<?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>S1646-58302016000300003</article-id>
<title-group>
<article-title xml:lang="pt"><![CDATA[Gravidez na doença renal crónica: da diálise peritoneal à hemodiálise]]></article-title>
<article-title xml:lang="en"><![CDATA[Pregnancy in chronic kidney disease: from peritoneal dialysis to hemodialysis]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Pinto]]></surname>
<given-names><![CDATA[Pedro Viana]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Nunes]]></surname>
<given-names><![CDATA[Ana Teresa]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Santos]]></surname>
<given-names><![CDATA[Carla]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Martins]]></surname>
<given-names><![CDATA[Patricia]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Machado]]></surname>
<given-names><![CDATA[Ana Paula]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Montenegro]]></surname>
<given-names><![CDATA[Nuno]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
<xref ref-type="aff" rid="A02"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Centro Hospitalar São João Serviço de Ginecologia/Obstetrícia ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<aff id="A02">
<institution><![CDATA[,Universidade do Porto Faculdade de Medicina ]]></institution>
<addr-line><![CDATA[Porto ]]></addr-line>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>09</month>
<year>2016</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>09</month>
<year>2016</year>
</pub-date>
<volume>10</volume>
<numero>3</numero>
<fpage>194</fpage>
<lpage>200</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_arttext&amp;pid=S1646-58302016000300003&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_abstract&amp;pid=S1646-58302016000300003&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_pdf&amp;pid=S1646-58302016000300003&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[Overview and Aims: pregnancy in women with chronic kidney disease (CKD), particularly in terminal CKD, remains a rare event. There are scarce reports of pregnancy in women undergoing peritoneal dialysis. Our study aims to evaluate the outcomes of pregnancies in women with CKD diagnosed at Hospital São João during the study period. Study design: retrospective case series. Population: pregnant women with chronic kidney disease diagnosed between January 2005 and December 2013. Methods: pregnancies in women with severe CKD (GFR <30mL in/1.73m2) were identified by using hospital electronic platforms with evaluation of maternal and fetal outcomes. Results: during the study period 4 cases of pregnancy in women with CKD were identified, including one of a woman in peritoneal dialysis prior to pregnancy - case 1. Case 1 progressed to hemodialysis at 17 weeks (due to haemoperitoneum subsequent to trauma by the peritoneal dialysis catheter) and had an eutocic late preterm delivery at 35 weeks. Case 2 began hemodialysis at 22 weeks, and was submitted to urgent cesarean section at 29 weeks. Case 3 started hemodialysis at 21 weeks, having also undergone urgent cesarean section at 31 weeks. Case 4 began hemodialysis at 21 weeks, presenting with an episode of hepatotoxicity secondary to darbopoietin at 26 weeks. Delivery occurred by Caesarean section at 32 weeks. Conclusion: despite the high fetal morbidity documented, with the strategies adopted there was no fetal or neonatal mortality. The monitoring of these pregnant in specialized consultation favored the positive outcomes.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Pregnancy]]></kwd>
<kwd lng="en"><![CDATA[Hemodialysis]]></kwd>
<kwd lng="en"><![CDATA[Chronic Kidney Disease]]></kwd>
