<?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>1688-0420</journal-id>
<journal-title><![CDATA[Revista Uruguaya de Cardiología]]></journal-title>
<abbrev-journal-title><![CDATA[Rev.Urug.Cardiol.]]></abbrev-journal-title>
<issn>1688-0420</issn>
<publisher>
<publisher-name><![CDATA[Sociedad Uruguaya de Cardiología]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1688-04202013000200020</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Estado actual del monitoreo ambulatorio de presión arterial]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Sandoya]]></surname>
<given-names><![CDATA[Edgardo]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Asociación Española Primra de Socorros Mútuos Servicio de Cardiología ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>08</month>
<year>2013</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>08</month>
<year>2013</year>
</pub-date>
<volume>28</volume>
<numero>2</numero>
<fpage>273</fpage>
<lpage>284</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.edu.uy/scielo.php?script=sci_arttext&amp;pid=S1688-04202013000200020&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.edu.uy/scielo.php?script=sci_abstract&amp;pid=S1688-04202013000200020&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.edu.uy/scielo.php?script=sci_pdf&amp;pid=S1688-04202013000200020&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen El monitoreo ambulatorio de presión arterial es una importante herramienta clínica, ya que mejora el diagnóstico de hipertensión arterial, detecta su presentación enmascarada así como su forma nocturna aislada, al igual que el ascenso matinal exagerado de la presión arterial, situaciones estas con implicancias pronóstico-terapéuticas. Mediante este estudio es posible diagnosticar la hipertensión de túnica blanca, particularmente frecuente en las primeras etapas del embarazo, evitando de esa forma tratamientos innecesarios. Dado que en las mujeres el control de la hipertensión arterial nocturna tiene marcado impacto en la reducción de eventos, este estudio debería ser considerado en todas quienes presentan hipertensión arterial o se tiene sospecha de ello. Todo esto ha llevado a que en el momento actual el monitoreo ambulatorio de presión arterial constituya un valioso aliado en el cuidado de la salud de los pacientes.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Summary Ambulatory blood pressure monitoring is an important clinical tool, as well as improving the diagnosis of hypertension, detect its masked presentation, its isolated nocturnal form and exaggerated morning surge in blood pressure, all situations with therapeutic and prognostic implications. Through this study it is possible to diagnose white coat hypertension, a situation particularly common in early pregnancy, thus avoiding unnecessary treatments. Since in women nocturnal hypertension control has marked impact in reducing events, this study should be considered in all those with hypertension or suspected it. All this makes the ambulatory blood pressure monitoring a valuable associate in patients' health care.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[HIPERTENSIÓN-diagnóstico]]></kwd>
<kwd lng="es"><![CDATA[HIPERTENSION ENMASCARADA-diagnóstico]]></kwd>
<kwd lng="es"><![CDATA[PRIMER TRIMESTRE DEL EMBARAZO]]></kwd>
<kwd lng="es"><![CDATA[MONITOREO AMBULATORIO]]></kwd>
<kwd lng="en"><![CDATA[HYPERTENSION-diagnosis]]></kwd>
<kwd lng="en"><![CDATA[MASKED HYPERTENSION-diagnosis]]></kwd>
<kwd lng="en"><![CDATA[PREGNANCY TRIMESTER, FIRST]]></kwd>
<kwd lng="en"><![CDATA[MONITORING, AMBULATORY]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[    <basefont size="3"> <multicol gutter="18" cols="2"></multicol>     <p align="left"><font face="Verdana" size="2"><b>HIPERTENSI&Oacute;N ARTERIAL</b>&nbsp; </font></p>       <p align="left"><font face="Verdana" size="2"><b>Art&iacute;culo original&nbsp;</b></font></p>       <p align="left"><b><font face="Verdana" size="4">Estado actual del monitoreo     ambulatorio de presi&oacute;n arterial&nbsp; </font></b></p>       <p align="left"><font face="Verdana" size="2"> Dr. Edgardo Sandoya</font><font color="#000000" face="Verdana" size="2">&nbsp;</font><font face="Verdana" size="2"> </font><font face="Verdana"><font size="2">    <br>   </font>   <basefont size="3"> </font> </p>       <p align="left"><font face="Verdana" size="2"> Asociaci&oacute;n Espa&ntilde;ola, Servicio de Cardiolog&iacute;a    <br>     Correspondencia: Dr. Edgardo   Sandoya. Correo electr&oacute;nico: </font> <font color="#1f1a17" face="Verdana" size="2"> <a href="edgardo.sandoya@gmail.com">edgardo.sandoya@gmail.com</a></font><font face="Verdana" size="2">&nbsp; </font></p>       <p align="left"><font face="Verdana" size="2"> <b>Resumen&nbsp;</b> </font></p>       <p align="left"><font face="Verdana" size="2"> El monitoreo ambulatorio de presi&oacute;n arterial es una importante herramienta  cl&iacute;nica, ya que mejora el diagn&oacute;stico de hipertensi&oacute;n arterial, detecta  su presentaci&oacute;n enmascarada as&iacute; como su forma nocturna aislada, al igual  que el ascenso matinal exagerado de la presi&oacute;n arterial, situaciones estas  con implicancias pron&oacute;stico-terap&eacute;uticas. Mediante este estudio es posible  diagnosticar la hipertensi&oacute;n de t&uacute;nica blanca, particularmente frecuente  en las primeras etapas del embarazo, evitando de esa forma tratamientos  innecesarios. Dado que en las mujeres el control de la hipertensi&oacute;n arterial  nocturna tiene marcado impacto en la reducci&oacute;n de eventos, este estudio  deber&iacute;a ser considerado en todas quienes presentan hipertensi&oacute;n arterial  o se tiene sospecha de ello. Todo esto ha llevado a que en el momento actual  el monitoreo ambulatorio de presi&oacute;n arterial constituya un valioso aliado  en el cuidado de la salud de los pacientes.&nbsp; </font></p>       ]]></body>
<body><![CDATA[<p align="left"> <font face="Verdana" size="2"><b>Palabras clave:</b>    <br>   &nbsp;&nbsp;&nbsp;&nbsp;HIPERTENSI&Oacute;N-diagn&oacute;stico    <br>   &nbsp;&nbsp;&nbsp;&nbsp;HIPERTENSION ENMASCARADA-diagn&oacute;stico    <br>   &nbsp;&nbsp;&nbsp;&nbsp;PRIMER  TRIMESTRE DEL EMBARAZO    <br>   &nbsp;&nbsp;&nbsp;&nbsp;MONITOREO AMBULATORIO&nbsp; </font></p>       <p align="left"><font face="Verdana" size="2">     <br>   </font></p>  <font face="Verdana" size="2">      <br>   </font>       <p align="left"><font face="Verdana" size="2"> <b>Summary&nbsp;</b> </font></p>       <p align="left"><font face="Verdana" size="2"> Ambulatory blood pressure monitoring is an important clinical tool, as  well as improving the diagnosis of hypertension, detect its masked presentation,  its isolated nocturnal form and exaggerated morning surge in blood pressure,  all situations with therapeutic and prognostic implications. Through this  study it is possible to diagnose white coat hypertension, a situation particularly  common in early pregnancy, thus avoiding unnecessary treatments. Since  in women nocturnal hypertension control has marked impact in reducing events,  this study should be considered in all those with hypertension or suspected  it. All this makes the ambulatory blood pressure monitoring a valuable  associate in patients' health care.&nbsp; </font></p>       ]]></body>
<body><![CDATA[<p align="left"> <font face="Verdana" size="2"><b>Key words:</b>    <br>   &nbsp;&nbsp;&nbsp;&nbsp;HYPERTENSION-diagnosis    <br>   &nbsp;&nbsp;&nbsp;&nbsp;MASKED HYPERTENSION-diagnosis    <br>   &nbsp;&nbsp;&nbsp;&nbsp;PREGNANCY  TRIMESTER, FIRST    <br>   &nbsp;&nbsp;&nbsp;&nbsp;MONITORING, AMBULATORY    <br>       <br>   &nbsp; </font></p>       <p align="left"><font face="Verdana" size="2">     <br>   </font></p>  <font face="Verdana" size="2">      <br>   </font>       ]]></body>
<body><![CDATA[<p align="left"><font face="Verdana" size="2"> <b>Introducci&oacute;n&nbsp;</b> </font></p>       <p align="left"><font face="Verdana" size="2"> En 1896, el m&eacute;dico italiano Scipione Riva-Rocci introdujo el esfigmoman&oacute;metro,  lo que permiti&oacute; por primera vez medir de forma no invasiva la presi&oacute;n arterial  (PA) sist&oacute;lica, y nueve a&ntilde;os despu&eacute;s el cirujano vascular ruso Nicolai  Korotkoff desarroll&oacute; la t&eacute;cnica auscultatoria, mediante la cual fue posible  medir sist&oacute;lica y diast&oacute;lica<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#1"><font face="Verdana"><sup>1</sup></font></a></font><font face="Verdana" size="2"><sup>)</sup><a name="-1"></a>. A partir de entonces, la determinaci&oacute;n  de la PA ha sido una de las maniobras m&aacute;s empleadas en la pr&aacute;ctica cl&iacute;nica  a escala universal. Si bien no existe una fecha precisa en la que la hipertensi&oacute;n  arterial (HTA) pas&oacute; a ser considerada una entidad patol&oacute;gica, ya en 1912  se dec&iacute;a que &ldquo;el t&eacute;rmino hipertensi&oacute;n actualmente es de uso com&uacute;n&rdquo;<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#2"><font face="Verdana"><sup>2</sup></font></a></font><font face="Verdana" size="2"><sup>)</sup><a name="-2"></a>,  plante&aacute;ndose por parte de los colegas de aquellos lejanos a&ntilde;os que era  &ldquo;dif&iacute;cil definir una l&iacute;nea definitiva de demarcaci&oacute;n entre PA normal y  anormal&rdquo;, algo que hoy sigue teniendo vigencia, y que plantea un problema  com&uacute;n a todas las afecciones que se definen a partir de un punto de corte  en una variable continua<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#3"><font face="Verdana"><sup>3</sup></font></a></font><font face="Verdana" size="2"><sup>)</sup>.