<?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>0001-6002</journal-id>
<journal-title><![CDATA[Acta Médica Costarricense]]></journal-title>
<abbrev-journal-title><![CDATA[Acta méd. costarric]]></abbrev-journal-title>
<issn>0001-6002</issn>
<publisher>
<publisher-name><![CDATA[Colegio de Médicos y Cirujanos de Costa Rica]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0001-60022009000300004</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Fibrilación atrial en los adultos mayores]]></article-title>
<article-title xml:lang="en"><![CDATA[Atrial Fibrillation in the Elderly]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Brizuela-Torres]]></surname>
<given-names><![CDATA[Jorge]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Morales-Martínez]]></surname>
<given-names><![CDATA[Fernando]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Hospital Nacionald e Geriatría y Gerontología Dr. Raúl Blanco Cervantes  ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>09</month>
<year>2009</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>09</month>
<year>2009</year>
</pub-date>
<volume>51</volume>
<numero>3</numero>
<fpage>138</fpage>
<lpage>146</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.sa.cr/scielo.php?script=sci_arttext&amp;pid=S0001-60022009000300004&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.sa.cr/scielo.php?script=sci_abstract&amp;pid=S0001-60022009000300004&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.sa.cr/scielo.php?script=sci_pdf&amp;pid=S0001-60022009000300004&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[La fibrilación atrial es la taquiarritmia más prevalente en los adultos mayores. La frecuencia de dicha arritmia aumenta con la edad, presentándose en un 1.5% de los 50 a 59 años a 10% de los 80 a 89 años. La fibrilación atrial no valvular incrementa el riesgo de sufrir un evento cerebrovascular isquémico cardioembólico en 5 veces y causa el 15% de todos los accidentes cerebrovasculares isquémicos en Estados Unidos de América. El manejo de la fibrilación atrial se enfoca, principalmente, en la prevención de los fenómenos tromboembólicos y en el control de la frecuencia y ritmo cardiaco. La anticoagulación, cuando está indicada, ha demostrado ser la principal herramienta en la prevención de dichos eventos. Sin embargo, aunque las complicaciones hemorrágicas son más frecuentes, en esta población, y aumentan con la edad, sobrepasa por mucho, el beneficio al riesgo. El control de la frecuencia cardiaca ha demostrado ser igual o mejor que el control del ritmo en cuanto a prevención de eventos cerebrovasculares y mortalidad en estos pacientes. La edad cronológica por sí sola, no es contraindicación alguna para ofrecer una terapia óptima. Debe tomarse en cuenta el estado funcional, cognitivo y social, así como aspectos fisiológicos del envejecimiento con respecto a la prescripción de medicamentos. Cuando, a pesar del tratamiento adecuado, la sintomatología persiste, las estrategias invasivas han demostrado ser beneficiosas, pero faltan estudios que involucren a individuos mayores.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Atrial fibrillation is the most prevalent arrhythmia in the elderly. Its frequency increases with age, being 1.5% from 50 to 59 years old and 10% from 80 to 89 years old. Non valvular atrial fibrillation increases 5 fold the risk of suffering an stroke and causes 15% of strokes in the USA. Atrial fibrillation management focuses in the prevention of thromboembolic phenomena and heart rate and rhythm control. Anticoagulation, when indicated, has demonstrated to be the main tool in the prevention of these events. Nevertheless, although bleeding complications are more frequent in this population and increase with age, anticoagulation benefits are greater than the risks. Heart rate control is better than rhythm control regarding cerebrovascular accidents and mortality. Age by itself is not a contraindication to offer optimal therapy. Functional, mental and social status, must be taken into account as well as physiological aspects of aging when it comes to prescribing medications. If symptoms persist in spite of adequate treatment, invasive strategies have demonstrated to be of benefit, however studies in elderly population are lacking.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[fibrilación atrial]]></kwd>
<kwd lng="es"><![CDATA[adulto mayor]]></kwd>
<kwd lng="es"><![CDATA[anticoagulación]]></kwd>
<kwd lng="es"><![CDATA[prevención]]></kwd>
<kwd lng="es"><![CDATA[antiplaquetarios]]></kwd>
<kwd lng="es"><![CDATA[accidente cerebrovascular]]></kwd>
<kwd lng="en"><![CDATA[atrial fibrillation]]></kwd>
<kwd lng="en"><![CDATA[elderly]]></kwd>
<kwd lng="en"><![CDATA[anticoagulation]]></kwd>
<kwd lng="en"><![CDATA[prevention]]></kwd>
<kwd lng="en"><![CDATA[antiplatelet agents]]></kwd>