<kwd lng="en"><![CDATA[Peritoneal Dialysis]]></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>Gravidez na doen&#231;a renal cr&#243;nica:&#160; da di&#225;lise peritoneal &#224; hemodi&#225;lise </b></font></p>     <p><font size="3"><b>Pregnancy in chronic kidney disease:&#160; from peritoneal dialysis to hemodialysis </b></font></p>     <p><b>Pedro Viana Pinto*, Ana Teresa Nunes*, Carla Santos**, Patricia Martins**, Ana Paula Machado***, Nuno Montenegro****</b></p>     <p>Servi&#231;o de Ginecologia/Obstetr&#237;cia, Centro Hospitalar S&#227;o Jo&#227;o</p>     <p>*Interno de Formac&#227;o Espec&#237;fica de Ginecologia e Obstetr&#237;cia, Centro Hospitalar de S&#227;o Jo&#227;o</p>     <p>**Interno de Formac&#227;o Espec&#237;fica de Nefrologia, Centro Hospitalar S&#227;o Jo&#227;o</p>     <p>***Assistente hospitalar, Servi&#231;o Nefrologia, Centro Hospitalar S&#227;o Jo&#227;o</p>     <p>****Assistente hospitalar, Servi&#231;o Ginecologia e Obstetr&#237;cia, Centro Hospitalar S&#227;o Jo&#227;o</p>     <p>*****Diretor do Servi&#231;o de Ginecologia e Obstetr&#237;cia, Centro Hospitalar de S&#227;o Jo&#227;o; Subdiretor da Faculdade de Medicina da Universidade do Porto</p>     ]]></body>
<body><![CDATA[<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>     <p><b>ABSTRACT</b></p>     <p><b>Overview and Aims: </b>pregnancy in women with chronic kidney disease (CKD), particularly in terminal CKD, remains a rare event. There are scarce reports of pregnancy in women undergoing peritoneal dialysis. Our study aims to evaluate the outcomes of pregnancies in women with CKD diagnosed at Hospital S&#227;o Jo&#227;o during the study period.</p>     <p><b>Study design: </b>retrospective case series.</p>     <p><b>Population: </b>pregnant women with chronic kidney disease diagnosed between January 2005 and December 2013.</p>     <p><b>Methods: </b>pregnancies in women with severe CKD (GFR &lt;30mL in/1.73m2) were identified by using hospital electronic platforms with evaluation of maternal and fetal outcomes.</p>     <p><b>Results: </b>during the study period 4 cases of pregnancy in women with CKD were identified, including one of a woman in peritoneal dialysis prior to pregnancy - case 1. Case 1 progressed to hemodialysis at 17 weeks (due to haemoperitoneum subsequent to trauma by the peritoneal dialysis catheter) and had an eutocic late preterm delivery at 35 weeks. Case 2 began hemodialysis at 22 weeks, and was submitted to urgent cesarean section at 29 weeks. Case 3 started hemodialysis at 21 weeks, having also undergone urgent cesarean section at 31 weeks. Case 4 began hemodialysis at 21 weeks, presenting with an episode of hepatotoxicity secondary to darbopoietin at 26 weeks. Delivery occurred by Caesarean section at 32 weeks.</p>     <p><b>Conclusion: </b>despite the high fetal morbidity documented, with the strategies adopted there was no fetal or neonatal mortality. The monitoring of these pregnant in specialized consultation favored the positive outcomes.</p>     <p><b>Palavras-chave: </b>Pregnancy; Hemodialysis; Chronic Kidney Disease; Peritoneal Dialysis.</p> <hr/>     ]]></body>
<body><![CDATA[<p>&nbsp;</p>     <p><b>Introdu&#231;&#227;o</b></p>     <p>Provavelmente nenhum outro insulto fisiol&#243;gico causa altera&#231;&#245;es t&#227;o marcadas na fun&#231;&#227;o renal como a gravidez. O volume renal aumenta cerca de 30%, a taxa de filtra&#231;&#227;o glomerular aumenta (n&#227;o por altera&#231;&#245;es histol&#243;gicas ou do n&#250;mero de nefr&#243;nios mas pelo aumento do d&#233;bito card&#237;aco e do fluxo sangu&#237;neo renal e por uma menor resposta a vasopressores como a angiotensina 2, noradrenalina e vasopressina)<sup>1-5</sup>, sendo que a alcalose respirat&#243;ria pr&#243;pria da gravidez e as maiores necessidades de hemoglobina imp&#245;em, tamb&#233;m, uma maior exig&#234;ncia aos rins maternos<sup>1</sup>. Contudo, na presen&#231;a de doen&#231;a renal cr&#243;nica (DRC) estas adapta&#231;&#245;es fisiol&#243;gicas ficam comprometidas ou at&#233; impossibilitadas, tornando a gravidez nestas situa&#231;&#245;es um desafio extremamente complexo<sup>6</sup>.</p>     <p>Mais de 40 anos ap&#243;s o primeiro caso descrito de gravidez numa mulher em di&#225;lise, a gravidez em mulheres com DRC grave continua um evento raro. H&#225; poucos dados sobre a taxa de concep&#231;&#227;o nestas mulheres, sendo a maioria provenientes de bases de dados antigas. No entanto, &#233; descrito um aumento significativo na taxa de concep&#231;&#227;o de mulheres em di&#225;lise - 0,9% em 1980 para 2,4% em 1998 - embora este valor possa estar subestimado dado que a maioria das gravidezes &#233; diagnosticada apenas no segundo trimestre, com perda dos casos de abortamentos precoces<sup>7, 8</sup>.