<a name="-3"></a>&nbsp; </font></p>       <p align="left"><font face="Verdana" size="2"> En los a&ntilde;os 50 diversas investigaciones epidemiol&oacute;gicas realizados en individuos  sin enfermedad cardiovascular mostraron que la PA elevada a&ntilde;os despu&eacute;s  se asociaba a una mayor tasa de eventos cardiovasculares<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#4"><font face="Verdana"><sup>4</sup></font></a></font><font face="Verdana" size="2"><sup>,</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#5"><font face="Verdana"><sup>5</sup></font></a></font><font face="Verdana" size="2"><sup>)</sup><a name="-4"></a><a name="-5"></a>. En 1973  un grupo de trabajo en Estados Unidos, al que se dio en llamar Joint National  Committee on Detection, Evaluation, and Treatment of High Blood Pressure,  desarroll&oacute; el primer reporte para la detecci&oacute;n, el seguimiento y el manejo  de los pacientes con HTA<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#6"><font face="Verdana"><sup>6</sup></font></a></font><font face="Verdana" size="2"><sup>)</sup>.<a name="-6"></a> A ese seguir&iacute;an otros seis, los que tendr&iacute;an  marcada influencia en el manejo de esta afecci&oacute;n en todo el mundo, encontr&aacute;ndose  actualmente el octavo de ellos en etapa de borrador<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#7"><font face="Verdana"><sup>7</sup></font></a></font><font face="Verdana" size="2"><sup>)</sup>.<a name="-7"></a>&nbsp; </font></p>        <p>&nbsp;</p>   <multicol gutter="18" cols="2"></multicol>     <p align="left"><font face="Verdana" size="2"> En 1990, una revisi&oacute;n de investigaciones epidemiol&oacute;gicas que incluy&oacute; a  420.000 individuos no tratados, estableci&oacute; que quienes tuvieron PA m&aacute;s  baja desarrollaron menos eventos cardiovasculares, sin que existiera un  l&iacute;mite inferior en que dicho beneficio se perdiera<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#8"><font face="Verdana"><sup>8</sup></font></a></font><font face="Verdana" size="2"><sup>)</sup>.<a name="-8"></a> Actualmente la mayor&iacute;a  de las gu&iacute;as internacionales consideran HTA a una PA </font> <font face="CentSchbook BT" size="2"> <font face="Verdana" size="2">&sup3; 140/90 mmHg, siendo  ese criterio el establecido por el III Consenso Uruguayo sobre Hipertensi&oacute;n  Arterial<a name="-9"></a></font><font face="Verdana"><sup>(</sup></font></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#9"><font face="Verdana"><sup>9</sup></font></a></font><font face="Verdana" size="2"><sup>)</sup>.&nbsp; </font></p>       <p align="left"><font face="Verdana" size="2"> Desde la primera mitad del siglo pasado se dudaba si la PA medida por el  m&eacute;dico en consultorio reflejaba el valor que ten&iacute;a el individuo en su vida  diaria<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#10"><font face="Verdana"><sup>10)</sup></font></a></font><font face="Verdana" size="2">.<a name="-10"></a> En los a&ntilde;os 80, registros de la PA intraarterial en pacientes  hospitalizados comprobaron que aquella preocupaci&oacute;n era v&aacute;lida, al comprobarse  que la misma variaba ampliamente, haci&eacute;ndolo incluso con cada latido card&iacute;aco<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#11"><font face="Verdana"><sup>11</sup></font></a></font><font face="Verdana" size="2"><sup>)</sup>.<a name="-11"></a>  Desde entonces existi&oacute; mucho inter&eacute;s por conocer cu&aacute;l era la PA de los  pacientes en su condiciones de vida habitual, lo que finalmente pudo lograrse  a partir de 1962, cuando fue introducido el monitoreo ambulatorio de la  PA (MAPA)<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#12"><font face="Verdana"><sup>12)</sup></font></a></font><font face="Verdana" size="2"><a name="-12"></a>. Desde entonces el avance tecnol&oacute;gico permiti&oacute; disponer de  equipos cada vez m&aacute;s peque&ntilde;os y confiables, lo que contribuy&oacute; a su uso  cada vez m&aacute;s extendido en la pr&aacute;ctica cl&iacute;nica.&nbsp; </font></p>       <p align="left"><font face="Verdana" size="2"> La investigaci&oacute;n ha comprobado mejor correlaci&oacute;n de la PA del MAPA que  con la de consultorio en relaci&oacute;n con eventos cardiovasculares<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#15"><font face="Verdana"><sup>15</sup></font></a></font><font face="Verdana" size="2"><sup>)</sup><a name="-15"></a>, hipertrofia  ventricular izquierda<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#13"><font face="Verdana"><sup>13</sup></font></a></font><font face="Verdana" size="2"><sup>)</sup>,<a name="-13"></a> as&iacute; como con marcadores subrogados de da&ntilde;o renal  como la microalbuminuria y de da&ntilde;o vascular como el espesor carot&iacute;deo<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#14"><font face="Verdana"><sup>14</sup></font></a></font><font face="Verdana" size="2"><sup>)</sup>.<a name="-14"></a>&nbsp; </font></p>       <p align="left"><font face="Verdana" size="2"> Actualmente se ha popularizado la medici&oacute;n de la PA por el propio paciente  en su domicilio, lo que se ha visto facilitado por el desarrollo de equipos  semiautom&aacute;ticos validados de costo razonable. Es as&iacute; que hoy se dispone  de tres formas de uso habitual para medir la PA en pacientes ambulatorios,  en muchos casos empleados de forma complementaria, y cada una de las cuales  tiene su propia utilidad (</font><font color="#1f1a17" face="Verdana" size="2"><a href="/img/revistas/ruc/v28n2/2a20t1.JPG">tabla 1</a></font><font face="Verdana" size="2">, modificada de<sup>[</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#15"><font face="Verdana"><sup>15</sup></font></a></font><font face="Verdana" size="2"><sup>]</sup>).&nbsp; </font> <font face="Verdana"><font size="2">    <br>   </font>   <basefont size="3"> </font> </p>   <font face="Verdana" size="2">    <br>   </font>       ]]></body>
<body><![CDATA[<p align="left"><font face="Verdana" size="2"> <b>Ventajas y desventajas del MAPA&nbsp;</b> </font></p>       <p align="left"><font face="Verdana" size="2"> Como todo m&eacute;todo diagn&oacute;stico, el MAPA posee ventajas y desventajas para  el manejo de los pacientes en la cl&iacute;nica habitual, las que se resumen en  la </font><font color="#1f1a17" face="Verdana" size="2"> <a href="/img/revistas/ruc/v28n2/2a20t2.JPG">tabla 2</a></font><font face="Verdana" size="2">. Entre las primeras, el registro de la PA durante las 24 horas  permite mejorar el diagn&oacute;stico de la HTA, as&iacute; como diagnosticar situaciones  con implicancia pron&oacute;stica que de otra forma no ser&iacute;an reconocidas. Por  otro lado, la medida de la PA, un acto m&eacute;dico importante, est&aacute; sujeta a  m&uacute;ltiples causas de error, debidas al equipo empleado, a las condiciones  del paciente, al observador, as&iacute; como a la t&eacute;cnica de medida. La causa  m&aacute;s frecuente de error es la preferencia por el d&iacute;gito, lo que lleva a  redondear de 10 en 10 mmHg valores que no son tales, no consign&aacute;ndose el  valor real de la PA. Esta tendencia al redondeo est&aacute; tan arraigada en la  pr&aacute;ctica m&eacute;dica de nuestro pa&iacute;s, que en una investigaci&oacute;n reciente comprobamos  que en la asistencia se registr&oacute; la PA de 10 en 10 mmHg a pesar que el  equipo semiautom&aacute;tico report&oacute; en su pantalla las cifras al mil&iacute;metro. En  ese sentido, el empleo del MAPA evita muchos de los errores en la medida,  particularmente los debidos al observador y a la t&eacute;cnica de medida.&nbsp; </font><font face="Verdana"><font size="2">    <br>   </font>   <basefont size="3"> </font> </p>        <p align="left"><font face="Verdana" size="2"> Entre las desventajas del MAPA, ocurre que a un porcentaje de pacientes,  su realizaci&oacute;n les genera molestias importantes, perturbando su sue&ntilde;o y/o  su vida habitual. De acuerdo a datos no publicados de nuestro estudio,  esto ocurri&oacute; en 6% de los casos, mientras que a 70% le molest&oacute; algo, pero  sin interferir con su vida, y a 24% no le molest&oacute;.&nbsp; </font></p>       <p align="left"><font face="Verdana" size="2"> Si bien el costo del MAPA es m&aacute;s elevado que la medici&oacute;n cl&iacute;nica convencional,  existe evidencia que ese costo adicional es compensado al establecerse  un diagn&oacute;stico m&aacute;s preciso de HTA, as&iacute; como una cuantificaci&oacute;n m&aacute;s precisa  del riesgo<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#16"><font face="Verdana"><sup>16</sup></font></a></font><font face="Verdana" size="2"><sup>)</sup><a name="-16"></a>. El costo de conseguir un buen control de la PA en un paciente  puede ser hasta cuatro veces m&aacute;s elevado empleando la medici&oacute;n convencional  de PA<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#17"><font face="Verdana"><sup>17</sup></font></a></font><font face="Verdana" size="2"><sup>)</sup>.