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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">As a centre for the comprehensive treatment of rheumatoid arthritis &#40;RA&#41; and as professionals who work in everyday practice to achieve better clinical results in patients treated with biological therapies&#44; we were interested in reviewing the paper recently published in the <span class="elsevierStyleItalic">Reumatolog&#237;a Cl&#237;nica</span> journal by &#193;lvaro-Gracia et al&#46; on the follow-up and monitoring of the use of biological agents in different medical specialities and diseases&#44; in a biological therapy unit &#40;BTU&#41; in a university hospital&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">The existence of a BTU is not only associated with the application of biological medication&#59; in our experience&#44; the BTU improves patient adherence to follow-up and treatment&#44; and it is associated with better education and clinical control&#44; above all in patients with a low socio-economic level and&#47;or those who lack a good family and&#47;or social support network&#59; it also leads to better control and the early identification of adverse events&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">This is why we are interested in the paper by &#193;lvaro-Gracia et al&#46;&#44; most particularly in the results of RA&#46; We found that the differences between survival rates of the therapies in the different diseases made complete sense&#44; and in particular the survival rate in RA &#40;38&#46;4 months&#41;&#46; This is the disease for which biological therapies are prescribed the most often&#44; and it has been proven that the reasons for interruption were lack of efficacy&#44; loss of effectiveness and adverse reactions&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">1</span></a></p><p id="par0020" class="elsevierStylePara elsevierViewall">The survival time of drugs in this report differs from the analysis of data by the CORRONA registry&#44; where the average time at which therapies were changed or interrupted was 25&#46;1 months for patients with RA&#46; The most common reason for interruption was loss of efficacy&#44; followed by questions of safety&#44; the preference of the doctor&#44; the preference of the patient and access to the treatment&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">2</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">In a 36-month follow-up of patients treated with 3 alternative anti-TNF in a cohort of 307 subjects with RA that was undertaken in our BTU&#44; it was found that 97&#37; completed the follow-up at 24 months and that 95&#37; did so at 36 months&#59; with an adverse events rate &#40;AER&#41; of 20&#37; per year that differed between different medications&#59; the lowest AER was for etanercept&#44; at 12&#37;&#44; and the highest was for infliximab&#44; at 24&#37;&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">3</span></a> The paper by &#193;lvaro-Gracia et al&#46;&#44; shows a very similar result for the same agent &#40;12&#37;&#41;&#44; while the biological agent used in rheumatology with the higher AER include anakinra &#40;28&#46;6&#37;&#41;&#44; followed by rituximab &#40;24&#46;6&#37;&#41; and infliximab &#40;24&#37;&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">1</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">The similarities between the results of both follow-up studies is consistent with previous studies&#44; showing that even when agents belong to the same pharmaceutical group&#44; as is the case with infliximab and etanercept&#44; they may differ in terms of response efficacy and the percentage of adverse effects&#44; as was previously described in several follow-up studies of patients under treatment with biological therapies&#46;<a class="elsevierStyleCrossRefs" href="#bib0065"><span class="elsevierStyleSup">4&#8211;9</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">It should be pointed out that in analyses of this type of medication survival rates&#44; the latter are also associated with external variables such as the type of coverage&#44; specialist and patient preferences and limited access to biological therapies&#44; as described in the CORRONA analysis<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">2</span></a>&#59; our recommendation for studies of this type is therefore that data should be analysed according to disease and type of medication&#44; and that when possible they should take into account variables connected with coverage&#44; specialist and patient preferences&#44; combinations of biological therapies with methotrexate and barriers against access&#44; most especially to offer more information about the reasons for treatment discontinuation&#46;</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Financing</span><p id="par0040" class="elsevierStylePara elsevierViewall">Pedro Santos-Moreno and Omaira Valencia declare that they received no financing for the preparation of this document&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Conflict of Interests</span><p id="par0045" class="elsevierStylePara elsevierViewall">Pedro Santos-Moreno declares that he has received fees for congresses&#44; advisory boards&#44; research and other items from Abbvie&#44; Abbott&#44; Janssen&#44; Pfizer&#44; UCB&#44; Biopas&#44; Pharmetique&#44; La Sante&#44; Lafrancol&#44; Bristol&#44; Roche&#44; Sanofi&#44; Lilly and Novartis&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">Omaira Valencia has no conflict of interests to declare&#46;</p></span></span>"
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Editorial
Experience of Biological Therapy Units in Rheumatoid Arthritis and Other Autoimmune Diseases
Experiencia de unidades de terapias biológicas en artritis reumatoide y otras enfermedades autoinmunes
Pedro Santos-Moreno
Corresponding author
pedrosantosmoreno@hotmail.com

Corresponding author.