</p>     <p>A disfun&#231;&#227;o reprodutiva feminina nesta popula&#231;&#227;o &#233; complexa e multi-factorial, envolvendo fatores fisiol&#243;gicos, condi&#231;&#245;es m&#233;dicas associadas e fatores psicossociais. Em mulheres com insufici&#234;ncia renal avan&#231;ada a secre&#231;&#227;o de GnRH encontra-se alterada, bem como o pico de LH, embora os n&#237;veis de LH basais tendam a ser mais elevados, com a consequente falha na ovula&#231;&#227;o<sup>9-11</sup>. Os n&#237;veis de prolactina e a sua actividade biol&#243;gica encontram-se aumentados nestas mulheres, com consequente diminui&#231;&#227;o da libido, infertilidade, amenorreia ou oligomenorreia e galactorreia<sup>12</sup>. A amenorreia surge tipicamente com taxas de filtra&#231;&#227;o glomerulares (TFGe) menores que 5mL inuto<sup>8</sup>. Altera&#231;&#245;es secund&#225;rias na morfologia endometrial (atrofia ou altera&#231;&#245;es proliferativas) s&#227;o, tamb&#233;m, comuns e podem dificultar a implanta&#231;&#227;o do blastocisto<sup>9</sup>. O transplante renal bem-sucedido rep&#245;e, na maioria dos casos, o ambiente hormonal necess&#225;rio &#224; reprodu&#231;&#227;o<sup>12</sup>.</p>     <p>Os enormes avan&#231;os nos cuidados materno-fetais bem como na frequ&#234;ncia e efici&#234;ncia das t&#233;cnicas substitutivas da fun&#231;&#227;o renal permitiram um aumento da sobrevida fetal de 20-23 % em 1980 para 75-80%&#160; atualmente<sup>13-17</sup>. A concep&#231;&#227;o bem como o desfecho favor&#225;vel da gravidez s&#227;o muito mais frequentes em mulheres com menos tempo em di&#225;lise, com manuten&#231;&#227;o de fun&#231;&#227;o renal residual e quando a gravidez se inicia antes da necessidade de di&#225;lise<sup>11,17</sup>. O fator progn&#243;stico mais importante para os desfechos materno e fetal &#233; o grau de comprometimento da fun&#231;&#227;o renal no momento da concep&#231;&#227;o<sup>18</sup>.</p>     <p>Nestas mulheres &#233; essencial um controlo adequado das complica&#231;&#245;es cl&#237;nicas associadas &#224; doen&#231;a renal independentemente da etiologia da mesma<sup>6</sup>. Apesar de toda a evolu&#231;&#227;o na vigil&#226;ncia destas gr&#225;vidas, a maioria dos rec&#233;m-nascidos s&#227;o prematuros (idade gestacional m&#233;dia de 32 semanas)<sup>19,20</sup> e complica&#231;&#245;es como a doen&#231;a hipertensiva da gravidez, a anemia, o hidr&#226;mnios e a restri&#231;&#227;o de crescimento fetal s&#227;o tamb&#233;m frequentes<sup>17,20,21</sup>.</p>     <p>A gravidez bem-sucedida &#233; poss&#237;vel com ambas as t&#233;cnicas substitutivas da fun&#231;&#227;o renal. S&#227;o, no entanto, menos frequentes os casos descritos na literatura de gravidez em mulheres em di&#225;lise peritoneal (DP)<sup>22</sup>. Neste trabalho, descrevemos uma s&#233;rie de casos de gravidezes em mulheres com DRC grave acompanhadas entre 2005 e 2013 no Centro Hospitalar S&#227;o Jo&#227;o, incluindo um caso de uma gravidez numa mulher j&#225; em di&#225;lise peritoneal antes da concep&#231;&#227;o.</p>     <p><b>M&#233;todos</b></p>     <p>Foi realizado uma pesquisa sistem&#225;tica na nossa institui&#231;&#227;o de todas as gr&#225;vidas portadoras de doen&#231;a renal cr&#243;nica. Todas as mulheres portadoras de doen&#231;a renal cr&#243;nica grave (TFGe &lt;30mL/ min/1,73m<sup>2</sup>) e com parto na nossa institui&#231;&#227;o foram inclu&#237;das. As mulheres expostas foram identificadas com recurso a uma base de dados electr&#243;nica e ao sistema inform&#225;tico da nossa institui&#231;&#227;o (OBSCARE&#174;, SCLINICO&#174;). Foram consultados os processos cl&#237;nicos individuais de forma a identificar as caracter&#237;sticas particulares dos casos em estudo, nomeadamente a doen&#231;a renal de base, presen&#231;a de outras co-morbilidades maternas associadas, a idade gestacional (IG) de diagn&#243;stico de gravidez, a t&#233;cnica de substitui&#231;&#227;o renal utilizada e com que IG foi iniciada, presen&#231;a de doen&#231;a hipertensiva da gravidez (HTA gestacional, pr&#233;-ecl&#226;mpsia/ecl&#226;mpsia, s&#237;ndrome HELLP), restri&#231;&#227;o crescimento fetal, hidr&#226;mnios ou anemia, IG do parto, peso do rec&#233;m-nascido, via de parto e principais complica&#231;&#245;es puerperais e neonatais.</p>     ]]></body>
