<?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>1646-5830</journal-id>
<journal-title><![CDATA[Acta Obstétrica e Ginecológica Portuguesa]]></journal-title>
<abbrev-journal-title><![CDATA[Acta Obstet Ginecol Port]]></abbrev-journal-title>
<issn>1646-5830</issn>
<publisher>
<publisher-name><![CDATA[Euromédice, Edições Médicas Lda.]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1646-58302018000400003</article-id>
<title-group>
<article-title xml:lang="pt"><![CDATA[Depressão pós-parto: deteção precoce e fatores associados]]></article-title>
<article-title xml:lang="en"><![CDATA[Postpartum depression: early detection and associated factors]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ferreira]]></surname>
<given-names><![CDATA[Cátia]]></given-names>
</name>
<xref ref-type="aff" rid="A1"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Silva]]></surname>
<given-names><![CDATA[Vanessa]]></given-names>
</name>
<xref ref-type="aff" rid="A1"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Guerra]]></surname>
<given-names><![CDATA[Cláudia]]></given-names>
</name>
<xref ref-type="aff" rid="A1"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Silva]]></surname>
<given-names><![CDATA[Ana Isabel]]></given-names>
</name>
<xref ref-type="aff" rid="A2 "/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Rosário]]></surname>
<given-names><![CDATA[Rafaela]]></given-names>
</name>
<xref ref-type="aff" rid="A3 "/>
</contrib>
</contrib-group>
<aff id="AA1">
<institution><![CDATA[,Hospital Senhora Oliveira Ginecologia e Obstetrícia ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<aff id="AA2">
<institution><![CDATA[,Universidade do Minho Escola de Educação ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<aff id="AA3">
<institution><![CDATA[,Universidade do Minho Centro de Investigação em Estudos da Criança ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<aff id="AA4">
<institution><![CDATA[,Universidade do Minho Escola de Enfermagem ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>12</month>
<year>2018</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>12</month>
<year>2018</year>
</pub-date>
<volume>12</volume>
<numero>4</numero>
<fpage>262</fpage>
<lpage>267</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_arttext&amp;pid=S1646-58302018000400003&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_abstract&amp;pid=S1646-58302018000400003&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_pdf&amp;pid=S1646-58302018000400003&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[Overview: Introduction: Postpartum depression is a common, often neglected problem and it has implications in the mother’s quality of life, her relationship with the newborn and child's development. The study of sociodemographic and obstetric risk factors for the development of puerperal depressive symptomatology assumes a crucial importance in the developing of diagnosis and treatment strategies for postpartum depression. Methods: A questionnaire consisting of the Edinburgh postpartum depression scale and six additional items was applied to the postpartum women in the Obstetrics Service of the Hospital Senhora Oliveira, between February 1, 2016 and January 31, 2017. The cut-off used for the presence of depressive symptomatology was a score =10. The electronic processes were subsequently consulted through the Obscare® program of the puerperal women who completed the questionnaire. Results: 857 women completed the questionnaire between the 2nd and 3rd day postpartum. The prevalence of depressive symptomatology was 10.6%. The factors associated with depressive symptomatology were: history of previous depressive disorder (17.2 vs 7.7%, p = 0.03), Diabetes Mellitus (2.2 vs. 0.1%, p = 0.018, OR 18, 5), fetal growth restriction (8.6 vs. 2.4%, p = 0.003, OR 3.8) and low birth weight (10.8% vs. 5.2%, p = 0.037, OR 2.41). The variables were adjusted to the potential confounding variable - history of previous depression. Conclusions: The history of prior depression, fetal growth restriction, Diabetes Mellitus and low birth weight are associated with higher scores on the Edinburgh postpartum depression scale.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Postpartum depression]]></kwd>
