<?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>0121-8123</journal-id>
<journal-title><![CDATA[Revista Colombiana de Reumatología]]></journal-title>
<abbrev-journal-title><![CDATA[Rev.Colomb.Reumatol.]]></abbrev-journal-title>
<issn>0121-8123</issn>
<publisher>
<publisher-name><![CDATA[Asociación Colombiana de Reumatología]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0121-81232022000400265</article-id>
<article-id pub-id-type="doi">10.1016/j.rcreu.2021.05.011</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Perception of quality of life in patients with systemic lupus erythematosus. A five-year study]]></article-title>
<article-title xml:lang="es"><![CDATA[Percepción de la calidad de vida en pacientes con lupus eritematoso sistémico. Estudio de cinco años]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Solis Cartas]]></surname>
<given-names><![CDATA[Urbano]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Martínez Larrarte]]></surname>
<given-names><![CDATA[José Pedro]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Valdés González]]></surname>
<given-names><![CDATA[Jorge Luis]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Gafas González]]></surname>
<given-names><![CDATA[Carlos]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad Nacional de Chimborazo Facultad de Ciencias de la Salud ]]></institution>
<addr-line><![CDATA[Riobamba ]]></addr-line>
<country>Ecuador</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Hospital Moguel Enríquez Laboratorio de Líquido Cefalorraquídeo ]]></institution>
<addr-line><![CDATA[La Habana ]]></addr-line>
<country>Cuba</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,Escuela Superior Politécnica de Chimborazo Facultad de Salud Pública ]]></institution>
<addr-line><![CDATA[Riobamba ]]></addr-line>
<country>Ecuador</country>
</aff>
<aff id="Af4">
<institution><![CDATA[,Universidad Nacional de Chimborazo Facultad de Ciencias de la Salud ]]></institution>
<addr-line><![CDATA[Riobamba ]]></addr-line>
<country>Ecuador</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>12</month>
<year>2022</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>12</month>
<year>2022</year>
</pub-date>
<volume>29</volume>
<numero>4</numero>
<fpage>265</fpage>
<lpage>273</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_arttext&amp;pid=S0121-81232022000400265&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_abstract&amp;pid=S0121-81232022000400265&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_pdf&amp;pid=S0121-81232022000400265&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[ABSTRACT  Introduction: Systemic lupus erythematosus is an autoimmune, inflammatory, and chronic disease that considerably affects the perception of health-related quality of life.  Objective: To determine the perception of quality of life in patients with systemic lupus erythematosus.  Methodology: Descriptive and correlational study; universe of 143 patients and a sample of 127 patients to whom the Short Form 36 questionnaire was applied to determine perception of health-related quality of life; the SLEDAI questionnaire to determine clinical activity, the SLICC to identify organic damage and the Morisky Green test to identify pharmacological adherence. Pearson's correlation coefficient was used to determine the association between the study variables.  Results: Mean age of 32.83 years, predominance of female patients (92.91%) and with disease progression of between one and 5 years (69.29%). Of the patients, 75.59% had at least one associated comorbidity and 80.31% were considered pharmacological adherents. The overall quality of life perception score was 61.02 points in women and 59.03 points in men. In general, the most affected dimensions were the emotional role in women and vitality in men.  Conclusions: The increase in disease progression time, the presence of associated comorbidities and pharmacological non-adherence were variables that determined a decrease in the mean scores of perception of quality of life. There was a strong negative correlation between clinical activity of the disease and perception of quality of life.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[RESUMEN  Introducción:  El lupus eritematoso sistémico es una enfermedad autoinmune, inflamatoria y crónica que afecta considerablemente la percepción de la calidad de vida relacionada con la salud.  Objetivo:  Determinar la percepción de la calidad de vida en pacientes con lupus eritematoso sistémico.  Metodología:  Estudio descriptivo y correlacional, universo de 143 pacientes y muestra de 127, a los cuales se les aplicó el cuestionario Short Form 36 para determinar la percepción de la calidad de vida relacionada con la salud, el cuestionario Systemic Lupus Erythematosus Disease Activity Index (SLEDAI), a fin de establecer la actividad clínica, el SLICC, con el propósito de identificar el daño orgánico, y el test de Morisky-Green, a efectos de evaluar la adherencia farmacológica. Se utilizó coeficiente de correlación de Pearson para determinarla asociación entre las variables del estudio.  Resultados:  Promedio de edad de 32,83 anos, predominio de pacientes femeninas (92,91%) y con tiempo de evolución entre uno y cinco anos (69,29%). El 75,59% de los pacientes presentó al menos una comorbilidad asociada y el 80,31% se consideró adherente farmacológico. La puntuación de percepción de la calidad de vida global fue de 61,02 puntos en mujeres y 59,03 puntos en hombres. De forma general, las dimensiones más afectadas fueron el rol emocional en las féminas y la vitalidad en los hombres.  Conclusiones:  El aumento del tiempo de evolución de la enfermedad, la presencia de comorbilidades asociadas y la no adherencia farmacológica constituyeron variables que determinaron una disminución de las puntuaciones medias de percepción de la calidad de vida. Hubo correlación negativa fuerte entre actividad clínica de la enfermedad y percepción de la calidad de vida.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Quality of life]]></kwd>
<kwd lng="en"><![CDATA[Autoimmune diseases]]></kwd>
<kwd lng="en"><![CDATA[Rheumatic diseases]]></kwd>
<kwd lng="en"><![CDATA[Systemic Lupus Erythematosus]]></kwd>
<kwd lng="es"><![CDATA[Calidad de vida]]></kwd>
<kwd lng="es"><![CDATA[Enfermedades autoinmunes]]></kwd>
<kwd lng="es"><![CDATA[Enfermedades reumáticas]]></kwd>
<kwd lng="es"><![CDATA[Lupus eritematoso sistémico]]></kwd>
</kwd-group>
</article-meta>
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