></font></p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">V&aacute;rias  estrat&eacute;gias t&ecirc;m sido propostas nos pa&iacute;ses em desenvolvimento  para o enfrentamento da DVA no per&iacute;odo de lacta&ccedil;&atilde;o, entre  as quais a suplementa&ccedil;&atilde;o de megadoses de vitamina A no p&oacute;s-parto  imediato<sup>33</sup> que, teoricamente, parece a estrat&eacute;gia mais efetiva  a curto prazo. Assim, seriam beneficiadas tanto a mulher, pela eleva&ccedil;&atilde;o  dos n&iacute;veis desse micronutriente em seu organismo, como a crian&ccedil;a,  via leite materno.<sup>23</sup> No entanto, desde a proposi&ccedil;&atilde;o original  da Organiza&ccedil;&atilde;o Mundial de Sa&uacute;de (OMS) de 200.000 UI,<sup>33</sup>  a posologia e os efeitos ben&eacute;ficos dessa estrat&eacute;gia ainda n&atilde;o  foram suficientemente avaliados.</font></p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Dentre  os indicadores de resposta &agrave; suplementa&ccedil;&atilde;o materna de megadoses  de vitamina A, as concentra&ccedil;&otilde;es de retinol no sangue e no leite  maternos t&ecirc;m sido assumidas como referenciais,<sup>17,23</sup> tendo como  principal fundamento o estudo de Vahlquist &amp; Nilsson<sup>26</sup>(1979).</font></p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">O  objetivo do presente estudo foi realizar uma revis&atilde;o sistem&aacute;tica  de estudos sobre o efeito da suplementa&ccedil;&atilde;o com megadoses de vitamina  A nas concentra&ccedil;&otilde;es de retinol no sangue e no leite maternos.</font></p>    ]]></body>
<body><![CDATA[<p>&nbsp;</p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="3"><b>M&Eacute;TODOS</b></font></p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Utilizando  a estrat&eacute;gia de revis&atilde;o sistem&aacute;tica do Centro Cochrane do  Brasil para ensaios cl&iacute;nicos aleat&oacute;rios,<a name="topa"></a><a href="#backa">ª</a>  a busca foi realizada na base de dados PubMed, no per&iacute;odo de 1980 a 2007,  mediante o uso dos seguintes descritores: "randomized controlled trial" &#91;Publication  Type&#93; OR "controlled clinical trial" &#91;Publication Type&#93; OR "randomized  controlled trials" &#91;MeSH Terms&#93; OR "random allocation" &#91;MeSH Terms&#93;  OR "double blind method" &#91;MeSH Terms&#93; OR "single blind method" &#91;MeSH  Terms&#93; OR "clinical trial" &#91;Publication Type&#93; OR "clinical trials"  &#91;MeSH Terms&#93; OR "(clinical* &#91;Text Word&#93; AND trial* &#91;Text Word&#93;)"  OR "single*" &#91;Text Word&#93; OR "double*" &#91;Text Word&#93; OR "treble*"  &#91;Text Word&#93; OR "triple*" &#91;Text Word&#93; OR "placebos" &#91;MeSH Terms&#93;  OR "placebo*" &#91;Text Word&#93; OR "random*" &#91;Text Word&#93; OR "research  design" &#91;MeSH Terms&#93; OR "comparative study" &#91;MeSH Terms&#93; OR "evaluation  studies" &#91;MeSH Terms&#93; OR "follow-up studies" &#91;MeSH Terms&#93; OR "prospective  studies" &#91;MeSH Terms&#93; OR "control*" &#91;Text Word&#93; OR "prospectiv*"  &#91;Text Word&#93; OR "volunteer*" &#91;Text Word&#93; AND "supplementation"  AND "vitamin A" AND "mothers". A consulta &agrave; base de dados identificou 115  publica&ccedil;&otilde;es.