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<front>
<journal-meta>
<journal-id>0120-5633</journal-id>
<journal-title><![CDATA[Revista Colombiana de Cardiología]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. Colomb. Cardiol.]]></abbrev-journal-title>
<issn>0120-5633</issn>
<publisher>
<publisher-name><![CDATA[Sociedad Colombiana de Cardiologia. Oficina de Publicaciones]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0120-56332012000400003</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[La importancia de las evaluaciones económicas de los medicamentos: el caso del metoprolol]]></article-title>
<article-title xml:lang="en"><![CDATA[Relevance of economical evaluation of medications: the metoprolol case]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[López-Jaramillo]]></surname>
<given-names><![CDATA[Patricio]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Camacho]]></surname>
<given-names><![CDATA[Paul A]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Fundación Oftalmológica de Santander  ]]></institution>
<addr-line><![CDATA[Floridablanca ]]></addr-line>
<country>Colombia</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>08</month>
<year>2012</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>08</month>
<year>2012</year>
</pub-date>
<volume>19</volume>
<numero>4</numero>
<fpage>169</fpage>
<lpage>171</lpage>
<copyright-statement/>
<copyright-year/>
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</front><body><![CDATA[  <font size="2" face="Verdana">     <p>    <center>La importancia de las evaluaciones econ&oacute;micas de los medicamentos: el caso del metoprolol</center></p>     <p>    <center>  Relevance of economical evaluation of medications:    the metoprolol case</center></p>     <p>    <center> Patricio L&oacute;pez-Jaramillo, MD., PhD., FACP.<sup>(1, 2)</sup>; Paul A. Camacho, MD.<sup>(1)</sup></center></p>     <p><sup>(1)</sup> Fundaci&oacute;n Oftalmol&oacute;gica de Santander&ndash;FOSCAL, Floridablanca&ndash;Santander, Colombia.    <br> <sup>(2)</sup> Instituto de Investigaciones, Facultad de Medicina, Universidad de Santander &ndash; UDES, Bucaramanga, Colombia.</p>     <p><b>Correspondencia</b>: Dr. Patricio L&oacute;pez-Jaramillo, correo electr&oacute;nico: <a href="mailto:jplopezj@gmail.com" target="_blank">jplopezj@gmail.com</a></p>     ]]></body>
<body><![CDATA[<p>Recibido: 13/08/2012. Aceptado:15/08/2012.</p>  <hr size="1">     <p> En la pr&aacute;ctica cl&iacute;nica, el desarrollo de nuevas tecnolog&iacute;as en salud ha significado enfrentarse a nuevos retos, dado que los sistemas de salud no cuentan con los recursos necesarios para el cubrimiento de medicamentos y procedimientos recientes (1). Con recursos limitados, cualquier gasto que se realice en nuevos medicamentos o procedimientos debe tener suficiente evidencia de beneficio que justifique su incorporaci&oacute;n al sistema (2). Hasta el a&ntilde;o 2011, el Plan Obligatorio de Salud de Colombia contaba con 6.503 tecnolog&iacute;as en salud (651 medicamentos y 5.832 procedimientos) definidos en el Acuerdo 008 de 2009 de la Comisi&oacute;n Regulatoria en Salud (CRES) (3), algunas de las cuales se encuentran en fase de declinaci&oacute;n u obsolescencia (4, 5).</p>       <p>De otro lado, los estudios de evaluaci&oacute;n econ&oacute;mica de medicamentos y procedimientos desempe&ntilde;an un papel importante en la planificaci&oacute;n de los sistemas de salud, ya que proporcionan informaci&oacute;n &uacute;til para la toma de decisiones sobre el uso de tecnolog&iacute;as en salud que permiten mejorar la pr&aacute;ctica cl&iacute;nica y obtener los mejores resultados a un costo sostenible (6). Como se indic&oacute;, en Colombia existen medicamentos del Plan Obligatorio en Salud (POS) del Sistema General de Seguridad en Salud (SGSS) que se encuentran en fase de declinaci&oacute;n u obsolescencia, por lo cual es necesaria la evaluaci&oacute;n de nuevas opciones bien para su inclusi&oacute;n o para la exclusi&oacute;n de los antiguos, analizando costos y consecuencias que permitan recomendar las mejores alternativas en un contexto de recursos limitados (7).