<kwd lng="en"><![CDATA[Obstetric complications]]></kwd>
<kwd lng="en"><![CDATA[Risk factors]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p align="right"><font size="2"><b>ESTUDO ORIGINAL/</B>ORIGINAL STUDY</font></p>     <p><font size="4"><b>Depressão pós-parto: deteção precoce e fatores associados</b></font></p>     <p><font size="3"><b>Postpartum depression: early detection and associated factors</b></font></p>     <p><b>Cátia Ferreira*, Vanessa Silva*, Cláudia Guerra**, Ana Isabel Silva***,    Rafaela Rosário*****</b></p>     <p>Hospital Senhora Oliveira</p>     <p>*Interna Complementar de Ginecologia e Obstetrícia, Hospital Senhora Oliveira</p>     <p>**Assistente Hospitalar de Ginecologia e Obstetrícia, Hospital Senhora Oliveira</p>     <p>***PhD Escola de Educação, Universidade do Minho; Investigadora no Centro de    Investigação em Estudos da Criança, Universidade do Minho</p>     <p>****PhD Escola de Enfermagem, Universidade do Minho; Investigadora no Centro    de Investigação em Estudos da Criança, Universidade do Minho </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/>     ]]></body>
<body><![CDATA[<p>&nbsp;</p>     <p><b>ABSTRACT</b></p>     <p><b>Overview:</b> Introduction: Postpartum depression is a common, often neglected    problem and it has implications in the mother’s quality of life, her relationship    with the newborn and child's development. The study of sociodemographic and    obstetric risk factors for the development of puerperal depressive symptomatology    assumes a crucial importance in the developing of diagnosis and treatment strategies    for postpartum depression.</p>     <p><b>Methods:</b> A questionnaire consisting of the Edinburgh postpartum depression    scale and six additional items was applied to the postpartum women in the Obstetrics    Service of the Hospital Senhora Oliveira, between February 1, 2016 and January    31, 2017. The cut-off used for the presence of depressive symptomatology was    a score &#8805;10. The electronic processes were subsequently consulted through    the Obscare® program of the puerperal women who completed the questionnaire.</p>     <p><b>Results:</b> 857 women completed the questionnaire between the 2nd and 3rd    day postpartum. The prevalence of depressive symptomatology was 10.6%. The factors    associated with depressive symptomatology were: history of previous depressive    disorder (17.2 vs 7.7%, p = 0.03), Diabetes Mellitus (2.2 <i>vs.</i> 0.1%, p    = 0.018, OR 18, 5), fetal growth restriction (8.6 <i>vs.</i> 2.4%, p = 0.003,    OR 3.8) and low birth weight (10.8% <i>vs.</i> 5.2%, p = 0.037, OR 2.41). The    variables were adjusted to the potential confounding variable - history of previous    depression.</p>     <p><b>Conclusions:</b> The history of prior depression, fetal growth restriction,    Diabetes Mellitus and low birth weight are associated with higher scores on    the Edinburgh postpartum depression scale.</p>     <p><b>Keywords:</b> Postpartum depression; Obstetric complications; Risk factors.</p> <hr/>     <p>&nbsp;</p>     <p><b>Introdução</b></p>     <p>A depressão pós-parto é um problema comum, muitas vezes negligenciado pela    própria puérpera, marido e familiares<sup>1,2</sup>. Está associada a diminuição    da qualidade de vida e pode interferir na interação entre a mãe e o recém-nascido,    bem como no desenvolvimento emocional, intelectual e cognitivo da criança<sup>3,4</sup>.    Neste sentido, torna-se relevante o seu diagnóstico precoce, bem como a deteção    de possíveis fatores associados<b>.</b></p>     ]]></body>