<body><![CDATA[<p><b>Resultados</b></p>     <p>Durante o per&#237;odo em estudo houve 24.308 partos na nossa institui&#231;&#227;o, tendo sido detectados 4 casos de gr&#225;vidas com DRC severa com necessidade de t&#233;cnicas de substitui&#231;&#227;o renal (incid&#234;ncia - 1/6.077 nascimentos).</p>     <p><b>Caso 1</b></p>     <p>Primigesta, 37 anos, DRC terminal em DP desde os 33 anos ap&#243;s glomerulosclerose segmentar e focal diagnosticada aos 24 anos de idade. Aos 36 anos apresenta epis&#243;dio de neuropatia &#243;ptica isqu&#233;mica anterior, tratado sem sequelas.</p>     <p>Em Abril de 2013, apresentando um quadro de n&#225;useas e v&#243;mitos recorre a urg&#234;ncia hospitalar tendo sido diagnosticada gravidez de 10 semanas. Nesta data apresentava-se com uma estrat&#233;gia de DP de 3 permutas/dias (com 2L de dialisante Physioneal&#174;), com boa adequa&#231;&#227;o dial&#237;tica e diurese residual de 1000mL. A sua medica&#231;&#227;o cr&#243;nica pr&#233;via ao diagn&#243;stico de gravidez inclu&#237;a rosuvastatina 20mg/d, alopurinol 100mg/d, sertralina 50mg/d, amitriptilina 10mg/d, darbopoietina, sulfato ferroso, &#225;cido f&#243;lico e complexo multivitam&#237;nico do grupo B. Ap&#243;s diagn&#243;stico de gravidez manteve apenas a sertralina 50mg/d, darbopoietina, sulfato ferroso, &#225;cido f&#243;lico 5mg/d e complexo multivitam&#237;nico do grupo B, aos quais acrescentou o &#225;cido acetilsalic&#237;lico 100mg/d, tendo sido aumentadas as permutas de DP para 4 vezes/dia. Foi orientada para vigil&#226;ncia em consulta multidisciplinar envolvendo Nefrologia, Obstetr&#237;cia e Nutri&#231;&#227;o.</p>     <p>Durante o primeiro trimestre apresentou duas infe&#231;&#245;es urin&#225;rias baixas n&#227;o complicadas. &#192;s 15 semanas de gesta&#231;&#227;o apresentou um epis&#243;dio de hemoperitoneu sem evid&#234;ncia de trauma pelo cat&#233;ter de DP e com culturas de l&#237;quido peritoneal negativas. Fez amniocentese &#224;s 16 semanas por rastreio combinado de 1&#186; trimestre positivo, sem intercorr&#234;ncias (cari&#243;tipo 46, XY).</p>     <p>Devido a queixas de distens&#227;o abdominal foi reduzido o volume de dialisante (1700ml) mas aumentada a frequ&#234;ncia (5 vezes/dia) de modo a manter efic&#225;cia dial&#237;tica adequada. &#192;s 17 semanas de gesta&#231;&#227;o apresenta novo hemoperitoneu com documenta&#231;&#227;o ecogr&#225;fica de contacto entre cat&#233;ter de DP com a serosa uterina. Neste contexto procedeu-se &#224; remo&#231;&#227;o urgente do cat&#233;ter de DP e iniciada hemodi&#225;lise por cat&#233;ter tunelizado no mesmo dia. Duas semanas ap&#243;s o inicio de hemodi&#225;lise foi poss&#237;vel o in&#237;cio de pun&#231;&#227;o da fistula arterio-venosa, j&#225; previamente intervencionada durante a gravidez na perspetiva de eventual necessidade de transi&#231;&#227;o de di&#225;lise peritoneal para hemodi&#225;lise. A estrat&#233;gia adotada consistiu em 24h/semana de di&#225;lise (4h/6 vezes por semana). Foi estimado um aumento de peso de 450g/semana, com controlo do mesmo com recurso a avalia&#231;&#227;o cl&#237;nica regular, avalia&#231;&#245;es seriadas de BNP, bioimped&#226;ncia e &#237;ndices de vol&#233;mia ecocardiogr&#225;ficos. O controlo tensional foi efetuado sem recurso a medica&#231;&#227;o anti-hipertensora at&#233; &#224;s 27 semanas, altura em que iniciou metildopa (750mg/d). Necessitou de aumento progressivo da dose de estimulador da eritropoiese (doses de darbopoietina de 100 mcg/semana no final da gravidez) de modo a que os n&#237;veis de hemoglobina (Hb) se mantivessem est&#225;veis (Hb ~10g/ /dL). Durante o per&#237;odo em que realizou hemodi&#225;lise os n&#237;veis sangu&#237;neos de ureia mantiveram-se &lt;60mg/ /dL.