</p>       <p>En lo que respecta a insuficiencia cardiaca congestiva (ICC), un problema mundial que sigue siendo una causa cada vez m&aacute;s importante de morbilidad y mortalidad en pa&iacute;ses con moderados y bajos ingresos econ&oacute;micos (8, 9), la incidencia aproximada es de 2% en la poblaci&oacute;n general (10, 11). Por su parte, la mortalidad por enfermedad cardiovascular secundaria a falla cardiaca y sus comorbilidades se encuentra &iacute;ntimamente relacionada con el nivel de desarrollo y el estado socioecon&oacute;mico de cada pa&iacute;s (12). La hipertensi&oacute;n arterial sist&eacute;mica (HAS) puede afectar 20% de la poblaci&oacute;n adulta y en individuos mayores de cincuenta a&ntilde;os aumenta al 50%, es adem&aacute;s, la primera causa de morbilidad y de motivo de consulta dentro de las enfermedades del sistema circulatorio (13, 14).</p>       <p>En consonancia con lo anterior, el uso de betabloqueadores para el tratamiento de la ICC mostr&oacute; ser beneficioso en el control de par&aacute;metros cl&iacute;nicos y hemodin&aacute;micos (15,16), pues mejora la funci&oacute;n cardiaca y disminuyen la mortalidad por cualquier causa y el riesgo de hospitalizaci&oacute;n, en 30% a 35% y en 25% a 30%, respectivamente (17, 18). Estos medicamentos producen un efecto de &quot;upregulation&quot; que aumenta la cantidad de receptores membranales, lo cual se traduce en un mejoramiento de cronotropismo e inotropismo card&iacute;aco (19). Adem&aacute;s, el uso de betabloqueadores reduce algunos factores proinflamatorios, citoquinas y factores vasoconstrictores (20, 21) y contribuye con la normalizaci&oacute;n de los genes mioc&aacute;rdicos relacionados con la contractibilidad y la hipertrofia (22), controlando el da&ntilde;o mioc&aacute;rdico en la insuficiencia cardiaca. El bisoprolol y el metoprolol ejercen su efecto en los receptores beta 1 y el carvedilol act&uacute;a sobre los receptores beta 2 y alfa 1.</p>       <p>El metoprolol es un antagonista beta 1 selectivo disponible como tartrato y succinato (de liberaci&oacute;n prolongada). La dosis &uacute;nica de tartrato no garantiza un efecto beta bloqueante durante 24 horas por su vida media corta y en el estudio MDC no se demostr&oacute; una disminuci&oacute;n de la mortalidad o de la morbilidad (23). Entretanto, y aunque se cuestion&oacute; este estudio por el tiempo de seguimiento muy corto (24), el US Carvedilol Heart Failure Study Group mostr&oacute; una disminuci&oacute;n significativa de la mortalidad de 64% en una poblaci&oacute;n con fracci&oacute;n de eyecci&oacute;n menor de 35% en clase funcional II &ndash; III, as&iacute; como una reducci&oacute;n en la tasa de hospitalizaci&oacute;n del 27%, y mejoramiento de la clase funcional y de la fracci&oacute;n de eyecci&oacute;n. En el estudio CIBIS II (Cardiac Insufficiency Bisoprolol Study) se ratific&oacute; el impacto beneficioso de los betabloqueadores en pacientes con ICC clase II&ndash;III, al demostrar una reducci&oacute;n de mortalidad y muerte s&uacute;bita de 35% y 42%, respectivamente (26). El estudio MERIT-HF utiliz&oacute; metoprolol de liberaci&oacute;n prolongada a dosis de 12,5 mg hasta 200 g/d&iacute;a en pacientes con clase funcional II-III, y mostr&oacute; disminuci&oacute;n de la mortalidad por todas las causas, muerte s&uacute;bita y muerte por progresi&oacute;n de la enfermedad en 34%, 41% y 49%, en su orden. La dosis promedio de metoprolol succinato fue 159 mg equivalente a 119 mg de metoprolol tartrato, si bien 64% de los pacientes llegaron a una dosis de 200 mg/d&iacute;a (27, 28). El estudio COPERNICUS en pacientes con clase funcional IV severa y fracci&oacute;n de eyecci&oacute;n menor al 25%, demostr&oacute; una reducci&oacute;n en la mortalidad global del 35% y del 42% en la mortalidd en pacientes hospitalizados con fracci&oacute;n de eyecci&oacute;n menor del 20 (29). Al cotejar los resultados de los estudios CAPRICORN y MERIT-HF se evidenci&oacute; una mejor tendencia de la respuesta del metoprolol de liberaci&oacute;n prolongada en comparaci&oacute;n con carvedilol en pacientes post-infarto (30, 31). El estudio COMET compar&oacute; carvedilol y metoprolol con una dosis m&aacute;xima de 50 mg y 100 mg respectivamente, observ&aacute;ndose un mejoramiento de la sobrevida del 17% con carvedilol en comparaci&oacute;n con metoprolol, lo cual confirma que el efecto combinado sobre los receptores beta 1, beta 2 y alfa 1 es superior al bloqueante beta 1 convencional selectivo (32).