<kwd lng="en"><![CDATA[stroke]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[  <b><font face="Verdana" size="4">     <p align="center">Fibrilaci&oacute;n atrial en los adultos mayores</p>     <p align="center">(Atrial Fibrillation in the Elderly)</p> </font><font face="Verdana" size="2"> </font></b>     <p><font face="Verdana" size="2">Jorge Brizuela-Torres,    <br> Fernando Morales-Mart&iacute;nez</font></p>     <p><font face="Verdana" size="2">Unidad de Postgrado. Hospital Nacional Geriatr&iacute;a y Gerontolog&iacute;a Dr. Ra&uacute;l Blanco Cervantes. UCR-CENDEISSSCCSS.    <br> <b>Correspondencia: </b>Jorge Brizuela Torres E-mail: <a href="mailto:jbrizuela5@hotmail.com">jbrizuela5@hotmail.com</a></font></p> <b><font face="Verdana" size="3">     <p>Resumen</p> </font></b><font face="Verdana" size="2"> </font>     <p><font face="Verdana" size="2">La fibrilaci&oacute;n atrial es la taquiarritmia m&aacute;s prevalente en los adultos mayores. La frecuencia de dicha arritmia aumenta con la edad, present&aacute;ndose en un 1.5% de los 50 a 59 a&ntilde;os a 10% de los 80 a 89 a&ntilde;os. La fibrilaci&oacute;n atrial no valvular incrementa el riesgo de sufrir un evento cerebrovascular isqu&eacute;mico cardioemb&oacute;lico en 5 veces y causa el 15% de todos los accidentes cerebrovasculares isqu&eacute;micos en Estados Unidos de Am&eacute;rica. El manejo de la fibrilaci&oacute;n atrial se enfoca, principalmente, en la prevenci&oacute;n de los fen&oacute;menos tromboemb&oacute;licos y en el control de la frecuencia y ritmo cardiaco. La anticoagulaci&oacute;n, cuando est&aacute; indicada, ha demostrado ser la principal herramienta en la prevenci&oacute;n de dichos eventos. Sin embargo, aunque las complicaciones hemorr&aacute;gicas son m&aacute;s frecuentes, en esta poblaci&oacute;n, y aumentan con la edad, sobrepasa por mucho, el beneficio al riesgo. El control de la frecuencia cardiaca ha demostrado ser igual o mejor que el control del ritmo en cuanto a prevenci&oacute;n de eventos cerebrovasculares y mortalidad en estos pacientes. La edad cronol&oacute;gica por s&iacute; sola, no es contraindicaci&oacute;n alguna para ofrecer una terapia &oacute;ptima. Debe tomarse en cuenta el estado funcional, cognitivo y social, as&iacute; como aspectos fisiol&oacute;gicos del envejecimiento con respecto a la prescripci&oacute;n de medicamentos. Cuando, a pesar del tratamiento adecuado, la sintomatolog&iacute;a persiste, las estrategias invasivas han demostrado ser beneficiosas, pero faltan estudios que involucren a individuos mayores.</font></p> <font face="Verdana" size="2"><b> </b></font>     <p><font face="Verdana" size="2"><b>Descriptores: </b>fibrilaci&oacute;n atrial, adulto mayor, anticoagulaci&oacute;n, prevenci&oacute;n, antiplaquetarios, accidente cerebrovascular.</font></p>     ]]></body>
<body><![CDATA[<p><b><font face="Verdana" size="3">Abstract</font></b></p> <font face="Verdana" size="2"> </font>     <p><font face="Verdana" size="2">Atrial fibrillation is the most prevalent arrhythmia in the elderly. Its frequency increases with age, being 1.5% from 50 to 59 years old and 10% from 80 to 89 years old. Non valvular atrial fibrillation increases 5 fold the risk of suffering an stroke and causes 15% of strokes in the USA. Atrial fibrillation management focuses in the prevention of thromboembolic phenomena and heart rate and rhythm control. Anticoagulation, when indicated, has demonstrated to be the main tool in the prevention of these events.</font></p>     <p><font face="Verdana" size="2">Nevertheless, although bleeding complications are more frequent in this population and increase with age, anticoagulation benefits are greater than the risks. Heart rate control is better than rhythm control regarding cerebrovascular accidents and mortality. Age by itself is not a contraindication to offer optimal therapy. Functional, mental and social status, must be taken into account as well as physiological aspects of aging when it comes to prescribing medications. If symptoms persist in spite of adequate treatment, invasive strategies have demonstrated to be of benefit, however studies in elderly population are lacking.</font></p> <font face="Verdana" size="2"><b> </b></font>     <p><font face="Verdana" size="2"><b>Key words: </b>atrial fibrillation, elderly, anticoagulation, prevention, antiplatelet agents, stroke.</font></p> <font face="Verdana" size="2"><i>     <p align="center"><span style="font-weight: bold;">Recibido:</span> 8 de agosto de 2008 <span style="font-weight: bold;">Aceptado:</span> 3 de febrero de 2009</p> </i></font>     <p><font face="Verdana" size="2">La fibrilaci&oacute;n atrial es, sin duda alguna, la arritmia cardiaca de mayor prevalencia en los adultos mayores, estim&aacute;ndose que el 5% de las personas de 65 a&ntilde;os y m&aacute;s, la presentan y un 10% en aquellos mayores de 80 a&ntilde;os. (<a  href="#figura1">Figura 1</a>).<sup>1,2    <br> </sup></font></p>     <p><font face="Verdana" size="2"><sup>    <br> </sup></font></p>     <div style="text-align: center;"><a name="figura1"></a><img  src="/img/fbpe/amc/v51n3/a04i1v51n3.jpg" title="" alt=""  style="width: 412px; height: 335px;">    
]]></body>
