<?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>0798-0264</journal-id>
<journal-title><![CDATA[Archivos Venezolanos de Farmacología y Terapéutica]]></journal-title>
<abbrev-journal-title><![CDATA[AVFT]]></abbrev-journal-title>
<issn>0798-0264</issn>
<publisher>
<publisher-name><![CDATA[Sociedad Venezolana de Farmacológia  y Farmacológia Clínica y Terapéutica. Escuela de MedicinaJosé Maria Vargas. Cátedra de Farmacológia, piso 3, esquina san jacinto, San José Caracas]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0798-02642004000200004</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Beneficios independientes de la reducción de la presión arterial en pacientes tratados con Nifedipina en microgránulos]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Téllez-Méndez]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Curiel]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Franco]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Medina]]></surname>
<given-names><![CDATA[G]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Sánchez]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[González Yibirín]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Anaya]]></surname>
<given-names><![CDATA[G]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Medina]]></surname>
<given-names><![CDATA[Y]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Hernández]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Espinoza]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Rico]]></surname>
<given-names><![CDATA[I]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Rondón]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Galdón]]></surname>
<given-names><![CDATA[E]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Durán]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Márquez]]></surname>
<given-names><![CDATA[E]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Hospital Dr. Jesús María Casal Ramos Unidad de Hipertensión Arterial ]]></institution>
<addr-line><![CDATA[Araure Portuguesa]]></addr-line>
<country>Venezuela</country>
</aff>
<aff id="A02">
<institution><![CDATA[,S.A.V. Lavoratorios Leti ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>07</month>
<year>2004</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>07</month>
<year>2004</year>
</pub-date>
<volume>23</volume>
<numero>2</numero>
<fpage>118</fpage>
<lpage>121</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://ve.scielo.org/scielo.php?script=sci_arttext&amp;pid=S0798-02642004000200004&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://ve.scielo.org/scielo.php?script=sci_abstract&amp;pid=S0798-02642004000200004&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://ve.scielo.org/scielo.php?script=sci_pdf&amp;pid=S0798-02642004000200004&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Introducción: El estado "dippers" es un factor de riesgo independiente en los pacientes hipertensos ("Risers"-R->"Non-dippers"-ND->"Dippers"-D>"Dippers extremos"-DE). Se evaluó el efecto de la nueva nifedipina en microgránulos (NMG) una vez al día en la disminución de la presión arterial nocturna medida a través del MAPA con Mobil-o-Graph -CE0434-(I.E.M.Gmbh-Cockerillstr. 69 D-Stolberg. Germany). Métodos: Se incluyeron pacientes hipertensos (PAS &#8805; 140 y/o PAD &#8805; 90 mmHg, medidas con esfigmomanómetro de Hg) que recibieron de 30 a 60 mgrs/día de NMG, en un estudio prospectivo abierto comparativo y cruzado en "time-doses" 8 am ó 8 pm; que luego de 6 semanas de tratamiento mantuvieran PAS < 140 mmHg. Resultados: Se reclutaron 73 pacientes. 