</font></p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Ap&oacute;s  a leitura dos t&iacute;tulos, resumos e, quando indicado, dos textos completos,  procedeu-se &agrave; sele&ccedil;&atilde;o dos artigos utilizando cinco crit&eacute;rios  de inclus&atilde;o: 1- ensaios cl&iacute;nicos controlados e randomizados; 2-  compara&ccedil;&atilde;o de suplementa&ccedil;&atilde;o isolada com megadoses  de vitamina A na forma de palmitato de retinol; 3- presen&ccedil;a de diferentes  esquemas posol&oacute;gicos, (200.000 UI, 300.000 UI e 400.000 UI); 4- que avaliaram  o efeito da suplementa&ccedil;&atilde;o nas concentra&ccedil;&otilde;es de retinol  no sangue materno; 5- que avaliaram, no leite materno, o poss&iacute;vel efeito  da suplementa&ccedil;&atilde;o de vitamina A nos n&iacute;veis de retinol. Com  estes cinco crit&eacute;rios b&aacute;sicos definiu-se o conjunto de trabalhos  da revis&atilde;o. A inclus&atilde;o de exig&ecirc;ncias adicionais sobre procedimentos  metodol&oacute;gicos resultaria num elenco final de artigos numericamente inadequados  para os objetivos do estudo. N&atilde;o houve restri&ccedil;&atilde;o quanto ao  ano e idioma da publica&ccedil;&atilde;o. Foram exclu&iacute;dos artigos de revis&atilde;o  e estudos experimentais com animais.</font></p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Os  115 estudos identificados pela estrat&eacute;gia de revis&atilde;o foram analisados  de forma criteriosa e independente por dois pesquisadores e a sele&ccedil;&atilde;o  dos artigos ocorreu quando havia concord&acirc;ncia e/ou desempate por um terceiro  pesquisador, com base nos crit&eacute;rios de inclus&atilde;o, totalizando 14  artigos.</font></p>    <p>&nbsp;</p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="3"><b>RESULTADOS</b></font></p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Dos  14 estudos selecionados, sete<sup>3-5,10,16,19,28</sup> avaliaram a dose &uacute;nica  de 200.000 UI, um<sup>22</sup> estudou os resultados da aplica&ccedil;&atilde;o  de 300.000 UI, tr&ecirc;s ensaios<sup>9,11,24</sup> realizaram uma compara&ccedil;&atilde;o  entre a aplica&ccedil;&atilde;o de 200.000 UI e 400.000 UI, enquanto tr&ecirc;s  outros experimentos<sup>1,14,34</sup> utilizaram a megadose de 400.000 UI.</font></p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">O  tempo de aplica&ccedil;&atilde;o da vitamina A ap&oacute;s o parto variou de 12  a 48 horas em seis estudos<sup>1,4,5,10,19,28</sup> e at&eacute; sete a 42 dias  em seis outros,<sup>3,9,11,16,22,24</sup> enquanto dois outros artigos,<sup>14,34</sup>  ministraram a suplementa&ccedil;&atilde;o vitam&iacute;nica ap&oacute;s 48 horas  de ocorr&ecirc;ncia do parto. Em um trabalho<sup>10</sup> o tempo de seguimento  entre a aplica&ccedil;&atilde;o de vitamina A e a avalia&ccedil;&atilde;o da resposta  foi de seis horas. Nas outras experi&ecirc;ncias relatadas, os casos experimentais  foram avaliados entre 45 dias<sup>14,34</sup> tr&ecirc;s meses,<sup>5,28</sup>  cinco a seis meses<sup>1,4,9,24</sup> e at&eacute; nove meses.<sup>3,11,16,19,22</sup>  Quatro trabalhos foram publicados na d&eacute;cada de 1990 e os demais, ap&oacute;s  o ano 2000.</font></p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Nove<sup>1,3,4,5,10,16,19,22,28</sup>  dos 11 artigos revisados resultaram em eleva&ccedil;&atilde;o dos n&iacute;veis  de retinol no leite materno, na compara&ccedil;&atilde;o com o resultado basal  (ponto zero do experimento) ou em compara&ccedil;&atilde;o com o grupo controle.  Quanto &agrave;s respostas ao retinol s&eacute;rico, entre nove trabalhos quatro<sup>14,19,22,34</sup>  revelaram um efeito positivo na eleva&ccedil;&atilde;o da vitamina A no soro dos  grupos acompanhados.</font></p>    ]]></body>