<body><![CDATA[<br>     <br> </div>     <p><font face="Verdana" size="2">La prevalencia de la fibrilaci&oacute;n atrial est&aacute; en incremento; en gran parte, por el aumento de la poblaci&oacute;n de 60 a&ntilde;os y m&aacute;s en todo el mundo. Como ya es sabido, Costa Rica no se excluye de este fen&oacute;meno demogr&aacute;fico. Para el a&ntilde;o 2050, se estima que habr&aacute; 5.6 millones de personas con fibrilaci&oacute;n atrial en los Estados Unidos de Am&eacute;rica (E.U.A.), de esos, el 50% tendr&aacute; 80 o m&aacute;s a&ntilde;os.<sup>1</sup></font></p>     <p><font face="Verdana" size="2">La fibrilaci&oacute;n atrial no valvular incrementa el riesgo de sufrir un evento cerebrovascular isqu&eacute;mico en 5 veces y causa el 15% de todos los accidentes vasculares cerebrales (AVC) isqu&eacute;micos en E.U.A. En personas de 80 a 89 a&ntilde;os, esto se incrementa aproximadamente, a un 24%.<sup>3</sup> Los eventos cerebrovasculares cardioemb&oacute;licos asociados a la fibrilaci&oacute;n atrial tienen una mortalidad del 25% en 30 d&iacute;as, y resultan en mayor discapacidad que los no cardioemb&oacute;licos.<sup>4, 5</sup></font></p>     <p><font face="Verdana" size="2">Es por eso, que la prevenci&oacute;n de los eventos cerebrovasculares en los pacientes portadores de una fibrilaci&oacute;n atrial es pilar en el tratamiento de dicha afecci&oacute;n, resultando en un impacto importante, en la reducci&oacute;n de costos, en la rehabilitaci&oacute;n y ulterior manejo del paciente con secuelas, desde el punto de vista m&eacute;dico, social y mental.<sup>4</sup> </font></p>     <p><font face="Verdana" size="2">Los anticoagulantes orales, cuando est&aacute;n indicados, han demostrado ser altamente efectivos en la prevenci&oacute;n de dicha cat&aacute;strofe. Sin embargo, por diversas razones, algunas de estas m&aacute;s mitos que realidades, son poco prescritos en los adultos mayores.<sup>6, 7</sup></font></p> <font face="Verdana" size="2"> </font>     <p style="font-weight: bold;"><font face="Verdana" size="3">Uso de la warfarina para prevenir AVC en acianos con fibrilaci&oacute;n atrial</font></p> <font face="Verdana" size="2"> </font>     <p><font face="Verdana" size="2">En el Hospital Nacional de Geriatr&iacute;a y Gerontolog&iacute;a "Dr. Ra&uacute;l Blanco Cervantes", los pacientes en que se determin&oacute; que hab&iacute;an sufrido un AVC isqu&eacute;mico cardioemb&oacute;lico secundario a fibrilaci&oacute;n atrial del 2005 al 2006, s&oacute;lo el 10%, estaban recibiendo un anticoagulante oral y menos de la mitad estaban con niveles &oacute;ptimos de INR (International Normalized Ratio) en el momento del evento. Por otra parte, de 1998 a 1999 en E.U.A, un estudio de Medicare report&oacute; que solo el 42% de los pacientes portadores de fibrilaci&oacute;n atrial, estaban recibiendo warfarina a la hora de darles de alta en distintos hospitales.<sup>8</sup> Existe amplia evidencia del beneficio y el uso seguro de la warfarina en los ancianos.<sup>9</sup></font></p>     <p><font face="Verdana" size="2">La warfarina reduce el riesgo relativo de un AVC isqu&eacute;mico en un 62-68% en pacientes con fibrilaci&oacute;n atrial y en un 33% la mortalidad por dicha causa.<sup>6, 9</sup></font></p>     <p><font face="Verdana" size="2">La dosis de warfarina, en esta poblaci&oacute;n, ha sido discutida ampliamente y en diversos estudios se ha documentado que los ancianos, por los cambios normales del envejecimiento en cuanto a la farmacocin&eacute;tica y farmacodinamia, requieren menor dosis de inicio y mantenimiento. Un estudio mostr&oacute; que se debe reducir la dosis de warfarina en 0.4mg/d&iacute;a por cada a&ntilde;o despu&eacute;s de los 70 a&ntilde;os, particularmente, en las mujeres, la dosis debe ser de 3 a 5 mg.<sup>10</sup></font></p>     ]]></body>
<body><![CDATA[<p><font face="Verdana" size="2">Independientemente de la dosis de inicio y de mantenimiento, lo crucial es mantener un INR de 2.0 a 3.0. Prescribir dosis menores logrando un INR &lt; 2.0 no brinda protecci&oacute;n de sufrir un AVC y no disminuye el riesgo de hemorragia intracraneal.<sup>11,12</sup> Tambi&eacute;n, el riesgo de sangrado es mayor proporcionalmente, al aumento de los niveles de INR sobre 4.0.<sup>6,14</sup></font></p>     <p><font face="Verdana" size="2">Los estudios no proveen evidencia clara sobre la frecuencia en que se debe controlar el INR en estos pacientes. <i>La Sociedad Americana de Geriatr&iacute;a </i>recomienda control diario hasta que se estabilicen los niveles de 2.0 a 3.0 en al menos dos ocasiones consecutivas, luego 2 a 3 veces por semana durante 2 semanas luego, semanalmente, por un mes y por &uacute;ltimo, mensualmente. Quiz&aacute; uno de los m&aacute;s grandes retos es el lograr un apego a los controles debido al poco acceso de laboratorios disponibles, en el primer y segundo nivel de atenci&oacute;n en el pa&iacute;s, as&iacute; como el estado f&iacute;sico, funcional, mental y social de los pacientes y la disponibilidad de los cuidadores. La educaci&oacute;n, en este sentido, es fundamental.<sup>13</sup></font></p>     <p><font face="Verdana" size="2">El riesgo de hemorragia asociado a la warfarina se incrementa con la edad. La tasa anual de sangrado en diversos estudios var&iacute;a desde un 0.3% a 10%.<sup>15, 16</sup></font></p>     <p><font face="Verdana" size="2">En un gran estudio de cohorte en pacientes con fibrilaci&oacute;n atrial, que estaban anticoagulados, se demostr&oacute; que la tasa de hemorragia intracraneana fue de 0.47% y de hemorragia extracraneana del 0.64% anual lo que significa decir que por 1 a&ntilde;o de terapia con warfarina, se estima 1 a 2 hemorragias intracraneanas por cada 1000 pacientes. (<a href="#figura2">Figura 2</a>).<sup>17    <br> </sup></font></p>     <p><font face="Verdana" size="2"><sup>    <br> </sup></font></p>     <div style="text-align: center;"><a name="figura2"></a><img  src="/img/fbpe/amc/v51n3/a04i2v51n3.jpg" title="" alt=""  style="width: 435px; height: 431px;">    