40 pacientes (54.8%), mantuvieron su estado: ND n = 22 (disminución de la PAS nocturna entre 0 y 10%), D n =16 (disminución de PAS nocturna entre 10 y 20%) y R n = 2 (incremento de la PAS nocturna). Los otros 33 pacientes (45.2%) modificaron su estado: cinco: 3D y 2ND cambiaron a DE (disminución de la PAS nocturna >20%), once: 2DE y 9ND se transformaron en D, catorce: 6R, 1DE y 7D hacia ND y 3D cambiaron a R. No hubo diferencias significativas en el cambio de estado "dippers" en ambos grupos (30 ó 60 mgrs), 17 pacientes mejoraron su estado (9ND y 2DE) se transformaron en D y 6R pasaron a ND; 16 pacientes "dippers" se mantuvieron. Conclusión: Estos resultados sugieren que la NMG ofrece en el 45% de los pacientes estudiados un beneficio independiente de la reducción de la presión arterial, manteniendo o mejorando el estado "dippers" ofreciendo una mejor predicción en la disminución de eventos cardiovasculares y del pronóstico de los accidentes cerebro-vasculares.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Background: The dipper status is an independent risk factor in the hypertensive patients (Risers-R->Non dipper-ND->Dipper-D->Extreme dipper-ED-). We evaluated the effect of new nifedipine once day in micro-granules (NMG) on the nocturnal blood pressure fall, measurement by ABPM. Methods: Were included hypertensive patient (SBP &#8805; 140 mmHg and/or DBP &#8805; 90 mmHg, measurement with sphygmomanometer) that received 30 o 60 mg/day in a prospective, open and crossed in the time-doses 8 am or 8 pm study and that after the six week of treatment if SBP were < 140 mmHg with. Results: We recruited 73 patients, 40 (54.8%) maintained their status: ND n = 22 (night SBP fall between 0 and 10%), D n = 16 (night SBP fall between 10 and 20%) and R n = 2 (nocturnal increase in SBP). The other 33 patients (45.2%) change their status, five: 3 D and 2 ND change to ED (night SBP fall > 20%), eleven: 2 ED and 9 ND change to D, fourteen: 6 R, 1 ED and 7 D changed to ND, and three: 3 D change to R. There were no statistical difference with nocturnal blood pressure dipping change among the groups (30 or 60 mg), 17 patients improved their status (9 ND and 2 ED to D and 6 R to ND) and 16 patients D, maintained it. Conclusions: These results suggest that NMP offers in the 45% of the patients maintained or improve the status like as an independent benefit for the reduction of the blood pressure that could result in a better prediction of cardiovascular events and influence the prognosis for stroke.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Nifedipina en microgránulos]]></kwd>
<kwd lng="es"><![CDATA[Estado dippers]]></kwd>
<kwd lng="es"><![CDATA[Hipertensión arterial]]></kwd>
<kwd lng="en"><![CDATA[Nifedipine in micro-granules]]></kwd>
<kwd lng="en"><![CDATA[Status dippers]]></kwd>
<kwd lng="en"><![CDATA[Blood pressure]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[   <B>    <P ALIGN="center"><font face="Times New Roman" size="4">Beneficios independientes de la reducci&oacute;n de la presi&oacute;n arterial en pacientes tratados con Nifedipina en microgr&aacute;nulos*</font></P> </B>    <P ALIGN="center"><font face="Times New Roman" size="3">R T&eacute;llez-M&eacute;ndez<sup>1</sup>, R Curiel<sup>1</sup>, A Franco<sup>1</sup>, G Medina<sup>1</sup>, M S&aacute;nchez<sup>1</sup>, M Gonz&aacute;lez Yibir&iacute;n<sup>2</sup>, G Anaya<sup>1</sup>, Y Medina<sup>1</sup>,</font></P>     <P ALIGN="center"><font face="Times New Roman" size="3">J Hern&aacute;ndez<sup>1</sup>, R Espinoza<sup>1</sup>, I Rico<sup>1</sup>, M Rond&oacute;n<sup>1</sup>, E Gald&oacute;n<sup>1</sup>, J Dur&aacute;n<sup>1</sup> y E M&aacute;rquez<sup>1</sup>.