<body><![CDATA[<p>A prevalência de depressão pós-parto nos países desenvolvidos varia entre 5,2    e 74%<sup>4</sup>. Esta amplitude de valores deve-se fundamentalmente à diversidade    nas metodologias de investigação, em termos dos instrumentos adotados para o    diagnóstico de depressão pós-parto, dos <i>timings</i> de avaliação e das amostras    consideradas<sup>5</sup>. </p>     <p>Vários estudos demonstram que existe uma boa correlação entre a sintomatologia    depressiva em fases precoces (ao 2º e 3º dias) e tardias (4 a 8 semanas) do    pós-parto, pelo que a existência de <i>scores</i> elevados em escalas de depressão    pós-parto à data de alta da maternidade é um bom preditor da ocorrência desta    patologia<sup>6-11</sup>.</p>     <p>A relação entre fatores sociodemográficos, psicológicos e obstétricos e a depressão    pós-parto tem sido alvo de diversos estudos, mantendo-se no entanto controversa<sup>1-5,9</sup>.    A história de patologia depressiva prévia é dos poucos fatores que aparece consensualmente    associado a depressão pós-parto, aumentando o seu risco<sup>1,4,12-20</sup>.    Os resultados em relação a outros fatores sociais e demográficos são divergentes:    se por um lado há estudos que mostram que a depressão pós-parto é mais frequente    em puérperas com estatuto socioeconómico e/ou habilitações literárias inferiores<sup>1,2,13,17,21-25</sup>,    outros não provaram essa associação<sup>4,5,19,20,26.</sup> A mesma questão    se levanta em relação a fatores obstétricos e neonatais como a restrição de    crescimento fetal (RCF), a diabetes gestacional (DG), o parto pré-termo (PPT),    a via de parto, o baixo peso ao nascimento e a admissão do recém-nascido (RN)    no Serviço de Neonatologia. Um exemplo desta discordância de resultados é a    associação entre a via de parto e a depressão pós-parto: alguns estudos mostram    que o parto por cesariana confere um risco acrescido de sintomatologia depressiva    no pós-parto<sup>3,13,22,23,26-28</sup>, enquanto outros estudos não demonstram    qualquer relação<sup>1,4,5,14,16,17,19,20,29,30</sup>.</p>     <p>O estudo e a compreensão da associação entre fatores sociodemográficos e obstétricos    e a sintomatologia depressiva no puerpério assume uma importância crucial para    o desenvolvimento de estratégias de diagnóstico e de tratamento<sup>22</sup>.    Assim, o objetivo do presente estudo é determinar a prevalência de sintomatologia    depressiva entre o 2º e o 3º dia pós-parto, bem como a sua potencial relação    com as seguintes variáveis: fatores sociodemográficos, antecedentes pessoais,    antecedentes obstétricos, complicações na gravidez (RCF, DG, alterações do líquido    amniótico (LA), complicações hipertensivas e ameaça de parto pré-termo (APPT),    características do parto (início do trabalho de parto - espontâneo ou induzido,    via de parto, idade gestacional (IG), analgesia epidural, realização de episiotomia    e existência de lacerações perineais de 3º ou 4º graus) e características do    RN (peso ao nascimento, índice de Apgar (IA) ao 1º e 5º minutos e necessidade    de internamento na Neonatologia).</p>     <p><b>Métodos</b></p>     <p>Foi aplicado um questionário constituído pela escala de depressão pós-parto    de Edimburgo - EDPPE e seis itens adicionais: peso no início e final da gravidez,    escolaridade, estado civil, profissão, história de depressão prévia ou durante    a gravidez e peso e comprimento do RN. </p>     <p>O uso da escala de depressão pós-parto de Edimburgo na população portuguesa    encontra-se validado e o <i>cut-off</i> utilizado para presença de sintomatologia    depressiva foi um <i>score</i> <i>&#8805;</i>10, à semelhança de estudos prévios    em Portugal, realizados no mesmo período pós-parto<sup>7,31</sup>.