<br>     <br> </div>     ]]></body>
<body><![CDATA[<p><font face="Verdana" size="2">En el per&iacute;odo de inicio de la terapia de anticoagulaci&oacute;n es donde se presentan m&aacute;s complicaciones hemorr&aacute;gicas, por lo que es importante el control estricto y seriado, desde el principio.<sup>17</sup></font></p>     <p><font face="Verdana" size="2">Se han identificado diversos factores de riesgo asociados a sangrado mayor que deben tomarse en cuenta en el adulto mayor: AVC previo, sangrado digestivo previo, hipertensi&oacute;n arterial, uso concomitante de aspirina, anemia, insuficiencia renal cr&oacute;nica, enfermedades neuropsiqui&aacute;tricas, polifarmacia (&gt; de 5 medicamentos), falta de educaci&oacute;n y c&aacute;ncer, todas muy frecuentes en esta poblaci&oacute;n.<sup>18,19</sup></font></p> <font face="Verdana" size="2"> </font>     <p style="font-weight: bold;"><font face="Verdana" size="3">Antiplaquetarios en la prevenci&oacute;n de AVC en ancianos con fibrilaci&oacute;n atrial</font></p> <font face="Verdana" size="2"> </font>     <p><font face="Verdana" size="2">Si la warfarina est&aacute; contraindicada o el paciente es de bajo riesgo, los antiplaquetarios tambi&eacute;n han demostrado ser beneficiosos en prevenir los eventos isqu&eacute;micos cerebrovasculares cardioemb&oacute;licos.<sup>20</sup></font></p>     <p><font face="Verdana" size="2">La aspirina reduce el riesgo de AVC en un 21% y tiene menos complicaciones hemorr&aacute;gicas que la warfarina. Algunas ventajas de esta sobre la warfarina es su costo, amplia disponibilidad, posee una vasta ventana terap&eacute;utica, menos interacciones droga-droga, dieta-droga y no necesita monitoreo. Debe tomarse en cuenta los sangrados digestivos y los efectos secundarios gastrointestinales en los adultos mayores. Un reciente estudio demostr&oacute; que los pacientes entre 80 y 90 a&ntilde;os abandonan, con mayor frecuencia, la aspirina que la warfarina precisamente, por los efectos secundarios reportados.<sup>20, 21</sup></font></p>     <p><font face="Verdana" size="2">El uso de la warfarina es superior al de aspirina combinada con clopidogrel, en la prevenci&oacute;n de eventos cerebrovasculares en pacientes con FA, con similares tasas de eventos hemorr&aacute;gicos en ambos grupos, demostrado en el estudio ACTIVE-W (Atrial fibrillation clopidogrel trial with Irbesartan for prevention of Vascular Events). El uso de clopidogrel solo, no es superior que la aspirina o la warfarina.<sup>21, 22</sup></font></p>     <p><font face="Verdana" size="2">Otros antitromb&oacute;ticos han sido estudiados, como el inhibidor directo de trombina, el ximelagatran, demostr&oacute; ser, al menos, igual de eficaz que la warfarina en la prevenci&oacute;n de AVC, pero nunca fue lanzado al mercado por su toxicidad hep&aacute;tica. El idraparinux, un inhibidor directo del factor Xa as&iacute; como el apixaban y rivoroxaban se encuentran en estudios, as&iacute; que por el momento no existe otro antitromb&oacute;tico que sea superior a la warfarina en la prevenci&oacute;n de eventos cerebrovasculares en ancianos con FA. <sup>22,23</sup></font></p> <font face="Verdana" size="3" style="font-weight: bold;">     <p>Anticoagulaci&oacute;n basada en la evidencia y en la estratificaci&oacute;n del riesgo</p> </font><font face="Verdana" size="2"> </font>     <p><font face="Verdana" size="2">Los ancianos reciben menos prescripci&oacute;n de anticoagulantes y cuando se les anticoagula, se hace de manera subterap&eacute;utica, a pesar de que tengan criterios para recibir dicha terapia. Algunos de los factores que influyen en esta omisi&oacute;n terap&eacute;utica, inciden en el temor de algunos m&eacute;dicos de recetar warfarina por creencias infundadas, como lo es el riesgo de un anciano a caerse y desarrollar grandes hematomas o trauma craneoencef&aacute;lico, el antecedente de sangrado previo, demencia y la poca adherencia al tratamiento. Como se apreci&oacute;, en el Hospital Nacional de Geriatr&iacute;a y Gerontolog&iacute;a y en otras partes del mundo, existe una tendencia de no ofrecer el beneficio de la anticoagulaci&oacute;n plena cuando esta se encuentra indicada y menos de la mitad de estos pacientes est&aacute;n anticoagulados de manera &oacute;ptima. <sup>24-27</sup> </font></p>     <p><font face="Verdana" size="2">Pocos estudios han logrado cuantificar el riesgo absoluto asociado a las ca&iacute;das y la warfarina, en parte porque la mayor&iacute;a de estos, excluyen a pacientes con riesgo de caerse. Uno de los estudios m&aacute;s influyentes en la decisi&oacute;n de anticoagular a estos pacientes, demostr&oacute; que es necesario caerse 300 veces al a&ntilde;o para que la warfarina no se indique como tratamiento de elecci&oacute;n cuando as&iacute; se requiera.28 Por otra parte, un estudio document&oacute; que los pacientes con alto riesgo de ca&iacute;das, pero bajo riesgo de presentar un evento cerebrovascular isqu&eacute;mico tromboemb&oacute;lico, no se ven beneficiados con el uso de warfarina.<sup>29</sup></font></p>     ]]></body>