</font> </P>     <P ALIGN="center"><font face="Times New Roman" size="3"><sup>1</sup> Unidad de Hipertensi&oacute;n Arterial. Hospital &quot;Dr. Jes&uacute;s Mar&iacute;a Casal Ramos&quot;, Araure. Estado Portuguesa. Venezuela.</font></P>     <P ALIGN="center"><font face="Times New Roman" size="3"><sup>2</sup> Lavoratorios Leti, S.A.V.</font></P>     <P ALIGN="center"><FONT face="Times New Roman" size=3> * La Nifedipina microgr&aacute;nulos fue suministrada por Laboratorios Biocontrolled. </FONT></P>     <P ALIGN="center"><font face="Times New Roman" size="3">E-mail: <A HREF="mailto:telsal@cantv.net">telsal@cantv.net</A></font></P> <B>    <P ALIGN="JUSTIFY"><font face="Times New Roman" size="3">RESUMEN</font></P>     <P ALIGN="JUSTIFY"><font face="Times New Roman" size="3">Introducci&oacute;n:</font></B> <font size="3"><font face="Times New Roman"> El estado &quot;dippers&quot; es un factor de riesgo independiente en los pacientes hipertensos (&quot;Risers&quot;-R-&gt;&quot;Non-dippers&quot;-ND-&gt;&quot;Dippers&quot;-D&gt;&quot;Dippers extremos&quot;-DE). Se evalu&oacute; el efecto de la nueva nifedipina en microgr&aacute;nulos (NMG) una vez al d&iacute;a en la disminuci&oacute;n de la presi&oacute;n arterial nocturna medida a trav&eacute;s del MAPA con Mobil-o-Graph -CE0434-(I.E.M.Gmbh-Cockerillstr. 69 D-Stolberg. Germany). <B>M&eacute;todos:</B><I> </I>Se incluyeron pacientes hipertensos (PAS &#8805; 140 y/o PAD &#8805; 90 mmHg, medidas con esfigmomanómetro de Hg) que recibieron de 30 a 60 mgrs/día de NMG, en un estudio prospectivo abierto comparativo y cruzado en “time-doses” 8 am ó 8 pm; que luego de 6 semanas de tratamiento mantuvieran PAS &lt; 140 mmHg. <B>Resultados: </B>Se reclutaron 73 pacientes. 40 pacientes (54.8%), mantuvieron su estado: ND n = 22 (disminuci&oacute;n de la PAS nocturna entre 0 y 10%), D n =16 (disminuci&oacute;n de PAS nocturna entre 10 y 20%) y R n = 2 (incremento de la PAS nocturna). Los otros 33 pacientes (45.2%) modificaron su estado: cinco: 3D y 2ND cambiaron a DE (disminuci&oacute;n de la PAS nocturna &gt;20%), once: 2DE y 9ND se transformaron en D, catorce: 6R, 1DE y 7D hacia ND y 3D cambiaron a R. No hubo diferencias significativas en el cambio de estado &quot;dippers&quot; en ambos grupos (30 &oacute; 60 mgrs), 17 pacientes mejoraron su estado (9ND y 2DE) se transformaron en D y 6R pasaron a ND; 16 pacientes &quot;dippers&quot; se mantuvieron. <B>Conclusi&oacute;n:</B> Estos resultados sugieren que la NMG ofrece en el 45% de los pacientes estudiados un beneficio independiente de la reducci&oacute;n de la presi&oacute;n arterial, manteniendo o mejorando el estado &quot;dippers&quot; ofreciendo una mejor predicci&oacute;n en la disminuci&oacute;n de eventos cardiovasculares y del pron&oacute;stico de los accidentes cerebro-vasculares.</font></font></P>     ]]></body>
<body><![CDATA[<P ALIGN="JUSTIFY"><FONT face="Times New Roman" size=3><b>Palabras Clave:</b> Nifedipina en microgr&aacute;nulos, Estado dippers, Hipertensi&oacute;n arterial. </FONT></P>  <B>     <P ALIGN="JUSTIFY"><FONT face="Times New Roman" size=3>ABSTRACT </FONT></P>      <P ALIGN="JUSTIFY"><font face="Times New Roman" size="3">Background:</font></B> <font size="3"><font face="Times New Roman"> The dipper status is an independent risk factor in the hypertensive patients (Risers-R-&gt;Non dipper–ND-&gt;Dipper–D-&gt;Extreme dipper-ED-). We evaluated the effect of new nifedipine once day in micro-granules (NMG) on the nocturnal blood pressure fall, measurement by ABPM. <B>Methods:</B> Were included hypertensive patient (SBP  &#8805; 140 mmHg and/or DBP &#8805; 90 mmHg, measurement with sphygmomanometer) that received 30 o 60 mg/day in a prospective, open and crossed in the time–doses 8 am or 8 pm study and that after the six week of treatment if