<a name="-17"></a>&nbsp; </font></p>  <font face="Verdana" size="2">      <br>   </font>       <p align="left"><font face="Verdana" size="2"> <b>Normalidad de la presi&oacute;n arterial en el MAPA&nbsp;</b> </font></p>       <p align="left"><font face="Verdana" size="2"> Tanto las investigaciones epidemiol&oacute;gicas que demostraron los da&ntilde;os de  la HTA, como los ensayos cl&iacute;nicos que mostraron el beneficio del tratamiento  antihipertensivo, tuvieron como base a la PA de consultorio<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#18"><font face="Verdana"><sup>18</sup></font></a></font><font face="Verdana" size="2"><sup>)</sup><a name="-18"></a>. La introducci&oacute;n  del MAPA plante&oacute; la necesidad de establecer cu&aacute;l era el valor normal de  la PA para este m&eacute;todo, necesariamente diferente al incluir datos de los  per&iacute;odos diurno y nocturno, los que est&aacute;n influenciados por la actividad  del individuo. Con la finalidad de definir estos l&iacute;mites, investigaciones  realizadas en poblaciones europeas y asi&aacute;ticas analizaron la relaci&oacute;n entre  la PA medida en consultorio y la del MAPA de 24 horas mediante diferentes  aproximaciones metodol&oacute;gicas<sup>(</sup></font><sup><font color="#1f1a17" face="Verdana" size="2"><a href="#19">19</a></font><font face="Verdana" size="2">-</font><font color="#1f1a17" face="Verdana" size="2"><a href="#23">23</a></font></sup><font face="Verdana" size="2"><sup>)</sup><a name="-19"></a><a name="-20"></a><a name="-21"></a>. <a name="-22"></a><a name="-23"></a>En 1999, nuestro grupo de trabajo  en hipertensi&oacute;n arterial (Hugo Senra, Carlos Schettini, Manuel Bianchi,  Fernando Nieto y Edgardo Sandoya) propuso, a partir de una investigaci&oacute;n  llevada a cabo en una muestra de 2.070 adultos seleccionados al azar, que  el valor normal era 125/80 mmHg, cifra que mejor se correlacion&oacute; con los  140/90 mmHg en el consultorio (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#figura_1">figura 1</a></font><font face="Verdana" size="2">)<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#24"><font face="Verdana"><sup>24</sup></font></a></font><font face="Verdana" size="2"><sup>)<a name="-24"></a></sup>. Eso llev&oacute; a que se propusieran  diferentes valores de normalidad del MAPA, existiendo consenso en que su  definici&oacute;n reci&eacute;n podr&iacute;a establecerse cuando se dispusiera de datos que  permitieran relacionar la PA del MAPA inicial con los eventos cardiovasculares  ocurridos a largo plazo&nbsp; </font></p>       <p align="left"><font size="2" face="Verdana">    <br>   </font><font size="2">   </p>       ]]></body>
<body><![CDATA[<p></font><font size="2" face="Verdana"><a name="figura_1"></a><img style="width: 397px; height: 283px;" alt="" src="/img/revistas/ruc/v28n2/2a20f1.JPG"></font></p>       <p></p>       <p align="left"><font face="Verdana" size="2">Con esa finalidad en 2006 se constituy&oacute; la International Database in Relation   to Cardiovascular Outcome (IDACO), la que incluy&oacute; investigaciones:&nbsp; </font></p>   <ul>        <ul>         <li><font face="Verdana" size="2">     con MAPA de 24 horas;&nbsp;   </font></li>         <li><font face="Verdana" size="2">     realizadas en una poblaci&oacute;n general seleccionada al azar y no solamente     entre hipertensos;&nbsp;   </font></li>         <li><font face="Verdana" size="2">     publicadas en revistas arbitradas;&nbsp;   </font></li>         <li><font face="Verdana" size="2">     que hubieran relevado factores de riesgo cardiovascular, y&nbsp; que tuvieran registro de los eventos ocurridos en el seguimiento</font><sup><font face="Verdana" size="2">(</font><font color="#1f1a17" face="Verdana" size="2"><a href="#25">25)</a></font></sup><font face="Verdana" size="2">.<a name="-25"></a></font></li>            </ul>     <multicol gutter="18" cols="2"></multicol>   <font face="Verdana" size="2">&nbsp; </font>          <p align="left"><font face="Verdana" size="2"> Este grupo, formado inicialmente por cohortes reclutadas en Copenhague  (Dinamarca), Noorderkempen (B&eacute;lgica), Ohasama (Jap&oacute;n), Uppsala (Suecia),  Jing Ning (China) y Montevideo, luego ser&iacute;a ampliado con cohortes de Dubl&iacute;n,  (Irlanda), Novosibirsk (Rusia), Cracovia (Polonia), Padua (Italia) y Pilsen  (Rep&uacute;blica Checa), comprendiendo actualmente 12.148 individuos. A partir  del metaan&aacute;lisis de los datos individuales de la PA del MAPA inicial y  de la incidencia de eventos cardiovasculares ocurridos en los diez a&ntilde;os  posteriores, se han definido valores de normalidad para los diferentes  per&iacute;odos del d&iacute;a (</font><font color="#1f1a17" face="Verdana" size="2"><a href="/img/revistas/ruc/v28n2/2a20t3.JPG">tabla 3</a></font><font face="Verdana" size="2">), ajustados por cohorte, PA convencional y factores  de riesgo cardiovascular</font><sup><font face="Verdana" size="2">(</font><font color="#1f1a17" face="Verdana" size="2"><a href="#26">26</a></font><font face="Verdana" size="2">)<a name="-26"></a></font></sup><font face="Verdana" size="2">.&nbsp; </font>   <font face="Verdana"><font size="2">    <br>     </font>     <basefont size="3">   </font>   </p>            ]]></body>
<body><![CDATA[<p align="left"><font face="Verdana" size="2">&nbsp;&nbsp;&nbsp;</font></p>            <p align="left"><font face="Verdana" size="2"> De acuerdo al III Consenso Uruguayo sobre Hipertensi&oacute;n Arterial, la HTA  se clasifica en tres categor&iacute;as: Grado 1 (ligera), Grado 2 (moderada) y  Grado 3 (severa)<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#9"><font face="Verdana"><sup>9</sup></font></a></font><font face="Verdana" size="2"><sup>)</sup>. Esta clasificaci&oacute;n y sus puntos de corte son empleados  por razones pr&aacute;cticas, estando claro que lo que gu&iacute;a el tratamiento en  cada paciente es su riesgo cardiovascular<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#27"><font face="Verdana"><sup>27</sup></font></a></font><font face="Verdana" size="2"><sup>)</sup><a name="-27"></a>, y que los l&iacute;mites establecidos  son arbitrarios, dado que el riesgo es un continuo sin que exista un valor  inferior por debajo del cual se pierda el beneficio<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#8"><font face="Verdana"><sup>8</sup></font></a></font><font face="Verdana" size="2"><sup>)</sup>.&nbsp; </font></p>            <p align="left"><font face="Verdana" size="2"> Dado que disponer de categor&iacute;as es pr&aacute;ctico en la cl&iacute;nica diaria, se ha  propuesto definir categor&iacute;as en el MAPA que se correlacionen con los diferentes  de HTA<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#28"><font face="Verdana"><sup>28</sup></font></a></font><font face="Verdana" size="2"><sup>)<a name="-28"></a></sup>. En la </font>   <font color="#1f1a17" face="Verdana" size="2">   <a href="/img/revistas/ruc/v28n2/2a20t4.JPG">tabla 4</a></font><font face="Verdana" size="2"> se presenta cada categor&iacute;a de HTA con su equivalente  en el MAPA de 24 horas (adaptado de<sup>[</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#26"><font face="Verdana"><sup>26</sup></font></a></font><font face="Verdana" size="2"><sup>,</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#28"><font face="Verdana"><sup>28</sup></font></a></font><font face="Verdana" size="2"><sup>]</sup>).&nbsp; </font>   <font face="Verdana"><font size="2">    <br>     </font>     <basefont size="3">   </font>   </p>            <p align="left"><font face="Verdana" size="2">&nbsp;     <br>  Por ejemplo, cifras de 168/101 mmHg en el MAPA corresponden a una HTA severa,  lo que obliga a indicar medidas en el estilo de vida y antihipertensivos  independientemente del riesgo cardiovascular global<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#9"><font face="Verdana"><sup>9</sup></font></a></font><font face="Verdana" size="2"><sup>)</sup>.&nbsp; </font></p>            <p align="left"><font face="Verdana" size="2"> Los valores a alcanzar en la PA de 24 horas con el tratamiento antihipertensivo  son m&aacute;s bajos que los medidos en consultorio, ya que el promedio incluye  los valores nocturnos, momento en que la PA es m&aacute;s baja. Al igual que con  la PA de consultorio, los valores de la PA ambulatoria a alcanzar dependen  del riesgo cardiovascular individual, siendo mayores para los pacientes  con riesgo elevado o que presentan da&ntilde;o de &oacute;rgano blanco. Del punto de  vista pr&aacute;ctico, en la   </font><font color="#1f1a17" face="Verdana" size="2">   <a href="/imgrevistas/ruc/v28n2//2a20t5.JPG">tabla 5</a></font><font face="Verdana" size="2"> se presentan los valores a alcanzar en el  MAPA, tomando como referencia el III Consenso Uruguayo y las sugerencias  de la Gu&iacute;a Australiana de Hipertensi&oacute;n Arterial de 2011<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#15"><font face="Verdana"><sup>15)</sup></font></a></font><font face="Verdana" size="2">.&nbsp; </font>   <font face="Verdana"><font size="2">    <br>     </font>     <basefont size="3">   </font>   </p>            <p><font face="Verdana" size="2">&nbsp; </font>   </p>           <p align="left"><font face="Verdana" size="2">   <b>Patrones de presi&oacute;n arterial en las 24 horas&nbsp;</b>   </font></p>            ]]></body>