<body><![CDATA[<p><font face="Verdana" size="2">La warfarina incrementa el riesgo en un 25% de sufrir fracturas patol&oacute;gicas ya que disminuye la densidad mineral &oacute;sea. En este estudio se demostr&oacute; que el deterioro cognitivo y las enfermedades neuropsiqui&aacute;tricas tambi&eacute;n son factores de riesgo para fracturas, por lo que se hace &eacute;nfasis en la importancia de analizar el estado cognitivo y funcional de los pacientes a los que se les prescribe warfarina.<sup>29, 38</sup></font></p>     <p><font face="Verdana" size="2">Existen algunos &iacute;ndices de evaluaci&oacute;n de riesgo para sufrir un evento cerebrovascular isqu&eacute;mico en los ancianos con FA. El m&aacute;s validado por la mayor&iacute;a de autores es el &iacute;ndice de CHADS<sub>2</sub> (<i style="font-weight: bold;">C</i>ongestive heart failure, <i style="font-weight: bold;">H</i>ipertensi&oacute;n, <i  style="font-weight: bold;">A</i>ge &gt; 75 a&ntilde;os, <i  style="font-weight: bold;">D</i>iabetes Mellitus, prior <i  style="font-weight: bold;">S</i>troke/transient ischemic attack).<sup>30-32</sup> Este &iacute;ndice muestra el riesgo anual de presentar un AVC en pacientes portadores de FA que no reciben anticoagulaci&oacute;n, el cual var&iacute;a de &lt; 1% con solo un punto a 20% en aquellos que tienen al menos un puntaje de 6. <sup>32</sup> (<a href="#cuadro1">Cuadro 1</a> y <a  href="#figura3">Figura 3</a>)    <br> </font></p>     <p style="text-align: center;"><font face="Verdana" size="2">    <br> <a name="cuadro1"></a><img src="/img/fbpe/amc/v51n3/a04i3v51n3.gif" title="" alt=""  style="width: 407px; height: 437px;">    
<br> </font></p>     <p style="text-align: center;"><font face="Verdana" size="2">    <br> <a name="figura3"></a><img src="/img/fbpe/amc/v51n3/a04i4v51n3.jpg" title="" alt=""  style="width: 435px; height: 335px;">    
<br>     <br> </font></p>     ]]></body>
<body><![CDATA[<p><font face="Verdana" size="2">Est&aacute; claro entonces, que los pacientes mayores que asocian, al menos, un factor de riesgo, se ven beneficiados de la anticoagulaci&oacute;n plena con respecto a la prevenci&oacute;n de AVC isqu&eacute;mico cardioemb&oacute;lico asociado a FA, evidencia que dista de la realidad, en la pr&aacute;ctica cl&iacute;nica, en nuestro medio.<sup>33</sup></font></p>     <p style="font-weight: bold;"><font face="Verdana" size="3">Control farmacol&oacute;gico de la frecuencia y el ritmo cardiaco en los ancianos</font></p> <font face="Verdana" size="2"> </font>     <p><font face="Verdana" size="2">Algunos estudios recientes han demostrado que el control del ritmo cardiaco no es superior al control de la frecuencia en el manejo de la FA en cuanto a mortalidad o aparici&oacute;n de AVC. Adem&aacute;s los f&aacute;rmacos antiarr&iacute;tmicos no previenen los eventos cerebrovasculares ni evitan la indicaci&oacute;n de anticoagulaci&oacute;n. De hecho, el control del ritmo cardiaco se ha asociado a un aumento, en la mortalidad, en el adulto mayor.<sup>34-37</sup></font></p>     <p><font face="Verdana" size="2">Un reciente metaan&aacute;lisis evidenci&oacute; que la incidencia de AVC isqu&eacute;mico entre los pacientes en que se control&oacute; el ritmo con los que se control&oacute; la frecuencia cardiaca fue similar (3.35% vs 3.9% respectivamente, OR=0.50, IC=95%).<sup>41</sup> (<a href="#figura4">Figura 4</a>)    <br> </font></p>     <p><font face="Verdana" size="2">    <br> </font></p>     <div style="text-align: center;"><a name="figura4"></a><img  src="/img/fbpe/amc/v51n3/a04i5v51n3.jpg" title="" alt=""  style="width: 437px; height: 426px;">    
<br>     <br> </div>     ]]></body>
<body><![CDATA[<p><font face="Verdana" size="2">Antes de iniciar cualquier tratamiento para una FA de inicio reciente se debe valorar el riesgo/beneficio, debido a que entre el 44% y el 78% de los pacientes con fibrilaci&oacute;n atrial de menos de 24 horas, sufren cardioversi&oacute;n espont&aacute;nea.<sup>36</sup></font></p>     <p><font face="Verdana" size="2">Los betabloqueadores, los calcioantagonistas no dihidropirid&iacute;nicos y la digoxina, son los f&aacute;rmacos mayormente recomendados y utilizados para controlar la frecuencia cardiaca en la fibrilaci&oacute;n auricular, pero todos ellos pueden inducir bradicardia o bloqueos de la conducci&oacute;n atrioventricular en los ancianos.<sup>37</sup> (<a href="#cuadro5">Cuadro 5</a> y <a href="#cuadro6">6</a>)</font></p>     <p><font face="Verdana" size="2">La amiodarona, un antiarr&iacute;tmico de clase III de Vaugham Williams, ha demostrado ser la droga m&aacute;s efectiva para mantener el ritmo sinusal. El 30% de los pacientes, con la dosis de carga, lo logran, a pesar de ser recomendaci&oacute;n Iia por la Asociaci&oacute;n Americana del Coraz&oacute;n.<sup>50</sup> Su metabolito activo, la desetilamiodarona metabolizada en el h&iacute;gado, bloquea los canales de sodio, potasio y calcio, as&iacute; como un relativo alfa y betabloqueo a nivel de los miocitos cardiacos. El m&aacute;s significativo es el bloqueo de los canales de potasio que enlentece la repolarizaci&oacute;n, prolongando el QT y previene el remodelado el&eacute;ctrico del miocardio.    <br> </font></p>     <p><font face="Verdana" size="2">Su gran volumen de distribuci&oacute;n, por ser lipof&iacute;lica, es de aproximadamente 66 litros por kilogramo de peso corporal, aspecto a tomar en cuenta ya que en el anciano aumenta en un 20% a 40% la grasa corporal total y disminuye en un 10%-15% el agua corporal total.<sup>43</sup> Su inicio de acci&oacute;n es de 2-3 d&iacute;as y tiene una eliminaci&oacute;n media de hasta 6 meses. No se ve alterada por la funci&oacute;n renal y es especialmente &uacute;til en pacientes con alteraci&oacute;n estructural del coraz&oacute;n o en aquellos que tienen insuficiencia cardiaca.<sup>44</sup></font></p>     <p><font face="Verdana" size="2">La dosis inicial es de 400 mg dos veces al d&iacute;a durante 2 semanas hasta acumular una dosis de 10 gr, seguida de 400 mg por d&iacute;a por 2 semanas m&aacute;s para luego continuar con 200 mg v&iacute;a oral por d&iacute;a de mantenimiento. (<a href="#cuadro2">Cuadros 2</a>, <a href="#cuadro3">3</a>, <a href="#cuadro4">4</a>).    <br> </font></p>     <p><font face="Verdana" size="2">    <br> </font></p>     <div style="text-align: center;"><a name="cuadro2"></a><img  src="/img/fbpe/amc/v51n3/a04i6v51n3.gif" title="" alt=""  style="width: 373px; height: 429px;">    
]]></body>
<body><![CDATA[<br>     <br>     <br> <a name="cuadro3"></a><img src="/img/fbpe/amc/v51n3/a04i7v51n3.gif" title="" alt=""  style="width: 376px; height: 401px;">    
<br>     <br>     <br> <a name="cuadro4"></a><img src="/img/fbpe/amc/v51n3/a04i8v51n3.gif" title="" alt=""  style="width: 762px; height: 524px;">    
<br>     <br> </div>     <p><font face="Verdana" size="2">En el anciano no deben variar las dosis de carga por el aumento en la grasa corporal descrito anteriormente sin embargo, aunque no hay estudios al respecto, se recomienda que la dosis de mantenimiento en algunos ancianos, sobre todo aquellos que tienen un IMC &lt; 18 Kg/m<sup>2</sup>, sea de 100 mg por d&iacute;a, aunado a la disminuci&oacute;n del metabolismo hep&aacute;tico de fase I y por la relativa disminuci&oacute;n de la alb&uacute;mina s&eacute;rica en estos pacientes, haci&eacute;ndolos m&aacute;s susceptibles a bradicardias, por lo que si el QT se prolonga por m&aacute;s de 550 mseg, debe reducirse la dosis.<sup>43</sup></font></p>     <p><font face="Verdana" size="2">El efecto indeseado m&aacute;s com&uacute;n en los ancianos es la bradicardia, el hipotiroidismo se presenta en un 20%, no debe suspenderse el f&aacute;rmaco y puede agregarse levotiroxina si se requiere.<sup>45</sup> El Hipertiroidismo var&iacute;a de un 3% a un 20%, se debe descontinuar la amiodarona si este se presenta. Los niveles de T<sub>4</sub> libre y TSH deben medirse al inicio y cada 6 meses.</font></p>     ]]></body>
<body><![CDATA[<p><font face="Verdana" size="2">La toxicidad pulmonar es la complicaci&oacute;n m&aacute;s seria y se presenta en un 3%, es dosis dependiente y su aparici&oacute;n requiere retirar el medicamento. Pruebas de funci&oacute;n pulmonar y la radiograf&iacute;a de t&oacute;rax deben realizarse al inicio de la terapia y anualmente.<sup>45,46</sup> La toxicidad hep&aacute;tica, una esteatohepatitis no alcoh&oacute;lica, es asintom&aacute;tica y se manifiesta por elevaci&oacute;n de dos veces los valores de las transaminasas, que puede resultar en cirrosis hep&aacute;tica si no se descontin&uacute;a la ingesta de amiodarona, aparece en un 15%. Deben solicitarse las pruebas de funci&oacute;n hep&aacute;tica al menos cada seis meses. Los efectos dermatol&oacute;gicos aparecen en un 25%- 75% con fotosensibilidad por lo que debe evitarse la exposici&oacute;n al sol. Los pacientes expuestos a la amiodarona por largos per&iacute;odos de tiempo pueden aquejar una coloraci&oacute;n gris&aacute;cea difusa y alopecia.<sup>47</sup> Microdep&oacute;sitos corn&eacute;ales aparecen en todos los pacientes sin tener repercusiones cl&iacute;nicas; la neuropat&iacute;a &oacute;ptica aparece en menos del 1% y es raz&oacute;n para suspender la amiodarona.<sup>44,46</sup></font></p>     <p><font face="Verdana" size="2">Ataxia, tremor, polineuropat&iacute;a, insomnio y deterioro en la memoria, son efectos neurol&oacute;gicos que se presentan hasta en un 30% y es dosis dependiente. En general, los efectos adversos pueden persistir hasta en un 13%-18% un a&ntilde;o despu&eacute;s de descontinuar la amiodarona.<sup>48</sup>Otras contraindicaciones para el uso de dicho f&aacute;rmaco son: disfunci&oacute;n del nodo y bloqueos atrioventriculares de alto grado (excepto los que tienen marcapaso artificial funcionante). La dosis de warfarina debe reducirse en un 25% con el uso concomitante de la amiodarona debido a la interacci&oacute;n de ambos, en el metabolismo hep&aacute;tico en el citocromo P450-2C9.<sup>49</sup></font></p>     <p><font face="Verdana" size="2">La dronedarona, un derivado benzofurano recientemente desarrollado, con propiedades electroestructurales similares a la amiodarona pero con un radical iod&iacute;nico menos, que busca reducir o eliminar la pneumo y tirotoxicidad, actua bloqueando canales de sodio, calcio, potasio y tambi&eacute;n tiene efectos antiadren&eacute;rgicos, con una vida media de 1 a 2 d&iacute;as comparado con la amiodarona que es de 30 a 55 d&iacute;as.