</p>     <p>O questionário, aprovado pela Comissão de Ética Hospitalar, foi fornecido a    todas as puérperas do serviço de Obstetrícia do Hospital Senhora Oliveira (HSO)    entre 1 de Fevereiro de 2016 e 31 de Janeiro de 2017, juntamente com o consentimento    informado. O seu preenchimento foi de carácter voluntário e realizou-se à data    de alta (2º dia após parto vaginal e 3º dia após parto por cesariana).</p>     <p>Foram posteriormente consultados os processos eletrónicos, através do programa    Obscare® das 857 puérperas que preencheram o questionário, de forma a obter    as seguintes informações: idade, hábitos tabágicos, hábitos alcoólicos, antecedentes    obstétricos, antecedentes pessoais, tipo de conceção (espontânea <i>Vs.</i>    após técnica de procriação medicamente assistida), tipo de gestação (unifetal    <i>Vs.</i> gestação múltipla), intercorrências da gravidez (RCF, DG, alterações    do LA, complicações hipertensivas e APPT), início do trabalho de parto (induzido    <i>Vs.</i> espontâneo), IG ao parto, via de parto, realização de analgesia epidural    e de episiotomia, lacerações perineais de 3º ou 4º graus, peso do RN, IA ao    1º e 5º minutos e admissão do RN na unidade de Neonatologia. </p>     <p>Definiu-se RCF como peso fetal estimado inferior ao percentil (P) 3 para a    idade gestacional ou inferior ao P 10, na presença de alterações fluxométricas.    PPT foi definido como parto que ocorreu antes da 37ª semana de gestação. O diagnóstico    de DG foi realizado com base nas recomendações nacionais em vigor: glicemia    em jejum no 1ºT e prova de tolerância oral com 75 g de glicose entre as 24 e    28 semanas de gestação.</p>     ]]></body>
<body><![CDATA[<p>A presença de sintomatologia depressiva constituiu a variável a analisar, tendo-se    constituído dois grupos (EDPPE <i>&#8805;</i>10 e EDPPE &lt;10), que foram comparados    em relação às variáveis anteriormente descritas. A análise estatística foi realizada    recorrendo ao programa SPSS v20.0<sup>®</sup>. Foi realizada uma estatística    descritiva e posteriormente uma estatística comparativa entre os dois grupos,    utilizando os testes <i>t-Student</i> <i>e</i> <i>Mann-Whitney</i> (dependendo    da distribuição de normalidade) nas variáveis quantitativas, e o teste <i>Qui</i><sup>2</sup>    nas variáveis categóricas. Nas variáveis nas quais se obteve uma diferença estatisticamente    significativa (<i>p-value</i> &lt;0,05), foi aplicada uma análise univariada    logística e posteriormente procedeu-se ao ajuste para a potencial variável confundidora    (história de depressão prévia ou durante a gravidez) através de uma análise    multivariada. Os resultados da análise multivariada são apresentados como <i>odds    ratio </i>(OR).</p>     <p><b>Resultados</b></p>     <p>De 1 de Fevereiro de 2016 até 31 de Janeiro de 2017, 857 puérperas preencheram    o questionário entre o 2º e o 3º dia pós-parto, sendo que 93 pacientes apresentaram    uma pontuação &#8805;10 na EDPPE, o que resultou numa prevalência de sintomatologia    depressiva de 10,6%. Os <i>scores</i> de depressão pós-parto variaram entre    0 e 20.</p>     <p>O <a href="#q1">Quadro I</a> descreve as características sociodemográficas    e os antecedentes pessoais e obstétricos de ambos os grupos. </p>     <p>&nbsp;</p>     <p align="center"><a name="q1"></a><img src="/img/revistas/aogp/v12n4/12n4a03q1.jpg"/></p>     