<body><![CDATA[<p align="left"><font face="Verdana" size="2"> El monitoreo ambulatorio de la PA a lo largo de todo el d&iacute;a, mientras los  individuos realizan sus actividades habituales, permiti&oacute; conocer su ritmo  circadiano, con descenso durante el sue&ntilde;o y elevaci&oacute;n al despertarse, al  tiempo que se identificaron diversos patrones de comportamiento durante  las 24 horas.&nbsp;   </font></p>            <p align="left"><font face="Verdana" size="2"> El registro invasivo en individuos hospitalizados hab&iacute;a mostrado una elevaci&oacute;n  de la PA ante la presencia del personal sanitario, a lo que se dio en llamar  hipertensi&oacute;n de t&uacute;nica blanca<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#29"><font face="Verdana"><sup>29</sup></font></a></font><font face="Verdana" size="2"><sup>)</sup><a name="-29"></a>. El MAPA confirm&oacute; este fen&oacute;meno a nivel  ambulatorio, al tiempo que permiti&oacute; reconocer un nuevo patr&oacute;n caracterizado  por PA normal en consultorio y elevada fuera del mismo, la hipertensi&oacute;n  enmascarada</font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#30"><font face="Verdana"><sup>(30)</sup></font></a></font><font face="Verdana" size="2"><a name="-30"></a>.&nbsp; </font></p>            <p align="left"><font face="Verdana" size="2"> Es as&iacute; que hoy en los registros de 24 horas se reconoce un patr&oacute;n normal  de PA y tres patrones patol&oacute;gicos:&nbsp;   </font></p>            <p align="left"><font face="Verdana" size="2"> 1)&nbsp;&nbsp;&nbsp;&nbsp;HTA;&nbsp;   </font></p>            <p align="left"><font face="Verdana" size="2"> 2)&nbsp;&nbsp;&nbsp;&nbsp;hipertensi&oacute;n de t&uacute;nica blanca e&nbsp;   </font></p>            <p align="left"><font face="Verdana" size="2"> 3)&nbsp;&nbsp;&nbsp;&nbsp;hipertensi&oacute;n enmascarada.&nbsp;   </font></p>            <p align="left"><font face="Verdana" size="2"> Se ha propuesto que cada uno de ellos se asociar&iacute;a a diferente pron&oacute;stico  en el largo plazo</font><sup><font face="Verdana" size="2">(</font><font color="#1f1a17" face="Verdana" size="2"><a href="#15">15</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2">. Un an&aacute;lisis realizado en 7.030 individuos de la  cohorte de IDACO (edad media 54,6 a&ntilde;os, sexo femenino 47,0%), mostr&oacute; que  la mitad era normotenso, un cuarto era hipertenso y que el otro cuarto  tuvo hipertensi&oacute;n de t&uacute;nica blanca o enmascarada (siendo este patr&oacute;n m&aacute;s  prevalente que el de t&uacute;nica blanca) (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#figura_2">figura 2</a></font><font face="Verdana" size="2">)</font><sup><font face="Verdana" size="2">(</font><font color="#1f1a17" face="Verdana" size="2"><a href="#31">31</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2">.<a name="-31"></a>&nbsp; </font>   <font size="2" face="Verdana">    <br>         <br>    </font><font size="2">    </p>            <p></font><font size="2" face="Verdana"><a name="figura_2"></a><img style="width: 310px; height: 310px;" alt="" src="/img/revistas/ruc/v28n2/2a20f2.JPG">    ]]></body>
<body><![CDATA[<br>    </font>    </p>            <p></p>            <p align="left"><font face="Verdana" size="2"> Luego de un seguimiento promedio de diez a&ntilde;os, la presencia de HTA se asoci&oacute;  a un 80% de aumento de riesgo de padecer un evento cardiovascular (muerte  de causa cardiovascular, infarto agudo de miocardio [IAM] no fatal, accidente  cerebrovascular, insuficiencia card&iacute;aca o revascularizaci&oacute;n coronaria)  en relaci&oacute;n con la normotensi&oacute;n: <i>hazard ratio</i> (HR) 1,80; IC 95% 1,54-2,09  (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#figura_3">figura 3</a></font><font face="Verdana" size="2">).&nbsp;   </font><font size="2" face="Verdana">    <br>         <br>    </font><font size="2">    </p>             <p><font face="Verdana"><a name="figura_3"></a><img style="width: 349px; height: 266px;" alt="" src="/img/revistas/ruc/v28n2/2a20f3.JPG"></font></p>     </font><font size="2" face="Verdana">         <br>        </font>            <p align="left"><font face="Verdana" size="2">   <b>Hipertensi&oacute;n de t&uacute;nica blanca&nbsp;</b>   </font></p>            <p align="left"><font face="Verdana" size="2"> La hipertensi&oacute;n de t&uacute;nica blanca ha sido asociada con niveles de ansiedad  elevados, pudiendo ser que el mecanismo que subyace al fen&oacute;meno sea una  respuesta condicionada<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#32"><font face="Verdana"><sup>32</sup></font></a></font><font face="Verdana" size="2"><sup>)</sup><a name="-32"></a>. Diversas investigaciones han comprobado que  quienes tienen esta entidad tiene mayor probabilidad de desarrollar HTA  en los diez a&ntilde;os siguientes<sup>(</sup></font><sup><font color="#1f1a17" face="Verdana" size="2"><a href="#33">33</a></font><font face="Verdana" size="2">,</font><font color="#1f1a17" face="Verdana" size="2"><a href="#34">34</a></font></sup><font face="Verdana" size="2"><sup>)</sup>.<a name="-33"></a><a name="-34"></a>&nbsp; </font></p>            <p align="left"><font face="Verdana" size="2"> La hipertensi&oacute;n de t&uacute;nica blanca se asocia a mayor masa ventricular izquierda  que la normotensi&oacute;n, habi&eacute;ndose postulado que tambi&eacute;n estar&iacute;a asociada  a mayor incidencia de eventos cardiovasculares<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#35"><font face="Verdana"><sup>35</sup></font></a></font><font face="Verdana" size="2"><sup>)</sup>.<a name="-35"></a> En la cohorte de IDACO,  si bien hubo mayor incidencia de eventos cardiovasculares con esta entidad,  luego de ajustar el riesgo inicial por cohorte, sexo, edad, &iacute;ndice de masa  corporal, colesterol, tabaquismo, consumo de alcohol, enfermedad cardiovascular,  diabetes y uso de antihipertensivos, no se observ&oacute; diferencia significativa  con la normotensi&oacute;n: HR 1,22; IC 95% 0,97-1,50 (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#figura_3">figura 3</a></font><font face="Verdana" size="2">). Al analizar  el riesgo en diferentes intervalos de tiempo, a los 12 a&ntilde;os se comprob&oacute;  aumento significativo del mismo HR 1,30 (p &lt; 0,05), lo que podr&iacute;a indicar  que los riesgos de esta entidad se manifestar&iacute;an luego de per&iacute;odos de tiempo  m&aacute;s prolongados.&nbsp; </font></p>            ]]></body>
<body><![CDATA[<p align="left"><font face="Verdana" size="2"> Al comparar el riesgo de la hipertensi&oacute;n de t&uacute;nica blanca con el de la  HTA, el mismo fue significativamente menor a los 12 a&ntilde;os (HR 0,68 p = 0,003)  y en todos los intervalos de tiempo analizados (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#figura_3">figura 3</a></font><font face="Verdana" size="2">).&nbsp;   </font></p>             <p><font face="Verdana" size="2">&nbsp;    <br>    </font>    </p>     <multicol gutter="18" cols="2"></multicol>          <p align="left"><font face="Verdana" size="2"> Dada la posibilidad de evolucionar hacia la HTA, estos pacientes deber&iacute;an  ser seguidos cada 1-2 a&ntilde;os mediante MAPA o autotoma domiciliaria de PA<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#36"><font face="Verdana"><sup>36</sup></font></a></font><font face="Verdana" size="2"><sup>)</sup>.<a name="-36"></a>&nbsp; </font></p>            <p align="left"><font face="Verdana" size="2"> Como vimos, el MAPA permiti&oacute; detectar a individuos con un patr&oacute;n de PA  normal en el consultorio y valores elevados fuera del mismo. Las posibles  razones para no detectar PA elevada en la cl&iacute;nica, en particular por la  ma&ntilde;ana, incluyen el consumo de alcohol vespertino, la variaci&oacute;n circadiana  de la PA o la apnea obstructiva del sue&ntilde;o<sup>(</sup></font><sup><font color="#1f1a17" face="Verdana" size="2"><a href="#37">37</a></font><font face="Verdana" size="2">,</font><font color="#1f1a17" face="Verdana" size="2"><a href="#38">38</a></font></sup><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#38"><font face="Verdana"><sup>)</sup></font></a></font><font face="Verdana" size="2">.<a name="-37"></a><a name="-38"></a> La incidencia de eventos  entre quienes ten&iacute;an hipertensi&oacute;n enmascarada fue mayor que la de los normotensos  (HR 1,62; IC 95% 1,27-1,95) y similar a la observada en la HTA (p = NS),  de ah&iacute; la importancia de diagnosticar esta entidad (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#figura_3">figura 3</a></font><font face="Verdana" size="2">).&nbsp; </font></p>            <p align="left"><font face="Verdana" size="2"> La hipertensi&oacute;n enmascarada debe sospecharse en sujetos con PA normal en  la cl&iacute;nica y que presentan alguno de los siguientes elementos<sup>()</sup>:&nbsp;   </font></p>        <ul>           <li><font face="Verdana" size="2"> hipertrofia ventricular izquierda o evidencia de otro da&ntilde;o de &oacute;rgano blanco;&nbsp;       </font></li>           <li><font face="Verdana" size="2"> m&uacute;ltiples factores de riesgo cardiovascular;&nbsp;       </font></li>           <li><font face="Verdana" size="2"> enfermedad renal cr&oacute;nica;&nbsp;       </font></li>           <li><font face="Verdana" size="2"> estr&eacute;s laboral importante;&nbsp;       </font></li>           ]]></body>