<body><![CDATA[<p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Os  resultados mostraram varia&ccedil;&atilde;o de procedimentos em rela&ccedil;&atilde;o  a: hor&aacute;rio, t&eacute;cnica de coleta de leite e outras diferen&ccedil;as  na avalia&ccedil;&atilde;o da linha basal de vitamina A nas amostras, conforme  apresentado na <a href="/img/revistas/rsp/v43n4/318t.gif">Tabela</a>.</font></p>    <p>&nbsp;</p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="3"><b>DISCUSS&Atilde;O</b></font></p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">A  quest&atilde;o fundamental da revis&atilde;o sistem&aacute;tica &eacute; se a  aplica&ccedil;&atilde;o de megadoses de vitamina A (200.000 UI, 300.00 UI ou 400.000  UI) seria suficiente para assegurar a provis&atilde;o adequada deste nutriente  para a cobertura das necessidades basais do lactente no per&iacute;odo cr&iacute;tico  do aleitamento materno (os quatro a seis primeiros meses de vida). Por conseguinte,  este se torna o desfecho desejado em primeiro plano, sendo os n&iacute;veis de  retinol s&eacute;rico da m&atilde;e um objetivo colinear ou um co-requisito para  se assegurar a primeira condi&ccedil;&atilde;o. Ainda, a biologia materno-fetal  pode recorrer a mecanismos compensat&oacute;rios em favor do feto ou do lactente,  a exemplo da deple&ccedil;&atilde;o de nutrientes do pr&oacute;prio organismo  materno.<sup>32</sup></font></p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Partindo  destas considera&ccedil;&otilde;es, dos 11 ensaios que analisaram a condi&ccedil;&atilde;o  do retinol no leite materno, nove<sup>1,3,4,5,10,16,19,22,28</sup> apresentaram  uma eleva&ccedil;&atilde;o de maior ou menor express&atilde;o ap&oacute;s a aplica&ccedil;&atilde;o  de megadoses de vitamina A, o que n&atilde;o ocorreu em dois estudos.<sup>9,11</sup>  Todavia, num dos casos<sup>11</sup> os valores basais de retinol no leite j&aacute;  eram bastante elevados (m&eacute;dia=4,34; desvio-padr&atilde;o=3,01 &#181;mol/L)  um m&ecirc;s ap&oacute;s o parto, de modo que uma maior eleva&ccedil;&atilde;o  j&aacute; n&atilde;o poderia se justificar como um objetivo necessariamente desej&aacute;vel.  Na pesquisa de Darboe et al<sup>9</sup> (2007), n&atilde;o h&aacute; informa&ccedil;&otilde;es  sobre a situa&ccedil;&atilde;o basal de retinol no leite materno, de modo que  o desfecho se limita a considerar a compara&ccedil;&atilde;o estat&iacute;stica  dos resultados entre duas posologias, n&atilde;o esclarecendo o impacto final  em rela&ccedil;&atilde;o a n&iacute;veis seguros de retinol no leite seis meses  depois. Trata-se, portanto, de um resultado cuja an&aacute;lise n&atilde;o pode  ser devidamente estabelecida.</font></p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Entre  os experimentos que mostraram respostas positivas em rela&ccedil;&atilde;o aos  interesses da revis&atilde;o, observa-se que no ensaio de Dimenstein et al<sup>10</sup>  (2007), o seguimento foi de apenas seis horas ap&oacute;s a administra&ccedil;&atilde;o  da vitamina A. N&atilde;o se enquadra, portanto, na perspectiva de um efeito protetor  efetivo. Segundo ensaio de Aza&iuml;s-Braesco &amp; Pascal<sup>2</sup> (2000),  o processo de transporte da vitamina A at&eacute; o f&iacute;gado se faz em cerca  de cinco horas. Portanto, o experimento de Dimenstein et al<sup>10</sup> (2007)  apenas confirmaria tal observa&ccedil;&atilde;o, tornando pertinente a constata&ccedil;&atilde;o  bem anterior de Vahlquist &amp; Nilsson<sup>26</sup> (1979), de que, ap&oacute;s  uma ingest&atilde;o de alimentos ricos em vitamina A, esse nutriente pode passar  diretamente da dieta para o leite materno, sem necessitar da regula&ccedil;&atilde;o  do f&iacute;gado. Assim, o efeito registrado no colostro das mulheres suplementadas  poderia refletir uma eleva&ccedil;&atilde;o de car&aacute;ter transit&oacute;rio.