</p>       <p>En este n&uacute;mero de la Revista Colombiana de Cardiolog&iacute;a se publica el art&iacute;culo de Romero y colaboradores sobre el an&aacute;lisis de costo-efectividad del uso de metoprolol succinato en el tratamiento de la hipertensi&oacute;n arterial y la falla card&iacute;aca en Colombia, basado en un estudio que tiene un enfoque econ&oacute;mico desde la perspectiva del tercer pagador. La efectividad se determin&oacute; por la medici&oacute;n de los desenlaces de muertes evitadas y el total de hospitalizaciones evitadas. Los autores concluyen que no es recomendable el uso del metoprolol tartrato en el manejo de falla cardiaca e hipertensi&oacute;n arterial ya que el metoprolol succinato es la opci&oacute;n menos costosa y m&aacute;s efectiva para evitar hospitalizaciones (33). El costo total del brazo tratado con metoprolol succinato fue menor comparado con los brazos de metoprolol tartrato y carvedilol. Los autores de este editorial consideramos que antes de tener conclusiones definitivas, en el an&aacute;lisis se debe comparar un brazo de metoprolol succinato a 150 mg/d&iacute;a similar al brazo de metoprolol tartrato y un brazo del metoprolol succinato a 200 mg/d&iacute;a como se hizo en el estudio MERIT-HF, ya que para lograr la dosis de metoprolol succinato necesaria para producir un efecto equivalente a tartrato debe ser 33% mayor que la dosis de metoprolol tartrato. En el estudio de Romero y colaboradores, la dosis media utilizada de metoprolol succinato fue 100 mg/d&iacute;a, menor a la del estudio MERIT-HF. Por otro lado, el estudio COMET evalu&oacute; cabeza a cabeza el metoprolol tartrato con carvedilol, evidenci&aacute;ndose desenlaces m&aacute;s favorables con este &uacute;ltimo (3). Sin duda, el uso de betabloqueadores en pacientes con ICC e hipertensi&oacute;n tiene suficiente evidencia positiva sobre el impacto beneficioso en las tasas de mortalidad por todas las causas y en morbilidad en general.</p>       <p>Como se coment&oacute; al inicio de este editorial, la inclusi&oacute;n o el cambio de un medicamento puede ser una carga adicional a considerar de frente a la limitaci&oacute;n de recursos del sistema de salud. Adicionalmente, se requieren estudios que indiquen cu&aacute;les son los niveles de adherencia de los m&eacute;dicos a las recomendaciones de las gu&iacute;as de atenci&oacute;n a pacientes con ICC, ya que, como se demostr&oacute; recientemente en Colombia, existe una muy baja utilizaci&oacute;n de medicamentos probadamente &uacute;tiles en pacientes en prevenci&oacute;n cardiovascular secundaria (34).</p>     <p>En conclusi&oacute;n, el trabajo de Romero y colaboradores es una aproximaci&oacute;n importante en el campo de las evaluaciones econ&oacute;micas en salud, las cuales son necesarias para depurar aquellas tecnolog&iacute;as en salud que est&aacute;n en fase de declinaci&oacute;n u obsolescencia del POS del SGSS. Recomendamos a los autores que en un pr&oacute;ximo art&iacute;culo, incluyan en sus evaluaciones el impacto presupuestario que tendr&iacute;a el cambio o la inclusi&oacute;n de un nuevo betabloqueante en la gu&iacute;a terap&eacute;utica del POS, pues estamos convencidos de que las evaluaciones de tecnolog&iacute;as en salud deben ser una herramienta eficiente que contribuya a la toma de decisiones por parte de los responsables de las pol&iacute;ticas p&uacute;blicas de salud de Colombia.</p>   <h4><b>Bibliograf&iacute;a</b></h4>       <!-- ref --><p>1.	Fuchs VR. The future of health economics. J Health Econ 2000; 19: 141-57.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000022&pid=S0120-5633201200040000300001&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>       <!-- ref --><p>2.	Pole JD. 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