SBP were &lt; 140 mmHg with. <B>Results:</B> We recruited 73 patients, 40 (54.8%) maintained their status: ND n = 22 (night SBP fall between 0 and 10%), D n = 16 (night SBP fall between 10 and 20%) and R n = 2 (nocturnal increase in SBP). The other 33 patients (45.2%) change their status, five: 3 D and 2  ND change to ED (night SBP fall &gt; 20%), eleven: 2 ED and 9 ND change to D, fourteen: 6 R, 1 ED and 7 D changed to ND, and three: 3 D change to R. There were no statistical difference with nocturnal blood pressure dipping change among the groups (30 or 60 mg), 17 patients improved their status (9 ND and 2 ED to D and 6 R to ND) and 16 patients D, maintained it. <B>Conclusions:</B> These results suggest that NMP offers in the 45% of the patients maintained or improve the status like as an independent benefit for the reduction of the blood pressure that could result in a better prediction of cardiovascular events and influence the prognosis for stroke.</font></font></P> <B>    <P ALIGN="JUSTIFY"><FONT face="Times New Roman" size=3>Key Words: </FONT> </B><FONT face="Times New Roman" size=3>Nifedipine in micro-granules, Status dippers, Blood pressure. </FONT></P> <B>    <P ALIGN="JUSTIFY"><font face="Times New Roman" size="3">Introducci&oacute;n</font></P> </B>    <P ALIGN="JUSTIFY"><font size="3"><font face="Times New Roman">Los beneficios del tratamiento antihipertensivo han sido estudiados y catalogados como beneficios dependientes de la reducci&oacute;n de cifras de la presi&oacute;n arterial y los beneficios independientes de &eacute;stas. Se sabe que una disminuci&oacute;n promedio de 5-6 mmHg para presi&oacute;n arterial diast&oacute;lica y de 10-12 mmHg para la sist&oacute;lica se asocia con una disminuci&oacute;n de un 21% en la mortalidad cardiovascular, de un 48% en accidentes cerebro vasculares fatales y no fatales y una disminuci&oacute;n del 14% en la enfermedad coronaria fatal y no fatal<sup>(1)</sup>. En los estudios UKPDS, HOT, ABCD, SHEP y SIST.-EUR, revelan un porcentaje de reducci&oacute;n de la mortalidad total entre un 18 al 64% como consecuencia de las disminuciones de las presiones arteriales sist&oacute;licas entre 4 y 10 mmHg y de la diast&oacute;lica entre 2 y 8 mmHg<sup>(2-6)</sup>. Estos beneficios dependientes del cambio de la presi&oacute;n arterial, tienen lugar a cualquier nivel de la presi&oacute;n arterial previa al tratamiento y son independientes del tipo de f&aacute;rmaco(s) utilizado(s)<sup>(7)</sup>.</font></font> </P>     <P ALIGN="JUSTIFY"><font size="3"><font face="Times New Roman">Se han demostrado dentro de los beneficios independientes de la reducci&oacute;n de las presiones arteriales, que en pacientes hipertensos en tratamiento con estados diferentes al dippers presentan un porcentaje mayor de accidentes cerebro vasculares silentes expresados por lagunas y radiolucidencias peri ventriculares, de hipertrofia del ventr&iacute;culo izquierdo y de micro albuminuria<sup>(8)</sup>. De igual manera se demostr&oacute; una mayor incidencia de accidentes cardiovasculares totales en la poblaci&oacute;n general si el estado era diferente al dippers con una acentuaci&oacute;n de &eacute;stos si los pacientes pertenec&iacute;an al sexo femenino<sup>(9)</sup>. El estudio OHASAMA que evalu&oacute; el valor pron&oacute;stico de la variabilidad circadiana de las presiones arteriales en el riesgo cardiovascular en la poblaci&oacute;n general, demostr&oacute; un incremento del riesgo relativo de la mortalidad cardiovascular y total cuando el estado era diferente al dippers y al dippers extremo, no existiendo diferencias en la mortalidad no cardiovascular, en el mismo trabajo se realiz&oacute; un seguimiento de la