<p>&nbsp;</p>     <p>O grupo que pontuou <i>scores</i> mais elevados apresentou mais frequentemente    história de patologia depressiva prévia (17,2 <i>Vs.</i> 7,7%, p=0,03). Neste    sentido, tal como efetuado em estudos prévios, esta variável foi analisada como    uma potencial variável confundidora.</p>     <p>Não foram observadas diferenças estatisticamente significativas entre os dois    grupos em relação à idade, escolaridade, profissão, aumento ponderal durante    gestação e consumo de álcool e tabaco.</p>     <p>No que diz respeito aos antecedentes pessoais, a Diabetes <i>Mellitus</i> surge    como um fator associado a sintomatologia depressiva no pós-parto, mesmo após    o ajuste para a variável confundidora (2,2 <i>Vs.</i> 0,1%, p= 0,018, OR 18,5).</p>     ]]></body>
<body><![CDATA[<p>Em relação aos antecedentes obstétricos, não foi encontrada nenhuma relação    entre o <i>score</i> de depressão pós-parto e a paridade. No entanto, constatou-se    uma diferença estatisticamente significativa entre os dois grupos em relação    à história de abortamentos prévios (8,6 <i>Vs.</i> 4,8%, p= 0,032), que não    se manteve após o ajuste para a variável confundidora.</p>     <p>O <a href="#q2">Quadro II</a> descreve as características da gestação e as    complicações obstétricas nos dois grupos. A RCF surge como fator associado a    <i>scores</i> de depressão pós-parto mais elevados, permanecendo esta relação    após o ajuste para a história de patologia depressiva prévia (8,6 <i>Vs.</i>    2,4%, p= 0,003, OR 3,8). </p>     <p>&nbsp;</p>     <p align="center"><a name="q2"></a><img src="/img/revistas/aogp/v12n4/12n4a03q2.jpg"/></p>     
<p>&nbsp;</p>     <p>Não foram observadas diferenças estatisticamente significativas entre os dois    grupos em relação a intercorrências da gravidez como PPT, complicações hipertensivas    ou DG.</p>     <p>O <a href="#q3">Quadro III</a> expõe os dados relativos ao parto e ao RN.</p>     <p>&nbsp;</p>     <p align="center"><a name="q3"></a><img src="/img/revistas/aogp/v12n4/12n4a03q3.jpg"/></p>     
<p>&nbsp;</p>     ]]></body>
<body><![CDATA[<p>Não foi encontrada qualquer associação entre a sintomatologia depressiva no    puerpério e a via de parto, indução do trabalho de parto, analgesia epidural,    episiotomia ou lacerações de 3º e 4º graus.</p>     <p>Em relação aos dados dos RN, foi constatada uma associação entre baixo peso    ao nascimento (&lt;2.500g.) e maiores <i>scores</i> na EDPPE, independentemente    da história de patologia depressiva prévia (10,8% <i>Vs.</i> 5,2%, p= 0,037,    OR 2,41).</p>     <p>O <a href="#q4">Quadro IV</a> resume os fatores associados a sintomatologia    depressiva no pós-parto, após ajuste para a potencial variável confundidora    - história de patologia depressiva prévia.</p>     <p>&nbsp;</p>     <p align="center"><a name="q4"></a><img src="/img/revistas/aogp/v12n4/12n4a03q4.jpg"/></p>     
<p>&nbsp;</p>     <p><b>Discussão</b></p>     <p>A incidência de sintomatologia depressiva encontrada (10,6%) foi concordante    com a descrita em estudos prévios (realizados no mesmo período pós-parto, com    recurso ao mesmo instrumento de medida - EDPPE e o mesmo <i>cut-off</i>: <i>score</i>    &#8805; 10), que relatam uma incidência entre 6% e 18%<sup>17,20,31-33</sup>.  </p>     <p>A existência de patologia depressiva prévia foi mais frequente no grupo com    resultados &#8805; 10 na EDPPE, tal como foi ampla e consensualmente descrito    em estudos prévios<sup>1,4,12-20,28</sup>.</p>     <p>No que diz respeito às características sociodemográficas, não foi encontrada    qualquer associação entre estes fatores e a presença de sintomatologia depressiva    no pós-parto, de acordo com o previamente defendido por alguns autores<sup>5,19,20,26</sup>.    Por outro lado, estes dados vão contra o descrito em outros estudos, que relatam    que menor idade materna, baixa escolaridade e estatuto socioeconómico inferior    estão associados a sintomatologia depressiva no pós-parto<sup>1,2,13,17,23-25</sup>.</p>     ]]></body>