</p>     <p>&#192;s 27 semanas de gesta&#231;&#227;o foi internada no servi&#231;o de Medicina Materno-Fetal no contexto de amea&#231;a de parto pr&#233;-termo, tendo iniciado toc&#243;lise com nifedipina e ciclo de matura&#231;&#227;o pulmonar fetal com betametasona. Diagnosticada restri&#231;&#227;o de crescimento fetal &#224;s 32 semanas (percentil 5), com fluxometria umbilical e da art&#233;ria cerebral m&#233;dia normais. &#192;s 35 semanas por HTA grave (apesar da terap&#234;utica com metildopa 1500mg/d) com tra&#231;ado cardiotocogr&#225;fico suspeito (variabilidade longa reduzida sustentada) foi induzido o trabalho de parto, tendo tido um parto eut&#243;cico, com rec&#233;m-nascido (RN) do sexo masculino com 1975g e &#237;ndice de Apgar de 7/8 ao 1&#186;/5&#186; minutos (<a href="#q1">Quadro I</a>). O RN apresentou diurese osm&#243;tica na depend&#234;ncia de azotemia materna, bem como uma dilata&#231;&#227;o pielocalicial ligeira &#224; esquerda (5mm), tendo tido alta ao 18&#186; dia de vida.</p>     <p>&nbsp;</p>     <p align="center"><a name="q1"></a><img src="/img/revistas/aogp/v10n3/10n3a03q1.jpg"/></p>     
]]></body>
<body><![CDATA[<p>&nbsp;</p>     <p>Teve alta ao 7&#186; dia de puerp&#233;rio em programa regular de hemodi&#225;lise 4 vezes/semana, tendo reiniciado DP 2 meses ap&#243;s o parto. Atualmente mant&#233;m DP com controlo adequado de volume e diurese residual de 1000mL.</p>     <p><b>Caso 2</b></p>     <p>Paciente de 40 anos de idade, gesta 7, 6 partos eut&#243;cicos, seguida por Nefrologia por DRC no contexto de nefroangiosclerose hipertensiva - suspeita de estenose da art&#233;ria renal (TFGe antes da gravidez de 13,6ml/&#160; in/1,73m2). Em ecografia (Novembro de 2005) realizada para estudo da doen&#231;a renal foi-lhe diagnosticada gravidez (cerca de 18 semanas). Foi alterada a medica&#231;&#227;o anti- hipertensora (suspendeu Enalapril) e orientada para consulta multidisciplinar de Obstetr&#237;cia e Nefrologia para acompanhamento especializado. &#192;s 21 semanas foi internada por HTA cr&#243;nica agravada (com agravamento da fun&#231;&#227;o renal), sem outras altera&#231;&#245;es anal&#237;ticas. Apresentava anemia grave com necessidade de suporte transfusional. Foi conseguido controlo tensional satisfat&#243;rio mas n&#227;o se verificou recupera&#231;&#227;o da fun&#231;&#227;o renal tendo iniciado hemodi&#225;lise &#224;s 22 semanas - estrat&#233;gia de 20h/semana (4h/5 vezes semana). Apesar da medica&#231;&#227;o anti-hipertensora (metildopa 1500g/d) e estrat&#233;gia dial&#237;tica frequente apresentou controlo tensional sub-&#243;timo procedendo-se a internamento &#224;s 27 semanas para realiza&#231;&#227;o de ciclo de matura&#231;&#227;o pulmonar fetal com betametasona. &#192;s 29 semanas tem parto por cesariana eletiva por mau controlo tensional associado a restri&#231;&#227;o crescimento fetal grave com altera&#231;&#245;es da fluxometria umbilical, com RN do sexo masculino, 1040g e &#237;ndice de Apgar 8/9 ao 1&#186;/5&#186; minutos (Quadro I). O RN apresentou v&#225;rias complica&#231;&#245;es no contexto de prematuridade, apresentando atualmente desenvolvimento psicomotor adequado. A m&#227;e tem alta ao 6&#186; dia de puerp&#233;rio, medicada com lisinopril. Foi submetida a transplante renal em 2011 e transplectomizada um m&#234;s depois por infe&#231;&#227;o de hematoma (hemorragia no p&#243;s-transplante imediato), com segundo transplante, bem sucedido, em 2013.</p>     <p><b>Caso 3</b></p>     <p>Primigesta de 25 anos, com DRC secund&#225;ria a nefropatia de refluxo, nefrectomia direita em 1996 e HTA. Gravidez diagnosticada &#224;s 8 semanas (Outubro de 2009), tendo sido encaminhada para consulta multidisciplinar de Obstetr&#237;cia e Nefrologia. Prevendo-se a necessidade de in&#237;cio de di&#225;lise a curto prazo (&#224; data de diagn&#243;stico de gravidez TFGe 19ml in/1,72m2) &#233; constru&#237;da f&#237;stula arterio-venosa, com fal&#234;ncia prim&#225;ria desta. &#192;s 20 semanas de gesta&#231;&#227;o &#233; internada por hipervol&#233;mia e agravamento da fun&#231;&#227;o renal com in&#237;cio de hemodi&#225;lise por cat&#233;ter venoso central tunelizado. Tem alta &#224;s 22 semanas de gravidez, medicada com &#225;cido acetilsalic&#237;lico (AAS) 100mg e metildopa 1500mg/d, com