supervivencia en la poblaci&oacute;n general en un lapso de 96 meses, demostrando que los pacientes de mayor riesgo eran &quot;risers&quot;&gt;non dippers&gt;dippers&gt;dippers extremo<sup>(10)</sup>. Otro estudio realizado para evaluar la variabilidad circadiana de la presi&oacute;n arterial y cambios de la funci&oacute;n renal a 3 a&ntilde;os en pacientes con insuficiencia renal cr&oacute;nica demostr&oacute;, una pendiente de descenso en la filtraci&oacute;n gromerular y de la excreci&oacute;n urinaria de alb&uacute;mina en 24 horas mayor en pacientes que no exhib&iacute;an el estado dippers<sup>(11)</sup>. La presi&oacute;n arterial ambulatoria como predictor del pron&oacute;stico en la hipertensi&oacute;n arterial esencial fue evaluada a trav&eacute;s de 400 semanas de seguimiento en donde se evidenci&oacute; la probabilidad de supervivencia libre de accidentes cardiovasculares, comprob&aacute;ndose que los pacientes de mayor riesgo son non dippers&gt;dippers&gt;HTA de bata blanca&gt;normotensos<sup>(14)</sup>.</font></font></P>     <P ALIGN="JUSTIFY"><font face="Times New Roman" size="3">Por ser el estado &quot;dippers&quot; un factor de riesgo independiente en los pacientes hipertensos, se evalu&oacute; el efecto de la nueva nifedipina de liberaci&oacute;n programada en micro-gr&aacute;nulos (NMG) una vez al d&iacute;a en la disminuci&oacute;n de la presi&oacute;n arterial nocturna medida a trav&eacute;s del monitoreo ambulatorio de la presi&oacute;n arterial (MAPA) y evidenciar la variabilidad circadiana de las presiones arteriales luego del tratamiento con esta mol&eacute;cula.</font></P> <B>    <P ALIGN="JUSTIFY"><FONT face="Times New Roman" size=3>Materiales y M&eacute;todos</FONT></P> </B>    <P ALIGN="JUSTIFY"><font size="3"><font face="Times New Roman">El estudio se realiz&oacute; en la Unidad de Hipertensi&oacute;n Arterial del Hospital Universitario &quot;Dr. Jes&uacute;s Mar&iacute;a Casal Ramos de Acarigua-Araure, Estado Portuguesa, Venezuela. Luego de su aceptaci&oacute;n por el Comit&eacute; de &Eacute;tica local, siguiendo con las regulaciones locales y seg&uacute;n enmienda de la Declaraci&oacute;n de Helsinki en la 52ª Asamblea General Edimburgo, Escocia, Octubre 2000<sup>(12)</sup>, fueron evaluados 73 pacientes, en un estudio abierto, prospectivo, comparativo y cruzado en &quot;time doses&quot;, con hipertensi&oacute;n arterial (HTA) esencial (sin causa secundaria). Se tomaron como criterios de admisi&oacute;n al estudio PAS igual o mayor a 140 mmHg o PAD igual o mayor a 90 mmHg cuantificadas en posici&oacute;n sentado, en dos ocasiones con intervalos de 15 minutos en la misma posici&oacute;n, medidas con el esfigmoman&oacute;metro de mercurio (EMPIRE, Riester<sup>&reg;</sup>. Germany) calibrado de manera habitual a hombres o mujeres entre 35 y 70 a&ntilde;os, pacientes en tratamiento antihipertensivo con monoterapia a dosis media, que despu&eacute;s de un per&iacute;odo de lavado de 2 semanas mantuvieran las cifras de presi&oacute;n diast&oacute;lica entre 90 y 110 mmHg y a todos &eacute;stos se le solicit&oacute; el consentimiento firmado por escrito.</font></font></P>     ]]></body>