</font></p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Por  outro lado, a an&aacute;lise comparativa da posologia das megadoses (200.000 UI,  300.000 UI e 400.000 UI) n&atilde;o possibilita esclarecer as poss&iacute;veis  diferen&ccedil;as de resultados em fun&ccedil;&atilde;o do esperado efeito dose-resposta  da carga crescente de vitamina A. Tal compara&ccedil;&atilde;o seria relevante  para a proposta mais recente da OMS<sup>18</sup> de aplica&ccedil;&atilde;o de  doses mais elevadas de vitamina A (400.000 UI) como uma estrat&eacute;gia mais  segura de preven&ccedil;&atilde;o de DVA no per&iacute;odo de aleitamento.<sup>23</sup></font></p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Entre  os nove estudos que consideraram o status da vitamina A no sangue materno,<sup>1,9,14,16,19,22,24,28,34</sup>  apenas quatro estudos encontraram eleva&ccedil;&atilde;o dos n&iacute;veis de  retinol s&eacute;rico em rela&ccedil;&atilde;o aos valores basais.<sup>14,19,22,34</sup>  Seriam, portanto, resultados pouco conclusivos em termos de estrat&eacute;gia  de interven&ccedil;&atilde;o efetivamente segura. Ademais, mesmo sendo um indicador  importante, os teores sangu&iacute;neos do status de vitamina A s&eacute;rica  seriam de import&acirc;ncia secund&aacute;ria em rela&ccedil;&atilde;o ao comportamento  dos n&iacute;veis de retinol no leite materno.</font></p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Quanto  aos limites da presente revis&atilde;o, dentro do pequeno conjunto de artigos  selecionados na triagem da revis&atilde;o sistem&aacute;tica, persistem condicionantes  que afetam a validade interna e externa dos seus resultados. Assim, dos estudos  que utilizaram a dose de 200.000 UI, proposta pela OMS<sup>33</sup> (1997) e que  seguiram prospectivamente as m&atilde;es por um m&ecirc;s ou mais,<sup>3,4,5,16,19,28</sup>  a eleva&ccedil;&atilde;o do retinol no leite materno variou de 45 dias<sup>5</sup>  ao sexto m&ecirc;s p&oacute;s-parto.<sup>19</sup> Ainda, tr&ecirc;s desses experimentos  n&atilde;o esclareceram adequadamente a t&eacute;cnica de coleta do leite materno.  O estudo de Bhaskaram et al<sup>5</sup> (1998) n&atilde;o levou em considera&ccedil;&atilde;o  o per&iacute;odo de coleta, assim como n&atilde;o referiu o instrumento utilizado  e o intervalo entre as mamadas, n&atilde;o distinguindo coleta de mama cheia ou  casual. Outros trabalhos n&atilde;o informaram o instrumento de coleta,<sup>19</sup>  assim como a mama utilizada.<sup>3,19</sup> Considerando-se os demais estudos  que utilizaram a dose referida de 200.000 UI<sup>4,16,28</sup> e que padronizaram  a t&eacute;cnica da coleta do leite, pode-se inferir um efeito positivo de cerca  de tr&ecirc;s meses de dura&ccedil;&atilde;o.</font></p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Por  outro lado, dois aspectos n&atilde;o foram devidamente considerados: a condi&ccedil;&atilde;o  de aleitamento materno exclusivo, face &agrave; recomenda&ccedil;&atilde;o universal  de que se trata de melhor op&ccedil;&atilde;o para a alimenta&ccedil;&atilde;o  da crian&ccedil;a nos seis primeiros meses de vida e, em segundo plano, a situa&ccedil;&atilde;o  basal no in&iacute;cio do experimento. Em rela&ccedil;&atilde;o &agrave; exclusividade  do aleitamento materno, seu prolongamento por seis meses implica, cumulativamente,  maiores demandas de vitamina A do que, por exemplo, nos casos de m&atilde;es que  praticam apenas uma, duas ou tr&ecirc;s mamadas di&aacute;rias. Nesse sentido,  apenas dois artigos<sup>4,28</sup> consideraram esta importante condi&ccedil;&atilde;o.</font></p>    ]]></body>