<body><![CDATA[<li><font face="Verdana" size="2"> respuesta exagerada de la PA al ejercicio.&nbsp;       </font></li>            </ul>            <p align="left"><font face="Verdana" size="2"> Si se sospecha hipertensi&oacute;n enmascarada debe realizarse un MAPA para confirmar  el diagn&oacute;stico, dado el aumento de riesgo que implica esta entidad y la  necesidad de su tratamiento en caso de confirmarse el diagn&oacute;stico.&nbsp;   </font></p>    <font face="Verdana" size="2">        <br>        </font>            <p align="left"><font face="Verdana" size="2">   <b>Otros elementos que aumentar&iacute;an el riesgo&nbsp;</b>   </font></p>            <p align="left"><font face="Verdana" size="2"> Se ha planteado que diversos elementos relevados en el MAPA se asociar&iacute;an  a aumento del riesgo de eventos cardiovasculares y/o de da&ntilde;o de &oacute;rgano  blanco, m&aacute;s all&aacute; del riesgo conferido por el promedio de la PA de 24 horas  y por el tipo de hipertensi&oacute;n. Entre estos se han descrito el ascenso matinal  brusco, la HTA nocturna aislada, la falta de descenso nocturno, la variabilidad  de la PA, las cargas diurnas y nocturnas, as&iacute; como la variabilidad de la  frecuencia card&iacute;aca.&nbsp;   </font></p>            <p align="left"><font face="Verdana" size="2">   <b>Ascenso matinal brusco de la presi&oacute;n arterial&nbsp;</b>   </font></p>            <p align="left"><font face="Verdana" size="2"> En las primeras horas de la ma&ntilde;ana existe mayor incidencia de IAM y de  otros eventos cardiovasculares que en el resto del d&iacute;a</font><sup><font face="Verdana" size="2">(</font><font color="#1f1a17" face="Verdana" size="2"><a href="#39">39)</a></font></sup><font face="Verdana" size="2"><a name="-39"></a>. Se ha postulado  que el ascenso matinal exagerado de la PA estar&iacute;a asociado a esa mayor  incidencia, pero los estudios al respecto no han mostrado resultados consistentes,  probablemente por un bajo n&uacute;mero de eventos, carencia de poder estad&iacute;stico  y/o la definici&oacute;n de ascenso matinal empleada</font><sup><font face="Verdana" size="2">(</font><font color="#1f1a17" face="Verdana" size="2"><a href="#40">40</a></font><font face="Verdana" size="2">,</font><font color="#1f1a17" face="Verdana" size="2"><a href="#41">41</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2"><a name="-40"></a><a name="-41"></a>. Para evaluar cu&aacute;nto  impacta este fen&oacute;meno a la estratificaci&oacute;n del riesgo cardiovascular se  analizaron 5.645 individuos de IDACO, los que fueron seguidos durante 11,4  a&ntilde;os. En el decil superior de ascenso hubo mayor mortalidad, riesgo relativo  (RR) 1,32; IC 95% 1,09-1,59) y de eventos cardiovasculares RR 1,30 (IC  95% 1,06-1,60), siendo consistente este hallazgo tanto para la PA sist&oacute;lica  como para la diast&oacute;lica.</font><font color="#000000" face="Verdana" size="2">&nbsp;</font><font face="Verdana" size="2">   </font></p>            <p align="left"><font face="Verdana" size="2"> Un ascenso matinal de la PA sist&oacute;lica por encima del percentil 90 (&sup3; 37  mmHg) predice de manera independiente la muerte y los eventos cardiovasculares,  mientras que un aumento matinal &pound; 20 mmHg probablemente no se asocie a  mayor riesgo de los mismos</font><sup><font face="Verdana" size="2">(</font><font color="#1f1a17" face="Verdana" size="2"><a href="#42">42</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2">.<a name="-42"></a> Si bien ning&uacute;n ensayo cl&iacute;nico ha explorado  si un tratamiento que modere este ascenso reduce los eventos m&aacute;s all&aacute; del  beneficio conferido por la reducci&oacute;n en el promedio de 24 horas, es razonable  tratar de atenuarlo en hipertensos con riesgo cardiovascular elevado.&nbsp; </font></p>            <p align="left"><font face="Verdana" size="2">   <b>Hipertensi&oacute;n nocturna aislada&nbsp;</b>   </font></p>            ]]></body>
<body><![CDATA[<p align="left">   <font face="Verdana" size="2">Se ha establecido que la presencia de HTA nocturna aislada se asocia con  da&ntilde;o de &oacute;rgano blanco, pero no se ha determinado si la misma se asocia  a aumento de eventos cardiovasculares</font><sup><font face="Verdana" size="2">(</font><font color="#1f1a17" face="Verdana" size="2"><a href="#43">43)</a></font></sup><font face="Verdana" size="2"><a name="-43"></a>. En IDACO, la HTA nocturna aislada  (PA diurna &lt; 135/85 mmHg y nocturna &sup3; 120/70 mmHg) tuvo mayor incidencia  en Sudam&eacute;rica (9,4%) que en Asia (7,2%) y en Europa (5,7%), p &lt; 0,05).  Entre los 577 individuos (de 8.711, 6,6%) con HTA nocturna aislada no tratados,  al cabo de 10,7 a&ntilde;os de seguimiento la HTA nocturna aislada se asoci&oacute; a  un aumento de mortalidad (HR 1,29; p = 0,045), y de eventos cardiovasculares  (HR 1,38; p = 0,037) en comparaci&oacute;n con la normotensi&oacute;n</font><sup><font face="Verdana" size="2">(</font><font color="#1f1a17" face="Verdana" size="2"><a href="#44">44</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2"><a name="-44"></a>.&nbsp; </font></p>             <p>   <font face="Verdana" size="2">   <a href="MasterFrame2_252.htm"></a></font></p>     <multicol gutter="18" cols="2"></multicol>          <p align="left"><font face="Verdana" size="2"> El estudio MAPEC mostr&oacute; que administrando los antihipertensivos en la noche  se consigui&oacute; un mejor control de la PA en las 24 horas y menor nivel de  marcadores de riesgo, siendo necesarios ensayos cl&iacute;nicos randomizados de  mayor tama&ntilde;o para ver si se confirman estos prometedores hallazgos<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#45."><font face="Verdana"><sup>45</sup></font></a></font><font face="Verdana" size="2"><sup>)</sup>.&nbsp;<a name="-45"></a> </font></p>            <p align="left"><font face="Verdana" size="2">   <b>Falta de descenso nocturno de la presi&oacute;n arterial&nbsp;</b>   </font></p>            <p align="left">   <font face="Verdana" size="2">El MAPA permiti&oacute; conocer que la PA mostraba un descenso fisiol&oacute;gico de  10%-20% durante el sue&ntilde;o. Este descenso obedece a la inactividad f&iacute;sica,  como se ha comprobado en quienes trabajan en turnos variables, en los cuales  la PA cae durante el sue&ntilde;o tanto en los d&iacute;as en que trabajan de noche como  cuando lo hacen de d&iacute;a</font><sup><font face="Verdana" size="2">(</font><font color="#1f1a17" face="Verdana" size="2"><a href="#46">46)</a></font></sup><font face="Verdana" size="2"><a name="-46"></a>. A los individuos que presentan este patr&oacute;n  normal de descenso se les ha denominado <i>dippers</i>, en tanto que a aquellos  que no tienen descenso nocturno son los <i>non dippers</i>. La mayor&iacute;a de los  estudios que investigaron este fen&oacute;meno reportaron que la presi&oacute;n nocturna  es m&aacute;s importante para predecir futuros eventos que la diurna</font><sup><font face="Verdana" size="2">(</font><font color="#1f1a17" face="Verdana" size="2"><a href="#47">47</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2"><a name="-47"></a>, particularmente  en hipertensos que no muestran reducci&oacute;n de PA durante el sue&ntilde;o</font><sup><font face="Verdana" size="2">(</font><font color="#1f1a17" face="Verdana" size="2"><a href="#48">48</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2">.<a name="-48"></a> Un  an&aacute;lisis de 7.458 individuos de IDACO mostr&oacute; que los valores nocturnos  predijeron la mortalidad de forma independiente de la PA diurna (HR 1,18;  p &lt; 0,01), pero los valores diurnos adem&aacute;s predijeron la muerte de causa  cardiovascular y los eventos cardiovasculares</font><sup><font face="Verdana" size="2">(</font><font color="#1f1a17" face="Verdana" size="2"><a href="#49">49</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2"><a name="-49"></a>. Un an&aacute;lisis por separado  de 23.856 hipertensos y de 9.641 participantes de IDACO mostr&oacute; que cuando  se realiza ajuste completo del riesgo por presi&oacute;n diurna, nocturna y de  24 horas, la ca&iacute;da nocturna de la PA es predictor significativo de pron&oacute;stico,  pero que agrega muy poco al que brinda el promedio de las 24 horas</font><sup><font face="Verdana" size="2">(</font><font color="#1f1a17" face="Verdana" size="2"><a href="#50">50</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2"><a name="-50"></a>.&nbsp; </font></p>            <p align="left"><font face="Verdana" size="2">   <b>Variabilidad de la presi&oacute;n arterial&nbsp;</b>   </font></p>            <p align="left">   <font face="Verdana" size="2">Se ha postulado que el aumento de la variabilidad de la PA durante las  24 horas impondr&iacute;a mayor sobrecarga al sistema cardiovascular, lo que se  asociar&iacute;a a mayor riesgo de eventos cardiovasculares, pero los datos al  respecto no han sido consistentes</font><sup><font face="Verdana" size="2">(</font><font color="#1f1a17" face="Verdana" size="2"><a href="#51">51</a></font><font face="Verdana" size="2">-</font><font color="#1f1a17" face="Verdana" size="2"><a href="#53">53</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2"><a name="-51"></a><a name="-52"></a><a name="-53"></a>. En IDACO, al cabo de 11,3 a&ntilde;os  de seguimiento hubo 1.242 muertes (487 de causa cardiovascular), 421 eventos  coronarios y 457 accidentes cerebrovasculares. El an&aacute;lisis multivariado  mostr&oacute; que la variabilidad en la PA de las 24 horas agreg&oacute; menos de 1%  a la capacidad de predicci&oacute;n de un evento cardiovascular. Los an&aacute;lisis  de sensibilidad en base a etnicidad, sexo, edad, antecedente de enfermedad  cardiovascular, tratamiento antihipertensivo, n&uacute;mero de mediciones y relaci&oacute;n  noche/d&iacute;a de la PA no modificaron ese hallazgo. De acuerdo a estos resultados,  surgidos de una cohorte de poblaci&oacute;n general con suficiente potencia estad&iacute;stica,  la variabilidad de la PA determinada por MAPA no contribuir&iacute;a a la estratificaci&oacute;n  de riesgo m&aacute;s all&aacute; que lo que lo hace el valor de las 24 horas</font><sup><font face="Verdana" size="2">(</font><font color="#1f1a17" face="Verdana" size="2"><a href="#54">54)</a></font></sup><font face="Verdana" size="2">.