estrat&#233;gia de di&#225;lise 20h/semana (4h/5 vezes semana), visando-se um aumento de peso seco de cerca 250-300g/semana. &#192;s 29 semanas apresenta pielonefrite aguda por <i>Escherichia coli</i> com resolu&#231;&#227;o com antibioterapia (ceftriaxone seguido de amoxicilina/ &#225;cido clavul&#226;nico), sendo re-internada &#224;s 31 semanas por restri&#231;&#227;o de crescimento fetal com altera&#231;&#245;es fluxom&#233;tricas. Faz ciclo de matura&#231;&#227;o pulmonar fetal com betametasona sendo submetida a cesariana emergente por estado fetal n&#227;o tranquilizador &#224;s 31 semanas, com RN do sexo feminino, 1250g e &#237;ndice de Apgar 8/9 ao 1&#186;/5&#186; minutos. O per&#237;odo neonatal evoluiu sem intercorr&#234;ncias. A m&#227;e teve alta ao 5&#186; dia de puerp&#233;rio, tendo optado por iniciar di&#225;lise peritoneal (Quadro I). Foi transplantada 2 anos depois e apresenta boa fun&#231;&#227;o do aloenxerto.</p>     <p><b>Caso 4</b></p>     <p>Primigesta com 31 anos, com DRC secund&#225;ria a glomerulopatia cr&#243;nica n&#227;o especificada, com uma TFGe antes da gravidez de 16ml in/1,72m2. Encaminhada para consulta multidisciplinar de Obstetr&#237;cia e Nefrologia &#224;s 13 semanas de gesta&#231;&#227;o (Julho de 2010), sendo medicada com metildopa 500mg/d, suplementa&#231;&#227;o de ferro, AAS 100mg id, &#225;cido f&#243;lico 5mg id e darbopoietina 10&#181;g/sem. &#192;s 21 semanas de gesta&#231;&#227;o, por agravamento da fun&#231;&#227;o renal, inicia hemodi&#225;lise por f&#237;stula arterio-venosa (15h - 3h/ 5 vezes semana) com um aumento de peso seco previsto de 500g/semana. &#192;s 26 semanas &#233; detectada cit&#243;lise hep&#225;tica com hiperbilirrubinemia, tendo sido internada para estudo. Realizou bi&#243;psia hep&#225;tica que revelou apenas siderose nas c&#233;lulas de Kupfer e, dada a melhoria anal&#237;tica ap&#243;s suspens&#227;o de darbopoietina, foi presumida hepatite t&#243;xica secund&#225;ria este f&#225;rmaco. Teve necessidade de suporte transfusional (6U de gl&#243;bulos rubros) durante a gravidez. &#192;s 31 semanas foi reinternada por hipervol&#233;mia associada a infe&#231;&#227;o respirat&#243;ria e agravamento do controlo tensional tendo sido medicada com amlodipina. &#192;s 32 semanas, ap&#243;s completar matura&#231;&#227;o pulmonar fetal com betametasona, no contexto de hipervol&#233;mia e HTA graves e insufici&#234;ncia respirat&#243;ria, foi submetida a cesariana urgente com rec&#233;m-nascido do sexo feminino, 1705g e &#237;ndice de Apgar 8/8 ao 1&#186;/5&#186; minutos (Quadro I). O RN desenvolveu uma s&#233;psis no per&#237;odo neonatal com posterior melhoria e recupera&#231;&#227;o. A doente permaneceu 24 horas em Unidade de Cuidados Intensivos, com alta hospitalar ao 11&#186; dia de puerp&#233;rio, ap&#243;s remo&#231;&#227;o de elevado volume de ultrafiltrado (13 L em 3 dias). Atualmente mant&#233;m-se em programa regular de hemodi&#225;lise, em lista de espera para transplante renal.</p>     <p><b>Discuss&#227;o</b></p>     <p>Esta s&#233;rie de casos permite constatar que, apesar da elevada morbilidade associada, a gravidez em mulheres com DRC grave &#233; poss&#237;vel, com desfecho materno-fetal aceit&#225;vel. Apesar da alta incid&#234;ncia de complica&#231;&#245;es observadas na nossa s&#233;rie (parto pr&#233;-termo, doen&#231;a hipertensiva da gravidez, agravamento da fun&#231;&#227;o renal, complica&#231;&#245;es infeciosas, hipersensibilidade medicamentosa) com as estrat&#233;gias adotadas n&#227;o existiu mortalidade fetal ou neonatal.</p>     ]]></body>