<body><![CDATA[<p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Sobre  a situa&ccedil;&atilde;o basal, dos 11 estudos que avaliaram o leite materno,  quatro n&atilde;o consideraram a situa&ccedil;&atilde;o inicial do retinol l&aacute;cteo,<sup>1,5,9,28</sup>  enquanto dos nove estudos que avaliaram o retinol s&eacute;rico, um n&atilde;o  considerou sua situa&ccedil;&atilde;o inicial.<sup>9</sup> Tr&ecirc;s implica&ccedil;&otilde;es  decorrem dessas observa&ccedil;&otilde;es: a) o seguimento prospectivo dos casos  que apresentam valores iniciais normais ou elevados n&atilde;o obedece ao mesmo  padr&atilde;o em rela&ccedil;&atilde;o aos casos que, j&aacute; no ponto zero,  apresentam valores baixos; b) a quest&atilde;o final do desfecho n&atilde;o se  limita &agrave; circunst&acirc;ncia de que os n&iacute;veis de vitamina A tenham  simplesmente aumentado ou diminu&iacute;do, mas a pergunta sobre se, nos casos  de diminui&ccedil;&atilde;o ou, eventualmente, de pequenos aumentos, os valores  do retinol n&atilde;o se situariam em n&iacute;veis inseguros, ou seja, baixos  e deficientes; c) finalmente, tal avalia&ccedil;&atilde;o bioqu&iacute;mica inicial  possibilitaria distinguir a evolu&ccedil;&atilde;o temporal dos n&iacute;veis  de retinol de forma distinta entre o sangue e o leite materno, considerando que  o colostro ou o leite dos primeiros dias apresenta, naturalmente teores mais elevados  de vitamina A que o leite maduro. Sete estudos oferecem algumas informa&ccedil;&otilde;es  sobre este aspecto. <sup>3,4,10,11,16,19,22</sup></font></p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">A  variabilidade do conte&uacute;do de gordura do leite deve ser considerada, uma  vez que a vitamina A &eacute; veiculada na fra&ccedil;&atilde;o lip&iacute;dica  deste alimento, sujeita a erros amostrais por procedimentos n&atilde;o padronizados  de coleta. A mais importante fonte desses erros se relaciona ao conte&uacute;do  da mama da qual a amostra &eacute; retirada. Quanto mais cheia a mama, mais baixo  &eacute; seu conte&uacute;do de gordura.<sup>23</sup> Outra fonte de varia&ccedil;&atilde;o  na gordura do leite que pode influir nos n&iacute;veis de vitamina A est&aacute;  relacionada &agrave; hora do dia em que a amostra &eacute; retirada. Assim, Ruel  et al<sup>20</sup> (1997) encontraram maior concord&acirc;ncia nas concentra&ccedil;&otilde;es  de lip&iacute;dios no leite materno coletado no per&iacute;odo de seis e oito  horas da manh&atilde; de m&atilde;es em jejum e maior varia&ccedil;&atilde;o entre  16-18 horas e 12-14 horas, o que poderia explicar diferen&ccedil;as entre os resultados  sem a devida homogeniza&ccedil;&atilde;o de procedimentos.</font></p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Em  alguns dos estudos em que se avaliou o retinol s&eacute;rico materno<sup>16,19,28</sup>  apenas um<sup>19</sup> encontrou diferen&ccedil;a estatisticamente significante  at&eacute; o sexto m&ecirc;s p&oacute;s-suplementa&ccedil;&atilde;o. Embora a  pesquisa de Rice et al<sup>16</sup> (1999) n&atilde;o tenha observado esse efeito  no sangue, verificou-se aos tr&ecirc;s meses eleva&ccedil;&atilde;o da deposi&ccedil;&atilde;o  hep&aacute;tica pelo teste <i>Modified relative dose responde</i> (MRDR) nas mulheres  suplementadas. Vinutha et al<sup>28</sup> (2000) observaram na linha de base que  27% das mulheres apresentavam n&iacute;veis de retinol