</font><font color="#000000" face="Verdana" size="2"><a name="-54"></a>&nbsp;</font><font face="Verdana" size="2">   </font></p>            <p align="left"><font face="Verdana" size="2">   <b>Cargas de presi&oacute;n arterial&nbsp;</b>   </font></p>            <p align="left">   <font face="Verdana" size="2">La proporci&oacute;n de tiempo durante la cual la presi&oacute;n est&aacute; por encima de los  valores de referencia durante el d&iacute;a y durante la noche puede ser definida  como la carga de PA. Este par&aacute;metro representar&iacute;a la sobrecarga cr&oacute;nica  de presi&oacute;n que induce al da&ntilde;o mioc&aacute;rdico y vascular asociados con el proceso  de la enfermedad hipertensiva. Esta medida est&aacute; directamente relacionada  a la PA media y a la variabilidad y se ha postulado que es un mejor predictor  de da&ntilde;o de &oacute;rgano blanco que la medida de consultorio</font><sup><font face="Verdana" size="2">(</font><font color="#1f1a17" face="Verdana" size="2"><a href="#55">55</a></font><font face="Verdana" size="2">,</font><font color="#1f1a17" face="Verdana" size="2"><a href="#56">56</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2">.</font><font color="#000000" face="Verdana" size="2"><a name="-55"></a><a name="-56"></a>&nbsp;</font><font face="Verdana" size="2">   </font></p>            <p align="left">   <font face="Verdana" size="2">Actualmente se est&aacute; investigando en este campo, dado que la evidencia disponible  es limitada y de acuerdo a an&aacute;lisis preliminares de expertos en el &aacute;rea,  este par&aacute;metro no agregar&iacute;a informaci&oacute;n pron&oacute;stica m&aacute;s all&aacute; de la que proporcionan  los par&aacute;metros disponibles</font><sup><font color="#1f1a17" face="Verdana" size="2"><a href="#57">(57</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2">.</font><font color="#000000" face="Verdana" size="2"><a name="-57"></a>&nbsp;</font><font face="Verdana" size="2">   </font></p>            ]]></body>
<body><![CDATA[<p align="left"><font face="Verdana" size="2">   <b>Variabilidad de la frecuencia card&iacute;aca&nbsp;</b>   </font></p>            <p align="left"><font face="Verdana" size="2"> Estudios realizados en hipertensos y en la poblaci&oacute;n general sugieren que  la frecuencia card&iacute;aca (FC) medida en reposo o mediante MAPA de 24 horas  podr&iacute;a ser un predictor de mortalidad, aunque la evidencia al respecto  es incompleta<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#58"><font face="Verdana"><sup>58</sup></font></a></font><font face="Verdana" size="2"><sup>)</sup>.<a name="-58"></a> En IDACO se analizaron los datos de FC en el MAPA de  6.928 sujetos que no recib&iacute;an tratamiento con beta-bloqueantes, a los que  se sigui&oacute; durante 9,6 a&ntilde;os. Cuando existi&oacute; una FC de 24 horas m&aacute;s elevada,  hubo mayor mortalidad, HR 1,15; IC 95% 1,06-1,25, lo que fue mediado por  una mayor mortalidad de causa no cardiovascular, no existiendo mayor mortalidad  cardiovascular. La FC elevada de 24 horas tampoco aument&oacute; el riesgo combinado  de muerte cardiovascular y eventos no fatales.&nbsp; </font></p>            <p align="left"><font face="Verdana" size="2"> En cambio, el incremento de la FC nocturna en diez latidos por minuto (un  desv&iacute;o est&aacute;ndar) se asoci&oacute; a 14% de aumento de riesgo de muerte cardiovascular;  del mismo modo la relaci&oacute;n noche/d&iacute;a aument&oacute; el riesgo de eventos coronarios  (HR 1,15; IC 95% 1,06-1,24). Pero estos hallazgos podr&iacute;an explicarse porque  los individuos con peor estado de salud y escasa movilidad tuvieran menor  PA y FC en el d&iacute;a, lo que en realidad har&iacute;a de que se tratase de un fen&oacute;meno  de causalidad reversa<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#59"><font face="Verdana"><sup>59</sup></font></a></font><font face="Verdana" size="2"><sup>)</sup><a name="-59"></a>.&nbsp; </font></p>      <multicol gutter="18" cols="2"></multicol>          <p align="left"><font face="Verdana" size="2">   <b>Situaciones especiales&nbsp;</b>   </font></p>            <p align="left"><font face="Verdana" size="2">   <b>Riesgo en la mujer&nbsp;</b>   </font></p>            <p align="left"><font face="Verdana" size="2"> En IDACO las mujeres tuvieron menor riesgo cardiovascular que los hombres,  pero la PA de 24 horas, y particularmente la nocturna, mostr&oacute; una relaci&oacute;n  m&aacute;s marcada con los eventos cardiovasculares que la observada entre los  hombres. La reducci&oacute;n de un desv&iacute;o est&aacute;ndar de la PA sist&oacute;lica en las mujeres  se asoci&oacute; a mayor reducci&oacute;n que en los hombres en mortalidad y en los eventos  cardiovasculares, cerebrovasculares y card&iacute;acos (</font><font color="#1f1a17" face="Verdana" size="2"><a href="/img/revistas/ruc/v28n2/2a20t6.JPG">tabla 6</a></font><font face="Verdana" size="2">). Ello muestra  la necesidad de definir la PA de 24 horas en las mujeres, puesto que si  bien tienen menor riesgo que los hombres, el conocimiento de sus valores  sist&oacute;licos nocturnos y de 24 horas permitir&iacute;an definir mejor su riesgo<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#60"><font face="Verdana"><sup>60</sup></font></a></font><font face="Verdana" size="2"><sup>)</sup><a name="-60"></a>.&nbsp; </font>   <font face="Verdana"><font size="2">    <br>     </font>     <basefont size="3">   </font>   </p>           <p align="left">&nbsp;</p>            <p align="left"><font face="Verdana" size="2"> El MAPA es particularmente &uacute;til en mujeres con PA sist&oacute;lica entre 130-139  y diast&oacute;lica entre 85-89 (normal alta) o en aquellas con HTA Grado 1<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#9"><font face="Verdana"><sup>9</sup></font></a></font><font face="Verdana" size="2"><sup>)</sup>.  Para un determinado valor de PA su riesgo puede ser bajo, moderado o alto  dependiendo de la coexistencia o no de factores de riesgo, de da&ntilde;o de &oacute;rgano  blanco o de enfermedad cardiovascular o renal. Integrando al c&aacute;lculo del  riesgo los valores de MAPA ser&iacute;a posible evitar el exceso de tratamiento  en las pacientes con riesgo bajo as&iacute; como el subtratamiento en aquellas  con riesgo alto derivado de una PA nocturna elevada<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#61"><font face="Verdana"><sup>61</sup></font></a></font><font face="Verdana" size="2"><sup>)</sup>.<a name="-61"></a>&nbsp; </font></p>            <p align="left"><font face="Verdana" size="2">   <b>Presi&oacute;n arterial elevada en el embarazo&nbsp;</b>   </font></p>            ]]></body>
<body><![CDATA[<p align="left"><font face="Verdana" size="2"> El papel principal del MAPA en el embarazo es descartar la hipertensi&oacute;n  de t&uacute;nica blanca en las primeras etapas del mismo, evitando as&iacute; el uso  de f&aacute;rmacos innecesarios. Los valores de normalidad del MAPA en el embarazo  ser&iacute;an &lt; 132/80 mmHg en el promedio diurno hasta las 30 semanas de gestaci&oacute;n  y &lt; 135/86 mmHg despu&eacute;s de ello<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#62"><font face="Verdana"><sup>62</sup></font></a><sup><a href="#61"><font face="Verdana">)</font></sup></font><sup><font face="Verdana" size="2"><a name="-62"></a></font></sup><font face="Verdana" size="2"></a>.&nbsp;   </font></p>            <p align="left"><font face="Verdana" size="2"> Hasta 30% de las embarazadas con cifras elevadas de PA presentan hipertensi&oacute;n  de t&uacute;nica blanca, lo que puede ser diagnosticado mediante el MAPA. evitando  as&iacute; el uso de f&aacute;rmacos y las internaciones<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#63"><font face="Verdana"><sup>63</sup></font></a></font><font face="Verdana" size="2"><sup>)</sup><a name="-63"></a>. Se ha visto que las cifras  elevadas de PA muchas veces llevan a la ces&aacute;rea, lo que podr&iacute;a ser evitado  si se demuestra que a lo largo de las 24 horas la PA tiene un promedio  normal<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#64"><font face="Verdana"><sup>64)</sup></font></a></font><font face="Verdana" size="2"><a name="-64"></a>.&nbsp; </font></p>            <p align="left"><font face="Verdana" size="2"> El MAPA, en cambio, no tiene ning&uacute;n papel en el manejo de la preeclampsia  establecida ni de la hipertensi&oacute;n gestacional<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#65"><font style="text-decoration: underline; font-weight: bold;" face="Verdana"><sup>65</sup></font></a></font><font face="Verdana" size="2"><sup>)</sup>.<a name="-65"></a>&nbsp; </font></p>            <p align="left"><font face="Verdana" size="2">   <b>Hipertensi&oacute;n y diabetes&nbsp;</b>   </font></p>            <p align="left"><font face="Verdana" size="2"> Existe abundante investigaci&oacute;n basada en medidas convencionales de la PA  que muestran que la existencia de HTA y diabetes aumentan el riesgo de  las complicaciones cardiovasculares</font><sup><font face="Verdana" size="2">(</font><font color="#1f1a17" face="Verdana" size="2"><a href="#66">66</a></font><font face="Verdana" size="2">,</font><font color="#1f1a17" face="Verdana" size="2"><a href="#67">67</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2">.