<body><![CDATA[<p>Relativamente aos antecedentes pessoais, observou-se uma associação entre existência    de Diabetes <i>Mellitus</i> e sintomatologia depressiva no pós-parto, conforme    o descrito por Kayton W., Russo J. e Gavin A. em 2014<sup>24</sup>. No que concerne    aos antecedentes obstétricos, não se constatou nenhuma diferença estatisticamente    significativa entre os dois grupos, à semelhança do demonstrado previamente<sup>1,16,19,34</sup>.</p>     <p>A RCF foi a única complicação obstétrica relacionada com sintomatologia depressiva    no puerpério, tal como referenciado Yang S. <i>et al</i> em 2011<sup>28</sup>.    Esta relação não foi observada para nenhuma outra complicação da gravidez, ao    contrário do descrito em trabalhos anteriores<sup>22,23,25,26,35</sup>. No seguimento    da RCF, o baixo peso ao nascimento (&lt; 2500g.) foi o único <i>outcome</i>    neonatal associado a <i>scores</i> &#8805; 10 na EDPPE, dado já sugerido previamente    por alguns autores<sup>24,34,35</sup>. </p>     <p>A associação entre a via de parto e a incidência de sintomatologia depressiva,    controversa e alvo de inúmeros estudos, não foi demonstrada no presente trabalho.    Apesar de algumas investigações descreverem o parto por cesariana como um fator    de risco para depressão pós-parto,<sup>22,26-28</sup> a maioria dos estudos    corroboram o resultado deste estudo e não descrevem essa associação<sup>1,5,16,17,19,20,25,29,30</sup>.    Ainda neste domínio, alguns trabalhos relatam maior prevalência de sintomatologia    depressiva nas cesarianas urgentes e emergentes<sup>3,13,23</sup>, fator que    também não se verificou na presente investigação.</p>     <p>O presente estudo apresenta algumas limitações: em primeiro lugar, a sintomatologia    depressiva sugerida por <i>scores</i> &#8805; 10 na EDPPE não foi medicamente    confirmada com recurso a uma entrevista clínica. Neste sentido, é importante    relembrar que a EDPPE é uma ferramenta de rastreio e não um teste de diagnóstico.    Uma outra limitação importante é o facto de que a escala foi aplicada à data    de alta e não foi repetida numa fase mais tardia do pós-parto. Apesar de vários    estudos mostrarem uma boa correlação entre os valores pontuados numa altura    precoce e os <i>scores</i> às 4-8 semanas após o parto<sup>6-11,36</sup>, seria    relevante a confirmação do resultado numa fase mais tardia. Pode também apontar-se    como limitação o facto de os questionários terem sido preenchidos em dias diferentes    (2º dia após parto vaginal e 3º dia após parto por cesariana), uma vez que a    perceção emocional das pacientes pode diferir de acordo com a altura em que    o questionário é aplicado, independentemente da via de parto. Por último, não    foram investigados alguns fatores potencialmente associados a sintomatologia    depressiva no puerpério descritos na literatura, como o suporte familiar e a    existência de eventos de vida traumáticos<sup>21,25</sup>.</p>     <p>Como conclusão, pode dizer-se que este trabalho permite avaliar a prevalência    de sintomatologia depressiva ao 2º-3º dia pós-parto e vem reafirmar a sua relação    com algumas variáveis: patologia depressiva prévia, Diabetes <i>Mellitus</i>,    RCF e baixo peso ao nascimento. Os resultados apoiam o rastreio precoce de mulheres    em risco de depressão pós-parto, com base na prevalência de sintomatologia depressiva    à data de alta hospitalar, que deve ter em conta os potenciais fatores de risco    associados. Investigação adicional é necessária no sentido de um conhecimento    mais aprofundado destes mesmos fatores de risco, de forma a possibilitar o desenvolvimento    de estratégias eficazes de rastreio e tratamento da depressão pós-parto.