considerados como baixos  (0,35-0,70 &#181;mol/L), enquanto no estudo de Rice et al<sup>16</sup> (1999),  o grupo placebo possu&iacute;a 54% das mulheres com as reservas hep&aacute;ticas  comprometidas aos tr&ecirc;s meses p&oacute;s-parto, o que leva a crer que o grupo  experimental teria evolu&iacute;do para essa situa&ccedil;&atilde;o caso n&atilde;o  tivesse sido suplementado. Como o status de vitamina A n&atilde;o estava adequado  na linha e base, e tendo em conta o papel homeost&aacute;tico das reservas em  situa&ccedil;&otilde;es especiais, como a amamenta&ccedil;&atilde;o, &eacute;  poss&iacute;vel que os n&iacute;veis s&eacute;ricos respondam menos ao uso de  megadoses que o leite.<sup>25</sup></font></p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">O  estudo de Roy et al<sup>19</sup> (1997) dosou o retinol s&eacute;rico na linha  de base at&eacute; 24h p&oacute;s-parto, o de Vinutha et al<sup>28</sup> (2000)  at&eacute; 48 h e o de Rice et al<sup>16</sup>(1999) at&eacute; 15 dias p&oacute;s  parto. &Eacute; admiss&iacute;vel que o processo inflamat&oacute;rio do parto/puerp&eacute;rio  em suas primeiras horas possa ter interferido nas concentra&ccedil;&otilde;es  s&eacute;ricas do retinol.<sup>12,13</sup> Ademais, se a linha de base no estudo  de Roy et al<sup>19</sup> (1997) apresentava n&iacute;veis de 1,38 (dp= 0,17 &#181;mol/L),  provavelmente essas mulheres dispunham de estoques hep&aacute;ticos relativamente  adequados, o que n&atilde;o deve ter ocorrido com os demais estudos. Isso explicaria  a eleva&ccedil;&atilde;o dos n&iacute;veis de retinol at&eacute; o sexo m&ecirc;s  p&oacute;s-suplementa&ccedil;&atilde;o, tanto no leite quanto no sangue materno.</font></p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">No  caso espec&iacute;fico da suplementa&ccedil;&atilde;o com 300.000 UI, apenas um  estudo foi identificado e selecionado,<sup>22</sup> relatando um efeito persistente  no leite at&eacute; o oitavo m&ecirc;s e nos n&iacute;veis s&eacute;ricos at&eacute;  o sexto m&ecirc;s. No entanto, o teste <i>Relative Dose Response</i> (RDR) n&atilde;o  detectou diferen&ccedil;a no grupo de mulheres suplementadas. Os estudos que compararam  a dose de 400.000 UI <i>vs</i> 200.000 UI, n&atilde;o mostraram efeito diferencial  quanto ao conte&uacute;do de vitamina A no leite materno,<sup>9,11</sup> s&eacute;rico  e hep&aacute;tico.<sup>24</sup> Possivelmente os m&eacute;todos usados n&atilde;o  foram apropriados para tal fim. Quanto &agrave; aus&ecirc;ncia de efeito nos dep&oacute;sitos  hep&aacute;ticos e no sangue, o estudo de Tchum et al<sup>24</sup> (2006) refere  que o percentual de mulheres com MRDR &gt; 0,060 diminuiu em todos os grupos e  que, no quinto m&ecirc;s, n&atilde;o havia nenhuma mulher em ambos os grupos com  MRDR &gt; 0,060. Os autores sugerem que a dose de 400.000 UI provavelmente aumentou  as reservas do f&iacute;gado mais do que a dose de 200.000UI, mas que n&atilde;o  p&ocirc;de ser mostrado pelo teste MRDR e, portanto, apenas indicou reservas normais  de vitamina A em todas as avalia&ccedil;&otilde;es p&oacute;s tratamento para  cada grupo.