<body><![CDATA[<P ALIGN="JUSTIFY"><font face="Times New Roman" size="3">Se excluyeron a los pacientes con PAD superior a 110 mmHg o PAS superior a 200 mmHg, sospecha de hipertensi&oacute;n secundaria o maligna, aquellos pacientes que normalizaran la presi&oacute;n arterial durante el per&iacute;odo de lavado, pacientes con enfermedad hep&aacute;tica o renal severa, accidente cerebro vascular o IM durante los &uacute;ltimos tres meses, angina inestable o arritmias card&iacute;acas, insuficiencia card&iacute;aca izquierda, cardiopat&iacute;a isqu&eacute;mica aguda, tuberculosis pulmonar, c&aacute;ncer, disfunci&oacute;n tiroidea, enfermedad mental, consumo de drogas no medicinales y alcoholismo, psicosis, &uacute;lcera, o alteraciones de la bioqu&iacute;mica sangu&iacute;nea. No se admitieron pacientes que se encuentren en tratamiento antihipertensivo con dosis m&aacute;xima en monoterapia o con terapia combinada de antihipertensivos, uso concomitante de litio o de cualquier medicaci&oacute;n con efectos conocidos sobre la presi&oacute;n arterial y pacientes con sensibilidad conocida a la nifedipina, y la intenci&oacute;n o necesidad de donar sangre durante el estudio o hasta un mes despu&eacute;s de finalizar el estudio.</font></P>     <P ALIGN="JUSTIFY"><font face="Times New Roman" size="3">Se evalu&oacute; el efecto de la NMG desarrollada por Laboratorios Biocontrolled Venezuela, administrada una vez al d&iacute;a en la disminuci&oacute;n de la presi&oacute;n arterial nocturna medida a trav&eacute;s del MAPA con Mobil-o-Graph -CE0434-(I.E.M.Gmbh-Cockerillstr. 69 D-Stolberg. Germany).</font></P>     <P ALIGN="JUSTIFY"><font size="3"><font face="Times New Roman">Se clasificaron el estado dippers en cuatro categor&iacute;as: dippers: aquellos pacientes con disminuci&oacute;n de PAS nocturna entre 10 y 20%, dippers extremos: los pacientes con disminuci&oacute;n de la PAS nocturna &gt;20%, non dippers: pacientes con disminuci&oacute;n de la PAS nocturna entre 0 y 10% y los non dippers extremos o &quot;risers&quot;: aquellos pacientes con incremento de la PAS nocturna<sup>(13)</sup>.</font></font></P>     <P ALIGN="JUSTIFY"><font face="Times New Roman" size="3">Las visitas hospitalarias se realizaron en la ma&ntilde;ana en el per&iacute;odo de inclusi&oacute;n en donde se les realiz&oacute; a los pacientes el MAPA en la etapa de pre-tratamiento y en el mismo horario luego de la administraci&oacute;n de NMG 30 mgrs &oacute; 60 mgrs administrados a las 8 am o a las 8 pm, y a la 6ta semana despu&eacute;s del inicio del tratamiento.</font></P>     <P ALIGN="JUSTIFY"><font face="Times New Roman" size="3">Los criterios de valoraci&oacute;n de la eficacia primaria fueron: los cambios en el estado nocturno dipper luego de la normalizaci&oacute;n de la presi&oacute;n arterial (la PAS &lt; 140 mmHg o la PAD &lt; 90 mmHg) con el esfigmoman&oacute;metro de mercurio.</font></P>     <P ALIGN="JUSTIFY"><font face="Times New Roman" size="3">A los resultados se les aplic&oacute; estad&iacute;sticas descriptivas, T-student y an&aacute;lisis de varianza.</font></P> <B>    <P ALIGN="JUSTIFY"><font face="Times New Roman" size="3">Resultados</font></P> </B>    <P ALIGN="JUSTIFY"><font face="Times New Roman" size="3">Se analizaron 73 pacientes con edades de 44.62 ± 0.9 a&ntilde;os. Las reducciones de las presiones arteriales de inicio y al final del tratamiento a las 6 semanas fueron: PAS de 148.04 ± 6.26 a 130.74 ± 4.43 mmHg (p&lt;0.05) y PAD de 96.98 ± 5.0 a 84.49 ± 2.79 mmHg (p&lt;0.05).</font></P>     <P ALIGN="JUSTIFY"><font face="Times New Roman" size="3">De estos pacientes, 40 (54.8%) mantuvieron su estado: 22 permanecieron en su estado non dippers, 16 conservaron su estado dippers y 2 preservaron su estado &quot;risers&quot;. Los otros 33 pacientes (45.2%) modificaron su estado: cinco (5): 3 dippers y 2 non dippers cambiaron su estado a dippers extremos, once (11): 2 dippers extremos y 9 non dippers se transformaron en dippers, catorce (14): 6 &quot;risers&quot;, 1 dippers extremo y 7 dippers se convirtieron en non dippers y 3 dippers cambiaron de status a &quot;risers&quot;.</font></P>     <P ALIGN="JUSTIFY"><font face="Times New Roman" size="3">No hubo diferencias significativas en el cambio de estado &quot;dippers&quot; en los pacientes que tomaron 30 &oacute; 60 mgrs de NMG. Los pacientes que mantuvieron o mejoraron el estado fueron 45% (n = 33 pacientes).</font></P> <B>    ]]></body>