</p>     <p>&nbsp;</p>     <p><b>REFER&Ecirc;NCIAS BIBLIOGR&Aacute;FICAS</b></p>     <!-- ref --><p>1. Ghosh A, Goswami S. Evaluation of Post Partum Depression in a Tertiary Hospital.    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<body><![CDATA[<!-- ref --><p>23. Blom EA, Jansen PW, Verhulst FC, Hofman A, Raat H, Jaddoe VW, et al. Perinatal    complications increase the risk of postpartum depression. The Generation R Study.    BJOG 2010;117(11): 1390-1398.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1872490&pid=S1646-5830201800040000300023&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --> </p>     <!-- ref --><p>24. Katon W, Russo J, Gavin A. Predictors of postpartum depression. J Womens    Health 2014;23(9):753-759.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1872492&pid=S1646-5830201800040000300024&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>     <!-- ref --><p>25. Tikmani SS, Soomro T, Tikmani P. Prevalence and determinants of postpartum    depression in a tertiary care hospital. Austin J Obstet Gynecol 2016;3(2):1-5.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1872494&pid=S1646-5830201800040000300025&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>     <!-- ref --><p>26. Adewuya AO, Fatoye FO, Ola BA, Ijaodola OR, Ibigbami SM. Sociodemographic    and obstetric risk factors for postpartum depressive symptoms in Nigerian women.    J Psychiatr Pract 2005;11(5):353-358.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1872496&pid=S1646-5830201800040000300026&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>     <!-- ref --><p>27. Zanardo V, Giliberti L, Volpe F, Parotto M, de Luca F, Straface G. Cohort    study of the depression, anxiety, and anhedonia components of the Edinburgh    Postnatal Depression Scale after delivery. Int J Gynaecol Obstet 2017;137(3):277-281.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1872498&pid=S1646-5830201800040000300027&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>33. Dubey C, Gupta N, Bhasin S, Muthal RA, Arora R. Prevalence and associated    risk factors for postpartum depression in women attending a tertiary hospital,    Delhi, India. Int J Soc Psychiatry 2012;58(6):577-580.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1872510&pid=S1646-5830201800040000300033&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>     <!-- ref --><p>34. Bergant AM, Heim K, Ulmer H, Illmensee K. Early postnatal depressive mood:    associations with obstetric and psychosocial factors. J Psychosom Res 1999;46(4):    391-394.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1872512&pid=S1646-5830201800040000300034&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --> </p>     <!-- ref --><p>35. Vigod SN, Villegas L, Dennis CL, Ross LE. Prevalence and risk factors for    postpartum depression among women with preterm and low-birth-weight infants:    a systematic review. BJOG 2010;117(5):540-550.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1872514&pid=S1646-5830201800040000300035&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>     <!-- ref --><p>36. Warzecha D, Gajda S, Kosinska-Kaczynska K, Szymusik I, Wielgos M. Risk    factors for depressive symptoms in early postpartum period and after puerperium    - are they the same? Neuro Endocrinol Lett 2016;37(6): 452-460.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1872516&pid=S1646-5830201800040000300036&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>     ]]></body>
<body><![CDATA[<p>Cátia Ferreira</p>     <p>E-mail: <a href="mailto:catia.lmferreira@gmail.com">catia.lmferreira@gmail.com</a></p>     <p>&nbsp;</p>     <p><b>Recebido em: </b>09/12/2017</p>     <p><b>Aceite para publicação: </b>30/09/2018</p>      ]]></body><back>
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