<a name="-66"></a><a name="-67"></a> Pero se duda acerca de si la  diabetes y la HTA son factores de riesgo aditivos o se potencian uno a  otro. Para tratar de dar respuesta a esta pregunta se analiz&oacute; la PA de  24 horas de 8.484 individuos de IDACO, entre los que 6,9% eran diab&eacute;ticos<sup>(</sup></font><font color="#1f1a17" face="CentSchbook BT" size="2"><a href="#68"><font face="Verdana"><sup>68)</sup></font></a></font><font face="Verdana" size="2">.<a name="-68"></a>  Mediante an&aacute;lisis multivariado se evalu&oacute; el valor aditivo versus el valor  sin&eacute;rgico de PA y diabetes en relaci&oacute;n con un evento cardiovascular combinado.  A 10,6 a&ntilde;os de seguimiento, 1.066 individuos tuvieron un evento, observ&aacute;ndose  que tanto la diabetes como la PA de 24 horas fueron predictores independientes  de los eventos cardiovasculares, no existiendo relaci&oacute;n sin&eacute;rgica entre  ambos (p = 0,09).&nbsp; </font></p>            <p align="left"><font face="Verdana" size="2"> De acuerdo a lo rese&ntilde;ado, se puede dividir a las indicaciones del MAPA  en aquellas que tienen finalidad diagn&oacute;stica y las que tienen finalidad  terap&eacute;utica (</font><font color="#1f1a17" face="Verdana" size="2"><a href="/img/revistas/ruc/v28n2/2a20t7.JPG">tabla 7</a></font><font face="Verdana" size="2">).&nbsp;   </font><font face="Verdana"><font size="2">    <br>     </font>     <basefont size="3">   </font>   </p>            <p align="left"><font face="Verdana" size="2"> En caso de hipertensi&oacute;n enmascarada, en mujeres con PA nocturna elevada,  as&iacute; como en personas con mucha variabilidad, el MAPA puede ser empleado  para guiar el tratamiento. En los casos de sospecha de hipertensi&oacute;n de  t&uacute;nica blanca, el MAPA debe repetirse peri&oacute;dicamente para ver si no se  ha establecido una HTA.&nbsp;   </font></p>             <p><font face="Verdana" size="2">&nbsp; </font>   </p>           <p align="left"><font face="Verdana" size="2">or otro lado, la frecuencia con que debe repetirse este estudio depende  del criterio cl&iacute;nico, teniendo en cuenta el riesgo cardiovascular del paciente  y si el objetivo de PA ha sido alcanzado.&nbsp;   </font></p>           ]]></body>
<body><![CDATA[<p align="left">&nbsp;</p>            <p align="left"><font face="Verdana" size="2"> M&uacute;ltiples medidas de la PA reflejan mejor la verdadera PA del individuo  que la toma casual, por lo que el MAPA mejora la precisi&oacute;n y reproducibilidad  de su medici&oacute;n, a la vez que elimina los sesgos que introduce el observador.  La investigaci&oacute;n ha permitido mejorar el conocimiento del comportamiento  de la PA a lo largo del d&iacute;a, as&iacute; como establecer patrones asociados a mayor  riesgo de eventos cardiovasculares, tales como la hipertensi&oacute;n enmascarada,  el ascenso matinal exagerado de la presi&oacute;n y la hipertensi&oacute;n nocturna.  Mediante este estudio es posible diagnosticar la hipertensi&oacute;n de t&uacute;nica  blanca, evitando de esa forma tratamientos innecesarios, algo que es frecuente  en las primeras etapas del embarazo. Dado que en las mujeres el control  de la hipertensi&oacute;n nocturna tiene marcado impacto en la reducci&oacute;n de eventos,  este estudio deber&iacute;a ser considerado en toda mujer con HTA o sospecha de  la misma. Por todo ello, el MAPA deber&iacute;a ser utilizado en el manejo de  los pacientes con PA elevada con mayor frecuencia de lo que se lo hace  actualmente, lo que se traducir&iacute;a en beneficio en la salud de los pacientes.&nbsp;   </font></p>    <font face="Verdana" size="2">        <br>        </font>            <p align="left"><font face="Verdana" size="2">   <b>Bibliograf&iacute;a&nbsp;</b>   </font></p>            <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="1"></a>   </font><font color="#1f1a17" face="Verdana" size="2">   <a href="#-1">1</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Verrij E, van Montfrans G, Bos WJ.</b> Reintroduction of Riva-Rocci measurements  to determine systolic blood pressure? Neth J Med 2008;66:480-2.    &nbsp;   </font></p>            <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="2"></a>   </font><font color="#1f1a17" face="Verdana" size="2">   <a href="#-2">2</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Rusell W.</b> A Post-graduate lecture on the estimation of heart power: and  the terms blood pressure; hypertension; hyperpiesis; hypertonus. BMJ 1912;1(2673):  659-62.    &nbsp;   </font></p>            <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="3"></a>   </font><font color="#1f1a17" face="Verdana" size="2">   <a href="#-3">3</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Cunningham RL.</b> Mechanism and clinical aspects of chronic arterial hypertension.  Cal State J Med 1912; 10(7): 303-5.    &nbsp;   </font></p>            ]]></body>
<body><![CDATA[<!-- ref --><p align="left"><font face="Verdana" size="2"><a name="4"></a>   </font><font color="#1f1a17" face="Verdana" size="2">   <a href="#-4">4</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Paul O, Lepper MH, Phelan WH, Dupertuis GW, Macmillan A, Mckean H, et  al. </b>A longitudinal study of coronary heart disease. Circulation 1963;28:20-31.    &nbsp;   </font></p>            <p align="left"><font face="Verdana" size="2"><a name="5"></a>   </font><font color="#1f1a17" face="Verdana" size="2">   <a href="#-5">5</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Stokes J 3rd, Kannel WB, Wolf PA, D&rsquo;Agostino RB, Cupples LA. </b>Blood pressure  as a risk factor for cardiovascular disease. The Framingham Study&mdash;30 years  of follow-up. Hypertension 1989;13(5Suppl): l13-8.&nbsp;   </font></p>            <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="6"></a>   </font><font color="#1f1a17" face="Verdana" size="2">   <a href="#-6">6</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;Report of the Joint National Committee on Detection, Evaluation, and  Treatment of High Blood Pressure. A cooperative study. JAMA 1977;237:255-61.    &nbsp;   </font></p>            <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="7"></a>   </font><font color="#1f1a17" face="Verdana" size="2"><a href="#-7"> 7</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>National Institutes of Health. National Heart, Lung and Blood Institute.</b>  Blood Pressure in Adults: Report from the Joint National Committee (JNC).  Disponible en:   </font><font color="#1f1a17" face="Verdana" size="2"> <a href="http://www.nhlbi.nih.gov/guidelines/hypertension/jnc8/index.htm">http://www.nhlbi.nih.gov/guidelines/hypertension/jnc8/index.htm</a></font><font face="Verdana" size="2">.  (Consultado 15/03/2013).    &nbsp;   </font></p>            <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="8"></a>   </font><font color="#1f1a17" face="Verdana" size="2">   <a href="#-8">8</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>MacMahon S, Peto R, Cutler J, Collins R, Sorlie P, Neaton J, et al.</b> Blood  pressure, stroke, and coronary heart disease. Part 1, Prolonged differences  in blood pressure: prospective observational studies corrected for the  regression dilution bias. Lancet 1990;335(8692):765-74.    &nbsp;   </font></p>            <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="9"></a>   </font><font color="#1f1a17" face="Verdana" size="2"><a href="#-9"> 9</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;Sociedad Uruguaya de Hipertensi&oacute;n Arterial. Tercer Consenso Uruguayo  sobre Hipertensi&oacute;n Arterial. Montevideo, 2005. Disponible en</font><font color="#1f1a17" face="Verdana" size="2"><a href="http://www.suc.org.%20uy/pdf/consenso%20ha3.pdf."> http://www.suc.org.  uy/pdf/consenso%20ha3.pdf.</a></font><font face="Verdana" size="2"> (Consultado 15/03/ 2013).    &nbsp;   </font></p>            <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="10"></a>   </font><font color="#1f1a17" face="Verdana" size="2">   <a href="#-10">10</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Kain Hk, Hinman AT, Sokolow M.</b> Arterial blood pressure measurements  with a portable recorder in hypertensive patients. I. Variability and correlation  with "casual" pressures. Circulation 1964;30:882-92.    &nbsp;   </font></p>             <p><font face="Verdana" size="2">&nbsp; </font>   </p>           <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="11"></a>   </font><font color="#1f1a17" face="Verdana" size="2"><a href="#-11">11</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Mancia G.</b> Methods for assessing blood pressure values in humans. Hypertension  1983;5(5Pt 2):III5-13.    &nbsp;   </font></p>            <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="12"></a>   </font><font color="#1f1a17" face="Verdana" size="2">   <a href="#-12">12</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Hinman A T, Engel BT, Bickford AF.</b> Portable blood pressure recorder:  Accuracy and preliminary use in evaluating intradaily variations in pressure.  Am Heart J 1962;63:663.    &nbsp;   </font></p>            <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="13"></a>   </font><font color="#1f1a17" face="Verdana" size="2">   <a href="#-13">13</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Fagard RH, Staessen JA, Thijs L.</b> Prediction of cardiac structure and  function by repeated clinic and ambulatory blood pressure. Hypertension  1997; 29:22-9.    &nbsp;   </font></p>            ]]></body>