<body><![CDATA[<P ALIGN="JUSTIFY"><FONT face="Times New Roman" size=3>Discusi&oacute;n</FONT></P> </B>    <P ALIGN="JUSTIFY"><font face="Times New Roman" size="3">La nifedipina para ser administrada cada 24 horas en microgr&aacute;nulos ha sido evaluada por nuestro grupo, demostrando una eficacia terap&eacute;utica como monoterapia en el 86.7% de los pacientes estudiados<sup>(15)</sup>, esto concuerda con estudios previos donde se observ&oacute; que en monoterapia la nifedipina de liberaci&oacute;n osm&oacute;tica logr&oacute; el control satisfactorio de la presi&oacute;n arterial, regresi&oacute;n de la hipertrofia ventricular izquierda y buena tolerancia despu&eacute;s de un a&ntilde;o de seguimiento<sup>(16)</sup>. En una poblaci&oacute;n china hipertensa y con diabetes tipo 2 estudiada con amlodipina y nifedipina retard, ambas drogas fueron efectivas en el control de la presi&oacute;n arterial en las 24 horas, al mismo tiempo encontraron que el 14,8%, de los pacientes restauraron el estado dipper nocturno normal. A estos pacientes se les realiz&oacute; seguimiento durante una a&ntilde;o, despu&eacute;s del cual se evidenci&oacute; que estos pacientes &quot;nuevos dippers&quot; ten&iacute;an un incremento significante de la fracci&oacute;n de eyecci&oacute;n sist&oacute;lica del ventr&iacute;culo izquierdo y un incremento del di&aacute;metro diast&oacute;lico del ventr&iacute;culo izquierdo con estos calcio-antagonistas<sup>(17)</sup>.</font></P>     <P ALIGN="JUSTIFY"><FONT face="Times New Roman" size=3>Lo que demuestra que mantener o mejorar el estado dipper durante el tratamiento antihipertensivo, se asocia a un beneficio sobre la funci&oacute;n card&iacute;aca.</FONT></P>     <P ALIGN="JUSTIFY"><font face="Times New Roman" size="3">En algunos estudios se ha visto que no hay beneficios de prevenci&oacute;n de accidentes cerebro vasculares entre los pacientes hipertensos medicados y no medicados que posean el estado dippers extremos y &quot;risers&quot;<sup>(18-19)</sup>, sin embargo en estudios con seguimientos m&aacute;s largos<sup>(9-10)</sup>, demuestran que los dippers extremos tienen mejor probabilidad de supervivencia libre de accidentes vasculares que los &quot;risers&quot;.</font></P>     <P ALIGN="JUSTIFY"><FONT face="Times New Roman" size=3>El mantenimiento o cambio del estado dippers no hab&iacute;a sido estudiado con NMG, en el presente estudio se tom&oacute; una poblaci&oacute;n de pacientes que respondieron a la medicaci&oacute;n antihipertensiva evalu&aacute;ndose adem&aacute;s la variaci&oacute;n del estado dippers, encontr&aacute;ndose que aparte de los beneficios directos de la reducci&oacute;n de la presi&oacute;n arterial, una buena parte de los pacientes mejoraron o mantuvieron su estado dippers como beneficio adicional en el tratamiento antihipertensivo.</FONT></P>     <P ALIGN="JUSTIFY"><FONT face="Times New Roman" size=3>En conclusi&oacute;n, estos resultados sugieren que la NMG ofrece el beneficio directo de la reducci&oacute;n de la presi&oacute;n arterial en el 100% de los pacientes estudiados, y en el 45% de los pacientes ofrece adicionalmente un beneficio independiente de la reducci&oacute;n de la presi&oacute;n arterial, manteniendo o mejorando el estado &quot;dippers&quot; y de esta manera podemos esperar en estos pacientes una disminuci&oacute;n de eventos cardiovasculares y una mejor&iacute;a del pron&oacute;stico en la incidencia de los accidentes cerebro-vasculares.