<body><![CDATA[<p>O agravamento da fun&#231;&#227;o renal &#233; mais frequente nas gr&#225;vidas com DRC avan&#231;ada e deve-se em particular &#224;s altera&#231;&#245;es hemodin&#226;micas t&#237;picas da gravidez com uma importante sobrecarga de volume materno, a maior incid&#234;ncia de HTA e s&#237;ndromes obst&#233;tricos associados e &#224;s complica&#231;&#245;es infeciosas, particularmente do tracto genito-urin&#225;rio<sup>17</sup>. Os tr&#234;s casos que iniciaram di&#225;lise durante a gravidez apresentavam j&#225; doen&#231;a renal cr&#243;nica avan&#231;ada e iniciaram di&#225;lise no contexto de hipertens&#227;o n&#227;o controlada, hipervol&#233;mia e agravamento da fun&#231;&#227;o renal.</p>     <p>O caso 1 reporta a &#250;nica gravidez numa mulher j&#225; em tratamento de substitui&#231;&#227;o renal, em di&#225;lise peritoneal. Esta situa&#231;&#227;o &#233; relativamente rara, com poucos casos descritos na literatura<sup>22</sup>. A di&#225;lise peritoneal permite trocas dial&#237;ticas cont&#237;nuas, com controlo metab&#243;lico mais suave, e altera&#231;&#245;es menos abruptas no volume intravascular materno, possivelmente diminuindo as altera&#231;&#245;es hemodin&#226;micas na circula&#231;&#227;o utero-placent&#225;ria e minimizando as flutua&#231;&#245;es na press&#227;o arterial materna. Por outro lado, traz tamb&#233;m o benef&#237;cio de n&#227;o ser necess&#225;ria anti-coagula&#231;&#227;o, com menor risco hemorr&#225;gico<sup>8,22</sup>. Contudo, as altera&#231;&#245;es de volume intra-abdominal causadas pelo aumento das dimens&#245;es uterinas podem obrigar &#224; diminui&#231;&#227;o dos volumes de dialisante e necessidade de aumento da frequ&#234;ncia das permutas de modo a manter uma efic&#225;cia dial&#237;tica adequada<sup>23</sup>. Outras complica&#231;&#245;es diretamente associadas &#224; di&#225;lise peritoneal s&#227;o a dor abdominal, o hemoperitoneu ou peritonite<sup>22</sup>. No caso em quest&#227;o foi necess&#225;rio transitar para hemodi&#225;lise &#224;s 17 semanas ap&#243;s um segundo epis&#243;dio de hemoperitoneu comprovadamente associado a les&#227;o uterina pelo cat&#233;ter de di&#225;lise.</p>     <p>Em mulheres com DRC o diagn&#243;stico de gravidez frequentemente &#233; tardio, dada a irregularidade menstrual pr&#243;pria das mulheres com doen&#231;a renal e a n&#227;o valoriza&#231;&#227;o de sintomas como n&#225;useas e v&#243;mitos, tradicionalmente associados a uremia. Ap&#243;s o diagn&#243;stico de gravidez, &#233; determinante a vigil&#226;ncia por equipa multidisciplinar, que inclua especialistas em Obstetr&#237;cia, Nefrologia e Nutri&#231;&#227;o, adaptados &#224;s caracter&#237;sticas particulares do acompanhamento destas doentes. Apesar de na nossa casu&#237;stica 3 dos casos terem sido diagnosticados no 1&#186; trimestre, &#233; desej&#225;vel que a interven&#231;&#227;o multidisciplinar seja o mais precoce poss&#237;vel.</p>     <p>Os melhores desfechos obst&#233;tricos descritos s&#227;o obtidos com hemodi&#225;lise intensiva com aumento da frequ&#234;ncia das trocas semanais (&gt;24h/semana)<sup>11,24</sup>. &#201; indispens&#225;vel um controlo adequado do ganho de peso e da tens&#227;o arterial (todos os nossos casos se acompanharam de HTA), devendo haver um limiar baixo de suspei&#231;&#227;o de doen&#231;as como pr&#233;-ecl&#226;mpsia e s&#237;ndrome HELLP cujo diagn&#243;stico por vezes pode ser complicado nestas pacientes. O controlo da tens&#227;o arterial deve ser conseguido pelo controlo da vol&#233;mia e, quando necess&#225;rio, pelo recurso a medica&#231;&#227;o anti-hipertensora. N&#227;o existe um valor alvo consensual de tens&#227;o arterial nas gr&#225;vidas com DRC, no entanto s&#227;o sugeridos valores &lt;140/90mmHg, n&#227;o sendo recomendadas valores de TA diast&#243;lica inferiores a 75mmHg de modo a n&#227;o comprometer a perfus&#227;o placentar<sup>18,25</sup>.</p>     <p>&#201; fundamental o controlo dos n&#237;veis de hemoglobina que diminuem por aumento das necessidades de s&#237;ntese de eritr&#243;citos, perdas de ferro e eritr&#243;citos durante a di&#225;lise, bem como aumento da resist&#234;ncia &#224; eritropoietina por citocinas circulantes. As gr&#225;vidas com doen&#231;a renal apresentam frequentemente necessidades muito elevadas de estimuladores da eritropoietina e de suplementa&#231;&#227;o de ferro para manuten&#231;&#227;o de n&#237;veis de hemoglobina entre 10-11g/dL<sup>8,18,25</sup>. Um adequado aporte nutricional &#233; promovido atrav&#233;s de liberaliza&#231;&#227;o da dieta, aumento de ingest&#227;o proteica (1,5-1,8g/ kg/dia) e suplementa&#231;&#227;o com vitaminas hidrossol&#250;veis com destaque para o acido f&#243;lico<sup>8,11</sup>. &#201; essencial a vigil&#226;ncia regular dos n&#237;veis de c&#225;lcio e f&#243;sforo, uma vez que a hipercalcemia materna pode causar hipocalcemia e hiperfosfatemia no rec&#233;m-nascido e afetar o seu desenvolvimento esquel&#233;tico<sup>25</sup>.