</font></p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Dos  estudos que utilizaram a dose de 400.000 UI e avaliaram o efeito da suplementa&ccedil;&atilde;o  no retinol s&eacute;rico,<sup>1,14,34</sup> e no leite materno,<sup>1</sup> Ayah  et al<sup>1</sup> (2007) encontraram diferen&ccedil;as nos teores de vitamina  A no leite materno entre os grupos at&eacute; o final de acompanhamento no sexto  m&ecirc;s. Todavia, n&atilde;o ocorreu o mesmo com o retinol s&eacute;rico, provavelmente  devido &agrave; defici&ecirc;ncia deste micronutriente nas mulheres na linha de  base. Malaba et al<sup>14</sup> (2005) encontraram efeito que se mantiveram at&eacute;  45 dias e Zvandsara et al<sup>34</sup> (2006) relacionaram o efeito positivo em  mulheres soronegativas para o HIV suplementadas em compara&ccedil;&atilde;o com  mulheres com o v&iacute;rus HIV, o que &eacute; consistente com a associa&ccedil;&atilde;o  conhecida entre processos infeciosos/inflamat&oacute;rios e diminui&ccedil;&atilde;o  de vitamina A no sangue.<sup>25</sup></font></p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Em  s&iacute;ntese, as pesquisas com a dose recomendada pela OMS (200.000 UI) foram  controversas em rela&ccedil;&atilde;o ao tempo de cobertura da vitamina A no leite  materno, possivelmente devido &agrave; diversidade de procedimentos de coleta  de leite materno. Em rela&ccedil;&atilde;o ao sangue, provavelmente ocorreriam  efeitos diferenciais em popula&ccedil;&otilde;es em que as reservas hep&aacute;ticas  n&atilde;o estivessem depletadas. Finalmente, pode-se concluir que v&aacute;rios  aspectos referentes &agrave; efetividade da suplementa&ccedil;&atilde;o com megadoses  de vitamina A em m&atilde;es lactantes n&atilde;o est&atilde;o devidamente esclarecidos,  recomendando-se a realiza&ccedil;&atilde;o de estudos mais aprofundados e controlados,  considerando as principais restri&ccedil;&otilde;es relacionadas &agrave;s varia&ccedil;&otilde;es  dos procedimentos discutidos, de modo a presumir seus potenciais resultados, e,  em conseq&uuml;&ecirc;ncia, fundamentar a recomenda&ccedil;&atilde;o de a&ccedil;&otilde;es  estrat&eacute;gicas. Tais quest&otilde;es s&atilde;o particularmente importantes  no Brasil, onde a aplica&ccedil;&atilde;o de megadoses de vitamina A no p&oacute;s-parto  vem se difundindo como uma estrat&eacute;gia potencialmente promissora para a  preven&ccedil;&atilde;o da DVA no bin&ocirc;mio m&atilde;e/filho.</font></p>    <p>&nbsp;</p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="3"><b>REFER&Ecirc;NCIAS</b></font></p>    <!-- ref --><p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">1  Ayah RA, Mwaniki DL, Magnussen P, Tedstone AE, Marshall T, Alusala D, et al. The  effects of maternal and infant vitamin A supplementation on vitamin A status:  a randomised trial in Kenya. <i>Br J Nutr</i>. 2007;98(2):422-30. 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<body><![CDATA[<br> 52060-590  Recife, PE, Brasil    <br> E-mail: <a href="mailto:fatimacaminha@imip.org.br">fatimacaminha@imip.org.br</a></font></p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Recebido:  13/06/2008    <br> Revisado: 12/11/2008    <br> Aprovado: 04/12/2008</font></p>    <p>&nbsp;</p>    <p>&nbsp;</p>    <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Artigo  baseado em tese de doutorado de Caminha MFC, apresentada ao Programa de P&oacute;s-Gradua&ccedil;&atilde;o  em Nutri&ccedil;&atilde;o da Universidade Federal de Pernambuco em 2009.    <br> <a name="backa"></a><a href="#topa">a</a>  Centro Cochrane do Brasil, Laborat&oacute;rio de Ensino a Dist&acirc;ncia. Escola  Paulista de Medicina. Universidade Federal de S&atilde;o Paulo. Curso de revis&atilde;o  sistem&aacute;tica e metan&aacute;lise &#91;Internet&#93;. &#91;citado 2006 dez  28&#93;. Dispon&iacute;vel em: <a href="http://www.virtual.epm.br/cursos/metanalise/" target="_blank">http://www.virtual.epm.br/cursos/metanalise/</a></font></p>      ]]></body><back>
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