, Omaira Valencia
Biomab – Centro de Artritis Reumatoide, Bogotá, Colombia
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">As a centre for the comprehensive treatment of rheumatoid arthritis &#40;RA&#41; and as professionals who work in everyday practice to achieve better clinical results in patients treated with biological therapies&#44; we were interested in reviewing the paper recently published in the <span class="elsevierStyleItalic">Reumatolog&#237;a Cl&#237;nica</span> journal by &#193;lvaro-Gracia et al&#46; on the follow-up and monitoring of the use of biological agents in different medical specialities and diseases&#44; in a biological therapy unit &#40;BTU&#41; in a university hospital&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">The existence of a BTU is not only associated with the application of biological medication&#59; in our experience&#44; the BTU improves patient adherence to follow-up and treatment&#44; and it is associated with better education and clinical control&#44; above all in patients with a low socio-economic level and&#47;or those who lack a good family and&#47;or social support network&#59; it also leads to better control and the early identification of adverse events&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">This is why we are interested in the paper by &#193;lvaro-Gracia et al&#46;&#44; most particularly in the results of RA&#46; We found that the differences between survival rates of the therapies in the different diseases made complete sense&#44; and in particular the survival rate in RA &#40;38&#46;4 months&#41;&#46; This is the disease for which biological therapies are prescribed the most often&#44; and it has been proven that the reasons for interruption were lack of efficacy&#44; loss of effectiveness and adverse reactions&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">1</span></a></p><p id="par0020" class="elsevierStylePara elsevierViewall">The survival time of drugs in this report differs from the analysis of data by the CORRONA registry&#44; where the average time at which therapies were changed or interrupted was 25&#46;1 months for patients with RA&#46; The most common reason for interruption was loss of efficacy&#44; followed by questions of safety&#44; the preference of the doctor&#44; the preference of the patient and access to the treatment&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">2</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">In a 36-month follow-up of patients treated with 3 alternative anti-TNF in a cohort of 307 subjects with RA that was undertaken in our BTU&#44; it was found that 97&#37; completed the follow-up at 24 months and that 95&#37; did so at 36 months&#59; with an adverse events rate &#40;AER&#41; of 20&#37; per year that differed between different medications&#59; the lowest AER was for etanercept&#44; at 12&#37;&#44; and the highest was for infliximab&#44; at 24&#37;&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">3</span></a> The paper by &#193;lvaro-Gracia et al&#46;&#44; shows a very similar result for the same agent &#40;12&#37;&#41;&#44; while the biological agent used in rheumatology with the higher AER include anakinra &#40;28&#46;6&#37;&#41;&#44; followed by rituximab &#40;24&#46;6&#37;&#41; and infliximab &#40;24&#37;&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">1</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">The similarities between the results of both follow-up studies is consistent with previous studies&#44; showing that even when agents belong to the same pharmaceutical group&#44; as is the case with infliximab and etanercept&#44; they may differ in terms of response efficacy and the percentage of adverse effects&#44; as was previously described in several follow-up studies of patients under treatment with biological therapies&#46;<a class="elsevierStyleCrossRefs" href="#bib0065"><span class="elsevierStyleSup">4&#8211;9</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">It should be pointed out that in analyses of this type of medication survival rates&#44; the latter are also associated with external variables such as the type of coverage&#44; specialist and patient preferences and limited access to biological therapies&#44; as described in the CORRONA analysis<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">2</span></a>&#59; our recommendation for studies of this type is therefore that data should be analysed according to disease and type of medication&#44; and that when possible they should take into account variables connected with coverage&#44; specialist and patient preferences&#44; combinations of biological therapies with methotrexate and barriers against access&#44; most especially to offer more information about the reasons for treatment discontinuation&#46;</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Financing</span><p id="par0040" class="elsevierStylePara elsevierViewall">Pedro Santos-Moreno and Omaira Valencia declare that they received no financing for the preparation of this document&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Conflict of Interests</span><p id="par0045" class="elsevierStylePara elsevierViewall">Pedro Santos-Moreno declares that he has received fees for congresses&#44; advisory boards&#44; research and other items from Abbvie&#44; Abbott&#44; Janssen&#44; Pfizer&#44; UCB&#44; Biopas&#44; Pharmetique&#44; La Sante&#44; Lafrancol&#44; Bristol&#44; Roche&#44; Sanofi&#44; Lilly and Novartis&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">Omaira Valencia has no conflict of interests to declare&#46;</p></span></span>"
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