</FONT></P> <B>    <P ALIGN="JUSTIFY"><FONT face="Times New Roman" size=3>referencias bibliogr&aacute;ficas</FONT></P>  </B>    <!-- ref --><P ALIGN="JUSTIFY"><FONT face="Times New Roman" size=3>1. 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Rev Esp Cardiol. 1997; 50(8): 567-72.  </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=582587&pid=S0798-0264200400020000400016&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><P ALIGN="JUSTIFY"><FONT face="Times New Roman" size=3>17. Ko GT, Chan HC. Restoration of nocturnal dip in blood pressure is associated with improvement in left ventricular ejection fraction. A 1-year clinical study comparing the effects of Amlodipine and Nifedipine retard on ambulatory blood pressure and left ventricular systolic function in Chinese hypertensive type 2 diabetic patients. Int J Cardiol. 2003; 89(2-3): 159-66.  </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=582588&pid=S0798-0264200400020000400017&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><P ALIGN="JUSTIFY"><FONT face="Times New Roman" size=3>18. Hoshide Y, Kario K, Schwartz JE, Hoshide S, Pickering TG, Shimada K. Incomplete benefit of antihypertensive therapy on stroke reduction in older hypertensives with abnormal nocturnal blood pressure dipping (extreme-dippers and reverse-dippers). 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<back>
<ref-list>
<ref id="B1">
<label>1</label><nlm-citation citation-type="">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Berthet]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
<name>
<surname><![CDATA[Neal]]></surname>
<given-names><![CDATA[BC]]></given-names>
</name>
<name>
<surname><![CDATA[Chalmers]]></surname>
<given-names><![CDATA[JP]]></given-names>
</name>
<name>
<surname><![CDATA[MacMahon]]></surname>
<given-names><![CDATA[SW]]></given-names>
</name>
<name>
<surname><![CDATA[Bousser]]></surname>
<given-names><![CDATA[MG]]></given-names>
</name>
<name>
<surname><![CDATA[Colman]]></surname>
<given-names><![CDATA[SA]]></given-names>
</name>
<name>
<surname><![CDATA[Woodward]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
</person-group>
<source><![CDATA[Perindopril Protection Against Recurrent Stroke Study Collaborative Group: Reductions in the risks of recurrent stroke in patients with and without diabetes: the PROGRESS Trial]]></source>
<year>2004</year>
<volume>13</volume>
<page-range>7-13</page-range></nlm-citation>
</ref>
<ref id="B2">
<label>2</label><nlm-citation citation-type="">
<collab>UKPDS. United Kingdom Prospective Diabetes Study Group</collab>
<source><![CDATA[Efficacy of atenolol and captopril in reducing risk of macrovascular and microvascular complications]]></source>
<year>1998</year>
<volume>317</volume>
<page-range>703-713</page-range></nlm-citation>
</ref>
<ref id="B3">
<label>3</label><nlm-citation citation-type="book">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Hansson]]></surname>
<given-names><![CDATA[L]]></given-names>
</name>
<name>
<surname><![CDATA[Zanchetti]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
</person-group>
<source><![CDATA[The Hypertension Optimal Treatment Study (HOT)]]></source>
<year>1993</year>
<volume>2</volume>
<page-range>62-68</page-range><publisher-name><![CDATA[Blood Press]]></publisher-name>
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</ref>
<ref id="B4">
<label>4</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
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<given-names><![CDATA[RO]]></given-names>
</name>
<name>
<surname><![CDATA[Jeffers]]></surname>
<given-names><![CDATA[BW]]></given-names>
</name>
<name>
<surname><![CDATA[Hiatt]]></surname>
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