</font></p>     <p><font face="Verdana" size="2">Algunos estudios recientes sugieren que la dronedarona tiene un impacto en la morbimortalidad relacionada con la fibrilaci&oacute;n atrial, como lo demostraron los meta-an&aacute;lisis EURIDIS (European Trial in Atrial Fibrillation Patients Receiving Dronedarone for the Maintenance of Sinus Rythm), y el estudio ADONIS (American-Australian Trial With Dronedarone in Atrial Fibrillation Patients for the Maintenance of Sinus Rythm); ambos mostraron una reducci&oacute;n de la tasa de recurrencia de episodios de fibrilaci&oacute;n atrial a 12 meses de seguimiento de 67.1% y 61.1% con dronedarona versus 77.5% y 72.8% con placebo respectivamente.<sup>50,51</sup></font></p>     <p><font face="Verdana" size="2">Estos beneficios se confirmaron m&aacute;s recientemente, con el estudio doble ciego controlado con placebo: ATHENA; realizado en 551 centros de 37 pa&iacute;ses alrededor del mundo, en donde se randomizaron sujetos mayores de 70 a&ntilde;os, portadores de fibrilaci&oacute;n atrial parox&iacute;stica o persistente asociado a un moderado/alto riesgo cardiovascular el cual mostr&oacute; una reducci&oacute;n del 24% en el riesgo de hospitalizaci&oacute;n o muerte cardiovascular en los sujetos que recibieron dronedarona 400 mg BID, as&iacute; como una reducci&oacute;n del 45% en la mortalidad asociada a arritmias y sin efectos secundarios superiores al placebo, por lo que parece ser una buena opci&oacute;n para evitar los efectos adversos de la amiodarona y se perfila a jugar un rol protag&oacute;nico en el manejo de pacientes portadores de fibrilaci&oacute;n atrial en el corto plazo.<sup>52</sup></font></p>     <p><font face="Verdana" size="2">La digoxina debe usarse con precauci&oacute;n por su toxicidad, estrecha ventana terap&eacute;utica y m&uacute;ltiples interacciones con otros medicamentos, sobre todo en los pacientes con falla renal. Su principal indicaci&oacute;n es en el control de la frecuencia en los pacientes con insuficiencia cardiaca o disfunci&oacute;n del ventr&iacute;culo izquierdo. La digoxina reduce la frecuencia cardiaca en reposo pero no as&iacute; en la actividad f&iacute;sica.<sup>49</sup> La dosis habitual es de 0.125mg a 0.5 mg por d&iacute;a v&iacute;a oral. (<a href="#cuadro5">Cuadros 5</a> y <a href="#cuadro6">6</a>) Un estudio reciente sugiere que mantener niveles s&eacute;ricos de 0.09 ng/ml es efectivo para reducir la tasa de eventos vasculares.<sup>53</sup> No existen recomendaciones avaladas por las diferentes autoridades mundiales para que se dosifique de lunes a viernes y no se administren las dosis correspondientes a los fines de semana en los ancianos, pr&aacute;ctica muy com&uacute;n en nuestro medio.<sup>49</sup> Lo m&aacute;s importante es cuantificar los niveles de manera peri&oacute;dica para mantenerlos dentro del rango terap&eacute;utico (0.2-2 ng/ml).<sup>53</sup>Las diferentes presentaciones de digoxina en la CCSS son: tabletas de 0.25 mg, frasco al 0.075% o 0.75mg/ml o sea cada gota contiene 16.6 mcgr y ampollas de 1 ml con 0.25 mg/ml.<sup>54    <br> </sup></font></p>     <p><font face="Verdana" size="2"><sup>    <br> </sup></font></p>     <div style="text-align: center;"><a name="cuadro5"></a><img  src="/img/fbpe/amc/v51n3/a04i9v51n3.gif" title="" alt=""  style="width: 768px; height: 497px;">    
]]></body>
<body><![CDATA[<br>     <br> <a name="cuadro6"></a><img src="/img/fbpe/amc/v51n3/a04i10v51n3.gif" title="" alt=""  style="width: 765px; height: 368px;">    
<br> </div>     <p><font face="Verdana" size="2">Las Gu&iacute;as de Pr&aacute;ctica Cl&iacute;nica Americanas recomiendan que el objetivo en el control de la frecuencia cardiaca en estos pacientes debe ser de 60-80 latidos por minuto en reposo y de 90 a 115 latidos durante la actividad f&iacute;sica moderada.<sup>49</sup></font></p> <font face="Verdana" size="3" style="font-weight: bold;">     <p>Tratamiento invasivo en ancianos con fibrilaci&oacute;n atrial</p> </font><font face="Verdana" size="2"> </font>     <p><font face="Verdana" size="2">Los pocos estudios que involucran el manejo invasivo para controlar la frecuencia y el ritmo cardiaco, en el adulto mayor, incluyen algunas estrategias como la ablaci&oacute;n del nodo atrioventricular con implantaci&oacute;n de marcapaso, ablaci&oacute;n focal de las venas pulmonares con cat&eacute;ter de radiofrecuencia y el procedimiento de Cox-Maze III.</font></p>     <p><font face="Verdana" size="2">Cuando est&aacute;n indicados, estos procedimientos han demostrado ser m&aacute;s efectivos que los agentes farmacol&oacute;gicos, sobre todo en pacientes que persisten sintom&aacute;ticos a pesar del tratamiento m&eacute;dico &oacute;ptimo.<sup>55, 57</sup></font></p>     <p><font face="Verdana" size="2">La ablaci&oacute;n del nodo atrioventricular se realiza mediante ablaci&oacute;n transvenosa con radiofrecuencia del nodo AV y colocaci&oacute;n de marcapaso atrial o bicameral, resultando en un bloqueo completo y control de la frecuencia. En un estudio de 350 pacientes (edad promedio 68&plusmn;11 a&ntilde;os), la supervivencia no fue inferior a la de aquellos pacientes controlados con tratamiento &oacute;ptimo. La anticoagulaci&oacute;n debe persistir a pesar de dicha estrategia.<sup>55</sup> La ablaci&oacute;n percut&aacute;nea con cat&eacute;ter de radiofrecuencia permite realizar la ablaci&oacute;n transvenosa en los focos de ectopia, los cuales se considera que se encuentran ubicados en un 80% al 90% en las venas pulmonares, seguidos de las venas cavas, los atrios y el seno coronario.