</p>     <p>Uma das principais complica&#231;&#245;es da gravidez em mulheres com DRC &#233; a prematuridade, na maioria dos casos iatrog&#233;nica, com uma preval&#234;ncia que varia entre os 67-100% em mulheres em di&#225;lise<sup>16</sup>. A prematuridade &#233; o determinante isolado mais importante de desfecho adverso infantil, quer em termos de morbilidade quer em termos de mortalidade<sup>26</sup>. Apesar do n&#250;mero limitado de casos na nossa s&#233;rie salienta-se que o caso 1, em que a concep&#231;&#227;o decorreu em doente em di&#225;lise, submetido a uma estrat&#233;gia de di&#225;lise mais intensiva, obteve o melhor desfecho obst&#233;trico com parto &#224;s 35 semanas (pr&#233;-termo tardio).</p>     <p>Outra complica&#231;&#227;o muito frequente nestas gr&#225;vidas &#233; a restri&#231;&#227;o de crescimento fetal (cerca de 36% dos casos)<sup>27</sup>, que deve ser orientada de acordo com os padr&#245;es obst&#233;tricos habituais com ecografias seriadas, avalia&#231;&#227;o da fluxometria Doppler das art&#233;rias umbilical<sup>28</sup> e cerebral m&#233;dia<sup>29</sup> e cardiotocografia. Por &#250;ltimo, refer&#234;ncia ao hidr&#226;mnios, secund&#225;rio a diurese osm&#243;tica fetal pelo aumento da ureia na urina<sup>25</sup>. A decis&#227;o quanto &#224; via de parto deve ser individualizada, tendo sempre o parto vaginal como via preferencial. A op&#231;&#227;o por uma cesariana dever&#225; estar de acordo com as indica&#231;&#245;es obst&#233;tricas habituais.</p>     <p>Esta pequena s&#233;rie de casos demonstra que, apesar da gravidez em pacientes com doen&#231;a renal cr&#243;nica avan&#231;ada apresentar elevada morbilidade, a monitoriza&#231;&#227;o fetal frequente e o controlo intensivo dos par&#226;metros bioqu&#237;micos e f&#237;sicos maternos, sob a supervis&#227;o de uma equipa multidisciplinar especializada tornam poss&#237;veis desfechos positivos. O ajuste das t&#233;cnicas dial&#237;ticas, em particular os esquemas de di&#225;lise intensiva e intera&#231;&#227;o frequente entre os profissionais permite otimizar a sa&#250;de materna sem comprometimento fetal e obter melhores desfechos obst&#233;tricos.</p>     <p>&nbsp;</p>     <p><b>REFER&#202;NCIAS BIBLIOGR&#193;FICAS</b></p>     ]]></body>
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<body><![CDATA[<!-- ref --><p>27. Manisco G, Poti M, Maggiulli G, Di Tullio M, Losappio V, Vernaglione L. Pregnancy in end- stage renal disease patients on dialysis: how to achieve a successful delivery. Clin Kidney J. 2015;8: 293-299.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1858129&pid=S1646-5830201600030000300027&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>     <!-- ref --><p>28. Alfirevic Z, Stampalija T, Gyte GM. Fetal and umbilical Doppler ultrasound in high-risk pregnancies. Cochrane Database Syst Rev. 2013;11:CD007529.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1858131&pid=S1646-5830201600030000300028&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>     <!-- ref --><p>29. Prior T, Mullins E, Bennett P, Kumar S. Prediction of intra<sub></sub>partum fetal compromise using the cerebroumbilical ratio: a prospective observational study. Am J Obstet Gynecol. 2013;208:124 e1-6.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1858133&pid=S1646-5830201600030000300029&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>Pedro Viana Pinto </p>     <p>Centro Hospitalar S&#227;o Jo&#227;o </p>     ]]></body>
<body><![CDATA[<p>E-mail: <a href="mailto:pedrovianapinto@gmail.com">pedrovianapinto@gmail.com</a> </p>     <p>&nbsp;</p>     <p><b>Conflitos de interesse</b></p>     <p>Os autores declaram n&#227;o haver qualquer conflito de interesses. </p>     <p>&nbsp;</p>     <p><b>Recebido em: </b>20/4/2015</p>     <p><b>Aceite para publica&#231;&#227;o: </b>3/12/2015</p>      ]]></body><back>
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