<body><![CDATA[<!-- ref --><p align="left"><font face="Verdana" size="2"><a name="14"></a>   </font><font color="#1f1a17" face="Verdana" size="2">   <a href="#-14">14</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Elliott HL.</b> 24-h blood pressure control: its relevance to cardiovascular  outcomes and the importance of long-acting antihypertensive drugs. J Hum  Hypertens 2004;18(8):539-43.    &nbsp;   </font></p>            <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="15"></a>   </font><font color="#1f1a17" face="Verdana" size="2">   <a href="#-15">15</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Head GA, McGrath BP, Mihailidou AS, Nelson MR, Schlaich MP, Stowasser  M, et al.</b> Ambulatory blood pressure monitoring in Australia: 2011 consensus  position statement. J Hypertens 2012; 30(2):253-66.    &nbsp;   </font></p>            <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="16"></a>   </font><font color="#1f1a17" face="Verdana" size="2">   <a href="#-16">16</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Krakoff LR.</b> Cost-effectiveness of ambulatory blood pressure: a reanalysis.  Hypertension 2006:47:29-34.    &nbsp;   </font></p>            <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="17"></a>   </font><font color="#1f1a17" face="Verdana" size="2">   <a href="#-17">17</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Rodriguez-Roca GC, Alonso-Moreno FJ, Garcia-Jimenez A, Hidalgo-Vega  A, Llisterri-Caro JL, Barrios-Alonso V, et al. </b>Cost-effectiveness of ambulatory  blood pressure monitoring in the follow-up of hypertension. Blood Press  2006; 15(1):27-36.    &nbsp;   </font></p>            <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="18"></a>   </font><font color="#1f1a17" face="Verdana" size="2">   <a href="#-18">18</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Collins R, Peto R, MacMahon S, Hebert P, Fiebach NH, Eberlein KA, et  al.</b> Blood pressure, stroke, and coronary heart disease. Part 2, Short-term  reductions in blood pressure: overview of randomised drug trials in their  epidemiological context. Lancet 1990;335:827-38.    &nbsp;   </font></p>            ]]></body>
<body><![CDATA[<!-- ref --><p align="left"><font face="Verdana" size="2"><a name="19"></a>   </font><font color="#1f1a17" face="Verdana" size="2">   <a href="#-19">19</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Ohkubo T, Imai Y, Tsuji I, Nagai K, Ito S, Satoh H, et al. </b>Reference  values for 24-hour ambulatory blood pressure monitoring based on a prognostic  criterion: the Ohasama Study. Hypertension 1998;32:255-9.    &nbsp;   </font></p>            <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="20"></a>   </font><font color="#1f1a17" face="Verdana" size="2">   <a href="#-20">20</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Imai Y, Nagai K, Sakuma M, Sakuma H, Nakatsuka H, Satoh H, et al.</b> Ambulatory  blood pressure of adults in Ohasama, Japan. Hypertension 1993;22:900-12.    &nbsp;   </font></p>            <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="21"></a>   </font><font color="#1f1a17" face="Verdana" size="2">   <a href="#-21">21</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Mancia G, Sega R, Bravi C, De Vito G, Valagussa F, Cesana G, et al.  </b>Ambulatory blood pressure normality: results from the PAMELA study. J Hypertens  1995;13:1377-90.    &nbsp;   </font></p>            <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="22"></a>   </font><font color="#1f1a17" face="Verdana" size="2">   <a href="#-22">22</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Staessen J, Fagard Rh, Lijnen PJ, Thijs L, Van Hulle S, Vyncke G, et  al.</b> Ambulatory blood pressure and blood pressure measurement at home: progress  report on a population study. J Cardiovasc Pharmacol 1994;23 (suppl 5):S5-S11.    &nbsp;   </font></p>            <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="23"></a>   </font><font color="#1f1a17" face="Verdana" size="2">   <a href="#-23">23</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Rasmussen SL, Torp-Pedersen C, Borch-Johnsen K, Ibsen H.</b> Normal values  for ambulatory blood pressure and differences between casual blood pressure  and ambulatory blood pressure: results from a Danish population survey.  J Hypertens 1998;16:1415-24.    &nbsp;   </font></p>            ]]></body>
<body><![CDATA[<!-- ref --><p align="left"><font face="Verdana" size="2"><a name="24"></a>   </font><font color="#1f1a17" face="Verdana" size="2">   <a href="#-24">24</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Schettini C, Bianchi M, Nieto F, Sandoya E, Senra H.</b> Ambulatory blood  pressure: normality and comparison with other measurements. Hypertension  Working Group. Hypertension 1999;34(Pt 2):818-25.    &nbsp;   </font></p>            <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="25"></a>   </font><font color="#1f1a17" face="Verdana" size="2">   <a href="#-25">25</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Thijs L, Hansen TW, Kikuya M, Bj&ouml;rklund-Bodeg&aring;rd K, Li Y, Dolan E, et  al.</b> The International Database of Ambulatory Blood Pressure in relation  to Cardiovascular Outcome (IDACO): protocol and research perspectives.  Blood Press Monit. 2007; 12:255-62.    &nbsp;   </font></p>            <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="26"></a>   </font><font color="#1f1a17" face="Verdana" size="2">   <a href="#-26">26</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Kikuya M, Hansen TW, Thijs L, Bj&ouml;rklund-Bodeg&aring;rd K, Kuznetsova T, Ohkubo  T, et al. International Database on Ambulatory blood pressure monitoring  in relation to Cardiovascular Outcomes Investigators.</b> Diagnostic thresholds  for ambulatory blood pressure monitoring based on 10-year cardiovascular  risk. Circulation 2007; 115:2145-52.    &nbsp;   </font></p>            <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="27"></a>   </font><font color="#1f1a17" face="Verdana" size="2">   <a href="#-27">27</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Natero, Ara&uacute;jo O, D&iacute;az-Arnesto O, Aguayo R, Sandoya E en nombre de los  redactores.</b> Gu&iacute;a pr&aacute;ctica de prevenci&oacute;n cardiovascular. Rev Urug Cardiol  2009;24:43-83.    &nbsp;   </font></p>            <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="28"></a>   </font><font color="#1f1a17" face="Verdana" size="2">   <a href="#-28">28</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Head G, Mihailidou A, Duggan K, Beilin L, Berry N, Brown M, et al.</b> Definition  of ambulatory blood pressure targets for diagnosis and treatment of hypertension  in relation to clinic blood pressure: prospective cohort study. BMJ 2010:  340:c1104.    &nbsp;   </font></p>            ]]></body>
<body><![CDATA[<p align="left"><font face="Verdana" size="2"><a name="29"></a>   </font><font color="#1f1a17" face="Verdana" size="2">   <a href="#-29">29</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Mancia G, Bertinieri G, Grassi G, Parati G, Pomidossi G, Ferrari A,  et al.</b> Effects of blood-pressure measurement by the doctor on patient&rsquo;s  blood pressure and heart rate. Lancet 1983 24;2(8352): 695-8.&nbsp;   </font></p>            <p align="left"><font face="Verdana" size="2"><a name="30"></a>   </font><font color="#1f1a17" face="Verdana" size="2">   <a href="#-30">30</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Staessen JA, O&rsquo;Brien ET, Thijs L, Fagard RH.</b> Modern approaches to blood  pressure measurement. Occup Environ Med 2000;57:510-20.&nbsp;   </font></p>            <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="31"></a>   </font><font color="#1f1a17" face="Verdana" size="2"><a href="#-31"> 31</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Boggia J, Hansen T, Asayama K, Luzardo L, Li Y, Staessen J. </b>White-coat  Hypertension on Automated Blood Pressure Measurement Implications for Clinical  Practice. Eur J Cardiovasc Med 2011;1: 17-21.    &nbsp;   </font></p>            <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="32"></a>   </font><font color="#1f1a17" face="Verdana" size="2">   <a href="#-32">32</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Ogedegbe G, Pickering TG, Clemow L, Chaplin W, Spaiill TM, Albanese  GM, et al.</b> The misdiagnosis of hypertension: the role of patient anxiety.  Arch Intern Med 2008;168:2459-65.    &nbsp;   </font></p>            <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="33"></a>   </font><font color="#1f1a17" face="Verdana" size="2">   <a href="#-33">33</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Ugajin T, Hozawa A, Ohkubo T, Asayama K, Kikuya M, Obara T, et al. </b>White-coat  hypertension as a risk factor for the development of home hypertension:  the Ohasama study. Arch Intern Med 2005; 165:1541-6.    &nbsp;   </font></p>            <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="34"></a>   </font><font color="#1f1a17" face="Verdana" size="2">   <a href="#-34">34</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Mancia G, Bombelli M, Facchetti R, Madotto F, Quarti-Trevano F, Polo  Friz H, et al.</b> Long-term risk of sustained hypertension in white-coat or  masked hypertension. Hypertension 2009:54:226-32.    &nbsp;   </font></p>             ]]></body>
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