<sup>56-58</sup></font></p>     <p><font face="Verdana" size="2">Las tasas de &eacute;xito son del 78% al 85% con un rango de complicaciones entre el 1% y el 5% en centros experimentados.<sup>59</sup> A&uacute;n no est&aacute; claro si la anticoagulaci&oacute;n debe continuarse luego de este procedimiento sin embargo, la mayor&iacute;a de los estudios se han efectuado en pacientes menores de 65 a&ntilde;os sin patolog&iacute;a estructural cardiaca y sin comorbilidades.<sup>60</sup> La cirug&iacute;a de Cox-Maze III consiste en realizar incisiones en el atrio, eliminando los ap&eacute;ndices auriculares, aislando las venas pulmonares y posterior reconstrucci&oacute;n del atrio. Tiene una tasa de curaci&oacute;n en un 90% a 10 a&ntilde;os plazo, con una mortalidad del 2% al 3% perioperatoria.<sup>61</sup></font></p> <font face="Verdana" size="2"> </font>     <p style="font-weight: bold;"><font face="Verdana" size="3">Conclusi&oacute;n</font></p> <font face="Verdana" size="2"> </font>     ]]></body>
<body><![CDATA[<p><font face="Verdana" size="2">La fibrilaci&oacute;n atrial es la arritmia m&aacute;s frecuente en el adulto mayor y es un importante factor de riesgo para desencadenar una cat&aacute;strofe tromboemb&oacute;lica, resultando en un accidente cerebrovascular isqu&eacute;mico. Los que sobreviven a dicho evento, arrastrar&aacute;n las secuelas f&iacute;sicas, mentales, funcionales y sociales, as&iacute; como sus familias y cuidadores. Actualmente, existe evidencia clara sobre las pautas que se deben asumir en el manejo &oacute;ptimo y oportuno de la fibrilaci&oacute;n atrial, enfocado principalmente, en la prevenci&oacute;n del fen&oacute;meno tromboemb&oacute;lico y en el control de la frecuencia cardiaca. Aunque son relativamente pocos los estudios en los ancianos, no existe contraindicaci&oacute;n absoluta para privar a estos pacientes, solo por la edad cronol&oacute;gica, de ofrecer el beneficio de la terapia recomendada siempre y cuando se individualice, integralmente, cada paciente.</font></p> <font face="Verdana" size="2"> </font>     <p><font face="Verdana" size="2"><span style="font-weight: bold;">Abreviaturas:</span> AAS, &aacute;cido acetil salic&iacute;lico; CCSS, Caja Costarricense del Seguro Social; AIT, accidente isqu&eacute;mico transitorio; AVC, accidente vascular cerebral; FC, frecuencia cardiaca; FE, fracci&oacute;n de eyecci&oacute;n del ventr&iacute;culo izquierdo; HTA, hipertensi&oacute;n arterial; ICC, insuficiencia cardiaca congestiva; INR, international normalized ratio.</font></p>     <p style="font-weight: bold;"><font face="Verdana" size="3">Referencias</font></p> <font face="Verdana" size="2"> </font>     <!-- ref --><p><font face="Verdana" size="2">1. Go AS, Hylek EM, Phillips KA. Prevalence of diagnosed atrial fibrillation in adults: national implications for rhythm management and stroke prevention: The Anticoagulation and Risk factors in Atrial Fibrillation (ATRIA) Study. JAMA. 2000; 285:2370-2375.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=039404&pid=S0001-6002200900030000400001&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p><font face="Verdana" size="2">2. Wolf PA, Abbott RD, Kannel WB. Atrial fibrillation as an independent risk factor for stroke: The Framingham Study. Stroke1991;22:983-988.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=039405&pid=S0001-6002200900030000400002&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p><font face="Verdana" size="2">3. Lakshminarayan K, Solid CA, Collins AJ. Atrial fibrillation and stroke in general medicare population: a 10 year perspective (1992-2002). Stroke.2006;37:1969-1974.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=039406&pid=S0001-6002200900030000400003&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p><font face="Verdana" size="2">4. Lin HJ, Wolf PA, Kelly Hayes M. Stroke severity in atrial fibrillation. The Framinghan Study. Stroke 1996;27:1760-4.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=039407&pid=S0001-6002200900030000400004&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p><font face="Verdana" size="2">5. Hylek EM, Go AS, Chang Y. Effect of intensity of oral anticoagulation on stroke severity and mortality in atrial fibrillation. N Engl J Med 2003;349:1019-26.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=039408&pid=S0001-6002200900030000400005&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p><font face="Verdana" size="2">6. Hart R, Benavente O, McBride R. Antithrombotic therapy to prevent stroke in patients with atrial fibrillation: a meta-analysis. Ann Intern Med 1999;131:492-501.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=039409&pid=S0001-6002200900030000400006&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p><font face="Verdana" size="2">7. Mccrory DC, Matchar DB, Samsa G. Physician attitudes about anticoagulation for nonvalvular atrial fibrillation in the elderly. Arch Intern Med 1995; 155:277-81.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=039410&pid=S0001-6002200900030000400007&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p><font face="Verdana" size="2">8. 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